✦ LIBER ✦

Tetrahydrothiophene nucleosides as potential anti-HIV agents

✍ Scribed by Martin F. Jones; Stewart A. Noble; Colin A. Robertson; Richard Storer

Publisher: Elsevier Science
Year: 1991
Tongue: French
Weight: 195 KB
Volume: 32
Category: Article
ISSN: 0040-4039
DOI: 10.1016/0040-4039(91)80867-6

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Synthesis of trideoxyhexopyranosylated a

Synthesis of trideoxyhexopyranosylated and hexenopyranosylated nucleoside analogues as potential anti-HIV agents

✍ P. Herdewijn; A. van Aerschot 📂 Article 📅 2010 🏛 Wiley (John Wiley & Sons) ⚖ 338 KB 👁 1 views

Synthesis and Mass Spectrometric Behavio

Synthesis and Mass Spectrometric Behaviour of Some New Nucleosides as Potential Anti-HIV Agents

✍ Anna Maria Fadda; Gianni Podda; Marta Teijeira; Eugenio Uriarte; Donata Favretto 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 166 KB 👁 2 views

The electron-impact (EI) mass spectrometric behaviour of a series of 8-aza-purines derivatized with hydroxymethylcyclopentane and exhibiting cis-trans isomerization in the cyclopentane ring has been studied in detail with the aid of metastable-ion data. Specific fragmentation processes, present in b

ChemInform Abstract: 6-Aminoquinolones a

ChemInform Abstract: 6-Aminoquinolones as New Potential Anti-HIV Agents.

✍ Manlio Palumbo; et al. et al. 📂 Article 📅 2001 🏛 John Wiley and Sons ⚖ 29 KB 👁 2 views

Cyclotides as natural anti-HIV agents

✍ David C. Ireland; Conan K. L. Wang; Jennifer A. Wilson; Kirk R. Gustafson; David 📂 Article 📅 2007 🏛 Wiley (John Wiley & Sons) 🌐 English ⚖ 327 KB 👁 2 views

## Abstract Cyclotides are disulfide rich macrocyclic plant peptides that are defined by their unique topology in which a head‐to‐tail cyclized backbone is knotted by the interlocking arrangement of three disulfide bonds. This cyclic cystine knot motif gives the cyclotides exceptional resistance to

Synthesis of new pyridazine derivatives

Synthesis of new pyridazine derivatives as potential anti-HIV-1 agents

✍ Stefania Ferro; Stefano Agnello; Maria Letizia Barreca; Laura De Luca; Frauke Ch 📂 Article 📅 2009 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 86 KB 👁 1 views

## Abstract magnified image We herein report conventional and microwave‐assisted methods for the synthesis of a series of compounds containing some bivalent ion chelating requirements useful to exert potential HIV‐1 integrase (IN) enzyme inhibition activity. The biological screening highlighted tha

4-(Arylamino)phenyl α-d-glucopyranosides

4-(Arylamino)phenyl α-d-glucopyranosides as potential anti-HIV agents

✍ Josie C. Briggs; Alan H. Haines 📂 Article 📅 1996 🏛 Elsevier Science 🌐 English ⚖ 446 KB

Our recent interest in aryl-substituted phenyl C~-D-glucopyranosides as potential anti-HIV agents [I-3] led us to examine 4-(arylamino)phenyl a-o-glucopyranosides (1) in this context, since we regarded these glycosides as a logical modification of 4-(arylsulfonylamino)phenyl a-D-glucopyranosides (2)