CAS 37682-72-7

L-Valinamid, N2-[[[(1S)-1-carboxy-2-phenylethyl]amino]carbonyl]-L-arginyl-N-[4-[(aminoiminomethyl)amino]-1-formylbutyl]-, hydrochlorid (1:2)

Beschreibung:

L-Valinamid, N2-[[[(1S)-1-carboxy-2-phenylethyl]amino]carbonyl]-L-arginyl-N-[4-[(aminoiminomethyl)amino]-1-formylbutyl]-, hydrochlorid (1:2) ist eine komplexe organische Verbindung, die durch ihre multifunktionale Struktur gekennzeichnet ist, die Aminosäurederivate und eine Hydrochloridsalzform umfasst. Diese Substanz weist eine Kombination aus einem L-Valinamid-Rückgrat und einem L-Arginin-Moiety auf, was auf ihre potenzielle Rolle in biologischen Systemen hinweist, insbesondere in der Peptidsynthese oder als pharmazeutischer Zwischenstoff. Das Vorhandensein mehrerer funktioneller Gruppen, wie Carbonsäuren, Amine und Iminen, deutet darauf hin, dass sie unterschiedliche Reaktivitäts- und Löslichkeitseigenschaften aufweisen kann. Die Hydrochloridform verbessert ihre Stabilität und Löslichkeit in wässrigen Umgebungen, was sie für verschiedene Anwendungen in der medizinischen Chemie geeignet macht. Darüber hinaus ist die Stereochemie der Verbindung, insbesondere die (1S)-Konfiguration, entscheidend für ihre biologische Aktivität und beeinflusst die Wechselwirkungen mit biologischen Zielen. Insgesamt positioniert die komplexe Struktur und funktionale Vielfalt dieser Verbindung sie als eine bedeutende Entität in der Studie von bioaktiven Molekülen und therapeutischen Wirkstoffen.

Formel: C₂₇H₄₄N₁₀O₆·2ClH

InChl: InChI=1S/C27H44N10O6.2ClH/c1-16(2)21(23(40)34-18(15-38)10-6-12-32-25(28)29)37-22(39)19(11-7-13-33-26(30)31)35-27(43)36-20(24(41)42)14-17-8-4-3-5-9-17;;/h3-5,8-9,15-16,18-21H,6-7,10-14H2,1-2H3,(H,34,40)(H,37,39)(H,41,42)(H4,28,29,32)(H4,30,31,33)(H2,35,36,43);2*1H

InChI Key: InChIKey=YAHXZYICKJUJEO-UHFFFAOYSA-N

SMILES: C(C(NC(C(NC(CCCNC(=N)N)C=O)=O)C(C)C)=O)(NC(NC(CC1=CC=CC=C1)C(O)=O)=O)CCCNC(=N)N.Cl

Synonyme:

• <span class="text-smallcaps">L</smallcap>-Valinamide, N²-[[[(1S)-1-carboxy-2-phenylethyl]amino]carbonyl]-<smallcap>L</span>-arginyl-N-[4-[(aminoiminomethyl)amino]-1-formylbutyl]-, dihydrochloride
• <span class="text-smallcaps">L</smallcap>-Valinamide, N²-[[[(1S)-1-carboxy-2-phenylethyl]amino]carbonyl]-<smallcap>L</span>-arginyl-N-[4-[(aminoiminomethyl)amino]-1-formylbutyl]-, hydrochloride (1:2)
• Antipain dihydrochloride
• L-Valinamide, N(sup 2)-(((1-carboxy-2-phenylethyl)amino)carbonyl)-L-arginyl-N-(4-((aminoiminomethyl)amino)-1-formylbutyl)-, dihydrochloride
• N-({(1S)-4-[(diaminomethylidene)amino]-1-[(N-{4-[(diaminomethylidene)amino]-1-formylbutyl}-L-valyl)carbamoyl]butyl}carbamoyl)phenylalanine dihydrochloride
• L-Valinamide, N2-[[[(1S)-1-carboxy-2-phenylethyl]amino]carbonyl]-L-arginyl-N-[4-[(aminoiminomethyl)amino]-1-formylbutyl]-, dihydrochloride
• L-Valinamide, N2-[[[(1S)-1-carboxy-2-phenylethyl]amino]carbonyl]-L-arginyl-N-[4-[(aminoiminomethyl)amino]-1-formylbutyl]-, hydrochloride (1:2)

Antipain dihydrochloride

CAS: 37682-72-7

Antipain inhibits trypsin, papain, and catherpsins A and B (a reversible inhibitor of cysteine and serine proteases). It is used to evaluate the role of proteases in cell transformations. It is used to help identify new proteases. This Thermo Scientific brand product was originally part of the Alfa

Formel: C₂₇H₄₄N₁₀O₆•2HCl

Farbe und Form: White, Powder

Molekulargewicht: 677.6

Ref: 02-J63680

Antipain dihydrochloride

CAS: 37682-72-7

Antipain dihydrochloride

Farbe und Form: White To Pale Yellow Powder

Molekulargewicht: 677.62g/mol

Ref: 54-BIA0201

Antipain dihydrochloride

CAS: 37682-72-7

Antipain dihydrochloride (Antipain 2HCl) is a protease inhibitor derived from Actinomycetes with analgesic activity.

Formel: C₂₇H₄₆Cl₂N₁₀O₆

Reinheit: 95%

Farbe und Form: White To Off-White Powder

Molekulargewicht: 677.62

Ref: TM-T26637

Antipain dihydrochloride

CAS: 37682-72-7

Formel: C₂₇H₄₄N₁₀O₆₂HCl

Molekulargewicht: 677.60

Ref: 7W-GL6582

Antipain (Synthetic)

CAS: 37682-72-7

Antipain (supplied as the HCl salt) is a cytosolic and bound form of antipain. It binds to ATP-binding cassette transporter proteins, which are involved in the transport of substances across cell membranes, and inhibits their enzymatic activity. Antipain 2HCI also has inhibitory properties on enzymes such as DNA polymerase II and pyruvate kinase. It has been shown to have an effect on biochemical properties such as protein synthesis, enzyme activities, and polymerase chain reactions. This drug has been shown to be effective in preventing myocardial infarcts and cellular apoptosis by inhibiting the release of cytochrome c from mitochondria. Antipain 2HCI may also have some anti-inflammatory effects due to its inhibition of prostaglandin synthesis.

Formel: C₂₇H₄₄N₁₀O₆·2HCl

Reinheit: Min. 95%

Molekulargewicht: 604.7 g/mol

Ref: 3D-IAP-3996-PI

Antipain dihydrochloride

CAS: 37682-72-7

Antipain 2HCI is a cytosolic and bound form of antipain. It binds to ATP-binding cassette transporter proteins, which are involved in the transport of substances across cell membranes, and inhibits their enzymatic activity. Antipain 2HCI also has inhibitory properties on enzymes such as DNA polymerase II and pyruvate kinase. It has been shown to have an effect on biochemical properties such as protein synthesis, enzyme activities, and polymerase chain reactions. This drug has been shown to be effective in preventing myocardial infarcts and cellular apoptosis by inhibiting the release of cytochrome c from mitochondria. Antipain 2HCI may also have some anti-inflammatory effects due to its inhibition of prostaglandin synthesis.

Formel: C₂₇H₄₄N₁₀O₆•(HCl)₂

Reinheit: Min. 95%

Molekulargewicht: 677.62 g/mol

Ref: 3D-FA29612