Carbazole scaffolds in cancer therapy: a review from 2012 to 2018

Article Properties
  • Language
    English
  • Publication Date
    2019/01/01
  • Indian UGC (journal)
  • Refrences
    106
  • Citations
    90
  • Samar Issa Ecole de Biologie Industrielle, EBInnov, Cergy-Pontoise, France; ORCID (unauthenticated)
  • Anthony Prandina Faculté de Pharmacie - ISPB, EA 4446 Bioactive Molecules and Medicinal Chemistry, SFR Santé Lyon-Est CNRS UMS3453 - INSERM US7, Université de Lyon, Université Claude Bernard Lyon 1, Lyon, France;Department of Pharmaceutical Chemistry, School of Pharmacy, University of Oslo, Oslo, Norway; ORCID (unauthenticated)
  • Nicolas Bedel Faculté de Pharmacie - ISPB, EA 4446 Bioactive Molecules and Medicinal Chemistry, SFR Santé Lyon-Est CNRS UMS3453 - INSERM US7, Université de Lyon, Université Claude Bernard Lyon 1, Lyon, France;
  • Pål Rongved Department of Pharmaceutical Chemistry, School of Pharmacy, University of Oslo, Oslo, Norway; ORCID (unauthenticated)
  • Saïd Yous Université Lille, Inserm, CHU Lille, UMR-S 1172 JPArc Centre de Recherche Jean-Pierre Aubert Neurosciences et Cancer, Lille, France ORCID (unauthenticated)
  • Marc Le Borgne Faculté de Pharmacie - ISPB, EA 4446 Bioactive Molecules and Medicinal Chemistry, SFR Santé Lyon-Est CNRS UMS3453 - INSERM US7, Université de Lyon, Université Claude Bernard Lyon 1, Lyon, France; ORCID (unauthenticated)
  • Zouhair Bouaziz Faculté de Pharmacie - ISPB, EA 4446 Bioactive Molecules and Medicinal Chemistry, SFR Santé Lyon-Est CNRS UMS3453 - INSERM US7, Université de Lyon, Université Claude Bernard Lyon 1, Lyon, France; ORCID (unauthenticated)
Cite
Issa, Samar, et al. “Carbazole Scaffolds in Cancer Therapy: A Review from 2012 to 2018”. Journal of Enzyme Inhibition and Medicinal Chemistry, vol. 34, no. 1, 2019, pp. 1321-46, https://doi.org/10.1080/14756366.2019.1640692.
Issa, S., Prandina, A., Bedel, N., Rongved, P., Yous, S., Le Borgne, M., & Bouaziz, Z. (2019). Carbazole scaffolds in cancer therapy: a review from 2012 to 2018. Journal of Enzyme Inhibition and Medicinal Chemistry, 34(1), 1321-1346. https://doi.org/10.1080/14756366.2019.1640692
Issa S, Prandina A, Bedel N, Rongved P, Yous S, Le Borgne M, et al. Carbazole scaffolds in cancer therapy: a review from 2012 to 2018. Journal of Enzyme Inhibition and Medicinal Chemistry. 2019;34(1):1321-46.
Refrences
Title Journal Journal Categories Citations Publication Date
Synthesis of hetero annulated isoxazolo-, pyrido- and pyrimido carbazoles: Screened for in vitro antitumor activity and structure activity relationships, a novel 2-amino-4-(3'-bromo-4'-methoxyphenyl)-8-chloro-11 H -pyrimido[4,5- a ]carbazole as an antitumor agent European Journal of Medicinal Chemistry
  • Medicine: Therapeutics. Pharmacology
  • Science: Chemistry: Analytical chemistry
  • Science: Chemistry
16 2017
Synthesis of hetero annulated isoxazolo-, pyrido- and pyrimido carbazoles: Screened for in vitro antitumor activity and structure activity relationships, a novel 2-amino-4-(3'-bromo-4'-methoxyphenyl)-8-chloro-11 H -pyrimido[4,5- a ]carbazole as an antitumor agent International Journal of Pharmacy and Pharmaceutical Sciences 2014
Synthesis of hetero annulated isoxazolo-, pyrido- and pyrimido carbazoles: Screened for in vitro antitumor activity and structure activity relationships, a novel 2-amino-4-(3'-bromo-4'-methoxyphenyl)-8-chloro-11 H -pyrimido[4,5- a ]carbazole as an antitumor agent International Journal of Pharmacy and Pharmaceutical Sciences 2012
Synthesis of hetero annulated isoxazolo-, pyrido- and pyrimido carbazoles: Screened for in vitro antitumor activity and structure activity relationships, a novel 2-amino-4-(3'-bromo-4'-methoxyphenyl)-8-chloro-11 H -pyrimido[4,5- a ]carbazole as an antitumor agent Berichte der deutschen chemischen Gesellschaft 1872
Medicinal and aromatic plants I. Biotechnology in agriculture and forestry 1988
Citations
Title Journal Journal Categories Citations Publication Date
Photocatalytic Dehydrogenative 6π‐Photocyclisation of Indole Derivatives via Successive Energy Transfer

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  • Science: Chemistry: Organic chemistry
  • Technology: Chemical technology: Polymers and polymer manufacture
  • Science: Chemistry
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Synthesis, spectral analysis, DFT studies and Biological application of (E)-3-benzylidene-9-methyl-1,2,3,9-tetrahydro-4H-carbazol-4-one Chemical Physics Impact
  • Science: Chemistry: Physical and theoretical chemistry
2024
Prediction of antibody production performance change in Chinese hamster ovary cells using morphological profiling Journal of Bioscience and Bioengineering
  • Technology: Chemical technology: Biotechnology
  • Technology: Chemical technology: Food processing and manufacture
  • Science: Biology (General)
  • Science: Chemistry: Organic chemistry: Biochemistry
1 2024
Biological evaluation of carbazoyl hydrazine derivatives as potential Pim-1 kinase inhibitors for the treatment of human liver cancer Journal of Molecular Structure
  • Science: Chemistry: Physical and theoretical chemistry
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New conjugated carbazole derivatives: synthesis and photophysical properties catalysed by Pd–Cu@rGO

New Journal of Chemistry
  • Science: Chemistry: General. Including alchemy
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2024
Citations Analysis
Category Category Repetition
Science: Chemistry58
Science: Chemistry: General. Including alchemy28
Science: Chemistry: Organic chemistry23
Technology: Chemical technology: Polymers and polymer manufacture22
Medicine: Therapeutics. Pharmacology21
Science: Chemistry: Analytical chemistry17
Medicine: Public aspects of medicine: Toxicology. Poisons14
Science: Biology (General)12
Science: Chemistry: Physical and theoretical chemistry8
Science: Chemistry: Organic chemistry: Biochemistry8
Medicine: Internal medicine: Neoplasms. Tumors. Oncology. Including cancer and carcinogens5
Technology: Electrical engineering. Electronics. Nuclear engineering: Materials of engineering and construction. Mechanics of materials4
Technology: Chemical technology4
Science: Physics3
Science: Chemistry: Inorganic chemistry2
Science: Physics: Nuclear and particle physics. Atomic energy. Radioactivity2
Technology: Engineering (General). Civil engineering (General)2
Technology: Technology (General): Industrial engineering. Management engineering2
Science: Science (General)2
Science: Biology (General): Cytology2
Science: Biology (General): Genetics2
Technology: Chemical technology: Biotechnology2
Technology: Chemical technology: Food processing and manufacture2
Medicine: Pharmacy and materia medica2
Medicine1
Science1
Technology: Environmental technology. Sanitary engineering1
Science: Biology (General): Ecology1
Medicine: Internal medicine: Infectious and parasitic diseases1
Science: Chemistry: Crystallography1
Technology: Home economics: Nutrition. Foods and food supply1
Medicine: Medicine (General)1
Social Sciences: Industries. Land use. Labor: Special industries and trades: Pharmaceutical industry1
The category Science: Chemistry 58 is the most commonly referenced area in studies that cite this article. The first research to cite this article was titled An Expeditious Benzannulation Reaction of Indol‐3‐yl‐but‐3‐yn‐2‐ols to Substituted 2‐Iodocarbazoles via Domino 5‐endo Spirocyclization/Selective Vinyl Shift and Aromatization and was published in 2019. The most recent citation comes from a 2024 study titled Pd-catalyzed three-component [2 + 2 + 1] cycloamination toward carbazoles. This article reached its peak citation in 2022, with 26 citations. It has been cited in 60 different journals, 21% of which are open access. Among related journals, the Organic & Biomolecular Chemistry cited this research the most, with 4 citations. The chart below illustrates the annual citation trends for this article.
Citations used this article by year