| Weight | 176.22 g/mol |
|---|---|
| Formula | C6H16N4O2+2 |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 5 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 5 |
arginine (74-79-3)
Score:
#1378 in Biochemistry
,
#3320 in Biology
,
#4141 in Chemistry
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- The L-Arginine-Nitric Oxide Pathway (The New England Journal of Medicine, 1993)
- Vascular endothelial cells synthesize nitric oxide from L-arginine. (Nature, 1988)
- ARGININE METABOLISM : NITRIC OXIDE AND BEYOND (Biochemical Journal, 1998)
- Macrophage oxidation of L-arginine to nitrite and nitrate: nitric oxide is an intermediate (Biochemistry, 1988)
- Formation of nitric oxide from L-arginine in the central nervous system: a transduction mechanism for stimulation of the soluble guanylate cyclase. (Proceedings of the National Academy of Sciences of the United States of America, 1989)
- Macrophage cytotoxicity: role for L-arginine deiminase and imino nitrogen oxidation to nitrite (Science, 1987)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC(CC(C(=O)O)[NH3+])C[NH+]=C(N)N
-
InChIKeyODKSFYDXXFIFQN-UHFFFAOYSA-P
- Pubchem - arginine
- Wikipedia - arginine
Arginine (abbreviated as Arg or R) is an -amino acid that is used in the biosynthesis of proteins. It is encoded by the codons CGU, CGC, CGA, CGG, AGA, and AGG. It contains an -amino group, an -carboxylic acid group, and a side chain consisting of a 3-carbon aliphatic straight chain ending in a guanidino group.
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