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Details

Stereochemistry ABSOLUTE
Molecular Formula C32H52O2
Molecular Weight 468.7541
Optical Activity UNSPECIFIED
Defined Stereocenters 10 / 10
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LUPEOL ACETATE

SMILES

[H][C@]12[C@@H](CC[C@]1(C)CC[C@]3(C)[C@]2([H])CC[C@]4([H])[C@@]5(C)CC[C@H](OC(C)=O)C(C)(C)[C@]5([H])CC[C@@]34C)C(C)=C

InChI

InChIKey=ODSSDTBFHAYYMD-YOJQYFTNSA-N
InChI=1S/C32H52O2/c1-20(2)22-12-15-29(6)18-19-31(8)23(27(22)29)10-11-25-30(7)16-14-26(34-21(3)33)28(4,5)24(30)13-17-32(25,31)9/h22-27H,1,10-19H2,2-9H3/t22-,23+,24-,25+,26-,27+,29+,30-,31+,32+/m0/s1

HIDE SMILES / InChI

Molecular Formula C32H52O2
Molecular Weight 468.7541
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 9 / 10
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
4.1 µM [IC50]
PubMed

PubMed

TitleDatePubMed
Assessment of antimycobacterial activity of a series of mainly marine derived natural products.
2000 May
Inhibitory effects of triterpenoids and sterols on human immunodeficiency virus-1 reverse transcriptase.
2001 May
A bioactive spirolactone iridoid and triterpenoids from Himatanthus sucuuba.
2001 Nov
Streblus asper Lour. (Shakhotaka): A Review of its Chemical, Pharmacological and Ethnomedicinal Properties.
2006 Jun
Daboia russellii and Naja kaouthia venom neutralization by lupeol acetate isolated from the root extract of Indian sarsaparilla Hemidesmus indicus R.Br.
2006 Jun 15
Seco-terpenoids and other constituents from Elateriospermum tapos.
2008 Feb
[Bioactive constituents from whole herbs of Vernonia cinerea (II)].
2009 Nov
Separation and identification of some common isomeric plant triterpenoids by thin-layer chromatography and high-performance liquid chromatography.
2009 Sep 18
Protective effect of Hemidesmus indicus R.Br. root extract against cisplatin-induced cytogenetic damage in mouse bone marrow cells.
2010 Jan
In vitro antituberculosis activities of the constituents isolated from Haloxylon salicornicum.
2010 Jul 15
Substance Class Chemical
Created
by admin
on Sat Dec 16 04:02:01 GMT 2023
Edited
by admin
on Sat Dec 16 04:02:01 GMT 2023
Record UNII
WJ3A89G0H6
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
LUPEOL ACETATE
MI  
Common Name English
LUPENYL ACETATE
Common Name English
LUP-20(29)-EN-3.BETA.-YL ACETATE
Common Name English
LUPEYL ACETATE
Common Name English
LUP-20(29)-EN-3-OL, ACETATE, (3.BETA.)-
Common Name English
LUPEOL 3-ACETATE
Common Name English
3-O-ACETYLLUPEOL
Common Name English
3-ACETYLLUPEOL
Common Name English
LUP-20(29)-EN-3.BETA.-OL, ACETATE
Common Name English
3.BETA.-OAC-20(29)-LUPENE
Common Name English
NSC-281806
Code English
CLERODOL ACETATE
Common Name English
LUPEOL ACETATE [MI]
Common Name English
ACETYLLUPEOL
Common Name English
LUP-20(30)-EN-3.BETA.-OL, ACETATE
Common Name English
Code System Code Type Description
EPA CompTox
DTXSID70936584
Created by admin on Sat Dec 16 04:02:01 GMT 2023 , Edited by admin on Sat Dec 16 04:02:01 GMT 2023
PRIMARY
ECHA (EC/EINECS)
216-575-8
Created by admin on Sat Dec 16 04:02:01 GMT 2023 , Edited by admin on Sat Dec 16 04:02:01 GMT 2023
PRIMARY
MESH
C055329
Created by admin on Sat Dec 16 04:02:01 GMT 2023 , Edited by admin on Sat Dec 16 04:02:01 GMT 2023
PRIMARY
CAS
1617-68-1
Created by admin on Sat Dec 16 04:02:01 GMT 2023 , Edited by admin on Sat Dec 16 04:02:01 GMT 2023
PRIMARY
MERCK INDEX
m6938
Created by admin on Sat Dec 16 04:02:01 GMT 2023 , Edited by admin on Sat Dec 16 04:02:01 GMT 2023
PRIMARY Merck Index
PUBCHEM
92157
Created by admin on Sat Dec 16 04:02:01 GMT 2023 , Edited by admin on Sat Dec 16 04:02:01 GMT 2023
PRIMARY
NSC
281806
Created by admin on Sat Dec 16 04:02:01 GMT 2023 , Edited by admin on Sat Dec 16 04:02:01 GMT 2023
PRIMARY
FDA UNII
WJ3A89G0H6
Created by admin on Sat Dec 16 04:02:01 GMT 2023 , Edited by admin on Sat Dec 16 04:02:01 GMT 2023
PRIMARY