Wen W. Jiang

发表

Original Open Access

M. Kiso, H. Ishida, M. Tako, 2013 .

Fluorescence-based Polymerase Amplification for the Sensitive Detection of DNA Methyltransferase Activity.

Xiao-Li Zhong, Wen W. Jiang, Xiao Zhang, 2018, Analytical sciences : the international journal of the Japan Society for Analytical Chemistry.

Design, synthesis and inhibitory activity of novel 2, 3-dihydroquinolin-4(1H)-one derivatives as potential succinate dehydrogenase inhibitors.

Wei Cheng, Wen W. Jiang, Yingkun Yan, 2021, European journal of medicinal chemistry.

Identification of halosalicylamide derivatives as a novel class of allosteric inhibitors of HCV NS5B polymerase.

L. Traphagen, U. Warrior, A. Molla, 2008, Bioorganic & medicinal chemistry letters.

Synthesis, Structure, and Characterisation of Two New Open-Framework Zinc Phosphites of Varying Dimensionality

Jin-Hua Li, Q. Wang, Wen W. Jiang, 2015 .

Hepatitis C NS5B polymerase inhibitors: 4,4-Dialkyl-1-hydroxy-3-oxo-3,4-dihydronaphthalene-3-yl benzothiadiazine derivatives.

V. Stoll, A. Molla, D. Kempf, 2008, Bioorganic & medicinal chemistry letters.

Inhibitors of HCV NS5B polymerase: synthesis and structure-activity relationships of unsymmetrical 1-hydroxy-4,4-dialkyl-3-oxo-3,4-dihydronaphthalene benzothiadiazine derivatives.

A. C. Krueger, A. Molla, D. Kempf, 2007, Bioorganic & medicinal chemistry letters.

Inhibitors of HCV NS5B polymerase: synthesis and structure-activity relationships of N-alkyl-4-hydroxyquinolon-3-yl-benzothiadiazine sulfamides.

A. C. Krueger, A. Molla, D. Kempf, 2006, Bioorganic & medicinal chemistry letters.

Antioxidant Activity and Characterization of One New Polysaccharide Obtained from Perigord Truffle (Tuber huidongense)

Jianmin Kan, Yong Liang, Wen W. Jiang, 2016, Evidence-based complementary and alternative medicine : eCAM.

Design, Synthesis and Biological Evaluation of HDAC and VEGFR Dual Inhibitors as a Multi-targeted Anticancer Agents

Y. Liu, Yingjie Zhang, Y. Luan, 2021 .

(C5H6N)4[Be6(HPO3)8]·H2O: A low-density open-framework beryllium phosphite with multidirectional 12-ring channels

Yingxia Wang, Jianhua Lin, Jin-Hua Li, 2014 .

Facile in situ syntheses of new templates and formations of three zinc phosphates

Yingxia Wang, Jianhua Lin, Jin-Hua Li, 2014 .

Des-A-ring benzothiadiazines: inhibitors of HCV genotype 1 NS5B RNA-dependent RNA polymerase.

A. Molla, D. Kempf, W. Kati, 2008, Bioorganic & medicinal chemistry letters.

Identification of aryl dihydrouracil derivatives as palm initiation site inhibitors of HCV NS5B polymerase.

A. Molla, J. Randolph, C. Flentge, 2012, Bioorganic & medicinal chemistry letters.

Mechanistic study of HCV polymerase inhibitors at individual steps of the polymerization reaction.

S. Vasavanonda, W. Kati, Wen W. Jiang, 2006, Biochemistry.

Design, synthesis and evaluation of highly selective pyridone-based class II MET inhibitors.

Wei Huang, Xiao-Lei Zhu, Zhi-Hui Ming, 2014, Bioorganic & medicinal chemistry letters.

Inhibitors of hepatitis C virus polymerase: synthesis and biological characterization of unsymmetrical dialkyl-hydroxynaphthalenoyl-benzothiadiazines.

A. C. Krueger, A. Molla, D. Kempf, 2009, Journal of medicinal chemistry.

Design and synthesis of highly selective pyruvate dehydrogenase complex E1 inhibitors as bactericides.

Lingling Feng, Wen W. Jiang, H. He, 2018, Bioorganic & medicinal chemistry.

Design, Synthesis, and Potency of Pyruvate Dehydrogenase Complex E1 Inhibitors against Cyanobacteria.

Lingling Feng, JiangTao Feng, Wen W. Jiang, 2017, Biochemistry.

Hepatitis C NS5B polymerase inhibitors: functional equivalents for the benzothiadiazine moiety.

V. Stoll, A. Molla, D. Kempf, 2011, Bioorganic & medicinal chemistry letters.

Synthesis and biological characterization of B-ring amino analogues of potent benzothiadiazine hepatitis C virus polymerase inhibitors.

A. Molla, D. Kempf, J. Randolph, 2009, Journal of medicinal chemistry.

Design and synthesis of potent, non-peptide inhibitors of HCV NS3 protease.

C. Decicco, Z. Wasserman, Carl P Decicco, 2003, Bioorganic & medicinal chemistry letters.

Inhibitors of HCV NS5B polymerase: synthesis and structure-activity relationships of N-1-benzyl and N-1-[3-methylbutyl]-4-hydroxy-1,8-naphthyridon-3-yl benzothiadiazine analogs containing substituents on the aromatic ring.

A. Molla, D. Kempf, D. Beno, 2006, Bioorganic & medicinal chemistry letters.

Synthesis and SAR of novel 1,1-dialkyl-2(1H)-naphthalenones as potent HCV polymerase inhibitors.

A. Molla, D. Kempf, H. Mo, 2008, Bioorganic & medicinal chemistry letters.