Synthesis and anti-inflammatory evaluation of some new 3,6-disubstituted-1, 2,4-triazolo-[3,4-b]-1,3,4-thiadiazoles bearing pyrazole moiety

dc.contributor.authorMalladi, S.
dc.contributor.authorIsloor, A.M.
dc.contributor.authorShetty, P.
dc.contributor.authorFun, H.-K.
dc.contributor.authorTelkar, S.
dc.contributor.authorMahmood, R.
dc.contributor.authorIsloor, N.
dc.date.accessioned2026-02-05T09:35:09Z
dc.date.issued2012
dc.description.abstractIn the present study, a new series of 3,6-disubstituted- 1,2,4-triazolo-[3,4-b]-1,3,4-thiadiazoles (4aj) have been synthesized by condensing 3-substituted-4-amino-5- mercapto-1,2,4-triazoles (1a-b) with various 3-substitutedpyrazole- 4-carboxylic acids (3a-e) in the presence ofPOCl3. The structures of newly synthesized compounds were characterized by elemental analysis, IR, 1H NMR, 13CNMR, and mass spectroscopic studies. Structure of the compound 4b was also confirmed by recording the single crystal X-ray structure. All the synthesized compounds were screened for their anti-inflammatory activities by carrageenan induced paw edema method. Anti-inflammatory screening indicated that, compounds 4d, 4e, and 4h were found to be biologically active whereas remaining compounds showed poor antiinflammatory activity. Also molecular docking studies were also performed for compounds which showed good antiinflammatory activity. © Springer Science+Business Media, LLC 2011.
dc.identifier.citationMedicinal Chemistry Research, 2012, 21, 10, pp. 3272-3280
dc.identifier.issn10542523
dc.identifier.urihttps://doi.org/10.1007/s00044-011-9865-0
dc.identifier.urihttps://idr.nitk.ac.in/handle/123456789/26953
dc.subject1,2,4 triazole derivative
dc.subject1,3,4 thiadiazole derivative
dc.subject3 ethyl 6 ( 3 ( 2,4 dichlorophenyl) 1h pyrazol 4 yl)[ 1,2,4 ]triazolo[3,4 b][ 1,3,4 ]thiadiazole
dc.subject3 ethyl 6 ( 3 ( 4 chlorophenyl) 1h pyrazol 4 yl)[ 1,2,4 ]triazolo[3,4 b][ 1,3,4 ]thiadiazole
dc.subject3 ethyl 6 ( 3 ( 4 fluorophenyl) 1h pyrazol 4 yl)[ 1,2,4 ]triazolo[3,4 b][ 1,3,4 ]thiadazole
dc.subject3 ethyl 6 ( 3 ( 4 methoxyphenyl) 1h pyrazol 4 yl)[ 1,2,4]triazolo[3,4 b][ 1,3,4 ]thiadiazole
dc.subject3 ethyl 6 ( 3 phenyl 1h pyrazol 4 yl)[ 1,2,4 ]triazolo[3,4 b][ 1,3,4 ]thiadiazole
dc.subject3 propyl 6 ( 3 ( 2,4 dichlorophenyl) 1h pyrazol 4 yl)[ 1,2,4 ]triazolo[3,4 b][ 1,3,4]thiadiazole
dc.subject3 propyl 6 ( 3 ( 4 chlorophenyl) 1h pyrazol 4 yl0[ 1,2,4 ]triazolo[3,4 b][ 1,3,4 ]thiadiazole
dc.subject3 propyl 6 ( 3 ( 4 fluorophenyl) 1h pyrazol 4 yl)[ 1,2,4 ]triazolo[3,4 b][ 1,3,4 ]thiadiazole
dc.subject3 propyl 6 ( 3 ( 4 methoxyphenyl) 1h pyrazol 4 yl)[ 1,2,4 ]triazolo[3,4 b][ 1,3,4 ]thiadiazole
dc.subject3 propyl 6 ( 3 phenyl 1h pyrazol 4 yl)[ 1,2,4 ]triazolo[3,4 b][ 1,3,4 ]thiadiazole
dc.subjectantiinflammatory agent
dc.subjectcarrageenan
dc.subjectdiclofenac
dc.subjectpyrazole
dc.subjectpyrazole derivative
dc.subjectunclassified drug
dc.subjectanimal experiment
dc.subjectantiinflammatory activity
dc.subjectarticle
dc.subjectcarbon nuclear magnetic resonance
dc.subjectchemical analysis
dc.subjectchemical structure
dc.subjectcomputer model
dc.subjectcontrolled study
dc.subjectcrystal structure
dc.subjectdrug screening
dc.subjectdrug synthesis
dc.subjectfemale
dc.subjectin vitro study
dc.subjectinfrared spectroscopy
dc.subjectmale
dc.subjectmass spectrometry
dc.subjectmolecular docking
dc.subjectnonhuman
dc.subjectpaw edema
dc.subjectproton nuclear magnetic resonance
dc.subjectrat
dc.subjectsubstitution reaction
dc.subjectX ray crystallography
dc.titleSynthesis and anti-inflammatory evaluation of some new 3,6-disubstituted-1, 2,4-triazolo-[3,4-b]-1,3,4-thiadiazoles bearing pyrazole moiety

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