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Benzothiazole-containing hydroxamic acids as histone deacetylase inhibitors and antitumor agents
- Dao Thi Kim Oanh;
- Hoang Van Hai;
- Park, Sang Ho;
- Kim, Hyun-Jung;
- Han, Byung-Woo;
- 외 5명
WEB OF SCIENCE
61SCOPUS
68초록
Data from clinical studies indicate that inhibitors of Class I and Class II histone deacetylase (HDAC) enzymes show great promise for the treatment of cancer. Zolinza (SAHA, Zolinza) was recently approved by the FDA for the treatment of the cutaneous manifestations of cutaneous T-cell lymphoma. As a part of our ongoing effort to identify novel small molecules to target these important enzymes, we have prepared two series of benzothiazole-containing analogues of SAHA. It was found that several compounds with 6C-bridge linking benzothiazole moiety and hydroxamic functional groups showed good inhibition against HDAC3 and 4 at as low as 1 mu g/ml and exhibited potent cytotoxicity against five cancer cell lines with average IC50 values of as low as 0.81 mu g/ml, almost equipotent to SAHA. (C) 2011 Published by Elsevier Ltd.
키워드
- 제목
- Benzothiazole-containing hydroxamic acids as histone deacetylase inhibitors and antitumor agents
- 저자
- Dao Thi Kim Oanh; Hoang Van Hai; Park, Sang Ho; Kim, Hyun-Jung; Han, Byung-Woo; Kim, Hyung-Sook; Hong, Jin-Tae; Han, Sang-Bae; Van Thi My Hue; Nguyen-Hai Nam
- 발행일
- 2011-12
- 유형
- Article
- 권
- 21
- 호
- 24
- 페이지
- 7509 ~ 7512
- 언어
- ENG
- 출판사
- PERGAMON-ELSEVIER SCIENCE LTD
- 발행국가
- 영국
- 분량
- 4 페이지
- ISSN
- E 1464-3405
P 0960-894X