|
[1]
|
Virtual Screening and Molecular Docking: Discovering Novel c-KIT Inhibitors
|
|
Current Medicinal …,
2022 |
|
|
|
[2]
|
Transition metal-free functionalization of 2-oxindoles via sequential aldol and reductive aldol reactions using rongalite as a C1 reagent
|
|
Organic & Biomolecular …,
2022 |
|
|
|
[3]
|
Designing and Synthesis of New Isatin Derivatives as Potential CDK2 Inhibitors
|
|
International journal of molecular …,
2022 |
|
|
|
[4]
|
The Development of 3-substituted Indolin-2-one Derivatives as Kinase Inhibitors for Cancer Therapy
|
|
Current Medicinal Chemistry,
2022 |
|
|
|
[5]
|
3-Substituted-2-oxindole derivatives: Design, synthesis and their anti-tuberculosis and radical scavenging dual-action studies
|
|
Journal of Molecular …,
2022 |
|
|
|
[6]
|
Molecular Docking and In Vitro Anticancer Screening of Synthesized Arylthiazole linked 2H-indol-2-one Derivatives as VEGFR-2 Kinase Inhibitors
|
|
Anti-Cancer Agents …,
2022 |
|
|
|
[7]
|
Logical synthetic strategies and structure-activity relationship of indolin-2-one hybrids as small molecule anticancer agents: An overview
|
|
Journal of Molecular …,
2022 |
|
|
|
[8]
|
Isatin-hydrazide conjugates as potent α-amylase and α-glucosidase inhibitors: Synthesis, structure and in vitro evaluations
|
|
Bioorganic …,
2021 |
|
|
|
[9]
|
Synthesis of the Kinase Inhibitors Nintedanib, Hesperadin, and Their Analogues Using the Eschenmoser Coupling Reaction
|
|
The Journal of Organic …,
2021 |
|
|
|
[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 …
|
|
2020 |
|
|
|
[12]
|
Anticancer compounds based on isatin-derivatives: strategies to ameliorate selectivity and efficiency
|
|
2020 |
|
|
|
[13]
|
Recent Advances in the Utility of Glycerol as a Benign and Biodegradable Medium in Heterocyclic Synthesis
|
|
2019 |
|
|
|
[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
|
|
Journal of heterocyclic chemistry,
2019 |
|
|
|
[15]
|
Oxidative Assets Toward Biomolecules and Cytotoxicity of New Oxindolimine-Copper (II) and Zinc (II) Complexes
|
|
2019 |
|
|
|
[16]
|
Novel 3-((2-chloroquinolin-3-yl) methylene) indolin-2-one derivatives produce anticancer efficacy in ovarian cancer in vitro
|
|
2019 |
|
|
|
[17]
|
Multicomponent reactions (MCRs): a useful access to the synthesis of benzo-fused γ-lactams
|
|
2019 |
|
|
|
[18]
|
DNA binding, cytotoxic effects and probable targets of an oxindolimine-vanadyl complex as an antitumor agent.
|
|
2019 |
|
|
|
[19]
|
The effect of combined drug treatment on HL60 cells
|
|
2019 |
|
|
|
[20]
|
Domino carbometalation/coupling reactions of N-arylpropiolamides: a novel and promising synthetic strategy toward stereocontrolled preparation of highly …
|
|
RSC Advances,
2017 |
|
|
|
[21]
|
Targeting of the breast cancer microenvironment with a potent and linkable oxindole based antiangiogenic small molecule
|
|
2017 |
|
|
|
[22]
|
Oxalic Acid as Sustainable CO Source for Pyrrolone‐Fused Benzosuberenes Synthesis through Palladium Catalyzed Carbonylative Cyclization
|
|
ChemistrySelect,
2017 |
|
|
|
[23]
|
Iodine-Catalyzed Regioselective Synthesis of Multisubstiuted Pyrrole Polyheterocycles Free from Rotamers and Keto–Enol Tautomers
|
|
The Journal of Organic Chemistry,
2017 |
|
|
|
[24]
|
Heterocyclic Analogues as Kinase Inhibitors: A Focus Review
|
|
Current Topics in Medicinal Chemistry,
2017 |
|
|
|
[25]
|
Domino carbometalation/coupling reactions of N-arylpropiolamides: a novel and promising synthetic strategy toward stereocontrolled preparation of highly …
|
|
RSC Advances,
2017 |
|
|
|
[26]
|
Peptide–Drug Conjugate GnRH–Sunitinib Targets Angiogenesis Selectively at the Site of Action to Inhibit Tumor Growth
|
|
2016 |
|
|
|
[27]
|
Imobilização de complexos oxindolimínicos de cobre e zinco em argilas beidelitas
|
|
Thesis,
2016 |
|
|
|
[28]
|
Peptide–Drug Conjugate GnRH–Sunitinib Targets Angiogenesis Selectively at the Site of Action to Inhibit Tumor GrowthA Potent Sunitinib–GnRH Conjugate for …
|
|
Cancer research,
2016 |
|
|
|
[29]
|
Prevalence of bacterial and fungal diseases in dromedary camels in the Rajasthan state of India.
|
|
2015 |
|
|
|
[30]
|
Design, synthesis and biological evaluation of bioconjugates for selective drug delivery and tumour targeting
|
|
2015 |
|
|
|
[31]
|
Highly efficient regioselective synthesis of pyrroles via a tandem enamine formation–Michael addition–cyclization sequence under catalyst-and solvent-free conditions
|
|
Green Chemistry,
2015 |
|
|
|
[32]
|
Highly efficient regioselective synthesis of pyrroles via a tandem enamine formation-Michael addition-cyclization sequence under catalyst-and solvent-free conditions
|
|
Green Chemistry,
2015 |
|
|
|
[33]
|
Proxy-PET Building Blocks as a Design Element for Library Synthesis
|
|
Dissertation, Wright State University,
2015 |
|
|
|
[34]
|
Design and Synthesis of 3-Substituted Indolin-2-one Derivatives with Methyl (E)-2-(3-Methoxy) acrylate Moiety
|
|
Asian Journal of Chemistry,
2015 |
|
|
|
[35]
|
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 |
|
|
|
[36]
|
A one-pot 'click'reaction from spiro-epoxides catalyzed by Cu (i)-pyrrolidinyl-oxazole-carboxamide
|
|
New Journal of Chemistry,
2015 |
|
|
|
[37]
|
Design and Synthesis of 3-Substituted Indolin-2-one Derivatives with Methyl (E)-2-(3-Methoxy) acrylate Moiety.
|
|
Asian Journal of Chemistry,
2015 |
|
|
|
[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
|
|
Synthetic Communications,
2015 |
|
|
|
[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
|
|
Chemistry–A European Journal,
2015 |
|
|
|
[43]
|
Peptide-drug conjugate GnRH-sunitinib targets angiogenesis selectively at the site of action to inhibit tumor growth
|
|
Cancer research,
2015 |
|
|
|
[44]
|
2-Indolinone a versatile scaffold for treatment of cancer: a patent review (2008–2014)
|
|
Expert opinion on therapeutic patents,
2015 |
|
|
|
[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 …
|
|
2014 |
|
|
|
[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
|
|
2014 |
|
|
|
[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
|
|
Tetrahedron,
2013 |
|
|
|
[58]
|
Cyclodextrin host as a supramolecular catalyst in nonpolar solvents: stereoselective synthesis of (< i> E)-3-alkylideneoxind
|
|
Tetrahedron,
2013 |
|
|
|
[59]
|
Libraries from Libraries Approach to the Synthesis of Arylidene Oxindoles
|
|
NULL
2013 |
|
|
|
[60]
|
Rational design of protein kinase inhibitors
|
|
Biopolymers and Cell,
2013 |
|
|
|
[61]
|
The design, synthesis, and biological evaluation of potent receptor tyrosine kinase inhibitors
|
|
NULL
2012 |
|
|