HIV Citation List: January 6 - January 19, 2010
Pubmed citations:
1. A lectin isolated from bananas is a potent inhibitor of HIV replication. Swanson MD, Winter HC, Goldstein IJ, Markovitz DM. J Biol Chem. 2010 Jan 15. [Epub ahead of print]PMID: 20080975
2. Different selection patterns of resistance and cross-resistance to HIV-1 agents targeting CCR5. Armand-Ugón M, Moncunill G, Gonzalez E, Mena M, Ballana E, Clotet B, Esté JA. J Antimicrob Chemother. 2010 Jan 12. [Epub ahead of print]PMID: 20067983
3. A novel lectin with highly potent antiproliferative and HIV-1 reverse transcriptase inhibitory activities from the edible wild mushroom Russula delica. Zhao S, Zhao Y, Li S, Zhao J, Zhang G, Wang H, Ng TB. Glycoconj J. 2010 Jan 12. [Epub ahead of print]PMID: 20066561
4. Progranulin (granulin/epithelin precursor) and its constituent granulin repeats repress transcription from cellular promoters. Hoque M, Mathews MB, Pe'ery T. J Cell Physiol. 2010 Jan 6. [Epub ahead of print]PMID: 20054825
5. Biochemical and Functional Properties of a Lectin Purified from Korean Large Black Soybeans - A Cultivar of Glycine Max. Fang EF, Wong JH, Lin P, Ng TB. Protein Pept Lett. 2010 Jan 10. [Epub ahead of print]PMID: 19715533
ISI Web of Knowledge citations:
6. Inhibition of HIV-1 integrase nuclear import and replication by a peptide bearing integrase putative nuclear localization signal. Levin, A; Armon-Omer, A; Rosenbluh, J; Melamed-Book, N; Graessmann, A; Waigmann, E; Loyter, A. RETROVIROLOGY, 2009; 6.
7. 3-O-Methylfunicone, a Selective Inhibitor of Mammalian Y-Family DNA Polymerases from an Australian Sea Salt Fungal Strain. Mizushina, Y; Motoshima, H; Yamaguchi, Y; Takeuchi, T; Hirano, K; Sugawara, F; Yoshida, H. MARINE DRUGS, 2009; 7(4): 624-639.
8. Synthesis of New Pyridazine Derivatives as Potential Anti-HIV-1 Agents. Ferro, S; Agnello, S; Barreca, ML; De Luca, L; Christ, F; Gitto, R. JOURNAL OF HETEROCYCLIC CHEMISTRY, 2009; 46(6): 1420-1424.
9. A Convenient Synthesis and Biological Evaluation of Novel Pseudonucleosides Bearing a Thiazolidin-4-one Moiety by Tandem Staudinger/Aza-Wittig/Cyclization. Chen, H; Zhang, HZ; Feng, JN; Li, XL; Jiao, LL; Qin, ZB; Yin, QM; Zhang, JC. EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2009; 35: 6100-6103.
10. Activity and molecular modeling of a new small molecule active against NNRTI-resistant HIV-1 mutants. Carta, A; Pricl, S; Piras, S; Fermeglia, M; La Colla, P; Loddo, R. EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2009; 44(12): 5117-5122.
11. Synthesis and Biological Activities of Quinoline Derivatives as HIV-1 Integrase Inhibitors. Luo, ZG; Zeng, CC; Wang, F; He, HQ; Wang, CX; Du, HG; Hu, LM. CHEMICAL RESEARCH IN CHINESE UNIVERSITIES, 2009; 25(6): 841-845.
12. Design and Synthesis of New Anti-AIDS Drugs-Introducing an Immunomodulator into Delavirdine Derivative. Lu, HB; Mi, HY; Cui, LL; Yu, XH; Liang, T; Wang, ES. CHEMICAL RESEARCH IN CHINESE UNIVERSITIES, 2009; 25(6): 856-860.
13. Unique metabolites of Pestalotiopsis fici suggest a biosynthetic; hypothesis involving a Diels-Alder reaction and then mechanistic diversification. Liu, L; Niu, SB; Lu, XH; Chen, XL; Zhang, H; Guo, LD; Che, YS. CHEMICAL COMMUNICATIONS, 2010; 46(3): 460-462.
14. Synthesis and evaluation of 3 '-azido-2 ',3 '-dideoxypurine nucleosides as inhibitors of human immunodeficiency virus. Zhang, HW; Coats, SJ; Bondada, L; Amblard, F; Detorio, M; Asif, G; Fromentin, E; Solomon, S; Obikhod, A; Whitaker, T; Sluis-Cremer, N; Mellors, JW; Schinazi, RF. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2010; 20(1): 60-64.
15. Structure-based design, synthesis and biological evaluation of new N-carboxyphenylpyrrole derivatives as HIV fusion inhibitors targeting gp41. ang, Y; Lu, H; Zhu, Q; Jiang, SB; Liao, Y. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2010; 20(1): 189-192.
16. Non-peptide entry inhibitors of HIV-1 that target the gp41 coiled coil pocket. Stewart, KD; Huth, JR; Ng, TI; McDaniel, K; Hutchinson, RN; Stoll, VS; Mendoza, RR; Matayoshi, ED; Carrick, R; Mo, HM; Severin, J; Walter, K; Richardson, PL; Barrett, LW; Meadows, R; Anderson, S; Kohlbrenner, W; Maring, C; Kempf, DJ; Molla, A; Olejniczak, ET. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2010; 20(2): 612-617.
17. Spirodiketopiperazine-based CCR5 antagonists: Improvement of their pharmacokinetic profiles. Nishizawa, R; Nishiyama, T; Hisaichi, K; Hirai, K; Habashita, H; Takaoka, Y; Tada, H; Sagawa, K; Shibayama, S; Maeda, K; Mitsuya, H; Nakai, H; Fukushima, D; Toda, M. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2010; 20(2): 763-766.
18. Synthesis, nanosizing and in vitro drug release of a novel anti-HIV polymeric prodrug: Chitosan-O-isopropyl-5 '-O-d4T monophosphate conjugate. Yang, L; Chen, LQ; Zeng, R; Li, C; Qiao, RZ; Hu, LM; Li, ZL. BIOORGANIC & MEDICINAL CHEMISTRY, 2010; 18(1): 117-123.
19. Characterization of a Peptide Domain within the GB Virus C NS5A Phosphoprotein that Inhibits HIV Replication. Xiang, JH; McLinden, JH; Chang, Q; Jordan, EL; Stapleton, JT. PLOS ONE, 2008; 3(7).
20. Facile Synthesis of Hydroxy Wilfordic Acid, A Esterifying Unit of Anti-HIV Sesquiterpene Pyridine Alkaloids. Eun, JS; Seo, SY. ARCHIVES OF PHARMACAL RESEARCH. 2009; 32(12): 1673-1679.