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Recent Development of Benzimidazole‐Containing Antibacterial Agents

https://doi.org/10.1002/cmdc.201600041

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Synthesis, antimicrobial, antiquorum-sensing and antitumor activities of new benzimidazole analogs

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Development of benzimidazole-based derivatives as antimicrobial agents and their synergistic effect with colistin against gram-negative bacteria

inferred← citeshttps://doi.org/10.1016/j.ejmech.2021.113826openalex-snapshot

Design, synthesis and bioevaluation of 6-aryl-1-(3,4,5-trimethoxyphenyl)-1H-benzo[d]imidazoles as tubulin polymerization inhibitors

inferred← citeshttps://doi.org/10.1016/j.ejmech.2021.113921openalex-snapshot

Coumarin–benzimidazole hybrids: A review of developments in medicinal chemistry

inferred← citeshttps://doi.org/10.1016/j.ejmech.2022.115040openalex-snapshot

SAR investigation and optimization of benzimidazole-based derivatives as antimicrobial agents against Gram-negative bacteria

inferred← citeshttps://doi.org/10.1016/j.envpol.2019.113877openalex-snapshot

Fungicides enhanced the abundance of antibiotic resistance genes in greenhouse soil

inferred← citeshttps://doi.org/10.1016/j.heliyon.2025.e42105openalex-snapshot

Microwave assisted palladium catalyzed carbon-carbon bond formation to synthesise novel benzimidazole derivatives and their Photophysical properties, molecular docking, and DFT study

inferred← citeshttps://doi.org/10.1016/j.ica.2022.121333openalex-snapshot

Cu(I)-benzimidazole complexes with triphenylphosphine as coligand: DNA lesion and reactive oxygen-dependent mitochondrial dysfunction inducing apoptosis

inferred← citeshttps://doi.org/10.1016/j.indcrop.2023.116705openalex-snapshot

Functional natural wood-plastic composites: A review of antimicrobial properties and their influencing factors

inferred← citeshttps://doi.org/10.1016/j.jddst.2023.105121openalex-snapshot

Nanoemulgel formulation of a benzimidazole derivative for wound healing

inferred← citeshttps://doi.org/10.1016/j.jics.2021.100236openalex-snapshot

A study on multifunctional protein fibre with UV protection, moth repellency and antibacterial properties using ESIPT core containing benzimidazole and benzothiazole based functional acid azo dyes

inferred← citeshttps://doi.org/10.1016/j.jiec.2026.07.040openalex-snapshot

Sustainable Dyeing, thermodynamic Investigation, and antimicrobial finishing of Nylon-6 fabrics using novel Benzimidazole-Based azo dyes in supercritical carbon dioxide

inferred← citeshttps://doi.org/10.1016/j.lddd.2026.100372openalex-snapshot

Benzimidazole derivatives as kinase inhibitors: Synthetic strategies, and therapeutic prospects in cancer

inferred← citeshttps://doi.org/10.1016/j.molliq.2018.01.140openalex-snapshot

Synthesis and characterization of ruthenium(III) complex containing 2-aminomethyl benzimidazole, and its anticancer activity of in vitro and in vivo models

inferred← citeshttps://doi.org/10.1016/j.molstruc.2020.128996openalex-snapshot

Exploring electronic structure, and substituent effect of some biologically active benzimidazole derivatives: Experimental insights and DFT calculations

inferred← citeshttps://doi.org/10.1016/j.molstruc.2020.129809openalex-snapshot

Structural elucidation, spectroscopic, and metallochromic studies of 2-(2-hydroxy phenyl)-1-H–benzimidazole complexes: Metal ions sensing, DNA binding, and antimicrobial activity evaluation

inferred← citeshttps://doi.org/10.1016/j.molstruc.2021.131473openalex-snapshot

Recent advancements and developments in search of anti-tuberculosis agents: A quinquennial update and future directions

inferred← citeshttps://doi.org/10.1016/j.molstruc.2022.134071openalex-snapshot

Molecular modelling, DFT, molecular dynamics simulations, synthesis and antimicrobial potential studies of heterocyclic nucleoside mimetics

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.molstruc.2024.139326openalex-snapshot

Synthesis and computational studies of 1,3,4-thiadiazole and benzothiazole clubbed benzimidazole analogous as anti-tubercular and anti-protozoal agent

inferred← citeshttps://doi.org/10.1016/j.molstruc.2024.140136openalex-snapshot

Exploring the anti-diabetic activity of benzimidazole containing Schiff base derivatives: In vitro α-amylase, α-glucosidase inhibitions and in silico studies

inferred← citeshttps://doi.org/10.1016/j.molstruc.2025.143700openalex-snapshot

Recent advances in the green synthesis and biological applications of 2-substituted benzazoles

inferred← citeshttps://doi.org/10.1016/j.molstruc.2025.144208openalex-snapshot

Exploring Cu-catalyzed intramolecular cyclization for the synthesis of benzimidazo-pyrrolo[3,4-b]pyridines: In silico, DFT and in vitro anti-lung cancer study

inferred← citeshttps://doi.org/10.1016/j.poly.2017.12.033openalex-snapshot

Synthesis, structural characterization and cytotoxicity studies of T-shaped silver(I) complexes derived from 1-benzyl-3H-benzimidazolium p-toluenesulfonates

inferred← citeshttps://doi.org/10.1016/j.poly.2025.117861openalex-snapshot

Novel benzimidazole based cobalt complex: synthesis, AChE enzyme inhibition, antibacterial and antibiofilm activity against multidrug-resistant bacteria, and computational analysis

inferred← citeshttps://doi.org/10.1016/j.tet.2017.05.018openalex-snapshot

Synthesis of benzimidazoles from o -phenylenediamines and DMF derivatives in the presence of PhSiH 3

inferred← citeshttps://doi.org/10.1016/j.tet.2018.03.049openalex-snapshot

Iodine-mediated direct synthesis of multifunctional 2-aminobenzimidazoles from N-substituted o-diaminoarenes and isothiocyanates

inferred← citeshttps://doi.org/10.1021/acs.bioconjchem.7b00416openalex-snapshot

DNA-Compatible Nitro Reduction and Synthesis of Benzimidazoles

inferred← citeshttps://doi.org/10.1021/acs.jcim.5c01275openalex-snapshot

Chemical Space Exploration and Reinforcement Learning for Discovery of Novel Benzimidazole Hybrid Antibiotics

inferred← citeshttps://doi.org/10.1021/acs.joc.0c02067openalex-snapshot

Construction of Binuclear Benzimidazole-Fused Quinazolinones and Pyrimidinones Using Aryl Isocyanates as Building Blocks by Transition-Metal-Free C(sp2)–N Coupling

inferred← citeshttps://doi.org/10.1021/acs.joc.7b00142openalex-snapshot

I2-Mediated Intramolecular C–H Amidation for the Synthesis of N-Substituted Benzimidazoles

inferred← citeshttps://doi.org/10.1021/acs.orglett.3c01905openalex-snapshot

Organocatalytic Atroposelective Construction of Axially Chiral Compounds Containing Benzimidazole and Quinoline Rings

inferred← citeshttps://doi.org/10.1021/acs.orglett.7b01356openalex-snapshot

Iridium(III)-Catalyzed Synthesis of Benzimidazoles via C–H Activation and Amidation of Aniline Derivatives

inferred← citeshttps://doi.org/10.1021/acs.orglett.8b02197openalex-snapshot

Chemoselective N–H or C-2 Arylation of Indole-2-carboxamides: Controllable Synthesis of Indolo[1,2-a]quinoxalin-6-ones and 2,3′-Spirobi[indolin]-2′-ones

inferred← citeshttps://doi.org/10.1021/acsanm.4c00378openalex-snapshot

Fabrication of Nanoporous 3D Carbon Nitride from Poly(ionic liquid)s for Regiospecific Synthesis of Benzimidazole Frameworks

inferred← citeshttps://doi.org/10.1021/acscombsci.8b00009openalex-snapshot

Development and Synthesis of DNA-Encoded Benzimidazole Library

inferred← citeshttps://doi.org/10.1021/acsmedchemlett.5c00650openalex-snapshot

Discovery and Optimization of a Trichloroacetamidine Scaffold as a Novel Antibacterial against Multidrug-Resistant Staphylococcus aureus

inferred← citeshttps://doi.org/10.1021/acsomega.5c02816openalex-snapshot

Facile Epitaxial Growth of Novel Nanoscale Ag-MAFs on Reverse Osmosis Membranes: Enhancing Performance, Antibacterial Activity, and (Bio)fouling Resistance

inferred← citeshttps://doi.org/10.1021/acsomega.5c03795openalex-snapshot

Targeting Cancer with New Morpholine-Benzimidazole-Oxadiazole Derivatives: Synthesis, Biological Evaluation, and Computational Insights

inferred← citeshttps://doi.org/10.1038/s41598-025-91410-4openalex-snapshot

High throughput screening identifies potential inhibitors targeting trimethoprim resistant DfrA1 protein in Klebsiella pneumoniae and Escherichia coli

inferred← citeshttps://doi.org/10.1039/c8ra07773hopenalex-snapshot

An efficient one-pot conversion of carboxylic acids into benzimidazoles via an HBTU-promoted methodology

inferred← citeshttps://doi.org/10.1039/c9nj03960kopenalex-snapshot

Antibacterial and aqueous dual-responsive sensing activities of monomeric complexes with uncoordinated imidazole sites

inferred← citeshttps://doi.org/10.1039/c9ob00639gopenalex-snapshot

A rearrangement involving a solid-state melt reaction for the synthesis of multifunctional tetrasubstituted olefins

inferred← citeshttps://doi.org/10.1039/d0cy00965bopenalex-snapshot

Theoretical elucidation of the multi-functional synthetic methodology for switchable Ni(0)-catalyzed C–H allylations, alkenylations and dienylations with allenes

inferred← citeshttps://doi.org/10.1039/d1dt02008kopenalex-snapshot

Water-soluble silver( i ) complexes with N-donor benzimidazole ligands containing an imidazolium core: stability and preliminary biological studies

inferred← citeshttps://doi.org/10.1039/d1ra00650aopenalex-snapshot

Preparation of 1,2-substituted benzimidazoles via a copper-catalyzed three component coupling reaction

inferred← citeshttps://doi.org/10.1039/d2md00143hopenalex-snapshot

Novel tetrahydropyrimidinyl-substituted benzimidazoles and benzothiazoles: synthesis, antibacterial activity, DNA interactions and ADME profiling

inferred← citeshttps://doi.org/10.1039/d2qo01644copenalex-snapshot

Hypervalent iodine( iii ) promoted C–H/C–H amination/annulation tandem reactions: synthesis of benzimidazoles from simple anilines and aldehydes

inferred← citeshttps://doi.org/10.1039/d3ce00529aopenalex-snapshot

Prolonged release of silver and iodine from ZIF-7 carrier with great antibacterial activity

inferred← citeshttps://doi.org/10.1039/d3dt01678aopenalex-snapshot

Novel valproate half-sandwich rhodium and iridium conjugates to fight against multidrug-resistant Gram-positive bacteria

inferred← citeshttps://doi.org/10.1039/d4ra08864fopenalex-snapshot

Benzimidazole(s): synthons, bioactive lead structures, total synthesis, and the profiling of major bioactive categories

inferred← citeshttps://doi.org/10.1039/d4tb02524eopenalex-snapshot

Novel functionalized benzimidazole-salicylic acid derivatives: synthesis, photophysical characteristics and biological applications

inferred← citeshttps://doi.org/10.1055/a-1790-2858openalex-snapshot

Bridging Chlorine Atoms Enable the Construction of a Novel Benzimidazole-Derived Fluorescent Molecule

inferred← citeshttps://doi.org/10.1055/a-2673-4657openalex-snapshot

Synthetic Strategies for Benzimidazole-Based Heterocycles via Transition Metal–Catalyzed C–H Annulation

inferred← citeshttps://doi.org/10.1055/s-0041-1737489openalex-snapshot

(2-Aminoaryl)iminophosphoranes as Versatile Starting Materials for the Synthesis of 1-Aryl-2-trifluoromethylbenzimidazoles

inferred← citeshttps://doi.org/10.1055/sos-sd-241-00259openalex-snapshot

3.2.1.1 Encoding Using Double-Stranded DNA: A Headpiece-Based DNA Ligation Strategy

inferred← citeshttps://doi.org/10.1080/00397911.2020.1803913openalex-snapshot

Efficient and simple synthesis of novel 1,2,3-triazolyl-linked benzimidazolone, molecular docking and evaluation of their antimicrobial activity

inferred← citeshttps://doi.org/10.1080/00958972.2020.1812587openalex-snapshot

Synthesis, antimicrobial properties, and theoretical analysis of benzimidazole-2-ylidene silver(I) complexes

inferred← citeshttps://doi.org/10.1080/10406638.2022.2061534openalex-snapshot

ESIPT Core Containing Benzothiazole and Benzimidazole Based Fluorescent Acid Azo Dyes for Protein Fiber: Synthesis, Spectral Characteristics, and Fastness Evaluation

inferred← citeshttps://doi.org/10.1080/10406638.2023.2273885openalex-snapshot

Synthesis and Insecticidal Activity of Novel Trifluoromethylbenzimidazole Linked N -Phenylamide Compounds

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/10.1080/15421406.2022.2142748openalex-snapshot

Synthesis, experimental and theoretical characterization of an unsymmetrical bis-benzimidazolium nitrate salt

inferred← citeshttps://doi.org/10.1080/17568919.2024.2393570openalex-snapshot

Benzimidazole-acrylonitrile hybrid derivatives act as potent urease inhibitors with possible fungicidal activity

inferred← citeshttps://doi.org/10.1080/17568919.2024.2401314openalex-snapshot

Potent α-glucosidase inhibitors with benzimidazole-propionitrile hybridization; synthesis, bioassay and docking study

inferred← citeshttps://doi.org/10.1101/2024.11.18.624070openalex-snapshot

High-Throughput Screening Reveals Potential Inhibitors Targeting Trimethoprim-Resistant DfrA1 Protein in Klebsiella pneumoniae and Escherichia coli

inferred← citeshttps://doi.org/10.1107/s2056989024011538openalex-snapshot

Synthesis, crystal structure and Hirshfeld surface analysis of bis(acetylacetonato-κ 2 O , O ′)(2-amino-1-methyl-1 H -benzimidazole-κ N 3 )copper(II)

inferred← citeshttps://doi.org/10.1134/s1068162024010096openalex-snapshot

Benzothiophene Schiff Bases Disrupt Cytoplasmic Membrane Integrity of Gram-Positive and -Negative Bacteria Cells

inferred← citeshttps://doi.org/10.1134/s1070363223060269openalex-snapshot

Synthesis of New 4-[{2′-(2H-Tetrazol-5-yl)-[1,1′-biphenyl]-4-yl)methyl}(2-R-2-oxoethyl)amino]benzoic Acid Derivatives as Potent Biological Agents with Docking Studies

inferred← citeshttps://doi.org/10.1139/cjc-2025-0154openalex-snapshot

Nucleophilic replacement by catalytic methanolysis: interaction of benzimidazole-2-thione with 2,3-dicholo-5,6-dicyano-1,4-benzoquinone involving substitution reaction via initial charge transfer complexation

inferred← citeshttps://doi.org/10.1186/s43094-024-00589-2openalex-snapshot

Design, synthesis and in-vitro anti-depressant activity evaluation of some 2-styrylbenzimidazole derivatives

inferred← citeshttps://doi.org/10.1248/cpb.c17-00922openalex-snapshot

Synthesis of Novel Thiophene, Thiazole and Coumarin Derivatives Based on Benzimidazole Nucleus and Their Cytotoxicity and Toxicity Evaluations

inferred← citeshttps://doi.org/10.1248/cpb.c24-00570openalex-snapshot

Facile Synthesis of 1,2-Disubstituted Benzimidazoles as Potent Cytotoxic Agents

inferred← citeshttps://doi.org/10.13040/ijpsr.0975-8232.14(2).674-87openalex-snapshot

inferred← citeshttps://doi.org/10.14233/ajchem.2024.31484openalex-snapshot

Novel Benzimidazole based Hydrazide-hydrazone Compounds: Synthesis, Characterization and Antimicrobial Assessment

inferred← citeshttps://doi.org/10.15446/rcciquifa.v48n3.84959openalex-snapshot

Síntesis, caracterización y evaluación farmacológica de nuevos complejos metálicos derivados de híbridos heteroaromáticos (benzimidazol/oxadiazol)

inferred← citeshttps://doi.org/10.17311/sciintl.2023.34.53openalex-snapshot

Biological Activities and Chelating Properties of New Benzoyl Derivatives of 2-Substituted Benzimidazoles

inferred← citeshttps://doi.org/10.17344/acsi.2020.6359openalex-snapshot

CO2 Improved Synthesis of Benzimidazole with the Catalysis of a New Calcium 4-Amino-3-hydroxybenzoate

inferred← citeshttps://doi.org/10.18231/j.ctppc.2024.008openalex-snapshot

Medicinal chemistry of benzimidazole, a versatile pharmacophore

inferred← citeshttps://doi.org/10.18596/jotcsa.546960openalex-snapshot

Synthesis, Characterization, and Carbonic Anhydrase Inhibitory Properties of Silver(I) Complexes of Benzimidazole Derivatives

inferred← citeshttps://doi.org/10.2139/ssrn.5158089openalex-snapshot

Facile Epitaxial Growth of Novel Nanoscale Ag-Mafs on Reverse Osmosis Membranes: Enhancing Performance, Antibacterial Activity, and (Bio)Fouling Resistance

inferred← citeshttps://doi.org/10.2139/ssrn.7451468openalex-snapshot

Glycerol-Mediated Green, Efficient and Mild Synthesis of 2-Arylbenzimidazoles from Aromatic Aldehydes and o-phenylenediamine at Ambient Temperature

inferred← citeshttps://doi.org/10.21608/aps.2022.126565.1083openalex-snapshot

Synthesis, Biological Evaluation and In-silico ADME Study of Novel Hybridized Benzimidazole-Chalcone Compounds with Potential Antimicrobial Activity

inferred← citeshttps://doi.org/10.21608/ejchem.2020.24418.2453openalex-snapshot

Synthesis and characterization of novel mixed complexes derived from 2-aminomethylbenzimidazole and 2-(1H-Benzimidazol-2-yl) aniline and theoretical prediction of toxicity

inferred← citeshttps://doi.org/10.21608/ejchem.2021.65196.3461openalex-snapshot

Synthesis and characterization of some new five and seven-membered heterocyclic compounds derived from mefenamic acid

inferred← citeshttps://doi.org/10.21608/ejchem.2021.87021.4207openalex-snapshot

Design and structure-activity relationships anticandidosic of diazaheteroaryl functionalized by Michaël acceptors

inferred← citeshttps://doi.org/10.2174/0113852728303189240321084818openalex-snapshot

Recent Progress in the Synthesis and Biological Assessment of Benzimidazole-1,2,3- Triazole Hybrids

inferred← citeshttps://doi.org/10.2174/0113852728348072250113115434openalex-snapshot

Synthesis of N-Heterocycles and Linear Adducts from Allyl-Containing Substrates and Sulfonamides

inferred← citeshttps://doi.org/10.2174/0113852728390615250917072619openalex-snapshot

Recent Insights into Benzimidazole Derivatives: From Synthesis to Medicinal Applications

inferred← citeshttps://doi.org/10.2174/0929867331666230915093928openalex-snapshot

State-of-the-art Review on the Antiparasitic Activity of Benzimidazolebased Derivatives: Facing Malaria, Leishmaniasis, and Trypanosomiasis

inferred← citeshttps://doi.org/10.2174/138527282499920092209094openalex-snapshot

Recent Advances in the Synthesis and Applications of Thiabendazole Derivatives: A Short Review

inferred← citeshttps://doi.org/10.2174/1570180820666221017155955openalex-snapshot

Review on the Discovery of New Benzimidazole Derivatives as Anticancer Agents: Synthesis and Structure-activity Relationship (2010-2022)

inferred← citeshttps://doi.org/10.2174/1871520619666191028101506openalex-snapshot

Synthesis and Biological Evaluation of Structurally Diverse Benzimidazole Scaffolds as Potential Chemotherapeutic Agents

inferred← citeshttps://doi.org/10.26434/chemrxiv-2024-0hzg8openalex-snapshot

Redefining Antibacterial Strategies with computational Screening of Benzimidazole Ligands Against VanZ Protein for Alternatives of Antibiotic.

inferred← citeshttps://doi.org/10.29413/abs.2022-7.3.14openalex-snapshot

Antibacterial and antibiofilm activity of polyfunctional benzimidazole derivatives

inferred← citeshttps://doi.org/10.31032/ijbpas/2021/10.10.5660openalex-snapshot

DRUG DESIGN, SYNTHESIS, CHARACTERIZATION AND ANTIBACTERIAL STUDIES OF NOVEL BENZIMIDAZOLE DERIVATIVES AS DNA GYRASE INHIBITOR IN ESCHERICHIA COLI

inferred← citeshttps://doi.org/10.31788/rjc.2022.1558222openalex-snapshot

A FACILE SYNTHESIS OF BENZAZOLYLSULFONYL PYRIMIDINYL ACETAMIDE DERIVATIVES WITH IONIC LIQUID UNDER ULTRASONIC IRRADIATION

inferred← citeshttps://doi.org/10.32388/r7liupopenalex-snapshot

Synthesis of 1, 2-Disubstituted Benzimidazoles at Ambient Temperature Catalyzed by 1-Methylimidazolium Tetraflouroborate ([Hmim] BF_4) and Investigating Their Anti-ovarian Cancer Properties Through Molecular Docking Studies and Calculations

inferred← citeshttps://doi.org/10.3390/ijms231710047openalex-snapshot

Ligand-Based Virtual Screening and Molecular Docking of Benzimidazoles as Potential Inhibitors of Triosephosphate Isomerase Identified New Trypanocidal Agents

inferred← citeshttps://doi.org/10.3390/molecules21111574openalex-snapshot

Synthesis and Biological Evaluation of Benzimidazole Phenylhydrazone Derivatives as Antifungal Agents against Phytopathogenic Fungi

inferred← citeshttps://doi.org/10.3390/molecules27113501openalex-snapshot

N-methyl Benzimidazole Tethered Cholic Acid Amphiphiles Can Eradicate S. aureus-Mediated Biofilms and Wound Infections

inferred← citeshttps://doi.org/10.3390/molecules28114435openalex-snapshot

Structure–Activity Relationships in NHC–Silver Complexes as Antimicrobial Agents

inferred← citeshttps://doi.org/10.3390/ph14121278openalex-snapshot

29th Annual GP2A Medicinal Chemistry Conference

inferred← citeshttps://doi.org/10.36329/jkcm/2023/v2.i10.13347openalex-snapshot

Synthesis and Characterization of New benzimidazole-nitrone Derivatives, and Study of Their Effect as Anti-bacterial.

inferred← citeshttps://doi.org/10.3987/com-19-14071openalex-snapshot

Facile Sodium Metabisulfite Mediated Synthesis of 1,2-Disubstituted Benzimidazoles and Cytotoxicity Evaluation

inferred← citeshttps://doi.org/10.4155/fmc-2023-0154openalex-snapshot

Novel Hydroxy- and Amidino-Substituted Benzimidazoles and Benzothiazoles as Antibacterial and Antiproliferative Agents

inferred← citeshttps://doi.org/10.46939/j.sci.arts-21.1-b05openalex-snapshot

BENZIMIDAZOLE AS A PROMISING ANTIVIRAL HETEROCYCLIC SCAFFOLD: A REVIEW

inferred← citeshttps://doi.org/10.47750/pnr.2022.13.s03.137openalex-snapshot

Synthesis New Benzimidazole Derivatives as Antibacterial

inferred← citeshttps://doi.org/10.48048/tis.2023.6110openalex-snapshot

In vitro Studies of Antibacterial and Antifungal Activity of Novel Substituted Benzimidazole Derivatives

inferred← citeshttps://doi.org/10.5564/mjc.v24i50.2435openalex-snapshot

Monte Carlo and DFT calculations on the corrosion inhibition efficiency of some benzimide molecules

inferred← citeshttps://doi.org/10.5772/intechopen.1001896openalex-snapshot

Recent Approaches for the Synthesis of Imidazoquinazolines and Benzimidazoquinazolines

inferred← citeshttps://doi.org/10.5772/intechopen.101702openalex-snapshot

Advances of Benzimidazole Derivatives as Anticancer Agents: Bench to Bedside

inferred← citeshttps://doi.org/10.6084/m9.figshare.26681134openalex-snapshot

Additional file 1 of Design, synthesis and in-vitro anti-depressant activity evaluation of some 2-styrylbenzimidazole derivatives

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.