Literature DB >> 1799953

KNI-102, a novel tripeptide HIV protease inhibitor containing allophenylnorstatine as a transition-state mimic.

T Mimoto1, J Imai, S Tanaka, N Hattori, S Kisanuki, K Akaji, Y Kiso.   

Abstract

HIV-1 protease inhibitors containing allophenylnorstatine [Apns; (2S,3S)-3-amino-2-hydroxy-4-phenylbutyric acid]-Pro (syn diastereomer) as a transition-state mimic were established to be potent and highly selective. Z-Asn-Apns-Pro-NHBut (KNI-102) is the only tripeptide exhibiting substantial anti-HIV activity and may be of minimum size for potent, selective inhibition of HIV protease. Ready availability due to its simple chemical structure and stability should make it valuable for studies of the development of metabolically stable anti-AIDS drugs.

Entities:  

Mesh:

Substances:

Year:  1991        PMID: 1799953     DOI: 10.1248/cpb.39.3088

Source DB:  PubMed          Journal:  Chem Pharm Bull (Tokyo)        ISSN: 0009-2363            Impact factor:   1.645


  7 in total

1.  Structural insights into the activation and inhibition of histo-aspartic protease from Plasmodium falciparum.

Authors:  Prasenjit Bhaumik; Huogen Xiao; Koushi Hidaka; Alla Gustchina; Yoshiaki Kiso; Rickey Y Yada; Alexander Wlodawer
Journal:  Biochemistry       Date:  2011-09-26       Impact factor: 3.162

2.  Crystal structures of multidrug-resistant HIV-1 protease in complex with two potent anti-malarial compounds.

Authors:  Ravikiran S Yedidi; Zhigang Liu; Yong Wang; Joseph S Brunzelle; Iulia A Kovari; Patrick M Woster; Ladislau C Kovari; Deepak Gupta
Journal:  Biochem Biophys Res Commun       Date:  2012-03-24       Impact factor: 3.575

3.  Crystal structures of the free and inhibited forms of plasmepsin I (PMI) from Plasmodium falciparum.

Authors:  Prasenjit Bhaumik; Yasumi Horimoto; Huogen Xiao; Takuya Miura; Koushi Hidaka; Yoshiaki Kiso; Alexander Wlodawer; Rickey Y Yada; Alla Gustchina
Journal:  J Struct Biol       Date:  2011-04-20       Impact factor: 2.867

4.  Antimalarial activity enhancement in hydroxymethylcarbonyl (HMC) isostere-based dipeptidomimetics targeting malarial aspartic protease plasmepsin.

Authors:  Koushi Hidaka; Tooru Kimura; Adam J Ruben; Tsuyoshi Uemura; Mami Kamiya; Aiko Kiso; Tetsuya Okamoto; Yumi Tsuchiya; Yoshio Hayashi; Ernesto Freire; Yoshiaki Kiso
Journal:  Bioorg Med Chem       Date:  2008-10-10       Impact factor: 3.641

5.  In vitro anti-human immunodeficiency virus (HIV) activities of transition state mimetic HIV protease inhibitors containing allophenylnorstatine.

Authors:  S Kageyama; T Mimoto; Y Murakawa; M Nomizu; H Ford; T Shirasaka; S Gulnik; J Erickson; K Takada; H Hayashi
Journal:  Antimicrob Agents Chemother       Date:  1993-04       Impact factor: 5.191

6.  Crystal structures of the histo-aspartic protease (HAP) from Plasmodium falciparum.

Authors:  Prasenjit Bhaumik; Huogen Xiao; Charity L Parr; Yoshiaki Kiso; Alla Gustchina; Rickey Y Yada; Alexander Wlodawer
Journal:  J Mol Biol       Date:  2009-03-11       Impact factor: 5.469

7.  Understanding the structural basis of substrate recognition by Plasmodium falciparum plasmepsin V to aid in the design of potent inhibitors.

Authors:  Rajiv K Bedi; Chandan Patel; Vandana Mishra; Huogen Xiao; Rickey Y Yada; Prasenjit Bhaumik
Journal:  Sci Rep       Date:  2016-08-17       Impact factor: 4.379

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.