Synthesis, Structure−Activity Relationship, and Biological Studies of Indolocarbazoles as Potent Cyclin D1-CDK4 Inhibitors

scientific article published on May 22, 2003

Synthesis, Structure−Activity Relationship, and Biological Studies of Indolocarbazoles as Potent Cyclin D1-CDK4 Inhibitors is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1021/JM0256169
P953full work available at URLhttps://pubs.acs.org/doi/pdf/10.1021/jm0256169
P698PubMed publication ID12747775

P2093author name stringRichard M. Schultz
Chuan Shih
Guoxin Zhu
Xun Zhou
Beverly Teicher
Bharvin Patel
Cathy Ogg
Eileen Considine
Margaret M. Faul
Robert Morris Campbell
Tiechao Li
Bryan D. Anderson
Charles D. Spencer
Harold B. Brooks
Jack A. Dempsey
Scott A. Watkins
Scott E. Conner
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Cell cycle control and cancerQ29617536
Four-dimensional control of the cell cycleQ33772655
Pharmacological inhibitors of cyclin-dependent kinasesQ34866778
Inhibition of cyclin-dependent kinase 2 by p21 is necessary for retinoblastoma protein-mediated G1 arrest after gamma-irradiationQ34946238
Regulation of transcription by proteins that control the cell cycleQ40882566
Purification, characterization, and kinetic mechanism of cyclin D1. CDK4, a major target for cell cycle regulationQ41005486
Phase I trial of continuous infusion flavopiridol, a novel cyclin-dependent kinase inhibitor, in patients with refractory neoplasms.Q52184569
P433issue11
P407language of work or nameEnglishQ1860
P921main subjectmolecular medicineQ3523816
proto-oncogene proteinQ66020913
P304page(s)2027-2030
P577publication date2003-05-01
2003-05-22
P1433published inJournal of Medicinal ChemistryQ900316
P1476titleSynthesis, structure-activity relationship, and biological studies of indolocarbazoles as potent cyclin D1-CDK4 inhibitors
Synthesis, Structure−Activity Relationship, and Biological Studies of Indolocarbazoles as Potent Cyclin D1-CDK4 Inhibitors
P478volume46

Reverse relations

cites work (P2860)
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