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2,4-二苯基呋喃二脒作为新型抗卡氏肺孢子虫肺炎药物。

2,4-Diphenyl furan diamidines as novel anti-Pneumocystis carinii pneumonia agents.

作者信息

Francesconi I, Wilson W D, Tanious F A, Hall J E, Bender B C, Tidwell R R, McCurdy D, Boykin D W

机构信息

Department of Chemistry and Center for Biotechnology and Drug Design, Georgia State University, Atlanta, Georgia 30303-3083, USA.

出版信息

J Med Chem. 1999 Jun 17;42(12):2260-5. doi: 10.1021/jm990071c.

Abstract

Dicationic 2,4-bis(4-amidinophenyl)furans 5-10 and 2, 4-bis(4-amidinophenyl)-3,5-dimethylfurans 14 and 15 have been synthesized. Thermal melting studies revealed high binding affinity of the compounds to poly(dA-dT) and to the duplex oligomer d(CGCGAATTCGCG)2. All of the new compounds were effective against Pneumocystis carinii pneumonia in the immunosuppressed rat model with up to 200-fold increase in activity compared to the control compound pentamidine. No toxicity was noted for 5, 7-10 at the dose of 10 micromol/kg/d; however, the isopropyl analogue 7 showed toxicity comparable to pentamidine at the dosage of 20 micromol/kg/d. Dimethylation of the parent compound on the furan ring resulted in reduced activity and increased toxicity.

摘要

已合成了双阳离子型2,4 - 双(4 - 脒基苯基)呋喃5 - 10以及2,4 - 双(4 - 脒基苯基)- 3,5 - 二甲基呋喃14和15。热熔研究表明这些化合物对聚(dA - dT)以及双链寡聚物d(CGCGAATTCGCG)₂具有高结合亲和力。所有新化合物在免疫抑制大鼠模型中对卡氏肺孢子虫肺炎有效,与对照化合物喷他脒相比,活性提高了200倍。在10微摩尔/千克/天的剂量下,5、7 - 10未观察到毒性;然而,异丙基类似物7在20微摩尔/千克/天的剂量下显示出与喷他脒相当的毒性。母体化合物在呋喃环上的二甲基化导致活性降低和毒性增加。

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