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Rohit Srivastava

Researcher at Central Drug Research Institute

Publications -  27
Citations -  539

Rohit Srivastava is an academic researcher from Central Drug Research Institute. The author has contributed to research in topics: Glucose uptake & Insulin. The author has an hindex of 10, co-authored 25 publications receiving 472 citations. Previous affiliations of Rohit Srivastava include Hebrew University of Jerusalem.

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Synthesis and bioevaluation of glycosyl ureas as α-glucosidase inhibitors and their effect on mycobacterium

TL;DR: Glycosyl amino esters on reaction with different isocyanates resulted in quantitative conversion to glycosyl ureas, which exhibited marginal antitubercular activity against Mycobacterium aurum and alpha-glucosidase.
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miR-135a targets IRS2 and regulates insulin signaling and glucose uptake in the diabetic gastrocnemius skeletal muscle.

TL;DR: In-vivo silencing of miR-135a alleviated hyperglycemia, improved glucose tolerance and significantly restored the levels of IRS2 and p-Akt in the gastrocnemius skeletal muscle of db/db mice without any effect on their hepatic levels, suggesting that miR -135a targets IRS2 levels by binding to its 3'UTR and this interaction regulates skeletal muscle insulin signaling.
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Synthesis of glycosylated β-amino acids as new class of antitubercular agents

TL;DR: Though most of the compounds exhibited little activity, however, one showed significant activity against all the strains in cell culture and activity was confirmed by B actec method.
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Elevated hepatic miR-22-3p expression impairs gluconeogenesis by silencing the Wnt-responsive transcription factor, Tcf7

TL;DR: A novel link between elevated hepatic miR-22-3p expression and impaired gluconeogenesis in diabetic db/db mice via the regulation of Tcf7 is unraveled via microRNA-mediated regulation of TCF7, and this microRNAs increases the expression of enzymes of the gluconeogenic pathway in HepG2 cells.
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Synthesis and antimycobacterial activity of 3,5-disubstituted thiadiazine thiones

TL;DR: A series of 3,5-disubstituted thiadiazine thiones synthesized by reaction of primary amines with carbon disulphide followed by cyclocondensation of the resulting intermediate with formaldehyde and primary amine or amino acids showed antimycobacterial activity in vitro and exhibited activity in vivo.