coprostanol

લેખ બનાવો

This is an automatic view based on data from વિકિડેટા.
There is not a complete article yet, but you can help creating one.

chemical compound

બાહ્ય સ્રોતો

ફ્રીબેઝ આઈડી	/m/0cjcrz
Microsoft Academic ID	2777585577
PubChem CID	221122^[૧]
DSSTOX compound identifier	DTXCID6030603
UniChem compound ID	10531484^[૨]
PDB ligand ID	QNJ
SPLASH	splash10-052u-9527000000-d23f4273340e8c85dc8a
NSC number	5060 18175
OpenAlex ID	C2910061293^[૩] C2777585577^[૩]
InChIKey	QYIXCDOBOSTCEI-NWKZBHTNSA-N^[૪]
Human Metabolome Database ID	HMDB0000577^[૫]^[૧]
ChEBI ID	89519^[૬]^[૭] mapping relation type: exact match
DSSTox substance ID	DTXSID1052036^[૮]^[૧]
SureChEMBL ID	SCHEMBL28410^[૫]^[૧]
UNII	PPT67I3S74^[૧]
KNApSAcK ID	C00061602^[૫]^[૧]
ECHA Substance Infocard ID	100.006.036^[૯]
MassBank accession ID	MSBNK-Fac_Eng_Univ_Tokyo-JP003428
ChemSpider ID	19951861
EC number	206-638-8^[૯]
InChI	InChI=1S/C27H48O/c1-18(2)7-6-8-19(3)23-11-12-24-22-10-9-20-17-21(28)13-15-26(20,4)25(22)14-16-27(23,24)5/h18-25,28H,6-17H2,1-5H3/t19-,20-,21+,22+,23-,24+,25+,26+,27-/m1/s1
NALT ID	28974
CAS Registry Number	360-68-9^[૧૦]
Probes And Drugs ID	PD121784
LIPID MAPS ID	LMST01010078^[૧૧]

ઉદાહરણ

type of chemical entity

નો પેટા-પ્રકાર

cholestanol^[૧૨]

(3R,5S,8R,9S,10S,13R,14S)-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol^[૧૨]

રાસાયણિક સંરચના

image of molecular model or crystal lattice model

દર્શાવે છે: ball-and-stick model

mass

૩૮૮.૩૭૦૫૧૬૧૫૬ dalton^[૧૩]

stereoisomer of

Epicholestanol^[૫]^[૧૪]

dihydrocholesterol^[૫]^[૧૪]

(3S,5R)-10,13-dimethyl-17-(6-methylheptan-2-yl)-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol^[૫]^[૧૪]

Cholestan-3-ol, (3beta,5alpha)-^[૫]^[૧૪]

epicoprosterol^[૫]^[૧૪]

epidihydrocholesterin^[૧૪]

cholestan-3-ol^[૧૪]

Cholestan-3-ol, (3.beta.)-^[૧૪]

(3S,5S,8S,9S,10S,13R,14S,17R)-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol^[૧૪]

(3S,5S,8R,9R,10S,13R,14S,17R)-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol^[૧૪]

5a-Cholestan-3beta-ol^[૧૪]

રાસાયણિક સૂત્ર

C₂₇H₄₈O

canonical SMILES

OC1CCC2(C)C(CCC3C4CCC(C(C)CCCC(C)C)C4(C)CCC32)C1

isomeric SMILES

O[C@H]4CC[C@]3([C@H](CC[C@H]2[C@@H]1CC[C@@H]([C@@]1(C)CC[C@@H]23)[C@H](C)CCCC(C)C)C4)C

found in taxon

Phallusia nigra^[૧૫]

Petrosia ficiformis^[૧૬]

Homo sapiens^[૧૭]

કોમન્સ શ્રેણી

Coprostanol

સંદર્ભ

↑ ^૧.૦ ^૧.૧ ^૧.૨ ^૧.૩ ^૧.૪ ^૧.૫ QYIXCDOBOSTCEI-NWKZBHTNSA-N, InChIKey
↑ UniChem
↑ ^૩.૦ ^૩.૧ OpenAlex, ૨૬ જાન્યુઆરી 2022, https://docs.openalex.org/download-snapshot/snapshot-data-format
↑ ChEBI release 2020-09-01
↑ ^૫.૦ ^૫.૧ ^૫.૨ ^૫.૩ ^૫.૪ ^૫.૫ ^૫.૬ ^૫.૭ inferred from InChIKey
↑ ChEBI release 2019-10-02
↑ InChI=1S/C27H48O/c1-18(2)7-6-8-19(3)23-11-12-24-22-10-9-20-17-21(28)13-15-26(20,4)25(22)14-16-27(23,24)5/h18-25,28H,6-17H2,1-5H3/t19-,20-,21+,22+,23-,24+,25+,26+,27-/m1/s1, International Chemical Identifier
↑ Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard
↑ ^૯.૦ ^૯.૧ ECHA Substance Infocard database, ૨૭ ડિસેમ્બર 2018, 100.006.036, 5-β-cholestan-3-β-ol, CAS no.: 360-68-9
↑ CAS Common Chemistry, ૯ એપ્રિલ 2021, https://commonchemistry.cas.org/detail?cas_rn=360-68-9, QYIXCDOBOSTCEI-NWKZBHTNSA-N
↑ LIPID MAPS, http://www.lipidmaps.org/rest/compound/lm_id/LM/all/download, ૩૦ જૂન 2018
↑ ^૧૨.૦ ^૧૨.૧ inferred from SMILES
↑ inferred from isomeric SMILES
↑ ^{૧૪.૦૦} ^{૧૪.૦૧} ^{૧૪.૦૨} ^{૧૪.૦૩} ^{૧૪.૦૪} ^{૧૪.૦૫} ^{૧૪.૦૬} ^{૧૪.૦૭} ^{૧૪.૦૮} ^{૧૪.૦૯} ^{૧૪.૧૦} inferred from InChI
↑ Minor sterols of marine invertebrates 37. Isolation of novel coprostanols and 4 alpha-methyl sterols from the tunicate Ascidia nigra
↑ Minor and trace sterols from marine invertebrates 56. Novel coprostanols from the marine sponge Petrosia ficiformis
↑ Global gas chromatography/time-of-flight mass spectrometry (GC/TOFMS)-based metabonomic profiling of lyophilized human feces

[r1f80b23e-1] ૧.૦ ^૧.૧ ^૧.૨ ^૧.૩ ^૧.૪ ^૧.૫ QYIXCDOBOSTCEI-NWKZBHTNSA-N, InChIKey

[rb4997d09-2] UniChem

[rf384841b-3] ૩.૦ ^૩.૧ OpenAlex, ૨૬ જાન્યુઆરી 2022, https://docs.openalex.org/download-snapshot/snapshot-data-format

[rdb8780da-4] ChEBI release 2020-09-01

[r2758fec3-5] ૫.૦ ^૫.૧ ^૫.૨ ^૫.૩ ^૫.૪ ^૫.૫ ^૫.૬ ^૫.૭ inferred from InChIKey

[r9d0da0c8-6] ChEBI release 2019-10-02

[refac1316-7] InChI=1S/C27H48O/c1-18(2)7-6-8-19(3)23-11-12-24-22-10-9-20-17-21(28)13-15-26(20,4)25(22)14-16-27(23,24)5/h18-25,28H,6-17H2,1-5H3/t19-,20-,21+,22+,23-,24+,25+,26+,27-/m1/s1, International Chemical Identifier

[r76075370-8] Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard

[r94a5080a-9] ૯.૦ ^૯.૧ ECHA Substance Infocard database, ૨૭ ડિસેમ્બર 2018, 100.006.036, 5-β-cholestan-3-β-ol, CAS no.: 360-68-9

[r88cb58f3-10] CAS Common Chemistry, ૯ એપ્રિલ 2021, https://commonchemistry.cas.org/detail?cas_rn=360-68-9, QYIXCDOBOSTCEI-NWKZBHTNSA-N

[r65f905ad-11] LIPID MAPS, http://www.lipidmaps.org/rest/compound/lm_id/LM/all/download, ૩૦ જૂન 2018

[r2e18fda9-12] ૧૨.૦ ^૧૨.૧ inferred from SMILES

[ra32331d2-13] rred from isomeric SMILES

[rf76af6ca-14] {૧૪.૦૦} ^{૧૪.૦૧} ^{૧૪.૦૨} ^{૧૪.૦૩} ^{૧૪.૦૪} ^{૧૪.૦૫} ^{૧૪.૦૬} ^{૧૪.૦૭} ^{૧૪.૦૮} ^{૧૪.૦૯} ^{૧૪.૧૦} inferred from InChI

[rdadb1c10-15] Minor sterols of marine invertebrates 37. Isolation of novel coprostanols and 4 alpha-methyl sterols from the tunicate Ascidia nigra

[r3e6b2149-16] Minor and trace sterols from marine invertebrates 56. Novel coprostanols from the marine sponge Petrosia ficiformis

[rd7ba76a6-17] Global gas chromatography/time-of-flight mass spectrometry (GC/TOFMS)-based metabonomic profiling of lyophilized human feces

[૧]

[૨]

[૩]

[૪]

[૫]

[૬]

[૭]

[૮]

[૯]

[૧૦]

[૧૧]

[૧૨]

[૧૩]

[૧૪]

[૧૫]

[૧૬]

[૧૭]