about
Novel Natural Product- and Privileged Scaffold-Based Tubulin Inhibitors Targeting the Colchicine Binding SiteIdentification of new drug targets and resistance mechanisms in Mycobacterium tuberculosisSynthesis of C-Pseudonucleosides Bearing Thiazolidin-4-one as a Novel Potential Immunostimulating AgentConformational space and vibrational spectra of 2-[(2,4-dimethoxyphenyl)amino]-1,3-thiazolidin-4-one.N-(2,4-Dioxo-1,3-thia-zolidin-3-yl)-2-(4-isobutyl-phen-yl)propanamide.Synthesis of new pyrazolyl-2, 4-thiazolidinediones as antibacterial and antifungal agents.5-Chloro-N-{4-oxo-2-[4-(trifluoro-meth-yl)phen-yl]-1,3-thia-zolidin-3-yl}-3-phenyl-1H-indole-2-carboxamideCrystal structure of (5Z)-5-(5-bromo-2-hy-droxy-benzyl-idene)-1,3-thia-zolidine-2,4-dione.Microwave assisted tandem reactions for the synthesis of 2-hydrazolyl-4-thiazolidinones.Medicinal significance of benzothiazole scaffold: an insight view.Synthesis and antibacterial and cytotoxic activities of new N-3 substituted thiazolidine-2,4-dione derivatives bearing the pyrazole moiety.Synthesis, cytotoxicity, and pro-apoptosis activity of etodolac hydrazide derivatives as anticancer agents.A convenient ultrasound-promoted synthesis of some new thiazole derivatives bearing a coumarin nucleus and their cytotoxic activity.Design and synthesis of 2-iminothiazolidin-4-one moiety-containing compounds as potent antiproliferative agents.Synthesis and antimicrobial activities of 5-Arylidene-thiazolidine-2,4-dione derivatives.New thiourea and 1,3-thiazolidin-4-one derivatives effective on the HIV-1 virus.Synthesis, antioxidant and antimicrobial activities of novel thiopyrano[2,3-d]thiazoles based on aroylacrylic acids.4-({(Z)-5-[(Z)-3-Eth-oxy-4-hy-droxy-benzyl-idene]-3-methyl-4-oxo-1,3-thia-zolidin-2-yl-idene}amino)-benzoic acid dimethyl-formamide monosolvate.Synthesis and biological evaluation of new 1,3-thiazolidine-4-one derivatives of 2-(4-isobutylphenyl)propionic acid.Synthesis, antimicrobial and antiviral testing of some new 1-adamantyl analogues.Crystal structure of (Z)-2-hy-droxy-4-methyl-N'-(4-oxo-1,3-thia-zolidin-2-yl-idene)benzohydrazide trihydrate.Crystal structure of (Z)-2-hy-droxy-N'-(4-oxo-1,3-thia-zolidin-2-yl-idene)benzohydrazide.Chemistry of polyhalogenated nitrobutadienes, 14: Efficient synthesis of functionalized (Z)-2-allylidenethiazolidin-4-ones.Efficient regioselective three-component domino synthesis of 3-(1,2,4-Triazol-5-yl)-1,3-thiazolidin-4-ones as potent antifungal and antituberculosis agents.Microwave-assisted synthesis of dinucleoside analogues containing a thiazolidin-4-one linkage via one-pot tandem Staudinger/aza-Wittig/cyclization.Synthesis and biological evaluation of (E)-1-(substituted)-3-phenylprop-2-en-1-ones bearing rhodanines as potent anti-microbial agents.Synthesis, in vitro antitubercular activity and 3D-QSAR of novel quinoxaline derivatives.Benign by design: catalyst-free in-water, on-water green chemical methodologies in organic synthesis.Synthesis of some heterofunctionalized penicillanic acid derivatives and investigation of their biological activities.Silver Nanoparticles Mediated by Costus afer Leaf Extract: Synthesis, Antibacterial, Antioxidant and Electrochemical Properties.Synthesis and pharmacological investigation of 2-(4-dimethylaminophenyl)-3,5-disubstituted thiazolidin-4-ones as anticonvulsants.A green, multicomponent, regio- and stereo-selective 1,3-dipolar cycloaddition of azides and azomethine ylides generated in situ with bifunctional dipolarophiles using PEG-400.In silico identification of targets for a novel scaffold, 2-thiazolylimino-5-benzylidin-thiazolidin-4-one.Synthesis and antifungal activity of dehydroabietic acid-based 1,3,4-thiadiazole-thiazolidinone compounds.Discovery of the highly potent fluoroquinolone-based benzothiazolyl-4-thiazolidinone hybrids as antibacterials.An asymmetric alkynylation/hydrothiolation cascade: an enantioselective synthesis of thiazolidine-2-imines from imines, acetylenes and isothiocyanates.Synthesis and Antifungal Screening of 2-{[1-(5-Alkyl/arylalkylpyrazin-2-yl)ethylidene]hydrazono}-1,3-thiazolidin-4-ones.Synthesis of 2-mercaptobenzimidazole derivatives as potential anti-microbial and cytotoxic agents.Thiopyrano[2,3-d]Thiazoles as New Efficient Scaffolds in Medicinal Chemistry.Novel thiazolidinone-containing compounds, without the well-known sulphonamide zinc-binding group acting as human carbonic anhydrase IX inhibitors
P2860
Q28067375-95A46343-9344-4556-A9CE-2A5AF584B121Q28533721-6FB84390-6C86-413C-8539-91E0E751288FQ28657565-527457BA-DE26-48A8-85A9-F98A70368A2AQ34071617-3504CAA9-40C4-402C-BA77-662C253B7B0CQ34265984-0909AA23-4ADD-44E3-BED1-F631F5CAC1CFQ35872366-77E5966F-BBD2-4E74-8660-CD9355059B03Q36314404-980C5059-642A-4FBE-B066-4F290D3536C6Q36482023-E95FFA71-A915-46D0-9629-294FFD1ED9E5Q37345501-DC3D8002-661E-4557-A265-748C212E46DAQ38048811-1033FCFA-C6D5-46A6-BD43-26BB282F2B53Q39004478-01EFFD26-3388-47C2-9C96-481DD346D51EQ39162073-AF4923C9-0BEA-465E-BB18-864A47C95481Q39302327-5E2010A5-A5A3-4DE5-AAE5-DA18400D339BQ39416611-AEF4BFB5-81D6-4D73-BC27-2F70CB3E4642Q39937286-23A341DB-0B02-446D-A698-76FA87F007C4Q40231384-D51B57C9-8705-4156-9BA0-C3C2E3352780Q40235335-061E1849-D3E5-419F-A9E0-87CEC3DADDA9Q41580363-457B0A4F-F1FF-49B2-BB4C-6D92C3D59497Q41733181-D0430462-AF0A-4C33-8B3F-5179AAEA3CBCQ41811192-B2C1805B-F819-436F-B78C-7F6885325E9EQ41845378-B8B26185-E776-4C2A-88D2-64F3414D3C24Q41932108-2C047754-694E-46CE-A48C-E4DFC0E8CB49Q42121724-41675535-DF34-4001-A8AF-64A3967C2A3DQ42726732-855AEA09-799B-4E96-BD59-A1911BA48DEBQ42731300-488B8D6E-71FF-49CE-93A5-9A09A4EE243BQ43559467-55B1539B-542F-42A0-B9E8-04028CC862EEQ44663921-E4BAA062-C860-4143-A339-00B2CFEFF310Q44767766-FDE11723-DEFF-4CB7-803A-6F1079FBF8B6Q46381177-A90773E5-22A6-4F3B-9FBE-DC745182B6AEQ46644230-C429723E-A651-42C8-A7AD-F582AFF66367Q48143337-0B9F8326-8B0A-41C6-8CE2-593F8D56D6F6Q50460476-CB5AA7AF-9494-43F9-B96D-3CD43EFE8813Q50927975-83811CF8-537F-49A2-8916-D248FC8ABE38Q51221077-43B32B64-3A4A-4B1E-B510-4FE8CAA9CE0FQ53295716-E1822AB0-6F66-4E4E-BC02-A4C8213D0BC2Q53587876-6D8F554C-1CA5-41DF-B6F3-F9A662657D20Q53663010-55292191-37EF-48D5-B1A5-C3AE0D4E10CDQ54369458-649A18A5-64F6-42C4-926D-440E33B1EC09Q55405195-D358595B-FAE9-4BA6-8067-D39D5ABB7946Q58700155-78FFE19B-B5D0-4104-8B1E-DC7A6E886011
P2860
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
2007年论文
@zh
2007年论文
@zh-cn
name
4-thiazolidinone--a biologically active scaffold.
@en
type
label
4-thiazolidinone--a biologically active scaffold.
@en
prefLabel
4-thiazolidinone--a biologically active scaffold.
@en
P1476
4-thiazolidinone--a biologically active scaffold
@en
P2093
Amit Verma
P304
P356
10.1016/J.EJMECH.2007.07.017
P577
2007-08-06T00:00:00Z