Synthesis and preliminary evaluation of new 5-pyrazolinone derivatives as analgesic agents
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Synthesis, characterization and anti-breast cancer activity of new 4-aminoantipyrine-based heterocycles.(2-Amino-phen-yl)[(5S)-5-hydr-oxy-3,5-dimethyl-4,5-dihydro-1H-pyrazol-1-yl]methanone.5-Ethyl-4-methyl-1H-pyrazol-3(2H)-one.5-Pentyl-4-phenyl-sulfonyl-1H-pyrazol-3-ol.Tert-butyl 3-oxo-2,3,4,5,6,7-hexa-hydro-1H-pyrazolo[4,3-c]pyridine-5-carboxyl-ate4-Methyl-5-phenyl-1H-pyrazol-3-ol.3-Ethyl-4-phen-oxy-1-(2,2,2-trifluoro-eth-yl)-1H-pyrazol-5-ol.2-[(1,5-Dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazol-4-yl)amino]-1-methyl-2-oxoethyl pyrrolidine-1-carbodithio-ate(Z)-4-{1-[(2-Hy-droxy-ethyl)-amino]-ethyl-idene}-3-methyl-1-phenyl-1H-pyrazol-5(4H)-one.On the Importance of the Aromatic Ring Parameter in Studies of the Solvolyses of Cinnamyl and Cinnamoyl Halides.4-[(E)-(4-Diethyl-amino-2-hy-droxy-benzyl-idene)amino]-1,5-dimethyl-2-phenyl-1H-pyrazol-3(2H)-one.1-(1,5-Diphenyl-4-phenyl-sulfonyl-1H-pyrazol-3-yl)ethanone.Synthesis, in-vitro antimicrobial and antitubercular screening of Schiff bases of 3-amino-1-phenyl-4- [2-(4-phenyl-1,3-thiazol-2-yl) hydrazin-1-ylidene]-4,5-dihydro-1H-pyrazol-5-oneNovel tetrazole and cyanamide derivatives as inhibitors of cyclooxygenase-2 enzyme: design, synthesis, anti-inflammatory evaluation, ulcerogenic liability and docking study.A convenient synthesis and molecular modeling study of novel pyrazolo[3,4-d]pyrimidine and pyrazole derivatives as anti-tumor agents.New pyrazole derivative 5-[1-(4-fluorophenyl)-1H-pyrazol-4-yl]-2H-tetrazole: synthesis and assessment of some biological activities.Synthesis of some imidazolyl-thioacetyl-pyrazolinone derivatives and their antinociceptive and anticancer activities.Masuda borylation-Suzuki coupling (MBSC) sequence of vinylhalides and its application in a one-pot synthesis of 3,4-biarylpyrazoles.Synthesis and anti-inflammatory activity of celecoxib like compounds.Synthesis and antimicrobial evaluation of novel pyrazolones and pyrazolone nucleosides.Synthesis and antioxidant evaluation of some new pyrazolopyridine derivatives.Solvent and Copper Ion-Induced Synthesis of Pyridyl-Pyrazole-3-One Derivatives: Crystal Structure, Cytotoxicity.Efficient synthesis of 1,2-bis(alkoxycarbonyl)pyrazol-3-ones from 2,3-allenoic acids, azodicarboxylates and PPh3.Catalyst-free, one-pot, three-component synthesis of 5-amino-1,3-aryl-₁Η-pyrazole-4-carbonitriles in green media.Formation and aromatization of strained bicyclic pyrazolidines via tandem reaction of alkyl 2-aroyl-1-chlorocyclopropanecarboxylates with acylhydrazones.Facile synthesis and antimicrobial evaluation of some new heterocyclic compounds incorporating a biologically active sulfamoyl moiety.Synthesis, antiviral, cytotoxicity and antitumor evaluations of A4 type of porphyrin derivativesThe Newly Synthesized Pyrazole Derivative 5-(1-(3 Fluorophenyl)-1-Pyrazol-4-yl)-2-Tetrazole Reduces Blood Pressure of Spontaneously Hypertensive Rats NO/cGMO Pathway
P2860
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P2860
Synthesis and preliminary evaluation of new 5-pyrazolinone derivatives as analgesic agents
description
2000 nî lūn-bûn
@nan
2000 թուականի Մարտին հրատարակուած գիտական յօդուած
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2000 թվականի մարտին հրատարակված գիտական հոդված
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2000年の論文
@ja
2000年学术文章
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2000年学术文章
@zh-cn
2000年学术文章
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2000年学术文章
@zh-my
2000年学术文章
@zh-sg
2000年學術文章
@yue
name
Synthesis and preliminary eval ...... erivatives as analgesic agents
@ast
Synthesis and preliminary eval ...... erivatives as analgesic agents
@en
Synthesis and preliminary eval ...... erivatives as analgesic agents
@nl
type
label
Synthesis and preliminary eval ...... erivatives as analgesic agents
@ast
Synthesis and preliminary eval ...... erivatives as analgesic agents
@en
Synthesis and preliminary eval ...... erivatives as analgesic agents
@nl
prefLabel
Synthesis and preliminary eval ...... erivatives as analgesic agents
@ast
Synthesis and preliminary eval ...... erivatives as analgesic agents
@en
Synthesis and preliminary eval ...... erivatives as analgesic agents
@nl
P2093
P1476
Synthesis and preliminary eval ...... erivatives as analgesic agents
@en
P2093
P304
P356
10.1016/S0223-5234(00)00117-3
P407
P577
2000-03-01T00:00:00Z