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Effective lowly cytotoxic analogs of an HIV-cell fusion inhibitor, T22 ([Tyr 5,12, Lys 7]-polyphemusin II)
A tachyplesin peptide analog, T22 ([Tyr 5,12, Lys 7]-polyphemusin II), and its shortened congener, TW70 (des-[Cys 8,13, Tyr 9,12]-[ d-Lys 10, Pro 11]-T22) have strong anti-human immunodeficiency virus (HIV) activity, comparable to that of 3′-azido-2′, 3′-dideoxythymidine (AZT). T22 and TW70 are extr...
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Published in: | Bioorganic & medicinal chemistry 1998-02, Vol.6 (2), p.231-238 |
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Main Authors: | , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | A tachyplesin peptide analog, T22 ([Tyr
5,12, Lys
7]-polyphemusin II), and its shortened congener, TW70 (des-[Cys
8,13, Tyr
9,12]-[
d-Lys
10, Pro
11]-T22) have strong anti-human immunodeficiency virus (HIV) activity, comparable to that of 3′-azido-2′, 3′-dideoxythymidine (AZT). T22 and TW70 are extremely basic peptides, containing 5 Arg residues and 3 Lys residues. The number of positive charges might be related in part to high collateral cytotoxicities of T22 and TW70. Here we have synthesized several analogs, in which the number of positive charges has been reduced through amino acid substitutions using Glu or
l-citrulline. As a result, several effective compounds have been found which possess higher selectivity indexes (SIs, 50% cytotoxic concentration/50% effective concentration) than those of T22 and TW70. Higher SIs were attributed mainly to a decrease in cytotoxicity. |
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ISSN: | 0968-0896 1464-3391 |
DOI: | 10.1016/S0968-0896(97)10037-2 |