CAS 4299-03-0

Benzamida, N-[1-(aminocarbonil)-4-[(aminoiminometil)amino]butil]-, monohidrocloreto, (S)-

Descrição:

Benzamida, N-[1-(aminocarbonil)-4-[(aminoiminometil)amino]butil]-, monohidrocloreto, (S)- é um composto químico caracterizado por sua estrutura complexa, que inclui um grupo benzamida e múltiplos grupos funcionais, como amino e carbonilo. Este composto é tipicamente um sólido branco a off-white e é solúvel em água devido à presença de grupos funcionais polares. A presença do cloridrato indica que é uma forma de sal, o que muitas vezes melhora sua estabilidade e solubilidade em soluções aquosas. A designação (S) refere-se à sua estereoisomeria específica, indicando que é um dos enantiômeros do composto. Os derivados de benzamida são frequentemente estudados por sua atividade biológica, incluindo potenciais aplicações farmacêuticas, devido à sua capacidade de interagir com vários alvos biológicos. A estrutura molecular do composto sugere que pode exibir propriedades relacionadas à inibição enzimática ou modulação de receptores, tornando-o de interesse na química medicinal e no desenvolvimento de medicamentos.

Fórmula: C₁₃H₁₉N₅O₂·ClH

InChI: InChI=1S/C13H19N5O2.ClH/c14-11(19)10(7-4-8-17-13(15)16)18-12(20)9-5-2-1-3-6-9;/h1-3,5-6,10H,4,7-8H2,(H2,14,19)(H,18,20)(H4,15,16,17);1H/t10-;/m0./s1

Chave InChI: InChIKey=PYZACNCNNFUUDO-PPHPATTJSA-N

SMILES: C(N[C@@H](CCCNC(=N)N)C(N)=O)(=O)C1=CC=CC=C1.Cl

Sinónimos:

• Benzamide, N-(1-carbamoyl-4-guanidinobutyl)-, monohydrochloride, <span class="text-smallcaps">L</span>-
• Benzamide, N-[1-(aminocarbonyl)-4-[(aminoiminomethyl)amino]butyl]-, monohydrochloride, (S)-
• Benzoyl-<span class="text-smallcaps">L</span>-arginine amide monohydrochloride
• Benzoyl-Arg-NH2.HCl
• Bz-Arg-NH2 . HCl
• N-carbamoyl-4-{4-[(diaminomethylidene)amino]butyl}benzamide hydrochloride (1:1)
• N-{1-amino-5-[(diaminomethylidene)amino]-1-oxopentan-2-yl}benzamide
• N-α-Benzoyl-<span class="text-smallcaps">L</span>-argininamide hydrochloride
• N2-(phenylcarbonyl)-L-argininamide hydrochloride
• NSC 343719
• α-N-Benzoyl-<span class="text-smallcaps">L</span>-argininamide hydrochloride
• Benzoyl-L-arginine amide monohydrochloride
• α-N-Benzoyl-L-argininamide hydrochloride

Nα-Benzoyl-L-argininamide Hydrochloride Monohydrate

CAS: 4299-03-0

Fórmula: C₁₃H₁₉N₅O₂·HCl·H₂O

Pureza: >98.0%(T)(HPLC)

Cor e Forma: White to Light yellow powder to crystal

Peso molecular: 331.81

Ref: 3B-B0102

N-α-benzoyl-l-argininamide HCl

CAS: 4299-03-0

Fórmula: C₁₃H₂₀ClN₅O₂

Pureza: 98.0%

Cor e Forma: Solid

Peso molecular: 313.7832

Ref: IN-DA003SPX

(S)-N-(1-Amino-5-guanidino-1-oxopentan-2-yl)benzamide hydrochloride

CAS: 4299-03-0

(S)-N-(1-Amino-5-guanidino-1-oxopentan-2-yl)benzamide hydrochloride

Pureza: 95%

Peso molecular: 313.79g/mol

Ref: 54-OR1054367

(S)-N-(1-Amino-5-guanidino-1-oxopentan-2-yl)benzamide hydrochloride

CAS: 4299-03-0

Fórmula: C₁₃H₂₀ClN₅O₂

Pureza: 95.0%

Cor e Forma: Solid

Peso molecular: 313.79

Ref: 10-F242800

N-alpha-Benzoyl-L-arginine amide hydrochloride

CAS: 4299-03-0

N-alpha-Benzoyl-L-arginine amide hydrochloride (BA) is a synthetic, noncompetitive inhibitor of phosphodiesterase. It has been shown to inhibit protease activity in vitro and rhizosphere enzyme activities in vivo. BA also inhibits the formation of hippuric acid from benzoic acid, which is a reaction catalyzed by the enzyme phosphatase. The kinetics of this inhibition have been studied using a number of different substrates and enzymes. BA binds to the catalytic site on the enzyme, sterically hindering binding of the substrate and preventing hydrolysis.

Fórmula: C₁₃H₁₉N₅O₂·HCl

Pureza: Min. 95%

Cor e Forma: Powder

Peso molecular: 313.78 g/mol

Ref: 3D-FB49071

Bz-Arg-NH2 • HCl • H20

CAS: 4299-03-0

Bz-Arg-NH2 is a proteolytic variant of the enzyme arginase. It is inactivated by ammonium sulfate and competitively by constant. The active site of Bz-Arg-NH2 contains an aldehyde group, which is responsible for its proteolytic activity. Peptides & Biochemicals offers this product as a solute to be used in affinity chromatography and filtration experiments. This product has been shown to be most active at pH 6.0 with an optimum temperature of 37°C. The chloromethyl ketone can be used as a marker for this product during fractionation due to its fluorescing properties.

Fórmula: C₁₃H₁₉N₅O₂•HCI•H₂O

Pureza: Min. 95%

Peso molecular: 331.8 g/mol

Ref: 3D-SRA-3002