Tri-substituted triazoles as potent non-nucleoside inhibitors of the HIV-1 reverse transcriptase

M De La Rosa, HW Kim, E Gunic, C Jenket…

Index: Bioorganic and Medicinal Chemistry Letters, , vol. 16, # 17 p. 4444 - 4449

Full Text: HTML

Citation Number: 92

Abstract

... Bioorganic & Medicinal Chemistry Letters. Volume 16, Issue 17, 1 September 2006, Pages 4444–4449. Cover image Cover image. Tri-substituted triazoles as potent non-nucleoside inhibitors of the HIV-1 reverse transcriptase. ...

Related Articles:

Synthesis of substituted 8-aminoquinolines and phenanthrolines through a Povarov approach

[De, Kavita; Legros, Julien; Crousse, Benoit; Chandrasekaran, Srinivasan; Bonnet-Delpon, Daniele Organic and Biomolecular Chemistry, 2011 , vol. 9, # 2 p. 347 - 350]

Synthesis of mono-and dialkylsubstituted 1, 10-phenanthrolines

[Belser, Peter; Bernhard, Stefan; Guerig, Urs Tetrahedron, 1996 , vol. 52, # 8 p. 2937 - 2944]

Substitution effect on the one-and two-photon sensitivity of DMAQ “caging” groups

[Organic Letters, , vol. 14, # 24 p. 6366 - 6369]

Synthesis of mono-and dialkylsubstituted 1, 10-phenanthrolines

[Tetrahedron, , vol. 52, # 8 p. 2937 - 2944]

More Articles...