UVAOL

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C30H50O2
Molecular Weight	442.7168
Optical Activity	UNSPECIFIED
Defined Stereocenters	10 / 10
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

C[C@@H]1CC[C@]2(CO)CC[C@]3(C)C(=CC[C@@H]4[C@@]5(C)CC[C@H](O)C(C)(C)[C@@H]5CC[C@@]34C)[C@@H]2[C@H]1C

InChI

InChIKey=XUARCIYIVXVTAE-ZAPOICBTSA-N

InChI=1S/C30H50O2/c1-19-10-15-30(18-31)17-16-28(6)21(25(30)20(19)2)8-9-23-27(5)13-12-24(32)26(3,4)22(27)11-14-29(23,28)7/h8,19-20,22-25,31-32H,9-18H2,1-7H3/t19-,20+,22+,23-,24+,25+,27+,28-,29-,30-/m1/s1

HIDE SMILES / InChI

Molecular Formula	C30H50O2
Molecular Weight	442.7168
Charge	0
Count

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	10 / 10
E/Z Centers	0
Optical Activity	UNSPECIFIED

Approval Year

PubMed

Title	Date	PubMed
CYP716A subfamily members are multifunctional oxidases in triterpenoid biosynthesis.	2011-12	22039103
Antitubercular activity of triterpenoids from Asteraceae flowers.	2005-01	15635183
Antimycobacterial plant terpenoids.	2001-11	11731906
Inhibitory effects of triterpenoids and sterols on human immunodeficiency virus-1 reverse transcriptase.	2001-05	11432464
Inhibitory effect of triterpenes from Crataegus pinatifida on HIV-I protease.	1999-05	10364847
Triterpenes as potential dimerization inhibitors of HIV-1 protease.	1996-10-14	8967903

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 19:57:35 GMT 2025` Edited by `admin` on `Mon Mar 31 19:57:35 GMT 2025`
Record UNII	W599R31ROT
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

NSC-159627

Preferred Name

English

UVAOL

Common Name

English

URS-12-EN-3.BETA.,28-DIOL

Common Name

English

UVALOL

Common Name

English

3,28-DIHYDROXYURS-12-ENE

Common Name

English

URS-12-ENE-3,28-DIOL, (3.BETA.)-

Common Name

English

URS-12-ENE-3.BETA.,28-DIOL

Common Name

English

3.BETA.,28-DIHYDROXYURS-12-ENE

Common Name

English

Code System Code Type Description

EPA CompTox

DTXSID901350099