These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
9. A comparative study of the solution structures of tachyplesin I and a novel anti-HIV synthetic peptide, T22 ([Tyr5,12, Lys7]-polyphemusin II), determined by nuclear magnetic resonance. Tamamura H; Kuroda M; Masuda M; Otaka A; Funakoshi S; Nakashima H; Yamamoto N; Waki M; Matsumoto A; Lancelin JM Biochim Biophys Acta; 1993 May; 1163(2):209-16. PubMed ID: 8490053 [TBL] [Abstract][Full Text] [Related]
10. Anti-human immunodeficiency virus activity of a novel synthetic peptide, T22 ([Tyr-5,12, Lys-7]polyphemusin II): a possible inhibitor of virus-cell fusion. Nakashima H; Masuda M; Murakami T; Koyanagi Y; Matsumoto A; Fujii N; Yamamoto N Antimicrob Agents Chemother; 1992 Jun; 36(6):1249-55. PubMed ID: 1384424 [TBL] [Abstract][Full Text] [Related]
11. Analysis of the interaction of an anti-HIV peptide, T22 ([Tyr5, 12, Lys7]-polyphemusin II), with gp120 and CD4 by surface plasmon resonance. Tamamura H; Ishihara T; Otaka A; Murakami T; Ibuka T; Waki M; Matsumoto A; Yamamoto N; Fujii N Biochim Biophys Acta; 1996 Nov; 1298(1):37-44. PubMed ID: 8948487 [TBL] [Abstract][Full Text] [Related]
12. Marked increase in anti-HIV activity, as well as inhibitory activity against HIV entry mediated by CXCR4, linked to enhancement of the binding ability of tachyplesin analogs to CXCR4. Xu Y; Tamamura H; Arakaki R; Nakashima H; Zhang X; Fujii N; Uchiyama T; Hattori T AIDS Res Hum Retroviruses; 1999 Mar; 15(5):419-27. PubMed ID: 10195751 [TBL] [Abstract][Full Text] [Related]
13. Lymphocytes and promonocytes attach to the synthetic [Tyr5,12, Lys7]- polyphemusin II peptide. Weeks BS; Nomizu M; Otaka A; Weston CA; Okusu A; Tamamura H; Matsumoto A; Yamamoto N; Fujii N Biochem Biophys Res Commun; 1994 Jul; 202(1):470-5. PubMed ID: 8037749 [TBL] [Abstract][Full Text] [Related]
14. 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 deprotection. Tamamura H; Otaka A; Takada W; Terakawa Y; Yoshizawa H; Masuda M; Ibuka T; Murakami T; Nakashima H; Waki M Chem Pharm Bull (Tokyo); 1995 Jan; 43(1):12-8. PubMed ID: 7895303 [TBL] [Abstract][Full Text] [Related]
15. A low-molecular-weight inhibitor against the chemokine receptor CXCR4: a strong anti-HIV peptide T140. Tamamura H; Xu Y; Hattori T; Zhang X; Arakaki R; Kanbara K; Omagari A; Otaka A; Ibuka T; Yamamoto N; Nakashima H; Fujii N Biochem Biophys Res Commun; 1998 Dec; 253(3):877-82. PubMed ID: 9918823 [TBL] [Abstract][Full Text] [Related]
16. An anti-HIV peptide, T22, forms a highly active complex with Zn(II). Tamamura H; Otaka A; Murakami T; Ibuka T; Sakano K; Waki M; Matsumoto A; Yamamoto N; Fujii N Biochem Biophys Res Commun; 1996 Dec; 229(2):648-52. PubMed ID: 8954952 [TBL] [Abstract][Full Text] [Related]
17. A small molecule CXCR4 inhibitor that blocks T cell line-tropic HIV-1 infection. Murakami T; Nakajima T; Koyanagi Y; Tachibana K; Fujii N; Tamamura H; Yoshida N; Waki M; Matsumoto A; Yoshie O; Kishimoto T; Yamamoto N; Nagasawa T J Exp Med; 1997 Oct; 186(8):1389-93. PubMed ID: 9334379 [TBL] [Abstract][Full Text] [Related]
18. Pharmacophore identification of a specific CXCR4 inhibitor, T140, leads to development of effective anti-HIV agents with very high selectivity indexes. Tamamura H; Omagari A; Oishi S; Kanamoto T; Yamamoto N; Peiper SC; Nakashima H; Otaka A; Fujii N Bioorg Med Chem Lett; 2000 Dec; 10(23):2633-7. PubMed ID: 11128640 [TBL] [Abstract][Full Text] [Related]