From snake venom toxins to therapeutics - Cardiovascular examples

被引:151
|
作者
Koh, Cho Yeow [1 ]
Kini, Manjunatha [1 ,2 ]
机构
[1] Natl Univ Singapore, Fac Sci, Prot Sci Lab, Dept Biol Sci, Singapore 117437, Singapore
[2] Virginia Commonwealth Univ, Med Coll Virginia, Dept Biochem & Mol Biophys, Richmond, VA 23298 USA
关键词
Toxins to therapeutics; Toxins to drugs; Drug discovery; Drug design; Antithrombotic agents; Anti-hypertensive agents; Anti-cancer; BRADYKININ-POTENTIATING PEPTIDES; ANGIOTENSIN-CONVERTING ENZYME; AMINO-ACID-SEQUENCE; AGKISTRODON-CONTORTRIX-CONTORTRIX; DECOMPENSATED HEART-FAILURE; BREAST-CANCER PROGRESSION; PROTEIN INTERACTION SITES; SHORT-NEUROTOXIN HOMOLOG; GLYCOPROTEIN-IIB-IIIA; ANGIOGENESIS IN-VITRO;
D O I
10.1016/j.toxicon.2011.03.017
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Snakes have fascinated the imaginations of people since the dawn of civilization. Their deadly venoms cause significant mortality and morbidity worldwide, and strike fear in most of us. Snake venoms contain a huge variety of molecules affecting vital physiological systems, and scientists are turning some of these life-threatening toxins into a source of life-saving therapeutics. Since the approval of captopril - the first drug based on snake venom protein - more than 30 years ago, snake venom toxins have become a valuable natural pharmacopeia of bioactive molecules that provide lead compounds for the development of new drugs. Many toxins are being explored and developed into drugs for the treatment of conditions such as hypertension, thrombosis and cancer. A number of new drugs are constantly emerging from this pipeline. In this review, we briefly highlight the molecular basis of developing therapeutic agents, such as Captopril, Tirofiban, and Eptifibatide, from snake venom proteins. We also discuss the successes and failures as an update to the advances in the field. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:497 / 506
页数:10
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