TY - JOUR
T1 - Synthetic approaches, structure activity relationship and biological applications for pharmacologically attractive pyrazole/pyrazoline-thiazolidine-based hybrids
AU - Havrylyuk, Dmytro
AU - Roman, Olexandra
AU - Lesyk, Roman
N1 - Publisher Copyright:
© 2016 Elsevier Masson SAS. All rights reserved.
PY - 2016/5/4
Y1 - 2016/5/4
N2 - The features of the chemistry of 4-thiazolidinone and pyrazole/pyrazolines as pharmacologically attractive scaffolds were described in a number of reviews in which the main approaches to the synthesis of mentioned heterocycles and their biological activity were analyzed. However, the pyrazole/pyrazoline-thiazolidine-based hybrids as biologically active compounds is poorly discussed in the context of pharmacophore hybrid approach. Therefore, the purpose of this review is to summarize the data about the synthesis and modification of heterocyclic systems with thiazolidine and pyrazoline or pyrazole fragments in molecules as promising objects of modern bioorganic and medicinal chemistry. The description of biological activity was focused on SAR analysis and mechanistic insights of mentioned hybrids.
AB - The features of the chemistry of 4-thiazolidinone and pyrazole/pyrazolines as pharmacologically attractive scaffolds were described in a number of reviews in which the main approaches to the synthesis of mentioned heterocycles and their biological activity were analyzed. However, the pyrazole/pyrazoline-thiazolidine-based hybrids as biologically active compounds is poorly discussed in the context of pharmacophore hybrid approach. Therefore, the purpose of this review is to summarize the data about the synthesis and modification of heterocyclic systems with thiazolidine and pyrazoline or pyrazole fragments in molecules as promising objects of modern bioorganic and medicinal chemistry. The description of biological activity was focused on SAR analysis and mechanistic insights of mentioned hybrids.
KW - Biological activity
KW - Pyrazole
KW - Pyrazoline
KW - Synthesis
KW - Thiazolidine
UR - http://www.scopus.com/inward/record.url?scp=84959143806&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84959143806&partnerID=8YFLogxK
U2 - 10.1016/j.ejmech.2016.02.030
DO - 10.1016/j.ejmech.2016.02.030
M3 - Short survey
C2 - 26922234
AN - SCOPUS:84959143806
SN - 0223-5234
VL - 113
SP - 145
EP - 166
JO - European Journal of Medicinal Chemistry
JF - European Journal of Medicinal Chemistry
ER -