Chemicals

Showing 5401–5550 of 41137 results

  • 3,3′-((2-Chlorophenyl)methylene)bis(4-hydroxy-2H-chromen-2-one) is a non-nucleotide inhibitor of ectonucleotide pyrophosphatase/phosphodiesterase 1 (ENPP1; Ki = 50 µM).{48700,50816} It also inhibits urease (IC50 = 84.53 µM for the Jack bean enzyme).{48701}  

     

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    Cayman
    SKU:29864 - 10 mg

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  • 3,3′-((2-Chlorophenyl)methylene)bis(4-hydroxy-2H-chromen-2-one) is a non-nucleotide inhibitor of ectonucleotide pyrophosphatase/phosphodiesterase 1 (ENPP1; Ki = 50 µM).{48700,50816} It also inhibits urease (IC50 = 84.53 µM for the Jack bean enzyme).{48701}  

     

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    Cayman
    SKU:29864 - 25 mg

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  • 3,3′-((2-Chlorophenyl)methylene)bis(4-hydroxy-2H-chromen-2-one) is a non-nucleotide inhibitor of ectonucleotide pyrophosphatase/phosphodiesterase 1 (ENPP1; Ki = 50 µM).{48700,50816} It also inhibits urease (IC50 = 84.53 µM for the Jack bean enzyme).{48701}  

     

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    Cayman
    SKU:29864 - 5 mg

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  • 3,3′-Dihexyloxacarbocyanine (DiOC6(3)) is a lipophilic fluorescent dye with excitation/emission spectra of 484/501 nm, respectively.{39274} At high concentrations, DiOC6(3) accumulates in the endoplasmic reticulum (ER) and has been used to visualize ER in moss, yeast, and muscle cells. At low concentrations, DiOC6(3) accumulates in mitochondria and has been used to assess mitochondrial dislocations, fusion, and fission in living cells, as well as to visualize cellular apoptosis. DiOC6(3) can also be used to assess cell membrane potential, as depolarization directly correlates with increased fluorescence.{39275,39276} DiOC6(3) photoexcitation inactivates intracellular organelle movement and inhibits microtubule polymerization in vitro.{39277}  

     

    Brand:
    Cayman
    SKU:23124 - 1 g

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  • 3,3′-Dihexyloxacarbocyanine (DiOC6(3)) is a lipophilic fluorescent dye with excitation/emission spectra of 484/501 nm, respectively.{39274} At high concentrations, DiOC6(3) accumulates in the endoplasmic reticulum (ER) and has been used to visualize ER in moss, yeast, and muscle cells. At low concentrations, DiOC6(3) accumulates in mitochondria and has been used to assess mitochondrial dislocations, fusion, and fission in living cells, as well as to visualize cellular apoptosis. DiOC6(3) can also be used to assess cell membrane potential, as depolarization directly correlates with increased fluorescence.{39275,39276} DiOC6(3) photoexcitation inactivates intracellular organelle movement and inhibits microtubule polymerization in vitro.{39277}  

     

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    Cayman
    SKU:23124 - 500 mg

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  • 3,3′-Diiodo-L-thyronine is a metabolite of thyroid hormone that is also known as T2 or 3,3’-T2.{27332} It is derived enzymatically from triiodothyronine isoforms T3 and reverse T3. T2 and its analog 3,5-T2 stimulate the activity of cytochrome c oxidase by blocking inhibition by ATP.{27333,27334}  

     

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  • 3,3′-Diiodo-L-thyronine is a metabolite of thyroid hormone that is also known as T2 or 3,3’-T2.{27332} It is derived enzymatically from triiodothyronine isoforms T3 and reverse T3. T2 and its analog 3,5-T2 stimulate the activity of cytochrome c oxidase by blocking inhibition by ATP.{27333,27334}  

     

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    Cayman
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  • 3,3′-Diiodo-L-thyronine is a metabolite of thyroid hormone that is also known as T2 or 3,3’-T2.{27332} It is derived enzymatically from triiodothyronine isoforms T3 and reverse T3. T2 and its analog 3,5-T2 stimulate the activity of cytochrome c oxidase by blocking inhibition by ATP.{27333,27334}  

     

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    Cayman
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  • 3,3′-Diiodo-L-thyronine is a metabolite of thyroid hormone that is also known as T2 or 3,3’-T2.{27332} It is derived enzymatically from triiodothyronine isoforms T3 and reverse T3. T2 and its analog 3,5-T2 stimulate the activity of cytochrome c oxidase by blocking inhibition by ATP.{27333,27334}  

     

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    Cayman
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  • 3,3′,5-Triiodo-L-thyronine (T3) is a thyroid hormone.{61095} It is produced by 5′-monodeiodination of the prohormone thyroxine (T4) in various tissues, including liver and kidney. T3 is an agonist of thyroid hormone receptors TRα and TRβ (Kis = 2.3 nM for both) that modulates diverse biological properties, including metabolism, cardiac function, growth, and redox signaling.{27008,27007,27010,27009} It also functions as an inhibitor of L-type amino acid transporter 1 (LAT1), inhibiting LAT1-mediated leucine uptake in HEK293 cells when used at a concentration of 10 µM.{59277}  

     

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    Cayman
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  • 3,3′,5-Triiodo-L-thyronine (T3) is a thyroid hormone.{61095} It is produced by 5′-monodeiodination of the prohormone thyroxine (T4) in various tissues, including liver and kidney. T3 is an agonist of thyroid hormone receptors TRα and TRβ (Kis = 2.3 nM for both) that modulates diverse biological properties, including metabolism, cardiac function, growth, and redox signaling.{27008,27007,27010,27009} It also functions as an inhibitor of L-type amino acid transporter 1 (LAT1), inhibiting LAT1-mediated leucine uptake in HEK293 cells when used at a concentration of 10 µM.{59277}  

     

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    Cayman
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  • 3,3′,5-Triiodo-L-thyronine (T3) is a thyroid hormone.{61095} It is produced by 5′-monodeiodination of the prohormone thyroxine (T4) in various tissues, including liver and kidney. T3 is an agonist of thyroid hormone receptors TRα and TRβ (Kis = 2.3 nM for both) that modulates diverse biological properties, including metabolism, cardiac function, growth, and redox signaling.{27008,27007,27010,27009} It also functions as an inhibitor of L-type amino acid transporter 1 (LAT1), inhibiting LAT1-mediated leucine uptake in HEK293 cells when used at a concentration of 10 µM.{59277}  

     

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    Cayman
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  • 3,3′,5-Triiodo-L-thyronine (T3) is a thyroid hormone.{61095} It is produced by 5′-monodeiodination of the prohormone thyroxine (T4) in various tissues, including liver and kidney. T3 is an agonist of thyroid hormone receptors TRα and TRβ (Kis = 2.3 nM for both) that modulates diverse biological properties, including metabolism, cardiac function, growth, and redox signaling.{27008,27007,27010,27009} It also functions as an inhibitor of L-type amino acid transporter 1 (LAT1), inhibiting LAT1-mediated leucine uptake in HEK293 cells when used at a concentration of 10 µM.{59277}  

     

    Brand:
    Cayman
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  • 3,3′,5’-Triiodo-L-thyronine, also known as reverse T3 (rT3), is a thyroid hormone generated by deiodination of the prohormone thyroxine. It is about 1,000-fold less active at the thyroid hormone receptors TRα and TRβ than 3,3′,5-triiodo-L-thyronine (Item No. 16028) and commonly described as inactive.{28789,28791} However, high serum levels of rT3 are found in neonates and in certain conditions.{28795,28793,28790,28792} It reportedly activates TRΔα1, a native form of TRα that lacks a nuclear localization signal and functions in the cytoplasm.{28794} Through this action, rT3 initiates actin polymerization, particularly in astrocytes and neurons.{28794}  

     

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    Cayman
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  • 3,3′,5’-Triiodo-L-thyronine, also known as reverse T3 (rT3), is a thyroid hormone generated by deiodination of the prohormone thyroxine. It is about 1,000-fold less active at the thyroid hormone receptors TRα and TRβ than 3,3′,5-triiodo-L-thyronine (Item No. 16028) and commonly described as inactive.{28789,28791} However, high serum levels of rT3 are found in neonates and in certain conditions.{28795,28793,28790,28792} It reportedly activates TRΔα1, a native form of TRα that lacks a nuclear localization signal and functions in the cytoplasm.{28794} Through this action, rT3 initiates actin polymerization, particularly in astrocytes and neurons.{28794}  

     

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    Cayman
    SKU:-

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  • 3,3′,5’-Triiodo-L-thyronine, also known as reverse T3 (rT3), is a thyroid hormone generated by deiodination of the prohormone thyroxine. It is about 1,000-fold less active at the thyroid hormone receptors TRα and TRβ than 3,3′,5-triiodo-L-thyronine (Item No. 16028) and commonly described as inactive.{28789,28791} However, high serum levels of rT3 are found in neonates and in certain conditions.{28795,28793,28790,28792} It reportedly activates TRΔα1, a native form of TRα that lacks a nuclear localization signal and functions in the cytoplasm.{28794} Through this action, rT3 initiates actin polymerization, particularly in astrocytes and neurons.{28794}  

     

    Brand:
    Cayman
    SKU:-

    Available on backorder

  • 3,3′,5’-Triiodo-L-thyronine, also known as reverse T3 (rT3), is a thyroid hormone generated by deiodination of the prohormone thyroxine. It is about 1,000-fold less active at the thyroid hormone receptors TRα and TRβ than 3,3′,5-triiodo-L-thyronine (Item No. 16028) and commonly described as inactive.{28789,28791} However, high serum levels of rT3 are found in neonates and in certain conditions.{28795,28793,28790,28792} It reportedly activates TRΔα1, a native form of TRα that lacks a nuclear localization signal and functions in the cytoplasm.{28794} Through this action, rT3 initiates actin polymerization, particularly in astrocytes and neurons.{28794}  

     

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    Cayman
    SKU:-

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  • 3,3′-Dioctadecyloxacarbocyanine is a lipophilic fluorescent dye. It exhibits polarity-dependent fluorescence that is enhanced when incorporated into membranes or lipophilic molecules. Upon membrane incorporation, 3,3′-dioctadecyloxacarbocyanine rapidly diffuses to stain the entire cell membrane.{43912} It has been used in the clonal analysis of S. purparatus embryos. 3,3′-Dioctadecyloxacarbocyanine displays excitation/emission maxima of 484/501 nm, respectively, and can be used for live cell applications.  

     

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    Cayman
    SKU:27876 - 10 mg

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  • 3,3′-Dioctadecyloxacarbocyanine is a lipophilic fluorescent dye. It exhibits polarity-dependent fluorescence that is enhanced when incorporated into membranes or lipophilic molecules. Upon membrane incorporation, 3,3′-dioctadecyloxacarbocyanine rapidly diffuses to stain the entire cell membrane.{43912} It has been used in the clonal analysis of S. purparatus embryos. 3,3′-Dioctadecyloxacarbocyanine displays excitation/emission maxima of 484/501 nm, respectively, and can be used for live cell applications.  

     

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    Cayman
    SKU:27876 - 25 mg

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  • 3,3′-Dioctadecyloxacarbocyanine is a lipophilic fluorescent dye. It exhibits polarity-dependent fluorescence that is enhanced when incorporated into membranes or lipophilic molecules. Upon membrane incorporation, 3,3′-dioctadecyloxacarbocyanine rapidly diffuses to stain the entire cell membrane.{43912} It has been used in the clonal analysis of S. purparatus embryos. 3,3′-Dioctadecyloxacarbocyanine displays excitation/emission maxima of 484/501 nm, respectively, and can be used for live cell applications.  

     

    Brand:
    Cayman
    SKU:27876 - 5 mg

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  • 3,3′-Dioctadecyloxacarbocyanine is a lipophilic fluorescent dye. It exhibits polarity-dependent fluorescence that is enhanced when incorporated into membranes or lipophilic molecules. Upon membrane incorporation, 3,3′-dioctadecyloxacarbocyanine rapidly diffuses to stain the entire cell membrane.{43912} It has been used in the clonal analysis of S. purparatus embryos. 3,3′-Dioctadecyloxacarbocyanine displays excitation/emission maxima of 484/501 nm, respectively, and can be used for live cell applications.  

     

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    Cayman
    SKU:27876 - 50 mg

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  • 3,4-Di-O-acetyl-L-fucal is a glycal precursor that has been used in the palladium-catalyzed stereoselective synthesis of glycosides.{56038} It has also been used as a precursor in the copper-catalyzed stereoselective synthesis of 2-deoxyglycosides.{56039}  

     

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    Cayman
    SKU:30864 - 100 mg

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  • 3,4-Di-O-acetyl-L-fucal is a glycal precursor that has been used in the palladium-catalyzed stereoselective synthesis of glycosides.{56038} It has also been used as a precursor in the copper-catalyzed stereoselective synthesis of 2-deoxyglycosides.{56039}  

     

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    Cayman
    SKU:30864 - 250 mg

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  • 3,4-Di-O-acetyl-L-fucal is a glycal precursor that has been used in the palladium-catalyzed stereoselective synthesis of glycosides.{56038} It has also been used as a precursor in the copper-catalyzed stereoselective synthesis of 2-deoxyglycosides.{56039}  

     

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    Cayman
    SKU:30864 - 50 mg

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  • 3,4-Dicaffeoylquinic acid (3,4-DCQA) is a polyphenol with diverse biological activities.{41896,41897,41898,41899} 3,4-DCQA (1-500 μg/ml) inhibits acetylcholinesterase (ACE) and α-glucosidase in a concentration-dependent manner.{41896,41898} It reduces mutagenicity of Trp-P-1 against S. typhimurium by 59% when used at a concentration of 0.57 mM.{41897} 3,4-DCQA has antioxidant activity in ferric reducing, β-carotene bleaching, and DPPH scavenging assays (EC50s = 2.18, 23.85, and 68.91 μg/ml, respectively).{41898} It is cytotoxic to NCI-H23 lung adenocarcinoma cells (EC50 = 3.26 μg/ml). In vivo, 3,4-DCQA (50 mg/kg) increases tumor necrosis factor-related apoptosis inducing ligand (TRAIL) mRNA, reduces influenza H1N1 hemagglutinin (HA) mRNA, and increases survival in a mouse model of influenza A infection.{41899}  

     

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    Cayman
    SKU:25053 - 10 mg

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  • 3,4-Dicaffeoylquinic acid (3,4-DCQA) is a polyphenol with diverse biological activities.{41896,41897,41898,41899} 3,4-DCQA (1-500 μg/ml) inhibits acetylcholinesterase (ACE) and α-glucosidase in a concentration-dependent manner.{41896,41898} It reduces mutagenicity of Trp-P-1 against S. typhimurium by 59% when used at a concentration of 0.57 mM.{41897} 3,4-DCQA has antioxidant activity in ferric reducing, β-carotene bleaching, and DPPH scavenging assays (EC50s = 2.18, 23.85, and 68.91 μg/ml, respectively).{41898} It is cytotoxic to NCI-H23 lung adenocarcinoma cells (EC50 = 3.26 μg/ml). In vivo, 3,4-DCQA (50 mg/kg) increases tumor necrosis factor-related apoptosis inducing ligand (TRAIL) mRNA, reduces influenza H1N1 hemagglutinin (HA) mRNA, and increases survival in a mouse model of influenza A infection.{41899}  

     

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    Cayman
    SKU:25053 - 25 mg

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  • 3,4-Dicaffeoylquinic acid (3,4-DCQA) is a polyphenol with diverse biological activities.{41896,41897,41898,41899} 3,4-DCQA (1-500 μg/ml) inhibits acetylcholinesterase (ACE) and α-glucosidase in a concentration-dependent manner.{41896,41898} It reduces mutagenicity of Trp-P-1 against S. typhimurium by 59% when used at a concentration of 0.57 mM.{41897} 3,4-DCQA has antioxidant activity in ferric reducing, β-carotene bleaching, and DPPH scavenging assays (EC50s = 2.18, 23.85, and 68.91 μg/ml, respectively).{41898} It is cytotoxic to NCI-H23 lung adenocarcinoma cells (EC50 = 3.26 μg/ml). In vivo, 3,4-DCQA (50 mg/kg) increases tumor necrosis factor-related apoptosis inducing ligand (TRAIL) mRNA, reduces influenza H1N1 hemagglutinin (HA) mRNA, and increases survival in a mouse model of influenza A infection.{41899}  

     

    Brand:
    Cayman
    SKU:25053 - 5 mg

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  • 3,4-Dicaffeoylquinic acid (3,4-DCQA) is a polyphenol with diverse biological activities.{41896,41897,41898,41899} 3,4-DCQA (1-500 μg/ml) inhibits acetylcholinesterase (ACE) and α-glucosidase in a concentration-dependent manner.{41896,41898} It reduces mutagenicity of Trp-P-1 against S. typhimurium by 59% when used at a concentration of 0.57 mM.{41897} 3,4-DCQA has antioxidant activity in ferric reducing, β-carotene bleaching, and DPPH scavenging assays (EC50s = 2.18, 23.85, and 68.91 μg/ml, respectively).{41898} It is cytotoxic to NCI-H23 lung adenocarcinoma cells (EC50 = 3.26 μg/ml). In vivo, 3,4-DCQA (50 mg/kg) increases tumor necrosis factor-related apoptosis inducing ligand (TRAIL) mRNA, reduces influenza H1N1 hemagglutinin (HA) mRNA, and increases survival in a mouse model of influenza A infection.{41899}  

     

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    SKU:25053 - 50 mg

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  • 3,4-Dichloroisocoumarin (3,4-DCI) is a serine protease inhibitor.{38255} It completely inhibits enzyme activity of 24 serine proteases including human leukocyte elastase, thrombin, plasmin, Factor Xa, and Factor XIIa in vitro. 3,4-DCI stimulates caseinolytic activity of bovine pituitary multicatalytic proteinase complex (MPC) by inducing a conformational change in the MPC that exposes the caseinolytic active site.{38256} It has been used to functionally characterize the catalytic activities of multiple proteases including rat liver MPC and extracellular lipase.{38257,38258}  

     

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    Cayman
    SKU:21194 -

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  • 3,4-Dichloroisocoumarin (3,4-DCI) is a serine protease inhibitor.{38255} It completely inhibits enzyme activity of 24 serine proteases including human leukocyte elastase, thrombin, plasmin, Factor Xa, and Factor XIIa in vitro. 3,4-DCI stimulates caseinolytic activity of bovine pituitary multicatalytic proteinase complex (MPC) by inducing a conformational change in the MPC that exposes the caseinolytic active site.{38256} It has been used to functionally characterize the catalytic activities of multiple proteases including rat liver MPC and extracellular lipase.{38257,38258}  

     

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    Cayman
    SKU:21194 -

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  • 3,4-Dichloroisocoumarin (3,4-DCI) is a serine protease inhibitor.{38255} It completely inhibits enzyme activity of 24 serine proteases including human leukocyte elastase, thrombin, plasmin, Factor Xa, and Factor XIIa in vitro. 3,4-DCI stimulates caseinolytic activity of bovine pituitary multicatalytic proteinase complex (MPC) by inducing a conformational change in the MPC that exposes the caseinolytic active site.{38256} It has been used to functionally characterize the catalytic activities of multiple proteases including rat liver MPC and extracellular lipase.{38257,38258}  

     

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    Cayman
    SKU:21194 -

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  • 3,4-Dichloromethcathinone (hydrochloride) (Item No. 25376) is an analytical reference standard categorized as a cathinone. This product is intended for research and forensic applications.  

     

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    SKU:25376 - 1 mg

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  • 3,4-Dichloromethcathinone (hydrochloride) (Item No. 25376) is an analytical reference standard categorized as a cathinone. This product is intended for research and forensic applications.  

     

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    SKU:25376 - 5 mg

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  • 3,4-difluoro U-50488 (hydrochloride) (Item No. 29566) is an analytical reference standard categorized as a utopioid. This product is intended for research and forensic applications.  

     

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    SKU:29566 - 1 mg

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  • 3,4-difluoro U-50488 (hydrochloride) (Item No. 29566) is an analytical reference standard categorized as a utopioid. This product is intended for research and forensic applications.  

     

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    SKU:29566 - 5 mg

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  • Naratriptan is a selective serotonin 5-HT1B agonist (pKi = 8.9 for human 5-HT1B) used in the treatment of severe cephalic pain, including migraine headaches.{25802,25801,29035} 3,4-dihydro Naratriptan is an impurity formed during the preparation of naratriptan.{29036}  

     

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  • Naratriptan is a selective serotonin 5-HT1B agonist (pKi = 8.9 for human 5-HT1B) used in the treatment of severe cephalic pain, including migraine headaches.{25802,25801,29035} 3,4-dihydro Naratriptan is an impurity formed during the preparation of naratriptan.{29036}  

     

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  • Naratriptan is a selective serotonin 5-HT1B agonist (pKi = 8.9 for human 5-HT1B) used in the treatment of severe cephalic pain, including migraine headaches.{25802,25801,29035} 3,4-dihydro Naratriptan is an impurity formed during the preparation of naratriptan.{29036}  

     

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  • Naratriptan is a selective serotonin 5-HT1B agonist (pKi = 8.9 for human 5-HT1B) used in the treatment of severe cephalic pain, including migraine headaches.{25802,25801,29035} 3,4-dihydro Naratriptan is an impurity formed during the preparation of naratriptan.{29036}  

     

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  • 3,4-Dihydroquinolin-2(1H)-one is a building block.{52836,52837} It has been used in the synthesis of compounds with antidepressant and anticonvulsant activities, as well as dual ligands of sigma (σ) receptors and the NMDA receptor GluN2b subunit that have antioxidant and neuroprotective properties.  

     

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    Cayman
    SKU:31701 - 1 g

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  • 3,4-Dihydroquinolin-2(1H)-one is a building block.{52836,52837} It has been used in the synthesis of compounds with antidepressant and anticonvulsant activities, as well as dual ligands of sigma (σ) receptors and the NMDA receptor GluN2b subunit that have antioxidant and neuroprotective properties.  

     

    Brand:
    Cayman
    SKU:31701 - 10 g

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  • 3,4-Dihydroquinolin-2(1H)-one is a building block.{52836,52837} It has been used in the synthesis of compounds with antidepressant and anticonvulsant activities, as well as dual ligands of sigma (σ) receptors and the NMDA receptor GluN2b subunit that have antioxidant and neuroprotective properties.  

     

    Brand:
    Cayman
    SKU:31701 - 25 g

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  • 3,4-Dihydroquinolin-2(1H)-one is a building block.{52836,52837} It has been used in the synthesis of compounds with antidepressant and anticonvulsant activities, as well as dual ligands of sigma (σ) receptors and the NMDA receptor GluN2b subunit that have antioxidant and neuroprotective properties.  

     

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    Cayman
    SKU:31701 - 5 g

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  • 3,4-Dihydroxyamphetamine (hydrochloride) (Item No. 30531) is an analytical reference standard categorized as an amphetamine. 3,4-Dihydroxyamphetamine is a metabolite of 3,4-MDMA (Item Nos. ISO60190 | 13971) via the intermediate (±)-MDA (Item Nos. ISO60189 | 11554).{23483,53703} This product is intended for research and forensic applications.  

     

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    SKU:30531 - 1 mg

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  • 3,4-Dihydroxyamphetamine (hydrochloride) (Item No. 30531) is an analytical reference standard categorized as an amphetamine. 3,4-Dihydroxyamphetamine is a metabolite of 3,4-MDMA (Item Nos. ISO60190 | 13971) via the intermediate (±)-MDA (Item Nos. ISO60189 | 11554).{23483,53703} This product is intended for research and forensic applications.  

     

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    SKU:30531 - 5 mg

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  • 3,4-Dihydroxybenzaldehyde is a polyphenol that has been found in S. miltiorrhiza and has diverse biological activities, including antibacterial, antioxidative, and anticancer properties.{45267,45268,45269,45270} It is active against methicillin-resistant S. aureus (MRSA) when used at a concentration of 0.01 µg/ml.{45268} It prevents hexavalent chromium-induced formation of reactive oxygen species (ROS) and reactive nitrogen species (RNS) in a concentration-dependent manner and increases glutathione (GSH) levels in isolated human erythrocytes.{45267} 3,4-Dihydroxybenzaldehyde selectively inhibits human DNA topoisomerase II (IC50 = 150 µM) over human topoisomerase I and a variety of mammalian polymerases (IC50s = >200 µM).{45269} It inhibits proliferation of HT-29 cells when used at a concentration of 362 µM but not HCT116 cells at a concentration of 100 µM.{45270,45269}  

     

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    Cayman
    SKU:27547 - 10 g

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  • 3,4-Dihydroxybenzaldehyde is a polyphenol that has been found in S. miltiorrhiza and has diverse biological activities, including antibacterial, antioxidative, and anticancer properties.{45267,45268,45269,45270} It is active against methicillin-resistant S. aureus (MRSA) when used at a concentration of 0.01 µg/ml.{45268} It prevents hexavalent chromium-induced formation of reactive oxygen species (ROS) and reactive nitrogen species (RNS) in a concentration-dependent manner and increases glutathione (GSH) levels in isolated human erythrocytes.{45267} 3,4-Dihydroxybenzaldehyde selectively inhibits human DNA topoisomerase II (IC50 = 150 µM) over human topoisomerase I and a variety of mammalian polymerases (IC50s = >200 µM).{45269} It inhibits proliferation of HT-29 cells when used at a concentration of 362 µM but not HCT116 cells at a concentration of 100 µM.{45270,45269}  

     

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    Cayman
    SKU:27547 - 100 g

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  • 3,4-Dihydroxybenzaldehyde is a polyphenol that has been found in S. miltiorrhiza and has diverse biological activities, including antibacterial, antioxidative, and anticancer properties.{45267,45268,45269,45270} It is active against methicillin-resistant S. aureus (MRSA) when used at a concentration of 0.01 µg/ml.{45268} It prevents hexavalent chromium-induced formation of reactive oxygen species (ROS) and reactive nitrogen species (RNS) in a concentration-dependent manner and increases glutathione (GSH) levels in isolated human erythrocytes.{45267} 3,4-Dihydroxybenzaldehyde selectively inhibits human DNA topoisomerase II (IC50 = 150 µM) over human topoisomerase I and a variety of mammalian polymerases (IC50s = >200 µM).{45269} It inhibits proliferation of HT-29 cells when used at a concentration of 362 µM but not HCT116 cells at a concentration of 100 µM.{45270,45269}  

     

    Brand:
    Cayman
    SKU:27547 - 25 g

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  • 3,4-Dihydroxybenzaldehyde is a polyphenol that has been found in S. miltiorrhiza and has diverse biological activities, including antibacterial, antioxidative, and anticancer properties.{45267,45268,45269,45270} It is active against methicillin-resistant S. aureus (MRSA) when used at a concentration of 0.01 µg/ml.{45268} It prevents hexavalent chromium-induced formation of reactive oxygen species (ROS) and reactive nitrogen species (RNS) in a concentration-dependent manner and increases glutathione (GSH) levels in isolated human erythrocytes.{45267} 3,4-Dihydroxybenzaldehyde selectively inhibits human DNA topoisomerase II (IC50 = 150 µM) over human topoisomerase I and a variety of mammalian polymerases (IC50s = >200 µM).{45269} It inhibits proliferation of HT-29 cells when used at a concentration of 362 µM but not HCT116 cells at a concentration of 100 µM.{45270,45269}  

     

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    Cayman
    SKU:27547 - 5 g

    Available on backorder

  • 3,4-Dihydroxyphenyl ethanol is a phenolic component of olive oil that inhibits both 12- and 5-LO. The IC50 values for the inhibition of rat platelet 12-LO and rat neutrophil 5-LO are 4.2 and 13 µM, respectively. It does not inhibit, and may actually enhance, COX activity.{4049} 3,4-Dihydroxyphenyl ethanol also protects LDL from both biological and chemical oxidation, suggesting a potential mechanism for the protective effects of olive oil against atherosclerosis.{6597}  

     

    Brand:
    Cayman
    SKU:70604 - 10 mg

    Available on backorder

  • 3,4-Dihydroxyphenyl ethanol is a phenolic component of olive oil that inhibits both 12- and 5-LO. The IC50 values for the inhibition of rat platelet 12-LO and rat neutrophil 5-LO are 4.2 and 13 µM, respectively. It does not inhibit, and may actually enhance, COX activity.{4049} 3,4-Dihydroxyphenyl ethanol also protects LDL from both biological and chemical oxidation, suggesting a potential mechanism for the protective effects of olive oil against atherosclerosis.{6597}  

     

    Brand:
    Cayman
    SKU:70604 - 100 mg

    Available on backorder

  • 3,4-Dihydroxyphenyl ethanol is a phenolic component of olive oil that inhibits both 12- and 5-LO. The IC50 values for the inhibition of rat platelet 12-LO and rat neutrophil 5-LO are 4.2 and 13 µM, respectively. It does not inhibit, and may actually enhance, COX activity.{4049} 3,4-Dihydroxyphenyl ethanol also protects LDL from both biological and chemical oxidation, suggesting a potential mechanism for the protective effects of olive oil against atherosclerosis.{6597}  

     

    Brand:
    Cayman
    SKU:70604 - 5 mg

    Available on backorder

  • 3,4-Dihydroxyphenyl ethanol is a phenolic component of olive oil that inhibits both 12- and 5-LO. The IC50 values for the inhibition of rat platelet 12-LO and rat neutrophil 5-LO are 4.2 and 13 µM, respectively. It does not inhibit, and may actually enhance, COX activity.{4049} 3,4-Dihydroxyphenyl ethanol also protects LDL from both biological and chemical oxidation, suggesting a potential mechanism for the protective effects of olive oil against atherosclerosis.{6597}  

     

    Brand:
    Cayman
    SKU:70604 - 50 mg

    Available on backorder

  • 3,4-dihydroxyphenylacetic acid (DOPAC) is a metabolite of dopamine (Item No. 21992) formed through deamination by monoamine oxidase (MAO).{36669} DOPAC is further metabolized by catechol-O-methyltransferase (COMT) to form homovanillic acid, and DOPAC levels are increased 5- to 6-fold compared to wild-type in the nucleus accumbens, striatum, and prefrontal cortex of COMT knockout mice. DOPAC oxidation is catalyzed by α-synuclein and oxidized DOPAC binds to monomeric α-synuclein preventing fibrillation.{36668} In vivo, foot shock stress increases DOPAC levels relative to control by approximately 45% in the prefrontal cortex and by 15% in the olfactory tubercles and ventral tegmental area (VTA) in rats.{36667}  

     

    Brand:
    Cayman
    SKU:24912 - 10 g

    Available on backorder

  • 3,4-dihydroxyphenylacetic acid (DOPAC) is a metabolite of dopamine (Item No. 21992) formed through deamination by monoamine oxidase (MAO).{36669} DOPAC is further metabolized by catechol-O-methyltransferase (COMT) to form homovanillic acid, and DOPAC levels are increased 5- to 6-fold compared to wild-type in the nucleus accumbens, striatum, and prefrontal cortex of COMT knockout mice. DOPAC oxidation is catalyzed by α-synuclein and oxidized DOPAC binds to monomeric α-synuclein preventing fibrillation.{36668} In vivo, foot shock stress increases DOPAC levels relative to control by approximately 45% in the prefrontal cortex and by 15% in the olfactory tubercles and ventral tegmental area (VTA) in rats.{36667}  

     

    Brand:
    Cayman
    SKU:24912 - 25 g

    Available on backorder

  • 3,4-dihydroxyphenylacetic acid (DOPAC) is a metabolite of dopamine (Item No. 21992) formed through deamination by monoamine oxidase (MAO).{36669} DOPAC is further metabolized by catechol-O-methyltransferase (COMT) to form homovanillic acid, and DOPAC levels are increased 5- to 6-fold compared to wild-type in the nucleus accumbens, striatum, and prefrontal cortex of COMT knockout mice. DOPAC oxidation is catalyzed by α-synuclein and oxidized DOPAC binds to monomeric α-synuclein preventing fibrillation.{36668} In vivo, foot shock stress increases DOPAC levels relative to control by approximately 45% in the prefrontal cortex and by 15% in the olfactory tubercles and ventral tegmental area (VTA) in rats.{36667}  

     

    Brand:
    Cayman
    SKU:24912 - 5 g

    Available on backorder

  • 3,4-dihydroxyphenylacetic acid (DOPAC) is a metabolite of dopamine (Item No. 21992) formed through deamination by monoamine oxidase (MAO).{36669} DOPAC is further metabolized by catechol-O-methyltransferase (COMT) to form homovanillic acid, and DOPAC levels are increased 5- to 6-fold compared to wild-type in the nucleus accumbens, striatum, and prefrontal cortex of COMT knockout mice. DOPAC oxidation is catalyzed by α-synuclein and oxidized DOPAC binds to monomeric α-synuclein preventing fibrillation.{36668} In vivo, foot shock stress increases DOPAC levels relative to control by approximately 45% in the prefrontal cortex and by 15% in the olfactory tubercles and ventral tegmental area (VTA) in rats.{36667}  

     

    Brand:
    Cayman
    SKU:24912 - 50 g

    Available on backorder

  • Methylenedioxy Pyrovalerone (MDPV) (Item No. 10624) is a cathinone commonly found in products sold as bath salts or plant food.{19193,20369} It is regulated as a Schedule 1 compound in the United States.{18947} 3,4-dimethoxy-α-Pyrrolidinopentiophenone is an analog of MDPV, differing only by an opening of the ring structure on the phenyl group. The physiological and toxicological properties of this compound have not been investigated. This product is intended for research and forensic applications.  

     

    Brand:
    Cayman
    SKU:-
  • Methylenedioxy Pyrovalerone (MDPV) (Item No. 10624) is a cathinone commonly found in products sold as bath salts or plant food.{19193,20369} It is regulated as a Schedule 1 compound in the United States.{18947} 3,4-dimethoxy-α-Pyrrolidinopentiophenone is an analog of MDPV, differing only by an opening of the ring structure on the phenyl group. The physiological and toxicological properties of this compound have not been investigated. This product is intended for research and forensic applications.  

     

    Brand:
    Cayman
    SKU:-
  • Methylenedioxy Pyrovalerone (MDPV) (Item No. 10624) is a cathinone commonly found in products sold as bath salts or plant food.{19193,20369} It is regulated as a Schedule 1 compound in the United States.{18947} 3,4-dimethoxy-α-Pyrrolidinopentiophenone is an analog of MDPV, differing only by an opening of the ring structure on the phenyl group. The physiological and toxicological properties of this compound have not been investigated. This product is intended for research and forensic applications.  

     

    Brand:
    Cayman
    SKU:-
  • 3,4-dimethoxy-α-Pyrrolidinopropiophenone (hydrochloride) (Item No. 30034) is an analytical reference standard categorized as a cathinone. This product is intended for research and forensic applications.  

     

    Brand:
    Cayman
    SKU:30034 - 1 mg

    Available on backorder

  • 3,4-dimethoxy-α-Pyrrolidinopropiophenone (hydrochloride) (Item No. 30034) is an analytical reference standard categorized as a cathinone. This product is intended for research and forensic applications.  

     

    Brand:
    Cayman
    SKU:30034 - 5 mg

    Available on backorder

  • 3,4-Dimethoxyphenethylamine (hydrochloride) (Item No. 14141) is an analytical reference standard that is structurally categorized as a phenethylamine. It inhibits the deamination of tyramine (Item No. 18601) and tryptamine by rat brain monoamine oxidase.{33002} This product is intended for research and forensic applications.  

     

    Brand:
    Cayman
    SKU:-
  • 3,4-Dimethoxyphenethylamine (hydrochloride) (Item No. 14141) is an analytical reference standard that is structurally categorized as a phenethylamine. It inhibits the deamination of tyramine (Item No. 18601) and tryptamine by rat brain monoamine oxidase.{33002} This product is intended for research and forensic applications.  

     

    Brand:
    Cayman
    SKU:-
  • 3,4-DMMC (hydrochloride) (Item No. 9001098) is a potential designer drug with combined features of amphetamines, cathinones, and phenethylamines. It is structurally related to 4-methylmethcathinone, a psychoactive compound that has been identified in products sold as bath salts and plant food.{19498,19499,19497} This metabolite of 3,4-DMMC features conversion of the β-keto group to β-hydroxy and is an enantiomeric mixture of the R,S and S,R orientations at carbons one and two, as in ephedrine. The physiological and toxicological properties of this compound have not been elucidated. This product is intended for research and forensic applications.  

     

    Brand:
    Cayman
    SKU:9001431 - 1 mg

    Available on backorder

  • 3,4-DMMC (hydrochloride) (Item No. 9001098) is a potential designer drug with combined features of amphetamines, cathinones, and phenethylamines. It is structurally related to 4-methylmethcathinone, a psychoactive compound that has been identified in products sold as bath salts and plant food.{19498,19499,19497} This metabolite of 3,4-DMMC features conversion of the β-keto group to β-hydroxy and is an enantiomeric mixture of the R,S and S,R orientations at carbons one and two, as in ephedrine. The physiological and toxicological properties of this compound have not been elucidated. This product is intended for research and forensic applications.  

     

    Brand:
    Cayman
    SKU:9001431 - 5 mg

    Available on backorder

  • 3,4-DMMC (hydrochloride) (Item No. 9001098) is a potential designer drug with combined features of amphetamines, cathinones, and phenethylamines. It is structurally related to 4-methylmethcathinone, a psychoactive compound that has been identified in products sold as bath salts and plant food.{19498,19499,19497} This metabolite of 3,4-DMMC features conversion of the β-keto group to β-hydroxy and is an enantiomeric mixture of the R,S and S,R orientations at carbons one and two, as in ephedrine. The physiological and toxicological properties of this compound have not been elucidated. This product is intended for research and forensic applications.  

     

    Brand:
    Cayman
    SKU:9001431 - 500 µg

    Available on backorder

  • 3,4-Dimethylmethcathinone (3,4-DMMC) (hydrochloride) ((±)-pseudoephedrine stereochemistry) (Item No. 9001098) is a potential designer drug with combined features of amphetamines, cathinones, and phenethylamines. It is structurally related to 4-methylmethcathinone, a psychoactive compound that has been identified in products sold as bath salts and plant food.{19498,19499,19497} This metabolite of 3,4-DMMC features conversion of the β-keto group to β-hydroxy and is an enantiomeric mixture of the R,R and S,S orientations at carbons one and two, as in pseudoephedrine. The physiological and toxicological properties of this compound have not been elucidated. This product is intended for research and forensic applications.  

     

    Brand:
    Cayman
    SKU:9001437 - 1 mg

    Available on backorder

  • 3,4-Dimethylmethcathinone (3,4-DMMC) (hydrochloride) ((±)-pseudoephedrine stereochemistry) (Item No. 9001098) is a potential designer drug with combined features of amphetamines, cathinones, and phenethylamines. It is structurally related to 4-methylmethcathinone, a psychoactive compound that has been identified in products sold as bath salts and plant food.{19498,19499,19497} This metabolite of 3,4-DMMC features conversion of the β-keto group to β-hydroxy and is an enantiomeric mixture of the R,R and S,S orientations at carbons one and two, as in pseudoephedrine. The physiological and toxicological properties of this compound have not been elucidated. This product is intended for research and forensic applications.  

     

    Brand:
    Cayman
    SKU:9001437 - 5 mg

    Available on backorder

  • 3,4-Dimethylmethcathinone (3,4-DMMC) (hydrochloride) ((±)-pseudoephedrine stereochemistry) (Item No. 9001098) is a potential designer drug with combined features of amphetamines, cathinones, and phenethylamines. It is structurally related to 4-methylmethcathinone, a psychoactive compound that has been identified in products sold as bath salts and plant food.{19498,19499,19497} This metabolite of 3,4-DMMC features conversion of the β-keto group to β-hydroxy and is an enantiomeric mixture of the R,R and S,S orientations at carbons one and two, as in pseudoephedrine. The physiological and toxicological properties of this compound have not been elucidated. This product is intended for research and forensic applications.  

     

    Brand:
    Cayman
    SKU:9001437 - 500 µg

    Available on backorder

  • 3,4-Dimethylpyrazole (phosphate) (3,4-DMPP) is an inhibitor of nitrification deemed safe by extensive standard toxicology and ecotoxicology tests.{34653} When utilized on crops, 3,4-DMPP prevents nitrogen loss from soil, increases nitrogen use efficiency, and boosts crop yields.{34653,34654} However, a meta-analysis found no influence of 3,4-DMPP on net crop yield, although it may boost yields in alkaline soil.{34655} 3,4-DMPP may be less effective in acidic soils and in the post-harvest period.{34656,34657} DMPP interferes with ammonia monooxygenase from ammonia-oxidizing bacteria (AOB) and archaea (AOA) but may not directly affect AOB, AOA, and non-target populations.{34658}  

     

    Brand:
    Cayman
    SKU:21887 -

    Out of stock

  • 3,4-Dimethylpyrazole (phosphate) (3,4-DMPP) is an inhibitor of nitrification deemed safe by extensive standard toxicology and ecotoxicology tests.{34653} When utilized on crops, 3,4-DMPP prevents nitrogen loss from soil, increases nitrogen use efficiency, and boosts crop yields.{34653,34654} However, a meta-analysis found no influence of 3,4-DMPP on net crop yield, although it may boost yields in alkaline soil.{34655} 3,4-DMPP may be less effective in acidic soils and in the post-harvest period.{34656,34657} DMPP interferes with ammonia monooxygenase from ammonia-oxidizing bacteria (AOB) and archaea (AOA) but may not directly affect AOB, AOA, and non-target populations.{34658}  

     

    Brand:
    Cayman
    SKU:21887 -

    Out of stock

  • 3,4-Dimethylpyrazole (phosphate) (3,4-DMPP) is an inhibitor of nitrification deemed safe by extensive standard toxicology and ecotoxicology tests.{34653} When utilized on crops, 3,4-DMPP prevents nitrogen loss from soil, increases nitrogen use efficiency, and boosts crop yields.{34653,34654} However, a meta-analysis found no influence of 3,4-DMPP on net crop yield, although it may boost yields in alkaline soil.{34655} 3,4-DMPP may be less effective in acidic soils and in the post-harvest period.{34656,34657} DMPP interferes with ammonia monooxygenase from ammonia-oxidizing bacteria (AOB) and archaea (AOA) but may not directly affect AOB, AOA, and non-target populations.{34658}  

     

    Brand:
    Cayman
    SKU:21887 -

    Out of stock

  • 3,4-Dimethylpyrazole (phosphate) (3,4-DMPP) is an inhibitor of nitrification deemed safe by extensive standard toxicology and ecotoxicology tests.{34653} When utilized on crops, 3,4-DMPP prevents nitrogen loss from soil, increases nitrogen use efficiency, and boosts crop yields.{34653,34654} However, a meta-analysis found no influence of 3,4-DMPP on net crop yield, although it may boost yields in alkaline soil.{34655} 3,4-DMPP may be less effective in acidic soils and in the post-harvest period.{34656,34657} DMPP interferes with ammonia monooxygenase from ammonia-oxidizing bacteria (AOB) and archaea (AOA) but may not directly affect AOB, AOA, and non-target populations.{34658}  

     

    Brand:
    Cayman
    SKU:21887 -

    Out of stock

  • 3,4-DMA (hydrochloride) (Item No. 14142) is an analytical reference standard that is structurally categorized as an amphetamine. The physiological and toxicological properties of this compound are not known. This product is intended for research and forensic applications.  

     

    Brand:
    Cayman
    SKU:-
  • 3,4-DMA (hydrochloride) (Item No. 14142) is an analytical reference standard that is structurally categorized as an amphetamine. The physiological and toxicological properties of this compound are not known. This product is intended for research and forensic applications.  

     

    Brand:
    Cayman
    SKU:-
  • 3,4-Dimethoxymethamphetamine (3,4-DMMA) (hydrochloride) is an analog of 3,4-methylenedioxymethamphetamine (MDMA), a psychoactive drug and research chemical of the phenethylamine and amphetamine chemical classes. DMMA appears to interfere with monoamine transport, inhibiting uptake of noradrenalin and serotonin transporters (Kis = 22.8 and 7.7 μM, IC50s = 253.4 and 108 μM, respectively).{20483} DMMA is significantly less potent than MDMA (Kis = 0.6 and 2.5 μM; IC50s = 6.6 and 34.8 μM for MDMA inhibition of noradrenalin and serotonin transporters, respectively).{20483}  

     

    Brand:
    Cayman
    SKU:11128 - 10 mg

    Available on backorder

  • 3,4-Dimethoxymethamphetamine (3,4-DMMA) (hydrochloride) is an analog of 3,4-methylenedioxymethamphetamine (MDMA), a psychoactive drug and research chemical of the phenethylamine and amphetamine chemical classes. DMMA appears to interfere with monoamine transport, inhibiting uptake of noradrenalin and serotonin transporters (Kis = 22.8 and 7.7 μM, IC50s = 253.4 and 108 μM, respectively).{20483} DMMA is significantly less potent than MDMA (Kis = 0.6 and 2.5 μM; IC50s = 6.6 and 34.8 μM for MDMA inhibition of noradrenalin and serotonin transporters, respectively).{20483}  

     

    Brand:
    Cayman
    SKU:11128 - 5 mg

    Available on backorder

  • 3,4-Dimethoxymethamphetamine (3,4-DMMA) (hydrochloride) is an analog of 3,4-methylenedioxymethamphetamine (MDMA), a psychoactive drug and research chemical of the phenethylamine and amphetamine chemical classes. DMMA appears to interfere with monoamine transport, inhibiting uptake of noradrenalin and serotonin transporters (Kis = 22.8 and 7.7 μM, IC50s = 253.4 and 108 μM, respectively).{20483} DMMA is significantly less potent than MDMA (Kis = 0.6 and 2.5 μM; IC50s = 6.6 and 34.8 μM for MDMA inhibition of noradrenalin and serotonin transporters, respectively).{20483}  

     

    Brand:
    Cayman
    SKU:11128 - 50 mg

    Available on backorder

  • Methylone (Item No. 10986) is designer cathinone that is structurally similar to the illicit, psychotropic drug 3,4-MDMA (Item No. 13971).{20370,20369} 3,4-EDMC is an analog of methylone. The physiological and toxicological properties of this compound are not known. This product is intended for forensic and research purposes.  

     

    Brand:
    Cayman
    SKU:-
  • Methylone (Item No. 10986) is designer cathinone that is structurally similar to the illicit, psychotropic drug 3,4-MDMA (Item No. 13971).{20370,20369} 3,4-EDMC is an analog of methylone. The physiological and toxicological properties of this compound are not known. This product is intended for forensic and research purposes.  

     

    Brand:
    Cayman
    SKU:-
  • Methylone (Item No. 10986) is designer cathinone that is structurally similar to the illicit, psychotropic drug 3,4-MDMA (Item No. 13971).{20370,20369} 3,4-EDMC is an analog of methylone. The physiological and toxicological properties of this compound are not known. This product is intended for forensic and research purposes.  

     

    Brand:
    Cayman
    SKU:-
  • 3,4-MDEA-d5 (hydrochloride) (exempt preparation) (Item No. 22876) is intended for use as an internal standard for the quantification of 3,4-MDEA (Item Nos. 14085 | ISO60196) by GC- or LC-MS. 3,4-MDEA is categorized as an amphetamine. It has similar psychotropic action to MDMA and shares the common name of “ecstasy”.{22187} Postmortem findings in human deaths associated with 3,4-MDEA as well as 3,4-MDMA indicate striking brain and myocardial damage as well as liver necrosis.{22188} 3,4-MDEA is regulated as a Schedule I compound in the United States. 3,4-MDEA-d5 (hydrochloride) (exempt preparation) (Item No. 22876) is provided as a DEA exempt preparation. This product is intended for research and forensic applications.  

     

    Brand:
    Cayman
    SKU:22876 - 1 mg

    Available on backorder

  • MDMA is a psychoactive drug, also known as ecstasy, that is banned in most countries, including the United States. 3,4-MDMA methylene homolog (hydrochloride) is a potential designer drug created by inserting a methylene group in the methylamphetamine portion of MDMA. The biological and toxicological activities of this compound have not been evaluated. This product is to be used in the forensic analysis of samples that may contain this compound.  

     

    Brand:
    Cayman
    SKU:10979 - 1 mg

    Available on backorder

  • MDMA is a psychoactive drug, also known as ecstasy, that is banned in most countries, including the United States. 3,4-MDMA methylene homolog (hydrochloride) is a potential designer drug created by inserting a methylene group in the methylamphetamine portion of MDMA. The biological and toxicological activities of this compound have not been evaluated. This product is to be used in the forensic analysis of samples that may contain this compound.  

     

    Brand:
    Cayman
    SKU:10979 - 10 mg

    Available on backorder

  • MDMA is a psychoactive drug, also known as ecstasy, that is banned in most countries, including the United States. 3,4-MDMA methylene homolog (hydrochloride) is a potential designer drug created by inserting a methylene group in the methylamphetamine portion of MDMA. The biological and toxicological activities of this compound have not been evaluated. This product is to be used in the forensic analysis of samples that may contain this compound.  

     

    Brand:
    Cayman
    SKU:10979 - 5 mg

    Available on backorder

  • 3,4-MDMA tert-butyl Carbamate (Item No. 22740) is an analytical reference standard that is structurally characterized as an amphetamine and is a precursor in the synthesis of 3,4-MDMA (Item Nos. 13971 | ISO60190).{18959} This product is intended for research and forensic applications.  

     

    Brand:
    Cayman
    SKU:22740 -

    Out of stock

  • 3,4-MDMA tert-butyl Carbamate (Item No. 22740) is an analytical reference standard that is structurally characterized as an amphetamine and is a precursor in the synthesis of 3,4-MDMA (Item Nos. 13971 | ISO60190).{18959} This product is intended for research and forensic applications.  

     

    Brand:
    Cayman
    SKU:22740 -

    Out of stock

  • 3,4-MDPA (hydrochloride) is a lesser known psychoactive substituted amphetamine of the phenethylamine class. Though little is known about the pharmacological properties, metabolism, and toxicity of 3,4-MDPA, it has been used as an internal standard for qualitative and quantitative analyses of hallucinogenic designer drugs in biological samples.{21380}. This compound is intended for forensic and research purposes only.  

     

    Brand:
    Cayman
    SKU:-
  • 3,4-MDPA (hydrochloride) is a lesser known psychoactive substituted amphetamine of the phenethylamine class. Though little is known about the pharmacological properties, metabolism, and toxicity of 3,4-MDPA, it has been used as an internal standard for qualitative and quantitative analyses of hallucinogenic designer drugs in biological samples.{21380}. This compound is intended for forensic and research purposes only.  

     

    Brand:
    Cayman
    SKU:-
  • 3,4-MDPA (hydrochloride) is a lesser known psychoactive substituted amphetamine of the phenethylamine class. Though little is known about the pharmacological properties, metabolism, and toxicity of 3,4-MDPA, it has been used as an internal standard for qualitative and quantitative analyses of hallucinogenic designer drugs in biological samples.{21380}. This compound is intended for forensic and research purposes only.  

     

    Brand:
    Cayman
    SKU:-
  • 3,4-Methylenedioxy PV9 (hydrochloride) (Item No. 16359) is an analytical reference standard that is structurally categorized as a cathinone. The physiological and toxicological properties of this compound are not known. This product is intended for research and forensic applications.  

     

    Brand:
    Cayman
    SKU:-

    Out of stock

  • 3,4-Methylenedioxy PV9 (hydrochloride) (Item No. 16359) is an analytical reference standard that is structurally categorized as a cathinone. The physiological and toxicological properties of this compound are not known. This product is intended for research and forensic applications.  

     

    Brand:
    Cayman
    SKU:-

    Out of stock

  • 3,4-Methylenedioxy PV9 (hydrochloride) (Item No. 16359) is an analytical reference standard that is structurally categorized as a cathinone. The physiological and toxicological properties of this compound are not known. This product is intended for research and forensic applications.  

     

    Brand:
    Cayman
    SKU:-

    Out of stock

  • Substituted cathinones are psychoactive compounds sold in packets labeled as bath salts or plant food.{21394,20369} 3,4-Methylenedioxy-N-benzylcathinone is a substituted cathinone that is structurally analogous to methylone, a narcotic that is regulated in the United States. This compound has a phenyl group added to the amino methyl group, substantially decreasing its solubility in aqueous solutions. The physiological and toxicological properties of this compound are not known. This product is intended for research and forensic applications.  

     

    Brand:
    Cayman
    SKU:9001330 - 10 mg

    Available on backorder

  • Substituted cathinones are psychoactive compounds sold in packets labeled as bath salts or plant food.{21394,20369} 3,4-Methylenedioxy-N-benzylcathinone is a substituted cathinone that is structurally analogous to methylone, a narcotic that is regulated in the United States. This compound has a phenyl group added to the amino methyl group, substantially decreasing its solubility in aqueous solutions. The physiological and toxicological properties of this compound are not known. This product is intended for research and forensic applications.  

     

    Brand:
    Cayman
    SKU:9001330 - 5 mg

    Available on backorder

  • Substituted cathinones are psychoactive compounds sold in packets labeled as bath salts or plant food.{21394,20369} 3,4-Methylenedioxy-N-benzylcathinone is a substituted cathinone that is structurally analogous to methylone, a narcotic that is regulated in the United States. This compound has a phenyl group added to the amino methyl group, substantially decreasing its solubility in aqueous solutions. The physiological and toxicological properties of this compound are not known. This product is intended for research and forensic applications.  

     

    Brand:
    Cayman
    SKU:9001330 - 50 mg

    Available on backorder

  • 3,4-Methylenedioxy-α-methylaminohexanophenone (hydrochloride) (Item No. 29753) is an analytical reference standard categorized as a cathinone. This product is intended for research and forensic applications.  

     

    Brand:
    Cayman
    SKU:29753 - 1 mg

    Available on backorder

  • 3,4-Methylenedioxy-α-methylaminohexanophenone (hydrochloride) (Item No. 29753) is an analytical reference standard categorized as a cathinone. This product is intended for research and forensic applications.  

     

    Brand:
    Cayman
    SKU:29753 - 5 mg

    Available on backorder

  • Pyrrolidinophenones (PPPs) are a family of compounds that feature a pyrrolidinyl group affixed to the narcotic cathinone. Many have been identified as components of designer drugs.{19508} 3,4-Methylenedioxy-α-Pyrrolidinobutiophenone (hydrochloride) shares structural features of the stimulants α-PPP (Item No. 10445) and methylenedioxypyrovalerone (Item No. 10684). This product is intended to be used for forensic applications.  

     

    Brand:
    Cayman
    SKU:10437 - 10 mg

    Available on backorder

  • Pyrrolidinophenones (PPPs) are a family of compounds that feature a pyrrolidinyl group affixed to the narcotic cathinone. Many have been identified as components of designer drugs.{19508} 3,4-Methylenedioxy-α-Pyrrolidinobutiophenone (hydrochloride) shares structural features of the stimulants α-PPP (Item No. 10445) and methylenedioxypyrovalerone (Item No. 10684). This product is intended to be used for forensic applications.  

     

    Brand:
    Cayman
    SKU:10437 - 5 mg

    Available on backorder

  • Pyrrolidinophenones (PPPs) are a family of compounds that feature a pyrrolidinyl group affixed to the narcotic cathinone. Many have been identified as components of designer drugs.{19508} 3,4-Methylenedioxy-α-Pyrrolidinobutiophenone (hydrochloride) shares structural features of the stimulants α-PPP (Item No. 10445) and methylenedioxypyrovalerone (Item No. 10684). This product is intended to be used for forensic applications.  

     

    Brand:
    Cayman
    SKU:10437 - 50 mg

    Available on backorder

  • 3,4-Methylenedioxy Pyrovalerone (3,4-MDPV, Item No. 10684) is a central nervous system stimulant that has been widely abused.{18947} 3,4-Methylenedioxy-α-pyrrolidinohexanophenone (3,4-MDPHP) is an analog of 3,4-MDPV that differs only by the addition of a single carbon to the alkyl chain. The physiological and toxicological properties of this compound are not known. This product is intended for forensic and research applications.  

     

    Brand:
    Cayman
    SKU:-

    Out of stock

  • 3,4-Methylenedioxy Pyrovalerone (3,4-MDPV, Item No. 10684) is a central nervous system stimulant that has been widely abused.{18947} 3,4-Methylenedioxy-α-pyrrolidinohexanophenone (3,4-MDPHP) is an analog of 3,4-MDPV that differs only by the addition of a single carbon to the alkyl chain. The physiological and toxicological properties of this compound are not known. This product is intended for forensic and research applications.  

     

    Brand:
    Cayman
    SKU:-

    Out of stock

  • 3,4-Methylenedioxy Pyrovalerone (3,4-MDPV, Item No. 10684) is a central nervous system stimulant that has been widely abused.{18947} 3,4-Methylenedioxy-α-pyrrolidinohexanophenone (3,4-MDPHP) is an analog of 3,4-MDPV that differs only by the addition of a single carbon to the alkyl chain. The physiological and toxicological properties of this compound are not known. This product is intended for forensic and research applications.  

     

    Brand:
    Cayman
    SKU:-

    Out of stock

  • Pyrrolidinophenones (PPPs) are a family of compounds that feature a pyrrolidinyl group affixed to the narcotic cathinone. Many have been identified as components of designer drugs.{19508} 3,4-Methylenedioxy-α-Pyrrolidinopropiophenone (3,4-MD-α-PPP) (hydrochloride) shares structural features of the stimulants α-PPP (Item No. 10445) and methylenedioxypyrovalerone (Item No. 10684). The metabolism of 3,4-MD-α-PPP in male Wistar rats has been characterized.{19736,19874} This product is intended to be used for forensic applications.  

     

    Brand:
    Cayman
    SKU:10439 - 10 mg

    Available on backorder

  • Pyrrolidinophenones (PPPs) are a family of compounds that feature a pyrrolidinyl group affixed to the narcotic cathinone. Many have been identified as components of designer drugs.{19508} 3,4-Methylenedioxy-α-Pyrrolidinopropiophenone (3,4-MD-α-PPP) (hydrochloride) shares structural features of the stimulants α-PPP (Item No. 10445) and methylenedioxypyrovalerone (Item No. 10684). The metabolism of 3,4-MD-α-PPP in male Wistar rats has been characterized.{19736,19874} This product is intended to be used for forensic applications.  

     

    Brand:
    Cayman
    SKU:10439 - 5 mg

    Available on backorder

  • Pyrrolidinophenones (PPPs) are a family of compounds that feature a pyrrolidinyl group affixed to the narcotic cathinone. Many have been identified as components of designer drugs.{19508} 3,4-Methylenedioxy-α-Pyrrolidinopropiophenone (3,4-MD-α-PPP) (hydrochloride) shares structural features of the stimulants α-PPP (Item No. 10445) and methylenedioxypyrovalerone (Item No. 10684). The metabolism of 3,4-MD-α-PPP in male Wistar rats has been characterized.{19736,19874} This product is intended to be used for forensic applications.  

     

    Brand:
    Cayman
    SKU:10439 - 50 mg

    Available on backorder

  • 3,4,5-Trimethoxyamphetamine (TMA), is a psychedelic hallucinogen that has appeared on the illicit drug market.{21281} Unlike amphetamines and cathinones, TMA has no effect on monoamine re-uptake.{19758} TMA has modest effects on the 5-HT2 serotonin receptors (pEC50s = 5.15 and 5.31 for phosphatidyl inositol release through 5-HT2A and 5-HT2C, respectively).{20772} This product is intended for research and forensic applications.  

     

    Brand:
    Cayman
    SKU:-
  • 3,4,6-Tri-O-benzyl-β-D-mannopyranose 1,2-(methyl orthoacetate) is a synthetic intermediate used in glycosylation reactions.{26790,26789} Typically, the methyl orthoester protecting group is first removed by mild acid hydrolysis, producing a glycosyl donor. Removal of the O-benzyl protecting groups is performed late in the synthesis.  

     

    Brand:
    Cayman
    SKU:-

    Out of stock

  • 3,4,6-Tri-O-benzyl-β-D-mannopyranose 1,2-(methyl orthoacetate) is a synthetic intermediate used in glycosylation reactions.{26790,26789} Typically, the methyl orthoester protecting group is first removed by mild acid hydrolysis, producing a glycosyl donor. Removal of the O-benzyl protecting groups is performed late in the synthesis.  

     

    Brand:
    Cayman
    SKU:-

    Out of stock

  • 3,4,6-Tri-O-benzyl-β-D-mannopyranose 1,2-(methyl orthoacetate) is a synthetic intermediate used in glycosylation reactions.{26790,26789} Typically, the methyl orthoester protecting group is first removed by mild acid hydrolysis, producing a glycosyl donor. Removal of the O-benzyl protecting groups is performed late in the synthesis.  

     

    Brand:
    Cayman
    SKU:-

    Out of stock

  • 3,4,6-Tri-O-benzyl-β-D-mannopyranose 1,2-(methyl orthoacetate) is a synthetic intermediate used in glycosylation reactions.{26790,26789} Typically, the methyl orthoester protecting group is first removed by mild acid hydrolysis, producing a glycosyl donor. Removal of the O-benzyl protecting groups is performed late in the synthesis.  

     

    Brand:
    Cayman
    SKU:-

    Out of stock

  • Resveratrol is a potent phenolic antioxidant found in natural sources that has antiproliferative activity.{9146} When the three phenolic hydroxyl groups of resveratrol are converted to methyl ethers, the inhibition of cell growth is enhanced.{10510} 3,4′,5-Trismethoxybenzophenone is an analog of trismethoxy resveratrol. It inhibits the growth of a variety of human tumor cell lines at concentrations from 0.4 to 2 µg/ml, which is 5-6 times more potent than resveratrol.{11554}  

     

    Brand:
    Cayman
    SKU:10004185 - 10 mg

    Available on backorder

  • Resveratrol is a potent phenolic antioxidant found in natural sources that has antiproliferative activity.{9146} When the three phenolic hydroxyl groups of resveratrol are converted to methyl ethers, the inhibition of cell growth is enhanced.{10510} 3,4′,5-Trismethoxybenzophenone is an analog of trismethoxy resveratrol. It inhibits the growth of a variety of human tumor cell lines at concentrations from 0.4 to 2 µg/ml, which is 5-6 times more potent than resveratrol.{11554}  

     

    Brand:
    Cayman
    SKU:10004185 - 100 mg

    Available on backorder

  • Resveratrol is a potent phenolic antioxidant found in natural sources that has antiproliferative activity.{9146} When the three phenolic hydroxyl groups of resveratrol are converted to methyl ethers, the inhibition of cell growth is enhanced.{10510} 3,4′,5-Trismethoxybenzophenone is an analog of trismethoxy resveratrol. It inhibits the growth of a variety of human tumor cell lines at concentrations from 0.4 to 2 µg/ml, which is 5-6 times more potent than resveratrol.{11554}  

     

    Brand:
    Cayman
    SKU:10004185 - 25 mg

    Available on backorder

  • Resveratrol is a potent phenolic antioxidant found in natural sources that has antiproliferative activity.{9146} When the three phenolic hydroxyl groups of resveratrol are converted to methyl ethers, the inhibition of cell growth is enhanced.{10510} 3,4′,5-Trismethoxybenzophenone is an analog of trismethoxy resveratrol. It inhibits the growth of a variety of human tumor cell lines at concentrations from 0.4 to 2 µg/ml, which is 5-6 times more potent than resveratrol.{11554}  

     

    Brand:
    Cayman
    SKU:10004185 - 50 mg

    Available on backorder

  • 3,5-Dicaffeoylquinic acid (3,5-DCQA) is a natural phenolic compound that has been found in L. japonica, I. kaushue, and other plants.{36684,36685} It has antioxidant, anti-inflammatory, and antiviral biological activities.{36685,36686,36687} 3,5-DCQA scavenges 2,2-diphenyl-1-picrylhydrazyl (DPPH; Item No. 14805) radicals in a cell-free assay (IC50 = 71.8 μM) and inhibits superoxide production in human neutrophils activated by N-formyl-Met-Leu-Phe (fMLF) and cytochalasin B (IC50 = 1.92 μM).{36685,36686} It inhibits HIV-1 integrase 3′-end processing, strand transfer, and disintegration in a cell-free assay (IC50s = 0.33, 0.34, and 0.66 μg/ml, respectively) and inhibits HIV-1-induced cytotoxicity in MT-2 cells (ED50 = 1 μg/ml).{36687} In vivo, 3,5-DCQA (25 mg/kg) protects mice from acute lung injury induced by LPS and decreases neutrophil count in bronchoalveolar lavage fluid (BALF).{36685}  

     

    Brand:
    Cayman
    SKU:24964 - 10 mg

    Available on backorder

  • 3,5-Dicaffeoylquinic acid (3,5-DCQA) is a natural phenolic compound that has been found in L. japonica, I. kaushue, and other plants.{36684,36685} It has antioxidant, anti-inflammatory, and antiviral biological activities.{36685,36686,36687} 3,5-DCQA scavenges 2,2-diphenyl-1-picrylhydrazyl (DPPH; Item No. 14805) radicals in a cell-free assay (IC50 = 71.8 μM) and inhibits superoxide production in human neutrophils activated by N-formyl-Met-Leu-Phe (fMLF) and cytochalasin B (IC50 = 1.92 μM).{36685,36686} It inhibits HIV-1 integrase 3′-end processing, strand transfer, and disintegration in a cell-free assay (IC50s = 0.33, 0.34, and 0.66 μg/ml, respectively) and inhibits HIV-1-induced cytotoxicity in MT-2 cells (ED50 = 1 μg/ml).{36687} In vivo, 3,5-DCQA (25 mg/kg) protects mice from acute lung injury induced by LPS and decreases neutrophil count in bronchoalveolar lavage fluid (BALF).{36685}  

     

    Brand:
    Cayman
    SKU:24964 - 25 mg

    Available on backorder

  • 3,5-Dicaffeoylquinic acid (3,5-DCQA) is a natural phenolic compound that has been found in L. japonica, I. kaushue, and other plants.{36684,36685} It has antioxidant, anti-inflammatory, and antiviral biological activities.{36685,36686,36687} 3,5-DCQA scavenges 2,2-diphenyl-1-picrylhydrazyl (DPPH; Item No. 14805) radicals in a cell-free assay (IC50 = 71.8 μM) and inhibits superoxide production in human neutrophils activated by N-formyl-Met-Leu-Phe (fMLF) and cytochalasin B (IC50 = 1.92 μM).{36685,36686} It inhibits HIV-1 integrase 3′-end processing, strand transfer, and disintegration in a cell-free assay (IC50s = 0.33, 0.34, and 0.66 μg/ml, respectively) and inhibits HIV-1-induced cytotoxicity in MT-2 cells (ED50 = 1 μg/ml).{36687} In vivo, 3,5-DCQA (25 mg/kg) protects mice from acute lung injury induced by LPS and decreases neutrophil count in bronchoalveolar lavage fluid (BALF).{36685}  

     

    Brand:
    Cayman
    SKU:24964 - 5 mg

    Available on backorder

  • 3,5-Dicaffeoylquinic acid (3,5-DCQA) is a natural phenolic compound that has been found in L. japonica, I. kaushue, and other plants.{36684,36685} It has antioxidant, anti-inflammatory, and antiviral biological activities.{36685,36686,36687} 3,5-DCQA scavenges 2,2-diphenyl-1-picrylhydrazyl (DPPH; Item No. 14805) radicals in a cell-free assay (IC50 = 71.8 μM) and inhibits superoxide production in human neutrophils activated by N-formyl-Met-Leu-Phe (fMLF) and cytochalasin B (IC50 = 1.92 μM).{36685,36686} It inhibits HIV-1 integrase 3′-end processing, strand transfer, and disintegration in a cell-free assay (IC50s = 0.33, 0.34, and 0.66 μg/ml, respectively) and inhibits HIV-1-induced cytotoxicity in MT-2 cells (ED50 = 1 μg/ml).{36687} In vivo, 3,5-DCQA (25 mg/kg) protects mice from acute lung injury induced by LPS and decreases neutrophil count in bronchoalveolar lavage fluid (BALF).{36685}  

     

    Brand:
    Cayman
    SKU:24964 - 50 mg

    Available on backorder

  • 3,5-Dihydroxybenzaldehyde is a building block.{46911,46912} It has been used in the synthesis of 2,4-dimethylbenzoylhydrazones with antileishmanial and antioxidant activities.  

     

    Brand:
    Cayman
    SKU:30445 - 1 g

    Available on backorder

  • 3,5-Dihydroxybenzaldehyde is a building block.{46911,46912} It has been used in the synthesis of 2,4-dimethylbenzoylhydrazones with antileishmanial and antioxidant activities.  

     

    Brand:
    Cayman
    SKU:30445 - 500 mg

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  • 3,5-Diiodothyroacetic acid (diac) is the acetic acid variant of thyroxine. Formulations containing dosages in the range of 100 mg/day decrease serum cholesterol and produce calorigenic effects in humans.{34677} Formulations containing diac also protect human LDL cholesterol from oxidation in vitro.{34678} Diac treatment prevents elevated liver cholesterol in rats fed a high-fat diet and reduces previously elevated liver cholesterol to control levels.{34679}  

     

    Brand:
    Cayman
    SKU:22108 -

    Out of stock

  • 3,5-Diiodothyroacetic acid (diac) is the acetic acid variant of thyroxine. Formulations containing dosages in the range of 100 mg/day decrease serum cholesterol and produce calorigenic effects in humans.{34677} Formulations containing diac also protect human LDL cholesterol from oxidation in vitro.{34678} Diac treatment prevents elevated liver cholesterol in rats fed a high-fat diet and reduces previously elevated liver cholesterol to control levels.{34679}  

     

    Brand:
    Cayman
    SKU:22108 -

    Out of stock

  • 3,5-Diiodothyroacetic acid (diac) is the acetic acid variant of thyroxine. Formulations containing dosages in the range of 100 mg/day decrease serum cholesterol and produce calorigenic effects in humans.{34677} Formulations containing diac also protect human LDL cholesterol from oxidation in vitro.{34678} Diac treatment prevents elevated liver cholesterol in rats fed a high-fat diet and reduces previously elevated liver cholesterol to control levels.{34679}  

     

    Brand:
    Cayman
    SKU:22108 -

    Out of stock

  • 3,5-Diiodothyroacetic acid (diac) is the acetic acid variant of thyroxine. Formulations containing dosages in the range of 100 mg/day decrease serum cholesterol and produce calorigenic effects in humans.{34677} Formulations containing diac also protect human LDL cholesterol from oxidation in vitro.{34678} Diac treatment prevents elevated liver cholesterol in rats fed a high-fat diet and reduces previously elevated liver cholesterol to control levels.{34679}  

     

    Brand:
    Cayman
    SKU:22108 -

    Out of stock

  • 3,5-Diiodothyropropionic acid (DITPA) is an inotropic thyroid hormone analogue of L-thyroxine (Item No. 14116) that binds to the thyroid hormone receptors TRα and TRβ (Kas = 2.4 and 4.06 x 107 M-1, respectively, for human recombinant receptors).{40907} DITPA increases mRNA expression of α-myosin heavy chain (α-MHC) in primary rat cardiomyocytes (EC50 = ~0.5 μM). Ex vivo, DITPA prevents myocardial infarction-induced loss of contractility in rabbit cardiomyocytes when administered at a dose of 3.75 mg/kg per day.{40908} DITPA (3.75 mg/kg per day) increases expression of VEGF, basic fibroblast growth factor (bFGF), angiopoietin-1, and angiopoietin-1 receptor (Tie-2) as well as angiogenesis in non-infarcted cardiac tissue in rats.{40909} It also decreases infarct size expansion, stimulates arteriolar growth, and inhibits ventricular remodeling post-myocardial infarction in rats when administered at a dose of 3.5 mg/kg per day.{40910}  

     

    Brand:
    Cayman
    SKU:23299 - 100 mg

    Available on backorder

  • 3,5-Diiodothyropropionic acid (DITPA) is an inotropic thyroid hormone analogue of L-thyroxine (Item No. 14116) that binds to the thyroid hormone receptors TRα and TRβ (Kas = 2.4 and 4.06 x 107 M-1, respectively, for human recombinant receptors).{40907} DITPA increases mRNA expression of α-myosin heavy chain (α-MHC) in primary rat cardiomyocytes (EC50 = ~0.5 μM). Ex vivo, DITPA prevents myocardial infarction-induced loss of contractility in rabbit cardiomyocytes when administered at a dose of 3.75 mg/kg per day.{40908} DITPA (3.75 mg/kg per day) increases expression of VEGF, basic fibroblast growth factor (bFGF), angiopoietin-1, and angiopoietin-1 receptor (Tie-2) as well as angiogenesis in non-infarcted cardiac tissue in rats.{40909} It also decreases infarct size expansion, stimulates arteriolar growth, and inhibits ventricular remodeling post-myocardial infarction in rats when administered at a dose of 3.5 mg/kg per day.{40910}  

     

    Brand:
    Cayman
    SKU:23299 - 25 mg

    Available on backorder

  • 3,5-Diiodothyropropionic acid (DITPA) is an inotropic thyroid hormone analogue of L-thyroxine (Item No. 14116) that binds to the thyroid hormone receptors TRα and TRβ (Kas = 2.4 and 4.06 x 107 M-1, respectively, for human recombinant receptors).{40907} DITPA increases mRNA expression of α-myosin heavy chain (α-MHC) in primary rat cardiomyocytes (EC50 = ~0.5 μM). Ex vivo, DITPA prevents myocardial infarction-induced loss of contractility in rabbit cardiomyocytes when administered at a dose of 3.75 mg/kg per day.{40908} DITPA (3.75 mg/kg per day) increases expression of VEGF, basic fibroblast growth factor (bFGF), angiopoietin-1, and angiopoietin-1 receptor (Tie-2) as well as angiogenesis in non-infarcted cardiac tissue in rats.{40909} It also decreases infarct size expansion, stimulates arteriolar growth, and inhibits ventricular remodeling post-myocardial infarction in rats when administered at a dose of 3.5 mg/kg per day.{40910}  

     

    Brand:
    Cayman
    SKU:23299 - 50 mg

    Available on backorder

  • PtdIns-(3,4,5)-P3 (PIP3) serves as an anchor for the binding of signal transduction proteins bearing pleckstrin homology (PH) domains such as phosphatidylinositol 3-kinase (PI3K) or PTEN. Protein binding to PIP3 is important for cytoskeletal rearrangement and membrane trafficking and initiates an intricate signaling cascade that has been implicated in cancer.{12235} 3,5-dimethyl PIT-1 is a dimethyl analog of PIT-1, the selective inhibitor of PIP3/Akt PH domain binding, that is designed for more favorable solubility in vivo. 3,5-dimethyl PIT-1 inhibits PI3K/Akt signaling (IC50 = 27 μM), suppressing PI3K-PDK1-Akt-dependent phosphorylation, which has been shown to reduce cell viability and induce apoptosis in PTEN-deficient U87MG glioblastoma cells (IC50 = 36 μM).{18957} 4T1 breast cancer growth is significantly attenuated in BALB/c mice with a dose of 1 mg/kg of 3,5-dimethyl PIT-1 per day.  

     

    Brand:
    Cayman
    SKU:10727 - 1 mg

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  • PtdIns-(3,4,5)-P3 (PIP3) serves as an anchor for the binding of signal transduction proteins bearing pleckstrin homology (PH) domains such as phosphatidylinositol 3-kinase (PI3K) or PTEN. Protein binding to PIP3 is important for cytoskeletal rearrangement and membrane trafficking and initiates an intricate signaling cascade that has been implicated in cancer.{12235} 3,5-dimethyl PIT-1 is a dimethyl analog of PIT-1, the selective inhibitor of PIP3/Akt PH domain binding, that is designed for more favorable solubility in vivo. 3,5-dimethyl PIT-1 inhibits PI3K/Akt signaling (IC50 = 27 μM), suppressing PI3K-PDK1-Akt-dependent phosphorylation, which has been shown to reduce cell viability and induce apoptosis in PTEN-deficient U87MG glioblastoma cells (IC50 = 36 μM).{18957} 4T1 breast cancer growth is significantly attenuated in BALB/c mice with a dose of 1 mg/kg of 3,5-dimethyl PIT-1 per day.  

     

    Brand:
    Cayman
    SKU:10727 - 10 mg

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  • PtdIns-(3,4,5)-P3 (PIP3) serves as an anchor for the binding of signal transduction proteins bearing pleckstrin homology (PH) domains such as phosphatidylinositol 3-kinase (PI3K) or PTEN. Protein binding to PIP3 is important for cytoskeletal rearrangement and membrane trafficking and initiates an intricate signaling cascade that has been implicated in cancer.{12235} 3,5-dimethyl PIT-1 is a dimethyl analog of PIT-1, the selective inhibitor of PIP3/Akt PH domain binding, that is designed for more favorable solubility in vivo. 3,5-dimethyl PIT-1 inhibits PI3K/Akt signaling (IC50 = 27 μM), suppressing PI3K-PDK1-Akt-dependent phosphorylation, which has been shown to reduce cell viability and induce apoptosis in PTEN-deficient U87MG glioblastoma cells (IC50 = 36 μM).{18957} 4T1 breast cancer growth is significantly attenuated in BALB/c mice with a dose of 1 mg/kg of 3,5-dimethyl PIT-1 per day.  

     

    Brand:
    Cayman
    SKU:10727 - 25 mg

    Available on backorder

  • PtdIns-(3,4,5)-P3 (PIP3) serves as an anchor for the binding of signal transduction proteins bearing pleckstrin homology (PH) domains such as phosphatidylinositol 3-kinase (PI3K) or PTEN. Protein binding to PIP3 is important for cytoskeletal rearrangement and membrane trafficking and initiates an intricate signaling cascade that has been implicated in cancer.{12235} 3,5-dimethyl PIT-1 is a dimethyl analog of PIT-1, the selective inhibitor of PIP3/Akt PH domain binding, that is designed for more favorable solubility in vivo. 3,5-dimethyl PIT-1 inhibits PI3K/Akt signaling (IC50 = 27 μM), suppressing PI3K-PDK1-Akt-dependent phosphorylation, which has been shown to reduce cell viability and induce apoptosis in PTEN-deficient U87MG glioblastoma cells (IC50 = 36 μM).{18957} 4T1 breast cancer growth is significantly attenuated in BALB/c mice with a dose of 1 mg/kg of 3,5-dimethyl PIT-1 per day.  

     

    Brand:
    Cayman
    SKU:10727 - 5 mg

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  • 3,5-Dinitrocatechol is a potent catechol O-methyltransferase (COMT) inhibitor (IC50 = 12 nM).{46554} It is selective for COMT over tyrosine hydroxylase, dopamine β-hydroxylase, dopamine decarboxylase, monoamine oxidase A (MAO-A), and MAO-B (IC50s = >14 μM for all). 3,5-Dintrocatechol (30 mg/kg), in combination with L-DOPA (Item No. 13248) and carbidopa (Item No. 23783), reduces 3-O-methyldopa (3-OMD) levels in rat serum, compared with control animals receiving only L-DOPA and carbidopa. Chronic administration of 3,5-dinitrocatechol (15 mg/kg per day for seven days) induces COMT-dependent thermal hyperalgesia and increases preference for dark in a light/dark preference test, indicating anxiety-like behavior, in rats, effects that can be prevented by the β-adrenergic receptor antagonist propranolol (Item No. 23349).{46555}  

     

    Brand:
    Cayman
    SKU:29180 - 1 mg

    Available on backorder

  • 3,5-Dinitrocatechol is a potent catechol O-methyltransferase (COMT) inhibitor (IC50 = 12 nM).{46554} It is selective for COMT over tyrosine hydroxylase, dopamine β-hydroxylase, dopamine decarboxylase, monoamine oxidase A (MAO-A), and MAO-B (IC50s = >14 μM for all). 3,5-Dintrocatechol (30 mg/kg), in combination with L-DOPA (Item No. 13248) and carbidopa (Item No. 23783), reduces 3-O-methyldopa (3-OMD) levels in rat serum, compared with control animals receiving only L-DOPA and carbidopa. Chronic administration of 3,5-dinitrocatechol (15 mg/kg per day for seven days) induces COMT-dependent thermal hyperalgesia and increases preference for dark in a light/dark preference test, indicating anxiety-like behavior, in rats, effects that can be prevented by the β-adrenergic receptor antagonist propranolol (Item No. 23349).{46555}  

     

    Brand:
    Cayman
    SKU:29180 - 10 mg

    Available on backorder

  • 3,5-Dinitrocatechol is a potent catechol O-methyltransferase (COMT) inhibitor (IC50 = 12 nM).{46554} It is selective for COMT over tyrosine hydroxylase, dopamine β-hydroxylase, dopamine decarboxylase, monoamine oxidase A (MAO-A), and MAO-B (IC50s = >14 μM for all). 3,5-Dintrocatechol (30 mg/kg), in combination with L-DOPA (Item No. 13248) and carbidopa (Item No. 23783), reduces 3-O-methyldopa (3-OMD) levels in rat serum, compared with control animals receiving only L-DOPA and carbidopa. Chronic administration of 3,5-dinitrocatechol (15 mg/kg per day for seven days) induces COMT-dependent thermal hyperalgesia and increases preference for dark in a light/dark preference test, indicating anxiety-like behavior, in rats, effects that can be prevented by the β-adrenergic receptor antagonist propranolol (Item No. 23349).{46555}  

     

    Brand:
    Cayman
    SKU:29180 - 5 mg

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  • 3,5-DMA (hydrochloride) (Item No. 19743) is an analytical reference standard that is structurally categorized as an amphetamine. The physiological and toxicological properties of this compound are not known. This product is intended for research and forensic applications.  

     

    Brand:
    Cayman
    SKU:19743 -

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  • 3,5-DMA (hydrochloride) (Item No. 19743) is an analytical reference standard that is structurally categorized as an amphetamine. The physiological and toxicological properties of this compound are not known. This product is intended for research and forensic applications.  

     

    Brand:
    Cayman
    SKU:19743 -

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  • 3,6-diacetoxy Phthalonitrile is a fluorescent probe for monitoring intracellular pH by flow cytometry in living cells.{29427} It rapidly crosses cell membranes and is cleaved by cytosolic esterases to form the fluorescent pH indicator 2,3-dicyano-hydroquinone (DCH), which is excited at UV wavelengths. DCH can be excited at 351 nm, with pH-dependent emission in the range of 450-476 nm (pH 5.0-10.0) using a potassium-based buffer.{29427}  

     

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    Cayman
    SKU:-

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  • 3,6-diacetoxy Phthalonitrile is a fluorescent probe for monitoring intracellular pH by flow cytometry in living cells.{29427} It rapidly crosses cell membranes and is cleaved by cytosolic esterases to form the fluorescent pH indicator 2,3-dicyano-hydroquinone (DCH), which is excited at UV wavelengths. DCH can be excited at 351 nm, with pH-dependent emission in the range of 450-476 nm (pH 5.0-10.0) using a potassium-based buffer.{29427}  

     

    Brand:
    Cayman
    SKU:-

    Available on backorder

  • 3,6-diacetoxy Phthalonitrile is a fluorescent probe for monitoring intracellular pH by flow cytometry in living cells.{29427} It rapidly crosses cell membranes and is cleaved by cytosolic esterases to form the fluorescent pH indicator 2,3-dicyano-hydroquinone (DCH), which is excited at UV wavelengths. DCH can be excited at 351 nm, with pH-dependent emission in the range of 450-476 nm (pH 5.0-10.0) using a potassium-based buffer.{29427}  

     

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    Cayman
    SKU:-

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  • 3,6-dichloro-benzo[b]thiophene-2-Carboxylic acid is an inhibitor of myeloid cell leukemia 1 (Mcl-1) with a Ki value of 59 μM for binding of FITC-Mcl-1-BH2 peptide binding to Mcl-1.{36227} It has been used as a building block in the synthesis of inhibitors of Mcl-1, the toll-like receptor 3/double-stranded RNA (TLR3/dsRNA) complex, and D-amino acid oxidase (DAO).{36227,36228,36229}  

     

    Brand:
    Cayman
    SKU:22948 - 100 mg

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  • 3,6-dichloro-benzo[b]thiophene-2-Carboxylic acid is an inhibitor of myeloid cell leukemia 1 (Mcl-1) with a Ki value of 59 μM for binding of FITC-Mcl-1-BH2 peptide binding to Mcl-1.{36227} It has been used as a building block in the synthesis of inhibitors of Mcl-1, the toll-like receptor 3/double-stranded RNA (TLR3/dsRNA) complex, and D-amino acid oxidase (DAO).{36227,36228,36229}  

     

    Brand:
    Cayman
    SKU:22948 - 250 mg

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  • 3,6-dichloro-benzo[b]thiophene-2-Carboxylic acid is an inhibitor of myeloid cell leukemia 1 (Mcl-1) with a Ki value of 59 μM for binding of FITC-Mcl-1-BH2 peptide binding to Mcl-1.{36227} It has been used as a building block in the synthesis of inhibitors of Mcl-1, the toll-like receptor 3/double-stranded RNA (TLR3/dsRNA) complex, and D-amino acid oxidase (DAO).{36227,36228,36229}  

     

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    Cayman
    SKU:22948 - 500 mg

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  • 3′-Azido-3′-deoxythymidine β-D-glucuronide is a metabolite of the nucleoside reverse transcriptase inhibitor, zidovudine (Item No. 15492), formed by direct conjugation by UDP-glucuronosyltransferase 2B7.{20875} The azido group of both zidovudine and its glucuronide metabolite can be reduced to an amino group by cytochrome P450 (CYP)3A, CYP2A6, or CYP2B1, forming 3’-amino-3’-deoxythymidine (AMT) and AMT glucuronide, respectively.{30307} Several compounds, including rifampicin (Item No. 14423), valproic acid (Item No. 13033), fluconazole (Item No. 11594), and efavirenz (Item No. 14412) are known to interfere with zidovudine glucuronidation in vitro in human liver microsomes.{30307,30306} Formation of AMT, which is 5-7-fold more toxic than the parent drug, is thought to be enhanced through inhibition of zidovudine glucuronidation.{30307}  

     

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    Cayman
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  • 3′-Azido-3′-deoxythymidine β-D-glucuronide is a metabolite of the nucleoside reverse transcriptase inhibitor, zidovudine (Item No. 15492), formed by direct conjugation by UDP-glucuronosyltransferase 2B7.{20875} The azido group of both zidovudine and its glucuronide metabolite can be reduced to an amino group by cytochrome P450 (CYP)3A, CYP2A6, or CYP2B1, forming 3’-amino-3’-deoxythymidine (AMT) and AMT glucuronide, respectively.{30307} Several compounds, including rifampicin (Item No. 14423), valproic acid (Item No. 13033), fluconazole (Item No. 11594), and efavirenz (Item No. 14412) are known to interfere with zidovudine glucuronidation in vitro in human liver microsomes.{30307,30306} Formation of AMT, which is 5-7-fold more toxic than the parent drug, is thought to be enhanced through inhibition of zidovudine glucuronidation.{30307}  

     

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    Cayman
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  • 3′-Azido-3′-deoxythymidine β-D-glucuronide is a metabolite of the nucleoside reverse transcriptase inhibitor, zidovudine (Item No. 15492), formed by direct conjugation by UDP-glucuronosyltransferase 2B7.{20875} The azido group of both zidovudine and its glucuronide metabolite can be reduced to an amino group by cytochrome P450 (CYP)3A, CYP2A6, or CYP2B1, forming 3’-amino-3’-deoxythymidine (AMT) and AMT glucuronide, respectively.{30307} Several compounds, including rifampicin (Item No. 14423), valproic acid (Item No. 13033), fluconazole (Item No. 11594), and efavirenz (Item No. 14412) are known to interfere with zidovudine glucuronidation in vitro in human liver microsomes.{30307,30306} Formation of AMT, which is 5-7-fold more toxic than the parent drug, is thought to be enhanced through inhibition of zidovudine glucuronidation.{30307}  

     

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    Cayman
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  • 3′-Deoxyguanosine is a ligand that can be complexed with enzymes, such as purine nucleoside phosphorylase, and receptors, in order to study structure-activity relationships.{29082,29083} This compound can also be used to selectively impair transcription.{29084}  

     

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    Cayman
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  • 3′-Deoxyguanosine is a ligand that can be complexed with enzymes, such as purine nucleoside phosphorylase, and receptors, in order to study structure-activity relationships.{29082,29083} This compound can also be used to selectively impair transcription.{29084}  

     

    Brand:
    Cayman
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