Xihong Wang, Ph.D.
Affiliations: | 2005 | University of North Carolina, Chapel Hill, Chapel Hill, NC |
Area:
Pharmaceutical Chemistry, OncologyGoogle:
"Xihong Wang"Mean distance: (not calculated yet)
Parents
Sign in to add mentorKuo-Hsing Lee | grad student | 2005 | UNC Chapel Hill | |
(Design, synthesis, and biological evaluation of neo-tanshinlactone and its analogs as potent antibreast cancer agents.) |
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Publications
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Wang SB, Cui MT, Wang XF, et al. (2016) Synthesis, biological evaluation, and physicochemical property assessment of 4-substituted 2-phenylaminoquinazolines as Mer tyrosine kinase inhibitors. Bioorganic & Medicinal Chemistry |
Wang SB, Wang XF, Qin B, et al. (2015) Optimization of N-aryl-6-methoxy-1,2,3,4-tetrahydroquinolines as tubulin polymerization inhibitors. Bioorganic & Medicinal Chemistry |
Li RJ, Sun Y, Sun B, et al. (2014) Phytotoxic cis-clerodane diterpenoids from the Chinese liverwort Scapania stephanii. Phytochemistry. 105: 85-91 |
Wang XF, Guan F, Ohkoshi E, et al. (2014) Optimization of 4-(N-cycloamino)phenylquinazolines as a novel class of tubulin-polymerization inhibitors targeting the colchicine site. Journal of Medicinal Chemistry. 57: 1390-402 |
Wang XF, Wang SB, Ohkoshi E, et al. (2013) N-aryl-6-methoxy-1,2,3,4-tetrahydroquinolines: a novel class of antitumor agents targeting the colchicine site on tubulin. European Journal of Medicinal Chemistry. 67: 196-207 |
Li WQ, Wang XL, Qian K, et al. (2013) Design, synthesis and potent cytotoxic activity of novel podophyllotoxin derivatives. Bioorganic & Medicinal Chemistry. 21: 2363-9 |
Wang XF, Ohkoshi E, Wang SB, et al. (2013) Synthesis and biological evaluation of N-alkyl-N-(4-methoxyphenyl)pyridin-2-amines as a new class of tubulin polymerization inhibitors. Bioorganic & Medicinal Chemistry. 21: 632-42 |
Wang XF, Tian XT, Ohkoshi E, et al. (2012) Design and synthesis of diarylamines and diarylethers as cytotoxic antitumor agents. Bioorganic & Medicinal Chemistry Letters. 22: 6224-8 |
Soares J, Keppler BR, Wang X, et al. (2011) ortho-Quinone tanshinones directly inhibit telomerase through an oxidative mechanism mediated by hydrogen peroxide. Bioorganic & Medicinal Chemistry Letters. 21: 7474-8 |
Liu X, Wang X, Li Q, et al. (2011) Synthesis and antimalarial activity of 2-guanidino-4-oxoimidazoline derivatives. Journal of Medicinal Chemistry. 54: 4523-35 |