Physicochemical Properties
Molecular Formula | C219H342F3N71O76S9 |
Molecular Weight | 5531.02 |
Related CAS # | Echistatin;154303-05-6 |
Appearance | White to off-white solid powder |
HS Tariff Code | 2934.99.9001 |
Storage |
Powder-20°C 3 years 4°C 2 years In solvent -80°C 6 months -20°C 1 month Note: Please store this product in a sealed and protected environment, avoid exposure to moisture. |
Shipping Condition | Room temperature (This product is stable at ambient temperature for a few days during ordinary shipping and time spent in Customs) |
Biological Activity
Targets | αvβ3 α5β1 αIIbβ3 |
References |
[1]. Inhibition of platelet adhesion to surfaces of extracorporeal circuits by disintegrins. RGD-containing peptides from viper venoms. Circulation. 1990 Jul;82(1):261-73. [2]. Echistatin is a potent inhibitor of bone resorption in culture. J Cell Biol. 1990 Oct;111(4):1713-23. [3]. Biochemical characterization of the binding of echistatin to integrin alphavbeta3 receptor. J Pharmacol Exp Ther. 1997 Nov;283(2):843-53. [4]. Structural requirements of echistatin for the recognition of alpha(v)beta(3) and alpha(5)beta(1) integrins. J Biol Chem. 1999 Dec 31;274(53):37809-14. |
Solubility Data
Solubility (In Vitro) | H2O :~50 mg/mL (~9.04 mM) |
Solubility (In Vivo) |
Solubility in Formulation 1: 50 mg/mL (9.04 mM) in PBS (add these co-solvents sequentially from left to right, and one by one), clear solution; with sonication.  (Please use freshly prepared in vivo formulations for optimal results.) |
Preparing Stock Solutions | 1 mg | 5 mg | 10 mg | |
1 mM | 0.1808 mL | 0.9040 mL | 1.8080 mL | |
5 mM | 0.0362 mL | 0.1808 mL | 0.3616 mL | |
10 mM | 0.0181 mL | 0.0904 mL | 0.1808 mL |