Electrophilic derivatives of purines as irreversible inhibitors of A1 adenosine receptors
KA Jacobson, S Barone, U Kammula…
Index: Jacobson; Barone; Kammula; Stiles Journal of Medicinal Chemistry, 1989 , vol. 32, # 5 p. 1043 - 1051
Full Text: HTML
Citation Number: 46
Abstract
Functionalized congeners derived from 1, 3-dipropyl-8-phenylxanthine and from p- phenyladenosine were derivatized to contain electrophilic groups (isothiocyanate, N- hydroxysuccinimide ester, maleimide, sulfonyl chloride, or a-haloacyl group) capable of reaction with nucleophiles on biopolymers. The goal was to inhibit chemically the AI adenosine receptor by using reactive agonist and antagonist ligands. Some of the ...
Related Articles:
[Zhang, Xuechun; Lee, Young K.; Kelley, James A.; Burke Jr., Terrence R. Journal of Organic Chemistry, 2000 , vol. 65, # 19 p. 6237 - 6240]
A general and facile one-pot process of isothiocyanates from amines under aqueous conditions
[Sun, Nan; Li, Bin; Shao, Jianping; Mo, Weimin; Hu, Baoxiang; Shen, Zhenlu; Hu, Xinquan Beilstein Journal of Organic Chemistry, 2012 , vol. 8, p. 61 - 70]
Facile and versatile synthesis of alkyl and aryl isothiocyanates by using triphosgene and cosolvent
[Liu, Pengfei; Li, Chunyan; Zhang, Jingwei; Xu, Xiaoyong Synthetic Communications, 2013 , vol. 43, # 24 p. 3342 - 3351]
[Chen, Kan; Tan, Zhiwu; He, Meizi; Li, Jiebo; Tang, Shixing; Hewlett, Indira; Yu, Fei; Jin, Yinxue; Yang, Ming Chemical Biology and Drug Design, 2010 , vol. 76, # 1 p. 25 - 33]