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Merck
CN

V8250

蛇毒 来源于锯鳞蝰

别名:

Saw-scaled Viper

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关于此项目

NACRES:
NA.25
UNSPSC Code:
12352200
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application(s)

metabolomics
vitamins, nutraceuticals, and natural products

storage temp.

−20°C

Quality Level

Application

Snake venom from Echis carinatus (Indian saw-scaled viper) which acts primarily on fibrinogen may be used as a source of anticoagulation factors and the prothrombin activator ecarin. It may also be used as an immunogen.

pictograms

Skull and crossbones

signalword

Danger

Hazard Classifications

Acute Tox. 2 Dermal - Acute Tox. 2 Oral

存储类别

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

法规信息

涉药品监管产品
此项目有

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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John Kim et al.
Xenobiotica; the fate of foreign compounds in biological systems, 45(8), 663-671 (2015-02-13)
1. The safety, tolerability, pharmacokinetics, pharmacodynamics, and food effect of LB30870, a new selective thrombin inhibitor, were studied in 16 healthy men. 2. A double-blind, placebo-controlled single ascending dose study was done at oral doses of 5, 15, 30, 60, 120, and
Isolation and partial purification of anticoagulant fractions , from the venom of the Iranian snake Echis carinatus.
Babaie M, Zolfagharian H, et al.
Bioengineered (2012)
K Paul et al.
Toxicon : official journal of the International Society on Toxinology, 50(7), 893-900 (2007-08-08)
High titer antibodies (IgY) were raised in egg yolk of white leghorn chicken (Gallus gallus domesticus) by immunizing with the venom of Echis carinatus (Saw scaled viper or carpet viper), an Indian venomous snake belonging to the family Viperidae. The
Effects of snake venom proteases on human fibrinogen chains.
Cortelazzo A, Guerranti R, Bini L, et al.
Blood, 8, 120-125 (2010)
Riley B Peacock et al.
Biochemistry, 57(18), 2694-2703 (2018-04-11)
Thrombin normally cleaves fibrinogen to promote coagulation; however, binding of thrombomodulin to thrombin switches the specificity of thrombin toward protein C, triggering the anticoagulation pathway. The W215A thrombin mutant was reported to have decreased activity toward fibrinogen without significant loss

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