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| Product | Description | |
|---|---|---|
| Chenodeoxycholic acid | 5g Pack Size. Group: Biochemicals, Detergents. Formula: C24H40O4. CAS No. 474-25-9. Prepack ID 31295558-5g. Molecular Weight 392.57. See USA prepack pricing. |  |
| Chenodeoxycholic Acid | Chenodeoxycholic Acid is a hydrophobic primary bile acid that activates nuclear receptors ( FXR ) involved in cholesterol metabolism. Uses: Scientific research. Group: Natural products. Alternative Names: CDCA. CAS No. 474-25-9. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg; 1 g; 5 g; 10 g. Product ID: HY-76847. |  |
| Chenodeoxycholic Acid | Chenodeoxycholic Acid - Product ID: NST-10-100. Category: Sterols. Alternative Names: Chenodiol. Purity: 98%. Test method: HPLC. CAS No. 474-25-9. Pack Sizes: 50g, 100g, 250g, 500g. Appearance: White to off-white powder. Molecular formula: C24H40O4. Mole weight: 392.57. Storage: +2 +8 °C. |  |
| Chenodeoxycholic Acid | Chenodeoxycholic Acid. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Deoxychenocholic acid. Product Category: Steroidal Compounds. Appearance: White to off-white powder. CAS No. 474-25-9. Molecular formula: C24H40O4. Mole weight: 392.57. Purity: 0.98. IUPACName: (4R)-4-[(3R,5S,7R,8R,9S,10S,13R,14S,17R)-3,7-Dihydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]pentanoic acid. Canonical SMILES: CC(CCC(=O)O)C1CCC2C1(CCC3C2C(CC4C3(CCC(C4)O)C)O)C. Density: 0.9985 g/cm³. ECNumber: 207-481-8. Product ID: ACM474259. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Chenodeoxycholic acid 24-acyl-b-D-glucuronide | Chenodeoxycholic acid 24-acyl-β-D-glucuronide is an indispensable constituent within the biomedical domain predominantly employed for the therapeutic research of hepatic ailments including cholestasand biliary cirrhosis. This compound exerts formidable hepatoprotective attributes and ensures the homeostasis of bile acid metabolism. Synonyms: 1-[(3a,5b,7a)-3,7-Dihydroxycholan-24-oate] b-D-glucopyranuronic acid. CAS No. 208038-27-1. Molecular formula: C30H48O10. Mole weight: 568.70. |  |
| Chenodeoxycholic Acid 24-Acyl- β-D-glucuronide | Chenodeoxycholic Acid 24-Acyl- β-D-glucuronide is a glucuronide metabolite of Chenodeoxycholic Acid (CDCA). Group: Biochemicals. Alternative Names: 1-[(3α,5 β,7α)-3,7-Dihydroxycholan-24-oate] β-D-Glucopyranuronic Acid. Grades: Highly Purified. CAS No. 208038-27-1. Pack Sizes: 2.5mg, 10mg. US Biological Life Sciences. |  Worldwide |
| Chenodeoxycholic Acid 24-Acyl- β-D-glucuronide Allyl Ester | A glucuronide metabolite of Chenodeoxycholic Acid (CDCA) (C291900). Group: Biochemicals. Alternative Names: 1-[(3α,5 β,7α)-3,7-Dihydroxycholan-24-oate] β-D-Glucopyranuronic Acid Allyl Ester. Grades: Highly Purified. Pack Sizes: 25mg. US Biological Life Sciences. | Worldwide |
| Chenodeoxycholic acid-3- β-D-glucuronide | Chenodeoxycholic acid-3- β-D-glucuronide is a derivative of chenodeoxycholic acid (C291900). Chenodeoxycholic acid 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. Fcilitates fat absorption in the small intestine by micellar solubilization of fatty acids and monoglycerides. Anticholelithogenic. Epimeric with Ursodiol. Group: Biochemicals. Grades: Highly Purified. CAS No. 58814-71-4. Pack Sizes: 5mg, 50mg. Molecular Formula: C30H48O10. US Biological Life Sciences. | Worldwide |
| Chenodeoxycholic acid, 95+% | 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. Fcilitates fat absorption in the small intestine by micellar solubilization of fatty acids and monoglycerides. Anticholelithogenic. Epimeric with Ursodiol. Group: Biochemicals. Alternative Names: (3α,5 β,7α)-3,7-Dihydroxycholan-24-oic Acid; (+)-Chenodeoxycholic Acid; 17 β - (1-Methyl-3-carboxypropyl) etiocholane-3α , 7α -diol; Chenodeoxycholic Acid; Chenodiol; CDCA; CDC; Chendol; Chenocol; Fluibil. Grades: Highly Purified. CAS No. 474-25-9. Pack Sizes: 25g, 50g, 100g, 250g, 500g. Molecular Formula: C24H40O4. US Biological Life Sciences. | Worldwide |
| Chenodeoxycholic Acid-d4 | Labeled Chenodiol (Chenodeoxycholic acid). 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. Fcilitates fat absorption in the small intestine by micellar solubilization of fatty acids and monoglycerides. Anticholelithogenic. Epimeric with Ursodiol. Group: Biochemicals. Alternative Names: (3α,5 β,7α)-3,7-Dihydroxycholan-24-oic Acid-d4; (+)-Chenodeoxycholic Acid-d4; 17 β - (1-Methyl-3-carboxypropyl) etiocholane-3α , 7α -diol-d4; Chenodeoxycholic Acid-d4; CDC-d4; Chendol-d4; Chenodiol-d4; Chenocol-d4; Fluibil-d4. Grades: Highly Purified. CAS No. 99102-69-9. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Chenodeoxycholic Acid-d5 (Major) | Labeled Chenodiol (Chenodeoxycholic acid). 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. Alternative Names: (3α,5 β,7α)-3,7-Dihydroxycholan-24-oic Acid-d5; (+)-Chenodeoxycholic Acid-d5; 17 β - (1-Methyl-3-carboxypropyl) etiocholane-3α , 7α -diol-d5; Chenodeoxycholic Acid-d5; CDC-d5; Chendol-d5; Chenodiol-d5; Chenocol-d5; Fluibil-d5. Grades: Highly Purified. CAS No. 52840-12-7. Pack Sizes: 2.5mg. Molecular Formula: C24H35D5O4. US Biological Life Sciences. | Worldwide |
| Chenodeoxycholic Acid-d7 (Major) | Chenodeoxycholic Acid-d7 is a labelled analogue of 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. Fcilitates fat absorption in the small intestine by micellar solubilization of fatty acids and monoglycerides. Anticholelithogenic. Epimeric with Ursodiol. In addition, Chenodeoxycholic Acid-d7 is an intermediate in synthesizing Glycochenodeoxycholic Acid-d7 Sodium Salt (G641257), which is a labelled Glycochenodeoxycholic Acid (G641255). A bile salt formed in the liver from chenodeoxycholate and glycine, usually as the sodium salt. It acts as a detergent to solubilize fats for absorption and is itself absorbed. It is a cholagogue and choleretic. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 2.5mg, 5mg. Molecular Formula: C24H33D7O4. US Biological Life Sciences. | Worldwide |
| Chenodeoxycholic acid diacetate methyl ester | Chenodeoxycholic acid diacetate methyl ester. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 3α,7α-Diacetoxy-5β-cholan-24-oic acid methyl ester. Product Category: Steroidal Compounds. CAS No. 2616-71-9. Molecular formula: C29H46O6. Mole weight: 490.67. Purity: 0.95. IUPACName: methyl (4R)-4-[(3R,5S,7R,8R,9S,10S,13R,14S,17R)-3,7-diacetyloxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]pentanoate. Canonical SMILES: CC(CCC(=O)OC)C1CCC2C1(CCC3C2C(CC4C3(CCC(C4)OC(=O)C)C)OC(=O)C)C. Density: 1.10±0.1 g/cm³ (Predicted). ECNumber: 636-755-3. Product ID: ACM2616719. Alfa Chemistry ISO 9001:2015 Certified. | |
| Chenodeoxycholic Acid Impurity 2 | Chenodeoxycholic Acid Impurity 2. Uses: For analytical and research use. Group: Impurity standards. CAS No. 15173-22-5. Molecular Formula: C24H40O3. Mole Weight: 376.58. Catalog: APB15173225. |  |
| Chenodeoxycholic Acid Impurity 3 | Chenodeoxycholic Acid Impurity 3. Uses: For analytical and research use. Group: Impurity standards. CAS No. 83896-19-9. Molecular Formula: C24H40N2O4. Mole Weight: 420.59. Catalog: APB83896199. | |
| Chenodeoxycholic Acid Impurity 4 | Chenodeoxycholic Acid Impurity 4. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1024498-33-6. Molecular Formula: C48H76N2O8. Mole Weight: 809.14. Catalog: APB1024498336. | |
| Chenodeoxycholic Acid Impurity 5 | Chenodeoxycholic Acid Impurity 5. Uses: For analytical and research use. Group: Impurity standards. CAS No. 96840-44-7. Molecular Formula: C24H42N2O3. Mole Weight: 406.61. Catalog: APB96840447. | |
| Chenodeoxycholic Acid Methyl Ester | A bile acid with hemolytic properties. Inhibits the initiation of Clostridium difficile spore germination. Anti-inflamatiory activity. Group: Biochemicals. Alternative Names: (3α,5 β,7α)-3,7-Dihydroxy-cholan-24-oic Acid Methyl Ester; Chenodeoxycholic Acid Methyl Ester; Methyl 3α,7α-Dihydroxy-5 β-cholan-24-oate; Methyl 3α,7α-Dihydroxy-5 β-cholanoate; Methyl Chenodeoxycholate. Grades: Highly Purified. CAS No. 3057-4-3. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
| Chenodeoxycholic acid sodium | Chenodeoxycholic acid sodium is a hydrophobic primary bile acid that activates nuclear receptors ( FXR ) involved in cholesterol metabolism. Uses: Scientific research. Group: Natural products. Alternative Names: CDCA sodium. CAS No. 2646-38-0. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg; 1 g; 5 g; 10 g. Product ID: HY-76847A. | |
| Chenodeoxycholic-2,2,4,4-d4 acid | Chenodeoxycholic-2,2,4,4-d4 acid. Uses: Designed for use in research and industrial production. Additional or Alternative Names: (3α,5β,7α)-3,7-Dihydroxycholan-24-oic acid-d4; 17β-(1-Methyl-3-carboxypropyl)etiocholane-3α,7α-diol-d4; CDC-d4. Product Category: Heterocyclic Organic Compound. Appearance: White solid. CAS No. 99102-69-9. Molecular formula: C24H36D4O4. Mole weight: 396.6. Purity: 98 atom % D. IUPACName: (4R)-4-[(3R,5S,7R,8R,9S,10S,13R,14S,17R)-2,2,4,4-tetradeuterio-3,7-dihydroxy-10,13-dimethyl-3,5,6,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]pentanoic acid. Canonical SMILES: CC(CCC(=O)O)C1CCC2C1(CCC3C2C(CC4C3(CCC(C4)O)C)O)C. Density: 1.14g/cm³. Product ID: ACM99102699. Alfa Chemistry ISO 9001:2015 Certified. Categories: Chenodeoxycholic Acid-d4. | |
| Glycochenodeoxycholic acid | Glycochenodeoxycholic acid (Chenodeoxycholylglycine) is a relatively toxic bile salt generated in the liver from chenodeoxycholic acid and glycine. Glycochenodeoxycholic acid inhibits Autophagosome formation and impairs lysosomal function by inhibiting lysosomal proteolysis and increasing lysosomal pH in human normal liver cells, leading to the Apoptosis of human hepatocyte cells. Glycochenodeoxycholic acid induces stemness and chemoresistance via activating STAT3 signaling pathway in hepatocellular carcinoma cells (HCC). Glycochenodeoxycholic acid is promising for research in the field of cholestasis desease, hepatocellular carcinoma and primary sclerosing cholangitis (PSC) [1] [2] [3] [4]. Uses: Scientific research. Group: Natural products. Alternative Names: Chenodeoxycholylglycine. CAS No. 640-79-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg. Product ID: HY-N2334. | |
| Glycochenodeoxycholic acid-d4 | Glycochenodeoxycholic acid-d 4 is the deuterium labeled Glycochenodeoxycholic acid. Glycochenodeoxycholic acid (Chenodeoxycholylglycine) is a bile acid formed in the liver from chenodeoxycholate and glycine. It acts as a detergent to solubilize fats for absorption and is itself absorbed. Glycochenodeoxycholic acid (Chenodeoxycholylglycine) induces hepatocyte apoptosis[1][2]. Uses: Scientific research. Group: Isotope-labeled compounds. Alternative Names: Chenodeoxycholylglycine-d4. CAS No. 1201918-16-2. Pack Sizes: 1 mg. Product ID: HY-N2334S. | |
| Glycochenodeoxycholic Acid-d5 3-Sulfate Disodium Salt | Labeled Glycochenodeoxycholic Acid 3-Sulfate. A bile salt formed in the liver from chenodeoxycholate and glycine, usually as the sodium salt. It acts as a detergent to solubilize fats for absorption and is itself absorbed. It is a cholagogue and choleretic. Group: Biochemicals. Alternative Names: N-[(3α,5 β,7α)-7-Hydroxy-24-oxo-3-(sulfooxy)cholan-24-yl]glycine-d5 Disodium Salt; Glycochenodeoxycholic Acid 3α-Sulfate-d5 Disodium Salt. Grades: Highly Purified. Pack Sizes: 500ug, 1mg. US Biological Life Sciences. | Worldwide |
| Glycochenodeoxycholic acid sodium salt | Glycochenodeoxycholic acid sodium salt (Sodium glycochenodeoxycholate) is a relatively toxic bile salt generated in the liver from chenodeoxycholic acid and glycine. Glycochenodeoxycholic acid sodium salt inhibits Autophagosome formation and impairs lysosomal function by inhibiting lysosomal proteolysis and increasing lysosomal pH in human normal liver cells, leading to the Apoptosis of human hepatocyte cells. Glycochenodeoxycholic acid sodium salt induces stemness and chemoresistance via activating STAT3 signaling pathway in hepatocellular carcinoma cells (HCC). Glycochenodeoxycholic acid sodium salt is promising for research in the field of cholestasis desease, hepatocellular carcinoma and primary sclerosing cholangitis (PSC) [1] [2] [3] [4]. Uses: Scientific research. Group: Natural products. Alternative Names: Chenodeoxycholylglycine sodium salt; Sodium glycochenodeoxycholate. CAS No. 16564-43-5. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-N2334A. | |
| Taurochenodeoxycholic acid | Taurochenodeoxycholic acid is a bile salt formed in the liver. It solubilizes fats in the small intestine and is itself absorbed. Synonyms: Taurochenodeoxycholate; Chenyltaurine; Chenodeoxycholyltaurine. CAS No. 516-35-8. Molecular formula: C26H45NO6S. Mole weight: 499.707. | |
| [(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,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,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 |
| 2-Ethoxy-1-ethoxycarbonyl-1,2-dihydroquinoline | 2-Ethoxy-1-ethoxycarbonyl-1,2-dihydroquinoline is used in the synthesis of Glycochenodeoxycholic Acid 3-Sulfate Disodium Salt which is a bile salt formed in the liver from chenodeoxycholate and glycine, usually as the sodium salt. It acts as a detergent to solubilize fats for absorption and is itself absorbed. It is a cholagogue and choleretic. Synonyms: 1-(Ethoxycarbonyl)-2-ethoxy-1,2-dihydroquinoline; 2-Ethoxy-1(2H)-quinolinecarboxylic acid ethyl ester; 2-Ethoxy-1-(ethoxycarbonyl)-1,2-dihydroquinoline; 2-Ethoxy-N-(ethoxycarbonyl)-1,2-dihydroquinoline; EEDQ; Ethyl 2-ethoxy-1(2H)-quinolinecarboxylate; N-(Ethoxycarbonyl)-2-ethoxy-1,2-dihydroquinoline; N-Carbethoxy-2-ethoxy-1,2-dihydroquinoline; NSC 147831; Ethyl N-(2-ethoxy-1,2-dihydroquinoline)carboxylate. Grades: 99 % (HPLC). CAS No. 16357-59-8. Molecular formula: C14H17NO3. Mole weight: 247.29. | |
| 3α,7α-Dihydroxycoprostanic acid | 3α, 7α-Dihydroxycoprostanic acid is an endogenous metabolite. 3α, 7α-Dihydroxycoprostanic acid, a bile acid, is the precursor to chenodeoxycholic acid [1]. Uses: Scientific research. Group: Natural products. CAS No. 17974-66-2. Pack Sizes: 1 mg. Product ID: HY-113097. | |
| 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. |  |
| 7α-hydroxycholest-4-en-3-one 12α-hydroxylase | A P-450 heme-thiolate protein. Requires EC 1.6.2.4, NADPH-hemoprotein reductase and cytochrome b5 for maximal activity. This enzyme is important in bile acid biosynthesis, being responsible for the balance between the formation of cholic acid and chenodeoxycholic acid. Group: Enzymes. Synonyms: 7α-hydroxy-4-cholesten-3-one 12α-monooxygenase; CYP12; sterol 12α-hydroxylase (ambiguous); HCO 12α-hydroxylase. Enzyme Commission Number: EC 1.14.18.8. 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-0970; 7α-hydroxycholest-4-en-3-one 12α-hydroxylase; EC 1.14.18.8; 7α-hydroxy-4-cholesten-3-one 12α-monooxygenase; CYP12; sterol 12α-hydroxylase (ambiguous); HCO 12α-hydroxylase. Cat No: EXWM-0970. | |
| 7α-Hydroxy Cholesterol | 7α-hydroxy Cholesterol is an oxysterol and a precursor in the biosynthesis of the bile acids cholic acid and chenodeoxycholic acid. 7α-Hydroxy Cholesterol is also a secondary metabolite of Cholesterol. 7α-hydroxy Cholesterol (40 μM) increases levels of the adhesion molecules ICAM-1, VCAM-1, and E-selectin in human umbilical vein endothelial cells (HUVECs). Synonyms: cholest-5-ene-3β,7α-diol; 7alpha-hydroxy-cholesterol; 7-alpha-OHC. Grades: > 95%. CAS No. 566-26-7. Molecular formula: C27H46O2. Mole weight: 402.65. | |
| Sodium Deoxycholate | Chenodeoxycholic Acid Sodium Salt; Chenodeoxycholic Acid Sodium Salt; 7-Deoxycholic Acid Sodium Salt. CAS No. 302-95-4. Product ID: 1-01530. Molecular formula: C24H39NaO4. Mole weight: 414.56. Properties: mp 172-175°C. MFCD No. MFCD00064139. |  |
| Sodium glycochenodeoxycholate | Sodium glycochenodeoxycholate is a bile salt formed in the liver from chenodeoxycholate and glycine, usually as the sodium salt. It acts as a detergent to solubilize fats for absorption and is itself absorbed. It is a cholagogue and choleretic. Synonyms: Glycochenodeoxycholic acid sodium salt. CAS No. 16564-43-5. Molecular formula: C26H42NNaO5. Mole weight: 471.614. | |
| 3α-hydroxy bile acid-CoA-ester 3-dehydrogenase | This bacterial enzyme is involved in the 7-dehydroxylation process associated with bile acid degradation. The enzyme has very little activity with unconjugated bile acid substrates. It has similar activity with choloyl-CoA, chenodeoxycholoyl-CoA, deoxycholoyl-CoA, and lithocholoyl-CoA. Group: Enzymes. Synonyms: baiA1 (gene name); baiA2 (gene name); baiA3 (gene name). Enzyme Commission Number: EC 1.1.1.395. 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-0315; 3α-hydroxy bile acid-CoA-ester 3-dehydrogenase; EC 1.1.1.395; baiA1 (gene name); baiA2 (gene name); baiA3 (gene name). Cat No: EXWM-0315. | |
| chenodeoxycholoyltaurine hydrolase | Some other taurine conjugates are hydrolysed, but not glycine conjugates of bile acids. Group: Enzymes. Enzyme Commission Number: EC 3.5.1.74. CAS No. 125752-75-2. 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-4465; chenodeoxycholoyltaurine hydrolase; EC 3.5.1.74; 125752-75-2. Cat No: EXWM-4465. | |
| 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. | |
| glycochenodeoxycholate sulfotransferase | The enzyme specifically sulfates glycochenodeoxycholate at the 7α-position (see also EC 2.8.2.14 bile-salt sulfotransferase). The monohydroxy bile acids glycolithocholate, chenodeoxycholate and ursodeoxycholate act as inhibitors. Group: Enzymes. Synonyms: bile acid:3'-phosphoadenosine-5'-phosphosulfate sulfotransferase; bile acid:PAPS:sulfotransferase; BAST. Enzyme Commission Number: EC 2.8.2.34. CAS No. 72668-90-7. 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-3394; glycochenodeoxycholate sulfotransferase; EC 2.8.2.34; 72668-90-7; bile acid:3'-phosphoadenosine-5'-phosphosulfate sulfotransferase; bile acid:PAPS:sulfotransferase; BAST. Cat No: EXWM-3394. | |
| taurochenodeoxycholate 6α-hydroxylase | A heme-thiolate protein (P-450). Requires cytochrome b5 for maximal activity. Acts on taurochenodeoxycholate, taurodeoxycholate and less readily on lithocholate and chenodeoxycholate. In adult pig (Sus scrofa), hyocholic acid replaces cholic acid as a primary bile acid. Group: Enzymes. Synonyms: CYP3A4; CYP4A21; taurochenodeoxycholate 6α-monooxygenase. Enzyme Commission Number: EC 1.14.13.97. CAS No. 105669-85-0. 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-0905; taurochenodeoxycholate 6α-hydroxylase; EC 1.14.13.97; 105669-85-0; CYP3A4; CYP4A21; taurochenodeoxycholate 6α-monooxygenase. Cat No: EXWM-0905. | |
| Taurochenodesoxycholic acid | Taurochenodesoxycholic acid - Product ID: NST-10-229. Category: Sterols. Alternative Names: 12-Deoxycholyltaurine, Chenodeoxycholyltaurine, Chenyltaurine. Purity: 98%. Test method: HPLC. CAS No. 516-35-8. Pack Sizes: 5g, 10g, 25g, 50g. Appearance: White Powder. Molecular formula: C26H45NO6S. Mole weight: 499.7. Storage: +2 +8 °C. | |
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