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Details of Camalexin

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Role	Metabolite
MPIMP ID	M000856
stereoisomer
isotopomer	ambient
formula	C11H8N2S
molecular mass	200.261
monoisotopic mass	200.04082
InChI	InChI=1S/C11H8N2S/c1-2-4-9-8(3-1)7-10(13-9)11-12-5-6-14-11/h1-7,13H
InChIKey	JWUOBSJPUNZMTG-UHFFFAOYSA-N
class	Alkaloid
application/atom+xml	http://gmd.mpimp-golm.mpg.de/REST/gmd.svc/Metabolite(guid%276074ff40-0627-4df8-af0f-327e128cb715%27)

Synonyms of Camalexin

property	value
CAS	135531-86-1
PubChem CID	20076847
PubChem SID	92297680
publication	Ayer WA, Craw PA, Ma YT, Miao S (1992) Synthesis of camalexin and related phytoalexins. Tetrahedron 48(14): 2919-24 [doi:10.1016/S0040-4020(01)90973-1]
synonym	1H-Indole, 3-(2-thiazolyl)- (9CI)
synonym	3-(1,3-thiazol-2-yl)-1H-indole
synonym	Camalexin
7 synonym(s)

Derivatives of Camalexin

analyte	stereoisomer	isotopomer
no hits!

Reference substances of Camalexin

reference substance	supplier	supplier code	lot
Camalexin
1 reference substance(s)

Isotopomers and stereoisomers of Camalexin

metabolite	stereoisomer	isotopomer
no hits!

Quantitative Camalexin 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 Camalexin Profile Data

species
no qualitative metabolite profile data available!

compound timestamp information
deposited	at 11/8/2006 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
last changed	at 8/9/2011 by Hummel J., Max Planck Institute of Molecular Plant Physiology, Bioinformatics, Am Muehlenberg 1, D-14476 Golm, Germany
modified by users	Kopka J., Hummel J.

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