About Author: Shekh Yunus1, Nirmal Das Adhikary2 and Partha Chattopadhyay*
National Institute of Pharmaceutical Education and Research
at IICB, Jadavpur, 4 Raja S.C. Mullick Road, Kolkata-700032, India
Source of Support: NIPER Kolkata and IICB
ABSTRACT:
Click chemistry is a modular approach that uses only the most practical and reliable chemical transformations. Its applications are increasingly found in all aspects of drug discovery, ranging from lead finding through combinatorial chemistry and target-templated in situ chemistry, to proteomics and DNA research, using bioconjugation reactions. The copper-(I)-catalyzed 1,2,3-triazole formation from azides and terminal acetylenes is a particularly powerful linking reaction, due to its high degree of dependability, complete specificity, and the bio-compatibility of the reactants. The triazole products are more than just passive linkers; they readily associate with biological targets, through hydrogen bonding and dipole interactions.