The chemical substance known as "({(2S)-1-amino-5-[(diaminomethylidene)ammonio]-1-oxopentan-2-yl}carbamoyl)benzene," with the CAS number 965-03-7, is a complex organic compound characterized by its amino acid structure and functional groups. It features a benzene ring substituted with a carbamoyl group, which is linked to a pentanoyl chain that contains multiple amino and oxo functional groups. This compound is likely to exhibit properties typical of amino acids and peptides, such as solubility in water due to its polar functional groups and potential for forming hydrogen bonds. Its structure suggests it may participate in various biochemical processes, possibly acting as a precursor or intermediate in the synthesis of more complex biomolecules. Additionally, the presence of multiple amine groups indicates potential basicity and reactivity, which could be relevant in biological systems or synthetic applications. Overall, this compound's unique structure contributes to its potential utility in medicinal chemistry and biochemistry.

({(2S)-1-amino-5-[(diaminomethylidene)ammonio]-1-oxopentan-2-yl}carbamoyl)benzene

Find at CymitQuimica all products linked to CAS 965-03-7. Enter now to get more information

N-alpha-Benzoyl-L-argininamide is a synthetic compound that is used as an enzyme inhibitor. It binds to the active site of proteases, thereby inhibiting their activity. This drug has been shown to inhibit the activities of phosphodiesterase and phosphatase enzymes in vitro. N-alpha-Benzoyl-L-argininamide also inhibits the proteolytic degradation of hippuric acid and casein in vitro. The binding affinity for this drug is due to its structural similarity with substrates such as glutamate and rhizosphere exudates.

CAS 965-03-7: ({(2S)-1-amino-5-[(diaminomethylidene)ammonio]-1-oxopentan-2-yl}carbamoyl)benzene

N-α-Benzoyl-L-argininamide

Ref: 3D-FB66544

Bz-Arg-NH2

Ref: IN-DA006QQW