# | Title | Journal | Year | Citations |
---|
1 | The Future of Peptide‐based Drugs | Chemical Biology and Drug Design | 2013 | 1,483 |
2 | Inhibition of Amyloid Fibril Formation by Polyphenols: Structural Similarity and Aromatic Interactions as a Common Inhibition Mechanism | Chemical Biology and Drug Design | 2006 | 859 |
3 | The Structure of Glycosaminoglycans and their Interactions with Proteins | Chemical Biology and Drug Design | 2008 | 820 |
4 | New Method for Fast and Accurate Binding-site Identification and Analysis | Chemical Biology and Drug Design | 2007 | 656 |
5 | Use of an Induced Fit Receptor Structure in Virtual Screening | Chemical Biology and Drug Design | 2006 | 550 |
6 | PHASE: A Novel Approach to Pharmacophore Modeling and 3D Database Searching | Chemical Biology and Drug Design | 2006 | 520 |
7 | Circular Dichroism Techniques: Biomolecular and Nanostructural Analyses‐ A Review | Chemical Biology and Drug Design | 2009 | 483 |
8 | Anti‐Inflammatory Property of n‐Hexadecanoic Acid: Structural Evidence and Kinetic Assessment | Chemical Biology and Drug Design | 2012 | 400 |
9 | Resveratrol is Not a Direct Activator of SIRT1 Enzyme Activity | Chemical Biology and Drug Design | 2009 | 379 |
10 | Probing the α‐Helical Structural Stability of Stapled p53 Peptides: Molecular Dynamics Simulations and Analysis | Chemical Biology and Drug Design | 2010 | 351 |
11 | Vicinal Diamino Functionalities as Privileged Structural Elements in Biologically Active Compounds and Exploitation of their Synthetic Chemistry | Chemical Biology and Drug Design | 2006 | 332 |
12 | Structure–activity Relationships of Amyloid Beta‐aggregation Inhibitors Based on Curcumin: Influence of Linker Length and Flexibility | Chemical Biology and Drug Design | 2007 | 282 |
13 | 1,3,4‐Thiadiazole and its Derivatives: A Review on Recent Progress in Biological Activities | Chemical Biology and Drug Design | 2013 | 263 |
14 | Antibiotic Adjuvants: Diverse Strategies for Controlling Drug‐Resistant Pathogens | Chemical Biology and Drug Design | 2015 | 245 |
15 | Comprehensive Review in Current Developments of Benzimidazole‐Based Medicinal Chemistry | Chemical Biology and Drug Design | 2015 | 243 |
16 | Two‐ and Three‐dimensional Rings in Drugs | Chemical Biology and Drug Design | 2014 | 235 |
17 | Structural Mechanism of the Pan‐BCR‐ABL Inhibitor Ponatinib (AP24534): Lessons for Overcoming Kinase Inhibitor Resistance | Chemical Biology and Drug Design | 2011 | 231 |
18 | Homology modeling in drug discovery: Overview, current applications, and future perspectives | Chemical Biology and Drug Design | 2019 | 229 |
19 | Antibody‐Drug Conjugates for the Treatment of Cancer | Chemical Biology and Drug Design | 2013 | 193 |
20 | Characteristics of flavonoids as potent MERS‐CoV 3C‐like protease inhibitors | Chemical Biology and Drug Design | 2019 | 191 |
21 | In Vitro Inhibition of Human Carbonic Anhydrase I and II Isozymes with Natural Phenolic Compounds | Chemical Biology and Drug Design | 2011 | 170 |
22 | Chemogenetic Analysis of Human Protein Methyltransferases | Chemical Biology and Drug Design | 2011 | 167 |
23 | Compensating Enthalpic and Entropic Changes Hinder Binding Affinity Optimization | Chemical Biology and Drug Design | 2007 | 163 |
24 | Expanding the Number of ‘Druggable’ Targets: Non‐Enzymes and Protein–Protein Interactions | Chemical Biology and Drug Design | 2013 | 161 |
25 | Peptide Nanoparticles as Novel Immunogens: Design and Analysis of a Prototypic Severe Acute Respiratory Syndrome Vaccine | Chemical Biology and Drug Design | 2009 | 158 |
26 | tRF‐Leu‐CAG promotes cell proliferation and cell cycle in non‐small cell lung cancer | Chemical Biology and Drug Design | 2017 | 148 |
27 | Atomic Interactions and Profile of Small Molecules Disrupting Protein–Protein Interfaces: the TIMBAL Database | Chemical Biology and Drug Design | 2009 | 144 |
28 | Insight into Amyloid Structure Using Chemical Probes | Chemical Biology and Drug Design | 2011 | 139 |
29 | Stability of Gold Nanoparticle-Bound DNA toward Biological, Physical, and Chemical Agents | Chemical Biology and Drug Design | 2006 | 138 |
30 | Triazole: A Promising Antitubercular Agent | Chemical Biology and Drug Design | 2015 | 138 |
31 | Carbonic Anhydrase Inhibitors: Inhibition of Human Erythrocyte Isozymes I and II with a Series of Phenolic Acids | Chemical Biology and Drug Design | 2010 | 134 |
32 | Conformational Adaptation Drives Potent, Selective and Durable Inhibition of the Human Protein Methyltransferase DOT1L | Chemical Biology and Drug Design | 2012 | 132 |
33 | A Chemical Genetic Screen for Cell Cycle Inhibitors in Zebrafish Embryos | Chemical Biology and Drug Design | 2006 | 127 |
34 | Crizotinib‐Resistant Mutants of EML4‐ALK Identified Through an Accelerated Mutagenesis Screen | Chemical Biology and Drug Design | 2011 | 127 |
35 | The Thermolysin Family (M4) of Enzymes: Therapeutic and Biotechnological Potential | Chemical Biology and Drug Design | 2009 | 125 |
36 | Structure‐based Drug Metabolism Predictions for Drug Design | Chemical Biology and Drug Design | 2010 | 124 |
37 | A Thermodynamic Approach to the Affinity Optimization of Drug Candidates | Chemical Biology and Drug Design | 2009 | 122 |
38 | Betulinic Acid: Recent Advances in Chemical Modifications, Effective Delivery, and Molecular Mechanisms of a Promising Anticancer Therapy | Chemical Biology and Drug Design | 2016 | 120 |
39 | Novel PPAR‐gamma Agonists Identified from a Natural Product Library: A Virtual Screening, Induced‐Fit Docking and Biological Assay Study | Chemical Biology and Drug Design | 2008 | 117 |
40 | Inhibitors of Apoptotic Proteins: New Targets for Anticancer Therapy | Chemical Biology and Drug Design | 2013 | 117 |
41 | Design features for optimization of tetrapyrrole macrocycles as antimicrobial and anticancer photosensitizers | Chemical Biology and Drug Design | 2017 | 117 |
42 | Overcoming Roadblocks in Lead Optimization: A Thermodynamic Perspective | Chemical Biology and Drug Design | 2006 | 116 |
43 | Synthesis, molecular modeling, and biological evaluation of 4‐[5‐aryl‐3‐(thiophen‐2‐yl)‐4,5‐dihydro‐1H‐pyrazol‐1‐yl] benzenesulfonamides toward acetylcholinesterase, carbonic anhydrase I and II enzymes | Chemical Biology and Drug Design | 2018 | 116 |
44 | Comparison of Biophysical and Biologic Properties of alpha-Helical Enantiomeric Antimicrobial Peptides | Chemical Biology and Drug Design | 2006 | 113 |
45 | Cell‐penetrating Peptides as a Novel Transdermal Drug Delivery System | Chemical Biology and Drug Design | 2012 | 112 |
46 | Searching for New Antimalarial Therapeutics amongst Known Drugs | Chemical Biology and Drug Design | 2006 | 110 |
47 | Synthesis and Anticonvulsant Activity of 6‐Alkoxy‐[1,2,4]Triazolo[3,4‐a]Phthalazines | Chemical Biology and Drug Design | 2009 | 110 |
48 | Antimicrobial β-Peptides and α-Peptoids | Chemical Biology and Drug Design | 2011 | 110 |
49 | New Force Field on Modeling Intrinsically Disordered Proteins | Chemical Biology and Drug Design | 2014 | 110 |
50 | Antimalarial Activity of Newly Synthesized Chalcone Derivatives In Vitro | Chemical Biology and Drug Design | 2012 | 109 |