about
Antinociceptive properties of new coumarin derivatives bearing substituted 3,4-dihydro-2H-benzothiazines.Induction of apoptosis through tubulin inhibition in human cancer cells by new chromene-based chalcones.Straightforward synthesis of thiazoline-incorporated chalconoids from phenacyl halides.Structural features of new quinolones and relationship to antibacterial activity against Gram-positive bacteria.Synthesis, in vitro antifungal evaluation and in silico study of 3-azolyl-4-chromanone phenylhydrazones.Synthesis and cytotoxic properties of novel (E)-3-benzylidene-7-methoxychroman-4-one derivatives.Synthesis and antibacterial activity of novel levofloxacin derivatives containing a substituted thienylethyl moietySynthesis and in vitro cytotoxic activity of novel chalcone-like agents.2-Amino-4-(nitroalkyl)-4H-chromene-3-carbonitriles as New Cytotoxic Agents.Recent advances of chroman-4-one derivatives: synthetic approaches and bioactivities.Recent applications of 1,3-thiazole core structure in the identification of new lead compounds and drug discovery.Current developments of coumarin-based anti-cancer agents in medicinal chemistry.Multi-structure docking analysis of BACE1 crystal structures and non-peptidic ligands.New racemic annulated pyrazolo[1,2-b]phthalazines as tacrine-like AChE inhibitors with potential use in Alzheimer's disease.Promising antileishmanial effectiveness of doxorubicin and Doxil against Leishmania major: An in vitro assay.The importance of triazole scaffold in the development of anticonvulsant agents.Facile synthesis and antiproliferative activity of 7H-benzo[7,8]chromeno[2,3-d]pyrimidin-8-amines.Synthesis and biological evaluation of novel imidazopyrimidin-3-amines as anticancer agents.β-Ionone and its analogs as promising anticancer agents.Recent advances of cytotoxic chalconoids targeting tubulin polymerization: Synthesis and biological activity.Synthesis and cytotoxic activity of novel poly-substituted imidazo[2,1-c][1,2,4]triazin-6-amines.Synthesis, in vitro cytotoxicity and apoptosis inducing study of 2-aryl-3-nitro-2H-chromene derivatives as potent anti-breast cancer agents.An overview of azoles targeting sterol 14α-demethylase for antileishmanial therapy.Synthesis and biological evaluation of 3-(trimethoxyphenyl)-2(3H)-thiazole thiones as combretastatin analogs.Polyoxygenated cinnamoylcoumarins as conformationally constrained analogs of cytotoxic diarylpentanoids: synthesis and biological activity.Cytotoxic activity evaluation and QSAR study of chromene-based chalcones.2H-chromene derivatives bearing thiazolidine-2,4-dione, rhodanine or hydantoin moieties as potential anticancer agents.Synthesis, in vitro antifungal activity and in silico study of 3-(1,2,4-triazol-1-yl)flavanones.Coumarin-based bioactive compounds: facile synthesis and biological evaluation of coumarin-fused 1,4-thiazepines.Isochaihulactone analogues: synthesis and anti-proliferative activity of novel dibenzylbutyrolactones.Synthesis and biological evaluation of 2-phenylthiazole-4-carboxamide derivatives as anticancer agents.Synthesis and in-vitro cytotoxicity of poly-functionalized 4-(2-arylthiazol-4-yl)-4H-chromenes.N-Substituted piperazinyl quinolones as potential cytotoxic agents: structure-activity relationships study.In Vitro Activities of Novel Azole Compounds ATTAF-1 and ATTAF-2 against Fluconazole-Susceptible and -Resistant Isolates of Candida Species.Functionalized N(2-oxyiminoethyl) piperazinyl quinolones as new cytotoxic agents.In vitro antileishmanial activity of novel azoles (3-imidazolylflavanones) against promastigote and amastigote stages of Leishmania major.Antituberculosis agents. V. Synthesis, evaluation of in vitro antituberculosis activity and cytotoxicity of some 2-(5-nitro-2-furyl)-1,3,4-thiadiazole derivatives.Hypothesis: The potential application of doxorubicin against cutaneous leishmaniasis.Utility of aptamers for antileishmanial drug targets: A potential hypothesis.Imidazolylchromanones containing non-benzylic oxime ethers: synthesis and molecular modeling study of new azole antifungals selective against Cryptococcus gattii.
P50
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P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Saeed Emami
@ast
Saeed Emami
@en
Saeed Emami
@es
Saeed Emami
@nl
Saeed Emami
@sl
type
label
Saeed Emami
@ast
Saeed Emami
@en
Saeed Emami
@es
Saeed Emami
@nl
Saeed Emami
@sl
prefLabel
Saeed Emami
@ast
Saeed Emami
@en
Saeed Emami
@es
Saeed Emami
@nl
Saeed Emami
@sl
P1053
K-1016-2015
P106
P1153
34871818800
P21
P31
P3829
P496
0000-0003-1665-6621
P569
2000-01-01T00:00:00Z