AbstractIn the present study, some pyrazolopyrimidin-6(7H)-ones and tricyclic 8-oxo-dihydrooxazolopyrazolopyrimidin-9-ium chloride derivatives were synthesized and tested for anti-inflammatory and analgesic activity and assessment of acute ulcerogenic propensity as compared to the standard drug indomethacin. Some of the compounds (2c–2e; 3c–3e) showed appreciable anti-inflammatory–analgesic activity at the evaluated equimolar dose with lower ulcerogenic profile when compared with the standard. Compounds containing fused dihydrooxazolo ring (3e) system were found to be more active than their corresponding congener pyrazolopyrimidine
New derivatives of pyrazolo[3,4-b]pyrazines and related heterocycles were synthesized using 5-amino-...
International audienceNew derivatives of pyrazolo[3,4-b]pyrazines and related heterocycles were synt...
AbstractIn the present research work, the motto was to develop new chemical entities as potential an...
In the present investigation, some new pyrazolo[3,4-d]pyrimidin-4(5H)-one derivatives (7–12) as well...
A main objective of the present research study is to synthesize series of novel fused 8-substituted ...
A new series of fused triazolo- and tetrazolopyrimidine derivatives 2–14 were synthesized and their ...
This study reports the synthesis of two series of new purine bioisosteres comprising a pyrazolo[3,4...
Purpose: Microbial infections often produce pain and inflammation. Chemotherapeutic, analgesic and ...
Purpose: Microbial infections often produce pain and inflammation. Chemotherapeutic, analgesic and a...
AbstractA new sequence of pyrazole derivatives (1–6) was synthesized from condensation technique und...
A new sequence of pyrazole derivatives (1–6) was synthesized from condensation technique under utili...
With the aim of developing novel anti-inflammatory scaffolds, a new series of pyrazole-substituted v...
The five-membered heterocyclic group of pyrazoles/pyrazolines plays important role in drug discovery...
2532-25373,5-Dimethyl pyrazole 3a-d and 3-methyl pyrazol-5-one 4a-d derivatives of diclofenac, ibupr...
Abstractp38α mitogen activated protein kinase (MAPK) inhibitors provide a novel approach for the tre...
New derivatives of pyrazolo[3,4-b]pyrazines and related heterocycles were synthesized using 5-amino-...
International audienceNew derivatives of pyrazolo[3,4-b]pyrazines and related heterocycles were synt...
AbstractIn the present research work, the motto was to develop new chemical entities as potential an...
In the present investigation, some new pyrazolo[3,4-d]pyrimidin-4(5H)-one derivatives (7–12) as well...
A main objective of the present research study is to synthesize series of novel fused 8-substituted ...
A new series of fused triazolo- and tetrazolopyrimidine derivatives 2–14 were synthesized and their ...
This study reports the synthesis of two series of new purine bioisosteres comprising a pyrazolo[3,4...
Purpose: Microbial infections often produce pain and inflammation. Chemotherapeutic, analgesic and ...
Purpose: Microbial infections often produce pain and inflammation. Chemotherapeutic, analgesic and a...
AbstractA new sequence of pyrazole derivatives (1–6) was synthesized from condensation technique und...
A new sequence of pyrazole derivatives (1–6) was synthesized from condensation technique under utili...
With the aim of developing novel anti-inflammatory scaffolds, a new series of pyrazole-substituted v...
The five-membered heterocyclic group of pyrazoles/pyrazolines plays important role in drug discovery...
2532-25373,5-Dimethyl pyrazole 3a-d and 3-methyl pyrazol-5-one 4a-d derivatives of diclofenac, ibupr...
Abstractp38α mitogen activated protein kinase (MAPK) inhibitors provide a novel approach for the tre...
New derivatives of pyrazolo[3,4-b]pyrazines and related heterocycles were synthesized using 5-amino-...
International audienceNew derivatives of pyrazolo[3,4-b]pyrazines and related heterocycles were synt...
AbstractIn the present research work, the motto was to develop new chemical entities as potential an...