A
Ashish Jain
Researcher at Indira Gandhi Centre for Atomic Research
Publications - 61
Citations - 699
Ashish Jain is an academic researcher from Indira Gandhi Centre for Atomic Research. The author has contributed to research in topics: Enthalpy & Boron. The author has an hindex of 15, co-authored 57 publications receiving 613 citations. Previous affiliations of Ashish Jain include Central Drug Research Institute.
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Synergistic chemoprotective mechanisms of dietary phytoestrogens in a select combination against prostate cancer
TL;DR: The findings suggest that selectively combining anticancer phytoestrogens could significantly increase the efficacy of individual components resulting in improved efficacy at physiologically achievable concentrations.
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Kinetics of oxidation of boron powder
TL;DR: In this article, the authors studied the kinetics of the oxidation of electrodeposited boron powder and the borton powder produced by the reduction process using thermogravimetry (TG).
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Studies on the ignition behaviour of boron powder
TL;DR: In this paper, the ignition behavior of boron powder, prepared through electrowinning process, was studied by using thermogravimetry coupled with simultaneous differential thermal analysis (TG-SDTA).
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Imidazole derivatives as possible microbicides with dual protection.
Lalit Kumar,Amit Sarswat,Nand Lal,Vishnu L. Sharma,Ashish Jain,Rajeev Kumar,Vikas Verma,Jagdamba P. Maikhuri,Awanit Kumar,Praveen K. Shukla,Gopal Gupta +10 more
TL;DR: It is concluded that introduction of the pharmacophore responsible for spermicidal activity into a proven anti-trichomonas structure may lead to a potent dual function microbicide better and safer than N-9.
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Carbodithioic acid esters of fluoxetine, a novel class of dual-function spermicides ☆
S.T.V.S. Kiran Kumar,Lalit Kumar,Vishnu L. Sharma,Ashish Jain,Rajeev K. Jain,Jagdamba P. Maikhuri,Manish Kumar,Praveen K. Shukla,Gopal Gupta +8 more
TL;DR: The study revealed that incorporation of carbodithioic acid residue directly into fluoxetine structure leads to compounds with better antifungal and anti-Trichomonas activities, and N-methyl-[3-phenyl-3-(4-trifluoromethyl-phenoxy)-propyl]carbodithIOic acid S-(2-pyrrolidino-ethyl) ester (14) has shown better profile than both fluoxettine