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Kartik Temburnikar

Researcher at University of Maryland, Baltimore County

Publications -  12
Citations -  234

Kartik Temburnikar is an academic researcher from University of Maryland, Baltimore County. The author has contributed to research in topics: Cell cycle checkpoint & Prodrug. The author has an hindex of 8, co-authored 11 publications receiving 194 citations. Previous affiliations of Kartik Temburnikar include Arizona State University & Johns Hopkins University School of Medicine.

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Evaluating TNA stability under simulated physiological conditions

TL;DR: It is shown that TNA remains undigested after 7days of incubation in the presence of either 50% human serum or human liver microsomes and is stable against snake venom phosphordiesterase and protected from nuclease digestion and complementary RNA strands from RNA degrading enzymes.
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Recent advances in synthetic approaches for medicinal chemistry of C-nucleosides.

TL;DR: Recent reports on the modular synthesis of C-nucleosides with a focus on D-ribonolactone and sugar modifications that have resulted in potent lead molecules are described.
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1-[2-(2-Benzoyl- and 2-benzylphenoxy)ethyl]uracils as potent anti-HIV-1 agents.

TL;DR: Evaluation revealed that the inhibitors were active against most nevirapine-resistant mono- and di-substituted RTs with the exception of the V106A RT, and can be regarded as potential lead compounds against the wild-type virus and drug-resistant forms.
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Antiproliferative activities of halogenated thieno[3,2-d]pyrimidines

TL;DR: The in vitro evaluation of thieno[3,2-d]pyrimidines identified halogenated compounds 1 and 2 with antiproliferative activity against three different cancer cell lines and the necessity of the chlorine at the C4-position for biological activity was indicated.
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Recognition of Artificial Nucleobases by E. coli Purine Nucleoside Phosphorylase versus its Ser90Ala Mutant in the Synthesis of Base-Modified Nucleosides.

TL;DR: It was found that the Ser90 residue of the PNP plays an important role in the binding and activation of 8-aza-7-deazapurines in the synthesis of their nucleosides and in the dephosphorylation of intermediary formed 2- deoxy-α-D-ribofuranose-1-phosphate in the trans-2-deoxyribosylation reaction.