CAS 37682-72-7

L-Valinamide, N2-[[[(1S)-1-carbossi-2-feniletil]amino]carbonil]-L-arginil-N-[4-[(aminoiminometil)amino]-1-formilbutil]-, cloridrato (1:2)

Descrizione:

L-Valinamide, N2-[[[(1S)-1-carbossi-2-feniletil]amino]carbonil]-L-arginil-N-[4-[(aminoiminometil)amino]-1-formilbutil]-, cloridrato (1:2) è un composto organico complesso caratterizzato dalla sua struttura multifunzionale, che include derivati degli amminoacidi e una forma di sale cloridrico. Questa sostanza presenta una combinazione di uno scheletro di L-valinamide e un frammento di L-arginina, indicando il suo potenziale ruolo nei sistemi biologici, in particolare nella sintesi di peptidi o come intermedio farmaceutico. La presenza di più gruppi funzionali, come acidi carbossilici, ammine e imine, suggerisce che possa mostrare diverse proprietà di reattività e solubilità. La forma cloridrica migliora la sua stabilità e solubilità in ambienti acquosi, rendendola adatta per varie applicazioni in chimica medicinale. Inoltre, la stereochimica del composto, in particolare la configurazione (1S), è cruciale per la sua attività biologica, influenzando le interazioni con i bersagli biologici. In generale, la struttura intricata e la diversità funzionale di questo composto lo posizionano come un'entità significativa nello studio di molecole bioattive e agenti terapeutici.

Formula: C₂₇H₄₄N₁₀O₆·2ClH

InChI: 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

Sinonimi:

• <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

Formula: C₂₇H₄₄N₁₀O₆•2HCl

Colore e forma: White, Powder

Peso molecolare: 677.6

Ref: 02-J63680

Antipain dihydrochloride

CAS: 37682-72-7

Antipain dihydrochloride

Colore e forma: White To Pale Yellow Powder

Peso molecolare: 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.

Formula: C₂₇H₄₆Cl₂N₁₀O₆

Purezza: 95%

Colore e forma: White To Off-White Powder

Peso molecolare: 677.62

Ref: TM-T26637

Antipain dihydrochloride

CAS: 37682-72-7

Formula: C₂₇H₄₄N₁₀O₆₂HCl

Peso molecolare: 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.

Formula: C₂₇H₄₄N₁₀O₆·2HCl

Purezza: Min. 95%

Peso molecolare: 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.

Formula: C₂₇H₄₄N₁₀O₆•(HCl)₂

Purezza: Min. 95%

Peso molecolare: 677.62 g/mol

Ref: 3D-FA29612