Comprehensive Review in Current Developments of Benzimidazole‐Based Medicinal Chemistry

Article Properties
  • Language
    English
  • DOI (url)
  • Publication Date
    2014/11/28
  • Indian UGC (journal)
  • Refrences
    277
  • Citations
    233
  • Rangappa S. Keri Centre for Nano and Material Sciences Jain University Jain Global Campus Bangalore Karnataka 562112 India
  • Asha Hiremathad Centre for Nano and Material Sciences Jain University Jain Global Campus Bangalore Karnataka 562112 India
  • Srinivasa Budagumpi Centre for Nano and Material Sciences Jain University Jain Global Campus Bangalore Karnataka 562112 India
  • Bhari Mallanna Nagaraja Centre for Nano and Material Sciences Jain University Jain Global Campus Bangalore Karnataka 562112 India
Abstract
Cite
Keri, Rangappa S., et al. “Comprehensive Review in Current Developments of Benzimidazole‐Based Medicinal Chemistry”. Chemical Biology &Amp; Drug Design, vol. 86, no. 1, 2014, pp. 19-65, https://doi.org/10.1111/cbdd.12462.
Keri, R. S., Hiremathad, A., Budagumpi, S., & Nagaraja, B. M. (2014). Comprehensive Review in Current Developments of Benzimidazole‐Based Medicinal Chemistry. Chemical Biology &Amp; Drug Design, 86(1), 19-65. https://doi.org/10.1111/cbdd.12462
Keri, Rangappa S., Asha Hiremathad, Srinivasa Budagumpi, and Bhari Mallanna Nagaraja. “Comprehensive Review in Current Developments of Benzimidazole‐Based Medicinal Chemistry”. Chemical Biology &Amp; Drug Design 86, no. 1 (2014): 19-65. https://doi.org/10.1111/cbdd.12462.
Keri RS, Hiremathad A, Budagumpi S, Nagaraja BM. Comprehensive Review in Current Developments of Benzimidazole‐Based Medicinal Chemistry. Chemical Biology & Drug Design. 2014;86(1):19-65.
Journal Categories
Medicine
Therapeutics
Pharmacology
Science
Biology (General)
Science
Chemistry
Organic chemistry
Biochemistry
Refrences
Title Journal Journal Categories Citations Publication Date
Design, synthesis, molecular docking and biological evaluation of new dithiocarbamates substituted benzimidazole and chalcones as possible chemotherapeutic agents 2013
Synthesis and biological activity of benzimidazoles 2011
Anti‐ulcerogeic effect of 2‐(pyrimidinylsulfinyl) benzimidazole derivative against different ulcerogenic agents in rats 2011
Synthesis and antiulcer, anti‐secretory activity of some new substituted 2‐(pyrimidinylsulfinyl) benzamidazoles derivatives 2011
Benzimidazoles in a wormy world 2010
Citations
Title Journal Journal Categories Citations Publication Date
Synthesis, Biological Investigation, and Molecular Docking of Novel Benzimidazole‐Hydrazone Hybrids as Potential Anticancer Agent Candidates

ChemistrySelect
  • Science: Chemistry: General. Including alchemy
  • Science: Chemistry
2024
Environmentally friendly and efficient TBHP-mediated catalytic reaction for the synthesis of substituted benzimidazole-2-ones: approach to pharmaceutical applications Environmental Research
  • Geography. Anthropology. Recreation: Environmental sciences
  • Medicine: Internal medicine: Special situations and conditions: Industrial medicine. Industrial hygiene
  • Technology: Environmental technology. Sanitary engineering
  • Science: Biology (General): Ecology
  • Medicine: Public aspects of medicine: Toxicology. Poisons
2024
Diaryl-substituted benzimidazole derivatives as antiproliferative agents: Design, synthesis, in vitro activity, and SAR analysis Journal of Molecular Structure
  • Science: Chemistry: Physical and theoretical chemistry
  • Science: Chemistry: Physical and theoretical chemistry
  • Science: Chemistry
2024
Fabrication, physicochemical characterization and theoretical studies of some new mixed ligands complexes based on N-(1H-benzimidazol-2-yl)-guanidine and 1, 10-phenanthroline: DNA interaction, biological applications and molecular docking approach Journal of Molecular Structure
  • Science: Chemistry: Physical and theoretical chemistry
  • Science: Chemistry: Physical and theoretical chemistry
  • Science: Chemistry
2024
Synthesis, spectroscopic, electrochemistry and antioxidant properties of benzofuroxan and 2H-benzimidazole 1,3-dioxide derivatives: Effects of conjugation with electron-acceptor 1,2,3-triazolyl-1,2,4-oxadiazole Journal of Molecular Structure
  • Science: Chemistry: Physical and theoretical chemistry
  • Science: Chemistry: Physical and theoretical chemistry
  • Science: Chemistry
2024
Citations Analysis
Category Category Repetition
Science: Chemistry155
Science: Chemistry: General. Including alchemy64
Science: Chemistry: Organic chemistry56
Technology: Chemical technology: Polymers and polymer manufacture47
Medicine: Therapeutics. Pharmacology46
Science: Chemistry: Analytical chemistry41
Medicine: Public aspects of medicine: Toxicology. Poisons30
Science: Biology (General)26
Science: Chemistry: Physical and theoretical chemistry20
Science: Chemistry: Inorganic chemistry16
Science: Physics: Nuclear and particle physics. Atomic energy. Radioactivity11
Science: Chemistry: Organic chemistry: Biochemistry11
Medicine: Internal medicine: Infectious and parasitic diseases6
Technology: Electrical engineering. Electronics. Nuclear engineering: Materials of engineering and construction. Mechanics of materials6
Technology: Chemical technology6
Technology: Chemical technology: Chemical engineering5
Geography. Anthropology. Recreation: Environmental sciences5
Science5
Technology: Environmental technology. Sanitary engineering4
Science: Science (General)4
Technology: Engineering (General). Civil engineering (General)3
Science: Chemistry: Crystallography3
Medicine3
Medicine: Internal medicine: Specialties of internal medicine: Immunologic diseases. Allergy3
Science: Microbiology3
Social Sciences: Industries. Land use. Labor: Special industries and trades: Energy industries. Energy policy. Fuel trade2
Medicine: Internal medicine: Special situations and conditions: Arctic medicine. Tropical medicine2
Technology: Engineering (General). Civil engineering (General): Environmental engineering2
Science: Biology (General): Ecology2
Science: Biology (General): Genetics2
Agriculture: Agriculture (General)1
Technology: Chemical technology: Food processing and manufacture1
Agriculture1
Medicine: Medicine (General)1
Technology: Chemical technology: Clay industries. Ceramics. Glass1
Science: Physics: Atomic physics. Constitution and properties of matter1
Technology: Mechanical engineering and machinery: Renewable energy sources1
Medicine: Pathology1
Science: Physics: Optics. Light1
Medicine: Internal medicine: Neoplasms. Tumors. Oncology. Including cancer and carcinogens1
Medicine: Internal medicine: Special situations and conditions: Industrial medicine. Industrial hygiene1
Science: Physics1
Technology: Chemical technology: Biotechnology1
Medicine: Public aspects of medicine1
Science: Biology (General): Cytology1
Medicine: Pharmacy and materia medica1
Medicine: Internal medicine: Specialties of internal medicine: Diseases of the endocrine glands. Clinical endocrinology1
Science: Zoology1
Science: Mathematics: Instruments and machines1
Science: Mathematics: Instruments and machines: Electronic computers. Computer science1
Medicine: Medicine (General): Computer applications to medicine. Medical informatics1
The category Science: Chemistry 155 is the most commonly referenced area in studies that cite this article. The first research to cite this article was titled Enantioselective Aza Michael‐Type Addition to Alkenyl Benzimidazoles Catalyzed by a Chiral Phosphoric Acid and was published in 2015. The most recent citation comes from a 2024 study titled Recent Advances in the Fixation of CO2 into Quinazoline and Benzimidazole. This article reached its peak citation in 2023, with 45 citations. It has been cited in 131 different journals, 16% of which are open access. Among related journals, the ChemistrySelect cited this research the most, with 13 citations. The chart below illustrates the annual citation trends for this article.
Citations used this article by year