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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[2] Transition metal-free functionalization of 2-oxindoles via sequential aldol and reductive aldol reactions using rongalite as a C1 reagent
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[3] Designing and Synthesis of New Isatin Derivatives as Potential CDK2 Inhibitors
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[4] The Development of 3-substituted Indolin-2-one Derivatives as Kinase Inhibitors for Cancer Therapy
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[5] 3-Substituted-2-oxindole derivatives: Design, synthesis and their anti-tuberculosis and radical scavenging dual-action studies
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[6] Molecular Docking and In Vitro Anticancer Screening of Synthesized Arylthiazole linked 2H-indol-2-one Derivatives as VEGFR-2 Kinase Inhibitors
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[7] Logical synthetic strategies and structure-activity relationship of indolin-2-one hybrids as small molecule anticancer agents: An overview
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[8] Isatin-hydrazide conjugates as potent α-amylase and α-glucosidase inhibitors: Synthesis, structure and in vitro evaluations
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[9] Synthesis of the Kinase Inhibitors Nintedanib, Hesperadin, and Their Analogues Using the Eschenmoser Coupling Reaction
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[10] Recent Advances in N‐Heterocyclic Carbene Catalyzed Oxidative Cyclization for the Formation of Heterocycles
Asian Journal of Organic Chemistry, 2021
[11] 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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[12] Anticancer compounds based on isatin-derivatives: strategies to ameliorate selectivity and efficiency
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[13] Recent Advances in the Utility of Glycerol as a Benign and Biodegradable Medium in Heterocyclic Synthesis
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[14] 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
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[15] Oxidative Assets Toward Biomolecules and Cytotoxicity of New Oxindolimine-Copper (II) and Zinc (II) Complexes
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[16] Novel 3-((2-chloroquinolin-3-yl) methylene) indolin-2-one derivatives produce anticancer efficacy in ovarian cancer in vitro
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[17] Multicomponent reactions (MCRs): a useful access to the synthesis of benzo-fused γ-lactams
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[18] DNA binding, cytotoxic effects and probable targets of an oxindolimine-vanadyl complex as an antitumor agent.
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[19] The effect of combined drug treatment on HL60 cells
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[20] Domino carbometalation/coupling reactions of N-arylpropiolamides: a novel and promising synthetic strategy toward stereocontrolled preparation of highly …
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[21] Targeting of the breast cancer microenvironment with a potent and linkable oxindole based antiangiogenic small molecule
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[22] Oxalic Acid as Sustainable CO Source for Pyrrolone‐Fused Benzosuberenes Synthesis through Palladium Catalyzed Carbonylative Cyclization
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[23] Iodine-Catalyzed Regioselective Synthesis of Multisubstiuted Pyrrole Polyheterocycles Free from Rotamers and Keto–Enol Tautomers
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[24] Heterocyclic Analogues as Kinase Inhibitors: A Focus Review
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[25] Domino carbometalation/coupling reactions of N-arylpropiolamides: a novel and promising synthetic strategy toward stereocontrolled preparation of highly …
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[26] Peptide–Drug Conjugate GnRH–Sunitinib Targets Angiogenesis Selectively at the Site of Action to Inhibit Tumor Growth
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[27] Imobilização de complexos oxindolimínicos de cobre e zinco em argilas beidelitas
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[28] Peptide–Drug Conjugate GnRH–Sunitinib Targets Angiogenesis Selectively at the Site of Action to Inhibit Tumor GrowthA Potent Sunitinib–GnRH Conjugate for …
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[29] Prevalence of bacterial and fungal diseases in dromedary camels in the Rajasthan state of India.
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[30] Design, synthesis and biological evaluation of bioconjugates for selective drug delivery and tumour targeting
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[31] 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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[32] 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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[33] Proxy-PET Building Blocks as a Design Element for Library Synthesis
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[34] Design and Synthesis of 3-Substituted Indolin-2-one Derivatives with Methyl (E)-2-(3-Methoxy) acrylate Moiety
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[35] Synthesis of 3‐(γ, δ‐Disubstituted) allylidene‐2‐Oxindoles from Isatins by Wittig Reaction with Morita–Baylis–Hillman Bromides
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[36] A one-pot 'click'reaction from spiro-epoxides catalyzed by Cu (i)-pyrrolidinyl-oxazole-carboxamide
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[37] Design and Synthesis of 3-Substituted Indolin-2-one Derivatives with Methyl (E)-2-(3-Methoxy) acrylate Moiety.
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[38] QSAR and molecular docking studies on oxindole derivatives as VEGFR-2 tyrosine kinase inhibitors
Journal of Receptors and Signal Transduction, 2015
[39] Inhibition of cyclin-dependent kinase CDK1 by oxindolimine ligands and corresponding copper and zinc complexes
JBIC Journal of Biological Inorganic Chemistry, 2015
[40] Microwave-Assisted, Multicomponent, Ecofriendly Synthesis of 3-Bihetaryl-2-Oxindole Derivatives Grafted with Phenothiazine Moiety
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[41] Molybdenum hexacarbonyl mediated synthesis of indolin-2-one & azaindolin-2-one under catalyst free conditions
Tetrahedron Letters, 2015
[42] Highly Stereoselective [4+ 2] and [3+ 2] Spiroannulations of 2‐(2‐Oxoindolin‐3‐ylidene) acetic Esters Catalyzed by Bifunctional Thioureas
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[43] Peptide-drug conjugate GnRH-sunitinib targets angiogenesis selectively at the site of action to inhibit tumor growth
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[44] 2-Indolinone a versatile scaffold for treatment of cancer: a patent review (2008–2014)
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[45] An expedient synthesis of 3-alkylideneoxindoles by Ti (O< sup> i Pr)< sub> 4/pyridine-mediated Knoevenagel condensat
Tetrahedron Letters, 2014
[46] 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
[47] Vinylogous< i> N,< i> N-dimethylaminomethylenation of 3-[(1-substituted) ethylidene]-oxindoles with< i> N,< i> N
Tetrahedron Letters, 2014
[48] Efficient synthesis of new oxindol-based heterocyclic entities via indolin-2-one derivatives
Arabian Journal of Chemistry, 2014
[49] 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
ACS chemical neuroscience, 2014
[50] Vinylogous N, N-dimethylaminomethylenation of 3-[(1-substituted) ethylidene]-oxindoles with N, N-dimethylformamide dimethylacetal
Tetrahedron Letters, 2014
[51] 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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[52] 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
[53] An expedient synthesis of 3-alkylideneoxindoles by Ti (OiPr) 4/pyridine-mediated Knoevenagel condensation
Tetrahedron Letters, 2014
[54] The Indolinone MAZ51 Induces Cell Rounding and G2
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[55] Synthesis, Structure-Activity Relationships and Biological Activity of New Isatin Derivatives as Tyrosinase Inhibitors
Current topics in medicinal chemistry, 2014
[56] 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
[57] Cyclodextrin host as a supramolecular catalyst in nonpolar solvents: stereoselective synthesis of (E)-3-alkylideneoxindoles
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[58] Cyclodextrin host as a supramolecular catalyst in nonpolar solvents: stereoselective synthesis of (< i> E)-3-alkylideneoxind
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[59] Libraries from Libraries Approach to the Synthesis of Arylidene Oxindoles
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[60] Rational design of protein kinase inhibitors
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[61] The design, synthesis, and biological evaluation of potent receptor tyrosine kinase inhibitors
2012
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