Inhibitors - Globe Thesis

Keyword [Inhibitors] Result: 21 - 40 \| Page: 2 of 10
21.	Theoretical Studies On The Potency And Selectivity Of Matrix Metalloproteinase Inhibitors And The Reaction Mechanism Catalyzed By Chalcone Synthase
22.	Study On Environment-Benign HABs-Inhibitors Based On Allelopathy
23.	The Rational Design, Synthesis And Bioactivity Of Structure-based Novel Protoporphyrinogen Oxidase Inhibitors
24.	Preparation And Structure-Activity Relationship Study Of PTP1B Inhibitors
25.	Structure-Based Design And Synthesis Of The Lead Compounds Of Novel D1 Protease Inhibitors
26.	Study On Synthesis Of Two Kinds Of Glycosides Compounds And Two Different Series Of Heterocycle Compounds And Biological Activities
27.	Study On Preparation And Properties Of Organic Conversion Coating On The Surface Of Magneium Alloy
28.	Theoretical Investigation On Corrosion Inhibition Mechanism Of Imidazoline Inhibitors
29.	Effects Of High Pressure Treatment On Lipoxygenase And Nutritional Inhibitors In Soybean And Properties Of Soybean Protein
30.	Theoretical Study On The Inhibition Mechanism Of β-lactamase By Inhibitors
31.	Environmental Quantitative Structure-Activity Relationship Studies On 2-Hydroxy-1,4-Naphthoquinones As Inhibitors Of PSII And Triazole Fungicides
32.	Design And Synthesis Of Novel Cholesterol Absorption Inhibitors
33.	Design, Synthesis And Antimicrobial Activities Of Novel Peptide Deformylase Inhibitors
34.	Molecular Modeling Study Of Some Kinase Inhibitors
35.	Research Of Nonnucleoside HIV-1 Reverse Transcriptase Inhibitors
36.	Research On The Multicomponent Synthesis And Bioactivities Of Aza-heterocyclic Compounds
37.	The Study Of HIV-1 Inhibitors
38.	Molecular Docking, Quantitative Structure-activity Relationship And De Novo Molecular Design Studies Of Neuraminidase Inhibitors
39.	Environmental Quantitative Structure-activity Relationship Studies On 2-hydroxy-1,4-naphthoquinones As Inhibitors Of Psii And Triazole Fungicides
40.	Design, Synthesis, And Structure-activity Relationships Study Of New N-Hydroxyamide Derivatives As Udp-(3-O-acyl)-N-acetylglucosamine Deacetylase (LpxC) Inhibitors
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