Glycocholic Acid-d5

CAS: 475-31-0

Ref. TR-G641352

Produktinformation

• Name: Glycocholic Acid-d5
• Synonyme: N-[(3a,5ß,7a,12a)-3,7,12-?rihydroxy-24-oxocholan-24-yl]glycine-d5, N-Choloylglycine-d5, Glycoreductodehydrocholic Acid-d5, 3a,7a,12a-Trihydroxy-5ß-cholanic ?cid-24-glycine-d5, Cholylglycine-d5, Glycine Cholate-d5, 3α,7α,12α-Trihydroxy-5β-cholan-24-oylglycine, 3α,7α,12α-Trihydroxy-5β-cholanic acid-24-glycine, 3α,7α,12α-Trihydroxy-N-(carboxymethyl)-5β-cholan-24-amide, 5β-Cholan-24-amide, N-(carboxymethyl)-3α,7α,12α-trihydroxy-, Cholane, glycine deriv., Cholylglycine, Glycine cholate, Glycine, N-[(3α,5β,7α,12α)-3,7,12-trihydroxy-24-oxocholan-24-yl]-, Glycine, N-choloyl-, Glycocholic Acid Free Acid, Glycocholic acid, Glycoreductodehydrocholic acid, Glycylcholic acid, N-(3-alpha,7-alpha,12-alpha-trihydroxycholan-24-oyl)glycine, N-(3-α,7-α,12-α-Trihydroxycholan-24-oyl)glycin, N-(3-α,7-α,12-α-trihydroxycholan-24-oyl)glycine, N-(3-α,7-α,12-α-trihydroxycholane-24-oyl)glycine, N-(3-α-7-α-12-α-trihidroxicolan-24-oil)glicina, N-Choloylglycine, N-[(3alpha,5beta,7alpha,12alpha)-3,7,12-trihydroxy-24-oxocholan-24-yl]glycine, N-[(3α,5β,7α,12α)-3,7,12-Trihydroxy-24-oxocholan-24-yl]glycine

Beschreibung

Stability Hygroscopic
Applications The product of conjugation of cholic acid with glycine; chief ingredient of the bile of herbivorous animals. In the weakly alkaline bile fluid glycocholic acid exists as the sodium salt.
References Ho, R., et al.: J. Biol. Chem., 279, 7213 (2004), Pasanen, M., et al.: Eur. J. Clin. Pharmacol., 62, 409 (2006), He, Y., et al.: Drug Metab. Dispos., 36, 1453 (2008),

• Marke: TRC

Chemische Eigenschaften

• Molekulargewicht: 470.65
• Formel: C₂₆H₃₈D₅NO₆
• Farbe/Form: Neat
• InChl: InChI=1S/C26H43NO6/c1-14(4-7-22(31)27-13-23(32)33)17-5-6-18-24-19(12-21(30)26(17,18)3)25(2)9-8-16(28)10-15(25)11-20(24)29/h14-21,24,28-30H,4-13H2,1-3H3,(H,27,31)(H,32,33)/t14-,15+,16-,17-,18+,19+,20-,21+,24+,25+,26-/m1/s1/i8D2,10D2,16D
• InChI Key: InChIKey=RFDAIACWWDREDC-IYHMEHENSA-N
• SMILES: [2H]C1([2H])C[C@]2(C)[C@H]3C[C@H](O)[C@@]4(C)[C@@H](CC[C@@H]4[C@H](C)CCC(=O)NCC(=O)O)[C@@H]3[C@H](O)C[C@@H]2C([2H])([2H])[C@]1([2H])O