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L-Canavanine

Catalog No. C1625 Name Sigma Aldrich
CAS Number 543-38-4 Website http://www.sigmaaldrich.com
M. F. C5H12N4O3 Telephone 1-800-521-8956
M. W. 176.17378 Fax
Purity ≥98% (TLC) Email
Storage Chembase ID: 1603

SYNONYMS

Title
L-刀豆氨酸
IUPAC name
(2S)-2-amino-4-(carbamimidamidooxy)butanoic acid
IUPAC Traditional name
canavanine
Synonyms
L-α-Amino-γ-(guanidinooxy)-n-butyric acid

DATABASE IDS

MDL Number MFCD00055781
PubChem SID 24892427
CAS Number 543-38-4

PROPERTIES

Biological Source from Canavalia ensiformis
Empirical Formula (Hill Notation) C5H12N4O3
Purity ≥98% (TLC)
Apperance powder
Solubility H2O: <100 mg/mL
GHS Pictograms GHS07
GHS Signal Word Warning
GHS Hazard statements H302-H312-H332
European Hazard Symbols Harmful Harmful (Xn)
MSDS Link Download
Personal Protective Equipment dust mask type N95 (US), Eyeshields, Gloves
GHS Precautionary statements P280
Risk Statements 20/21/22
RTECS ES7002000
Safety Statements 36
Storage Temperature 2-8°C
German water hazard class 3

DETAILS

Description (English)
Biochem/physiol Actions
A naturally occurring L-amino acid that interferes with L-arginine-utilizing enzymes due to its structural similarity. It is a selective inhibitor of inducible nitric oxide synthase (iNOS). Overproduction of NO by iNOS plays a crucial role in the pathophysiology of septic shock and chronic inflammation.
Canavanine is a naturally occurring L-amino acid that interferes with L-arginine-utilizing enzymes due to its structural similarity. It is a selective inhibitor of inducible nitric oxide synthase (iNOS). Overproduction of NO by iNOS plays a crucial role in the pathophysiology of septic shock and chronic inflammation.
Other Notes
Tandem Mass Spectrometry data independently generated by Scripps Center for Metabolomics is available to view or download in PDF. C1625.pdf Tested metabolites are featured on Scripps Center for Metabolomics METLIN Metabolite Database. To learn more, visit sigma.com/metlin.
Description (简体中文)
Biochem/physiol Actions
A naturally occurring L-amino acid that interferes with L-arginine-utilizing enzymes due to its structural similarity. It is a selective inhibitor of inducible nitric oxide synthase (iNOS). Overproduction of NO by iNOS plays a crucial role in the pathophysiology of septic shock and chronic inflammation.
Other Notes
Tandem Mass Spectrometry data independently generated by Scripps Center for Metabolomics is available to view or download in PDF. C1625.pdf Tested metabolites are featured on Scripps Center for Metabolomics METLIN Metabolite Database. To learn more, visit sigma.com/metlin.

REFERENCES