about
New 1H-pyrazole-containing polyamine receptors able to complex L-glutamate in water at physiological pH values.Computed coupling constants in X(CH3)nH(4-n) moieties where X = 13C and 15N+, and n = 0-4: comparisons with experimental data.Structural and spectral assignment of a new diterpenoid isolated from Ballota undulata and a complete (1)H and (13)C NMR data assignment for three other structurally related compounds.Hydrogen-bond-mediated self-assembly of 26-membered diaza tetraester crowns of 3,5-disubstituted 1H-pyrazole. Dimerization study in the solid state and in CDCl3 solution.Structural characterization of highly glucosylated crocins and regulation of their biosynthesis during flower development in CrocusNew polyhydroxylated sterols from Palythoa tuberculosa and their apoptotic activity in cancer cells.9-Arylpurines as a novel class of enterovirus inhibitors.Bioactive diterpenes from Orthosiphon labiatus and Salvia africana-lutea.Abasic analogues of TSAO-T as the first sugar derivatives that specifically inhibit HIV-1 reverse transcriptase.Synthesis and anti-HIV activity of [AZT]-[TSAO-T] and [AZT]-[HEPT] dimers as potential multifunctional inhibitors of HIV-1 reverse transcriptase.Enzymatic synthesis and characterization of fructooligosaccharides and novel maltosylfructosides by inulosucrase from Lactobacillus gasseri DSM 20604.Enzymatic synthesis and identification of two trisaccharides produced from lactulose by transgalactosylation.Characterization of a glucosyltransferase enzyme involved in the formation of kaempferol and quercetin sophorosides in Crocus sativus.Intramolecular cation-pi interactions as the driving force to restrict the conformation of certain nucleosides.Characterization of galactosyl derivatives obtained by transgalactosylation of lactose and different polyols using immobilized beta-galactosidase from Aspergillus oryzae.One-pot synthesis of polycyclic nucleosides with unusual molecular skeletons."Second generation" of TSAO compounds directed against HIV-1 TSAO-resistant strains.Synthesis and structural characterization of pyrimidine bi- and tricyclic nucleosides with sugar puckers conformationally locked into the eastern region of the pseudorotational cycle.Structure of a 4-nitroso-5-aminopyrazole and its salts: tautomerism, protonation, and E/Z isomerism.NMR and x-ray conformational study of artemisiifolin and three other related germacranolides.Homoheteroaromaticity: the case study of azepine and dibenzazepine.Synthesis of novel Bi-, Tri-, and tetracyclic nucleosides by reaction of a common cyclic enamine derived from TSAO-T with nucleophiles.The structure of Rimonabant in the solid state and in solution: an experimental and theoretical study.From kinase to cyclase: an unusual example of catalytic promiscuity modulated by metal switching.Analogues of the neuroprotective tripeptide Gly-Pro-Glu (GPE): synthesis and structure-activity relationships.Experimental measurements and theoretical calculations of the chemical shifts and coupling constants of three azines (benzalazine, acetophenoneazine and cinnamaldazine).Inositol phosphate profiling of fermented cowpeas by 1H NMR spectroscopy.A new Delta7,22 sterol from the bulbs of Autonoë madeirensis.New Gly-Pro-Glu (GPE) analogues: expedite solid-phase synthesis and biological activity.7,5'-O-dibenzylinosines: synthesis and studies on their conformational properties.Synthesis of highly condensed polycyclic carbohydrates by reaction of a spirocyclic enamino sulfonate derived from d-xylofuranose with bifunctional reagents.Unprecedented lability of the 5'-O-tert-butyldimethylsilyl group from 3'-spiro-5''-(4''-acylamino-1'',2''-oxathiole-2'',2''-dioxide) nucleoside derivatives via neighboring group participation of the 4''-acylamino residue.Synthesis of potentially-bioactive lactosyl-oligofructosides by a novel bi-enzymatic system using bacterial fructansucrases.Multitarget-Directed Ligands Combining Cholinesterase and Monoamine Oxidase Inhibition with Histamine H3 R Antagonism for Neurodegenerative Diseases.Stereochemical and Steric Control of Photophysical and Chiroptical Properties in Bichromophoric Systems.Novel tacrine-grafted Ugi adducts as multipotent anti-Alzheimer drugs: a synthetic renewal in tacrine-ferulic acid hybrids.The neuroprotective activity of GPE tripeptide analogues does not correlate with glutamate receptor binding affinity.The Antioxidant Additive Approach for Alzheimer's Disease Therapy: New Ferulic (Lipoic) Acid Plus Melatonin Modified Tacrines as Cholinesterases Inhibitors, Direct Antioxidants, and Nuclear Factor (Erythroid-Derived 2)-Like 2 Activators.Synthesis and structural characterization of raffinosyl-oligofructosides upon transfructosylation by Lactobacillus gasseri DSM 20604 inulosucrase.TSAO Derivatives: Highly Specific Inhibitors of Human Immunodeficiency Virus Type-1 (HIV-1) Replication
P50
Q30888867-00FCB349-D27D-4312-AE24-9DD6AE523C3EQ31039325-7E3E7CE8-EC6F-4CA4-97A5-8AF83F3C9C5EQ33292205-8D5795C8-2E77-4737-8D63-770A06F73FCBQ34016924-7DFFAEED-A54B-4045-BE86-C58CC4663A3AQ36245693-8BFB3B3B-B3D6-4677-8CF1-4E2B5FB68ED6Q38861683-DC04BBED-480F-40D5-8E75-259BE9D536DBQ39772818-8AABC307-4566-4ED8-8DE3-A5AC73E44CA0Q40178504-59AC54FA-327B-43A6-99F8-C49EECBFFE31Q40996897-4AC01C49-07F0-49D8-A159-FB2565F50FA0Q41346144-48EF7676-2050-422A-8114-D12EB3CAC12DQ41434016-51711614-D4B3-47E2-81C1-AD2D4D2DAD15Q42640490-124A1DCE-44E2-4BA0-98C0-1046A0D15989Q42717803-D65C14D3-635C-4DAB-8EEA-E358CBE43E24Q43146344-4B5019E7-7C07-45E1-8569-1A10550DF6C3Q43248069-BD64BC2A-3FB6-41E5-8BF4-D05A1A78C5BFQ43248789-3557E569-349F-4610-96A4-14302AD53B44Q43741929-95EEFD92-5E04-41F6-89AC-BC384F494A9FQ44549875-D45C0919-B63C-47C9-8346-86EBD469975EQ44646349-31C5AA83-3EBC-4843-B84B-78B19A06427FQ44850305-5530490A-51EF-4168-A3BC-ADEEFD638672Q44909934-7A13C8DF-5B42-4401-AD3B-E6F4B33661AFQ45170833-2335D6DD-FF31-4485-B8E2-6506BB95B4B2Q46199092-79C95E25-B08C-4963-91F6-A07637259B3AQ46213065-24C90C42-5C14-4E8B-BE10-AC267A623E43Q46443161-9D5410A3-A305-4DF9-8F3C-1D5935723A16Q46476721-836E176D-64E8-4CC0-B646-1D95FDEFD180Q46532590-C65C548C-EE84-438C-8F80-6A15DAC5A3D3Q46763439-89F9E3A5-18CF-4030-8E0E-F84E6219BB17Q46830554-59132320-8565-4134-8A64-C5FE354BEDDEQ46860516-BA5B48AE-CBFF-4764-B806-CC3EF54168B8Q46902346-193C944A-D7B6-49B4-8845-2C2F3F8914ECQ46936338-C3F6D035-9338-46F2-907C-3BFC5673B082Q47894780-0C1FD2C5-1406-4F72-BA9C-52CE7458141FQ48130975-CEA32F5A-3E2C-4FF1-AE71-5197BC5EEAD3Q48287608-7EA8EDEB-4175-4462-85ED-608CF1EA52C4Q48401352-587AD208-B9D8-43EB-BCC6-BDFE5177D970Q48559355-F49B82BE-E4C7-42AE-A03B-D72069A8A256Q48950857-1E214F87-2B69-434C-A1FB-CFFF1765F9D9Q51471047-C351823B-3534-45C7-9308-DFC8C950747BQ57977646-A3412684-48BD-4F14-94D2-DEA836EDFDAE
P50
description
hulumtuese
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Maria Luisa Jimeno
@ast
Maria Luisa Jimeno
@en
Maria Luisa Jimeno
@es
Maria Luisa Jimeno
@nl
Maria Luisa Jimeno
@sl
type
label
Maria Luisa Jimeno
@ast
Maria Luisa Jimeno
@en
Maria Luisa Jimeno
@es
Maria Luisa Jimeno
@nl
Maria Luisa Jimeno
@sl
prefLabel
Maria Luisa Jimeno
@ast
Maria Luisa Jimeno
@en
Maria Luisa Jimeno
@es
Maria Luisa Jimeno
@nl
Maria Luisa Jimeno
@sl
P1053
G-8723-2015
P106
P1153
7003949931
P21
P31
P3829
P496
0000-0001-6784-162X