Syntheses of phenylpyrazolodiazepin-7-ones as conformationally rigid analogs of aminopyrazole amide scaffold and their antiproliferative effects on cancer cells

• Published in: Bioorganic & medicinal chemistry 2011-11, Vol.19 (22), p.6760-6767
• Main Authors: Kim, Hyangmi, Kim, Minjung, Lee, Junghun, Yu, Hana, Hah, Jung-Mi
• Format: Article
• Language: English
• Subjects: Amides - chemical synthesis; Amides - chemistry; Amides - pharmacology; Antineoplastic agents; Antiproliferative activity; Azepines - chemical synthesis; Azepines - chemistry; Azepines - pharmacology; Biological and medical sciences; Cancer cell line; Cell Growth Processes - drug effects; Cell Line, Tumor; chemistry; Dihydropyrazolodiazepinone; General aspects; Humans; Kinase inhibitor; Kinase selectivity; Medical sciences; melanoma; Melanoma - drug therapy; Melanoma - pathology; Models, Molecular; Nuclear Magnetic Resonance, Biomolecular; Pharmacology. Drug treatments; phosphotransferases (kinases); Pyrazoles - chemical synthesis; Pyrazoles - chemistry; Pyrazoles - pharmacology; Structure-Activity Relationship; U937 Cells
• ISSN: 0968-0896; 1464-3391
• DOI: 10.1016/j.bmc.2011.09.042

The synthesis of a novel series of phenylpyrazolodiazepin-7-one derivatives 7a–g, 8a–o and their antiproliferative activities against A375P melanoma cell line and U937 hematopoietic cell line were described. Recently, we have reported the syntheses and antiproliferative activities of N-(5-amino-1-(4-methoxybenzyl)-1H-pyrazol-4-yl amide derivatives on melanoma cells. As a continuous work for antiproliferative agents in melanoma, here we report the synthesis of conformationally rigid analogs, phenyl-6,8-dihydropyrazolo[3,4-b][1,4]diazepin-7(1H)-one derivatives 7a–g, 8a–o and their antiproliferative activities against A375P melanoma cell line and U937 hematopoietic cell line. Most compounds showed competitive antiproliferative activities to sorafenib, the reference standard. Among them, N-(3-(1-benzyl-7-oxo-1,6,7,8-tetrahydropyrazolo[3,4-b][1,4]diazepin-5-yl)phenyl)-4-chloro-3-(trifluoro methyl)benzamide-amino-1-(4-methoxybenzyl)-1H-pyrazol-4-yl)-5-(3-(4-chloro-3-(trifluoromethyl) phenyl) ureido)-2-methylbenzamide (7b) exhibited potent activities (GI50=0.43μM and 0.06μM) on both cell lines. It has been further confirmed to be a potent and selective Raf kinases inhibitor and also mild inhibitor of PI3Kα.