Raj Kumar

Prof. Raj Kumar

orcid

Research Focus & Metrics

Academic Career Length

16Years (2011-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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22 February 2021 in Journal of Medicinal Chemistry
Verified
Journal Article
Closed access
PBPriyadeep Bhutani
Priyadeep Bhutani
GJGaurav Joshi
Gaurav Joshi
NRNivethitha Raja
Nivethitha Raja
NBNamrata Bachhav
Namrata Bachhav
PRPrabhakar K. Rajanna
Prabhakar K. Rajanna
RKRaj Kumar
Raj Kumar

3 July 2017 in Medicinal Research Reviews
Verified
Journal Article
Closed access
PDF file
RKRaj Kumar
Raj Kumar
GJGaurav Joshi
Gaurav Joshi
HKHarveen Kler
Harveen Kler
SKSourav Kalra
Sourav Kalra
MKManpreet Kaur
Manpreet Kaur
RARamandeep Arya
Ramandeep Arya

7 April 2022 in Journal of Molecular Structure
Verified
Journal Article
Closed access
MKMadhurendra K. Katiyar
Madhurendra K. Katiyar
GDGovind Kumar Dhakad
Govind Kumar Dhakad
SHShivani
Shivani
SASahil Arora
Sahil Arora
SBSrikant Bhagat
Srikant Bhagat
RKRaj Kumar
Raj Kumar

21 April 2011 in Expert Opinion on Therapeutic Patents
Verified
Journal Article
Closed access
RKRaj Kumar
Raj Kumar
DADarpan
Darpan
Sahil SharmaSahil Sharma
Sahil Sharma
RSRajveer Singh
Rajveer Singh
(2011). Xanthine oxidase inhibitors: a patent survey. Expert Opinion on Therapeutic Patents: Vol. 21, No. 7, pp. 1071-1108. doi: 10.1517/13543776.2011.577417

1 July 2013 in Journal of Enzyme Inhibition and Medicinal Chemistry
Verified
Journal Article
Closed access
JAJimi Marin Alex
Jimi Marin Alex
RKRaj Kumar
Raj Kumar
Pyrazoles, categorized as nitrogen-containing heterocycles, are well known for their interminable participation in the field of perpetual research and development of therapeutical active agents. As a consequence pyrazoles became an inevitable core of numerous drugs having diverse activities. The broad spectrum of activities portrayed by the pyrazoles instigated the researchers to modify the pyrazole ring as 4,5-dihydro-1H-pyrazoles commonly known as 2-pyrazolines. The present review is a concerted effort to retrace compounds covered from 2009-till date which owe diverse biological activities to the 2-pyrazoline scaffold and also condenses the retro-synthetic approaches employed for their synthesis. This endeavor culminated in revelation that inhibitory potential varied when the substituents in particular N-substituents of 2-pyrazolines were altered.

1 December 2017 in European Journal of Medicinal Chemistry
Verified
Journal Article
Closed access
SKSourav Kalra
Sourav Kalra
GJGaurav Joshi
Gaurav Joshi
AMAnjana Munshi
Anjana Munshi
RKRaj Kumar
Raj Kumar