Multivalent Agents: A Novel Concept and Preliminary Practice in Anti-HIV Drug Discovery

被引:12
作者
Song, Yu'ning [2 ]
Zhan, Peng [1 ]
Li, Xiao [1 ]
Rai, Diwakar [1 ]
De Clercq, Erik [3 ]
Liu, Xinyong [1 ]
机构
[1] Shandong Univ, Dept Med Chem, Sch Pharmaceut Sci, Jinan 250012, Shandong, Peoples R China
[2] Shandong Univ, Dept Pharmacol, Key Lab Chem Biol, Minist Educ,Sch Pharmaceut Sci, Jinan 250012, Shandong, Peoples R China
[3] Katholieke Univ Leuven, Rega Inst Med Res, B-3000 Louvain, Belgium
基金
中国博士后科学基金; 中国国家自然科学基金; 高等学校博士学科点专项科研基金;
关键词
HIV; AIDS; multivalency/polyvalency approach; drug design; chemical space; mixed sites inhibitor; REVERSE-TRANSCRIPTASE INHIBITORS; POTENTIAL MULTIFUNCTIONAL INHIBITORS; TYPE-1 PROTEASE INHIBITOR; SMALL-MOLECULE INHIBITORS; GP41 FUSION INTERMEDIATE; STRUCTURE-BASED DESIGN; NONNUCLEOSIDE INHIBITORS; WILD-TYPE; CHEMICAL SPACE; BIOLOGICAL-ACTIVITY;
D O I
暂无
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
The term multivalency (polyvalency) in the biological science is defined as the simultaneous binding of multiple ligands to one receptor (or multiple receptors to one ligand). The possibility of gaining potency and selectivity was significantly increased through the use of multivalent ligand as a homo- or hetero-dimer, thus multivalent ligands provided a more attractive strategy to design novel anti-HIV agents with therapeutic applications. Moreover, similar to phenomenon of multivalency, an alternative strategy is called the "mixed sites inhibitor", viz. a single molecule that possesses enough chemical space to maximize interactions with its complementary binding pocket, or to bind simultaneously in more than one regions in a target. Actually, the addition of a third heterocyclic nucleus to the parent compound resulted in "mixed sites" anti-HIV agents with broad spectrum of activities against the mutant HIV-1 strains. Based on current representative examples, the present article provided a brief review on the rationale for the design of different classes of multivalency anti-HIV agents and also discussed the advantages over their monomeric counterparts, providing a novel paradigm to facilitate the development of anti-HIV/AIDS therapeutic agents in treatment of HIV infected community.
引用
收藏
页码:815 / 832
页数:18
相关论文
共 150 条
[1]
ADAMS D., 1979, HITCH HIKERS GUIDE G
[2]
Inhibitor selectivity of a new class of oseltamivir analogs against viral neuraminidase over human neuraminidase enzymes [J].
Albohy, Amgad ;
Mohan, Sankar ;
Zheng, Ruixiang Blake ;
Pinto, B. Mario ;
Cairo, Christopher W. .
BIOORGANIC & MEDICINAL CHEMISTRY, 2011, 19 (09) :2817-2822
[3]
Anderson K.S., 2009, Patent No. [WO2009126293, 2009126293]
[4]
[Anonymous], Substituted benzimidazoles as non-nucleoside inhibitors of reverse transcriptase, Patent No. [WO 9837072 A1 19980827, 9837072]
[5]
Aslanyan S., 2011, 51 INT C ANT CHEM CH
[6]
Characteristics of known drug space. Natural products, their derivatives and synthetic drugs [J].
Bade, Richard ;
Chan, Ho-Fung ;
Reynisson, Johannes .
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2010, 45 (12) :5646-5652
[7]
Multivalent Anti-CCR5 ribozymes for stem cell-based HIV type 1 gene therapy [J].
Bai, JR ;
Rossi, J ;
Akkina, R .
AIDS RESEARCH AND HUMAN RETROVIRUSES, 2001, 17 (05) :385-399
[8]
An alternative strategy for inhibiting multidrug-resistant mutants of the dimeric HIV-1 protease by targeting the subunit interface [J].
Bannwarth, L. ;
Reboud-Ravaux, M. .
BIOCHEMICAL SOCIETY TRANSACTIONS, 2007, 35 :551-554
[9]
Inhibition of Herpes Simplex Virus Type 1 Infection by Silver Nanoparticles Capped with Mercaptoethane Sulfonate [J].
Baram-Pinto, Dana ;
Shukla, Sourabh ;
Perkas, Nina ;
Gedanken, Aharon ;
Sarid, Ronit .
BIOCONJUGATE CHEMISTRY, 2009, 20 (08) :1497-1502
[10]
Highly active antiretroviral therapy: Current state of the art, new agents and their pharmacological interactions useful for improving therapeutic outcome [J].
Barbaro, G ;
Scozzafava, A ;
Mastrolorenzo, A ;
Supuran, CT .
CURRENT PHARMACEUTICAL DESIGN, 2005, 11 (14) :1805-1843