Advances in diarylpyrimidines and related analogues as HIV-1 nonnucleoside reverse transcriptase inhibitors

被引:41
作者
Gu, Shuang-Xi [1 ]
Lu, Huan-Huan [2 ]
Liu, Gen-Yan [1 ]
Ju, Xiu-Lian [1 ]
Zhu, Yuan-Yuan [3 ]
机构
[1] Wuhan Inst Technol, Sch Chem Engn & Pharm, Minist Educ, Key Lab Green Chem Proc, Wuhan 430205, Hubei, Peoples R China
[2] Yichang Humanwell Pharmaceut Co Ltd, Yichang 443005, Peoples R China
[3] Wuhan Inst Technol, Sch Chem & Environm Engn, Wuhan 430205, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
AIDS; HIV-1; NNRTIs; Diarylpyrimidines; Structural modifications; SAR; BEARING BRIDGEHEAD NITROGEN; AIDED DRUG DESIGN; DUAL STRUCTURAL CONFORMATIONS; BIOLOGICAL EVALUATION; WILD-TYPE; PATENT EVALUATION; ENTRANCE CHANNEL; SUBSTITUTED DIARYLPYRIMIDINES; DIARYLPYRIDINE DERIVATIVES; POSITIONAL ADAPTABILITY;
D O I
10.1016/j.ejmech.2018.09.013
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
HIV-1 nonnucleoside reverse transcriptase inhibitors (NNRTIs) have been playing an important role in the fight against acquired immunodeficiency syndrome (AIDS). Diarylpyrimidines (DAPYs) as the second generation NNRTIs, represented by etravirine (TMC125) and rilpivirine (TMC278), have attracted extensive attention due to their extraordinary potency, high specificity and low toxicity. However, the rapid emergence of drug-resistant virus strains and dissatisfactory pharmacokinetics of DAPY5 present new challenges. In the past two decades, an increasing number of novel DAPY derivatives have emerged, which significantly enriched the structure-activity relationship of DAPYs. Studies of crystallography and molecular modeling have afforded a lot of useful information on structural requirements of NNRTIs, which contributes greatly to the improvement of their resistance profiles. In this review, we reviewed the discovery history and their evolution of DAPYs including their structural modification, derivatization and scaffold hopping in continuous pursuit of excellent anti-HIV drugs. And also, we discussed the prospect of DAPYs and the directions of future efforts. (C) 2018 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:371 / 392
页数:22
相关论文
共 110 条
[1]   Computer Aided Drug Design for Multi-Target Drug Design: SAR/QSAR, Molecular Docking and Pharmacophore Methods [J].
Abdolmaleki, Azizeh ;
Ghasemi, Jahan B. ;
Ghasemi, Fatemeh .
CURRENT DRUG TARGETS, 2017, 18 (05) :556-575
[2]   TMC125, a novel next-generation nonnucleoside reverse transcriptase inhibitor active against nonnucleoside reverse transcriptase inhibitor-resistant human immunodeficiency virus type 1 [J].
Andries, K ;
Azijn, H ;
Thielemans, T ;
Ludovici, D ;
Kukla, M ;
Heeres, J ;
Janssen, P ;
De Corte, B ;
Vingerhoets, J ;
Pauwels, R ;
de Béthune, MP .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2004, 48 (12) :4680-4686
[3]   Computer Aided Drug Design: Success and Limitations [J].
Baig, Mohammad Hassan ;
Ahmad, Khurshid ;
Roy, Sudeep ;
Ashraf, Jalaluddin Mohammad ;
Adil, Mohd ;
Siddiqui, Mohammad Haris ;
Khan, Saif ;
Kamal, Mohammad Amjad ;
Provaznik, Ivo ;
Choi, Inho .
CURRENT PHARMACEUTICAL DESIGN, 2016, 22 (05) :572-581
[4]   ISOLATION OF A T-LYMPHOTROPIC RETROVIRUS FROM A PATIENT AT RISK FOR ACQUIRED IMMUNE-DEFICIENCY SYNDROME (AIDS) [J].
BARRESINOUSSI, F ;
CHERMANN, JC ;
REY, F ;
NUGEYRE, MT ;
CHAMARET, S ;
GRUEST, J ;
DAUGUET, C ;
AXLERBLIN, C ;
VEZINETBRUN, F ;
ROUZIOUX, C ;
ROZENBAUM, W ;
MONTAGNIER, L .
SCIENCE, 1983, 220 (4599) :868-871
[5]  
Boone LR, 2006, CURR OPIN INVESTIG D, V7, P128
[6]   Non-nucleoside HIV-1 reverse transcriptase (RT) inhibitors: Past, present, and future perspectives [J].
Campiani, G ;
Ramunno, A ;
Maga, G ;
Nacci, V ;
Fattorusso, C ;
Catalanotti, B ;
Morelli, E ;
Novellino, E .
CURRENT PHARMACEUTICAL DESIGN, 2002, 8 (08) :615-657
[7]   Covalent inhibitors for eradication of drug-resistant HIV-1 reverse transcriptase: From design to protein crystallography [J].
Chan, Albert H. ;
Lee, Won-Gil ;
Spasov, Krasimir A. ;
Cisneros, Jose A. ;
Kudalkar, Shalley N. ;
Petrova, Zaritza O. ;
Buckingham, Amanda B. ;
Anderson, Karen S. ;
Jorgensen, William L. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2017, 114 (36) :9725-9730
[8]   Discovery of 2-pyridone derivatives as potent HIV-1 NNRTIs using molecular hybridization based on crystallographic overlays [J].
Chen, Wenmin ;
Zhan, Peng ;
Rai, Diwakar ;
De Clercq, Erik ;
Pannecouque, Christophe ;
Balzarini, Jan ;
Zhou, Zhongxia ;
Liu, Huiqing ;
Liu, Xinyong .
BIOORGANIC & MEDICINAL CHEMISTRY, 2014, 22 (06) :1863-1872
[9]   The Development of HEPT-Type HIV Non-Nucleoside Reverse Transcriptase Inhibitors and Its Implications for DABO Family [J].
Chen, Wenmin ;
Zhan, Peng ;
Wu, Jingde ;
Li, Zhenyu ;
Liu, Xinyong .
CURRENT PHARMACEUTICAL DESIGN, 2012, 18 (27) :4165-4186
[10]   Design, Synthesis, and Anti-HIV Evaluation of Novel Triazine Derivatives Targeting the Entrance Channel of the NNRTI Binding Pocket [J].
Chen, Xuwang ;
Meng, Qing ;
Qiu, Liyun ;
Zhan, Peng ;
Liu, Huiqing ;
De Clercq, Erik ;
Pannecouque, Christophe ;
Liu, Xinyong .
CHEMICAL BIOLOGY & DRUG DESIGN, 2015, 86 (01) :122-128