BS
Bharvi Sharma
Poseida Therapeutics (United States), AxisPharm, Guru Nanak Dev University, Khalsa College for Women
About
Bharvi Sharma is a researcher specializing in synthetic organic chemistry, Lipid Chemistry, click chemistry, mRNA delivery, medicinal chemistry, and bioconjugation. Her research interests focus on the development and application of innovative chemical strategies for biologically relevant molecules and therapeutic applications. Her current research interests include advanced click reactions, bioconjugation chemistry, ADCs, LNPs and the development of chemical tools for biomedical applications.
Employment
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Poseida Therapeutics (United States) Research Scientist2024 - 2026
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AxisPharm Scientist -I2022 - 2024
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Khalsa College for Women Assistant professor2015 - 2016
Education
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Guru Nanak Dev University M.S. (Honors School)2013 - 2015
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Guru Nanak Dev University B.S. (Honors School) Chemistry2010 - 2013
Projects & Funding
Projects & funding information is unavailable.
Publications (10)
- Designing quinoline-isoniazid hybrids as potent anti-tubercular agents inhibiting mycolic acid biosynthesis Save
- Functionalized 3-hydroxy-3-aminoquinoline-oxindole hybrids as promising dual-function anti-plasmodials Save
- Has Ferrocene Really Delivered Its Role in Accentuating the Bioactivity of Organic Scaffolds? Save
- 1 H ‐1,2,3‐triazole embedded Isatin‐Benzaldehyde‐bis(heteronuclearhydrazones): design, synthesis, antimycobacterial, and cytotoxic evaluation Save
- Recent accomplishments on the synthetic/biological facets of pharmacologically active 1H-1,2,3-triazoles Save
- Design, Synthesis, Antiproliferative Evaluation, and Molecular Docking Studies of N-(3-Hydroxyindole)-Appended β-Carbolines/Tetrahydro-β-Carbolines Targeting Triple-Negative and Non-Triple-Negative Breast Cancer Save
- Synthesis, anti-plasmodial and cytotoxic evaluation of 1H-1,2,3-triazole/acyl hydrazide integrated tetrahydro-β-carboline-4-aminoquinoline conjugates Save
- Design, synthesis, and anti-proliferative evaluation of 1H-1,2,3-triazole grafted tetrahydro-β-carboline-chalcone/ferrocenylchalcone conjugates in estrogen responsive and triple negative breast cancer cells Save
- Diastereoselective approach to rationally design tetrahydro-β-carboline–isatin conjugates as potential SERMs against breast cancer Save
- β -Lactam-Synthon Interceded Diastereoselective Synthesis of 2-Azido-γ -amino Alcohols with Subsequent Transformations to Functionally Enriched Heterocycles Save