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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|August 16, 2014
Exploiting the anti-HIV 6-desfluoroquinolones to design multiple ligandsLuca Sancineto, Nunzio Iraci, Maria Letizia Barreca, et al.
Bioorganic & Medicinal Chemistry|September 24, 2013
Towards new C6-rigid S-DABO HIV-1 reverse transcriptase inhibitors: synthesis, biological investigation and molecular modeling studiesHai-Qiu Wu, Zi-Hong Yan, Wen-Xue Chen, et al.
Journal of Virology|June 29, 2012
Intracytoplasmic trapping of influenza virus by a lipophilic derivative of aglycoristocetinEvelien Vanderlinden, Els Vanstreels, Eline Boons, et al.
Bioorganic & Medicinal Chemistry|April 25, 2015
Anti-HIV diarylpyrimidine-quinolone hybrids and their mode of actionTian-Qi Mao, Qiu-Qin He, Zheng-Yong Wan, et al.
European Journal of Medicinal Chemistry|January 24, 2016
Design, synthesis and anti-HIV evaluation of novel diarylpyridine derivatives targeting the entrance channel of NNRTI binding pocketJiapei Yang, Wenmin Chen, Dongwei Kang, et al.
Cell and Tissue Research|October 1, 2017
Comparative study of the organisation and phenotypes of bladder interstitial cells in human, mouse and ratThomas Gevaert, Jochen Neuhaus, Els Vanstreels, et al.
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