LUPEOL ACETATE

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 Search

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

Primary Target	Pharmacology	Condition	Potency
nitric oxide biosynthetic process 17 Target ID: GO:0006809 Sources: https://www.ncbi.nlm.nih.gov/pubmed/23243439	Inhibitor 8297		4.1 µM [IC50]

PubMed

Title	Date	PubMed
Assessment of antimycobacterial activity of a series of mainly marine derived natural products.	2000 May	10865450
Inhibitory effects of triterpenoids and sterols on human immunodeficiency virus-1 reverse transcriptase.	2001 May	11432464
A bioactive spirolactone iridoid and triterpenoids from Himatanthus sucuuba.	2001 Nov	11724243
Cytotoxic constituents from Plumbago zeylanica.	2004 Jul	15261389
Streblus asper Lour. (Shakhotaka): A Review of its Chemical, Pharmacological and Ethnomedicinal Properties.	2006 Jun	16786051
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	16426782
Oxyfunctionalization products of terpenoids with dimethyldioxirane and their biological activity.	2007 Feb	17268097
Seco-terpenoids and other constituents from Elateriospermum tapos.	2008 Feb	18179177
Chemical investigation of Finlaysonia obovata: part I--a rare triterpene acid showing antibacterial activity against fish pathogens.	2008 Jun 15	18569719
Gastroprotective effect of Benincasa hispida fruit extract.	2008 Nov	21279184
[Triterpenoids and steroids of root of Rubus biflorus].	2008 Nov	19260277
Anti-inflammatory and chemopreventive effects of triterpene cinnamates and acetates from shea fat.	2010	20484832
Protective effect of Hemidesmus indicus R.Br. root extract against cisplatin-induced cytogenetic damage in mouse bone marrow cells.	2010 Jan	21637624
Antioxidant Properties of the Methanol Extract of the Wood and Pericarp of Caesalpinia decapetala.	2010 Jan	21331190
In vitro antituberculosis activities of the constituents isolated from Haloxylon salicornicum.	2010 Jul 15	20542692
[Studies on the chemical constituents of Ficus microcarpa].	2010 Jun	21049616

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

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Name

Type

Language

LUPEOL ACETATE

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