volume 60 issue 9 pages 1818-1827

Design, Synthesis, Molecular Docking, and Anti-inflammatory Activity of 2-[(E)-{1-[4-(4-Chlorophenyl)-1,3-thiazol-2-yl]-1H-pyrazol-4-yl}(hydroxyimino)methyl]phenol and {1-[4-(4-Chlorophenyl)-1,3-thiazol-2-yl]-1H-pyrazol-4-yl}(2-hydroxyphenyl)methanone Derivatives

N R Darekar 1, 2
SUSHAMA J. TAKATE 2
Hemantkumar N Akolkar 3
Mubarak H Shaikh 1
V M Khedkar 4
Dipak Raut 5
S. D Mhaske 2, 6
1
 
P.G. and Research Department of Chemistry, Radhabai Kale Mahila Mahavidyalaya, Ahmednagar, India
2
 
P.G. and Research Department of Chemistry, New Arts, Science and Commerce College, Ahmednagar, India
3
 
Department of Chemistry, Abasaheb Marathe Arts and New Commerce, Science College, Rajapur, India
5
 
Department of Pharmacognosy, Amrutvahini College of Pharmacy, Sangamner, India
6
 
Department of Chemistry, Dadapatil Rajale Arts, Science and Commerce College, Adinathnagar, Ahmednagar, India
Publication typeJournal Article
Publication date2024-09-01
scimago Q4
wos Q4
SJR0.190
CiteScore1.3
Impact factor0.9
ISSN10704280, 16083393
Abstract
A series of {1-[4-(4-chlorophenyl)-1,3-thiazol-2-yl]-1H-pyrazol-4-yl}(2-hydroxyphenyl)metha­nones 5 were synthesized from 1-[4-(4-chlorophenyl)-1,3-thiazol-2-yl]hydrazine 3 and substituted 3-formyl­chromones 4. Compounds 5 were converted into 2-[(E)-{1-[4-(4-chlorophenyl)-1,3-thiazol-2-yl]-1H-pyrazol-4-yl}(hydroxyimino)methyl]phenols 6. The synthesized compounds were characterized by spectral techniques screened for their anti-inflammatory activity. Compounds 6c and 6e showed good percent inhibition of haemolysis when compared with the standard drug celecoxib. The molecular docking study explored the essential binding mode and possible thermodynamic interactions within the binding site of COX-2 enzyme.
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Darekar N. R. et al. Design, Synthesis, Molecular Docking, and Anti-inflammatory Activity of 2-[(E)-{1-[4-(4-Chlorophenyl)-1,3-thiazol-2-yl]-1H-pyrazol-4-yl}(hydroxyimino)methyl]phenol and {1-[4-(4-Chlorophenyl)-1,3-thiazol-2-yl]-1H-pyrazol-4-yl}(2-hydroxyphenyl)methanone Derivatives // Russian Journal of Organic Chemistry. 2024. Vol. 60. No. 9. pp. 1818-1827.
GOST all authors (up to 50) Copy
Darekar N. R., TAKATE S. J., Akolkar H. N., Shaikh M. H., Khedkar V. M., Raut D., Mhaske S. D. Design, Synthesis, Molecular Docking, and Anti-inflammatory Activity of 2-[(E)-{1-[4-(4-Chlorophenyl)-1,3-thiazol-2-yl]-1H-pyrazol-4-yl}(hydroxyimino)methyl]phenol and {1-[4-(4-Chlorophenyl)-1,3-thiazol-2-yl]-1H-pyrazol-4-yl}(2-hydroxyphenyl)methanone Derivatives // Russian Journal of Organic Chemistry. 2024. Vol. 60. No. 9. pp. 1818-1827.
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TY - JOUR
DO - 10.1134/s1070428024090264
UR - https://link.springer.com/10.1134/S1070428024090264
TI - Design, Synthesis, Molecular Docking, and Anti-inflammatory Activity of 2-[(E)-{1-[4-(4-Chlorophenyl)-1,3-thiazol-2-yl]-1H-pyrazol-4-yl}(hydroxyimino)methyl]phenol and {1-[4-(4-Chlorophenyl)-1,3-thiazol-2-yl]-1H-pyrazol-4-yl}(2-hydroxyphenyl)methanone Derivatives
T2 - Russian Journal of Organic Chemistry
AU - Darekar, N R
AU - TAKATE, SUSHAMA J.
AU - Akolkar, Hemantkumar N
AU - Shaikh, Mubarak H
AU - Khedkar, V M
AU - Raut, Dipak
AU - Mhaske, S. D
PY - 2024
DA - 2024/09/01
PB - Pleiades Publishing
SP - 1818-1827
IS - 9
VL - 60
SN - 1070-4280
SN - 1608-3393
ER -
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@article{2024_Darekar,
author = {N R Darekar and SUSHAMA J. TAKATE and Hemantkumar N Akolkar and Mubarak H Shaikh and V M Khedkar and Dipak Raut and S. D Mhaske},
title = {Design, Synthesis, Molecular Docking, and Anti-inflammatory Activity of 2-[(E)-{1-[4-(4-Chlorophenyl)-1,3-thiazol-2-yl]-1H-pyrazol-4-yl}(hydroxyimino)methyl]phenol and {1-[4-(4-Chlorophenyl)-1,3-thiazol-2-yl]-1H-pyrazol-4-yl}(2-hydroxyphenyl)methanone Derivatives},
journal = {Russian Journal of Organic Chemistry},
year = {2024},
volume = {60},
publisher = {Pleiades Publishing},
month = {sep},
url = {https://link.springer.com/10.1134/S1070428024090264},
number = {9},
pages = {1818--1827},
doi = {10.1134/s1070428024090264}
}
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Darekar, N. R., et al. “Design, Synthesis, Molecular Docking, and Anti-inflammatory Activity of 2-[(E)-{1-[4-(4-Chlorophenyl)-1,3-thiazol-2-yl]-1H-pyrazol-4-yl}(hydroxyimino)methyl]phenol and {1-[4-(4-Chlorophenyl)-1,3-thiazol-2-yl]-1H-pyrazol-4-yl}(2-hydroxyphenyl)methanone Derivatives.” Russian Journal of Organic Chemistry, vol. 60, no. 9, Sep. 2024, pp. 1818-1827. https://link.springer.com/10.1134/S1070428024090264.