about
Identification of NF-κB as Determinant of Posttraumatic Stress Disorder and Its Inhibition by the Chinese Herbal Remedy Free and Easy Wanderer.Polyethylene bio-degradation by caterpillars?Radical addition to iminium ions and cationic heterocycles.Chemoenzymatic synthesis of functional sialyl Lewis(x) mimetics with a heteroaromatic core.Carbohydrate nanocarriers in biomedical applications: functionalization and construction.Synthesis and biological evaluation of a D-ring-contracted analogue of lamellarin D.Total synthesis and biological evaluation of the natural product (-)-cyclonerodiol, a new inhibitor of IL-4 signaling.Elatumic acid: a new ursolic acid congener from Omphalocarpum elatum Miers (Sapotaceae).Chromatographically separable rotamers of an unhindered amide.Characterization of the synthetic cannabinoid MDMB-CHMCZCA.ESI-MS2 and Anti-inflammatory Studies of Cyclopropanic Triterpenes. UPLC-ESI-MS and MS2 Search of Related Metabolites from Donella ubanguiensis.Terphenyl Derivatives from Allantophomopsis lycopodina.3'-Demethyldihydromaldoxin and dihydromaldoxin, two anti-inflammtory diaryl ethers from a Steganospora species.The endoperoxide ascaridol shows strong differential cytotoxicity in nucleotide excision repair-deficient cells.GKK1032A₂, a secondary metabolite from Penicillium sp. IBWF-029-96, inhibits conidial germination in the rice blast fungus Magnaporthe oryzae.Structure elucidation of hypocreolide A by enantioselective total synthesis.New caloporoside derivatives and their inhibition of fungal spore germination.rac-4-{(E)-[1-Cyano-1-cyclo-hexyl-2-(1H-indol-3-yl)eth-yl]imino-meth-yl}benzonitrile.New naphthoquinone derivatives from the ascomycete IBWF79B-90A.Oxacyclododecindione, a novel inhibitor of IL-4 signaling from Exserohilum rostratum.Isolation and biological activity of new norhirsutanes from Creolophus cirrhatus.Phytotoxic dioxolanones are potential virulence factors in the infection process of Guignardia bidwellii.Bioconjugation of Small Molecules to RNA Impedes Its Recognition by Toll-Like Receptor 7.Unravelling the biosynthesis of pyriculol in the rice blast fungus Magnaporthe oryzae.Anti-inflammatory tetraquinane diterpenoids from a Crinipellis species.The Chinese herbal formula Free and Easy Wanderer ameliorates oxidative stress through KEAP1-NRF2/HO-1 pathwayA new member of the fusaricidin family - structure elucidation and synthesis of fusaricidin E.N-[(1S,2S)-2-Amino-1,2-diphenyl-eth-yl]-4-methyl-benzene-sulfonamide [(S,S)-TsDPEN].Simple two-step synthesis of 2,4-disubstituted pyrroles and 3,5-disubstituted pyrrole-2-carbonitriles from enones.(Z)-Amino-(2-methyl-3-oxoisoindolin-1-yl-idene)acetonitrileTanzawaic acids I-L: Four new polyketides from Penicillium sp. IBWF104-06.Screening of ligands for the Ullmann synthesis of electron-rich diaryl ethers.SF002-96-1, a new drimane sesquiterpene lactone from an Aspergillus species, inhibits survivin expression.Anti-inflammatory drimane sesquiterpene lactones from an Aspergillus species.(2E,4R,5R,6S)-2-(4,5,6-Trihy-droxy-cyclo-hex-2-en-1-yl-idene)acetonitrile.Caripyrin, a new inhibitor of infection-related morphogenesis in the rice blast fungus Magnaporthe oryzae.Racemization-free synthesis of (S)-(+)-tylophorine from L-proline by radical cyclization.Hirsutane-type sesquiterpenes with uncommon modifications from three basidiomycetes.Cyclocondensation of alpha-aminonitriles and enones: a short access to 3,4-dihydro-2H-pyrrole 2-carbonitriles and 2,3,5-trisubstituted pyrroles.D-glucose as a multivalent chiral scaffold for combinatorial chemistry.
P50
Q37739136-48EDB69E-7DA8-4ED1-BC8D-E9986C6987DEQ38252826-46BCA6E9-33B1-4366-8AD5-4B13E2F90578Q38259607-C89F725B-45FF-4142-975C-3A1946003F5CQ38306662-701BBB19-52AD-422F-8348-BAA0C0E48FD7Q38567851-4B65D3A4-A752-4708-809F-718E0678A9A4Q38715074-6B121850-7ADF-44BE-90F4-3B8E9583931EQ38944559-DA6CAA84-EA07-46B9-B7F9-7B012F2AB82BQ38952291-CA33864D-C093-4878-91EE-C8387155484BQ38969537-051F67A1-3B88-40FB-9D0B-47CCFA4A5750Q38987989-9B59BCD0-AC65-4F3A-9B62-CD8A40D82CAAQ39099602-75B01E9B-6AA7-4E7D-A17B-D6DCE1B9FBCDQ39299648-A6A051A9-E90D-4AD9-A950-6E8129BFD062Q39332364-AFDB1A3D-B819-4291-A223-49E956F53E61Q39405723-9EE8D610-C470-4B66-862D-6710CD98FB1FQ39428937-BA63AFDC-DD8B-4F30-8136-98515E0795EAQ39713471-ABBE26D3-27F3-4D2C-B72A-AB8829E05CCEQ39793398-4CC85A23-3EA8-4E2D-8F03-8694A8F898BDQ39822760-7B922084-6834-41B9-AA95-7C5AFFB3DB8CQ39868004-6465CE58-B8E7-4430-A8BB-39942401002DQ39957495-76AD8B2B-8AF1-477E-BFA2-6B67113E18D6Q39974925-95B2C8CB-C15D-4C0D-9ECB-4096D69228C5Q40085063-2C7474A4-8EE4-4820-82E3-EA489AC5E193Q40258598-95EB6833-8BDD-4307-B5C4-AB58C3B74220Q40429698-72187604-2934-41A3-A3DE-6065B88C81BFQ40435675-068CCCC3-F62E-4CE3-A274-5EA8D0CA0080Q41052057-D56663E1-E816-48CE-9C34-C7D3321F95C8Q41147691-8EDB7AE9-862D-4B5A-B98B-4E80789B6D39Q41511156-1F5837BB-DF8E-449B-B40D-34CADE5955F5Q41841541-A85B31D6-7F36-4195-BA29-0410582BB581Q41918733-F3CAB162-4373-42BF-897E-A6C432B34CB8Q42002073-7E4914B1-CCAA-4C89-9F2A-630D7789F6C6Q42007789-888912DE-EF84-46E9-B4F1-7207ED6FA3C9Q42066106-1EF0570B-724E-4D26-A49C-8BEEF0A2825BQ42216787-4671EEA0-9321-4E90-8841-6AA1EFC4CFE5Q42323558-5E00721C-9A60-43E6-9A19-581EFAF92514Q43105397-F002F3C5-321E-4B8A-BBBD-19C1C2D9EC8AQ43106128-E64B4BE3-33E6-4708-9100-3F8D0B647022Q43117627-F3BAC65E-D4DA-46CF-B873-68F582A278E3Q43270315-A7633A2E-7220-42E2-A0C5-DA248486088DQ44217602-CD9279A8-745D-42DA-A5D0-F707ED9F9263
P50
description
investigador
@es
researcher
@en
wetenschapper
@nl
name
Till Opatz
@en
Till Opatz
@nl
type
label
Till Opatz
@en
Till Opatz
@nl
prefLabel
Till Opatz
@en
Till Opatz
@nl
P31
P496
0000-0002-3266-4050