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Details

Stereochemistry ABSOLUTE
Molecular Formula C30H44O2
Molecular Weight 436.6692
Optical Activity UNSPECIFIED
Defined Stereocenters 7 / 7
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of DEHYDROERGOSTEROL ACETATE

SMILES

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

InChI

InChIKey=USXNJOVHHSKEBV-RDQHZIOXSA-N
InChI=1S/C30H44O2/c1-19(2)20(3)8-9-21(4)26-12-13-27-25-11-10-23-18-24(32-22(5)31)14-16-29(23,6)28(25)15-17-30(26,27)7/h8-11,15,19-21,24,26-27H,12-14,16-18H2,1-7H3/b9-8+/t20-,21+,24-,26+,27-,29-,30+/m0/s1

HIDE SMILES / InChI

Description

Dehydroergosterol acetate is ergosterol derivative that can be used in photochemical reactions.

Originator

Auwers, K.V.|Wolter, E.
1
Sources: achr. Ges. Wiss. Gottingen Math.-physik. Klasse (1931), 101-19.

Approval Year

Unknown
149124
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
PubMed

PubMed

TitleDatePubMed
Inhibitory effects of sterols isolated from Chlorella vulgaris on 12-0-tetradecanoylphorbol-13-acetate-induced inflammation and tumor promotion in mouse skin.
1996-04
Patents

Patents

US2576949
1

Sample Use Guides

In Vivo Use Guide
Unknown
Route of Administration: Unknown
In Vitro Use Guide
Unknown
Name Type Language
DEHYDROERGOSTEROL ACETATE
MI  
Common Name English
DEHYDROERGOSTEROL ACETATE [MI]
Preferred Name English
ERGOSTA-5,7,9(11),22-TETRAEN-3-OL, 3-ACETATE, (3.BETA.,22E)-
Systematic Name English
Code System Code Type Description
MERCK INDEX
m4147
Created by admin on Mon Mar 31 22:38:29 GMT 2025 , Edited by admin on Mon Mar 31 22:38:29 GMT 2025
PRIMARY Merck Index
FDA UNII
H762V3R6G7
Created by admin on Mon Mar 31 22:38:29 GMT 2025 , Edited by admin on Mon Mar 31 22:38:29 GMT 2025
PRIMARY
CAS
1060-56-6
Created by admin on Mon Mar 31 22:38:29 GMT 2025 , Edited by admin on Mon Mar 31 22:38:29 GMT 2025
PRIMARY
PUBCHEM
69827569
Created by admin on Mon Mar 31 22:38:29 GMT 2025 , Edited by admin on Mon Mar 31 22:38:29 GMT 2025
PRIMARY
NIH
NCATS
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