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Details

Stereochemistry ABSOLUTE
Molecular Formula C28H44O
Molecular Weight 396.6484
Optical Activity UNSPECIFIED
Defined Stereocenters 8 / 8
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of ERGOSTEROL

SMILES

[H][C@@]1(CC[C@@]2([H])C3=CC=C4C[C@@H](O)CC[C@]4(C)[C@@]3([H])CC[C@]12C)[C@H](C)\C=C\[C@H](C)C(C)C

InChI

InChIKey=DNVPQKQSNYMLRS-APGDWVJJSA-N
InChI=1S/C28H44O/c1-18(2)19(3)7-8-20(4)24-11-12-25-23-10-9-21-17-22(29)13-15-27(21,5)26(23)14-16-28(24,25)6/h7-10,18-20,22,24-26,29H,11-17H2,1-6H3/b8-7+/t19-,20+,22-,24+,25-,26-,27-,28+/m0/s1

HIDE SMILES / InChI

Molecular Formula C28H44O
Molecular Weight 396.6484
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 8 / 8
E/Z Centers 1
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 15:21:19 UTC 2023
Edited
by admin
on Fri Dec 15 15:21:19 UTC 2023
Record UNII
Z30RAY509F
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ERGOSTEROL
HSDB   INCI   MI   USP-RS  
INCI  
Official Name English
ERGOSTEROL (CONSTITUENT OF GANODERMA LUCIDUM FRUITING BODY) [DSC]
Common Name English
ERGOSTERIN
Common Name English
ERGOSTEROL [INCI]
Common Name English
ERGOSTEROL [MI]
Common Name English
ERGOSTEROL [HSDB]
Common Name English
PROVITAMIN D2
Common Name English
(22E)-ERGOSTA-5,7,22-TRIEN-3.BETA.-OL
Systematic Name English
ERGOSTEROL [USP-RS]
Common Name English
ERGOCALCIFEROL IMPURITY B [EP IMPURITY]
Common Name English
(3.BETA.,22E)-ERGOSTA-5,7,22-TRIEN-3-OL
Systematic Name English
Classification Tree Code System Code
LOINC 15411-2
Created by admin on Fri Dec 15 15:21:19 UTC 2023 , Edited by admin on Fri Dec 15 15:21:19 UTC 2023
NCI_THESAURUS C843
Created by admin on Fri Dec 15 15:21:19 UTC 2023 , Edited by admin on Fri Dec 15 15:21:19 UTC 2023
Code System Code Type Description
NCI_THESAURUS
C83810
Created by admin on Fri Dec 15 15:21:19 UTC 2023 , Edited by admin on Fri Dec 15 15:21:19 UTC 2023
PRIMARY
RS_ITEM_NUM
1241007
Created by admin on Fri Dec 15 15:21:19 UTC 2023 , Edited by admin on Fri Dec 15 15:21:19 UTC 2023
PRIMARY
CHEBI
16933
Created by admin on Fri Dec 15 15:21:19 UTC 2023 , Edited by admin on Fri Dec 15 15:21:19 UTC 2023
PRIMARY
HSDB
395
Created by admin on Fri Dec 15 15:21:19 UTC 2023 , Edited by admin on Fri Dec 15 15:21:19 UTC 2023
PRIMARY
WIKIPEDIA
ERGOSTEROL
Created by admin on Fri Dec 15 15:21:19 UTC 2023 , Edited by admin on Fri Dec 15 15:21:19 UTC 2023
PRIMARY
ECHA (EC/EINECS)
200-352-7
Created by admin on Fri Dec 15 15:21:19 UTC 2023 , Edited by admin on Fri Dec 15 15:21:19 UTC 2023
PRIMARY
FDA UNII
Z30RAY509F
Created by admin on Fri Dec 15 15:21:19 UTC 2023 , Edited by admin on Fri Dec 15 15:21:19 UTC 2023
PRIMARY
PUBCHEM
444679
Created by admin on Fri Dec 15 15:21:19 UTC 2023 , Edited by admin on Fri Dec 15 15:21:19 UTC 2023
PRIMARY
CAS
57-87-4
Created by admin on Fri Dec 15 15:21:19 UTC 2023 , Edited by admin on Fri Dec 15 15:21:19 UTC 2023
PRIMARY
DRUG BANK
DB04038
Created by admin on Fri Dec 15 15:21:19 UTC 2023 , Edited by admin on Fri Dec 15 15:21:19 UTC 2023
PRIMARY
MERCK INDEX
m4986
Created by admin on Fri Dec 15 15:21:19 UTC 2023 , Edited by admin on Fri Dec 15 15:21:19 UTC 2023
PRIMARY Merck Index
EPA CompTox
DTXSID90878679
Created by admin on Fri Dec 15 15:21:19 UTC 2023 , Edited by admin on Fri Dec 15 15:21:19 UTC 2023
PRIMARY
Related Record Type Details
PARENT -> CONSTITUENT ALWAYS PRESENT
USP
INHIBITOR -> TARGET
INHIBITOR -> TARGET
Related Record Type Details
PARENT -> IMPURITY