An improved synthesis of haloaceteamidine-based inactivators of protein arginine deiminase 4 (PAD4).

An improved synthesis of haloaceteamidine-based inactivators of protein arginine deiminase 4 (PAD4).
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DOI:
10.1016/j.tetlet.2008.05.021
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发表时间:
2008-07-07
影响因子:
1.8
通讯作者:
Thompson, Paul R.
Thompson, Paul R.
中科院分区:
化学4区
文献类型:
--
作者:
Causey, Corey P.;Thompson, Paul R.

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蛋白质精氨酸脱亚胺酶4(PAD 4)是水解肽基精氨酸残基以形成瓜氨酸和氨的酶。这种酶与几种疾病状态有关,例如类风湿性关节炎,因此代表了开发新型治疗剂的独特靶标。已开发了迄今为止描述的最有效的PAD 4灭活剂Cl-脒的液相合成。该合成在4个步骤中以80%的产率以显著(12倍)较低的成本进行。
Protein arginine deiminase 4 (PAD4) is an enzyme that hydrolyzes peptidyl arginine residues to form citrulline and ammonia. This enzyme has been implicated in several disease states, e.g. rheumatoid arthritis, and therefore represents a unique target for the development of a novel therapeutic. A solution-phase synthesis of Cl-amidine, the most potent PAD4 inactivator described to date, has been developed. This synthesis proceeds in 80% yield over 4 steps at a significantly (12-fold) lower cost.
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