Neidio i'r cynnwys

coprostanol

Ni chefnogir cynnwys y dudalen mewn ieithoedd eraill.

cyfansoddyn cemegol

Adnoddau allanol

dynodwr Freebase
dynodwr Microsoft Academic
PubChem CID
DSSTOX compound identifier
UniChem compound ID
PDB Ligand
SPLASH
NSC number
OpenAlex ID
InChIKey
dynodwr HMDB
ChEBI ID
89519[6][7]

mapping relation type: exact match

DSSTox substance ID
SureChEMBL ID
UNII
KNApSAcK ID
ECHA Substance Infocard ID
MassBank accession ID
ChemSpider ID
EC number
206-638-8[9]
InChI
ID NALT
Rhif Cofrestru CAS
Probes And Drugs ID
LIPID MAPS ID

enghraifft o'r canlynol

math o endid cemegol

isddosbarth o'r canlynol

cholestanol[12]
(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[12]

adeiledd gemegol

image of molecular model or crystal lattice model

yn portreadu: ball-and-stick model

màs

388.370516156 uned Dalton[13]

stereoisomer of

Epicholestanol[5][14]
dihydrocholesterol[5][14]
(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[5][14]
Cholestan-3-ol, (3beta,5alpha)-[5][14]
epicoprosterol[5][14]
epidihydrocholesterin[14]
cholestan-3-ol[14]
Cholestan-3-ol, (3.beta.)-[14]
(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[14]
(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[14]
5a-Cholestan-3beta-ol[14]

fformwla gemegol

C₂₇H₄₈O

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[15]
Petrosia ficiformis[16]

categori Comin

Coprostanol

Cyfeiriadau

  1. 1.0 1.1 1.2 1.3 1.4 1.5 QYIXCDOBOSTCEI-NWKZBHTNSA-N, InChIKey
  2. UniChem
  3. 3.0 3.1 OpenAlex, 26 Ionawr 2022, https://docs.openalex.org/download-snapshot/snapshot-data-format
  4. ChEBI release 2020-09-01
  5. 5.0 5.1 5.2 5.3 5.4 5.5 5.6 5.7 inferred from InChIKey
  6. ChEBI release 2019-10-02
  7. International Chemical Identifier, 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
  8. Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard
  9. 9.0 9.1 ECHA Substance Infocard database, 27 Rhagfyr 2018, 100.006.036, 5-β-cholestan-3-β-ol, CAS no.: 360-68-9
  10. CAS Common Chemistry, 9 Ebrill 2021, QYIXCDOBOSTCEI-NWKZBHTNSA-N, https://commonchemistry.cas.org/detail?cas_rn=360-68-9
  11. LIPID MAPS, http://www.lipidmaps.org/rest/compound/lm_id/LM/all/download, 30 Mehefin 2018
  12. 12.0 12.1 inferred from SMILES
  13. inferred from isomeric SMILES
  14. 14.00 14.01 14.02 14.03 14.04 14.05 14.06 14.07 14.08 14.09 14.10 inferred from InChI
  15. Minor sterols of marine invertebrates 37. Isolation of novel coprostanols and 4 alpha-methyl sterols from the tunicate Ascidia nigra
  16. Minor and trace sterols from marine invertebrates 56. Novel coprostanols from the marine sponge Petrosia ficiformis
  17. Global gas chromatography/time-of-flight mass spectrometry (GC/TOFMS)-based metabonomic profiling of lyophilized human feces