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Letters in Drug Design and Discovery, ISSN 1570-1808, 2016, Volume 13, Issue 1, pp. 64 - 76
A series of 6,7-disubstituted-3-{2-[4-(substituted) piperazin-1-yl]-2-oxoethyl}quinazoline-2,4(1H, 3H)-dione derivatives (7-34) were synthesized and their... 
Cytotoxicity | Sulforhodamine B method | Quinazoline | Anticancer | Quinazoline-2,4(1H,3H)-dione | Piperazine | SUBSTITUTED QUINAZOLINEDIONES | DESIGN | CHEMISTRY, MEDICINAL | AMPA | PROTEIN | piperazine | sulforhodamine B method | ANTICONVULSANT | anticancer | QUINAZOLINE-2,4-DIONE | IN-VITRO | DNA GYRASE | INHIBITORS | TOPOISOMERASE-IV | cytotoxicity | quinazoline-2,4(1H,3H)-dione
Journal Article
1996, The chemistry of heterocyclic compounds, ISBN 0471145653, Volume 55., xx, 736
Book
Book
Tetrahedron Letters, ISSN 0040-4039, 10/2019, Volume 60, Issue 44, p. 151186
An alternative green protocol and step economy for the synthesis of quinazoline has been developed. The reaction of readily available 2-aminobenzonitriles with... 
Water | Isothiocyanate | Quinazoline | Base
Journal Article
Phosphorus, Sulfur, and Silicon and the Related Elements, ISSN 1042-6507, 11/2017, Volume 192, Issue 11, pp. 1165 - 1170
Journal Article
Journal Article
Journal Article
European Journal of Medicinal Chemistry, ISSN 0223-5234, 08/2016, Volume 118, pp. 276 - 289
Three series of novel quinazoline and pyrido[2,3- ]pyrimidine derivatives were designed, synthesized and evaluated for their ability to inhibit EGFR tyrosine... 
Molecular dynamics simulation | Quinazoline and pyrido[2,3-d]pyrimidine derivatives | EGFR inhibitor | Molecular docking | Antitumor | Quinazoline and pyrido[2,3-d]pyrimidine | derivatives | CHEMISTRY, MEDICINAL | PARTICLE MESH EWALD | DISCOVERY | LAPATINIB | BREAST-CANCER CELLS | THERAPY | AMBER | ZD1839 IRESSA | DYNAMICS | TYROSINE KINASE INHIBITOR | AGENTS | Quinazolines - chemical synthesis | Pyrimidines - chemical synthesis | Antineoplastic Agents - chemical synthesis | Humans | Structure-Activity Relationship | Pyrimidines - chemistry | Pyrimidines - metabolism | Antineoplastic Agents - metabolism | Protein Kinase Inhibitors - chemistry | Receptor, Epidermal Growth Factor - metabolism | Quinazolines - metabolism | Drug Design | Antineoplastic Agents - pharmacology | Quinazolines - chemistry | Protein Kinase Inhibitors - chemical synthesis | Chemistry Techniques, Synthetic | Pyrimidines - pharmacology | Antineoplastic Agents - chemistry | Receptor, Epidermal Growth Factor - chemistry | Cell Line, Tumor | Receptor, Epidermal Growth Factor - antagonists & inhibitors | Protein Conformation | Cell Proliferation - drug effects | Molecular Docking Simulation | Protein Kinase Inhibitors - pharmacology | Quinazolines - pharmacology | Drug Screening Assays, Antitumor | Protein Kinase Inhibitors - metabolism | Tyrosine | Molecular dynamics | Pyrimidines | Models | Epidermal growth factor | Tumors
Journal Article
by Zhang, JT and Zhu, DP and Yu, CM and Wan, CF and Wang, ZY
ORGANIC LETTERS, ISSN 1523-7060, 06/2010, Volume 12, Issue 12, pp. 2841 - 2843
A facile and novel approach to the synthesis of 2-phenylquinazolines was developed via a tandem reaction following sp(3) C-H functionalization. Twenty-five... 
CHEMISTRY, ORGANIC | QUINOLINE | QUINAZOLINE | ACRIDONE ALKALOIDS | BONDS
Journal Article
Asian Journal of Chemistry, ISSN 0970-7077, 07/2015, Volume 27, Issue 7, pp. 2460 - 2462
Journal Article
Russian Journal of Organic Chemistry, ISSN 1070-4280, 6/2019, Volume 55, Issue 6, pp. 748 - 754
Journal Article
Chemical Biology & Drug Design, ISSN 1747-0277, 07/2016, Volume 88, Issue 1, pp. 88 - 96
Journal Article
Tetrahedron Letters, ISSN 0040-4039, 12/2015, Volume 56, Issue 49, pp. 6882 - 6885
The amination of quinazoline-based heterocyclics is of significant interest due to its privileged structure and application in the development of bioactive... 
Urea | Quinazoline | Amination | Azide
Journal Article
European Journal of Medicinal Chemistry, ISSN 0223-5234, 06/2014, Volume 80, pp. 447 - 501
Journal Article
Journal of Clinical Oncology, ISSN 0732-183X, 09/2013, Volume 31, Issue 27, pp. 3327 - 3334
Journal Article
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