CAS 4299-03-0

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

Descripción:

Benzamida, N-[1-(aminocarbonil)-4-[(aminoiminometil)amino]butil]-, monohidrocloruro, (S)- es un compuesto químico caracterizado por su estructura compleja, que incluye un grupo benzamida y múltiples grupos funcionales como amino y carbonilo. Este compuesto es típicamente un sólido blanco a blanco sucio y es soluble en agua debido a la presencia de grupos funcionales polares. La presencia del clorhidrato indica que es una forma de sal, lo que a menudo mejora su estabilidad y solubilidad en soluciones acuosas. La designación (S) se refiere a su estereoequilibrio específico, indicando que es uno de los enantiómeros del compuesto. Los derivados de benzamida se estudian a menudo por su actividad biológica, incluidas las posibles aplicaciones farmacéuticas, debido a su capacidad para interactuar con varios objetivos biológicos. La estructura molecular del compuesto sugiere que puede exhibir propiedades relacionadas con la inhibición enzimática o la modulación de receptores, lo que lo hace de interés en la química medicinal y el desarrollo de fármacos.

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

Clave 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)

Forma y color: 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%

Forma y color: 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%

Forma y color: 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%

Forma y color: 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