Pharmacology & Pharmacy

Pharmacology & Pharmacy

ISSN Print: 2157-9423
ISSN Online: 2157-9431
www.scirp.org/journal/pp
E-mail: pp@scirp.org
"Indolin-2-Ones in Clinical Trials as Potential Kinase Inhibitors: A Review"
written by Chinnasamy Rajaram Prakash, Panneerselvam Theivendren, Sundararajan Raja,
published by Pharmacology & Pharmacy, Vol.3 No.1, 2012
has been cited by the following article(s):
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[1] Ultrasound‐assisted synthesis of 3‐(1‐(2‐(1H‐indol‐3‐yl)ethyl)‐2‐aryl‐6,6‐dimethyl‐4‐oxo‐4,5,6,7‐tetrahydro‐1H‐indol‐3‐yl)indolin‐2‐ones by novel core‐shell bio‐based nanocatalyst anchoring sulfonated L‐histidine on …
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[2] Recent Advances in the Utility of Glycerol as a Benign and Biodegradable Medium in Heterocyclic Synthesis
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[3] Eco‐friendly Polyethylene Glycol‐400 as a Rapid and Efficient Recyclable Reaction Medium for the Synthesis of Anticancer Isatin‐linked Chalcones and Their 3‐Hydroxy Precursor
Journal of heterocyclic chemistry, 2019
[4] Oxidative Assets Toward Biomolecules and Cytotoxicity of New Oxindolimine-Copper (II) and Zinc (II) Complexes
2019
[5] Novel 3-((2-chloroquinolin-3-yl) methylene) indolin-2-one derivatives produce anticancer efficacy in ovarian cancer in vitro
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[6] Multicomponent reactions (MCRs): a useful access to the synthesis of benzo-fused γ-lactams
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[7] DNA binding, cytotoxic effects and probable targets of an oxindolimine-vanadyl complex as an antitumor agent.
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[8] Domino carbometalation/coupling reactions of N-arylpropiolamides: a novel and promising synthetic strategy toward stereocontrolled preparation of highly …
RSC Advances, 2017
[9] Targeting of the breast cancer microenvironment with a potent and linkable oxindole based antiangiogenic small molecule
2017
[10] Oxalic Acid as Sustainable CO Source for Pyrrolone‐Fused Benzosuberenes Synthesis through Palladium Catalyzed Carbonylative Cyclization
ChemistrySelect, 2017
[11] Iodine-Catalyzed Regioselective Synthesis of Multisubstiuted Pyrrole Polyheterocycles Free from Rotamers and Keto–Enol Tautomers
The Journal of Organic Chemistry, 2017
[12] Heterocyclic Analogues as Kinase Inhibitors: A Focus Review
Current Topics in Medicinal Chemistry, 2017
[13] Domino carbometalation/coupling reactions of N-arylpropiolamides: a novel and promising synthetic strategy toward stereocontrolled preparation of highly …
RSC Advances, 2017
[14] Peptide–Drug Conjugate GnRH–Sunitinib Targets Angiogenesis Selectively at the Site of Action to Inhibit Tumor Growth
2016
[15] Imobilização de complexos oxindolimínicos de cobre e zinco em argilas beidelitas
Thesis, 2016
[16] Prevalence of bacterial and fungal diseases in dromedary camels in the Rajasthan state of India.
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[17] Highly efficient regioselective synthesis of pyrroles via a tandem enamine formation–Michael addition–cyclization sequence under catalyst-and solvent-free conditions
Green Chemistry, 2015
[18] Highly efficient regioselective synthesis of pyrroles via a tandem enamine formation-Michael addition-cyclization sequence under catalyst-and solvent-free conditions
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[19] Proxy-PET Building Blocks as a Design Element for Library Synthesis
Dissertation, Wright State University, 2015
[20] Design and Synthesis of 3-Substituted Indolin-2-one Derivatives with Methyl (E)-2-(3-Methoxy) acrylate Moiety
Asian Journal of Chemistry, 2015
[21] Synthesis of 3‐(γ, δ‐Disubstituted) allylidene‐2‐Oxindoles from Isatins by Wittig Reaction with Morita–Baylis–Hillman Bromides
Bulletin of the Korean Chemical Society, 2015
[22] A one-pot 'click'reaction from spiro-epoxides catalyzed by Cu (i)-pyrrolidinyl-oxazole-carboxamide
New Journal of Chemistry, 2015
[23] Design and Synthesis of 3-Substituted Indolin-2-one Derivatives with Methyl (E)-2-(3-Methoxy) acrylate Moiety.
Asian Journal of Chemistry, 2015
[24] QSAR and molecular docking studies on oxindole derivatives as VEGFR-2 tyrosine kinase inhibitors
Journal of Receptors and Signal Transduction, 2015
[25] Inhibition of cyclin-dependent kinase CDK1 by oxindolimine ligands and corresponding copper and zinc complexes
JBIC Journal of Biological Inorganic Chemistry, 2015
[26] Microwave-Assisted, Multicomponent, Ecofriendly Synthesis of 3-Bihetaryl-2-Oxindole Derivatives Grafted with Phenothiazine Moiety
Synthetic Communications, 2015
[27] Molybdenum hexacarbonyl mediated synthesis of indolin-2-one & azaindolin-2-one under catalyst free conditions
Tetrahedron Letters, 2015
[28] Highly Stereoselective [4+ 2] and [3+ 2] Spiroannulations of 2‐(2‐Oxoindolin‐3‐ylidene) acetic Esters Catalyzed by Bifunctional Thioureas
Chemistry–A European Journal, 2015
[29] Peptide-drug conjugate GnRH-sunitinib targets angiogenesis selectively at the site of action to inhibit tumor growth
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[30] 2-Indolinone a versatile scaffold for treatment of cancer: a patent review (2008–2014)
Expert opinion on therapeutic patents, 2015
[31] An expedient synthesis of 3-alkylideneoxindoles by Ti (O< sup> i Pr)< sub> 4/pyridine-mediated Knoevenagel condensat
Tetrahedron Letters, 2014
[32] The Indolinone MAZ51 Induces Cell Rounding and G2/M Cell Cycle Arrest in Glioma Cells without the Inhibition of VEGFR-3 Phosphorylation: Involvement of the RhoA and Akt/GSK3β Signaling Pathways
PloS one, 2014
[33] Vinylogous< i> N,< i> N-dimethylaminomethylenation of 3-[(1-substituted) ethylidene]-oxindoles with< i> N,< i> N
Tetrahedron Letters, 2014
[34] Efficient synthesis of new oxindol-based heterocyclic entities via indolin-2-one derivatives
Arabian Journal of Chemistry, 2014
[35] Syntheses and Evaluation of Carbon-11-and Fluorine-18-Radiolabeled pan-Tropomyosin Receptor Kinase (Trk) Inhibitors: Exploration of the 4-Aza-2-oxindole Scaffold as Trk PET Imaging Agents
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[36] Vinylogous N, N-dimethylaminomethylenation of 3-[(1-substituted) ethylidene]-oxindoles with N, N-dimethylformamide dimethylacetal
Tetrahedron Letters, 2014
[37] The indolinone MAZ51 induces cell rounding and G2/M cell cycle arrest in glioma cells without the inhibition of VEGFR-3 phosphorylation: involvement of the …
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[38] Syntheses and evaluation of carbon-11-and fluorine-18-radiolabeled pan-tropomyosin receptor kinase (Trk) inhibitors: exploration of the 4-aza-2-oxindole scaffold as …
ACS Chemical Neuroscience, 2014
[39] An expedient synthesis of 3-alkylideneoxindoles by Ti (OiPr) 4/pyridine-mediated Knoevenagel condensation
Tetrahedron Letters, 2014
[40] The Indolinone MAZ51 Induces Cell Rounding and G2
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[41] Synthesis, Structure-Activity Relationships and Biological Activity of New Isatin Derivatives as Tyrosinase Inhibitors
Current topics in medicinal chemistry, 2014
[42] The indolinone MAZ51 induces cell rounding and G2/M cell cycle arrest in glioma cells without the inhibition of VEGFR-3 phosphorylation: involvement of the …
PLOS ONE, 2014
[43] Cyclodextrin host as a supramolecular catalyst in nonpolar solvents: stereoselective synthesis of (E)-3-alkylideneoxindoles
Tetrahedron, 2013
[44] Cyclodextrin host as a supramolecular catalyst in nonpolar solvents: stereoselective synthesis of (< i> E)-3-alkylideneoxind
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[45] Libraries from Libraries Approach to the Synthesis of Arylidene Oxindoles
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[46] Rational design of protein kinase inhibitors
Biopolymers and Cell, 2013
[47] The design, synthesis, and biological evaluation of potent receptor tyrosine kinase inhibitors
2012
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