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Synthesis and biological evaluation of 3,5-diaryl isoxazoline/isoxazole linked 2,3-dihydroquinazolinone hybrids as anticancer agents
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Every reference with a DOI in the deposited reference list resolved to a known work in Crossref or DataCite at the dated check, and none carried a retraction, withdrawal, or removal notice.
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The 26 checked references that resolve
resolves10.1016/j.tet.2006.07.098
The chemistry of recently isolated naturally occurring quinazolinone alkaloids
resolves10.1021/jm00073a024
A potent, orally active, balanced affinity angiotensin II AT1 antagonist and AT2 binding inhibitor
resolves10.1016/S0960-894X(98)00047-X
Nonpeptide glycoprotein IIb/IIIa inhibitors: Substituted quinazolinediones and quinazolinones as potent fibrinogen receptor antagonists
resolves10.1021/cc000113e
A Polymer-Bound Iminophosphorane Approach for the Synthesis of Quinazolines
resolves10.1021/cc000017d
Combinatorial Synthesis of Heterocycles: Solid-Phase Synthesis of 2-Amino-4(1<i>H</i>)-quinazolinone Derivatives
resolves10.1016/0223-5234(87)90015-8
Synthesis of substituted 2,3-dihydro-1-(β-phenylethyl)-2-aryl and 2,3-diaryl-4(1H)-quinazolinones and their pharmacological activities
resolves10.1021/jm000151c
6-Alkylamino- and 2,3-Dihydro-3‘-methoxy-2-phenyl-4-quinazolinones and Related Compounds: Their Synthesis, Cytotoxicity, and Inhibition of Tubulin Polymerization
resolves10.1021/jm00315a010
Substituted 2,3-Dihydro-4(1H)-quinazolinones. A New Class of Inhibitors of Cell Multiplication
resolves10.1021/bi00443a031
Antimitotic natural products combretastatin A-4 and combretastatin A-2: studies on the mechanism of their inhibition of the binding of colchicine to tubulin
resolves10.1021/jm00112a036
Synthesis and evaluation of stilbene and dihydrostilbene derivatives as potential anticancer agents that inhibit tubulin polymerization
resolves10.1021/jm00090a021
Synthesis and evaluation of analogs of (Z)-1-(4-methoxyphenyl)-2-(3,4,5-trimethoxyphenyl)ethene as potential cytotoxic and antimitotic agents
resolves10.1021/jm010523x
Potent, Orally Active Heterocycle-Based Combretastatin A-4 Analogues: Synthesis, Structure−Activity Relationship, Pharmacokinetics, and In Vivo Antitumor Activity Evaluation
resolves10.1021/jm049622b
Heterocyclic and Phenyl Double-Bond-Locked Combretastatin Analogues Possessing Potent Apoptosis-Inducing Activity in HL60 and in MDR Cell Lines
resolves10.1016/j.bmc.2006.02.001
Isoxazole-type derivatives related to combretastatin A-4, synthesis and biological evaluation
resolves10.1111/j.1747-0285.2007.00609.x
Synthesis, Structural Characterization and Biological Evaluation of Novel [1,2,4]triazolo [1,5‐<i>b</i>][1,2,4]benzothiadiazine‐benzothiazole Conjugates as Potential Anticancer Agents
resolves10.1016/j.bmc.2008.01.040
Phosphonate-linked pyrrolo[2,1-c][1,4]benzodiazepine conjugates: Synthesis, DNA-binding affinity and cytotoxicity
resolves10.1016/j.bmc.2009.12.015
Quinazolinone linked pyrrolo[2,1-c][1,4]benzodiazepine (PBD) conjugates: Design, synthesis and biological evaluation as potential anticancer agents
resolves10.1016/j.ejmech.2010.01.054
Synthesis and potential cytotoxic activity of new phenanthrylphenol-pyrrolobenzodiazepines
resolves10.1016/S0002-9440(10)63398-6
The Tubulin-Binding Agent Combretastatin A-4-Phosphate Arrests Endothelial Cells in Mitosis and Induces Mitotic Cell Death
resolves10.1016/S0021-9258(18)53096-9
G2 delay induced by nitrogen mustard in human cells affects cyclin A/cdk2 and cyclin B1/cdc2-kinase complexes differently.
resolves10.1038/sj.cr.7290210
LIGHT sensitizes IFNγ–mediated apoptosis of HT-29 human carcinoma cells through both death receptor and mitochondria pathways
The 3 references without a DOI — listed, not checked
no DOI — not checked10.1016/j.ejmech.2010.12.004_bib3
no DOI — not checked10.1016/j.ejmech.2010.12.004_bib11
no DOI — not checked10.1016/j.ejmech.2010.12.004_bib13
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