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| Product | Description | |
|---|---|---|
| Cholestane-3,7,26,27-tetrol | Heterocyclic Organic Compound. CAS No. 107088-80-2. Catalog: ACM107088802. |  |
| Cholestane-3b,5a,6b-triol | Steroidal Compounds. Alternative Names: 3beta,5alpha,6beta-Trihydroxycholestane; 3beta,5alpha,6beta-Cholestanetriol; Cholestane-3beta,5alpha,6beta-triol; Cholesta-3beta,5alpha,6beta-triol; cholestanetriol; 5alpha,6beta-Dihydroxycholestanol; 5alpha-cholestane-3beta,5,6beta-triol; (3S, 5R, 6R, 8S, 9S, 10R, 13R, 14S, 17R) -10, 13-dimethyl-17- [ (2R) -6-methylheptan-2-yl]-1, 2, 3, 4, 6, 7, 8, 9, 11, 12, 14, 15, 16, 17-tetradecahydrocyclopenta [a]phenanthrene-3, 5, 6-triol. CAS No. 1253-84-5. Molecular formula: C27H48O3. Mole weight: 420.68. Purity: 0.95. IUPACName: (3S, 5R, 6R, 8S, 9S, 10R, 13R, 14S, 17R) -10, 13-dimethyl-17- [ (2R) -6-methylheptan-2-yl]-1, 2, 3, 4, 6, 7, 8, 9, 11, 12, 14, 15, 16, 17-tetradecahydrocyclopenta [a]phenanthrene-3, 5, 6-triol. Canonical SMILES: CC (C)CCCC (C)C1CCC2C1 (CCC3C2CC (C4 (C3 (CCC (C4)O)C)O)O)C. Density: 1.065g/cm³. Catalog: ACM1253845. | |
| cholestanetriol 26-monooxygenase | This mitochondrial cytochrome P-450 enzyme requires adrenodoxin. It catalyses the first three sterol side chain oxidations in bile acid biosynthesis via the neutral (classic) pathway. Can also act on cholesterol, cholest-5-ene-3β,7α-diol, 7α-hydroxycholest-4-en-3-one, and 5β-cholestane-3α,7α-diol. The enzyme can also hydroxylate cholesterol at positions 24 and 25. The initial source of the electrons is NADPH, which transfers the electrons to the adrenodoxin via EC 1.18.1.6, adrenodoxin-NADP+ reductase. Group: Enzymes. Synonyms: 5β-cholestane-3α,7α,12α-triol 26-hydroxylase; 5β-cholestane-3α,7α,12α-triol hydroxylase; cholestanetriol 26-hydroxylase; sterol 27-hydroxylase; sterol 26-hydroxylase; cholesterol 27-hydroxyla. Enzyme Commission Number: EC 1.14.15.15. CAS No. 52227-77-7. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0940; cholestanetriol 26-monooxygenase; EC 1.14.15.15; 52227-77-7; 5β-cholestane-3α,7α,12α-triol 26-hydroxylase; 5β-cholestane-3α,7α,12α-triol hydroxylase; cholestanetriol 26-hydroxylase; sterol 27-hydroxylase; sterol 26-hydroxylase; cholesterol 27-hydroxylase; CYP27A; CYP27A1; cytochrome P450 27A1'. Cat No: EXWM-0940. |  |
| Cholestanol, 5β,6β-epoxy-d7 | Steroids2H Labeled Compounds. Alternative Names: 5β,6β-Epoxycholestanol-d7. CAS No. 127684-06-4. Molecular formula: C27H39O2D7. Mole weight: 409.7. Catalog: ACM127684064. | |
| Cholestanol acetate | Heterocyclic Organic Compound. Alternative Names: CHOLESTANOL ACETATE;DIHYDROCHOLESTEROL ACETATE;5-ALPHA-CHOLESTAN-3-BETA-OL ACETATE. CAS No. 1255-88-5. Molecular formula: C29H50O2. Mole weight: 430.71. Catalog: ACM1255885. | |
| cholestanol-d5 | cholestanol-d5. Group: Others. Purity: >99%. Mole weight: 393.7. Stability: 6 Months. Storage: -20°C. Avanti Polar Lipids; lipid products; sterols; sterols products; singnal transduction; cell pathways; cholestanol-d5; 2,2,3,4,4-pentadeuterio-5a-cholestan-3ss-ol. Cat No: STEZ-073. | |
| 25R-3α, 7α, 12α-Trihydroxy-5 β-cholestanoic Acid | 25R-3α, 7α, 12α-Trihydroxy-5 β-cholestanoic acid is an intermediate in the synthesis of (25R)-3 β, 7α, 12α-Trihydroxy-5-cholestenoic Acid (T795130), which is an oxysterol, an oxidized derivatives of cholesterol (C432501), which may be important in many biological processes, including cholesterol homeostasis, atherosclerosis, sphingolipid metabolism, platelet aggregation, apoptosis, and protein prenylation,[1] though their roles are poorly understood. Group: Biochemicals. Grades: Highly Purified. CAS No. 23740-14-9. Pack Sizes: 10mg, 25mg. Molecular Formula: C27H46O5. US Biological Life Sciences. |  Worldwide |
| [(25R)-3α,7α-Dihydroxy-5 β-cholestan-26-oyl]taurine-d4 Sodium Salt | [(25R)-3α,7α-Dihydroxy-5 β-cholestan-26-oyl]taurine-d4 Sodium Salt is the labeled deuterium form of [(25R)-3α,7α-Dihydroxy-5 β-cholestan-26-oyl]taurine Sodium Salt (D452630) that is derived from Chenodeoxycholic Acid (C291900), which is a major bile acid in many vertebrates, occurring as the N-glycine and/or N-taurine conjugate. With other bile acids, forms mixed micelles with lecithin in bile which solubilize cholesterol and thus facilitates its excretion. Facilitates fat absorption in the small intestine by micellar solubilization of fatty acids and monoglycerides. Anticholelithogenic. Epimeric with Ursodiol. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 500ug, 2.5mg. Molecular Formula: C29H46D4NNaO6S, Molecular Weight: 567.79. US Biological Life Sciences. | Worldwide |
| [(25R)-3α,7α-Dihydroxy-5 β-cholestan-26-oyl]taurine Sodium Salt | [(25R)-3α,7α-Dihydroxy-5 β-cholestan-26-oyl]taurine Sodium Salt is derived from Chenodeoxycholic Acid (C291900), which is a major bile acid in many vertebrates, occurring as the N-glycine and/or N-taurine conjugate. With other bile acids, forms mixed micelles with lecithin in bile which solubilize cholesterol and thus facilitates its excretion. Facilitates fat absorption in the small intestine by micellar solubilization of fatty acids and monoglycerides. Anticholelithogenic. Epimeric with Ursodiol. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 500ug, 2.5mg. Molecular Formula: C29H50NNaO6S, Molecular Weight: 563.77. US Biological Life Sciences. | Worldwide |
| (25R)-5 β-Cholestane-3α, 7α, 12α, 26-tetrol | (3α,5 β, 7α, 12α, 25R)-Cholestane-3, 7, 12, 26-tetrol, is used in the study of stereospecific modulation of the calcium channel in human erythrocytes by cholesterol derivatives. Group: Biochemicals. Grades: Highly Purified. CAS No. 27857-14-3. Pack Sizes: 2.5mg, 5mg. Molecular Formula: C27H48O4, Molecular Weight: 436.67. US Biological Life Sciences. | Worldwide |
| (25R)-5 β-Cholestane-3α,7α,26-triol | (25S)-5 β-Cholestane-3α,7α,26-triol, can be used in the study of stereospecific side-chain hydroxylations in the biosynthesis of chenodeoxycholic acid. Group: Biochemicals. Grades: Highly Purified. CAS No. 66807-58-7. Pack Sizes: 2.5mg, 5mg. Molecular Formula: C27H48O3, Molecular Weight: 420.67. US Biological Life Sciences. | Worldwide |
| (25S)-5 β-Cholestane-3α, 7α, 12α, 26-tetrol | (25S)-5 β-Cholestane-3α, 7α, 12α, 26-tetrol, can be used in the study of High-performance liquid chromatographic separation of bile acids and bile alcohols diastereoisomeric at C-25. Group: Biochemicals. Grades: Highly Purified. CAS No. 134002-65-6. Pack Sizes: 2.5mg, 5mg. Molecular Formula: C27H48O4, Molecular Weight: 436.67. US Biological Life Sciences. | Worldwide |
| (25S)-5 β-Cholestane-3α,7α,26-triol | (25S)-5 β-Cholestane-3α,7α,26-triol, can be used in the study of stereospecific side-chain hydroxylations in the biosynthesis of chenodeoxycholic acid. Group: Biochemicals. Grades: Highly Purified. CAS No. 66807-59-8. Pack Sizes: 2.5mg, 5mg. Molecular Formula: C27H48O3, Molecular Weight: 420.67. US Biological Life Sciences. | Worldwide |
| (3a,5b,7a,12a)-3,7,12,24-Tetrahydroxy-cholestan-26-oic acid | Heterocyclic Organic Compound. Alternative Names: TTHCA; 3alpha,7alpha,12alpha,24xi-tetrahydroxy-5beta-cholestan-26-oic acid; 3,7,12,24-Tetrahydroxycholestanoic acid; 3alpha,7alpha,12alpha,24-tetrahydroxy-5beta-cholestanoic acid; 3alpha,7alpha,12alpha,24-Tetrahydroxy-5beta-cholestan-26-oic acid; Varanic. CAS No. 1061-64-9. Molecular formula: C26H44O5. Mole weight: 466.650540 [g/mol]. Purity: 0.96. IUPACName: (6R)-3-hydroxy-2-methyl-6-[(3R, 5S, 7R, 8R, 9S, 10S, 12S, 13R, 14S, 17R)-3, 7, 12-trihydroxy-10, 13-dimethyl-2, 3, 4, 5, 6, 7, 8, 9, 11, 12, 14, 15, 16, 17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]heptanoic acid. Canonical SMILES: CC (CCC (C (C)C (=O)O)O)C1CCC2C1 (C (CC3C2C (CC4C3 (CCC (C4)O)C)O)O)C. Density: 1.188g/cm³. Catalog: ACM1061649. | |
| 3α,7α,12α-trihydroxy-5β-cholestanoyl-CoA 24-hydroxylase | Requires ATP. The reaction in mammals possibly involves dehydrogenation to give a 24(25)-double bond followed by hydration. However, in amphibians such as the Oriental fire-bellied toad (Bombina orientalis), it is probable that the product is formed via direct hydroxylation of the saturated side chain of (25R)-3α,7α,12α-trihydroxy-5β-cholestan-26-oate and not via hydration of a 24(25) double bond. In microsomes, the free acid is preferred to the coenzyme A ester, whereas in mitochondria, the coenzyme A ester is preferred to the free-acid form of the substrate. Group: Enzymes. Synonyms: trihydroxycoprostanoyl-CoA oxidase; THC-CoA oxidase; THCA-CoA oxidase; 3α,7α,12α-trihydroxy-5β-cholestanoyl-CoA oxidase; 3α,. Enzyme Commission Number: EC 1.17.99.3. CAS No. 119799-47-2. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1103; 3α,7α,12α-trihydroxy-5β-cholestanoyl-CoA 24-hydroxylase; EC 1.17.99.3; 119799-47-2; trihydroxycoprostanoyl-CoA oxidase; THC-CoA oxidase; THCA-CoA oxidase; 3α,7α,12α-trihydroxy-5β-cholestanoyl-CoA oxidase; 3α,7α,12α-trihydroxy-5β-cholestan-26-oate 24-hydroxylase. Cat No: EXWM-1103. | |
| 3α,7α-dihydroxy-5β-cholestanate-CoA ligase | This enzyme belongs to the family of ligases, specifically those forming carbon-sulfur bonds as acid-thiol ligases. This enzyme participates in bile acid biosynthesis. Group: Enzymes. Synonyms: 3α,7α-dihydroxy-5β-cholestanoyl coenzyme A synthetase; DHCA-CoA ligase; 3α,7α-dihydroxy-5β-cholestanate:CoA ligase (AMP-forming). Enzyme Commission Number: EC 6.2.1.28. CAS No. 118732-03-9. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-5686; 3α,7α-dihydroxy-5β-cholestanate-CoA ligase; EC 6.2.1.28; 118732-03-9; 3α,7α-dihydroxy-5β-cholestanoyl coenzyme A synthetase; DHCA-CoA ligase; 3α,7α-dihydroxy-5β-cholestanate:CoA ligase (AMP-forming). Cat No: EXWM-5686. | |
| 3α-Aminocholestane | 3α-Aminocholestane is an inhibitor of SH2 domain-containing inositol-5'-phosphatase 1 (SHP-1; IC50=~2.5 μM). It is selective for SHP-1 over SHP-2 and phosphatase and tensin homolog (PTEN; IC50s=>20 μM). Synonyms: 3AC; 5alpha-Cholestane-3alpha-amine. Grades: ≥95%. CAS No. 2206-20-4. Molecular formula: C27H49N. Mole weight: 387.7. |  |
| 3 β,5α,6 β-Trihydroxycholestane | Cholesterol analog. Useful for treatment of hyperlipemia, arteriosclerosis, diabetes, obesity. Group: Biochemicals. Alternative Names: (3 β,5α,6 β)-Cholestane-3,5,6-triol; 3 β-Hydroxycholestane-5α,6 β-diol; 5α,6 β-Dihydroxycholestanol; Cholesta-3 β,5α,6 β-triol; Cholestane-3 β,5α,6 β-triol; NSC 124751; NSC 18178. Grades: Highly Purified. CAS No. 1253-84-5. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| 3β,5α,6β-Trihydroxycholestane | 3β,5α,6β-Trihydroxycholestane is useful for treatment of hyperlipemia, arteriosclerosis, diabetes, obesity. Synonyms: Cholestane-3beta,5alpha,6beta-triol; 5alpha,6beta-Dihydroxycholestanol; Cholesta-3beta,5alpha,6beta-triol; 3beta,5alpha,6beta-trihydroxycholestane. Grades: >99%. CAS No. 1253-84-5. Molecular formula: C27H48O3. Mole weight: 420.68. | |
| 3 β,5α,6 β-Trihydroxycholestane-d7 | Labeled Cholesterol analog. Useful for treatment of hyperlipemia, arteriosclerosis, diabetes, obesity. Group: Biochemicals. Alternative Names: (3 β,5α,6 β)-Cholestane-3,5,6-triol-d7; 3 β-Hydroxycholestane-5α,6 β-diol-d7; 5α,6 β-Dihydroxycholestanol-d7; Cholesta-3 β,5α,6 β-triol-d7; Cholestane-3 β,5α,6 β-triol-d7; NSC 124751-d7; NSC 18178-d7. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| 5a-Bromo-6,19-epoxycholestanol 3-acetate | 5a-Bromo-6,19-epoxycholestanol 3-acetate. Group: Biochemicals. Alternative Names: (3b,5a,6b)-5-Bromo-6,19-epoxy-cholestan-3-ol Acetate. Grades: Highly Purified. CAS No. 1258-07-7. Pack Sizes: 5mg, 10mg, 25mg, 50mg, 100mg. Molecular Formula: C29H47BrO3. US Biological Life Sciences. | Worldwide |
| 5-a-Cholestan-3-one | 5-a-Cholestan-3-one. Group: Biochemicals. Grades: Highly Purified. CAS No. 566-88-1. Pack Sizes: 1g, 2g, 5g. Molecular Formula: C27H46O. US Biological Life Sciences. | Worldwide |
| 5α,6α-Epoxycholestanol-d7 | Steroids2H Labeled Compounds. Alternative Names: Cholestanol, 5α,6α-epoxy-d7. CAS No. 127685-38-5. Molecular formula: C27H39O2D7. Mole weight: 409.7. Catalog: ACM127685385. | |
| 5α, 6β-Dihydroxycholestanol-d7 | Steroids2H Labeled Compounds. Alternative Names: Cholestane-25,26,26,26,27,27,27-d7-3β,5α,6β-triol; 5α,6β-di-OHC-d7; Cholestanetriol-d7. CAS No. 127684-07-5. Molecular formula: C27H41D7O3. Mole weight: 427.7. Appearance: Solid. IUPACName: (3S, 5R, 6R, 8S, 9S, 10R, 13R, 14S, 17R) -10, 13-dimethyl-17- [ (2R) -6, 7, 7, 7-tetradeuterio-6- (trideuteriomethyl) heptan-2-yl]-1, 2, 3, 4, 6, 7, 8, 9, 11, 12, 14, 15, 16, 17-tetradecahydrocyclopenta [a]phenanthrene-3, 5, 6-triol. Catalog: ACM127684075. | |
| 5α-Bromo-6,19-epoxycholestanol 3-acetate | Heterocyclic Organic Compound. Alternative Names: (3β,5α,6β)-. CAS No. 1258-07-7. Molecular formula: C29H47BrO3. Mole weight: 523.59. Appearance: White Solid. Purity: 0.96. IUPACName: 6β,19-epoxy-5-bromo-5α-cholestane-3β-ol 3-acetate. Catalog: ACM1258077. | |
| 5-ALPHA-CHOLESTAN-3-ALPHA-OL ACETATE | 5-ALPHA-CHOLESTAN-3-ALPHA-OL ACETATE. CAS No. 1107-59-1. Molecular formula: C29H50O2. Mole weight: 430.71. Catalog: ACM1107591. | |
| 5α-Cholestan-3 β-ol | 5α-Cholestan-3 β-ol is a carbon stanol formed from biohydrogenation of Cholesterol (C432501) in the gut. Studies have also examined the conversion of 5α-Cholestan-3 β-ol catalyzed by 3- β-hydroxysteroid dehydrogenase of rat liver. Group: Biochemicals. Alternative Names: (3 β,5α)-Cholestan-3-ol; 3 β-Hydroxy-5α-cholestane; 3 β-Hydroxycholestane; 5α(H)-Cholestan-3 β-ol; 5α-Cholestanol; 5α-Dihydrocholesterol; Cholestan-3 β-ol; Cholestanol; Dihydrocholesterin; Dihydrocholesterol; Dihydrolathosterol; Lathostanol; NSC 18188; Zymostanol; β-Cholestanol. Grades: Highly Purified. CAS No. 80-97-7. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
| 5α-Cholestan-3 β-ol-d7 | 5α-Cholestan-3 β-ol-d7 is the isotope labelled analog of 5α-Cholestan-3 β-ol. 5α-Cholestan-3 β-ol is a carbon stanol formed from biohydrogenation of Cholesterol (C432501) in the gut. Group: Biochemicals. Alternative Names: (3 β,5α)-Cholestan-25,26,26,26,27,27,27-d7-3-ol; (3 β,5α)-Cholestan-3-ol-d7; 3 β-Hydroxy-5α-cholestane-d7; 3 β-Hydroxycholestane-d7; 5α(H)-Cholestan-3 β-ol-d7; 5α-Cholestanol-d7; 5α-Dihydrocholesterol-d7; Cholestan-3 β-ol-d7; Cholestanol-d7; Dihydrocholesterin-d7; Dihydrocholesterol-d7; Dihydrolathosterol-d7; Lathostanol-d7; NSC 18188-d7; Zymostanol-d7; β-Cholestanol-d7. Grades: Highly Purified. CAS No. 84061-69-8. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| 5α-Cholestan-3-one | 5α-Cholestan-3-one is an endogenous metabolite. Uses: Scientific research. Group: Natural products. Alternative Names: 5α-Cholestanone. CAS No. 566-88-1. Pack Sizes: 10 mM * 1 mL; 100 mg; 250 mg. Product ID: HY-107826. |  |
| 5α-Cholestane | 5α-Cholestane is a biochemical reagent that can be used as a biological material or organic compound for life science related research [1]. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 481-21-0. Pack Sizes: 25 mg; 50 mg; 100 mg. Product ID: HY-133970. | |
| 5Alpha-cholestane-3,3-d2 | Heterocyclic Organic Compound. Alternative Names: CHOLESTANE-3,3-D2;D2 C27 ALPHA ALPHA ALPHA (20R) CHOLESTANE;5alpha-Cholestane-3,3-D2;d2 C27 ααα (20R)-Cholestane. CAS No. 122241-86-5. Molecular formula: C27H46D2. Mole weight: 374.69. Purity: 98 atom % D. Catalog: ACM122241865. | |
| 5-b-Cholestan-3-one | 5-b-Cholestan-3-one. Group: Biochemicals. Grades: Highly Purified. CAS No. 601-53-6. Pack Sizes: 5mg, 10mg, 25mg. Molecular Formula: C27H46O. US Biological Life Sciences. | Worldwide |
| 5β-cholestane-3α,7α-diol 12α-hydroxylase | A heme-thiolate protein (P-450). This is the key enzyme in the biosynthesis of the bile acid cholic acid (3α,7α,12α-trihydroxy-5β-cholanoic acid). The activity of this enzyme determines the biosynthetic ratio between cholic acid and chenodeoxycholic acid. The enzyme can also hydroxylate the substrate at the 25 and 26 position, but to a lesser extent. Group: Enzymes. Synonyms: 5β-cholestane-3α,7α-diol 12α-monooxygenase; sterol 12α-hydroxylase (ambiguous); CYP8B1; cytochrome P450 8B1. Enzyme Commission Number: EC 1.14.13.96. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0904; 5β-cholestane-3α,7α-diol 12α-hydroxylase; EC 1.14.13.96; 5β-cholestane-3α,7α-diol 12α-monooxygenase; sterol 12α-hydroxylase (ambiguous); CYP8B1; cytochrome P450 8B1. Cat No: EXWM-0904. | |
| 5-Bromo-5a-cholestane-3,6-diol 3-acetate | 5-Bromo-5a-cholestane-3,6-diol 3-acetate. Group: Biochemicals. Alternative Names: 3b-Acetoxy-5-bromo-5a-cholestan-6b-ol. Grades: Highly Purified. CAS No. 1258-35-1. Pack Sizes: 10mg, 25mg, 50mg, 100mg, 250mg. Molecular Formula: C29H49BrO3. US Biological Life Sciences. | Worldwide |
| 5-Bromo-5α-cholestane-3,6-diol 3-acetate | Heterocyclic Organic Compound. Alternative Names: 3β-Acetoxy-5-bromo-5α-cholestan-6β-ol. CAS No. 1258-35-1. Molecular formula: C29H49BrO3. Mole weight: 525.6. Appearance: White Solid. Purity: 0.96. IUPACName: [ (3R, 5R, 6R, 8S, 9S, 10R, 13R, 14S) -5-bromo-6-hydroxy-10, 13-dimethyl-17- [ (2R) -6-methylheptan-2-yl]-1, 2, 3, 4, 6, 7, 8, 9, 11, 12, 14, 15, 16, 17-tetradecahydrocyclopenta [a]phenanthren-3-yl] acetate. Canonical SMILES: CC (C)CCCC (C)C1CCC2C1 (CCC3C2CC (C4 (C3 (CCC (C4)OC (=O)C)C)Br)O)C. Catalog: ACM1258351. | |
| 5-Bromo-5α-cholestane-3,6-diol 3-Acetate | Intermediate in the production of cholesterol derivatives. Group: Biochemicals. Alternative Names: 3 β-Acetoxy-5-bromo-5α-cholestan-6 β-ol. Grades: Highly Purified. CAS No. 1258-35-1. Pack Sizes: 25mg. US Biological Life Sciences. | Worldwide |
| 6α-Hydroxy-5α-cholestanol-d7 | Steroids2H Labeled Compounds. Alternative Names: 6alpha-Hydroxy-5alpha-cholestanol-d7. CAS No. 1246302-83-9. Molecular formula: C27H41O2D7. Mole weight: 411.71. Catalog: ACM1246302839. | |
| 6-Keto cholestanol | 6-Keto cholestanol. Group: Biochemicals. Alternative Names: 5a-Cholestan-6-one; 6-Oxocholestanol; 3b-Hydroxy-5a-cholestan-6-one. Grades: Highly Purified. CAS No. 1175-06-0. Pack Sizes: 1g, 2g, 5g, 10g, 25g. Molecular Formula: C27H46O2. US Biological Life Sciences. | Worldwide |
| 6-Keto cholestanol | Steroidal Compounds. Alternative Names: 6-Ketocholestanol, AKJ-90705, CID301398, NSC178278, LT00440814, 5.alpha.-Cholestan-6-one, 3.beta.-hydroxy-, Cholestan-6-one, 3-hydroxy-, (3.beta.,5.alpha.)-, 1175-06-0, (3 beta -Hydroxy-5 alpha -cholestan-6-one, 5 alpha -Cholestan-3 beta -ol-6-one). CAS No. 1175-06-0. Molecular formula: C27H46O2. Mole weight: 402.65. Appearance: WHITE TO SLIGHTLY YELLOW FINE CRYSTALLINE POWDER. Purity: 0.95. IUPACName: 3-hydroxy-10, 13-dimethyl-17- (6-methylheptan-2-yl) -1, 2, 3, 4, 5, 7, 8, 9, 11, 12, 14, 15, 16, 17-tetradecahydrocyclopenta [a]phenanthren-6-one. Canonical SMILES: CC (C)CCCC (C)C1CCC2C1 (CCC3C2CC (=O)C4C3 (CCC (C4)O)C)C. Density: 1 g/cm³. ECNumber: 214-640-5. Catalog: ACM1175060. | |
| 6-Ketocholestanol (5a-Cholestan-6-one) | An oxygenated cholesterol which can be used as a ligand for cytosolic-nuclear tumor promoter binding protein. Group: Biochemicals. Alternative Names: 5a-Cholestan-6-one. Grades: Highly Purified. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| 7α,12α-Dihydroxy-5 β-cholestan-3-one | Substrate for 3α-Hydroxysteroid Dehydrogenase in primary bile acid biosynthesis. Group: Biochemicals. Alternative Names: (5 β, 7α, 12α)-7, 12-Dihydroxy-cholestan-3-one. Grades: Highly Purified. CAS No. 547-97-7. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| a-Cholestane | a-Cholestane. Group: Biochemicals. Alternative Names: (5a)-Cholestane; (20R)-5a(H),14a(H),17a(H)-Cholestane; (20R)-5a(H),14a(H),17a(H)-Cholestane. Grades: Highly Purified. CAS No. 481-21-0. Pack Sizes: 100mg, 250mg, 500mg, 1g, 2g. Molecular Formula: C27H48. US Biological Life Sciences. | Worldwide |
| b-Cholestanol | b-Cholestanol. Group: Biochemicals. Alternative Names: 5a-Cholestan-3b-ol. Grades: Highly Purified. CAS No. 80-97-7. Pack Sizes: 2g, 5g, 10g, 25g, 50g. Molecular Formula: C27H48O. US Biological Life Sciences. | Worldwide |
| I-Cholestane | Synonyms: i-Cholestane; 3,5-Cyclocholestane; (3aR, 3bS, 5aR, 6R, 8aS, 8bS) -3a, 5a-dimethyl-6- ( (R) -6-methylheptan-2-yl) hexadecahydrocyclopenta [a]cyclopropa [2, 3]cyclopenta [1, 2-f]naphthalene; (3α,5α)-3,5-Cyclocholestane. CAS No. 465-56-5. Molecular formula: C27H46. Mole weight: 370.65. | |
| 20(R), 22(R)-Dihydroxy Cholesterol | Synonyms: (20R,22R)-5α-Cholestane-3β,20,22-triol. Grades: > 95%. CAS No. 53448-11-6. Molecular formula: C27H46O3. Mole weight: 418.67. | |
| 2-[(3 β)-Cholesta-5,24-dien-3-yloxy]tetrahydro-2H-pyran | 2-[(3 β)-Cholesta-5,24-dien-3-yloxy]tetrahydro-2H-pyran is an protected intermediate in the synthesis of Desmosterol (D296860), a metabolite of Cholesterol (C432501). Group: Biochemicals. Alternative Names: Cholestane, 2H-Pyran Deriv. Grades: Highly Purified. CAS No. 51231-31-3. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| 3α,7α,12α-trihydroxy-5β-cholest-24-enoyl-CoA hydratase | This enzyme forms part of the rat peroxisomal multifunctional enzyme perMFE-2, which also exhibits a dehydrogenase activity. The enzyme is involved in the β-oxidation of the cholesterol side chain in the cholic-acid-biosynthesis pathway. Group: Enzymes. Synonyms: 46 kDa hydratase 2; (24R,25R)-3α,7α,12α,24-tetrahydroxy-5β-cholestanoyl-CoA hydro-lyase. Enzyme Commission Number: EC 4.2.1.107. CAS No. 152787-68-3. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4946; 3α,7α,12α-trihydroxy-5β-cholest-24-enoyl-CoA hydratase; EC 4.2.1.107; 152787-68-3; 46 kDa hydratase 2; (24R,25R)-3α,7α,12α,24-tetrahydroxy-5β-cholestanoyl-CoA hydro-lyase. Cat No: EXWM-4946. | |
| [[(3 β , 24E) -Cholesta-5, 24-dien-3-yl-26-13C]oxy] (1, 1-dimethylethyl) dimethylsilane-d6 | [[(3 β , 24E) -Cholesta-5, 24-dien-3-yl-26-13C]oxy] (1, 1-dimethylethyl) dimethylsilane is an protected intermediate in the synthesis of Desmosterol (D296860), a metabolite of Cholesterol (C432501). Group: Biochemicals. Alternative Names: Cholestane Silane Derivative-d6. Grades: Highly Purified. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| 7-Dehydrocholesterol | A vitamin precursor. Uses: Provitamins. Synonyms: Cholecalciferol EP Impurity B; (3β)-7-Dehydro Cholesterol; Dehydrocholesterol; 7,8-Didehydrocholesterol; Cholesta-5,7-dien-3beta-ol; 5,7-Cholestandien-3beta-ol; provitamin D3. Grades: > 95%. CAS No. 434-16-2. Molecular formula: C27H44O. Mole weight: 384.64. | |
| Atheronal A | Atheronal A. Group: Others. Purity: >99%. Mole weight: 418.652. Stability: 6 Months. Storage: -20°C. Avanti Polar Lipids; lipid products; sterols; sterols products; singnal transduction; cell pathways; Atheronal A; 3b-hydroxy-5-oxo-5,6-seco-cholestan-6-al. Cat No: STEZ-044. | |
| Atheronal A | Atheronal A is a product of cholesterol ozonolysis. It is produced in the neutrophils post oxidative burst. Atheronal molecules may be a new association, in the already complex inter-relationship, between inflammation, cholesterol oxidation, the tissue macrophage, and atherosclerosis. Synonyms: 3b-hydroxy-5-oxo-5,6-seco-cholestan-6-al; 3β-hydroxy-5-oxo-5,6-seco-cholestan-6-al. Grades: >99%. Molecular formula: C27H46O3. Mole weight: 418.65. | |
| Campestanol | Campestanol. Group: Biochemicals. Alternative Names: 5a-Cholestan-24(RS)-methyl-3b-ol; (3b,5a,24R)-Ergostan-3-ol; 24b-Ethylcholestanol. Grades: Highly Purified. CAS No. 474-60-2. Pack Sizes: 1mg. Molecular Formula: C28H50O. US Biological Life Sciences. | Worldwide |
| cholate-CoA ligase | Requires Mg2+ for activity. The mammalian enzyme is membrane-bound and catalyses the first step in the conjugation of bile acids with amino acids, converting bile acids into their acyl-CoA thioesters. Chenodeoxycholate, deoxycholate, lithocholate and trihydroxycoprostanoate can also act as substrates. The bacterial enzyme is soluble and participates in an anaerobic bile acid 7 α-dehydroxylation pathway. Group: Enzymes. Synonyms: BAL; bile acid CoA ligase; bile acid co. Enzyme Commission Number: EC 6.2.1.7. CAS No. 9027-90-1. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-5709; cholate-CoA ligase; EC 6.2.1.7; 9027-90-1; BAL; bile acid CoA ligase; bile acid coenzyme A ligase; choloyl-CoA synthetase; choloyl coenzyme A synthetase; cholic thiokinase; cholate thiokinase; cholic acid:CoA ligase; 3α,7α,12α-trihydroxy-5β-cholestanoyl coenzyme A synthetase; 3α,7α,12α-trihydroxy-5β-cholestanoate-CoA ligase; 3α,7α,12α-trihydroxy-5β-cholestanoate-CoA synthetase; THCA-CoA ligase; 3α,7α,12α-trihydroxy-5β-cholestanate-CoA ligase; 3α,7α,12α-trihydroxy-5β-cholestanate:CoA ligase (AMP-forming); cholyl-CoA synthetase; trihydroxycoprostanoyl-CoA synthetase. Cat No: EXWM-5709. | |
| Cholesterol | Cholesterol occurs as white or faintly yellow, almost odorless, pearly leaflets, needles, powder, or granules. On prolonged exposure to light and air, cholesterol acquires a yellow to tan color. Synonyms: Cholesterin; cholesterolum. CAS No. 57-88-5. Product ID: PE-0519. Molecular formula: C27H46O. Mole weight: 386.67. Category: Emollient; Emulsifying Agents. Product Keywords: Excipients for Liquid Dosage Form; Emulsifier Excipients; PE-0519; Cholesterol; Emollient; Emulsifying Agents; C27H46O; 57-88-5. UNII: 97C5T2UQ7J. Chemical Name: Cholest-5-en-3β-ol. Grade: Pharmceutical Excipients. Administration route: Injections; ophthalmic, topical, and vaginal. Dosage Form: Injections; ophthalmic, topical, and vaginal preparations. Stability and Storage Conditions: Cholesterol is stable and should be stored in a well-closed container, protected from light. Source and Preparation: The commercial material is normally obtained from the spinal cord of cattle by extraction with petroleum ethers, but it may also be obtained from wool fat. Purification is normally accomplished by repeated bromination. Cholesterol may also be produced by entirely synthetic means. Cholesterol produced from animal organs will always contain cholestanol and other saturated sterols. Applications: Cholesterol is used in cosmetics and topical pharmaceutical formulations at concentrations of 0.3-5.0% w/w as an emulsifying agent. It imparts water-absorbi |  |
| Cholesterol-5α,6α-epoxide | Steroidal Compounds. Alternative Names: 5,6alpha-epoxy-5alpha-cholestan-3beta-ol; cholestanol; Cholesterol epoxide; Cholesterol-5α,6α-epoxide; Epoxycholesterol; Cholesterol-5alpha,6alpha-epoxide. CAS No. 1250-95-9. Molecular formula: C27H46O2. Mole weight: 402.65. Purity: 0.95. IUPACName: 5,6α-epoxy-5α-cholestan-3β-ol. Canonical SMILES: CC (C)CCCC (C)C1CCC2C1 (CCC3C2CC4C5 (C3 (CCC (C5)O)C)O4)C. Density: 1.04g/cm³. ECNumber: 215-007-6. Catalog: ACM1250959. | |
| FUSIDIC ACID | Fusidic acid is a steroid antibiotic that is isolated from the fermentation broth of Fusidium coccineum. It has a role as a protein synthesis inhibitor, an EC 2.7.1.33 (pantothenate kinase) inhibitor and an Escherichia coli metabolite. It is a 3alpha-hydroxy steroid, an 11alpha-hydroxy steroid, a sterol ester, a steroid acid, an alpha,beta-unsaturated monocarboxylic acid and a steroid antibiotic. It is a conjugate acid of a fusidate. It derives from a hydride of a 5alpha-cholestane. CAS No. 6990-6-3. Product ID: PAP-0038. Molecular formula: C31H48O6. Category: Antibacterial, anti-inflammatory and antiviral. Product Keywords: Antibacterial, Anti-inflammatory and Antiviral Series; FUSIDIC ACID; PAP-0038; Antibacterial, anti-inflammatory and antiviral; C31H48O6; 6990-06-3. Standard: EP/ BP. Color: White to Off-White. EC Number: 230-256-0. Physical State: neat. Solubility: Practically insoluble in water, freely soluble in ethanol (96 per cent). Storage: Sealed in dry,2-8°C. Applications: Fusidic acid is an antibiotic that is often used topically in creams or ointments and eyedrops but may also be given systemically as tablets or injections. Boiling Point: 521.49°C (rough estimate). Melting Point: 190-192°C. Density: 1.0389 (rough estimate). Product Description: Fusidic acid is an antibiotic that is often used topically in creams or ointments and eyedrops but may also be given systemically as tablets or injections. | |
| Lathosterol | A Cholesterol metabolite. Lathosterol (indicating cholesterol synthesis) and Sitosterol (indicating cholesterol absorption) also decreased with deteriorating health. Low Lathosterol, Sitosterol and Cholesterol predicted mortality additively and independently of each other. Group: Biochemicals. Alternative Names: (3 β,5α)-Cholest-7-en-3-ol; 5α-Cholest-7-en-3 β-ol; 3 β-Hydroxy-5α-cholest-7-ene; 7-En-3-cholestanol; Cholest-7-en-3-ol; Lathosterol; Δ7-Cholestenol; γ-Cholestenol. Grades: Highly Purified. CAS No. 80-99-9. Pack Sizes: 10mg, 25mg, 50mg, 100mg, 250mg. Molecular Formula: C??H??O, Molecular Weight: 386.65. US Biological Life Sciences. | Worldwide |
| propanoyl-CoA C-acyltransferase | Also acts on dihydroxy-5β-cholestanoyl-CoA and other branched chain acyl-CoA derivatives. The enzyme catalyses the penultimate step in the formation of bile acids. The bile acid moiety is transferred from the acyl-CoA thioester (RCO-SCoA) to either glycine or taurine (NH2R') by EC 2.3.1.65, bile acid-CoA:amino acid N-acyltransferase. Group: Enzymes. Synonyms: SCP2 (gene name); peroxisomal thiolase 2; sterol carrier protein-χ; SCPχ; PTE-2 (ambiguous); propionyl-CoA C2-trimethyltridecanoyltransferase; 3-oxopristanoyl-CoA hydrolase; 3-oxopristanoyl-CoA thiolase; peroxisome sterol carrier protein thiolase; sterol carrier protein; oxopristanoyl-CoA thiolase; . Enzyme Commission Number: EC 2.3.1.176. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2117; propanoyl-CoA C-acyltransferase; EC 2.3.1.176; SCP2 (gene name); peroxisomal thiolase 2; sterol carrier protein-χ; SCPχ; PTE-2 (ambiguous); propionyl-CoA C2-trimethyltridecanoyltransferase; 3-oxopristanoyl-CoA hydrolase; 3-oxopristanoyl-CoA thiolase; peroxisome sterol carrier protein thiolase; sterol carrier protein; oxopristanoyl-CoA thiolase; peroxisomal 3-oxoacyl coenzyme A thiolase; SCPx; 4,8,12-trimethyltridecanoyl-CoA:propanoyl-CoA 2-C-4,8,12-trimethyltridecanoyltransferase. Cat No: EXWM-2117. | |
| Solanidine | Solanidine is a cholestane alkaloid isolated from several potato species including Solanum demissum , Solanum acaule , and Solanum tuberosum. Solanidine can inhibit proliferation and exhibit obvious antitumor effect [1]. Uses: Scientific research. Group: Natural products. CAS No. 80-78-4. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-N7271. | |
| Squalamine | Squalamine is an aminosterol compound with potent broad spectrum antiviral activity. Group: Inhibitors. Alternative Names: 3beta-N-1-(N-[3-(4-Aminobutyl)]- 1,3-diaminopropane)-7alpha,24R-dihydroxy-5alpha-cholestane 24-sulfate. CAS No. 148717-90-2. Molecular formula: C34H65N3O5S. Mole weight: 628. Appearance: Solid. Purity: 95%+. IUPACName: [(3R,6R)-6-[(3S,5R,7R,8R,9S,10S,13R,14S,17R)-3-[3-(4-Aminobutylamino)propylamino]-7-hydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]-2-methylheptan-3-yl] hydrogen sulfate. Canonical SMILES: C[C@@]12[C@] (C[C@@H] (O)[C@]3 ([H])[C@]2 ([H])CC[C@@]4 (C)[C@@]3 ([H])CC[C@]4 ([H])[C@@H] (CC[C@H] (C (C)C)OS (=O) (O)=O)C) ([H])C[C@@H] (NCCCNCCCCN)CC1. Density: 1.13±0.1 g/cm³. Catalog: ACM148717902. | |
| Trihydroxycoprostane | A sterol, similar to cholesterol and is a substrate for the sterol 27-hydroxylase enzyme in the bile salt synthetic pathway. The accumulation of this compound in urine can manifest as jaundice or, in more extreme cases, is a sign of Xanthomatosis. Group: Biochemicals. Alternative Names: (3α,5 β, 7α, 12α)-Cholestane-3, 7, 12-triol; 3α, 7α, 12α-Trihydroxycoprostane. Grades: Highly Purified. CAS No. 547-96-6. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Trodusquemine | Trodusquemine, also called as MSI-1436 or Aminosterol-1436, with the potential to treat type 2 diabetes and obesity, it is a non-competitive cholestane inihbitor that specifically targets the enzyme protein tyrosine phosphatase 1B (PTB-1B) with 200-fold s. Synonyms: [ (3R, 6R) -6-[ (3S, 5R, 7R, 8R, 9S, 10S, 13R, 14S, 17R) -3-[3-[4- (3-aminopropylamino) butylamino]propylamino]-7-hydroxy-10, 13-dimethyl-2, 3, 4, 5, 6, 7, 8, 9, 11, 12, 14, 15, 16, 17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]-2-methylheptan-3-yl] hydrogen sulfate 3-N-1(sperm. CAS No. 186139-09-3. Molecular formula: C37H72N4O5S. Mole weight: 685.06. | |
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