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SAR and QSAR in Environmental Research|September 23, 2014
Docking-based CoMFA and CoMSIA studies on naphthyl-substituted diarylpyrimidines as NNRTIsHai-Qiu Wu, Jin Yao, Qiu-Qin He, et al.Journal of Enzyme Inhibition and Medicinal Chemistry|April 4, 2012
Synthesis and biological evaluation of 5-fluoroquinolone-3-carboxylic acids as potential HIV-1 integrase inhibitorsQiu-Qin He, Xuan Zhang, Liu-Meng Yang, et al.Bioorganic & Medicinal Chemistry|December 25, 2014
Synthesis and biological evaluation of DAPY-DPEs hybrids as non-nucleoside inhibitors of HIV-1 reverse transcriptaseHai-Qiu Wu, Jin Yao, Qiu-Qin He, et al.Current Pharmaceutical Design|November 24, 2016
Structural Modifications of Diarylpyrimidine-quinolone Hybrids as Potent HIV-1 NNRTIs with an Improved Drug Resistance ProfileTian-Qi Mao, Qiu-Qin He, Wen-Xue Chen, et al.Bioorganic & Medicinal Chemistry|July 6, 2010
Hybrid diarylbenzopyrimidine non-nucleoside reverse transcriptase inhibitors as promising new leads for improved anti-HIV-1 chemotherapyZhao-Sen Zeng, Qiu-Qin He, Yong-Hong Liang, et al.Chemmedchem|October 13, 2011
Synthesis and anti-HIV activity of aryl-2-[(4-cyanophenyl)amino]-4-pyrimidinone hydrazones as potent non-nucleoside reverse transcriptase inhibitorsXiao-Dong Ma, Shi-Qiong Yang, Shuang-Xi Gu, et al.Bioorganic & Medicinal Chemistry|July 19, 2011
Structural modifications of quinolone-3-carboxylic acids with anti-HIV activityQiu-Qin He, Shuang-Xi Gu, Jia Liu, et al.Bioorganic & Medicinal Chemistry|August 10, 2011
Synthesis and structure-activity relationship of novel diarylpyrimidines with hydromethyl linker (CH(OH)-DAPYs) as HIV-1 NNRTIsShuang-Xi Gu, Qiu-Qin He, Shi-Qiong Yang, et al.Bioorganic & Medicinal Chemistry|June 22, 2011
Synthesis and biological evaluation of naphthyl phenyl ethers (NPEs) as novel nonnucleoside HIV-1 reverse transcriptase inhibitorsShuang-Xi Gu, Xuan Zhang, Qiu-Qin He, et al.Bioorganic & Medicinal Chemistry|August 25, 2011
Synthesis and biological evaluation of HQCAs with aryl or benzyl substituents on N-1 position as potential HIV-1 integrase inhibitorsQiu-Qin He, Xuan Zhang, Hai-Qiu Wu, et al.Pageof 2