| Identification | Back Directory | [Name]
CARCININE HYDROCHLORIDE | [CAS]
56897-53-1 | [Synonyms]
β-Alanylhistamine
H-b-Ala-histaMine
β-Alanylhistamine
N-(2-(1H-Imidazol-5-yl)
CARCININE HYDROCHLORIDE
Carcinine dihydrochloride
Carcinine hydrochloride salt
Carcinine ditrifluoroacetate
β-Alanylhistamine dihydrochloride
β-Alanylhistamine dihydrochloride
Carcinine ditrifluoroacetate Acetate
N-(2-(1H-IMidazol-5-yl)ethyl)-3-aMinopropanaMide
3-Amino-N-[2-(1H-imidazol-4-yl)ethyl]propionamide
Propanamide, 3-amino-N-[2-(1H-imidazol-5-yl)ethyl]-
Carcinine ditrifluoroacetate Acetate (56897-53-1 Free base)
3-Amino-N-[2-(1H-imidazol-4-yl)ethyl]propanamideditrifluoroacetate | [Molecular Formula]
C8H14N4O | [MDL Number]
MFCD16618412 | [MOL File]
56897-53-1.mol | [Molecular Weight]
182.22 |
| Chemical Properties | Back Directory | [Boiling point ]
547.6±40.0 °C(Predicted) | [density ]
1.191±0.06 g/cm3(Predicted) | [storage temp. ]
Sealed in dry,2-8°C | [solubility ]
Soluble to 100 mM in water and to 100 mM in DMSO | [form ]
Powder | [pka]
14.37±0.10(Predicted) | [Sequence]
H-β-Ala-histamine hydrochloride salt |
| Hazard Information | Back Directory | [Uses]
Carcinine is a highly selective H3 antagonist. | [Definition]
ChEBI: A beta-alanine derivative that is the amide obtained by formal condensation of the carboxy group of beta-alanine with the primary amino group of histamine. | [Biological Activity]
Highly selective H 3 receptor antagonist (K i values are 0.30, 365 and 3621 μ M for H 3 , H 2 and H 1 receptors respectively). Acts as a natural antioxidant with hydroxyl radical scavenging and lipid peroxidase activities. |
|
|