hyodeoxycholic acid (Q5957042)

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chemical compound

7-Deoxyhyocholic acid
Hyodesoxycholic acid
3alpha,6alpha-Dihydroxy-5beta-cholanic acid
6alpha-Hydroxylithocholate
Iodeoxycholic acid
4-[(10R)-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]valeric acid
4-[(10R)-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
3a,6a-Dihydroxy-5b-cholanate
6a-Hydroxylithocholate
a-Hyodeoxycholic acid
7-Deoxyhyocholate
6a-Hydroxylithocholic acid
3a,6a-Dihydroxy-5b-cholanic acid
Hyodesoxycholate
3a,6a-Dihydroxy-5b-cholanoic acid
3a,6a-Dihydroxy-5b-cholanoate
alpha-Hyodeoxycholate
Hyodeoxycholate
3a,6a-Dihydroxy-5b-cholan-24-oic acid
a-Hyodeoxycholate
(4R)-4-[(1S,2R,5R,8S,10S,11S,14R,15R)-5,8-dihydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecan-14-yl]pentanoic acid
Iodeoxycholate
3a,6a-Dihydroxy-5b-cholan-24-oate
alpha-Hyodeoxycholic acid

Language	Label	Description	Also known as
English	hyodeoxycholic acid	chemical compound	7-Deoxyhyocholic acid Hyodesoxycholic acid 3alpha,6alpha-Dihydroxy-5beta-cholanic acid 6alpha-Hydroxylithocholate Iodeoxycholic acid 4-[(10R)-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]valeric acid 4-[(10R)-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 3a,6a-Dihydroxy-5b-cholanate 6a-Hydroxylithocholate a-Hyodeoxycholic acid 7-Deoxyhyocholate 6a-Hydroxylithocholic acid 3a,6a-Dihydroxy-5b-cholanic acid Hyodesoxycholate 3a,6a-Dihydroxy-5b-cholanoic acid 3a,6a-Dihydroxy-5b-cholanoate alpha-Hyodeoxycholate Hyodeoxycholate 3a,6a-Dihydroxy-5b-cholan-24-oic acid a-Hyodeoxycholate (4R)-4-[(1S,2R,5R,8S,10S,11S,14R,15R)-5,8-dihydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecan-14-yl]pentanoic acid Iodeoxycholate 3a,6a-Dihydroxy-5b-cholan-24-oate alpha-Hyodeoxycholic acid

Statements

type of chemical entity

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chemical structure

Hyodeoxycholic acid acsv.svg
1,655 × 1,125; 30 KB

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392.29266 dalton

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language of work or name

HYODEOXYCHOLIC ACID (English)

6 October 2016

stereoisomer of

3alpha,6alpha-Dihydroxy-5alpha-cholan-24-oic Acid

2 references

based on heuristic

inferred from InChIKey

based on heuristic

inferred from InChI

2 references

based on heuristic

inferred from InChIKey

based on heuristic

inferred from InChI

1 reference

based on heuristic

inferred from InChI

1 reference

based on heuristic

inferred from InChI

3beta,6beta-dihydroxy-5beta-cholan-24-oic acid

1 reference

based on heuristic

inferred from InChI

1 reference

based on heuristic

inferred from InChI

murideoxycholic acid

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based on heuristic

inferred from InChI

chemical formula

C₂₄H₄₀O₄

1 reference

language of work or name

HYODEOXYCHOLIC ACID (English)

6 October 2016

canonical SMILES

CC(CCC(=O)O)C1CCC2C1(CCC3C2CC(C4C3(CCC(C4)O)C)O)C

1 reference

language of work or name

HYODEOXYCHOLIC ACID (English)

6 October 2016

isomeric SMILES

C[C@H](CCC(=O)O)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2C[C@@H]([C@H]4[C@@]3(CC[C@H](C4)O)C)O)C

1 reference

language of work or name

HYODEOXYCHOLIC ACID (English)

6 October 2016

198.0 degree Celsius

1 reference

Jean-Claude Bradley Open Melting Point Dataset

1 reference

Hyodeoxycholic acid improves HDL function and inhibits atherosclerotic lesion formation in LDLR-knockout mice

Identifiers

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

1 reference

language of work or name

HYODEOXYCHOLIC ACID (English)

6 October 2016

DGABKXLVXPYZII-SIBKNCMHSA-N

2 references

language of work or name

HYODEOXYCHOLIC ACID (English)

6 October 2016

ChEBI release 2020-09-01

CAS Registry Number

2 references

language of work or name

hyodeoxycholic acid (English)

6 October 2016

DGABKXLVXPYZII-SIBKNCMHSA-N

CAS Common Chemistry

10 April 2021

https://commonchemistry.cas.org/detail?cas_rn=83-49-8

1 reference

language of work or name

Hyodeoxycholic acid (English)

6 October 2016

1 reference

language of work or name

HYODEOXYCHOLIC ACID (English)

6 October 2016

Reaxys registry number

3218394

1 reference

language of work or name

hyodeoxycholic acid (English)

6 October 2016

mapping relation type

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language of work or name

hyodeoxycholic acid (English)

6 October 2016

1 reference

language of work or name

HYODEOXYCHOLIC_ACID (English)

6 October 2016

UniChem compound ID

1 reference

MassBank accession ID

MSBNK-Metabolon-MT000122

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MSBNK-Nihon_Univ-NU000461

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MSBNK-Nihon_Univ-NU000462

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splash10-03di-6900000000-4fd08adbf84490eccc8d

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splash10-014i-9100000000-f9b18d5a5d1db2f8d606

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201-483-2

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Global Substance Registration System

language of work or name

HYODEOXYCHOLIC ACID (English)

6 October 2016

ECHA Substance Infocard ID

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

27 December 2018

3-α,6-α-dihydroxy-5-β-cholan-24-oic acid (English)

CAS no.: 83-49-8 (English)

1 reference

6 July 2021

CAS no.: 83-49-8 (English)

Hyodeoxycholic Acid (English)

Human Metabolome Database ID

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1 reference

language of work or name

hyodeoxycholic acid (English)

6 October 2016

1 reference

Global Substance Registration System

language of work or name

HYODEOXYCHOLIC ACID (English)

6 October 2016

Probes And Drugs ID

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1 reference

language of work or name

hyodeoxycholic acid (English)

6 October 2016

0 references

1 reference

6 April 2020

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Microsoft Academic ID

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Sitelinks

Wikipedia(7 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

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