Synthesis of Symmetrical and Asymmetrical Phenethyl Thiourea Compounds as Nonnucleoside Inhibitors of HIV‐1 Reverse Transcriptase-Reference-Cited by-同舟云学术

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Synthesis of Symmetrical and Asymmetrical Phenethyl Thiourea Compounds as Nonnucleoside Inhibitors of HIV‐1 Reverse Transcriptase

Published:2005-08-01 Issue:15 Volume:35 Page:2039-2056
ISSN:0039-7911
Container-title:Synthetic Communications
language:en
Short-container-title:Synthetic Communications

Author:

Venkatachalam T. K.¹²,Uckun F. M.²³

Affiliation:

1. a Department of Chemistry , Parker Hughes Institute , Roseville, Minnesota, USA

2. b Drug Discovery Program, Parker Hughes Cancer Center , Roseville, Minnesota, USA

3. c Departments of Virology and Immunology , Parker Hughes Institute , Roseville, Minnesota, USA

Publisher

Informa UK Limited

Subject

Organic Chemistry

Link

https://www.tandfonline.com/doi/pdf/10.1081/SCC-200066677

Reference18 articles.

1. Phenethylthiazolylthiourea (PETT) Compounds as a New Class of HIV-1 Reverse Transcriptase Inhibitors. 2. Synthesis and Further Structure−Activity Relationship Studies of PETT Analogs

2. Phenethylthiazolethiourea (PETT) Compounds, a New Class of HIV-1 Reverse Transcriptase Inhibitors. 1. Synthesis and Basic Structure-Activity Relationship Studies of PETT Analogs

3. Structure-based design of N-[2-(1-piperidinylethyl)]-N′-[2-(5-bromopyridyl)]-thiourea and N-[2-(1-piperazinylethyl)]-N′-[2-(5-bromopyridyl)]-thiourea as potent non-nucleoside inhibitors of HIV-1 reverse transcriptase

4. Rational design of N-[2-(2,5-dimethoxyphenylethyl)]-N′-[2-(5-bromopyridyl)]-thiourea (HI-236) as a potent non-nucleoside inhibitor of drug-resistant human immunodeficiency virus

5. Structure-based drug design of non-nucleoside inhibitors for wild-type and drug-resistant HIV reverse transcriptase

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2. Cardioprotective Activity of Some 2-Arylimino-1,3-Thiazole Derivatives;Scientia Pharmaceutica;2019-03-18

3. Synthesis and computational study of new meta- and para-substituted ferrocenyl thioureas as potent protein kinase inhibitors and cytotoxic agents;Inorganica Chimica Acta;2019-03

4. Synthesis, spectroscopic investigation, and DFT study of N,N′-disubstituted ferrocene-based thiourea complexes as potent anticancer agents;Dalton Transactions;2018

5. Green Process Development for the Synthesis of Aliphatic SymmetricalN,N′-Disubstituted Thiourea Derivatives in Aqueous Medium;Synthetic Communications;2014-12-13

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