| Weight | 176.176 g/mol |
|---|---|
| Formula | C5H12N4O3 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 4 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 5 |
L-canavanine (543-38-4)
Score:
#276 in Biochemistry
,
#1062 in Biology
,
#1187 in Chemistry
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- Sigma-Aldrich - L-canavanine93.90 - 470.00 USD
- Fisher Scientific - Search for L-canavanine
- TCI - Search for L-canavanine
- The biological effects and mode of action of L-canavanine, a structural analogue of L-arginine. (The Quarterly Review of Biology, 1977)
- l-Canavanine Made by Medicago sativa Interferes with Quorum Sensing in Sinorhizobium meliloti (Journal of Bacteriology, 2005)
- A novel means for dealing with L-canavanine, a toxic metabolite (Science, 1976)
- Quercetin, Coenzyme Q10, and l -canavanine as protective agents against lipid peroxidation and nitric oxide generation in endotoxin-induced shock in rat brain (Pharmacological Research, 2001)
- Preparation and colorimetric analysis of l-Canavanine (Analytical Biochemistry, 1977)
- Investigations of Canavanine Biochemistry in the Jack Bean Plant, Canavalia ensiformia (L.) DC: I. Canavanine Utilization in the Developing Plant (Plant Physiology, 1970)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC(CON=C(N)N)C(C(=O)O)N
-
InChIKeyFSBIGDSBMBYOPN-UHFFFAOYSA-N
- Pubchem - L-canavanine
- Wikipedia - canavanine
L-(+)-(S)-Canavanine is a non-proteinogenic amino acid found in certain leguminous plants. It is structurally related to the proteinogenic -amino acid L-arginine, the sole difference being the replacement of a methylene bridge (-CH 2- unit) in arginine with an oxa group (i.e., an oxygen atom) in canavanine. Canavanine is accumulated primarily in the seeds of the organisms which produce it, where it serves both as a highly deleterious defensive compound against herbivores and a vital source of nitrogen for the growing embryo (see also L-canaline).
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L-canavanine
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