Synthesis of Pyrrolo[2,3-d]Pytimidines and Pytimido[4,5-b]Indoles as Inhibitors of Multiple Receptor Tyrosine Kinases, Folate Metabolizing Enzymes and Tubulin
Defense Date
10-19-2009
Graduation Date
Fall 1-1-2009
Availability
Immediate Access
Submission Type
dissertation
Degree Name
PhD
Department
Medicinal Chemistry
School
School of Pharmacy
Committee Chair
Aleem Gangjee
Committee Member
Marc W Harrold
Committee Member
Patrick T Flaherty
Committee Member
David J Lapinsky
Committee Member
David A Johnson
Committee Member
J. Douglas Bricker
Keywords
Antifolate, Antitubulin, pyrimido[4, 5-b]indoles, pyrrolo[2, 3-d]pyrimidines, Receptor tyrosine kinase
Abstract
This dissertation deals with the synthesis of substituted pyrrolo[2,3-d]pyrimidines and pyrimido[4,5-b]indoles as potential antitumor agents. The approaches to target tumor cells include inhibition of tumor induced angiogenesis via multiple receptor tyrosine kinase (RTK) inhibition (or) inhibition of the folate metabolizing enzymes - dihydrofolate reductase (DHFR) or thymidylate synthase (TS) (or) inhibition of tubulin.
Format
Language
English
Recommended Citation
Zaware, N. (2009). Synthesis of Pyrrolo[2,3-d]Pytimidines and Pytimido[4,5-b]Indoles as Inhibitors of Multiple Receptor Tyrosine Kinases, Folate Metabolizing Enzymes and Tubulin (Doctoral dissertation, Duquesne University). Retrieved from https://dsc.duq.edu/etd/1539