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V0882

Sigma-Aldrich

D-Val-Leu-Lys 4-nitroanilide dihydrochloride

plasmin substrate

Sinonimo/i:

D-Val-Leu-Lys-pNA dihydrochloride, D-Valyl-L-leucyl-L-lysine 4-nitroanilide dihydrochloride

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5 MG
CHF 221.00
25 MG
CHF 827.00

CHF 221.00

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5 MG
CHF 221.00
25 MG
CHF 827.00

About This Item

Formula empirica (notazione di Hill):
C23H38N6O5 · 2HCl
Numero CAS:
62354-43-2
Peso molecolare:
551.51
Numero MDL:
MFCD00077899
Codice UNSPSC:
12352204
ID PubChem:
24900701
NACRES:
NA.32

CHF 221.00

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Saggio

≥98% (TLC)

Stato

powder

Solubilità

water: 50 mg/mL, clear, colorless to yellow

Temperatura di conservazione

−20°C

Stringa SMILE

Cl.Cl.CC(C)C[C@H](NC(=O)[C@H](N)C(C)C)C(=O)N[C@@H](CCCCN)C(=O)Nc1ccc(cc1)[N+]([O-])=O

InChI

1S/C23H38N6O5.2ClH/c1-14(2)13-19(28-23(32)20(25)15(3)4)22(31)27-18(7-5-6-12-24)21(30)26-16-8-10-17(11-9-16)29(33)34;;/h8-11,14-15,18-20H,5-7,12-13,24-25H2,1-4H3,(H,26,30)(H,27,31)(H,28,32);2*1H/t18-,19-,20+;;/m0../s1
VESQMNNSPPEOSZ-ZLARAOTRSA-N

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Applicazioni

D-Val-Leu-Lys 4-nitroanilide dihydrochloride has been used as a chromogenic substrate to determine the formation of plasmin from plasminogen in amidolytic activity assay[1] and plasminogen activating assay.[2]

Pittogrammi

Health hazardExclamation mark
GHS08,GHS07

Avvertenze

Warning

Classi di pericolo

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Repr. 2 - Skin Irrit. 2 - STOT SE 3

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

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Certificati d'analisi (COA)

Lot/Batch Number
0000400603
0000376518
0000296059
0000352710
0000352708

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S Ueshima et al.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis, 7(5), 522-529 (1996-07-01)
Staphylokinase (SAK), produced by Staphylococcus aureus, induces fibrinolytic activity in circulation without systemic fibrinolytic activation. Since the effect of blood vessels on the activity of SAK has not yet been clarified, plasminogen activator (PA) activity of SAK in the presence
I A Taitzoglou et al.
Reproduction (Cambridge, England), 121(1), 131-137 (2001-02-28)
The effect of tannic acid, a common flavonoid, on the acrosin and plasminogen activator activity and plasmin activity of human and ram spermatozoa was evaluated. Acrosin and plasminogen activator activity were determined by spectrophotometry using the chromogenic substrates N-alpha-benzoyl-DL-arginine para-nitroanilide-HCl
K M Rippel et al.
Journal of dairy science, 87(8), 2344-2350 (2004-08-26)
The plasmin system native to bovine milk consists of the caseinolytic serine proteinase plasmin; its inactive zymogen, plasminogen; plasminogen activators; and inhibitors. Evidence in the literature indicates that whey proteins may inhibit plasmin activity, but there is very little mention
Genetic modification of the streptokinase gene to study the interaction of streptokinase with plasminogen.
S Lizano et al.
Developments in biological standardization, 85, 195-198 (1995-01-01)
L C Petersen
European journal of biochemistry, 245(2), 316-323 (1997-04-15)
The two zymogens, plasminogen and pro-urokinase plasminogen activator (pro-uPA), constitute a system of reciprocal activation, since plasmin, generated by uPA-catalysed plasminogen activation, can activate pro-uPA to uPA. Two such zymogens, when mixed, will undergo autocatalytic, reciprocal activation resulting in generation
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Protocolli

Enzymatic Assay of Plasmin with D-Val-Leu-Lys-p-Nitroanilide Dihydrochloride

Protocol for Enzymatic Assay of Plasmin with D-Val-Leu-Lys-p-Nitroanilide Dihydrochloride

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