On the public citation graph
Synthesis and Biological Evaluation of Novel Bisbenzimidazoles as Escherichia coli Topoisomerase IA Inhibitors and Potential Antibacterial Agents
0 signed · 135 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/chin.199504173openalex-snapshot
ChemInform Abstract: DNA Binding Compounds. Part 6. Synthesis and Characterization of 2,5′‐ Disubstituted Bibenzimidazoles Related to the DNA Minor Groove Binder Hoechst 33258.
inferredcites →https://doi.org/10.1007/s10822-006-9078-7openalex-snapshot
Efficient overlay of small organic molecules using 3D pharmacophores
inferredcites →https://doi.org/10.1007/s10822-013-9673-3openalex-snapshot
Molecular dynamics simulation and linear interaction energy study of d-Glu-based inhibitors of the MurD ligase
inferredcites →https://doi.org/10.1007/s11010-007-9546-yopenalex-snapshot
Nuclear condensation and free radical scavenging: a dual mechanism of bisbenzimidazoles to modulate radiation damage to DNA
inferredcites →https://doi.org/10.1016/0162-0134(91)80035-gopenalex-snapshot
Mechanistic studies on E. coli DNA topoisomerase I: Divalent ion effects
inferredcites →https://doi.org/10.1016/j.ab.2007.02.029openalex-snapshot
Streptococcus pneumononiae gyrase ATPase: Development and validation of an assay for inhibitor discovery and characterization
inferredcites →https://doi.org/10.1016/j.abb.2012.12.013openalex-snapshot
A derivative of the natural compound kakuol affects DNA relaxation of topoisomerase IB inhibiting the cleavage reaction
inferredcites →https://doi.org/10.1016/j.addr.2005.04.006openalex-snapshot
Novel target sites in bacteria for overcoming antibiotic resistance
inferredcites →https://doi.org/10.1016/j.bmcl.2011.09.114openalex-snapshot
Novel cyclohexyl-amides as potent antibacterials targeting bacterial type IIA topoisomerases
inferredcites →https://doi.org/10.1016/j.bmcl.2012.01.116openalex-snapshot
Design of oxobenzimidazoles and oxindoles as novel androgen receptor antagonists
inferredcites →https://doi.org/10.1016/j.chembiol.2010.04.012openalex-snapshot
DNA Topoisomerases and Their Poisoning by Anticancer and Antibacterial Drugs
inferredcites →https://doi.org/10.1016/j.ejmech.2010.11.046openalex-snapshot
Synthesis and biological activity of novel inhibitors of topoisomerase I: 2-Aryl-substituted 2-bis-1H-benzimidazoles
inferredcites →https://doi.org/10.1016/s0960-894x(01)00457-7openalex-snapshot
Structure–activity relationship studies of a bisbenzimidazole-based, Zn2+-dependent inhibitor of HCV NS3 serine protease
inferredcites →https://doi.org/10.1021/bi00417a026openalex-snapshot
Cleavage of dT8 and dT8 phosphorothioyl analogues by Escherichia coli DNA topoisomerase I: product and rate analysis
inferredcites →https://doi.org/10.1021/bi0159837openalex-snapshot
DNA Gyrase Interaction with Coumarin-Based Inhibitors: The Role of the Hydroxybenzoate Isopentenyl Moiety and the 5‘-Methyl Group of the Noviose
inferredcites →https://doi.org/10.1021/ci049885eopenalex-snapshot
LigandScout: 3-D Pharmacophores Derived from Protein-Bound Ligands and Their Use as Virtual Screening Filters
inferredcites →https://doi.org/10.1021/cr030101qopenalex-snapshot
Bacterial Topoisomerase Inhibitors: Quinolone and Pyridone Antibacterial Agents
inferredcites →https://doi.org/10.1021/jm201465wopenalex-snapshot
Fluorocyclines. 1. 7-Fluoro-9-pyrrolidinoacetamido-6-demethyl-6-deoxytetracycline: A Potent, Broad Spectrum Antibacterial Agent
inferredcites →https://doi.org/10.1021/jm300395dopenalex-snapshot
Structure-Based Discovery of Substituted 4,5′-Bithiazoles as Novel DNA Gyrase Inhibitors
inferredcites →https://doi.org/10.1021/jm300690sopenalex-snapshot
Novel N-Linked Aminopiperidine Inhibitors of Bacterial Topoisomerase Type II with Reduced pKa: Antibacterial Agents with an Improved Safety Profile
inferredcites →https://doi.org/10.1021/jm950412wopenalex-snapshot
Substituted 2,5‘-Bi-1H-benzimidazoles: Topoisomerase I Inhibition and Cytotoxicity
inferredcites →https://doi.org/10.1038/367138a0openalex-snapshot
Three-dimensional structure of the 67K N-terminal fragment of E. coli DNA topoisomerase I
inferredcites →https://doi.org/10.1038/nature09197openalex-snapshot
Type IIA topoisomerase inhibition by a new class of antibacterial agents
inferredcites →https://doi.org/10.1039/c3mb70169gopenalex-snapshot
Bi and tri-substituted phenyl rings containing bisbenzimidazoles bind differentially with DNA duplexes: a biophysical and molecular simulation study
inferredcites →https://doi.org/10.1071/ch9940247openalex-snapshot
DNA Binding Compounds. V. Synthesis and Characterization of Boron Containing Bibenzimidazoles Related to the DNA Minor Groove Binder, Hoechst-33258
inferredcites →https://doi.org/10.1071/ch9941751openalex-snapshot
DNA Binding Compounds. VI. Synthesis and Characterization of 2,5'-Disubstituted Bibenzimidazoles Related to the DNA Minor Groove Binder Hoechst-33258
inferredcites →https://doi.org/10.1073/pnas.1100300108openalex-snapshot
Crystal structure of a covalent intermediate in DNA cleavage and rejoining by Escherichia coli DNA topoisomerase I
inferredcites →https://doi.org/10.1074/jbc.271.4.2262openalex-snapshot
Selected Novel Flavones Inhibit the DNA Binding or the DNA Religation Step of Eukaryotic Topoisomerase I
inferredcites →https://doi.org/10.1074/jbc.273.11.6050openalex-snapshot
Identification of Active Site Residues in Escherichia coli DNA Topoisomerase I
inferredcites →https://doi.org/10.1074/jbc.275.8.5318openalex-snapshot
The Acidic Triad Conserved in Type IA DNA Topoisomerases Is Required for Binding of Mg(II) and Subsequent Conformational Change
inferredcites →https://doi.org/10.1074/jbc.m110.148148openalex-snapshot
New Alkaloid Antibiotics That Target the DNA Topoisomerase I of Streptococcus pneumoniae
inferredcites →https://doi.org/10.1080/07391102.2005.10507045openalex-snapshot
Theoretical Study of Molecular Recognition by Hoechst 33258 Derivatives
inferredcites →https://doi.org/10.1086/499819openalex-snapshot
Bad Bugs Need Drugs: An Update on the Development Pipeline from the Antimicrobial Availability Task Force of the Infectious Diseases Society of America
inferredcites →https://doi.org/10.1093/jac/dkl556openalex-snapshot
Compounds with antibacterial activity that enhance DNA cleavage by bacterial DNA topoisomerase I
inferredcites →https://doi.org/10.1093/jac/dks322openalex-snapshot
3,4-Dimethoxyphenyl bis-benzimidazole, a novel DNA topoisomerase inhibitor that preferentially targets Escherichia coli topoisomerase I
inferredcites →https://doi.org/10.1093/nar/24.24.4882openalex-snapshot
Designer DNA-Binding Drugs: The Crystal Structure of a Meta-Hydroxy Analogue of Hoechst 33258 Bound to d(CGCGAATTCGCG)2
inferredcites →https://doi.org/10.1093/nar/25.8.1510openalex-snapshot
Structure of a Bis-Amidinium Derivative of Hoechst 33258 Complexed to Dodecanucleotide D(CGCGAATTCGCG)2: The Role of Hydrogen Bonding in Minor Groove Drug-DNA Recognition
inferredcites →https://doi.org/10.1093/nar/gkn1009openalex-snapshot
Structural studies of type I topoisomerases
inferredcites →https://doi.org/10.1093/nar/gkn460openalex-snapshot
Inhibition of Mg 2+ binding and DNA religation by bacterial topoisomerase I via introduction of an additional positive charge into the active site region
inferredcites →https://doi.org/10.1093/nar/gkn936openalex-snapshot
Bacterial topoisomerase I as a target for discovery of antibacterial compounds
inferredcites →https://doi.org/10.1093/nar/gkp024openalex-snapshot
Effects of magnesium and related divalent metal ions in topoisomerase structure and function
inferredcites →https://doi.org/10.1093/nar/gkt124openalex-snapshot
Topoisomerase IV-quinolone interactions are mediated through a water-metal ion bridge: mechanistic basis of quinolone resistance
inferredcites →https://doi.org/10.1107/s1600536802015842openalex-snapshot
2-(2,4-Dichlorophenyl)-5-fluoro-6-morpholin-4-yl-1H-benzimidazole monohydrate
inferredcites →https://doi.org/10.1111/j.1432-1033.1994.tb18917.xopenalex-snapshot
Three‐dimensional crystal structure of the A‐tract DNA dodecamer d(CGCAAATTTGCG) complexed with the minor‐groove‐binding drug Hoechst 33258
inferredcites →https://doi.org/10.1126/science.279.5356.1534openalex-snapshot
A Model for the Mechanism of Human Topoisomerase I
inferredcites →https://doi.org/10.1128/aac.00496-08openalex-snapshot
Mechanism of Action of the Antibiotic NXL101, a Novel Nonfluoroquinolone Inhibitor of Bacterial Type II Topoisomerases
inferredcites →https://doi.org/10.1128/aac.00862-10openalex-snapshot
In Vivo Efficacy of the Novel Aminoglycoside ACHN-490 in Murine Infection Models
inferredcites →https://doi.org/10.1128/aac.01584-08openalex-snapshot
In Vivo Pharmacodynamic Characterization of a Novel Plectasin Antibiotic, NZ2114, in a Murine Infection Model
inferredcites →https://doi.org/10.1128/aac.01617-06openalex-snapshot
Quinolone-Mediated Bacterial Death
inferredcites →https://doi.org/10.1128/aac.19.6.1050openalex-snapshot
Minimum inhibitory and bactericidal concentrations of 44 antimicrobial agents against three standard control strains in broth with and without human serum
inferredcites →https://doi.org/10.1146/annurev.bi.58.070189.002031openalex-snapshot
DNA TOPOISOMERASE POISONS AS ANTITUMOR DRUGS
inferredcites →https://doi.org/10.1146/annurev.biochem.70.1.369openalex-snapshot
DNA Topoisomerases: Structure, Function, and Mechanism
inferredcites →https://doi.org/10.1177/30.2.7061816openalex-snapshot
Cytotoxicity, Mutagenicity and DNA damage by Hoechst 33342.
inferredcites →https://doi.org/10.1186/1471-2091-10-18openalex-snapshot
Analysis of DNA relaxation and cleavage activities of recombinant Mycobacterium tuberculosis DNA topoisomerase I from a new expression and purification protocol
inferredcites →https://doi.org/10.1186/1471-2334-6-55openalex-snapshot
Neutropenia induced in outbred mice by a simplified low-dose cyclophosphamide regimen: characterization and applicability to diverse experimental models of infectious diseases
inferredcites →https://doi.org/10.1186/1756-0500-4-445openalex-snapshot
AUDocker LE: A GUI for virtual screening with AUTODOCK Vina
inferredcites →https://doi.org/10.1371/journal.pone.0051354openalex-snapshot
Binding of an Indenoisoquinoline to the Topoisomerase-DNA Complex Induces Reduction of Linker Mobility and Strengthening of Protein-DNA Interaction
inferredcites →https://doi.org/10.1371/journal.pone.0060770openalex-snapshot
Identification of Anziaic Acid, a Lichen Depside from Hypotrachyna sp., as a New Topoisomerase Poison Inhibitor
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/asia.202300054openalex-snapshot
2‐Hydroxypropyl Group Linked Derivatives of Indole Azoles as Potential Multifunctional Antibacterial Candidates for Effectively Inhibiting the Activity of MRSA and Responding Inflammatory Factors
inferred← citeshttps://doi.org/10.1002/cbdv.201800510openalex-snapshot
Design, Microwave‐Assisted Synthesis and in Vitro Antibacterial and Antifungal Activity of 2,5‐Disubstituted Benzimidazole
inferred← citeshttps://doi.org/10.1002/cmdc.201600041openalex-snapshot
Recent Development of Benzimidazole‐Containing Antibacterial Agents
inferred← citeshttps://doi.org/10.1002/ejoc.201600720openalex-snapshot
Palladium‐Catalysed Carbo‐ and Hydroamination of Allenyl Ethers and Aminoallenes: Available Entry to Nitrogen‐Containing Benzo‐Fused Rings
inferred← citeshttps://doi.org/10.1002/jcc.26712openalex-snapshot
Exploration of potential inhibitors for tuberculosis via structure‐based drug design, molecular docking, and molecular dynamics simulation studies
inferred← citeshttps://doi.org/10.1002/masy.202400111openalex-snapshot
Exploring the DNA Recognition of Compounds Based on Benzimidazole and Benzothiazole: A Concise Review
inferred← citeshttps://doi.org/10.1002/med.21417openalex-snapshot
Topoisomerases: Resistance versus Sensitivity, How Far We Can Go?
inferred← citeshttps://doi.org/10.1002/slct.202406021openalex-snapshot
Recent Expansions in the Potential of Uracil Derivatives as Chemotherapeutic, Antimicrobial, and Antiviral Agents: A Review
inferred← citeshttps://doi.org/10.1002/slct.202503714openalex-snapshot
Unveiling the Multifaceted Bioactivities of Benzimidazolium Salts: Synthesis, Characterization, and Computational Insights Into AChE Inhibition and Antimicrobial Action Against Multidrug Resistance Bacteria MRSA and MDR E. coli
inferred← citeshttps://doi.org/10.1007/s10593-017-2163-0openalex-snapshot
New method for the synthesis of 2-substituted benzimidazole-5(6)-carboxylic acids
inferred← citeshttps://doi.org/10.1007/s11094-019-01976-3openalex-snapshot
Recent Advances in Antiviral Benzimidazole Derivatives: A Mini Review
inferred← citeshttps://doi.org/10.1007/s11094-021-02389-xopenalex-snapshot
Bisbenzimidazole Derivatives as Potential Antimicrobial Agents: Design, Synthesis, Biological Evaluation and Pharmacophore Analysis
inferred← citeshttps://doi.org/10.1007/s40242-020-0274-0openalex-snapshot
Microwave-assisted Catalyzed Synthesis and In vitro Bioactivity Evaluation of Benzimidazoles Bearing Phenolic Hydroxyl
inferred← citeshttps://doi.org/10.1016/j.abb.2025.110630openalex-snapshot
Multifunctional benzimidazolium derivatives as anticancer, antibacterial, and acetylcholinesterase inhibitors: In vitro and molecular docking studies
inferred← citeshttps://doi.org/10.1016/j.arabjc.2023.105078openalex-snapshot
Synthesis, in vitro biological analysis and molecular docking studies of new thiadiazole-based thiourea derivatives as dual inhibitors of a-amylase and a-glucosidase
inferred← citeshttps://doi.org/10.1016/j.bbagen.2019.05.015openalex-snapshot
PPEF: A bisbenzimdazole potent antimicrobial agent interacts at acidic triad of catalytic domain of E. coli topoisomerase IA
inferred← citeshttps://doi.org/10.1016/j.bbrc.2019.06.034openalex-snapshot
Crystal structure of the 65-kilodalton amino-terminal fragment of DNA topoisomerase I from the gram-positive model organism Streptococcus mutans
inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.104266openalex-snapshot
Recent advancements in the medicinal chemistry of bacterial type II topoisomerase inhibitors
inferred← citeshttps://doi.org/10.1016/j.bioorg.2021.105096openalex-snapshot
Potential antibacterial ethanol-bridged purine azole hybrids as dual-targeting inhibitors of MRSA
inferred← citeshttps://doi.org/10.1016/j.bmc.2016.06.010openalex-snapshot
Synthesis and investigation of novel benzimidazole derivatives as antifungal agents
inferred← citeshttps://doi.org/10.1016/j.bmcl.2016.04.036openalex-snapshot
Design, synthesis and biological evaluation of 5-fluorouracil-derived benzimidazoles as novel type of potential antimicrobial agents
inferred← citeshttps://doi.org/10.1016/j.cclet.2016.03.009openalex-snapshot
Study on the inclusion behavior and solid inclusion complex of 5-amino-6-methyl-2-benzimidazolone with cyclodextrins
inferred← citeshttps://doi.org/10.1016/j.drudis.2016.11.006openalex-snapshot
DNA topoisomerase I and DNA gyrase as targets for TB therapy
inferred← citeshttps://doi.org/10.1016/j.ejmech.2016.01.052openalex-snapshot
Discovery of membrane active benzimidazole quinolones-based topoisomerase inhibitors as potential DNA-binding antimicrobial agents
inferred← citeshttps://doi.org/10.1016/j.ejmech.2016.12.010openalex-snapshot
Therapeutic evolution of benzimidazole derivatives in the last quinquennial period
inferred← citeshttps://doi.org/10.1016/j.ejmech.2017.05.064openalex-snapshot
Synthesis, antimicrobial, antiquorum-sensing and antitumor activities of new benzimidazole analogs
inferred← citeshttps://doi.org/10.1016/j.ejmech.2017.11.027openalex-snapshot
Novel aminopyrimidinyl benzimidazoles as potentially antimicrobial agents: Design, synthesis and biological evaluation
inferred← citeshttps://doi.org/10.1016/j.ijpharm.2024.123982openalex-snapshot
Polydispersity-mediated high efficacy of an in-situ aqueous nanosuspension of PPEF.3HCl in methicillin resistant Staphylococcus aureus sepsis model
inferred← citeshttps://doi.org/10.1016/j.jinorgbio.2020.111102openalex-snapshot
Influence of the introduction of a triphenylphosphine group on the anticancer activity of a copper complex
inferred← citeshttps://doi.org/10.1016/j.molstruc.2023.135367openalex-snapshot
Self-assembled crystals of nonplanar benzimidazole macrocycles: Synthesis, characterization, crystal structure, SEM, and DFT studies
inferred← citeshttps://doi.org/10.1016/j.molstruc.2024.137714openalex-snapshot
Synthesis of benzimidazoles containing piperazine ring as potential therapeutic agents against diabetes mellitus and antioxidant activities
inferred← citeshttps://doi.org/10.1016/j.pep.2016.04.010openalex-snapshot
A simplified protocol for high-yield expression and purification of bacterial topoisomerase I
inferred← citeshttps://doi.org/10.1016/j.poly.2018.10.020openalex-snapshot
Synthesis, DNA binding and antibacterial activity of metal(II) complexes of a benzimidazole Schiff base
inferred← citeshttps://doi.org/10.1016/j.tube.2017.01.005openalex-snapshot
Machine learning and docking models for Mycobacterium tuberculosis topoisomerase I
inferred← citeshttps://doi.org/10.1021/acs.biochem.8b01102openalex-snapshot
Benzimidazoles: Selective Inhibitors of Topoisomerase I with Differential Modes of Action
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.6b00966openalex-snapshot
Type I DNA Topoisomerases
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.7b00108openalex-snapshot
Triaryl Benzimidazoles as a New Class of Antibacterial Agents against Resistant Pathogenic Microorganisms
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.7b00191openalex-snapshot
Selective Inhibition of Escherichia coli RNA and DNA Topoisomerase I by Hoechst 33258 Derived Mono- and Bisbenzimidazoles
inferred← citeshttps://doi.org/10.1021/acs.joc.0c00421openalex-snapshot
Molecular Iodine-Promoted [3 + 2] Oxidative Cyclization for the Synthesis of Heteroarene-Fused [1,2,4] Thiadiazoles/Selenadiazoles
inferred← citeshttps://doi.org/10.1021/acs.joc.6b00186openalex-snapshot
Copper(II)-Catalyzed Oxidative Cross-Coupling of Anilines, Primary Alkyl Amines, and Sodium Azide Using TBHP: A Route to 2-Substituted Benzimidazoles
inferred← citeshttps://doi.org/10.1021/acs.joc.7b00265openalex-snapshot
Stereoselective Copper-Catalyzed Cross-Coupling of Aziridines with Benzimidazoles via Nucleophilic Ring Opening and C(sp 2 )–H Functionalization
inferred← citeshttps://doi.org/10.1021/acs.joc.7b01746openalex-snapshot
Chemo-, Regio-, and Stereoselective N-Alkenylation of Pyrazoles/Benzpyrazoles Using Activated and Unactivated Alkynes
inferred← citeshttps://doi.org/10.1021/acs.joc.8b01642openalex-snapshot
Substrate-Controlled Regio- and Stereoselective Synthesis of (Z)- and (E)-N-Styrylated Carbazoles, Aza-carbazoles, and γ-Carbolines via Hydroamination of Alkynes
inferred← citeshttps://doi.org/10.1021/acsomega.1c05743openalex-snapshot
Synthesis and Biological Evaluation of Novel 1H-Benzo[d]imidazole Derivatives as Potential Anticancer Agents Targeting Human Topoisomerase I
inferred← citeshttps://doi.org/10.1021/acsomega.6b00523openalex-snapshot
Naphthalenediimide-Linked Bisbenzimidazole Derivatives as Telomeric G-Quadruplex-Stabilizing Ligands with Improved Anticancer Activity
inferred← citeshttps://doi.org/10.1021/acsptsci.2c00118openalex-snapshot
Synthesis of Morpholine-, Piperidine-, and N-Substituted Piperazine-Coupled 2-(Benzimidazol-2-yl)-3-arylquinoxalines as Novel Potent Antitumor Agents
inferred← citeshttps://doi.org/10.1021/acsptsci.2c00205openalex-snapshot
New Xanthone Derivatives as Potent G-Quadruplex Binders for Developing Anti-Cancer Therapeutics
inferred← citeshttps://doi.org/10.1021/jm500853vopenalex-snapshot
Synthesis, Structure–Activity Relationship Studies, and Antibacterial Evaluation of 4-Chromanones and Chalcones, as Well as Olympicin A and Derivatives
inferred← citeshttps://doi.org/10.1038/s41598-019-48898-4openalex-snapshot
Gram-negative synergy and mechanism of action of alkynyl bisbenzimidazoles
inferred← citeshttps://doi.org/10.1038/s42003-023-04412-1openalex-snapshot
Unraveling topoisomerase IA gate dynamics in presence of PPEF and its preclinical evaluation against multidrug-resistant pathogens
inferred← citeshttps://doi.org/10.1038/srep44419openalex-snapshot
Synergistic efficacy of Bisbenzimidazole and Carbonyl Cyanide 3-Chlorophenylhydrazone combination against MDR bacterial strains
inferred← citeshttps://doi.org/10.1039/c5nj02943kopenalex-snapshot
Small heterocycles as highly luminescent building blocks in the solid state for organic synthesis
inferred← citeshttps://doi.org/10.1039/c5ra22568jopenalex-snapshot
Discovering new DNA gyrase inhibitors using machine learning approaches
inferred← citeshttps://doi.org/10.1039/c6cc01828aopenalex-snapshot
Copper catalyzed aerobic oxidative cyclization and ketonization: one pot synthesis of benzoimidazo[1,2-a]imidazolones
inferred← citeshttps://doi.org/10.1039/c6qo00733copenalex-snapshot
One-pot synthesis of benzazoles and quinazolinones via iron pentacarbonyl mediated carbonylation of aryl iodides under microwave irradiation
inferred← citeshttps://doi.org/10.1039/c8nj01571fopenalex-snapshot
Novel triple responsive polybenzimidazole synthesized via amine-ene Michael addition
inferred← citeshttps://doi.org/10.1039/c9bm01367aopenalex-snapshot
Facile core–shell nanoparticles with controllable antibacterial activity assembled by chemical and biological molecules
inferred← citeshttps://doi.org/10.1055/a-2735-9398openalex-snapshot
A Synthesis of Functionalized Benzimidazoles via the Three-Component Reaction of Terminal Alkynes, Phenylsulfonyl Azide, and Phenylenediamine-1,3-dicarbonyl Adducts
inferred← citeshttps://doi.org/10.1080/07391102.2023.2263569openalex-snapshot
An insight into the cytotoxic, antimicrobial, antioxidant, and biocontrol perspective of novel Iron(III) complexes of substituted benzimidazoles: Inhibition kinetics and molecular simulations
inferred← citeshttps://doi.org/10.1080/14756366.2018.1484733openalex-snapshot
Synthesis, anti-bacterial and anti-protozoal activities of amidinobenzimidazole derivatives and their interactions with DNA and RNA
inferred← citeshttps://doi.org/10.1111/cbdd.14605openalex-snapshot
Elucidation of the Microwave‐Assisted Synthesis and Characterization of Heteronuclear Complexes of Bisbenzimidazole Derivatives and Their Biological Activities by In Vitro and In Silico Assays
inferred← citeshttps://doi.org/10.1128/aac.00288-16openalex-snapshot
Small-Molecule Inhibitors Targeting Topoisomerase I as Novel Antituberculosis Agents
inferred← citeshttps://doi.org/10.1128/spectrum.02974-24openalex-snapshot
Adaptive laboratory-evolved MRSA with PPEF manifests cross-susceptibility to oxacillin and hypersensitivity to ciprofloxacin
inferred← citeshttps://doi.org/10.1155/2023/2881582openalex-snapshot
Discovery of New Ligand with Quinoline Scaffold as Potent Allosteric Inhibitor of HIV-1 and Its Copper Complexes as a Powerful Catalyst for the Synthesis of Chiral Benzimidazole Derivatives, and in Silico Anti-HIV-1 Studies
inferred← citeshttps://doi.org/10.21007/etd.cghs.2019.0491openalex-snapshot
Investigation of Narrow Spectrum Targets in Antibacterial Drug Discovery
inferred← citeshttps://doi.org/10.21608/ejchem.2021.75953.3714openalex-snapshot
Design, Synthesis and Molecular Docking of New Benzimidazole Derivatives of Potential Antimicrobial Activity as DNA Gyrase and Topoisomerase IV Inhibitors
inferred← citeshttps://doi.org/10.2174/1573406415666190416120801openalex-snapshot
Recent Advances in Therapeutic Applications of Bisbenzimidazoles
inferred← citeshttps://doi.org/10.25148/etd.fidc001958openalex-snapshot
Protein-protein Interactions of Bacterial Topoisomerase I
inferred← citeshttps://doi.org/10.3389/fchem.2020.00433openalex-snapshot
Synthesis and Antimycobacterial Activity of 2,5-Disubstituted and 1,2,5-Trisubstituted Benzimidazoles
inferred← citeshttps://doi.org/10.3390/antibiotics10060728openalex-snapshot
In Vitro Evaluation of the Potential Pharmacological Activity and Molecular Targets of New Benzimidazole-Based Schiff Base Metal Complexes
inferred← citeshttps://doi.org/10.3390/microorganisms9010086openalex-snapshot
Type IA Topoisomerases as Targets for Infectious Disease Treatments
inferred← citeshttps://doi.org/10.4155/fmc.14.157openalex-snapshot
Targeting Bacterial Topoisomerase I to Meet the Challenge of Finding New Antibiotics
inferred← citeshttps://doi.org/10.5772/intechopen.1004465openalex-snapshot
The Impact of Incorporating Piperazine on Biological Activities of Benzazoles
inferred← citeshttps://doi.org/10.5772/intechopen.104908openalex-snapshot
Synthesis, Characterization and Antimicrobial Properties of Novel Benzimidazole Amide Derivatives Bearing Thiophene Moiety
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.