about
In vitro bactericidal activity of 4- and 5-chloro-2-hydroxy-N-[1-oxo-1-(phenylamino)alkan-2-yl]benzamides against MRSA.Antiviral activity of substituted salicylanilides--a review.Advances in mycobacterial isocitrate lyase targeting and inhibitors.Sulphur-Containing Heterocycles as Antimycobacterial Agents: Recent Advances in Thiophene and Thiadiazole Derivatives.Combating highly resistant emerging pathogen Mycobacterium abscessus and Mycobacterium tuberculosis with novel salicylanilide esters and carbamates.Salicylanilide N-monosubstituted carbamates: Synthesis and in vitro antimicrobial activity.Synthesis and in vitro biological evaluation of 2-(phenylcarbamoyl)phenyl 4-substituted benzoates.Synthesis and biological activity of new salicylanilide N,N-disubstituted carbamates and thiocarbamates.Vibrational spectroscopic investigations and computational study of 5-chloro-2-[4-(trifluoromethyl)phenylcarbamoyl]phenyl acetate.Salicylanilide acetates: synthesis and antibacterial evaluation.In vitro biological evaluation of new antimycobacterial salicylanilide-tuftsin conjugates.Synthesis and antimicrobial evaluation of new 2-substituted 5,7-di-tert-butylbenzoxazoles.Novel Sulfamethoxazole Ureas and Oxalamide as Potential Antimycobacterial Agents.Synthesis of readily available fluorophenylalanine derivatives and investigation of their biological activity.N-substituted 2-isonicotinoylhydrazinecarboxamides--new antimycobacterial active molecules.Salicylanilide diethyl phosphates: synthesis, antimicrobial activity and cytotoxicity.Salicylanilide pyrazinoates inhibit in vitro multidrug-resistant Mycobacterium tuberculosis strains, atypical mycobacteria and isocitrate lyase.New derivatives of salicylamides: Preparation and antimicrobial activity against various bacterial species.Antimycobacterial assessment of Salicylanilide benzoates including multidrug-resistant tuberculosis strains.New series of isoniazid hydrazones linked with electron-withdrawing substituents.New amino acid esters of salicylanilides active against MDR-TB and other microbes.Synthetic route for the preparation of 2-hydroxy-N-[1-(2-hydroxyphenylamino)-1-oxoalkan-2-yl]benzamides.Preparation, in vitro evaluation and molecular modelling of pyridinium-quinolinium/isoquinolinium non-symmetrical bisquaternary cholinesterase inhibitors.FT-IR, FT-Raman and DFT calculations of 4-chloro-2-(3,4-dichlorophenylcarbamoyl)phenyl acetate.Salicylanilide esters of N-protected amino acids as novel antimicrobial agents.Sulfadiazine Salicylaldehyde-Based Schiff Bases: Synthesis, Antimicrobial Activity and Cytotoxicity.Novel derivatives of nitro-substituted salicylic acids: Synthesis, antimicrobial activity and cytotoxicity.Highly lipophilic benzoxazoles with potential antibacterial activity.Substituted pyrazinecarboxamides: synthesis and biological evaluation.Antifungal Activity of Salicylanilides and Their Esters with 4-(Trifluoromethyl)benzoic Acid.Synthesis and antimycobacterial and photosynthesis-inhibiting evaluation of 2-[(E)-2-substituted-ethenyl]-1,3-benzoxazoles.Effect of alaptide, its analogues and oxiracetam on memory for an elevated plus-maze in mice.Corrigendum to "Novel salicylanilides from 4,5-dihalogenated salicylic acids: Synthesis, antimicrobial activity and cytotoxicity" [Bioorg. Med. Chem. 25 (2017) 1524-1532].Antimicrobial activity of rhodanine-3-acetic acid derivatives.Novel salicylanilides from 4,5-dihalogenated salicylic acids: Synthesis, antimicrobial activity and cytotoxicity.Investigating Spectrum of Biological Activity of 4- and 5-Chloro-2-hydroxy-N-[2-(arylamino)-1-alkyl-2-oxoethyl]benzamidesAntistaphylococcal Activity of Novel Salicylanilide DerivativesAntibacterial Activity of Salicylanilide 4-(Trifluoromethyl)-benzoatesIn vitro antibacterial and antifungal activity of salicylanilide benzoatesSalicylanilide diethyl phosphates as potential inhibitors of some mycobacterial enzymes
P50
Q35063799-19E282C1-1F51-4DCD-AF77-37295FCDDF6FQ37901506-85B8DBB3-BAE8-40A8-A994-A8404686338AQ38054775-AB1C4138-41F8-4FCE-8459-B690A7741358Q38826871-33D7470C-1D94-4697-8036-081D3EB80877Q38849377-1834503B-C38D-48A9-A8DB-EB691D88D351Q38907920-C9CAC51C-859B-42BB-A5E5-A62A42EDCE47Q39057110-30B3F44D-EB36-4938-88AD-6603E7E1C72DQ39171946-B679342C-5A0C-46BC-B48A-88058F5F1687Q39420502-A75D03CE-65EB-4467-9902-0F5F642CFB31Q40095099-38BE9602-5C69-421B-95BB-086251B799E4Q40261992-B9B766D5-7D67-412C-AB1B-98F40E11DC76Q40265709-7B116916-1DF4-4FD3-88D4-CF02F7406A74Q40275284-9E03BC75-62C5-4F23-A9EE-C9003B9949B6Q40314053-C6754293-5C08-4C72-9491-223FA5827DA6Q42706161-E8041D7B-06D2-4F8B-94DD-0DA64D558C10Q42707770-333AC33D-E10F-4F8B-A139-9B514A070EC2Q42707928-758EDA7F-D994-40B9-8367-B60A964573C6Q42709366-26F55D6D-4F0F-4E14-975F-43CC20C76F45Q42714559-E04344EC-F2A2-40E9-BCB8-A4DA0C6BA96CQ42725784-BA36F4F3-61F6-47E7-95C2-192260076B42Q42862183-5453D489-982B-4DC9-8DD2-53B0449DDE6EQ43078375-E7E8C780-525C-4801-A6DD-4B5828C0775EQ43612984-201303CA-5804-4CD4-BA32-6CC04CF7D88AQ46177508-C73C7750-2F77-4B5E-835D-762FD64411B9Q46199045-E87959D9-1C25-4756-A26D-C97C22C7BBA3Q46304589-13285D4C-BA2C-4D77-8C26-BF9369973298Q46645003-6ECC6030-6BA0-472A-A533-003126243A95Q46897105-48628728-5034-4DDA-8F06-3A3DEFF979EDQ46930090-62DA63F1-9890-4528-BA2A-AD7330E7D263Q47292921-5702C06C-AED9-4C03-9341-1ADAFCCA8340Q51411495-BC318AE5-8315-42F5-8447-4427704D9CDDQ52046063-E35A5CEA-F9BC-40A1-9C19-5D1EF3921B3EQ53442127-BE9983A4-D72D-4124-A4CC-353DB9610F46Q53750818-86E8CB85-22C9-446D-A0CA-65B4C677BAE1Q53752600-3465FD84-FE16-4CB9-9975-9406F782CA00Q58260478-BBCFD88E-CA55-4D12-9A66-A5971B946E5CQ58359132-7D0A2D7F-4C76-468A-867F-C23F5117B561Q58851373-6BDD3BDC-C7A4-4B1A-B196-EFAE05DAC1FDQ58914729-0F0640BC-DFA6-4B97-A266-71EE5D518E70Q58929979-3E29B110-212F-483C-B3AB-A7F23FB4A38D
P50
description
hulumtuese
@sq
onderzoeker
@nl
researcher
@en
ricercatrice
@it
հետազոտող
@hy
name
Jarmila Vinsova
@ast
Jarmila Vinsova
@en
Jarmila Vinsova
@es
Jarmila Vinsova
@nl
Jarmila Vinsova
@sl
Jarmila Vinšová
@cs
type
label
Jarmila Vinsova
@ast
Jarmila Vinsova
@en
Jarmila Vinsova
@es
Jarmila Vinsova
@nl
Jarmila Vinsova
@sl
Jarmila Vinšová
@cs
altLabel
Jarmila Vinsova
@en
prefLabel
Jarmila Vinsova
@ast
Jarmila Vinsova
@en
Jarmila Vinsova
@es
Jarmila Vinsova
@nl
Jarmila Vinsova
@sl
Jarmila Vinšová
@cs
P214
P1053
A-9068-2008
P106
P1153
6701677200
P21
P214
P31
P3829
P496
0000-0002-3272-1158
P569
1951-03-17T00:00:00Z
P691
nlk19990073991
P735
P7859
lccn-n2010180386