Solution-phase synthesis of an anti-human immunodeficiency virus peptide, T22 ([Tyr5,12, Lys7]-polyphemusin II), and the modification of Trp by the p-methoxybenzyl group of cys during trimethylsilyl trifluoromethanesulfonate deprotec

DOI: 10.1248/cpb.43.12

Source and publish data:

Chemical and Pharmaceutical Bulletin p. 12 - 18 (1995)

Update date:2022-07-31

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Authors:

Tamamura

Otaka Otaka

Takada Takada

Terakawa

Yoshizawa

Masuda Masuda

Ibuka Ibuka

Murakami

Nakashima

Waki Waki

Matsumoto

Yamamoto

Fujii Fujii

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Article abstract of DOI:10.1248/cpb.43.12

T22 ([Tyr^5,12, Lys⁷]-polyphemusin II) was previously synthesized by a solid-phase method and was found to have a strong anti-human immunodeficiency virus (HIV) activity, comparable to that of 3'-azido-2',3'-dideoxy- thymidine (AZT).

Full text of DOI:10.1248/cpb.43.12

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