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Discovery and initial SAR of pyrimidin-4-yl-1H-imidazole derivatives with antiproliferative activity against melanoma cell lines
- Lee, Junghun;
- Kim, Hwan;
- Yu, Hana;
- Chung, Jae Yoon;
- Oh, Chang-Hyun;
- ... Hah, Jung-Mi;
- 외 2명
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35초록
The synthesis of a novel series of pyrimidin-4-yl-1H-imidazol-2-yl derivatives 7, 8, 9 and their antiproliferative activities against A375P human melanoma cell line and WM3629 cell line were described. Most compounds showed superior antiproliferative activities compared to Sorafenib, the well-known RAF inhibitor. Among them, 7a exhibited potent activities on both cell lines (IC50 = 0.62 and 4.49 mu M, respectively) and turned out to be a selective and potent CRAF inhibitor. (C) 2010 Elsevier Ltd. All rights reserved.
키워드
Pyrimidin-4-yl-1H-imidazol-2-yl derivatives; Antiproliferative activity; Melanoma cell line; BRAF; CRAF; Selectivity; MALIGNANT-MELANOMA; BRAF; KINASE; INHIBITOR; MUTATIONS; CRAF; SORAFENIB; CANCER; RAF; ERK
- 제목
- Discovery and initial SAR of pyrimidin-4-yl-1H-imidazole derivatives with antiproliferative activity against melanoma cell lines
- 저자
- Lee, Junghun; Kim, Hwan; Yu, Hana; Chung, Jae Yoon; Oh, Chang-Hyun; Yoo, Kyung Ho; Sim, Taebo; Hah, Jung-Mi
- 발행일
- 2010-03
- 유형
- Article
- 권
- 20
- 호
- 5
- 페이지
- 1573 ~ 1577
- 언어
- ENG
- 출판사
- PERGAMON-ELSEVIER SCIENCE LTD
- 발행국가
- 영국
- 분량
- 5 페이지
- ISSN
- E 1464-3405
P 0960-894X