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Methyl 2-({6-[(1-meth-oxy-2-methyl-1-oxopropan-2-yl)carbamo-yl]pyridin-2-yl}formamido)-2-methyl-propano-ate.Ethyl 2-amino-4-(4-fluoro-phen-yl)-6-meth-oxy-4H-benzo[h]chromene-3-carboxyl-ate.Methyl 2-{6-[(1-meth-oxy-1-oxopropan-2-yl)amino-carbon-yl]pyridine-2-carboxamido}-propano-ate2-Methyl-sulfanyl-1,2,4-triazolo[1,5-a]quinazoline-5(4H)-thione.3-Amino-1-(4-fluoro-phen-yl)-8-meth-oxy-1H-benzo[f]chromene-2-carbonitrile2-Amino-4-(4-bromo-phen-yl)-6-meth-oxy-4H-benzo[h]chromene-3-carbonitrile.2-(4-Fluoro-benzyl-idene)propane-dinitrile: monoclinic polymorph.Synthesis and biological activities of some new (Nα-dinicotinoyl)-bis-L-leucyl linear and macrocyclic peptides.Heterocyclic compounds based on 3-(4-bromophenyl) azo-5-phenyl-2(3H)-furanone: anti-avian influenza virus (H5N1) activity.A new investigation for some steroidal derivatives as anti-Alzheimer agents.5α-reductase inhibitors, antiviral and anti-tumor activities of some steroidal cyanopyridinone derivatives.Androgen receptor antagonists and anti-prostate cancer activities of some synthesized steroidal candidates.Design, synthesis and structure-activity relationship study of novel pyrazole-based heterocycles as potential antitumor agents.Synthesis and structure-activity relationship studies of pyrazole-based heterocycles as antitumor agents.Anticancer activities of some newly synthesized pyridine, pyrane, and pyrimidine derivatives.SYNTHESIS AND BIOLOGICAL EVALUATION OF SOME NOVEL FUSED THIAZOLO[3,2A]PYRIMIDINES AS POTENTIAL ANALGESIC AND ANTI-INFLAMMATORY AGENTS.Anti-inflammatory, analgesic, anticonvulsant and antiparkinsonian activities of some pyridine derivatives using 2,6-disubstituted isonicotinic acid hydrazides.Synthesis of chiral macrocyclic or linear pyridine carboxamides from pyridine-2,6-dicarbonyl dichloride as antimicrobial agents.Synthesis of some new pyridine-2,6-carboxamide-derived Schiff bases as potential antimicrobial agents.Analgesic, anticonvulsant and anti-inflammatory activities of some synthesized benzodiazipine, triazolopyrimidine and bis-imide derivatives.New steroidal derivatives synthesized using 3beta-hydroxyandrosten-17-one as starting material.Synthesis and pharmacological activities of some new triazolo- and tetrazolopyrimidine derivatives.Pharmacological activities of some new polycyclic triazolopyrazolopyridazine derivatives.Anti-arthritic and immunosuppressive activities of substituted triterpenoidal candidates.Synthesis of Some Novel Heterocyclic and Schiff Base Derivatives as Antimicrobial Agents.Synthesis and Antimicrobial Evaluation of a New Series of Heterocyclic Systems Bearing a Benzosuberone Scaffold.Synthesis, Anticancer Screening and Molecular docking studies of New Heterocycles with Trimethoxyphenyl Scaffold as Combretastatin Analogues.Synthesis and reactions of some new substituted pyridine and pyrimidine derivatives as analgesic, anticonvulsant and antiparkinsonian agents.Anti-inflammatory and analgesic activities of newly synthesized chiral peptide derivatives using (3-benzoyl- 4,5-dioxo-2-phenyl-pyrrolidin-1-yl)acetic acid ethyl ester as starting material.Synthesis of new macrocyclic polyamides as antimicrobial agent candidates.Anti-inflammatory profile of some synthesized heterocyclic pyridone and pyridine derivatives fused with steroidal structure.Synthesis and Characterization of Some New N-Glycosides of Pyridine-2,6-bis-Carboxamides Derivatives.Design, Synthesis and Docking Studies of Novel Macrocyclic Pentapeptides as Anticancer Multi-Targeted Kinase InhibitorsAntimelanomal Activities of some Newly Synthesized Pyrrolotriazolopyrimidines and Pyrrolotetrazolopyrimidines and their DerivativesSynthesis and Reactions of 2-(Phenylthiocarbamoyl)-N-(Benzothiazol-2-Yl)-3-Phenyl-3-Oxopropanamide With Activated ChlorocompoundsSingle-Piece Solid Contact Cu-Selective Electrodes Based on a Synthesized Macrocyclic Calix[4]arene Derivative as a Neutral Carrier IonophoreDesign, Synthesis, Anticancer Evaluation and Molecular Modeling of Novel Estrogen DerivativesCytotoxic Effects of Newly Synthesized Heterocyclic Candidates Containing Nicotinonitrile and Pyrazole Moieties on Hepatocellular and Cervical Carcinomas.Synthesis of new (Nalpha-dipicolinoyl)-bis-L-valyl-L-phenylalanyl linear and macrocyclic bridged peptides as anti-inflammatory agentsPVC membrane sensor for potentiometric determination of iron (II) in some pharmaceutical formulations based on a new neutral ionophore
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Q35934601-22C4494A-464B-4F4B-8D5A-6513FE049FCDQ36046583-A423942E-7544-4695-AA40-E29AD7468BF7Q36046632-B1EEAAC4-8500-49B0-BB53-1C776CEF6584Q36657373-E52D0CF8-0463-4CBB-AE6C-340B10B6F259Q36775581-C4FDF222-0684-45BC-9287-C8C18376DBECQ36775587-454A435A-C8BD-4F46-B836-556510C9CE59Q36775829-87367747-C855-4BD5-A202-104FDF154598Q38971793-B789D2A8-89C1-4AD6-8131-838C2D547CBAQ39207880-5C65C6CB-297E-46DD-B1C7-D6A17D6B84F4Q39357050-9571171C-AE20-4C77-BE9E-03D13F03E4EDQ39447444-BCDFE978-E5E1-47EB-A92C-8D029C57B9DEQ39450163-494BD214-40E1-4ADF-A78D-8956408D6811Q39643577-C39361AF-AEC2-4CFD-A390-199C93D0488CQ39714128-6E714B9A-F8CD-4EFC-960F-4E5557492480Q40277559-727F1BB8-8F2C-40EA-9493-489D2D725DAAQ40747691-C40E4DDD-9FE4-42A4-9615-06E0554F0F4AQ42791814-A8E2C214-0DF6-47E1-B299-61BBA84272D7Q42874490-63912CD3-475E-4A3E-A082-F4281ECA06E9Q42958870-FCB8E570-6A01-42F5-9CF3-9EA13A902359Q43291564-A4835CAC-0B31-42F0-9615-CAB6232B6481Q44198828-45124CCB-315A-41D6-BF61-D70977895106Q45419394-77D342B6-91C5-4520-89E3-0D218E164FF5Q46113039-D2C876A2-BE8C-4A59-BA64-2210CDE96042Q46316897-45A1643E-4FF7-41FB-83C4-14112997027BQ46446250-27AAC483-DE64-4E4B-8A95-64016C83432BQ46547408-471FE9E0-A3B2-4223-B4BA-868F8D6D3FD8Q46665206-5ED320B5-0FC5-4CDE-9942-E4D5CE05A58FQ46679941-DDFDC3A2-4572-4943-A5AC-B18A3791FFD5Q46795178-5EC91BC0-F23E-4BCB-89DE-DD0B0867C14EQ46873584-1C6FCBE4-8AC2-47A7-9940-7216AE1F7A17Q46887537-AB8A5372-EA04-48E9-A868-6D13288980C1Q53753225-D7FF01F5-E855-494B-B10F-22E5ECB2F09EQ58697467-9316CAEA-C298-4F60-8D12-9EF6A07D65B8Q59569619-F4D63281-0397-44D4-A3A7-8489A95CE0A3Q59569620-D5C51DE4-16BB-4CEC-B9B3-01B0C1072651Q64057956-D5C9C732-D7B4-4529-B6A0-66B77A78D55FQ64270215-68341C3F-5BEB-4CCB-9405-528242299BA4Q64939571-7278880F-557D-45E9-A25F-69817641CEABQ80464738-089BB58F-FE3D-4F63-B1B6-4EE6476DFCB1Q84426581-2E06DE29-68A3-4E17-8C3E-8E4F2CE51B56
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description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Abd El-Galil E Amr
@ast
Abd El-Galil E Amr
@en
Abd El-Galil E Amr
@es
Abd El-Galil E Amr
@nl
type
label
Abd El-Galil E Amr
@ast
Abd El-Galil E Amr
@en
Abd El-Galil E Amr
@es
Abd El-Galil E Amr
@nl
prefLabel
Abd El-Galil E Amr
@ast
Abd El-Galil E Amr
@en
Abd El-Galil E Amr
@es
Abd El-Galil E Amr
@nl
P1153
P106
P1153
55538111500
57191625402
57194148938
57195693294
P31
P496
0000-0002-1338-706X