CAS 4299-03-0

Benzamide, N-[1-(aminocarbonyl)-4-[(aminoiminomethyl)amino]butyl]-, monohydrochloride, (S)-

Description:

Benzamide, N-[1-(aminocarbonyl)-4-[(aminoiminomethyl)amino]butyl]-, monohydrochloride, (S)-, is a chemical compound characterized by its complex structure, which includes a benzamide moiety and multiple functional groups such as amino and carbonyl groups. This compound is typically a white to off-white solid and is soluble in water due to the presence of polar functional groups. The presence of the hydrochloride indicates that it is a salt form, which often enhances its stability and solubility in aqueous solutions. The (S)- designation refers to its specific stereochemistry, indicating that it is one of the enantiomers of the compound. Benzamide derivatives are often studied for their biological activity, including potential pharmaceutical applications, due to their ability to interact with various biological targets. The compound's molecular structure suggests it may exhibit properties related to enzyme inhibition or receptor modulation, making it of interest in medicinal chemistry and drug development.

Formula: 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

InChI key: InChIKey=PYZACNCNNFUUDO-PPHPATTJSA-N

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

Synonyms:

• 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

Formula: C₁₃H₁₉N₅O₂·HCl·H₂O

Purity: >98.0%(T)(HPLC)

Color and Shape: White to Light yellow powder to crystal

Molecular weight: 331.81

Ref: 3B-B0102

N-α-benzoyl-l-argininamide HCl

CAS: 4299-03-0

Formula: C₁₃H₂₀ClN₅O₂

Purity: 98.0%

Color and Shape: Solid

Molecular weight: 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

Purity: 95%

Molecular weight: 313.79g/mol

Ref: 54-OR1054367

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

CAS: 4299-03-0

Formula: C₁₃H₂₀ClN₅O₂

Purity: 95.0%

Color and Shape: Solid

Molecular weight: 313.79

Ref: 10-F242800

N-α-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.

Formula: C₁₃H₁₉N₅O₂·HCl

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 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.

Formula: C₁₃H₁₉N₅O₂•HCI•H₂O

Purity: Min. 95%

Molecular weight: 331.8 g/mol

Ref: 3D-SRA-3002