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Ester and hydroxamate analogues of methionyl and isoleucyl adenylates as inhibitors of methionyl-tRNA and isoleucyl-tRNA synthetases
被引:31
作者:

Lee, J
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Seoul Natl Univ, Coll Pharm, Med Chem Lab, Kwanak Ku, Seoul 151742, South Korea Seoul Natl Univ, Coll Pharm, Med Chem Lab, Kwanak Ku, Seoul 151742, South Korea

Kang, SU
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机构: Seoul Natl Univ, Coll Pharm, Med Chem Lab, Kwanak Ku, Seoul 151742, South Korea

Kim, SY
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机构: Seoul Natl Univ, Coll Pharm, Med Chem Lab, Kwanak Ku, Seoul 151742, South Korea

Kim, SE
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机构: Seoul Natl Univ, Coll Pharm, Med Chem Lab, Kwanak Ku, Seoul 151742, South Korea

Kang, MK
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机构: Seoul Natl Univ, Coll Pharm, Med Chem Lab, Kwanak Ku, Seoul 151742, South Korea

Jo, YJ
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机构: Seoul Natl Univ, Coll Pharm, Med Chem Lab, Kwanak Ku, Seoul 151742, South Korea

Kim, S
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机构: Seoul Natl Univ, Coll Pharm, Med Chem Lab, Kwanak Ku, Seoul 151742, South Korea
机构:
[1] Seoul Natl Univ, Coll Pharm, Med Chem Lab, Kwanak Ku, Seoul 151742, South Korea
[2] Sungkyunkwan Univ, ImaGene Co, Suwon 440746, South Korea
[3] Sungkyunkwan Univ, Natl Creative Res Initiat Ctr ARS Network, Suwon 440746, South Korea
关键词:
D O I:
10.1016/S0960-894X(01)00095-6
中图分类号:
R914 [药物化学];
学科分类号:
100701 ;
摘要:
The structure-activity relationship on a series of ester and hydroxamate analogues of methionyl and isoleucyl adenylate has been investigated through introducing linkers between the 1'-position of ribose and adenine surrogates as methionyl-tRNA. and isoleucyl-tRNA synthetase: inhibitors, respectively. The results indicate that ester analogue 23 was found to be a potent inhibitor of Escherichia coli methionyl-tRNA synthetase, and its interaction with the active site was proposed by a molecular modeling study. (C) 2001 Elsevier Science Ltd. All rights reserved.
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页码:961 / 964
页数:4
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