User profiles for Aleem Gangjee
Aleem Gangjeeprofessor medicinal chemistry Verified email at duq.edu Cited by 1365 |
Design and Synthesis of Classical and Nonclassical 6-Arylthio-2,4-diamino-5-ethylpyrrolo[2,3-d]pyrimidines as Antifolates
A Gangjee, Y Zeng, T Talreja, JJ McGuire… - Journal of medicinal …, 2007 - ACS Publications
The classical antifolate N-{4-[(2,4-diamino-5-ethyl-7H-pyrrolo[2,3-d]pyrimidin-6-yl)sulfanyl]benzoyl}-l-glutamic
acid (2) and 15 nonclassical analogues (3−17) were synthesized as …
acid (2) and 15 nonclassical analogues (3−17) were synthesized as …
Classical and nonclassical furo [2, 3-d] pyrimidines as novel antifolates: synthesis and biological activities
A Gangjee, R Devraj, JJ McGuire… - Journal of medicinal …, 1994 - ACS Publications
Classical antifolate analogues containing a novel furo [2, 3-d] pyrimidine ring system which
include 2V-[4-[N-[(2, 4-diaminofuro [2, 3-d] pyrimidin-5-yl) methyl] amino] benzoyl]-L-glutamic …
include 2V-[4-[N-[(2, 4-diaminofuro [2, 3-d] pyrimidin-5-yl) methyl] amino] benzoyl]-L-glutamic …
Effect of bridge region variation on antifolate and antitumor activity of classical 5-substituted 2, 4-diaminofuro [2, 3-d] pyrimidines
A Gangjee, R Devraj, JJ McGuire… - Journal of medicinal …, 1995 - ACS Publications
Variation of the bridge linking the heterocyclic ring and p-aminobenzoyl-L-glutamate
portions of our previously descibed classical2, 4-diaminofuro [2, 3-d] pyrimidines 1 and 2 are …
portions of our previously descibed classical2, 4-diaminofuro [2, 3-d] pyrimidines 1 and 2 are …
Targeting the proton-coupled folate transporter for selective delivery of 6-substituted pyrrolo [2, 3-d] pyrimidine antifolate inhibitors of de novo purine biosynthesis in …
…, MH Chang, MF Romero, C Cherian, A Gangjee… - Molecular …, 2010 - ASPET
The proton-coupled folate transporter (PCFT) is a folate-proton symporter with an acidic pH
optimum, approximating the microenvironments of solid tumors. We tested 6-substituted …
optimum, approximating the microenvironments of solid tumors. We tested 6-substituted …
Design, synthesis, and X-ray crystal structures of 2, 4-diaminofuro [2, 3-d] pyrimidines as multireceptor tyrosine kinase and dihydrofolate reductase inhibitors
A Gangjee, W Li, L Lin, Y Zeng, M Ihnat… - Bioorganic & medicinal …, 2009 - Elsevier
To optimize dual receptor tyrosine kinase (RTK) and dihydrofolate reductase (DHFR)
inhibition, the E- and Z-isomers of 5-[2-(2-methoxyphenyl)prop-1-en-1-yl]furo[2,3-d]pyrimidine-2,4-…
inhibition, the E- and Z-isomers of 5-[2-(2-methoxyphenyl)prop-1-en-1-yl]furo[2,3-d]pyrimidine-2,4-…
The human proton-coupled folate transporter: Biology and therapeutic applications to cancer
This review summarizes the biology of the proton-coupled folate transporter (PCFT). PCFT
was identified in 2006 as the primary transporter for intestinal absorption of dietary folates, as …
was identified in 2006 as the primary transporter for intestinal absorption of dietary folates, as …
2,4-Diamino-5-deaza-6-Substituted Pyrido[2,3-d]pyrimidine Antifolates as Potent and Selective Nonclassical Inhibitors of Dihydrofolate Reductases
A Gangjee, A Vasudevan, SF Queener… - Journal of medicinal …, 1996 - ACS Publications
Fifteen novel nonclassical and two classical 2,4-diamino-6-(benzylamino)pyrido[2,3-d]pyrimidine
antifolates were synthesized as potential inhibitors of Pneumocystis carinii, (pc) …
antifolates were synthesized as potential inhibitors of Pneumocystis carinii, (pc) …
Pneumocystis carinii and Toxoplasma gondii Dihydrofolate Reductase Inhibitors and Antitumor Agents: Synthesis and Biological Activities of 2,4-Diamino-5-methyl-6 …
A Gangjee, O Adair, SF Queener - Journal of medicinal chemistry, 1999 - ACS Publications
Thirteen 2,4-diamino-5-methyl-6-[(monosubstituted anilino)methyl]pyrido[2,3-d]pyrimidines 5−17
were synthesized as potential Pneumocystis carinii (pc) and Toxoplasma gondii (tg) …
were synthesized as potential Pneumocystis carinii (pc) and Toxoplasma gondii (tg) …
Synthesis and Biological Activity of a Novel Series of 6-Substituted Thieno[2,3-d]pyrimidine Antifolate Inhibitors of Purine Biosynthesis with Selectivity for High Affinity Folate …
…, Z Hou, LH Matherly, A Gangjee - Journal of medicinal …, 2009 - ACS Publications
A series of seven 2-amino-4-oxo-6-substituted thieno[2,3-d]pyrimidines with bridge length
variations (from 2 to 8 carbon atoms) were synthesized as selective folate receptor (FR) α and …
variations (from 2 to 8 carbon atoms) were synthesized as selective folate receptor (FR) α and …
Synthesis and discovery of high affinity folate receptor-specific glycinamide ribonucleotide formyltransferase inhibitors with antitumor activity
…, Z Hou, SA Buck, LH Matherly, A Gangjee - Journal of medicinal …, 2008 - ACS Publications
6-Substituted classical pyrrolo[2,3-d]pyrimidine antifolates with a three- to six-carbon bridge
between the heterocycle and the benzoyl-l-glutamate (compounds 2−5, respectively) were …
between the heterocycle and the benzoyl-l-glutamate (compounds 2−5, respectively) were …