Cayman
Showing 4651–4800 of 45550 results
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2,3-Dichlorophenylpiperazine is an analog of 3-chlorophenylpiperazine, a psychoactive drug of abuse.{20497,21515,19874} The physiological and toxicological properties of this analog have not been evaluated. This product is intended for forensic and research purposes.
Brand:CaymanSKU:-2,3-Dichlorophenylpiperazine is an analog of 3-chlorophenylpiperazine, a psychoactive drug of abuse.{20497,21515,19874} The physiological and toxicological properties of this analog have not been evaluated. This product is intended for forensic and research purposes.
Brand:CaymanSKU:-1,2,3-Thiadiazoles have diverse applications in medicine and agriculture, such as bactericides, fungicides, and antiviral agents. 2,3-dihydrothieno-Thiadiazole carboxylate (MTCC), 100 µM, both inhibits and inactivates certain microsomal CYP450 enzymes (CYP2E1 and CYP2B4), but not others (CYP1A2), with inactivation occurring in a mechanism-based manner.{15950}
Brand:CaymanSKU:10011048 - 10 mgAvailable on backorder
1,2,3-Thiadiazoles have diverse applications in medicine and agriculture, such as bactericides, fungicides, and antiviral agents. 2,3-dihydrothieno-Thiadiazole carboxylate (MTCC), 100 µM, both inhibits and inactivates certain microsomal CYP450 enzymes (CYP2E1 and CYP2B4), but not others (CYP1A2), with inactivation occurring in a mechanism-based manner.{15950}
Brand:CaymanSKU:10011048 - 100 mgAvailable on backorder
1,2,3-Thiadiazoles have diverse applications in medicine and agriculture, such as bactericides, fungicides, and antiviral agents. 2,3-dihydrothieno-Thiadiazole carboxylate (MTCC), 100 µM, both inhibits and inactivates certain microsomal CYP450 enzymes (CYP2E1 and CYP2B4), but not others (CYP1A2), with inactivation occurring in a mechanism-based manner.{15950}
Brand:CaymanSKU:10011048 - 50 mgAvailable on backorder
2,3-Dimethoxy-5-methyl-p-benzoquinone, also known as coenzyme Q0, is a key intermediate in the synthesis of coenzyme Q, coenzyme Q10, other ubiquinones, and vitamin E.{43190,43191} It inhibits the growth of SKOV-3, A2780, and A2870/CP70 human ovarian carcinoma cells (IC50s = 26.6, 27.3, and 28.4 µM, respectively) with a cytotoxic concentration of greater than 40 µM for non-cancerous ovarian surface epithelial cells.{43192} It halts the cell cycle at the G2/M phase, increases the production of reactive oxygen species (ROS), and induces autophagy and apoptosis in SKOV-3 cells. 2,3-Dimethoxy-5-methyl-p-benzoquinone downregulates the protooncogene HER-2 and decreases the protein levels of phosphorylated AKT and mTOR in SKOV-3 cells. It also decreases the incidence of tumors and tumor burden in a SKOV-3 human ovarian carcinoma mouse xenograft model when administered at a dose of 2.5 mg/kg every four days.
Brand:CaymanSKU:20504 -Available on backorder
2,3-Dimethoxy-5-methyl-p-benzoquinone, also known as coenzyme Q0, is a key intermediate in the synthesis of coenzyme Q, coenzyme Q10, other ubiquinones, and vitamin E.{43190,43191} It inhibits the growth of SKOV-3, A2780, and A2870/CP70 human ovarian carcinoma cells (IC50s = 26.6, 27.3, and 28.4 µM, respectively) with a cytotoxic concentration of greater than 40 µM for non-cancerous ovarian surface epithelial cells.{43192} It halts the cell cycle at the G2/M phase, increases the production of reactive oxygen species (ROS), and induces autophagy and apoptosis in SKOV-3 cells. 2,3-Dimethoxy-5-methyl-p-benzoquinone downregulates the protooncogene HER-2 and decreases the protein levels of phosphorylated AKT and mTOR in SKOV-3 cells. It also decreases the incidence of tumors and tumor burden in a SKOV-3 human ovarian carcinoma mouse xenograft model when administered at a dose of 2.5 mg/kg every four days.
Brand:CaymanSKU:20504 -Available on backorder
2,3-Dimethoxy-5-methyl-p-benzoquinone, also known as coenzyme Q0, is a key intermediate in the synthesis of coenzyme Q, coenzyme Q10, other ubiquinones, and vitamin E.{43190,43191} It inhibits the growth of SKOV-3, A2780, and A2870/CP70 human ovarian carcinoma cells (IC50s = 26.6, 27.3, and 28.4 µM, respectively) with a cytotoxic concentration of greater than 40 µM for non-cancerous ovarian surface epithelial cells.{43192} It halts the cell cycle at the G2/M phase, increases the production of reactive oxygen species (ROS), and induces autophagy and apoptosis in SKOV-3 cells. 2,3-Dimethoxy-5-methyl-p-benzoquinone downregulates the protooncogene HER-2 and decreases the protein levels of phosphorylated AKT and mTOR in SKOV-3 cells. It also decreases the incidence of tumors and tumor burden in a SKOV-3 human ovarian carcinoma mouse xenograft model when administered at a dose of 2.5 mg/kg every four days.
Brand:CaymanSKU:20504 -Available on backorder
2,3-Dimethoxy-5-methyl-p-benzoquinone, also known as coenzyme Q0, is a key intermediate in the synthesis of coenzyme Q, coenzyme Q10, other ubiquinones, and vitamin E.{43190,43191} It inhibits the growth of SKOV-3, A2780, and A2870/CP70 human ovarian carcinoma cells (IC50s = 26.6, 27.3, and 28.4 µM, respectively) with a cytotoxic concentration of greater than 40 µM for non-cancerous ovarian surface epithelial cells.{43192} It halts the cell cycle at the G2/M phase, increases the production of reactive oxygen species (ROS), and induces autophagy and apoptosis in SKOV-3 cells. 2,3-Dimethoxy-5-methyl-p-benzoquinone downregulates the protooncogene HER-2 and decreases the protein levels of phosphorylated AKT and mTOR in SKOV-3 cells. It also decreases the incidence of tumors and tumor burden in a SKOV-3 human ovarian carcinoma mouse xenograft model when administered at a dose of 2.5 mg/kg every four days.
Brand:CaymanSKU:20504 -Available on backorder
2,3-Dimethylmethcathinone (hydrochloride) is a potential designer drug with combined features of amphetamines, cathinones, and phenethylamines. It is structurally related to 4-methylmethcathinone, (Item No. 10801), a psychoactive compound that has been identified in products sold as bath salts and plant food.{19498,19499,19497} The physiological and toxicological properties of this compound have not been elucidated. This product is intended for research and forensic applications.
Brand:CaymanSKU:11225 - 10 mgAvailable on backorder
2,3-Dimethylmethcathinone (hydrochloride) is a potential designer drug with combined features of amphetamines, cathinones, and phenethylamines. It is structurally related to 4-methylmethcathinone, (Item No. 10801), a psychoactive compound that has been identified in products sold as bath salts and plant food.{19498,19499,19497} The physiological and toxicological properties of this compound have not been elucidated. This product is intended for research and forensic applications.
Brand:CaymanSKU:11225 - 5 mgAvailable on backorder
2,3-Dimethylmethcathinone (hydrochloride) is a potential designer drug with combined features of amphetamines, cathinones, and phenethylamines. It is structurally related to 4-methylmethcathinone, (Item No. 10801), a psychoactive compound that has been identified in products sold as bath salts and plant food.{19498,19499,19497} The physiological and toxicological properties of this compound have not been elucidated. This product is intended for research and forensic applications.
Brand:CaymanSKU:11225 - 50 mgAvailable on backorder
Prostaglandin E1 (PGE1) is not a major naturally occurring prostaglandin, but it is widely administered clinically for several indications including peripheral occlusive vascular disease, erectile dysfunction and in neonatal cardiology.{22,3803} The metabolism of PGE1 is normally initiated by oxidation at C-15, resulting in 13,14-dihydro-15-keto PGE1 as the major metabolite. However, inhibition of this pathway or saturation by excess substrate could theoretically lead to enhanced production of 2,3-dinor metabolites, including 2,3-dinor PGE1. The biological activity of 2,3-dinor PGE1 has not been published. Cayman Chemical is a leading supplier of prostaglandins and their metabolites, and is currently the exclusive manufacturer of 2,3-dinor PGE1.
Brand:CaymanSKU:-Prostaglandin E1 (PGE1) is not a major naturally occurring prostaglandin, but it is widely administered clinically for several indications including peripheral occlusive vascular disease, erectile dysfunction and in neonatal cardiology.{22,3803} The metabolism of PGE1 is normally initiated by oxidation at C-15, resulting in 13,14-dihydro-15-keto PGE1 as the major metabolite. However, inhibition of this pathway or saturation by excess substrate could theoretically lead to enhanced production of 2,3-dinor metabolites, including 2,3-dinor PGE1. The biological activity of 2,3-dinor PGE1 has not been published. Cayman Chemical is a leading supplier of prostaglandins and their metabolites, and is currently the exclusive manufacturer of 2,3-dinor PGE1.
Brand:CaymanSKU:-Prostaglandin E1 (PGE1) is not a major naturally occurring prostaglandin, but it is widely administered clinically for several indications including peripheral occlusive vascular disease, erectile dysfunction and in neonatal cardiology.{22,3803} The metabolism of PGE1 is normally initiated by oxidation at C-15, resulting in 13,14-dihydro-15-keto PGE1 as the major metabolite. However, inhibition of this pathway or saturation by excess substrate could theoretically lead to enhanced production of 2,3-dinor metabolites, including 2,3-dinor PGE1. The biological activity of 2,3-dinor PGE1 has not been published. Cayman Chemical is a leading supplier of prostaglandins and their metabolites, and is currently the exclusive manufacturer of 2,3-dinor PGE1.
Brand:CaymanSKU:-Thromboxane B2 (TXB2) is released in substantial quantities from aggregating platelets and metabolized during circulation to 11-dehydro TXB2 and 2,3-dinor TXB2.{1410} In rats and rabbits, 2,3-dinor TXB1 has been identified as another urinary metabolite of TXB2.{12600,12599} However in human urine, only trace amounts of 2,3-dinor TXB1 have been identified.{12600} In rats, 2,3-dinor TXB1 is excreted at a much higher rate than 2,3-dinor TXB2 (19.2 ± 4.9 ng/24 hr and 1.6 ± 0.3 ng/24 hr, respectively).{12600} Therefore, urinary 2,3-dinor TXB1 is a suitable marker of thromboxane biosynthesis in rats.
Brand:CaymanSKU:10006330 - 100 µgAvailable on backorder
Thromboxane B2 (TXB2) is released in substantial quantities from aggregating platelets and metabolized during circulation to 11-dehydro TXB2 and 2,3-dinor TXB2.{1410} In rats and rabbits, 2,3-dinor TXB1 has been identified as another urinary metabolite of TXB2.{12600,12599} However in human urine, only trace amounts of 2,3-dinor TXB1 have been identified.{12600} In rats, 2,3-dinor TXB1 is excreted at a much higher rate than 2,3-dinor TXB2 (19.2 ± 4.9 ng/24 hr and 1.6 ± 0.3 ng/24 hr, respectively).{12600} Therefore, urinary 2,3-dinor TXB1 is a suitable marker of thromboxane biosynthesis in rats.
Brand:CaymanSKU:10006330 - 25 µgAvailable on backorder
Thromboxane B2 (TXB2) is released in substantial quantities from aggregating platelets and metabolized during circulation to 11-dehydro TXB2 and 2,3-dinor TXB2.{1410} In rats and rabbits, 2,3-dinor TXB1 has been identified as another urinary metabolite of TXB2.{12600,12599} However in human urine, only trace amounts of 2,3-dinor TXB1 have been identified.{12600} In rats, 2,3-dinor TXB1 is excreted at a much higher rate than 2,3-dinor TXB2 (19.2 ± 4.9 ng/24 hr and 1.6 ± 0.3 ng/24 hr, respectively).{12600} Therefore, urinary 2,3-dinor TXB1 is a suitable marker of thromboxane biosynthesis in rats.
Brand:CaymanSKU:10006330 - 50 µgAvailable on backorder
Thromboxane B2 (TXB2) is released in substantial quantities from aggregating platelets and metabolized during circulation to 11-dehydro TXB2 and 2,3-dinor TXB2.{1410} 2,3-dinor TXB2 is an abundant urinary metabolite of TXB2 and can be used as a marker for in vivo TXA2 synthesis.{1410,629,717} In healthy male volunteers, the median excretion of 2,3-dinor TXB2 is 10.3 ng/hour (138 pg/mg creatine).{629}
Brand:CaymanSKU:-Available on backorder
Thromboxane B2 (TXB2) is released in substantial quantities from aggregating platelets and metabolized during circulation to 11-dehydro TXB2 and 2,3-dinor TXB2.{1410} 2,3-dinor TXB2 is an abundant urinary metabolite of TXB2 and can be used as a marker for in vivo TXA2 synthesis.{1410,629,717} In healthy male volunteers, the median excretion of 2,3-dinor TXB2 is 10.3 ng/hour (138 pg/mg creatine).{629}
Brand:CaymanSKU:-Available on backorder
Thromboxane B2 (TXB2) is released in substantial quantities from aggregating platelets and metabolized during circulation to 11-dehydro TXB2 and 2,3-dinor TXB2.{1410} 2,3-dinor TXB2 is an abundant urinary metabolite of TXB2 and can be used as a marker for in vivo TXA2 synthesis.{1410,629,717} In healthy male volunteers, the median excretion of 2,3-dinor TXB2 is 10.3 ng/hour (138 pg/mg creatine).{629}
Brand:CaymanSKU:-Available on backorder
Thromboxane B2 (TXB2) is released in substantial quantities from aggregating platelets and metabolized during circulation to 11-dehydro TXB2 and 2,3-dinor TXB2.{1410} 2,3-dinor TXB2 is an abundant urinary metabolite of TXB2 and can be used as a marker for in vivo TXA2 synthesis.{1410,629,717} In healthy male volunteers, the median excretion of 2,3-dinor TXB2 is 10.3 ng/hour (138 pg/mg creatine).{629}
Brand:CaymanSKU:-Available on backorder
2,3-dinor-11β-Prostaglandin F2α (2,3-dinor-11β-PGF2α) was recovered from the urine of both normal monkeys and humans when infused with radiolabeled PGD2, where it represented approximately 1% and 4% of the infused radiolabeled dose, respectively.{418} 2,3-dinor-11β-PGF2α has also been recovered from the urine of mastocytosis patients, where it is excreted in large amounts.{416} In human asthmatic patients, 2,3-dinor-11β-PGF2α represents about 40% (as determined by GC/MS) of the immunoreactive 11β-PGF2α when measured using Cayman’s 11β-PGF2α EIA Kit (Item No. 516521). The excretion rate for 2,3-dinor-11β-PGF2α is approximately 200-250 ng/24 hours in a normal adult.{7577}
Brand:CaymanSKU:-Out of stock
2,3-dinor-11β-Prostaglandin F2α (2,3-dinor-11β-PGF2α) was recovered from the urine of both normal monkeys and humans when infused with radiolabeled PGD2, where it represented approximately 1% and 4% of the infused radiolabeled dose, respectively.{418} 2,3-dinor-11β-PGF2α has also been recovered from the urine of mastocytosis patients, where it is excreted in large amounts.{416} In human asthmatic patients, 2,3-dinor-11β-PGF2α represents about 40% (as determined by GC/MS) of the immunoreactive 11β-PGF2α when measured using Cayman’s 11β-PGF2α EIA Kit (Item No. 516521). The excretion rate for 2,3-dinor-11β-PGF2α is approximately 200-250 ng/24 hours in a normal adult.{7577}
Brand:CaymanSKU:-Out of stock
2,3-dinor-11β-Prostaglandin F2α (2,3-dinor-11β-PGF2α) was recovered from the urine of both normal monkeys and humans when infused with radiolabeled PGD2, where it represented approximately 1% and 4% of the infused radiolabeled dose, respectively.{418} 2,3-dinor-11β-PGF2α has also been recovered from the urine of mastocytosis patients, where it is excreted in large amounts.{416} In human asthmatic patients, 2,3-dinor-11β-PGF2α represents about 40% (as determined by GC/MS) of the immunoreactive 11β-PGF2α when measured using Cayman’s 11β-PGF2α EIA Kit (Item No. 516521). The excretion rate for 2,3-dinor-11β-PGF2α is approximately 200-250 ng/24 hours in a normal adult.{7577}
Brand:CaymanSKU:-Out of stock
8-iso Prostaglandin F2α (8-iso PGF2α; 8-isoprostane) is a prostaglandin-like product of non-specific lipid peroxidation.{320} 2,3-dinor-8-iso PGF2α is a metabolite of 8-iso PGF2α in humans and rats.{6907} In these species, exogenously infused 8-iso PGF2α is converted to 2,3-dinor-8-iso PGF1α and (2,3-dinor-8-iso PGF2α.{6907,3026} Rat hepatocytes further metabolize 8-iso PGF2α to another β-oxidation product, 2,3,4,5-tetranor-8-iso PGF2α.{6907} 2,3-dinor-8-iso PGF2α is present in normal human urine at concentrations of 200-300 pg/ml.{6907} Its concentration is increased in conditions of oxidative injury (for example, smoking), and correlates well with that of the parent isoprostane, 8-iso PGF2α.{6907}
Brand:CaymanSKU:-8-iso Prostaglandin F2α (8-iso PGF2α; 8-isoprostane) is a prostaglandin-like product of non-specific lipid peroxidation.{320} 2,3-dinor-8-iso PGF2α is a metabolite of 8-iso PGF2α in humans and rats.{6907} In these species, exogenously infused 8-iso PGF2α is converted to 2,3-dinor-8-iso PGF1α and (2,3-dinor-8-iso PGF2α.{6907,3026} Rat hepatocytes further metabolize 8-iso PGF2α to another β-oxidation product, 2,3,4,5-tetranor-8-iso PGF2α.{6907} 2,3-dinor-8-iso PGF2α is present in normal human urine at concentrations of 200-300 pg/ml.{6907} Its concentration is increased in conditions of oxidative injury (for example, smoking), and correlates well with that of the parent isoprostane, 8-iso PGF2α.{6907}
Brand:CaymanSKU:-8-iso Prostaglandin F2α (8-iso PGF2α; 8-isoprostane) is a prostaglandin-like product of non-specific lipid peroxidation.{320} 2,3-dinor-8-iso PGF2α is a metabolite of 8-iso PGF2α in humans and rats.{6907} In these species, exogenously infused 8-iso PGF2α is converted to 2,3-dinor-8-iso PGF1α and (2,3-dinor-8-iso PGF2α.{6907,3026} Rat hepatocytes further metabolize 8-iso PGF2α to another β-oxidation product, 2,3,4,5-tetranor-8-iso PGF2α.{6907} 2,3-dinor-8-iso PGF2α is present in normal human urine at concentrations of 200-300 pg/ml.{6907} Its concentration is increased in conditions of oxidative injury (for example, smoking), and correlates well with that of the parent isoprostane, 8-iso PGF2α.{6907}
Brand:CaymanSKU:-2,3-Isopropylidene-D-ribonolactone is a building block.{46908} It has been used in the stereocontrolled synthesis of the carbohydrates 6-epi-trehazolin and 6-epi-trehalamine.
Brand:CaymanSKU:30479 - 1 gAvailable on backorder
2,3-Isopropylidene-D-ribonolactone is a building block.{46908} It has been used in the stereocontrolled synthesis of the carbohydrates 6-epi-trehazolin and 6-epi-trehalamine.
Brand:CaymanSKU:30479 - 500 mgAvailable on backorder
3,4-Methylenedioxyamphetamine (MDA) is psychedelic and entactogenic drug that is scheduled as a controlled substance in the United States.{21366} 2,3-MDA is a structural isomer of MDA which differs only in the placement of the methyledioxy group. The physiological and toxicological properties of this compound are not known. This product is intended for forensic and research applications.
Brand:CaymanSKU:-3,4-Methylenedioxyamphetamine (MDA) is psychedelic and entactogenic drug that is scheduled as a controlled substance in the United States.{21366} 2,3-MDA is a structural isomer of MDA which differs only in the placement of the methyledioxy group. The physiological and toxicological properties of this compound are not known. This product is intended for forensic and research applications.
Brand:CaymanSKU:-3,4-Methylenedioxyamphetamine (MDA) is psychedelic and entactogenic drug that is scheduled as a controlled substance in the United States.{21366} 2,3-MDA is a structural isomer of MDA which differs only in the placement of the methyledioxy group. The physiological and toxicological properties of this compound are not known. This product is intended for forensic and research applications.
Brand:CaymanSKU:-2,3-MDMA is an aromatic positional isomer of 3,4-MDMA (ecstasy, Item No. 13971), a euphoric entactogen that is illegal in most countries and is regulated (Schedule I) in the United States.{22085,21236} While 2,3-MDMA exhibits a similar potency to 3,4-MDMA for inhibition of the noradrenalin transporter (IC50s = 6.2 and 6.6 μM, respectively), it is less potent than 3,4-MDMA for inhibition of the serotonin transporter (IC50s = 82 μM and 34.8 μM, respectively).{20483} This compound is intended for forensic and research purposes only.
Brand:CaymanSKU:-2,3-MDMA is an aromatic positional isomer of 3,4-MDMA (ecstasy, Item No. 13971), a euphoric entactogen that is illegal in most countries and is regulated (Schedule I) in the United States.{22085,21236} While 2,3-MDMA exhibits a similar potency to 3,4-MDMA for inhibition of the noradrenalin transporter (IC50s = 6.2 and 6.6 μM, respectively), it is less potent than 3,4-MDMA for inhibition of the serotonin transporter (IC50s = 82 μM and 34.8 μM, respectively).{20483} This compound is intended for forensic and research purposes only.
Brand:CaymanSKU:-2,3-MDMA is an aromatic positional isomer of 3,4-MDMA (ecstasy, Item No. 13971), a euphoric entactogen that is illegal in most countries and is regulated (Schedule I) in the United States.{22085,21236} While 2,3-MDMA exhibits a similar potency to 3,4-MDMA for inhibition of the noradrenalin transporter (IC50s = 6.2 and 6.6 μM, respectively), it is less potent than 3,4-MDMA for inhibition of the serotonin transporter (IC50s = 82 μM and 34.8 μM, respectively).{20483} This compound is intended for forensic and research purposes only.
Brand:CaymanSKU:-2,3,3-Trimethylindolenine-5-sulfonic Acid is a water soluble, fluorescent near-infrared dye that can be conjugated to peptides, proteins, nucleic acids, RNA, DNA, carbohydrates, polymers, and small molecules via a sulfonyl substituent.{28772,28771}
Brand:CaymanSKU:-Available on backorder
2,3,3-Trimethylindolenine-5-sulfonic Acid is a water soluble, fluorescent near-infrared dye that can be conjugated to peptides, proteins, nucleic acids, RNA, DNA, carbohydrates, polymers, and small molecules via a sulfonyl substituent.{28772,28771}
Brand:CaymanSKU:-Available on backorder
2,3,3-Trimethylindolenine-5-sulfonic Acid is a water soluble, fluorescent near-infrared dye that can be conjugated to peptides, proteins, nucleic acids, RNA, DNA, carbohydrates, polymers, and small molecules via a sulfonyl substituent.{28772,28771}
Brand:CaymanSKU:-Available on backorder
2,3,3-Trimethylindolenine-5-sulfonic Acid is a water soluble, fluorescent near-infrared dye that can be conjugated to peptides, proteins, nucleic acids, RNA, DNA, carbohydrates, polymers, and small molecules via a sulfonyl substituent.{28772,28771}
Brand:CaymanSKU:-Available on backorder
2,3,4-Tri-O-acetyl-β-D-glucuronide methyl ester is a synthetic intermediate in the synthesis of prodrug forms of the antitumor antibiotic daunomycin (daunorubicin; Item No. 14159).{55086}
Brand:CaymanSKU:30540 - 1 gAvailable on backorder
2,3,4-Tri-O-acetyl-β-D-glucuronide methyl ester is a synthetic intermediate in the synthesis of prodrug forms of the antitumor antibiotic daunomycin (daunorubicin; Item No. 14159).{55086}
Brand:CaymanSKU:30540 - 100 mgAvailable on backorder
2,3,4-Tri-O-acetyl-β-D-glucuronide methyl ester is a synthetic intermediate in the synthesis of prodrug forms of the antitumor antibiotic daunomycin (daunorubicin; Item No. 14159).{55086}
Brand:CaymanSKU:30540 - 250 mgAvailable on backorder
2,3,4-Tri-O-acetyl-β-D-glucuronide methyl ester is a synthetic intermediate in the synthesis of prodrug forms of the antitumor antibiotic daunomycin (daunorubicin; Item No. 14159).{55086}
Brand:CaymanSKU:30540 - 500 mgAvailable on backorder
2,3,4-Trimethoxyamphetamine (hydrochloride) (Item No. 26491) is an analytical reference standard categorized as an amphetamine. It has hallucinogenic properties.{46060,49066} This product is intended for research and forensic applications.
Brand:CaymanSKU:26491 - 1 mgAvailable on backorder
2,3,4-Trimethoxyamphetamine (hydrochloride) (Item No. 26491) is an analytical reference standard categorized as an amphetamine. It has hallucinogenic properties.{46060,49066} This product is intended for research and forensic applications.
Brand:CaymanSKU:26491 - 5 mgAvailable on backorder
2,3,4,5-Tetrachlorophenol is a metabolite of the insecticide γ-lindane.{53465} It is toxic to fathead minnows and rainbow trout (LC50s = 0.496 and 0.304 mg/L, respectively, in tank water).{53466}
Brand:CaymanSKU:29743 - 100 mgAvailable on backorder
2,3,4,5-Tetrachlorophenol is a metabolite of the insecticide γ-lindane.{53465} It is toxic to fathead minnows and rainbow trout (LC50s = 0.496 and 0.304 mg/L, respectively, in tank water).{53466}
Brand:CaymanSKU:29743 - 25 mgAvailable on backorder
2,3,4,5-Tetrachlorophenol is a metabolite of the insecticide γ-lindane.{53465} It is toxic to fathead minnows and rainbow trout (LC50s = 0.496 and 0.304 mg/L, respectively, in tank water).{53466}
Brand:CaymanSKU:29743 - 50 mgAvailable on backorder
2,3,4,6-Tetra-O-benzoyl-β-D-glucopyranose is a D-glucopyranose derivative that has been used in glucosylation reactions.{33825,33826,33827,33828}
Brand:CaymanSKU:-Out of stock
2,3,4,6-Tetra-O-benzoyl-β-D-glucopyranose is a D-glucopyranose derivative that has been used in glucosylation reactions.{33825,33826,33827,33828}
Brand:CaymanSKU:-Out of stock
2,3,4,6-Tetra-O-benzoyl-β-D-glucopyranose is a D-glucopyranose derivative that has been used in glucosylation reactions.{33825,33826,33827,33828}
Brand:CaymanSKU:-Out of stock
2,3,5-Trimethoxyamphetamine (hydrochloride) (Item No. 25396) is an analytical reference standard categorized as an amphetamine. It has hallucinogenic, psychotomimetic, and stimulant properties.{46060,46061} This product is intended for research and forensic applications.
Brand:CaymanSKU:25396 - 1 mgAvailable on backorder
2,3,5-Trimethoxyamphetamine (hydrochloride) (Item No. 25396) is an analytical reference standard categorized as an amphetamine. It has hallucinogenic, psychotomimetic, and stimulant properties.{46060,46061} This product is intended for research and forensic applications.
Brand:CaymanSKU:25396 - 5 mgAvailable on backorder
2,3,5,6-Tetramethylpyrazine is an alkaloid that has been found in L. wallichii and has diverse biological activities.{54098,54099,54100} It reduces kainate-induced increases in production of reactive oxygen species (ROS) and cytotoxicity in primary rat hippocampal neurons when used at a concentration of 5 µM.{54098} 2,3,5,6-Tetramethylpyrazine (0.1 mM) induces vasodilation in precontracted isolated and endothelium-denuded rat tail artery strips and reduces blood pressure in anesthetized rats.{54099} It decreases infarct volume, caspase-3 activation, and hypoxia-inducible factor-1α (HIF-1α) levels in a rat model of focal cerebral ischemia induced by middle cerebral artery occlusion (MCAO) when administered at a dose of 20 mg/kg.{54100}
Brand:CaymanSKU:30281 - 100 gAvailable on backorder
2,3,5,6-Tetramethylpyrazine is an alkaloid that has been found in L. wallichii and has diverse biological activities.{54098,54099,54100} It reduces kainate-induced increases in production of reactive oxygen species (ROS) and cytotoxicity in primary rat hippocampal neurons when used at a concentration of 5 µM.{54098} 2,3,5,6-Tetramethylpyrazine (0.1 mM) induces vasodilation in precontracted isolated and endothelium-denuded rat tail artery strips and reduces blood pressure in anesthetized rats.{54099} It decreases infarct volume, caspase-3 activation, and hypoxia-inducible factor-1α (HIF-1α) levels in a rat model of focal cerebral ischemia induced by middle cerebral artery occlusion (MCAO) when administered at a dose of 20 mg/kg.{54100}
Brand:CaymanSKU:30281 - 25 gAvailable on backorder
2,3,5,6-Tetramethylpyrazine is an alkaloid that has been found in L. wallichii and has diverse biological activities.{54098,54099,54100} It reduces kainate-induced increases in production of reactive oxygen species (ROS) and cytotoxicity in primary rat hippocampal neurons when used at a concentration of 5 µM.{54098} 2,3,5,6-Tetramethylpyrazine (0.1 mM) induces vasodilation in precontracted isolated and endothelium-denuded rat tail artery strips and reduces blood pressure in anesthetized rats.{54099} It decreases infarct volume, caspase-3 activation, and hypoxia-inducible factor-1α (HIF-1α) levels in a rat model of focal cerebral ischemia induced by middle cerebral artery occlusion (MCAO) when administered at a dose of 20 mg/kg.{54100}
Brand:CaymanSKU:30281 - 50 gAvailable on backorder
2,3,5,6-Tetramethylpyrazine is an alkaloid that has been found in L. wallichii and has diverse biological activities.{54098,54099,54100} It reduces kainate-induced increases in production of reactive oxygen species (ROS) and cytotoxicity in primary rat hippocampal neurons when used at a concentration of 5 µM.{54098} 2,3,5,6-Tetramethylpyrazine (0.1 mM) induces vasodilation in precontracted isolated and endothelium-denuded rat tail artery strips and reduces blood pressure in anesthetized rats.{54099} It decreases infarct volume, caspase-3 activation, and hypoxia-inducible factor-1α (HIF-1α) levels in a rat model of focal cerebral ischemia induced by middle cerebral artery occlusion (MCAO) when administered at a dose of 20 mg/kg.{54100}
Brand:CaymanSKU:30281 - 500 gAvailable on backorder
2,3,6-Trimethoxyamphetamine (hydrochloride) (Item No. 26492) is an analytical reference standard categorized as an amphetamine.{46061} 2,3,6-Trimethoxyamphetamine has hallucinogenic properties.{23274,45177} This product is intended for research and forensic applications.
Brand:CaymanSKU:26492 - 1 mgAvailable on backorder
2,3,6-Trimethoxyamphetamine (hydrochloride) (Item No. 26492) is an analytical reference standard categorized as an amphetamine.{46061} 2,3,6-Trimethoxyamphetamine has hallucinogenic properties.{23274,45177} This product is intended for research and forensic applications.
Brand:CaymanSKU:26492 - 5 mgAvailable on backorder
2,4-Diacetylphloroglucinol is a non-nitrogen-containing compound produced by some isolates of P. fluorescens and is active against numerous plant pathogenic fungi, viruses, bacteria, and nematodes.{29713,29711} It has been used to increase crop yield by controlling plant root diseases.{29713,29711}
Brand:CaymanSKU:-Out of stock
2,4-Diacetylphloroglucinol is a non-nitrogen-containing compound produced by some isolates of P. fluorescens and is active against numerous plant pathogenic fungi, viruses, bacteria, and nematodes.{29713,29711} It has been used to increase crop yield by controlling plant root diseases.{29713,29711}
Brand:CaymanSKU:-Out of stock
2,4-Diacetylphloroglucinol is a non-nitrogen-containing compound produced by some isolates of P. fluorescens and is active against numerous plant pathogenic fungi, viruses, bacteria, and nematodes.{29713,29711} It has been used to increase crop yield by controlling plant root diseases.{29713,29711}
Brand:CaymanSKU:-Out of stock
2,4-Diamino-6-hydroxypyrimidine (DAHP) is a selective, specific inhibitor of GTP cyclohydrolase I, the rate limiting step for de novo pterin synthesis. In HUVEC cells, the IC50 for inhibition of BH4 biosynthesis is about 0.3 mM. DAHP can be used to effectively block NO production in several cell types.{1910,1263,1387}
Brand:CaymanSKU:81260 - 1 gAvailable on backorder
2,4-Diamino-6-hydroxypyrimidine (DAHP) is a selective, specific inhibitor of GTP cyclohydrolase I, the rate limiting step for de novo pterin synthesis. In HUVEC cells, the IC50 for inhibition of BH4 biosynthesis is about 0.3 mM. DAHP can be used to effectively block NO production in several cell types.{1910,1263,1387}
Brand:CaymanSKU:81260 - 10 gAvailable on backorder
2,4-Diamino-6-hydroxypyrimidine (DAHP) is a selective, specific inhibitor of GTP cyclohydrolase I, the rate limiting step for de novo pterin synthesis. In HUVEC cells, the IC50 for inhibition of BH4 biosynthesis is about 0.3 mM. DAHP can be used to effectively block NO production in several cell types.{1910,1263,1387}
Brand:CaymanSKU:81260 - 25 gAvailable on backorder
2,4-Diamino-6-hydroxypyrimidine (DAHP) is a selective, specific inhibitor of GTP cyclohydrolase I, the rate limiting step for de novo pterin synthesis. In HUVEC cells, the IC50 for inhibition of BH4 biosynthesis is about 0.3 mM. DAHP can be used to effectively block NO production in several cell types.{1910,1263,1387}
Brand:CaymanSKU:81260 - 5 gAvailable on backorder
2,4-Dichlorobenzenesulfonyl chloride is a heterocyclic building block.{52643} It has been used in the synthesis of nicotinyl arylsulfonylhydrazides that have anticancer and antibacterial activities in vitro.
Brand:CaymanSKU:30450 - 1 gAvailable on backorder
2,4-Dichlorobenzenesulfonyl chloride is a heterocyclic building block.{52643} It has been used in the synthesis of nicotinyl arylsulfonylhydrazides that have anticancer and antibacterial activities in vitro.
Brand:CaymanSKU:30450 - 5 gAvailable on backorder
2,4-Dichlorophenoxy acetic acid is a synthetic auxin, a class of plant growth regulators, that is often used as a supplement in plant cell culture media. It is also an active ingredient in herbicides that controls root elongation and cell production by disrupting the actin cytoskeleton.{16947}
Brand:CaymanSKU:10190 - 100 mgAvailable on backorder
2,4-Dichlorophenoxy acetic acid is a synthetic auxin, a class of plant growth regulators, that is often used as a supplement in plant cell culture media. It is also an active ingredient in herbicides that controls root elongation and cell production by disrupting the actin cytoskeleton.{16947}
Brand:CaymanSKU:10190 - 50 mgAvailable on backorder
2,4-Dimethylthiazole-5-carboxylic acid is a highly functionalized and biased thiazole used for drug discovery. It is used as a heterocyclic building block to specifically modify lead compounds.
Brand:CaymanSKU:-2,4-Dimethylthiazole-5-carboxylic acid is a highly functionalized and biased thiazole used for drug discovery. It is used as a heterocyclic building block to specifically modify lead compounds.
Brand:CaymanSKU:-2,4-Dimethylthiazole-5-carboxylic acid is a highly functionalized and biased thiazole used for drug discovery. It is used as a heterocyclic building block to specifically modify lead compounds.
Brand:CaymanSKU:-2,4-Dimethylthiazole-5-carboxylic acid is a highly functionalized and biased thiazole used for drug discovery. It is used as a heterocyclic building block to specifically modify lead compounds.
Brand:CaymanSKU:-2,4-DMA (hydrochloride) (Item No. 19746) is an analytical reference standard that is classified as an amphetamine. It is a serotonin 5-HT2 receptor agonist with an apparent pA2 value of 5.6.{31587} This product is intended for research and forensic applications.
Brand:CaymanSKU:19746 -Available on backorder
2,4-DMA (hydrochloride) (Item No. 19746) is an analytical reference standard that is classified as an amphetamine. It is a serotonin 5-HT2 receptor agonist with an apparent pA2 value of 5.6.{31587} This product is intended for research and forensic applications.
Brand:CaymanSKU:19746 -Available on backorder
The pro-angiogenic factor HIF-1α is targeted for destruction in normoxic environments by the hydroxylation of a specific proline residue, P564, by the oxygen-sensing enzyme HIF-α prolyl hydroxylase (HIF-PH).{8840} 2,4-DPD is a cell permeable, competitive inhibitor of HIF-PH. 2,4-DPD inhibits the hydroxylation of P564 by acting as a competitive inhibitor of the HIF-PH cofactor α-keto glutarate, with effective concentrations in the low µM range.{9005} 2,4-DPD is therefore expected to act as a pro-angiogenic compound, via the HIF-1α system.{9790,8799}
Brand:CaymanSKU:71200 - 10 mgAvailable on backorder
The pro-angiogenic factor HIF-1α is targeted for destruction in normoxic environments by the hydroxylation of a specific proline residue, P564, by the oxygen-sensing enzyme HIF-α prolyl hydroxylase (HIF-PH).{8840} 2,4-DPD is a cell permeable, competitive inhibitor of HIF-PH. 2,4-DPD inhibits the hydroxylation of P564 by acting as a competitive inhibitor of the HIF-PH cofactor α-keto glutarate, with effective concentrations in the low µM range.{9005} 2,4-DPD is therefore expected to act as a pro-angiogenic compound, via the HIF-1α system.{9790,8799}
Brand:CaymanSKU:71200 - 100 mgAvailable on backorder
The pro-angiogenic factor HIF-1α is targeted for destruction in normoxic environments by the hydroxylation of a specific proline residue, P564, by the oxygen-sensing enzyme HIF-α prolyl hydroxylase (HIF-PH).{8840} 2,4-DPD is a cell permeable, competitive inhibitor of HIF-PH. 2,4-DPD inhibits the hydroxylation of P564 by acting as a competitive inhibitor of the HIF-PH cofactor α-keto glutarate, with effective concentrations in the low µM range.{9005} 2,4-DPD is therefore expected to act as a pro-angiogenic compound, via the HIF-1α system.{9790,8799}
Brand:CaymanSKU:71200 - 25 mgAvailable on backorder
The pro-angiogenic factor HIF-1α is targeted for destruction in normoxic environments by the hydroxylation of a specific proline residue, P564, by the oxygen-sensing enzyme HIF-α prolyl hydroxylase (HIF-PH).{8840} 2,4-DPD is a cell permeable, competitive inhibitor of HIF-PH. 2,4-DPD inhibits the hydroxylation of P564 by acting as a competitive inhibitor of the HIF-PH cofactor α-keto glutarate, with effective concentrations in the low µM range.{9005} 2,4-DPD is therefore expected to act as a pro-angiogenic compound, via the HIF-1α system.{9790,8799}
Brand:CaymanSKU:71200 - 50 mgAvailable on backorder