about
Synthesis and cytotoxic evaluation of some new[1,3]dioxolo[4,5-g]chromen-8-one derivatives.Design, synthesis, docking study and cytotoxic activity evaluation of some novel letrozole analogs.A systematic review of drugs in late-stage development for the treatment of multiple sclerosis: a focus on oral synthetic drugs.Synthesis and cytotoxic properties of novel (E)-3-benzylidene-7-methoxychroman-4-one derivatives.Synthesis and In vitro cytotoxic activity evaluation of (E)-16-(substituted benzylidene) derivatives of dehydroepiandrosteroneSynthesis and evaluation of antiproliferative activity of substituted N-(9-oxo-9H-xanthen-4-yl)benzenesulfonamides.New methods for the discovery and synthesis of PDE7 inhibitors as new drugs for neurological and inflammatory disorders.The importance of synthetic drugs for type 2 diabetes drug discovery.Medicinal plants in the treatment of Helicobacter pylori infections.Discovery Approaches for Novel Dyslipidemia Drugs.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.In vitro and in vivo evaluation of paclitaxel-lapatinib-loaded F127 pluronic micelles.Anticancer effects of synthetic hexahydrobenzo [g]chromen-4-one derivatives on human breast cancer cell lines.Design, synthesis, in vitro cytotoxic activity evaluation, and apoptosis-induction study of new 9(10H)-acridinone-1,2,3-triazoles.The development of biomarkers to reduce attrition rate in drug discovery focused on oncology and central nervous system.Synthesis and cytotoxic activity of novel poly-substituted imidazo[2,1-c][1,2,4]triazin-6-amines.Cytotoxic and apoptotic effects of synthetic benzochromene derivatives on human cancer cell lines.Synthesis, in vitro cytotoxicity and apoptosis inducing study of 2-aryl-3-nitro-2H-chromene derivatives as potent anti-breast cancer agents.Synthesis, crystal structure, and cytotoxic activity of novel cyclic systems in [1,2,4]thiadiazolo[2,3-a]pyridine benzamide derivatives and their copper(II) complexes.Synthesis and biological evaluation of 3-(trimethoxyphenyl)-2(3H)-thiazole thiones as combretastatin analogs.Cytotoxic activity evaluation and QSAR study of chromene-based chalcones.2-Amino-3-cyano-4-(5-arylisoxazol-3-yl)-4H-chromenes: synthesis and in vitro cytotoxic activity.Coumarin-based bioactive compounds: facile synthesis and biological evaluation of coumarin-fused 1,4-thiazepines.Synthesis and in-vitro cytotoxicity of poly-functionalized 4-(2-arylthiazol-4-yl)-4H-chromenes.Complexes of 2-hydroxyacetophenone semicarbazones: A novel series of superoxide dismutase mimetics.Chemodiversity of Nepeta menthoides Boiss. & Bohse. essential oil from Iran and antimicrobial, acetylcholinesterase inhibitory and cytotoxic properties of 1,8-cineole chemotype.Caspase-dependent apoptosis induced by two synthetic halogenated flavanones, 3',7-dichloroflavanone and 3',6-dichloroflavanone, on human breast and prostate cancer cells.Bio-guided isolation of Centaurea bruguierana subsp. belangerana cytotoxic components.Synthesis and biological evaluation of 4-amino-5-cinnamoylthiazoles as chalcone-like anticancer agents.Novel Tacrine-Based Pyrano[3',4':5,6]pyrano[2,3-b]quinolinones: Synthesis and Cholinesterase Inhibitory Activity.Novel quinazolin-4(3H)-one linked to 1,2,3-triazoles: Synthesis and anticancer activity.Design, Synthesis, Biological Evaluation, and Docking Study of Acetylcholinesterase Inhibitors: New Acridone-1,2,4-oxadiazole-1,2,3-triazole Hybrids.Synthesis of novel chromenones linked to 1,2,3-triazole ring system: Investigation of biological activities against Alzheimer's disease.In-vitro evaluation of apoptotic effect of OEO and thymol in 2D and 3D cell cultures and the study of their interaction mode with DNADesign and synthesis of novel quinazolinone-1,2,3-triazole hybrids as new anti-diabetic agents: In vitro α-glucosidase inhibition, kinetic, and docking studyIn vitro antibacterial activity of some Iranian medicinal plant extracts against Helicobacter pyloriPhotocatalytic inactivation of Vibrio fischeri using Fe2O3-TiO2-based nanoparticlesDesign, synthesis, docking study, α-glucosidase inhibition, and cytotoxic activities of acridine linked to thioacetamides as novel agents in treatment of type 2 diabetesAsymmetrical 2,6-bis(benzylidene)cyclohexanones: Synthesis, cytotoxic activity and QSAR study
P50
Q33606317-9F53F93E-396C-4679-A167-5BFA385E4EF6Q34837553-680DA10E-86D8-4CE8-9221-D5D9C2668FEDQ35645303-A4B6C8DF-CEE0-4BCD-8927-11BF6EEF3680Q36891470-F77B2C6D-081A-4C2C-896B-A2C1236E3A1FQ36905760-D9E450ED-9A11-4105-830F-EB16A9D888E2Q37492732-0F8A0E0B-CD19-4012-97D4-2FA52312D08DQ38097492-CE3B8FCC-9B48-459E-A36F-DF1114AA19EEQ38139508-0DD042A9-C743-4AA6-AD37-C5BA40C1DD15Q38272171-8CE03183-DB5D-4677-8800-8BB2BA8D8818Q38541986-704A0753-0E3A-48C9-8EA5-029E8391361DQ38723452-5FFB45F8-4AB5-4701-A15A-8C8E35EAFD6DQ38730486-DF175DE2-EB25-4865-9F0D-49A5C6BF99BBQ38735063-3D3905E6-15BC-4938-86C4-0AA6BE6055D7Q38767142-0D3979F7-2A1C-4A94-B696-867C83ECD9CAQ38853487-9CCB9BFD-8D31-4F4B-947A-ABC582221A62Q38907580-5DA1D759-7020-48C1-AC49-C98BA7F1E7A1Q38917296-B71B2D8D-5A17-4617-A0D8-6ECCA2B571EAQ38952905-02D72B2D-4F16-4C1A-913B-0C11A59E6E72Q38957118-309FA995-97EF-4DB7-8B8E-90CE3C61195CQ39006093-09510BA5-4899-4627-A8FC-AE075058D18BQ39064042-164F3468-4F32-4FFF-BE72-EDA775C18ADEQ39221532-2BC88B4C-788B-4A24-B287-D1254D384903Q39408226-0B0E9834-B701-4763-A760-F6934A406F45Q39510300-9F7246BC-BDEE-4FB8-8B2D-00F0DA265030Q39724448-E07339D3-A468-4163-AE68-6CBE9B34B057Q43095021-9D170A73-13EE-49B0-B534-0AEF07AD074AQ48183667-71C861BF-2B1F-40A7-965C-EAB7F84A5EE8Q49629883-0D3977FE-BDEE-4E33-B9FF-B2A9191BB4A5Q49851499-A122E476-42FC-498E-A174-16953AB0A974Q50043567-434839BE-9372-4B23-920B-576FDA642D53Q51290528-716BE103-4350-40A5-9AE1-EF9BFBE677CEQ52594647-12BABB37-6E98-4D55-9856-009628476B89Q53365323-7CFB7B11-078E-4E85-AC75-F80BDB216F50Q53384400-383E8AE5-FE6C-4855-A338-F386B35E2DDCQ58562849-2E711607-1D0C-46AA-A03B-03F13F09F71CQ58571818-D31721D4-31C4-4882-BEF9-987BA9E6DD8EQ59255770-29D59615-4B02-44A9-80E1-FE19F512C986Q61759032-6355A0B7-41FC-43A5-BDB0-DE793455A7A5Q62104705-A721E1EB-5561-4378-AA6D-1FF4BF87D1C1Q83461930-681F3503-52B3-4114-8045-6E26AB4E664E
P50
description
Forscher
@de
chercheur
@fr
investigador
@es
researcher
@en
հետազոտող
@hy
研究者
@zh
name
Maliheh Safavi
@ast
Maliheh Safavi
@en
Maliheh Safavi
@es
Maliheh Safavi
@nl
type
label
Maliheh Safavi
@ast
Maliheh Safavi
@en
Maliheh Safavi
@es
Maliheh Safavi
@nl
prefLabel
Maliheh Safavi
@ast
Maliheh Safavi
@en
Maliheh Safavi
@es
Maliheh Safavi
@nl
P1153
25227167300
P31
P496
0000-0003-0950-3141