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Synthesis and biological evaluation of certain hydrazonoindolin-2-one derivatives as new potent anti-proliferative agents

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Outgoing claims: the papers this work cites, builds on, or argues with.

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Design, Synthesis and In Vitro Antiproliferative Activity of Novel Isatin‐Quinazoline Hybrids
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ChemInform Abstract: Heterocyclic Systems Containing Bridgehead Nitrogen Atom. Part 60. Synthesis of Thiazolo(2′,3′:3,4) (1,2,4)triazino(5,6‐b)indoles.
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ChemInform Abstract: Heterocyclic Systems Containing Bridgehead Nitrogen Atom: Synthesis of Thiazolo(3′,2′:2,3) (1,2,4)triazino(5,6‐b)indoles and Isomeric Thiazolo(2′,3′:3,4) (1,2,4)triazino(5,6‐b)indoles.
inferredcites →https://doi.org/10.1002/chin.199220225openalex-snapshot
ChemInform Abstract: Heterocyclic Systems Containing a Bridgehead Nitrogen Atom. Part 72. Reaction of 5H‐2,3‐Dihydro‐1,2,4‐triazino(5,6‐b)indole‐3‐thiones with Phenacyl Bromide, 1,2‐Dibromoethane and Chloroacetic Acid.
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(3Z)-3-(2-[4-(aryl)-1,3-thiazol-2-yl]hydrazin-1-ylidene)-2,3-dihydro-1H-indol-2-one derivatives as dual inhibitors of HIV-1 reverse transcriptase
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Indoline ureas as potential anti-hepatocellular carcinoma agents targeting VEGFR-2: Synthesis, in vitro biological evaluation and molecular docking
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Amido/ureidosubstituted benzenesulfonamides-isatin conjugates as low nanomolar/subnanomolar inhibitors of the tumor-associated carbonic anhydrase isoform XII
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Isatin-β-thiocarbohydrazones: Microwave-assisted synthesis, antitumor activity and structure-activity relationship
inferredcites →https://doi.org/10.1016/j.tet.2007.01.059openalex-snapshot
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Phase I clinical trial of nintedanib plus paclitaxel in early HER-2-negative breast cancer (CNIO-BR-01-2010/GEICAM-2010-10 study)
inferredcites →https://doi.org/10.1038/nrd1984openalex-snapshot
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inferredcites →https://doi.org/10.1073/pnas.94.7.2776openalex-snapshot
The cell cycle and cancer
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The potential role of nintedanib in treating colorectal cancer
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Synthesis and in vitro anti-proliferative activity of some novel isatins conjugated with quinazoline/phthalazine hydrazines against triple-negative breast cancer MDA-MB-231 cells as apoptosis-inducing agents
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One-pot three-component synthesis of novel spirooxindoles with potential cytotoxic activity against triple-negative breast cancer MDA-MB-231 cells
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Epithelioid cell cultures from rat small intestine. Characterization by morphologic and immunologic criteria.
inferredcites →https://doi.org/10.1158/1078-0432.ccr-06-2328openalex-snapshot
Approval Summary: Sunitinib for the Treatment of Imatinib Refractory or Intolerant Gastrointestinal Stromal Tumors and Advanced Renal Cell Carcinoma
inferredcites →https://doi.org/10.1248/bpb.24.1149openalex-snapshot
Synthesis and Pharmacological Activities of Hydrazones, Schiff and Mannich Bases of Isatin Derivatives.
inferredcites →https://doi.org/10.1371/journal.pone.0181241openalex-snapshot
New hydrazonoindolin-2-ones: Synthesis, exploration of the possible anti-proliferative mechanism of action and encapsulation into PLGA microspheres
inferredcites →https://doi.org/10.2147/dddt.s140164openalex-snapshot
Isatin-benzoazine molecular hybrids as potential antiproliferative agents: synthesis and in vitro pharmacological profiling
inferredcites →https://doi.org/10.2174/138161210791033914openalex-snapshot
Cell Cycle as a Target of Antineoplastic Drugs
inferredcites →https://doi.org/10.3390/molecules20058800openalex-snapshot
Design, Synthesis and Antitubercular Activity of Certain Nicotinic Acid Hydrazides
inferredcites →https://doi.org/10.3390/molecules21060762openalex-snapshot
Synthesis and Cytotoxic Activity of Biphenylurea Derivatives Containing Indolin-2-one Moieties
inferredcites →https://doi.org/10.3390/molecules22040659openalex-snapshot
Synthesis, Biological Evaluation, and Molecular Docking Studies of Novel Isatin-Thiazole Derivatives as α-Glucosidase Inhibitors
inferredcites →https://doi.org/10.3390/molecules22111958openalex-snapshot
Synthesis, Spectroscopic Characterization and Antimicrobial Potential of Certain New Isatin-Indole Molecular Hybrids
inferredcites →https://doi.org/10.4172/2161-0444.1000179openalex-snapshot
Isatins: A Diversity Orientated Biological Profile

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Incoming claims: where this work appears in other papers’ reference lists and arguments.

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TCS-isatin-INH triads as potent and selective anti-mycobacterial with high efficacy against Mycobacterium tuberculosis
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Enhancement of the tail hydrophobic interactions within the carbonic anhydrase IX active site via structural extension: Design and synthesis of novel N-substituted isatins-SLC-0111 hybrids as carbonic anhydrase inhibitors and antitumor agents
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