Gangadhar J. Sanjayan
Also known as: Sanjayan, Sanjayan G J
National Chemical Laboratory, Banaras Hindu University, University of Kerala
About
After completing his PhD studies in heterocyclic chemistry from Banaras Hindu University (advisor: Prof. A.K. Mukherjee), Sanjayan joined the group of Prof. K. N. Ganesh (CSIR-National Chemical Laboratory, NCL-Pune, India) for his first stint of post-doctoral studies (peptide nucleic acids & molecular self-assembly). Later, he moved to the University of Oxford, UK, to work with Prof. George. W. J. Fleet (carbohydrates & peptidomimetics).
Sanjayan is leading a group of synthetic chemists at National Chemical Laboratory, Pune, India - working on various projects including molecular recognition and self-assembly, medical chemistry, and peptides / peptidomimetics, We apply our skill and knowledge of synthetic organic chemistry to create novel molecules with potential applications in polymer/material chemistry and medicinal and. Our research interests lie primarily in the area of supramolecular chemistry, peptide chemistry, medicinal chemistry, and methodology/process development. We are developing diverse classes of self-assembling systems and investigating their application potential in polymer/material science. In medicinal chemistry, we apply our focus on anticancer drug development – and lately SARS-CoV-2 drug discovery as well. We have more than two decades of extensive experience in developing synthetic amino acids, peptides and their mimetics and their incorporation into bioactive peptides to modulate bioactivity. We also work on synthetic methodology and process development.
Visit our research group website to learn more about our research activities: https://gjsanjayan.wixsite.com/csir-ncl
Employment
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National Chemical Laboratory Chief Scientist & AcSIR Professor of Chemistry
Education
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Banaras Hindu University Ph.D? - 1994
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Banaras Hindu University M.Sc? - 1990
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University of Kerala B.Sc? - 1988
Projects & Funding
Projects & funding information is unavailable.
Publications (62)
- Dynamic Janus Hydrogen Bond Mimicry Unlocks Tough, Flexible Supramolecular Elastomers for Strain Sensing Save
- Photolabile-Protected Triazine-Based Janus G-C and Triple G-C-T Base-Coded Nucleobases for Supramolecular Polymer Construction Save
- Repurposed ciprofloxacin derivatives as potent autophagic-type anticancer agents Save
- Triple G–C–T Base-Coded Nucleobase Self-Assembling Monomers Featuring Polymerizable Groups for 3D Printing Save
- Morphology Rearrangement by Mixing of Internally Hydrogen-Bonded Nanoparticles Comprising Triazine-Based Amphiphilic Diblock Copolymers Save
- Triple G-C-T Base-Coded Self-Assembling Water-Soluble Nucleobase Monomers with a Broad Scope for Biomaterial and Protein Bioconjugation Applications Save
- Synthesis and Film Formation of Aqueous Emulsion Polymer Latexes Featuring Hydrogen Bonding via a Janus Guanine-Cytosine Base Monomer Save
- Block Copolymer Self‐assembly: Exploitation of Hydrogen Bonding for Nanoparticle Morphology Control via Incorporation of Triazine Based Comonomers by RAFT Polymerization Save
- Creep resistance in doubly crosslinked dynamic covalent networks Save
- Triazine-based self-assembling system Save