| Weight | 226.236 g/mol |
|---|---|
| Formula | C9H14N4O3 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 4 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 6 |
L-Carnosine (305-84-0)
Carnosine · Carnosine Hydrochloride · Carnosine, (D-His)-Isomer
Score:
#1234 in Biochemistry
,
#3069 in Biology
,
#3838 in Chemistry
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- Antioxidant activity of carnosine, homocarnosine, and anserine present in muscle and brain. (Proceedings of the National Academy of Sciences of the United States of America, 1988)
- Carnosine and related substances in animal tissues (Comparative Biochemistry and Physiology, 1970)
- The absorption of orally supplied -alanine and its effect on muscle carnosine synthesis in human vastus lateralis (Amino Acids, 2006)
- Influence of -alanine supplementation on skeletal muscle carnosine concentrations and high intensity cycling capacity (Amino Acids, 2007)
- Carnosine, homocarnosine and anserine: could they act as antioxidants in vivo? (Biochemical Journal, 1989)
- Carnosine: Its properties, functions and potential therapeutic applications (Molecular Aspects of Medicine, 1992)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Carnosine
- Carnosine Hydrochloride
- Carnosine, (D-His)-Isomer
- beta Alanylhistidine
- L Carnosine
- beta-Alanylhistidine
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SMILESC1=C(NC=N1)CC(C(=O)O)NC(=O)CCN
-
InChIKeyCQOVPNPJLQNMDC-UHFFFAOYSA-N
- Pubchem - L-Carnosine
- Wikipedia - carnosine
Carnosine (beta-alanyl-L-histidine), featuring the characteristic Imidazole-ring, is a dipeptide molecule, made up of the amino acids beta-alanine and histidine. It is highly concentrated in muscle and brain tissues. Carnosine and carnitine were discovered by Russian chemist Vladimir Gulevich.
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L-Carnosine
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