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Awantika Singh

Researcher at Central Drug Research Institute

Publications -  39
Citations -  793

Awantika Singh is an academic researcher from Central Drug Research Institute. The author has contributed to research in topics: Mass spectrometry & High-performance liquid chromatography. The author has an hindex of 16, co-authored 38 publications receiving 558 citations. Previous affiliations of Awantika Singh include Academy of Scientific and Innovative Research.

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Identification and characterization of phenolics and terpenoids from ethanolic extracts of Phyllanthus species by HPLC-ESI-QTOF-MS/MS

TL;DR: This method was developed using high-pressure liquid chromatography coupled with quadrupole time-of-flight tandem mass spectrometry for the identification and characterization of quercetin, kaempferol, ellagic acid and their derivatives in ethanolic extracts of Phyllanthus species.
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Rapid qualitative and quantitative analysis of bioactive compounds from Phyllanthus amarus using LC/MS/MS techniques

TL;DR: In this article, the authors developed a method for rapid screening of phytochemicals using high-pressure liquid chromatography hyphenated with quadrupole time-of-flight mass spectrometer (HPLC/ESI-QTOF-MS/MS).
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Analysis of phytochemical variations in dioecious Tinospora cordifolia stems using HPLC/QTOF MS/MS and UPLC/QqQLIT -MS/MS.

TL;DR: Phytochemicals in the stem of male and female Tinospora cordifolia showed significant qualitative and quantitative variations and LC-MS and MS/MS methods can be used to differentiate between male andFemale plants based on their chemical profiles and quantities of the marker bioactive alkaloids.
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Structural characterization of monoterpene indole alkaloids in ethanolic extracts of Rauwolfia species by liquid chromatography with quadrupole time-of-flight mass spectrometry.

TL;DR: An efficient and reliable liquid chromatography-tandem mass spectrometry (LC–MS/MS) method for ethanolic root extract of Rauwolfia species is developed to elucidate the fragmentation pathways for dereplication of bioactive MIAs.