Our principal goal is to discover new anti-HIV clinical trial candidates based on natural products from higher plants. Correspondingly, with the prior support of this grant, we developed the modified triterpene bevirimat (BVM), the first-in-class HIV maturation inhibitor, which successfully reached Phase IIb clinical trials, and discovered the gnidimacrin (GM)-related daphnane-type diterpenes, which exhibit extremely potent dichotomous activity for activation of latent HIV-1 replication and inhibition of de novo HIV infection at low picomolar concentration. We hypothesize that new anti-HIV-1 compounds with unique structures, extremely potent activity, and novel mechanism of action (MOA) can be identified from natural products and their derivatives. We will carry out the following specific studies to accomplish our objectives: 1. Discovery of new leads from natural products. We will identify potent anti-HIV principles from extracts of previously unexplored rainforest and medicinal plant species 2. Optimization of identified leads using rational synthetic modifications to yield promising compounds suitable for future preclinical studies and clinical trials. Two major research areas are 1) Development of a second-generation BVM-analog to overcome issues of Gag polymorphism in the viral target and continue clinical development of triterpenoid maturation inhibitors as a new anti-HIV therapy. 2) Modification of GM-related diterpenes to identify drug candidates for HIV-1 eradication. 3. Determination of anti-HIV-1 activity and MOA for new and already identified promising candidates. We will conduct both HIV drug screening and mechanistic assays, respectively. We plan to identify novel compounds with potent anti-HIV-1 activity and novel MOA, including families of compounds with activity against HIV isolates resistant to currently approved drugs. We also expect to identify the drug targets. A distinctive and valuable collaboration between two academic institutions [Dr. K.H. Lee, Natural Products Research Laboratories (NPRL), UNC and Dr. C.H. Chen, Duke University] has been established and is ongoing to discover and develop novel small molecule HIV inhibitors from natural products and their synthetic analogs. The NPRL has expertise in the bioactivity-directed fractionation and isolation (BDFI) and characterization of bioactive natural products coupled with structural modification of the new leads to optimize their pharmaceutical profiles. Dr. Chen's laboratory at Duke University has the needed expertise, experience, and resources to perform initial activity screening, as well as further mechanistic and pharmacological studies to develop the natural product-based inhibitors through preclinical studies. Based on these current lead compounds as well as future novel active constituents to be identified from medicinal plants, this anti-HIV research program will be able to successfully discover and develop new anti-HIV drug candidates for AIDS treatment and HIV-1 eradication.
New AIDS drugs are continually needed, particularly as HIV strains resistant to different current anti- retroviral therapies continue to emerge. One compound resulting from this research has already reached Phase IIb clinical trials and another compound is currently in-hand that shows extremely potent activity. Based on these current lead compounds as well as future novel active constituents to be identified from medicinal plants, this anti-HIV research program will be able to successfully discover and develop new anti-HIV drug candidates for AIDS treatment and HIV-1 eradication.
|Hung, Hsin-Yi; Nakagawa-Goto, Kyoko; Tokuda, Harukuni et al. (2014) A-ring modified betulinic acid derivatives as potent cancer preventive agents. Bioorg Med Chem Lett 24:1005-8|
|Wu, Zhi-Yuan; Liu, Na; Qin, Bingjie et al. (2014) Optimization of the antiviral potency and lipophilicity of halogenated 2,6-diarylpyridinamines as a novel class of HIV-1 NNRTIS. ChemMedChem 9:1546-55|
|Liu, Na; Qin, Bingjie; Sun, Lian-Qi et al. (2014) Physicochemical property-driven optimization of diarylaniline compounds as potent HIV-1 non-nucleoside reverse transcriptase inhibitors. Bioorg Med Chem Lett 24:3719-23|
|Asada, Yoshihisa; Sukemori, Aya; Watanabe, Takashi et al. (2013) Isolation, structure determination, and anti-HIV evaluation of tigliane-type diterpenes and biflavonoid from Stellera chamaejasme. J Nat Prod 76:852-7|
|Zhou, Ting; Shi, Qian; Chen, Chin-Ho et al. (2012) Anti-AIDS agents 85. Design, synthesis, and evaluation of 1R,2R-dicamphanoyl-3,3-dimethyldihydropyrano-[2,3-c]xanthen-7(1H)-one (DCX) derivatives as novel anti-HIV agents. Eur J Med Chem 47:86-96|
|Sun, Lian-Qi; Qin, Bingjie; Huang, Li et al. (2012) Optimization of 2,4-diarylanilines as non-nucleoside HIV-1 reverse transcriptase inhibitors. Bioorg Med Chem Lett 22:2376-9|
|Huang, Li; Ho, Phong; Yu, Jie et al. (2011) Picomolar dichotomous activity of gnidimacrin against HIV-1. PLoS One 6:e26677|
|Wang, Qiang; Hu, Weidong; Wang, Shuyang et al. (2011) Synthesis of new 2'-deoxy-2'-fluoro-4'-azido nucleoside analogues as potent anti-HIV agents. Eur J Med Chem 46:4178-83|
|Liu, Hong-Shan; Xu, Shi-Qing; Cheng, Ming et al. (2011) Anti-AIDS agents 87. New bio-isosteric dicamphanoyl-dihydropyranochromone (DCP) and dicamphanoyl-khellactone (DCK) analogues with potent anti-HIV activity. Bioorg Med Chem Lett 21:5831-4|
|Chen, Ying; Cheng, Ming; Liu, Fa-Qiang et al. (2011) Anti-AIDS agents 86. Synthesis and anti-HIV evaluation of 2',3'-seco-3'-nor DCP and DCK analogues. Eur J Med Chem 46:4924-36|
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