Empirical Formula (Hill Notation): | C9H14N4O3 |
CAS Number: | 305-84-0 |
Molecular Weight: | 226.23 |
Beilstein: | 87671 |
EC Number: | 206-169-9 |
MDL number: | MFCD00005207 |
UNSPSC Code: | 12352209 |
PubChem Substance ID: | 24893178 |
NACRES: | NA.26 |
Product Name | L-Carnosine, ~99%, crystalline |
Assay | ~99% |
form | crystalline |
color | white to off-white |
mp | 253 °C (dec.) (lit.) |
application(s) | cell analysis |
storage temp. | −20°C |
SMILES string | NCCC(=O)N[C@@H](Cc1c[nH]cn1)C(O)=O |
InChI | 1S/C9H14N4O3/c10-2-1-8(14)13-7(9(15)16)3-6-4-11-5-12-6/h4-5,7H,1-3,10H2,(H,11,12)(H,13,14)(H,15,16)/t7-/m0/s1 |
InChI key | CQOVPNPJLQNMDC-ZETCQYMHSA-N |
L-Carnosine has been used to study its effects as an antioxidant on meat quality of pigs. It has also been used to study its effects on brain injury in a rat intracerebral hemorrhage model.
L-Carosine is a dipeptide found at millimolar concentration in brain, muscle and the lens of the eye. In model systems it is a potent antioxidant that scavenges oxygen free radicals and transition metal ions. It blocks protein-protein and protein-DNA cross-links induced by hypochlorite anions and toxic aldehydes such as acetaldehyde, formaldehyde, and malondialdehyde, the primary product of lipid peroxidation. It also inhibits nonenzymatic protein glycation induced by aldose and ketose reducing sugars and inhibits the formation of toxic advanced glycation end products (AGE). These activities make it of interest in studies of aging, atherosclerosis, Alzheimer′s disease, and the secondary effects of diabetes.
Dipeptide with potent antioxidant and antiglycation activity; blocks nonenzymatic glycosylation and protein cross-linking induced by reactive aldehydes.
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ORID products are tested extensively in-house and supplied worldwide to the Life Sciences industries.
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