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Details

Stereochemistry ABSOLUTE
Molecular Formula C27H46O
Molecular Weight 386.6535
Optical Activity UNSPECIFIED
Defined Stereocenters 7 / 7
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Doristerol

SMILES

[H][C@@]1(CCC2=C3CC[C@@]4([H])C[C@@H](O)CC[C@]4(C)[C@@]3([H])CC[C@]12C)[C@H](C)CCCC(C)C

InChI

InChIKey=ONYPIMNXSARKFQ-NFTYELEKSA-N
InChI=1S/C27H46O/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/h18-21,23,25,28H,6-17H2,1-5H3/t19-,20+,21+,23-,25+,26+,27-/m1/s1

HIDE SMILES / InChI

Molecular Formula C27H46O
Molecular Weight 386.6535
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 7 / 7
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 16:34:03 GMT 2023
Edited
by admin
on Sat Dec 16 16:34:03 GMT 2023
Record UNII
TPL64BMT8B
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
Doristerol
Common Name English
(3S,5S,9S,10R,13S,17R)-10,13-DIMETHYL-17-((2R)-6-METHYLHEPTAN-2-YL)-2,3,4,5,6,7,9,11,12,15,16,17-DODECAHYDRO-1H-CYCLOPENTA(A)PHENANTHREN-3-OL
Systematic Name English
(3s,5s,9r,10s,13r,17r)-10,13-dimethyl-17-[(2r)-6-methylheptan-2-yl]-2,3,4,5,6,7,9,11,12,15,16,17-dodecahydro-1h-cyclopenta[a]phenanthren-3-ol
Systematic Name English
(3β,5α)-Cholest-8(14)-en-3-ol
Common Name English
Δ8(14)-Cholestenol
Common Name English
5α-Cholest-8(14)-ene-3β-ol
Common Name English
Cholest-8(14)-en-3-ol, (3β,5α)-
Common Name English
Code System Code Type Description
PUBCHEM
5283665
Created by admin on Sat Dec 16 16:34:03 GMT 2023 , Edited by admin on Sat Dec 16 16:34:03 GMT 2023
PRIMARY
EPA CompTox
DTXSID901312065
Created by admin on Sat Dec 16 16:34:03 GMT 2023 , Edited by admin on Sat Dec 16 16:34:03 GMT 2023
PRIMARY
FDA UNII
TPL64BMT8B
Created by admin on Sat Dec 16 16:34:03 GMT 2023 , Edited by admin on Sat Dec 16 16:34:03 GMT 2023
PRIMARY
CAS
566-99-4
Created by admin on Sat Dec 16 16:34:03 GMT 2023 , Edited by admin on Sat Dec 16 16:34:03 GMT 2023
PRIMARY