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A galloylated dimeric proanthocyanidin from grape seed exhibits dentin biomodification potential.Chlorinated Coumarins from the Polypore MushroomFomitopsis officinalisand Their Activity againstMycobacterium tuberculosisImportance of purity evaluation and the potential of quantitative ¹H NMR as a purity assay.Dentin biomodification potential depends on polyphenol source.Essential parameters for structural analysis and dereplication by (1)H NMR spectroscopy.Marine macrolides, a promising source of antitumor compounds.New finding of an anti-TB compound in the genus Marsypopetalum (Annonaceae) from a traditional herbal remedy of Laos.The tandem of full spin analysis and qHNMR for the quality control of botanicals exemplified with Ginkgo biloba.Complete 1H NMR spectral analysis of ten chemical markers of Ginkgo biloba.HiFSA fingerprinting applied to isomers with near-identical NMR spectra: the silybin/isosilybin caseUniversal quantitative NMR analysis of complex natural samples.Lipidated steroid saponins from Dioscorea villosa (wild yam).Belizeanolide, a cytotoxic macrolide from the dinoflagellate Prorocentrum belizeanum.Galloyl moieties enhance the dentin biomodification potential of plant-derived catechins.Digital NMR profiles as building blocks: assembling ¹H fingerprints of steviol glycosides.Discovery and characterization of the tuberculosis drug lead ecumicin.Proton fingerprints portray molecular structures: enhanced description of the 1H NMR spectra of small molecules.K-targeted metabolomic analysis extends chemical subtraction to DESIGNER extracts: selective depletion of extracts of hops (Humulus lupulus).Hytramycins V and I, anti-Mycobacterium tuberculosis hexapeptides from a Streptomyces hygroscopicus strain.Corozalic acid: a key okadaic acid biosynthetic precursor with phosphatase inhibition activity.Correction to Importance of Purity Evaluation and the Potential of Quantitative (1)H NMR as a Purity Assay.Antitumor activity of Lepidium latifolium and identification of the epithionitrile 1-cyano-2,3-epithiopropane as its major active component.On the configuration of five-membered rings: a spin-spin coupling constant approach.Structural Sequencing of Oligopeptides Aided by 1H Iterative Full-Spin Analysis.Belizentrin, a highly bioactive macrocycle from the dinoflagellate Prorocentrum belizeanum.Micromelones A and B, noncontiguous polypropionates from Micromelo undata.Computer-assisted 1 H NMR analysis of the anti-tuberculosis drug lead ecumicin.Identification and characterization of DTX-5c and 7-hydroxymethyl-2-methylene-octa-4,7-dienyl okadaate from Prorocentrum belizeanum cultures by LC-MSPd-Catalyzed Synthesis of Aryl and Heteroaryl Triflones from Reactions of Sodium Triflinate with Aryl (Heteroaryl) TriflatesCopper-Catalyzed Aerobic Oxidative Amidation of Benzyl AlcoholsLigand-Controlled Synthesis of Azoles via Ir-Catalyzed Reactions of Sulfoxonium Ylides with 2-Amino Heterocycles
P50
Q27311285-9B16B43C-D668-46AA-9251-E3BABF3025F8Q29037987-7B957FE2-3FC3-4C06-BFD4-29221C631EDDQ30370490-D360816D-DF64-4BAA-94EC-A0BB5AAEEA74Q30574299-4C792568-62D0-4E0D-AA60-CC05E32A82ABQ33824909-30848B31-0E13-48C6-91E2-0E4AAE4E2873Q34604323-AAD3ADCB-4699-4A51-B3DF-EC1760B300A5Q35066117-E973DF53-0C64-45D0-A22C-28C386F2A4B7Q36073688-8FE464FD-EBFB-440A-81B7-77373E9A7E79Q36661741-FA775266-DB00-44CD-BFFD-7E9ED7CBD061Q36807240-2C88C297-8487-4A92-8793-950E3A189AC3Q37550389-8FAF6874-7F20-42C6-AA3A-EFDE999D2B93Q37604312-B5F0F969-53CB-449E-81A0-EEB4A1ECFEE0Q39902562-FE2B6CE5-93AC-456E-B1BE-39F4A0055BD1Q40176868-D2D184D7-DB1A-40DB-ADCD-BE2C64D1C460Q40259482-FF4D2CED-4DB8-47E4-8C25-C86A3700B7EDQ41809992-ECFD8D55-0900-4229-9E9D-D566E6B9786EQ42156135-19561B64-0F7A-4412-9AAB-083C14A031FCQ42552795-BB398B01-D50A-4B92-9931-D1DF526262DAQ42708429-385365BA-829A-43C4-B82D-A15D3358A62BQ42922603-26B638EF-A65A-447B-87BF-8A0204648639Q43145923-BDB7671D-774A-447A-9347-F91C0BB2B0D3Q46274016-AF64F746-EB8B-40D5-B101-9392498DCD83Q46900046-0B416D17-FCE6-4CA3-A5C2-5F05FCAFF2FEQ47789093-94EBBC0F-C894-4747-ADF2-925C04677A02Q51418597-769606D4-265A-44A6-B2DE-0934A7E91E98Q51694648-B5510398-24F3-41B0-B9A5-36C8F01BEA85Q54857901-8CB21166-35BD-435F-B484-7B195E23ECAAQ80411230-A46364F6-A4E6-4C04-8D65-7C5E4A45DB9EQ87023592-5EC8FF9D-3B7B-4185-B773-4C01D3412200Q88551817-E7F8D95B-55CB-48A5-8493-40720DC343B3Q89277189-72B2CB77-66A4-4DD5-87B3-C011F4871EBD
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
José G Napolitano
@ast
José G Napolitano
@en
José G Napolitano
@es
José G Napolitano
@nl
José G Napolitano
@sl
type
label
José G Napolitano
@ast
José G Napolitano
@en
José G Napolitano
@es
José G Napolitano
@nl
José G Napolitano
@sl
prefLabel
José G Napolitano
@ast
José G Napolitano
@en
José G Napolitano
@es
José G Napolitano
@nl
José G Napolitano
@sl
P108
P106
P21
P31
P496
0000-0003-1250-2262