Lin Ma

发表

Synthesis and biological evaluation of phosphorylated flavonoids as potent and selective inhibitors of cholesterol esterase.

Yingling Wei, A. Peng, Bo-Chi Wang, 2014, European journal of medicinal chemistry.

Phosphaisocoumarins as a new class of potent inhibitors for pancreatic cholesterol esterase.

A. Peng, Lin Ma, Baojian Li, 2010, European journal of medicinal chemistry.

Novel core-shell nanoparticles and their application in high-capacity immobilization of enzymes

Pei Li, Zhishu Huang, Lin Ma, 2006 .

A novel method to prepare chitosan powder and its application in cellulase immobilization

Pei Li, Zhishu Huang, Lin Ma, 2006 .

Methyl 2-(2-(4-formylphenoxy)acetamido)-2-substituted acetate derivatives: a new class of acetylcholinesterase inhibitors.

Huacan Song, Lin Ma, Zihou Wang, 2007, Bioorganic & medicinal chemistry letters.

Curcumin Analogs as Potent Aldose Reductase Inhibitors

A. Chan, Wei Qiao, Zhishu Huang, 2006, Archiv der Pharmazie.

WITHDRAWN: Polyhydroxybenzaldehyde azines: A novel competitive α-glucosidase inhibitor

Hao Wu, Jingwei Zheng, Xinhua Li, 2013 .

Synthesis and biological evaluation of helicid analogues as novel acetylcholinesterase inhibitors.

Y. Wan, R. Cao, Huacan Song, 2008, European journal of medicinal chemistry.

Synthesis and biological evaluation of functionalized coumarins as acetylcholinesterase inhibitors.

A. Chan, Zhishu Huang, Xufeng Liu, 2005, European journal of medicinal chemistry.

Biological evaluations of novel vitamin C esters as mushroom tyrosinase inhibitors and antioxidants

Huacan Song, Lin Ma, Xiao-qin Wu, 2009 .

Silver(I) complexes of 2,4-dihydroxybenzaldehyde-amino acid Schiff bases-Novel noncompetitive α-glucosidase inhibitors.

Jingwei Zheng, Lin Ma, 2015, Bioorganic & medicinal chemistry letters.

Metal complexes of anthranilic acid derivatives: A new class of non-competitive α-glucosidase inhibitors

Lin Ma, Jing Zheng, 2016 .

Synthesis of 4-[(diethylamino)methyl]-phenol derivatives as novel cholinesterase inhibitors with selectivity towards butyrylcholinesterase.

R. Cao, Huacan Song, Lin Ma, 2010, Bioorganic & medicinal chemistry letters.

Synthesis and pharmacological activities of xanthone derivatives as alpha-glucosidase inhibitors.

Yan Liu, Wen-Hua Chen, Bo-Chi Wang, 2006, Bioorganic & medicinal chemistry.

Synthesis of 3-acyloxyxanthone derivatives as α-glucosidase inhibitors: A further insight into the 3-substituents' effect.

Yan Liu, Bo-Chi Wang, Lin Ma, 2016, Bioorganic & medicinal chemistry.

Binding mechanism and synergetic effects of xanthone derivatives as noncompetitive α-glucosidase inhibitors: a theoretical and experimental study.

Yan Liu, Hwangseo Park, Zhuofeng Ke, 2013, The journal of physical chemistry. B.

Synthesis, inhibitory activities, and QSAR study of xanthone derivatives as alpha-glucosidase inhibitors.

Yan Liu, Jianfang Cui, Zhuofeng Ke, 2008, Bioorganic & medicinal chemistry.

Synthesis of xanthone derivatives with extended π-systems as α-glucosidase inhibitors: Insight into the probable binding mode

Lin Ma, Yan Liu, Wen-Hua Chen, 2007 .

Synergetic inhibition of metal ions and genistein on α‐glucosidase

Zhishu Huang, Lin Ma, Xiao-dong Wang, 2004 .

Evaluation of Polyhydroxybenzophenones as α‐Glucosidase Inhibitors

Lin Ma, Xuesen Hu, Yang Xiao, 2011, Archiv der Pharmazie.

Synthesis, antioxidant, and antimicrobial evaluation of some 2-arylbenzimidazole derivatives.

Lin Ma, Baojian Li, Binhua Zhou, 2013, Bioorganic & medicinal chemistry letters.

Assessment of silver(I) complexes of salicylaldehyde derivatives—histidine Schiff base as novel α -glucosidase inhibitors

Lin Ma, Jing Zheng, 2016 .

Rational design and synthesis of 4-o-substituted phenylmethylenethiosemicarbazones as novel tyrosinase inhibitors.

R. Cao, Huacan Song, Lin Ma, 2010, Chemical & pharmaceutical bulletin.

Synthesis and biological evaluation of novel 4-hydroxybenzaldehyde derivatives as tyrosinase inhibitors.

R. Cao, Huacan Song, Lin Ma, 2010, European journal of medicinal chemistry.

A class of potent tyrosinase inhibitors: alkylidenethiosemicarbazide compounds.

Y. Wan, R. Cao, Huacan Song, 2009, European journal of medicinal chemistry.

1-(1-Arylethylidene)thiosemicarbazide derivatives: a new class of tyrosinase inhibitors.

Y. Wan, Huacan Song, Lin Ma, 2008, Bioorganic & medicinal chemistry.

Inhibitory effects of 5-benzylidene barbiturate derivatives on mushroom tyrosinase and their antibacterial activities.

R. Cao, Huacan Song, Lin Ma, 2009, European journal of medicinal chemistry.

Synthesis and biological evaluation of functionalized coumarins as acetylcholinesterase inhibitors.

A. Chan, Zhishu Huang, Xufeng Liu, 2005, European journal of medicinal chemistry.

Alpha-glucosidase inhibition of natural curcuminoids and curcumin analogs.

Lin Ma, A. Chan, Zhishu Huang, 2006, European journal of medicinal chemistry.

Synthesis and biological evaluation of helicid analogues as mushroom tyrosinase inhibitors.

Y. Wan, R. Cao, Huacan Song, 2008, Bioorganic & medicinal chemistry letters.

Synthesis and evaluation of 5-benzylidene(thio)barbiturate-beta-D-glycosides as mushroom tyrosinase inhibitors.

R. Cao, Huacan Song, Lin Ma, 2009, Bioorganic & medicinal chemistry letters.

Design, synthesis and biological evaluation of hydroxy- or methoxy-substituted phenylmethylenethiosemicarbazones as tyrosinase inhibitors.

R. Cao, Zhi-yong Chen, Lin Ma, 2009, Chemical & pharmaceutical bulletin.

Synthesis of new 1,1-dimethyl-1,2,3,4-tetrahydrophenanthrene derivatives

Zhishu Huang, Lin Ma, L. Gu, 2001 .

Synthesis and evaluation of quindoline derivatives as G-quadruplex inducing and stabilizing ligands and potential inhibitors of telomerase.

Lin Ma, Lian-Quan Gu, Zhi-Shu Huang, 2005, Journal of medicinal chemistry.

Synthesis of 6-substituted-3-hydroxy-4(1H)-pyridinones: Oxidation-Michael addition of 3-hydroxy-4(1H)-pyridinones

Zhishu Huang, Lin Ma, L. Gu, 1999 .

Synthesis of substituted 1,2-benzoquinones and substituted 3-hydroxy-4 (1H)-pyridinones: Application of oxidation—Michael addition in organic synthesis

Zhishu Huang, Lin Ma, L. Gu, 2010 .

1,2-Dihydro-1,6-dimethylphenanthro[1,2-b]furan-10,11-dione hemihydrate

Lin Ma, L. Gu, Xuepu Mao, 2005 .

Design and synthesis of 3,5-diaryl-4,5-dihydro-1H-pyrazoles as new tyrosinase inhibitors.

Lin Ma, Sujun Yan, Zhi-Fen Zhou, 2013, Bioorganic & medicinal chemistry.

Design, synthesis and evaluation of difunctionalized 4-hydroxybenzaldehyde derivatives as novel cholinesterase inhibitors.

R. Cao, Huacan Song, Lin Ma, 2010, Chemical & pharmaceutical bulletin.

Synthesis and biological evaluation of polyhydroxy benzophenone as mushroom tyrosinase inhibitors

Lin Ma, Xuesen Hu, Jianlong Wu, 2011, Journal of enzyme inhibition and medicinal chemistry.

Discovery of 4-functionalized phenyl-O-beta-D-glycosides as a new class of mushroom tyrosinase inhibitors.

R. Cao, Huacan Song, Lin Ma, 2009, Bioorganic & Medicinal Chemistry Letters.

Benzyl benzoates: New phlorizin analogs as mushroom tyrosinase inhibitors.

Lin Ma, Yaozong Chen, Y. Fang, 2011, Bioorganic & medicinal chemistry.

Synthesis of zwitterionic 4-hydroxycoumarin derivatives through a unique reaction of 4-hydroxycoumarins with p- benzoquinone and pyridine.

A. Chan, Zhishu Huang, Lin Ma, 2004, Organic letters.

Discovery of 4‐Functionalized Phenyl‐O‐β‐D‐glycosides as a New Class of Mushroom Tyrosinase Inhibitors.

R. Cao, Huacan Song, Lin Ma, 2010 .

Hydroxycoumarin derivatives: novel and potent α-glucosidase inhibitors.

A. Chan, Lin Ma, L. Gu, 2010, Journal of medicinal chemistry.

Synergetic inhibition of genistein and D-glucose on α-glucosidase

Zhishu Huang, Lin Ma, L. Gu, 2004 .

1,2-Diethyl-3-hydroxy-6-phenylthiopyridin-4(1H)-one

Lin Ma, L. Gu, Cai-Hong Chen, 2002 .

Synthesis, biological evaluation and molecular modeling of oxoisoaporphine and oxoaporphine derivatives as new dual inhibitors of acetylcholinesterase/butyrylcholinesterase.

Wei Qiao, Zhishu Huang, Lin Ma, 2009, European journal of medicinal chemistry.

Reaction of tanshinones with biogenic amine metabolites in vitro

Lin Ma, L. Gu, Hai-qiang Wu, 2002 .

Curcumin Analogues as Potent Aldose Reductase Inhibitors.

A. Chan, Wei Qiao, Zhishu Huang, 2006 .

Synthesis and Cytotoxicity of 9‐Substituted Benzo[de]chromene‐7,8‐dione and 5‐Benzyl‐9‐substituted Benzo[de]chromene‐7,8‐dione

A. Chan, Z. Liu, Zhishu Huang, 2006 .

(2E,6E)‐2,6‐Bis(3,5‐di‐tert‐butyl‐4‐hydroxybenzylidene)cyclohexanone acetic acid solvate

Lin Ma, L. Gu, Xuepu Mao, 2005 .