Chemicals
Showing 40951–41100 of 41137 results
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Hydrogen sulfide (H2S) is a naturally-occurring gasotransmitter with vasodilator and inflammatory modulating activity.{15636,13678} H2S is synthesized naturally in a range of mammalian tissues principally by the activity of two enzymes, cystathionine γ lyase (CSE) and cystathionine β synthetase (CBS). β-cyano-L-Alanine (BCA) is a reversible inhibitor of the H2S-synthesizing enzyme CSE.{16454} BCA blocks H2S synthesis in rat liver preparations with an IC50 value of 6.5 µM and increases blood pressure in anaesthetized rats induced with hemorrhagic shock by inhibiting endogenous H2S synthesis.{16094} BCA at 50 mg/kg blocked both L-cysteine- and LPS-induced hyperalgesia in rats.{16455}
Brand:CaymanSKU:10010947 - 10 mgAvailable on backorder
Hydrogen sulfide (H2S) is a naturally-occurring gasotransmitter with vasodilator and inflammatory modulating activity.{15636,13678} H2S is synthesized naturally in a range of mammalian tissues principally by the activity of two enzymes, cystathionine γ lyase (CSE) and cystathionine β synthetase (CBS). β-cyano-L-Alanine (BCA) is a reversible inhibitor of the H2S-synthesizing enzyme CSE.{16454} BCA blocks H2S synthesis in rat liver preparations with an IC50 value of 6.5 µM and increases blood pressure in anaesthetized rats induced with hemorrhagic shock by inhibiting endogenous H2S synthesis.{16094} BCA at 50 mg/kg blocked both L-cysteine- and LPS-induced hyperalgesia in rats.{16455}
Brand:CaymanSKU:10010947 - 100 mgAvailable on backorder
Hydrogen sulfide (H2S) is a naturally-occurring gasotransmitter with vasodilator and inflammatory modulating activity.{15636,13678} H2S is synthesized naturally in a range of mammalian tissues principally by the activity of two enzymes, cystathionine γ lyase (CSE) and cystathionine β synthetase (CBS). β-cyano-L-Alanine (BCA) is a reversible inhibitor of the H2S-synthesizing enzyme CSE.{16454} BCA blocks H2S synthesis in rat liver preparations with an IC50 value of 6.5 µM and increases blood pressure in anaesthetized rats induced with hemorrhagic shock by inhibiting endogenous H2S synthesis.{16094} BCA at 50 mg/kg blocked both L-cysteine- and LPS-induced hyperalgesia in rats.{16455}
Brand:CaymanSKU:10010947 - 250 mgAvailable on backorder
Hydrogen sulfide (H2S) is a naturally-occurring gasotransmitter with vasodilator and inflammatory modulating activity.{15636,13678} H2S is synthesized naturally in a range of mammalian tissues principally by the activity of two enzymes, cystathionine γ lyase (CSE) and cystathionine β synthetase (CBS). β-cyano-L-Alanine (BCA) is a reversible inhibitor of the H2S-synthesizing enzyme CSE.{16454} BCA blocks H2S synthesis in rat liver preparations with an IC50 value of 6.5 µM and increases blood pressure in anaesthetized rats induced with hemorrhagic shock by inhibiting endogenous H2S synthesis.{16094} BCA at 50 mg/kg blocked both L-cysteine- and LPS-induced hyperalgesia in rats.{16455}
Brand:CaymanSKU:10010947 - 50 mgAvailable on backorder
β-Cyclodextrin (β-CD) is a cyclic oligosaccharide that contains seven D-(+)-glucopyranose units and has been used to improve the aqueous solubility of various compounds, especially those containing a phenyl group.{26620,26432} The circular arrangement of its glucose units produces a torus-shaped ring configuration in which the CH2 groups and ether linkages of the molecule face the hollow interior, resulting in a nonpolar, hydrophobic cavity and a polar, hydrophilic exterior. When combined in solution with other compounds, the nonpolar aromatic portions of that compound interact with the nonpolar interior of the β-CD molecule, thus isolating the aromatic portion of the molecule from the water and thereby increasing its aqueous solubility.{26620,21228}
Brand:CaymanSKU:23387 - 100 gAvailable on backorder
β-Cyclodextrin (β-CD) is a cyclic oligosaccharide that contains seven D-(+)-glucopyranose units and has been used to improve the aqueous solubility of various compounds, especially those containing a phenyl group.{26620,26432} The circular arrangement of its glucose units produces a torus-shaped ring configuration in which the CH2 groups and ether linkages of the molecule face the hollow interior, resulting in a nonpolar, hydrophobic cavity and a polar, hydrophilic exterior. When combined in solution with other compounds, the nonpolar aromatic portions of that compound interact with the nonpolar interior of the β-CD molecule, thus isolating the aromatic portion of the molecule from the water and thereby increasing its aqueous solubility.{26620,21228}
Brand:CaymanSKU:23387 - 25 gAvailable on backorder
β-Cyclodextrin (β-CD) is a cyclic oligosaccharide that contains seven D-(+)-glucopyranose units and has been used to improve the aqueous solubility of various compounds, especially those containing a phenyl group.{26620,26432} The circular arrangement of its glucose units produces a torus-shaped ring configuration in which the CH2 groups and ether linkages of the molecule face the hollow interior, resulting in a nonpolar, hydrophobic cavity and a polar, hydrophilic exterior. When combined in solution with other compounds, the nonpolar aromatic portions of that compound interact with the nonpolar interior of the β-CD molecule, thus isolating the aromatic portion of the molecule from the water and thereby increasing its aqueous solubility.{26620,21228}
Brand:CaymanSKU:23387 - 50 gAvailable on backorder
β-D-Glucosamine pentaacetate is an N-acetylglucosamine derivative that has been shown to promote hyaluronic acid production.{29024,29025}
Brand:CaymanSKU:-Available on backorder
β-D-Glucosamine pentaacetate is an N-acetylglucosamine derivative that has been shown to promote hyaluronic acid production.{29024,29025}
Brand:CaymanSKU:-Available on backorder
β-D-Glucosamine pentaacetate is an N-acetylglucosamine derivative that has been shown to promote hyaluronic acid production.{29024,29025}
Brand:CaymanSKU:-Available on backorder
D-Glucose, a naturally occurring monosaccharide found in plants, is the primary energy source for living organisms.{14802} It is utilized as a metabolic intermediate by cells for either aerobic or anaerobic respiration. D-Glucose exists in two cyclic forms, α-D-glucose and β-D-glucose, based on the position of the substituent at the anomeric center.{19676} α-D-Glucose is the monomer unit in starch, whereas β-D-glucose is the monomer unit in cellulose.{19676} When one of these anomers is added to solution, it undergoes reversible epimerization to the other via an open-chain form, during which the specific rotation of the solution changes gradually until it reaches equilibrium. The existence of multiple binding modes of this single monosaccharide has been studied as a model scaffold to design compounds with increased probability of ligand binding.{27288}
Brand:CaymanSKU:-Out of stock
D-Glucose, a naturally occurring monosaccharide found in plants, is the primary energy source for living organisms.{14802} It is utilized as a metabolic intermediate by cells for either aerobic or anaerobic respiration. D-Glucose exists in two cyclic forms, α-D-glucose and β-D-glucose, based on the position of the substituent at the anomeric center.{19676} α-D-Glucose is the monomer unit in starch, whereas β-D-glucose is the monomer unit in cellulose.{19676} When one of these anomers is added to solution, it undergoes reversible epimerization to the other via an open-chain form, during which the specific rotation of the solution changes gradually until it reaches equilibrium. The existence of multiple binding modes of this single monosaccharide has been studied as a model scaffold to design compounds with increased probability of ligand binding.{27288}
Brand:CaymanSKU:-Out of stock
β-D-Ribofuranose 1,2,3,4-tetraacetate is a precursor in the synthesis of nucleosides with antiproliferative activity against cancer cells.{46967,46968}
Brand:CaymanSKU:30408 - 10 gAvailable on backorder
β-D-Ribofuranose 1,2,3,4-tetraacetate is a precursor in the synthesis of nucleosides with antiproliferative activity against cancer cells.{46967,46968}
Brand:CaymanSKU:30408 - 25 gAvailable on backorder
β-D-Ribofuranose 1,2,3,4-tetraacetate is a precursor in the synthesis of nucleosides with antiproliferative activity against cancer cells.{46967,46968}
Brand:CaymanSKU:30408 - 5 gAvailable on backorder
β-D-Ribofuranose 1,2,3,4-tetraacetate is a precursor in the synthesis of nucleosides with antiproliferative activity against cancer cells.{46967,46968}
Brand:CaymanSKU:30408 - 50 gAvailable on backorder
β-Defensin-4 is a peptide with antimicrobial properties that protects the skin and mucosal membranes of the respiratory, genitourinary, and gastrointestinal tracts.{41472} It induces migration of monocytes in vitro when used at a concentration of 10 nM but does not affect migration of neutrophils and eosinophils.{38795} β-Defensin-4 (30 μg/ml) stimulates gene expression and production of IL-6, IL-10, CXCL10, CCL2, MIP-3α, and RANTES by keratinocytes.{38796} It also stimulates calcium mobilization, migration, and proliferation of keratinocytes when used at concentrations of 30, 10, and 40 μg/ml, respectively. β-Defensin-4 induces IL-31 production by human peripheral blood-derived mast cells in vitro when used at a concentration of 10 μg/ml and by rat mast cells in vivo following a 500 ng intradermal dose.{38797} It also inhibits growth of E. coli, P. aeruginosa, and S. aureus with lethal concentration (LC) values of 5, 12, and 15 μM, respectively, of S. carnosus (MIC = 4.5 μg/ml), and of C. albicans with a minimum fungicidal concentration (MFC) value of 7.5 μM.{38795,38798}
Brand:CaymanSKU:24579 - 100 µgAvailable on backorder
β-Elemene is a monoterpene that has been found in C. sativa.{42314} It is intended for use as an analytical standard for the detection of β-elemene by GC- or LC-MS.
Brand:CaymanSKU:19641 -Available on backorder
β-Elemene is a monoterpene that has been found in C. sativa.{42314} It is intended for use as an analytical standard for the detection of β-elemene by GC- or LC-MS.
Brand:CaymanSKU:19641 -Available on backorder
β-Elemene is a monoterpene that has been found in C. sativa.{42314} It is intended for use as an analytical standard for the detection of β-elemene by GC- or LC-MS.
Brand:CaymanSKU:19641 -Available on backorder
β-Elemene is a monoterpene that has been found in C. sativa.{42314} It is intended for use as an analytical standard for the detection of β-elemene by GC- or LC-MS.
Brand:CaymanSKU:19641 -Available on backorder
β-Elemonic acid is a triterpene isolated from Boswellia (Burseraceae) that exhibits anticancer activity.{35033,35034} It inhibits growth of non-small cell lung cancer (NSCLC) A549 cells (IC50 = 6.92 µM) in vitro.{35034} β-Elemonic acid induces apoptosis and cytotoxicity in A549 cells in a dose-dependent manner but has no effect on normal epithelial WI-38 cells. It inhibits phosphorylation of p42/44, MAPK/JNK, and p38 and induces production of reactive oxygen species (ROS) and COX-2 expression in vitro. β-Elemonic acid also inhibits prolyl endopeptidase (IC50 = 39.74 µM) in vitro.{35033}
Brand:CaymanSKU:11712 - 1 mgAvailable on backorder
β-Elemonic acid is a triterpene isolated from Boswellia (Burseraceae) that exhibits anticancer activity.{35033,35034} It inhibits growth of non-small cell lung cancer (NSCLC) A549 cells (IC50 = 6.92 µM) in vitro.{35034} β-Elemonic acid induces apoptosis and cytotoxicity in A549 cells in a dose-dependent manner but has no effect on normal epithelial WI-38 cells. It inhibits phosphorylation of p42/44, MAPK/JNK, and p38 and induces production of reactive oxygen species (ROS) and COX-2 expression in vitro. β-Elemonic acid also inhibits prolyl endopeptidase (IC50 = 39.74 µM) in vitro.{35033}
Brand:CaymanSKU:11712 - 10 mgAvailable on backorder
β-Elemonic acid is a triterpene isolated from Boswellia (Burseraceae) that exhibits anticancer activity.{35033,35034} It inhibits growth of non-small cell lung cancer (NSCLC) A549 cells (IC50 = 6.92 µM) in vitro.{35034} β-Elemonic acid induces apoptosis and cytotoxicity in A549 cells in a dose-dependent manner but has no effect on normal epithelial WI-38 cells. It inhibits phosphorylation of p42/44, MAPK/JNK, and p38 and induces production of reactive oxygen species (ROS) and COX-2 expression in vitro. β-Elemonic acid also inhibits prolyl endopeptidase (IC50 = 39.74 µM) in vitro.{35033}
Brand:CaymanSKU:11712 - 25 mgAvailable on backorder
β-Elemonic acid is a triterpene isolated from Boswellia (Burseraceae) that exhibits anticancer activity.{35033,35034} It inhibits growth of non-small cell lung cancer (NSCLC) A549 cells (IC50 = 6.92 µM) in vitro.{35034} β-Elemonic acid induces apoptosis and cytotoxicity in A549 cells in a dose-dependent manner but has no effect on normal epithelial WI-38 cells. It inhibits phosphorylation of p42/44, MAPK/JNK, and p38 and induces production of reactive oxygen species (ROS) and COX-2 expression in vitro. β-Elemonic acid also inhibits prolyl endopeptidase (IC50 = 39.74 µM) in vitro.{35033}
Brand:CaymanSKU:11712 - 5 mgAvailable on backorder
β-Endorphin (β-EP) is an endogenous opioid neuropeptide with diverse biological activities.{37350} It is produced via piomelanocortin cleavage in the pituitary gland, hypothalamus, and in lymphocytes, then migrates to its sites of action which include plasma, gut, skin, placenta, cerebrospinal fluid, and cardiac tissues. β-EP induces concentration-dependent decreases in electrically stimulated contraction of the mouse vas deferens that can be reversed by the μ-opioid antagonist CTP and Δ-opioid antagonist ICI 174,864.{37351} In vivo, β-EP (5 μg, i.c.v.) slows gastrointestinal transit in mice. β-EP (0.5 or 5 μg, i.c.v.) stimulates food intake in rats for 4 to 6 hours, however, this effect is not prolonged with continuous infusion.{37352} It antagonizes the appetite-suppressive effects of α-melanocyte-stimulating hormone (α-MSH) for the first three days post administration. β-EP also reduces paralytic demyelination induced by the murine coronavirus MHV-JHM in immunocompetent, but not irradiated or immune-incompetent, mice and rats.{37353}
Brand:CaymanSKU:24153 - 500 µgAvailable on backorder
β-Estradiol 17-valerate is a synthetic estrogen. Formulations containing β-Estradiol 17-valerate in combination with dienogest (Item No. 21257) have been used to treat endometriosis.{37057} Clinical trials have shown improvement in pelvic pain and quality of life as well as reduced dysmenorrhea and bleeding following β-Estradiol 17-valerate administration.{37057},{37058} Formulations containing β-Estradiol 17-valerate have also been used in hormone replacement therapy post oophorectomy as they do not activate the renin-angiotensin system, thereby preventing cardiac hypertension often associated with synthetic estrogen therapies.{37059}
Brand:CaymanSKU:22221 -Out of stock
β-Estradiol 17-valerate is a synthetic estrogen. Formulations containing β-Estradiol 17-valerate in combination with dienogest (Item No. 21257) have been used to treat endometriosis.{37057} Clinical trials have shown improvement in pelvic pain and quality of life as well as reduced dysmenorrhea and bleeding following β-Estradiol 17-valerate administration.{37057},{37058} Formulations containing β-Estradiol 17-valerate have also been used in hormone replacement therapy post oophorectomy as they do not activate the renin-angiotensin system, thereby preventing cardiac hypertension often associated with synthetic estrogen therapies.{37059}
Brand:CaymanSKU:22221 -Out of stock
β-Estradiol 17-valerate is a synthetic estrogen. Formulations containing β-Estradiol 17-valerate in combination with dienogest (Item No. 21257) have been used to treat endometriosis.{37057} Clinical trials have shown improvement in pelvic pain and quality of life as well as reduced dysmenorrhea and bleeding following β-Estradiol 17-valerate administration.{37057},{37058} Formulations containing β-Estradiol 17-valerate have also been used in hormone replacement therapy post oophorectomy as they do not activate the renin-angiotensin system, thereby preventing cardiac hypertension often associated with synthetic estrogen therapies.{37059}
Brand:CaymanSKU:22221 -Out of stock
β-Eudesmol is a sesquiterpene that has been found in a variety of plants, including Cannabis, and has diverse biological activities.{42303,36865} It is a noncompetitive antagonist of nicotinic acetylcholine receptors (nAChRs) that decreases the open time and opening frequency of nAChR channels when used at concentrations of 40 and 80 µM and increases the decay phase of depolarization when used at a concentration of 100 µM in isolated mouse diaphragm muscle.{36866} β-Eudesmol (50-100 µM) inhibits VEGF- and bFGF-induced proliferation in human umbilical vein endothelial cells (HUVECs).{36867} It also inhibits proliferation of HeLa, SGC-7901, and BEL-7402 cells when used at concentrations ranging from 10 to 100 µM and reduces tumor growth in H22 and S-180 mouse tumor models when administered at doses ranging from 2.5 to 5 mg/kg. β-Eudesmol is an agonist of the transient receptor potential (TRP) receptor subtypes TRPA1, TRPV3, and TRPM8 and increases food intake and plasma levels of ghrelin in rats.{36868,36869}
Brand:CaymanSKU:25771 - 1 mgAvailable on backorder
β-Eudesmol is a sesquiterpene that has been found in a variety of plants, including Cannabis, and has diverse biological activities.{42303,36865} It is a noncompetitive antagonist of nicotinic acetylcholine receptors (nAChRs) that decreases the open time and opening frequency of nAChR channels when used at concentrations of 40 and 80 µM and increases the decay phase of depolarization when used at a concentration of 100 µM in isolated mouse diaphragm muscle.{36866} β-Eudesmol (50-100 µM) inhibits VEGF- and bFGF-induced proliferation in human umbilical vein endothelial cells (HUVECs).{36867} It also inhibits proliferation of HeLa, SGC-7901, and BEL-7402 cells when used at concentrations ranging from 10 to 100 µM and reduces tumor growth in H22 and S-180 mouse tumor models when administered at doses ranging from 2.5 to 5 mg/kg. β-Eudesmol is an agonist of the transient receptor potential (TRP) receptor subtypes TRPA1, TRPV3, and TRPM8 and increases food intake and plasma levels of ghrelin in rats.{36868,36869}
Brand:CaymanSKU:25771 - 500 µgAvailable on backorder
β-Gal-NONOate is a nitric oxide (NO) donor which releases NO following activation by β-galactosidase.{9700} β-Gal-NONOate is stabile in aqueous solution at neutral and acidic pH for several hours, exhibits good water solubility, and is able to cross the cell membrane. Following enzymatic hydrolysis, β-Gal-NONOate decomposes with a half-life of six minutes at pH 5.6.{9700} β-Gal-NONOate is cytotoxic to a number of cancer cell-lines and exhibits high bactericidal activity against E. coli transformed with the β-galactosidase gene.{9700,14266}
Brand:CaymanSKU:10009137 - 1 mgAvailable on backorder
β-Gal-NONOate is a nitric oxide (NO) donor which releases NO following activation by β-galactosidase.{9700} β-Gal-NONOate is stabile in aqueous solution at neutral and acidic pH for several hours, exhibits good water solubility, and is able to cross the cell membrane. Following enzymatic hydrolysis, β-Gal-NONOate decomposes with a half-life of six minutes at pH 5.6.{9700} β-Gal-NONOate is cytotoxic to a number of cancer cell-lines and exhibits high bactericidal activity against E. coli transformed with the β-galactosidase gene.{9700,14266}
Brand:CaymanSKU:10009137 - 10 mgAvailable on backorder
β-Gal-NONOate is a nitric oxide (NO) donor which releases NO following activation by β-galactosidase.{9700} β-Gal-NONOate is stabile in aqueous solution at neutral and acidic pH for several hours, exhibits good water solubility, and is able to cross the cell membrane. Following enzymatic hydrolysis, β-Gal-NONOate decomposes with a half-life of six minutes at pH 5.6.{9700} β-Gal-NONOate is cytotoxic to a number of cancer cell-lines and exhibits high bactericidal activity against E. coli transformed with the β-galactosidase gene.{9700,14266}
Brand:CaymanSKU:10009137 - 5 mgAvailable on backorder
β-Glycerophosphate is a protein phosphatase inhibitor that acts as a phosphate group donor in matrix mineralization studies.{22569,22570,22571} It promotes bone matrix mineralization when delivered to osteoblasts by providing a source of phosphate ions.{22569} β-Glycerophosphate (10 mM) accelerates calcification of cultured vascular smooth muscle cells through an alkaline phosphatase-related mechanism.{22568}
Brand:CaymanSKU:- β-Glycerophosphate is a protein phosphatase inhibitor that acts as a phosphate group donor in matrix mineralization studies.{22569,22570,22571} It promotes bone matrix mineralization when delivered to osteoblasts by providing a source of phosphate ions.{22569} β-Glycerophosphate (10 mM) accelerates calcification of cultured vascular smooth muscle cells through an alkaline phosphatase-related mechanism.{22568}
Brand:CaymanSKU:-
β-hydroxy 2C-B (hydrochloride) (Item No. 30520) is an analytical reference standard categorized as a phenethylamine. This product is intended for research and forensic applications.
Brand:CaymanSKU:30520 - 1 mgAvailable on backorder
β-hydroxy 2C-B (hydrochloride) (Item No. 30520) is an analytical reference standard categorized as a phenethylamine. This product is intended for research and forensic applications.
Brand:CaymanSKU:30520 - 5 mgAvailable on backorder
β-L-Gulopyranosyl-caldarchaetidyl-glycerol is the main polar lipid of the archaeon T. acidophilum.{42663} Cellular levels of β-L-gulopyranosyl-caldarchaetidyl-glycerol in T. acidophilum HO-62 positively and negatively correlate with increases in culture pH and temperature, respectively. β-L-gulopyranosyl-caldarchaetidyl-glycerol has been used as a standard for the quantification of polar lipids extracted from T. acidophilum HO-62. [Matreya, LLC. Catalog No. 1303]
Brand:CaymanSKU:27203 - 1 mgAvailable on backorder
β-L-Gulopyranosyl-caldarchaetidyl-glycerol is the main polar lipid of the archaeon T. acidophilum.{42663} Cellular levels of β-L-gulopyranosyl-caldarchaetidyl-glycerol in T. acidophilum HO-62 positively and negatively correlate with increases in culture pH and temperature, respectively. β-L-gulopyranosyl-caldarchaetidyl-glycerol has been used as a standard for the quantification of polar lipids extracted from T. acidophilum HO-62. [Matreya, LLC. Catalog No. 1303]
Brand:CaymanSKU:27203 - 500 µgAvailable on backorder
β-Lapachone is a natural quinone with diverse anti-cancer and anti-inflammatory effects. It inhibits topoisomerase I at 25 μM and transglutaminase (IC50 = 5 μM).{22728,22726} In cancer cells which overexpress NAD(P)H:quinone oxidoreductase, β-lapachone is reduced to β-lapachone hydroquinone, which generates reactive oxygen species during its reversion to β-lapachone.{22729} This process sensitizes cancer cells to radiation, suppresses NF-κB activation, and drives apoptosis.{22729,22725,22727}
Brand:CaymanSKU:- β-Lapachone is a natural quinone with diverse anti-cancer and anti-inflammatory effects. It inhibits topoisomerase I at 25 μM and transglutaminase (IC50 = 5 μM).{22728,22726} In cancer cells which overexpress NAD(P)H:quinone oxidoreductase, β-lapachone is reduced to β-lapachone hydroquinone, which generates reactive oxygen species during its reversion to β-lapachone.{22729} This process sensitizes cancer cells to radiation, suppresses NF-κB activation, and drives apoptosis.{22729,22725,22727}
Brand:CaymanSKU:- β-Lapachone is a natural quinone with diverse anti-cancer and anti-inflammatory effects. It inhibits topoisomerase I at 25 μM and transglutaminase (IC50 = 5 μM).{22728,22726} In cancer cells which overexpress NAD(P)H:quinone oxidoreductase, β-lapachone is reduced to β-lapachone hydroquinone, which generates reactive oxygen species during its reversion to β-lapachone.{22729} This process sensitizes cancer cells to radiation, suppresses NF-κB activation, and drives apoptosis.{22729,22725,22727}
Brand:CaymanSKU:- β-Lapachone is a natural quinone with diverse anti-cancer and anti-inflammatory effects. It inhibits topoisomerase I at 25 μM and transglutaminase (IC50 = 5 μM).{22728,22726} In cancer cells which overexpress NAD(P)H:quinone oxidoreductase, β-lapachone is reduced to β-lapachone hydroquinone, which generates reactive oxygen species during its reversion to β-lapachone.{22729} This process sensitizes cancer cells to radiation, suppresses NF-κB activation, and drives apoptosis.{22729,22725,22727}
Brand:CaymanSKU:-
β-Mangostin is a xanthone originally isolated from G. mangostana with diverse biological activites.{39821,39822,39823,39824,39825,39826} It inhibits growth of methicillin-resistant S. aureus (MRSA) and methicillin-susceptible S. aureus (MSSA; MICs = 6.25-12.5 and 6.25-25 μg/ml, respectively), P. falciparum (IC50 = 3 μg/ml), and M. tuberculosis (MIC = 6.25 μg/ml).{39821,39822,39823} β-Mangostin inhibits fatty acid synthase (FASN) with an IC50 value of 24.83 μM.{39824} It induces cell cycle arrest at the G2/M phase and intrinsic and mitochondrial apoptosis in MCF-7 breast cancer cells.{39825} β-Mangostin also inhibits LPS-induced nitric oxide and prostaglandin E2 (PGE2; Item No. 14010) production in RAW264.7 cells and reduces neutrophil infiltration and TNF-α and IL-1β production in a mouse model of carrageenan-induced peritonitis.{39826}
Brand:CaymanSKU:25071 - 1 mgAvailable on backorder
β-Mangostin is a xanthone originally isolated from G. mangostana with diverse biological activites.{39821,39822,39823,39824,39825,39826} It inhibits growth of methicillin-resistant S. aureus (MRSA) and methicillin-susceptible S. aureus (MSSA; MICs = 6.25-12.5 and 6.25-25 μg/ml, respectively), P. falciparum (IC50 = 3 μg/ml), and M. tuberculosis (MIC = 6.25 μg/ml).{39821,39822,39823} β-Mangostin inhibits fatty acid synthase (FASN) with an IC50 value of 24.83 μM.{39824} It induces cell cycle arrest at the G2/M phase and intrinsic and mitochondrial apoptosis in MCF-7 breast cancer cells.{39825} β-Mangostin also inhibits LPS-induced nitric oxide and prostaglandin E2 (PGE2; Item No. 14010) production in RAW264.7 cells and reduces neutrophil infiltration and TNF-α and IL-1β production in a mouse model of carrageenan-induced peritonitis.{39826}
Brand:CaymanSKU:25071 - 10 mgAvailable on backorder
β-Mangostin is a xanthone originally isolated from G. mangostana with diverse biological activites.{39821,39822,39823,39824,39825,39826} It inhibits growth of methicillin-resistant S. aureus (MRSA) and methicillin-susceptible S. aureus (MSSA; MICs = 6.25-12.5 and 6.25-25 μg/ml, respectively), P. falciparum (IC50 = 3 μg/ml), and M. tuberculosis (MIC = 6.25 μg/ml).{39821,39822,39823} β-Mangostin inhibits fatty acid synthase (FASN) with an IC50 value of 24.83 μM.{39824} It induces cell cycle arrest at the G2/M phase and intrinsic and mitochondrial apoptosis in MCF-7 breast cancer cells.{39825} β-Mangostin also inhibits LPS-induced nitric oxide and prostaglandin E2 (PGE2; Item No. 14010) production in RAW264.7 cells and reduces neutrophil infiltration and TNF-α and IL-1β production in a mouse model of carrageenan-induced peritonitis.{39826}
Brand:CaymanSKU:25071 - 5 mgAvailable on backorder
β-Methylamino-L-alanine (BMAA) is a neurotoxic non-proteinogenic amino acid that has been found in cyanobacteria.{59025,59026} It is cytotoxic to mouse primary cortical neurons when used at a concentration of 3 mM in the presence of bicarbonate, an effect that can be blocked by the NMDA receptor antagonist MK-801 or the mGluR5 receptor antagonist MPEP (Item No. 14536).{59027} BMAA (3 mM) stimulates release of glutamate and induces oxidative stress in the same cells.{59028} It also enhances neuronal cell death induced by amyloid-β (25-35) in mouse primary cortical neurons when used at a concentration of 0.1 mM.{59027} Intracerebroventricular administration of BMAA (500 µg/animal) induces wet-dog shakes, rigidity, and clonic convulsions in rats.{59029} It induces parkinsonism in cynomolgus monkeys.{59030} BMAA has been found in commercial seafood.{59031}
Brand:CaymanSKU:23287 - 10 mgAvailable on backorder
β-Methylamino-L-alanine (BMAA) is a neurotoxic non-proteinogenic amino acid that has been found in cyanobacteria.{59025,59026} It is cytotoxic to mouse primary cortical neurons when used at a concentration of 3 mM in the presence of bicarbonate, an effect that can be blocked by the NMDA receptor antagonist MK-801 or the mGluR5 receptor antagonist MPEP (Item No. 14536).{59027} BMAA (3 mM) stimulates release of glutamate and induces oxidative stress in the same cells.{59028} It also enhances neuronal cell death induced by amyloid-β (25-35) in mouse primary cortical neurons when used at a concentration of 0.1 mM.{59027} Intracerebroventricular administration of BMAA (500 µg/animal) induces wet-dog shakes, rigidity, and clonic convulsions in rats.{59029} It induces parkinsonism in cynomolgus monkeys.{59030} BMAA has been found in commercial seafood.{59031}
Brand:CaymanSKU:23287 - 5 mgAvailable on backorder
β-Muricholic acid (β-MCA) is a murine-specific primary bile acid.{30824,45190} Dietary administration of β-MCA reduces HMG-CoA reductase activity in liver microsomes from mice fed a high cholesterol and cholic acid diet.{33864} Dietary administration of β-MCA also dissolves 100% of gallstones in a gallstone-susceptible mouse model of diet-induced cholesterol gallstones.{33865}
Brand:CaymanSKU:20287 -Available on backorder
β-Muricholic acid (β-MCA) is a murine-specific primary bile acid.{30824,45190} Dietary administration of β-MCA reduces HMG-CoA reductase activity in liver microsomes from mice fed a high cholesterol and cholic acid diet.{33864} Dietary administration of β-MCA also dissolves 100% of gallstones in a gallstone-susceptible mouse model of diet-induced cholesterol gallstones.{33865}
Brand:CaymanSKU:20287 -Available on backorder
β-Muricholic acid (β-MCA) is a murine-specific primary bile acid.{30824,45190} Dietary administration of β-MCA reduces HMG-CoA reductase activity in liver microsomes from mice fed a high cholesterol and cholic acid diet.{33864} Dietary administration of β-MCA also dissolves 100% of gallstones in a gallstone-susceptible mouse model of diet-induced cholesterol gallstones.{33865}
Brand:CaymanSKU:20287 -Available on backorder
β-Myrcene is a terpene that has been found in Cannabis and has antioxidative properties.{37666} It reduces thiobarbituric acid reactive substance (TBARS) and increases glutathione (GSH), catalase, GSH peroxidase, and CuZn superoxide dismutase levels in a rat model of persistent environmental pollutant-induced oxidative stress when administered at a dose of 200 mg/kg per day.{37667}
Brand:CaymanSKU:21720 -Out of stock
β-Myrcene is a terpene that has been found in Cannabis and has antioxidative properties.{37666} It reduces thiobarbituric acid reactive substance (TBARS) and increases glutathione (GSH), catalase, GSH peroxidase, and CuZn superoxide dismutase levels in a rat model of persistent environmental pollutant-induced oxidative stress when administered at a dose of 200 mg/kg per day.{37667}
Brand:CaymanSKU:21720 -Out of stock
β-Nicotinamide mononucleotide (β-NMN) is an intermediate in the biosynthesis of nicotinamide adenine dinucleotide (NAD+; Item No. 16077). Nicotinamide phosphoribosyltransferase (Nampt) catalyzes the condensation of nicotinamide with 5-phosphoribosyl-1-pyrophosphate to generate β-NMN, which is subsequently converted to NAD+ by β-NMN adenyltransferase.{19182} At 50-100 µM, β-NMN has been used to enhance NAD biosynthesis and glucose-stimulated insulin secretion in a Nampt+/- mouse model of metabolic disease, demonstrating a role for Nampt in β cell function.{19185} Furthermore, at 500 mg/kg/day, it has been shown to ameliorate glucose intolerance in high-fat diet-induced type 2 diabetes mice by restoring NAD+ levels.{20366}
Brand:CaymanSKU:-Out of stock
β-Nicotinamide mononucleotide (β-NMN) is an intermediate in the biosynthesis of nicotinamide adenine dinucleotide (NAD+; Item No. 16077). Nicotinamide phosphoribosyltransferase (Nampt) catalyzes the condensation of nicotinamide with 5-phosphoribosyl-1-pyrophosphate to generate β-NMN, which is subsequently converted to NAD+ by β-NMN adenyltransferase.{19182} At 50-100 µM, β-NMN has been used to enhance NAD biosynthesis and glucose-stimulated insulin secretion in a Nampt+/- mouse model of metabolic disease, demonstrating a role for Nampt in β cell function.{19185} Furthermore, at 500 mg/kg/day, it has been shown to ameliorate glucose intolerance in high-fat diet-induced type 2 diabetes mice by restoring NAD+ levels.{20366}
Brand:CaymanSKU:-Out of stock
β-Nicotinamide mononucleotide (β-NMN) is an intermediate in the biosynthesis of nicotinamide adenine dinucleotide (NAD+; Item No. 16077). Nicotinamide phosphoribosyltransferase (Nampt) catalyzes the condensation of nicotinamide with 5-phosphoribosyl-1-pyrophosphate to generate β-NMN, which is subsequently converted to NAD+ by β-NMN adenyltransferase.{19182} At 50-100 µM, β-NMN has been used to enhance NAD biosynthesis and glucose-stimulated insulin secretion in a Nampt+/- mouse model of metabolic disease, demonstrating a role for Nampt in β cell function.{19185} Furthermore, at 500 mg/kg/day, it has been shown to ameliorate glucose intolerance in high-fat diet-induced type 2 diabetes mice by restoring NAD+ levels.{20366}
Brand:CaymanSKU:-Out of stock
β-Nicotinamide mononucleotide (β-NMN) is an intermediate in the biosynthesis of nicotinamide adenine dinucleotide (NAD+; Item No. 16077). Nicotinamide phosphoribosyltransferase (Nampt) catalyzes the condensation of nicotinamide with 5-phosphoribosyl-1-pyrophosphate to generate β-NMN, which is subsequently converted to NAD+ by β-NMN adenyltransferase.{19182} At 50-100 µM, β-NMN has been used to enhance NAD biosynthesis and glucose-stimulated insulin secretion in a Nampt+/- mouse model of metabolic disease, demonstrating a role for Nampt in β cell function.{19185} Furthermore, at 500 mg/kg/day, it has been shown to ameliorate glucose intolerance in high-fat diet-induced type 2 diabetes mice by restoring NAD+ levels.{20366}
Brand:CaymanSKU:-Out of stock
β-Nicotyrine is an alkaloid metabolite of nicotine as well as a major product of its pyrolysis.{26726,26727} It binds comparably to two cytochrome P450 (CYP) isoforms, CYP2A6 and CYP2A13 (Kis = 7.5 and 5.6 µM, respectively), which are prominently involved in the metabolism of xenobiotics in the airways.{26724} However, β-nicotyrine appears to more effectively inactivate CYP2A6, leaving only 49% activity after a 10 minute exposure with 20 µM β-nicotyrine, as opposed to 87% remaining activity for CYP2A13 treated identically.{26722} Presumably through this effect, β-nicotyrine inhibits DNA strand breaks induced by the genotoxic tobacco metabolite (4-(methylnitrosamino)-1-(2-pyridyl)-1-butanone), which is bioactivated by CYP2A isoforms.{26723}
Brand:CaymanSKU:-Out of stock
β-Nicotyrine is an alkaloid metabolite of nicotine as well as a major product of its pyrolysis.{26726,26727} It binds comparably to two cytochrome P450 (CYP) isoforms, CYP2A6 and CYP2A13 (Kis = 7.5 and 5.6 µM, respectively), which are prominently involved in the metabolism of xenobiotics in the airways.{26724} However, β-nicotyrine appears to more effectively inactivate CYP2A6, leaving only 49% activity after a 10 minute exposure with 20 µM β-nicotyrine, as opposed to 87% remaining activity for CYP2A13 treated identically.{26722} Presumably through this effect, β-nicotyrine inhibits DNA strand breaks induced by the genotoxic tobacco metabolite (4-(methylnitrosamino)-1-(2-pyridyl)-1-butanone), which is bioactivated by CYP2A isoforms.{26723}
Brand:CaymanSKU:-Out of stock
β-Nicotyrine is an alkaloid metabolite of nicotine as well as a major product of its pyrolysis.{26726,26727} It binds comparably to two cytochrome P450 (CYP) isoforms, CYP2A6 and CYP2A13 (Kis = 7.5 and 5.6 µM, respectively), which are prominently involved in the metabolism of xenobiotics in the airways.{26724} However, β-nicotyrine appears to more effectively inactivate CYP2A6, leaving only 49% activity after a 10 minute exposure with 20 µM β-nicotyrine, as opposed to 87% remaining activity for CYP2A13 treated identically.{26722} Presumably through this effect, β-nicotyrine inhibits DNA strand breaks induced by the genotoxic tobacco metabolite (4-(methylnitrosamino)-1-(2-pyridyl)-1-butanone), which is bioactivated by CYP2A isoforms.{26723}
Brand:CaymanSKU:-Out of stock
β-Nicotyrine is an alkaloid metabolite of nicotine as well as a major product of its pyrolysis.{26726,26727} It binds comparably to two cytochrome P450 (CYP) isoforms, CYP2A6 and CYP2A13 (Kis = 7.5 and 5.6 µM, respectively), which are prominently involved in the metabolism of xenobiotics in the airways.{26724} However, β-nicotyrine appears to more effectively inactivate CYP2A6, leaving only 49% activity after a 10 minute exposure with 20 µM β-nicotyrine, as opposed to 87% remaining activity for CYP2A13 treated identically.{26722} Presumably through this effect, β-nicotyrine inhibits DNA strand breaks induced by the genotoxic tobacco metabolite (4-(methylnitrosamino)-1-(2-pyridyl)-1-butanone), which is bioactivated by CYP2A isoforms.{26723}
Brand:CaymanSKU:-Out of stock
β-Ocimene is a monoterpene that has been found in a variety of plants and is a volatile compound involved in plant-plant signaling and plant defense against pests.{42453,42454} It is emitted by tea (C. sinensis) plants in response to a jasmonic acid combined with mechanical damage (JAMD) model of herbivore attack.{42453} β-Ocimene reduces the number of winged aphids (M. persicae) that settle on Chinese cabbage and the feeding time and number of nymphs produced by aphids on leaves.{42454} The aphid endoparasitoid A. gifuensis demonstrates a preference for β-ocimene-treated Chinese cabbage over control plants in a wind tube two-choice test. β-Ocimene (100-1,000 ppm) also has antioxidant activity in a thiobarbituric acid reactive substances (TBARS) assay.{2762}
Brand:CaymanSKU:23466 - 100 mgAvailable on backorder
β-Ocimene is a monoterpene that has been found in a variety of plants and is a volatile compound involved in plant-plant signaling and plant defense against pests.{42453,42454} It is emitted by tea (C. sinensis) plants in response to a jasmonic acid combined with mechanical damage (JAMD) model of herbivore attack.{42453} β-Ocimene reduces the number of winged aphids (M. persicae) that settle on Chinese cabbage and the feeding time and number of nymphs produced by aphids on leaves.{42454} The aphid endoparasitoid A. gifuensis demonstrates a preference for β-ocimene-treated Chinese cabbage over control plants in a wind tube two-choice test. β-Ocimene (100-1,000 ppm) also has antioxidant activity in a thiobarbituric acid reactive substances (TBARS) assay.{2762}
Brand:CaymanSKU:23466 - 250 mgAvailable on backorder
β-Ocimene is a monoterpene that has been found in a variety of plants and is a volatile compound involved in plant-plant signaling and plant defense against pests.{42453,42454} It is emitted by tea (C. sinensis) plants in response to a jasmonic acid combined with mechanical damage (JAMD) model of herbivore attack.{42453} β-Ocimene reduces the number of winged aphids (M. persicae) that settle on Chinese cabbage and the feeding time and number of nymphs produced by aphids on leaves.{42454} The aphid endoparasitoid A. gifuensis demonstrates a preference for β-ocimene-treated Chinese cabbage over control plants in a wind tube two-choice test. β-Ocimene (100-1,000 ppm) also has antioxidant activity in a thiobarbituric acid reactive substances (TBARS) assay.{2762}
Brand:CaymanSKU:23466 - 50 mgAvailable on backorder
β-Ocimene is a monoterpene that has been found in a variety of plants and is a volatile compound involved in plant-plant signaling and plant defense against pests.{42453,42454} It is emitted by tea (C. sinensis) plants in response to a jasmonic acid combined with mechanical damage (JAMD) model of herbivore attack.{42453} β-Ocimene reduces the number of winged aphids (M. persicae) that settle on Chinese cabbage and the feeding time and number of nymphs produced by aphids on leaves.{42454} The aphid endoparasitoid A. gifuensis demonstrates a preference for β-ocimene-treated Chinese cabbage over control plants in a wind tube two-choice test. β-Ocimene (100-1,000 ppm) also has antioxidant activity in a thiobarbituric acid reactive substances (TBARS) assay.{2762}
Brand:CaymanSKU:23466 - 500 mgAvailable on backorder
β-Pseudouridine is the C-5 glycoside isomer of the nucleoside uridine (Item No. 20300).{37180} It is formed when uridine in RNA undergoes site-specific isomerization by a pseudouridine synthase enzyme. β-pseudouridine is found in tRNAs from bacteria, archaea, and eukaryotes.{37181} In vitro, it reduces the number of X-ray-induced chromosomal aberrations in human lymphocytes isolated from whole blood in a dose-dependent manner.{37182}
Brand:CaymanSKU:23383 - 10 mgAvailable on backorder
β-Pseudouridine is the C-5 glycoside isomer of the nucleoside uridine (Item No. 20300).{37180} It is formed when uridine in RNA undergoes site-specific isomerization by a pseudouridine synthase enzyme. β-pseudouridine is found in tRNAs from bacteria, archaea, and eukaryotes.{37181} In vitro, it reduces the number of X-ray-induced chromosomal aberrations in human lymphocytes isolated from whole blood in a dose-dependent manner.{37182}
Brand:CaymanSKU:23383 - 25 mgAvailable on backorder
β-Pseudouridine is the C-5 glycoside isomer of the nucleoside uridine (Item No. 20300).{37180} It is formed when uridine in RNA undergoes site-specific isomerization by a pseudouridine synthase enzyme. β-pseudouridine is found in tRNAs from bacteria, archaea, and eukaryotes.{37181} In vitro, it reduces the number of X-ray-induced chromosomal aberrations in human lymphocytes isolated from whole blood in a dose-dependent manner.{37182}
Brand:CaymanSKU:23383 - 5 mgAvailable on backorder
β-Rubromycin is a bacterial metabolite originally isolated from Streptomyces that has diverse biological activities.{49077} It inhibits the growth of HMO2, KATO-III, and MCF-7 cells with GI50 values of 0.5, 0.84, and ortho-quinone group, but it was revised to a para-quinone group in 2000 using organic and biosynthetic methods, as well as spectroscopic analysis.{49077,49076,49078}
Brand:CaymanSKU:27477 - 1 mgAvailable on backorder
β-Rubromycin is a bacterial metabolite originally isolated from Streptomyces that has diverse biological activities.{49077} It inhibits the growth of HMO2, KATO-III, and MCF-7 cells with GI50 values of 0.5, 0.84, and ortho-quinone group, but it was revised to a para-quinone group in 2000 using organic and biosynthetic methods, as well as spectroscopic analysis.{49077,49076,49078}
Brand:CaymanSKU:27477 - 5 mgAvailable on backorder
β-Secretase inhibitor IV is an inhibitor of β-site amyloid protein cleaving enzymes (BACE/β-secretase) 1 and 2 (IC50s = 15 and 230 nM for human BACE1 and 2, respectively).{16820} It has >500-fold selectivity for BACE1 and 2 over the aspartyl proteases renin and cathepsin D. β-Secretase inhibitor IV inhibits secretion of amyloid-β (Aβ) precursor protein (APP; IC50 = 29 nM) in HEK293T cells transfected with a truncated APP. It also inhibits formation of the Aβ peptides Aβ38, Aβ40, and Aβ42 in primary chick neurons (IC50s = 3.7, 4.7, and 4.8 nM, respectively).{40417}
Brand:CaymanSKU:23388 - 1 mgAvailable on backorder
β-Secretase inhibitor IV is an inhibitor of β-site amyloid protein cleaving enzymes (BACE/β-secretase) 1 and 2 (IC50s = 15 and 230 nM for human BACE1 and 2, respectively).{16820} It has >500-fold selectivity for BACE1 and 2 over the aspartyl proteases renin and cathepsin D. β-Secretase inhibitor IV inhibits secretion of amyloid-β (Aβ) precursor protein (APP; IC50 = 29 nM) in HEK293T cells transfected with a truncated APP. It also inhibits formation of the Aβ peptides Aβ38, Aβ40, and Aβ42 in primary chick neurons (IC50s = 3.7, 4.7, and 4.8 nM, respectively).{40417}
Brand:CaymanSKU:23388 - 5 mgAvailable on backorder
β-Secretase inhibitor IV is an inhibitor of β-site amyloid protein cleaving enzymes (BACE/β-secretase) 1 and 2 (IC50s = 15 and 230 nM for human BACE1 and 2, respectively).{16820} It has >500-fold selectivity for BACE1 and 2 over the aspartyl proteases renin and cathepsin D. β-Secretase inhibitor IV inhibits secretion of amyloid-β (Aβ) precursor protein (APP; IC50 = 29 nM) in HEK293T cells transfected with a truncated APP. It also inhibits formation of the Aβ peptides Aβ38, Aβ40, and Aβ42 in primary chick neurons (IC50s = 3.7, 4.7, and 4.8 nM, respectively).{40417}
Brand:CaymanSKU:23388 - 500 µgAvailable on backorder
The four tocopherols (α, β, δ, and γ) and four tocotrienols (α, β, δ, and γ) are forms of vitamin E, which is known for its antioxidant activity.{3679} Tocotrienols are found in high concentrations in palm oil and wheat germ. β-Tocotrienol is a less potent antioxidant than α-tocotrienol (Item No. 10008377).{3679} A high cholesterol diet supplemented with a mixture of α- and β-tocopherols and tocotrienols has been shown to lower hepatic cholesterol and cholesterol ester concentration and to reduce atherosclerotic lesions in ApoE+/- mice.{25617}
Brand:CaymanSKU:9001533 - 1 mgAvailable on backorder
The four tocopherols (α, β, δ, and γ) and four tocotrienols (α, β, δ, and γ) are forms of vitamin E, which is known for its antioxidant activity.{3679} Tocotrienols are found in high concentrations in palm oil and wheat germ. β-Tocotrienol is a less potent antioxidant than α-tocotrienol (Item No. 10008377).{3679} A high cholesterol diet supplemented with a mixture of α- and β-tocopherols and tocotrienols has been shown to lower hepatic cholesterol and cholesterol ester concentration and to reduce atherosclerotic lesions in ApoE+/- mice.{25617}
Brand:CaymanSKU:9001533 - 10 mgAvailable on backorder
The four tocopherols (α, β, δ, and γ) and four tocotrienols (α, β, δ, and γ) are forms of vitamin E, which is known for its antioxidant activity.{3679} Tocotrienols are found in high concentrations in palm oil and wheat germ. β-Tocotrienol is a less potent antioxidant than α-tocotrienol (Item No. 10008377).{3679} A high cholesterol diet supplemented with a mixture of α- and β-tocopherols and tocotrienols has been shown to lower hepatic cholesterol and cholesterol ester concentration and to reduce atherosclerotic lesions in ApoE+/- mice.{25617}
Brand:CaymanSKU:9001533 - 25 mgAvailable on backorder
The four tocopherols (α, β, δ, and γ) and four tocotrienols (α, β, δ, and γ) are forms of vitamin E, which is known for its antioxidant activity.{3679} Tocotrienols are found in high concentrations in palm oil and wheat germ. β-Tocotrienol is a less potent antioxidant than α-tocotrienol (Item No. 10008377).{3679} A high cholesterol diet supplemented with a mixture of α- and β-tocopherols and tocotrienols has been shown to lower hepatic cholesterol and cholesterol ester concentration and to reduce atherosclerotic lesions in ApoE+/- mice.{25617}
Brand:CaymanSKU:9001533 - 5 mgAvailable on backorder
β-Zearalenol is a hepatic metabolite of zearalenone (Item No. 11353), a mycotoxin produced by fungi in food and animal feeds.{20562,27394} It is a less potent agonist of estrogen receptors than the parent compound.{27392} However, β-zearalenol has pronounced effects on uterotropic activity and sperm acrosome reaction.{27393,27396,27395}
Brand:CaymanSKU:-Available on backorder
β-Zearalenol is a hepatic metabolite of zearalenone (Item No. 11353), a mycotoxin produced by fungi in food and animal feeds.{20562,27394} It is a less potent agonist of estrogen receptors than the parent compound.{27392} However, β-zearalenol has pronounced effects on uterotropic activity and sperm acrosome reaction.{27393,27396,27395}
Brand:CaymanSKU:-Available on backorder
β-Zearalenol is a hepatic metabolite of zearalenone (Item No. 11353), a mycotoxin produced by fungi in food and animal feeds.{20562,27394} It is a less potent agonist of estrogen receptors than the parent compound.{27392} However, β-zearalenol has pronounced effects on uterotropic activity and sperm acrosome reaction.{27393,27396,27395}
Brand:CaymanSKU:-Available on backorder