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Details of Oleanolic acid, 3-acetyl-

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Role	Metabolite
MPIMP ID	M000255
stereoisomer
isotopomer	ambient
formula	C32H50O4
molecular mass	498.738
monoisotopic mass	498.37091
InChI
InChIKey	XELCDNMMZPLOCA-SLHMZFGRSA-N
class	Terpenoid (Ursolic Acids)
application/atom+xml	http://gmd.mpimp-golm.mpg.de/REST/gmd.svc/Metabolite(guid%270f83f7ce-f715-4fa4-853f-0de7e0a1c3bd%27)

Synonyms of Oleanolic acid, 3-acetyl-

property	value
CAS	4339-72-4
ChemSpider ID	19005188
MAPMAN	Acetyloleanoleate
PubChem CID	21337502
PubChem SID	92297493
synonym	Acetyloleanolic acid
synonym	Olean-12-en-28-oic acid, 3-(acetyloxy)-, (3beta)-
synonym	Oleanolic acid, 3-(acetoxy)-, (3beta-)-
synonym	Oleanolic acid, 3-acetoxy-
9 synonym(s)

Derivatives of Oleanolic acid, 3-acetyl-

analyte	stereoisomer	isotopomer
Oleanolic acid, 3-acetyl- (1TMS)		ambient
1 analyte(s)

Reference substances of Oleanolic acid, 3-acetyl-

reference substance	supplier	supplier code
Oleanolic acid, 3-acetyl-	Aldrich	S962880
Oleanolic acid, 3-acetyl-	Aldrich	S962880
2 reference substance(s)

Isotopomers and stereoisomers of Oleanolic acid, 3-acetyl-

metabolite	stereoisomer	isotopomer
no hits!

Quantitative Oleanolic acid, 3-acetyl- Profile Data

Each graph visualises metabolite concentrations across a single metabolite profiling experiment. Each box plot represents relative (normalised) metabolite concentrations for single replica groups in the specific metabolite profiling experiment.

Name	Organism	Factor	Heatmap	Box plot	Variance	Anova F score
no metabolite profile(s) found.

Qualitative Oleanolic acid, 3-acetyl- Profile Data

species
no qualitative metabolite profile data available!

compound timestamp information
deposited	at 8/29/2006 by Hummel J., Max Planck Institute of Molecular Plant Physiology, Bioinformatics, Am Muehlenberg 1, D-14476 Golm, Germany
last changed	at 12/20/2012 by Kopka J., Max Planck Institute of Molecular Plant Physiology, Department of Molecular Plant Physiology (Prof. Willmitzer L), Am Muehlenberg 1, D-14476 Golm, Germany
modified by users	Strehmel N., Hummel J., Kopka J.

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