New indolylarylsulfones as highly potent and broad spectrum HIV-1 non-nucleoside reverse transcriptase inhibitors

V Famiglini, G La Regina, A Coluccia, S Pelliccia…

Index: European Journal of Medicinal Chemistry, , vol. 80, p. 101 - 111

Full Text: HTML

Citation Number: 11

Abstract

... JavaScript is disabled on your browser. Please enable JavaScript to use all the features on this page. European Journal of Medicinal Chemistry. Volume 80, 10 June 2014, Pages 101–111. ... 19 j, nd, nd, nd, 91 ± 9, nd. 20 j, 19,937 ± 5223, 0.21 h, 94,938, nd, nd. ...

Related Articles:

Novel non-vanilloid VR1 antagonist of high analgesic effects and its structural requirement for VR1 antagonistic effects

[Bioorganic and Medicinal Chemistry Letters, , vol. 13, # 24 p. 4389 - 4393]

Novel non-vanilloid VR1 antagonist of high analgesic effects and its structural requirement for VR1 antagonistic effects

[Bioorganic and Medicinal Chemistry Letters, , vol. 13, # 24 p. 4389 - 4393]

Synthesis of N-benzyl-and N-phenyl-2-amino-4, 5-dihydrothiazoles and thioureas and evaluation as modulators of the isoforms of nitric oxide synthase

[Bioorganic and Medicinal Chemistry, , vol. 11, # 19 p. 4189 - 4206]

Nonsolvent application of ionic liquids: organo-catalysis by 1-alkyl-3-methylimidazolium cation based room-temperature ionic liquids for chemoselective N-tert- …

[Journal of Organic Chemistry, , vol. 76, # 17 p. 7132 - 7140]

Tricyclic indole-2-carboxylic acids: highly in vivo active and selective antagonists for the glycine binding site of the NMDA receptor

[Journal of Medicinal Chemistry, , vol. 46, # 5 p. 691 - 701]

More Articles...