α-Hyodeoxycholic Acid-d5

CAS : 83-49-8

Ref. TR-H998102

Informations sur le produit

• Nom: α-Hyodeoxycholic Acid-d5
• Synonymes: (3a,5ß,6a)-3,6-Dihydroxycholan-24-oic Acid-d5, 3a,6a-Dihydroxy-5ß-cholan-24 -oate-d5, 3a,6a-Dihydroxy-5ß-cholan-24-oic Acid-d5, 6a-Hydroxylithocholic Acid-d5, 7-Deoxyhyocholic Acid-d5, Hyodeoxycholic Acid-d5, Hyodesoxycholic Acid-d5, Iodeoxycholic Acid-d5, NSC 60672-d5, (3Alpha,5Beta,6Alpha)-3,6-Dihydroxycholan-24-Oate, (3Alpha,5Beta,6Alpha)-3,6-Dihydroxycholan-24-Oic Acid, (3Alpha,5Beta,6Alpha,8Xi,9Xi,14Xi)-3,6-Dihydroxycholan-24-Oic Acid, (3Alpha,6Alpha)-3,6-Dihydroxycholan-24-Oic Acid, (3α,5β,6α)-3,6-Dihydroxycholan-24-oic acid, 3,6-Dihydroxycholan-24-Oic Acid, 3alpha,6alpha-Dihydroxy-5beta-cholan-24-oic acid, 3α,6α-Dihydroxy-5β-cholan-24-oate, 3α,6α-Dihydroxy-5β-cholan-24-oic acid, 3α,6α-Dihydroxy-5β-cholanic acid, 3α,6α-Dihydroxy-5β-cholanoic acid, 4-[(3R,5R,6S,10R,13R,17R)-3,6-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, 5β-Cholan-24-oic acid, 3α,6α-dihydroxy-, 5β-Cholanic acid, 3α,6α-dihydroxy-, 6α-Hydroxylithocholic acid, 7-Deoxyhyocholic acid, Cholan-24-oic acid, 3,6-dihydroxy-, (3α,5β,6α)-, Hyodesoxycholic acid, Iodeoxycholic acid, NSC 60672, Pig Hyodeoxycholic acid, α-Hyodeoxycholic acid

Description

Applications Labelled Hyodeoxycholic Acid. Unlabelled version is isolated from pig bile. Antitumor agent.
References Abadie, C., et al.: Biochem. J., 299, 725 (1994), Taniguchi, T., et al.: J. Biol. Chem., 269, 10071 (1994), Davis, R., et al.: J. Lipid Res., 43, 533 (2002),

• Marque: TRC

Propriétés chimiques

• Masse moléculaire: 397.6
• Formule: C₂₄H₃₅D₅O₄
• Couleur/Forme: Neat
• InChI: InChI=1S/C24H40O4/c1-14(4-7-22(27)28)17-5-6-18-16-13-21(26)20-12-15(25)8-10-24(20,3)19(16)9-11-23(17,18)2/h14-21,25-26H,4-13H2,1-3H3,(H,27,28)/t14-,15-,16+,17-,18+,19+,20+,21+,23-,24-/m1/s1/i8D2,12D2,15D
• Code InChI: InChIKey=DGABKXLVXPYZII-QJMAJIAASA-N
• SMILES: [2H]C1([2H])C[C@]2(C)[C@H]3CC[C@@]4(C)[C@@H](CC[C@@H]4[C@H](C)CCC(=O)O)[C@@H]3C[C@H](O)[C@@H]2C([2H])([2H])[C@]1([2H])O