about
NAPROC-13: a database for the dereplication of natural product mixtures in bioassay-guided protocols.A new cytotoxic friedelane acid--pluricostatic acid--and other compounds from the leaves of Marila pluricostata.4-Phenylcoumarins as HIV transcription inhibitors.Uprolides N, O and P from the Panamanian Octocoral Eunicea succinea.3-Phenylcoumarins as inhibitors of HIV-1 replication.Synthesis and antimitotic and tubulin interaction profiles of novel pinacol derivatives of podophyllotoxins.Synthesis, bioevaluation and structural study of substituted phthalazin-1(2H)-ones acting as antifungal agents.Antimalarial activity of imidazo[2,1-a]isoindol-5-ol derivatives and related compounds.Antileishmanial activity and tubulin polymerization inhibition of podophyllotoxin derivatives on Leishmania infantum.Neoflavonoids as Inhibitors of HIV-1 Replication by Targeting the Tat and NF-κB Pathways.Bioactive phenolic derivatives from Acaena splendens methanol extract.Homocoupling versus reduction of radicals: an experimental and theoretical study of Ti(III)-mediated deoxygenation of activated alcohols.Triterpenes from Warszewiczia coccinea (Rubiaceae) as inhibitors of acetylcholinesterase.Simple dihydrosphyngosine analogues with potent activity against MDR-Mycobacterium tuberculosis.Leishmanicidal activity of some stilbenoids and related heterocyclic compounds.Anti-inflammatory activity of leaf extract and fractions of Bursera simaruba (L.) Sarg (Burseraceae).Vasorelaxant properties of acid and neutral fractions of Dimerocostus strobilaceus Kuntze used by Kuna Indians of Panama.Analgesic-antiinflammatory properties of Proustia pyrifolia.Cytotoxic 4-phenylcoumarins from the leaves of Marila pluricostata.Mesuol, a natural occurring 4-phenylcoumarin, inhibits HIV-1 replication by targeting the NF-kappaB pathway.Anxiolytic effects of benzalphthalides.Two new dammarane triterpenoids from Kageneckia angustifolia D. Don.Preliminary study of the anti-inflammatory activity of hexane extract and fractions from Bursera simaruba (Linneo) Sarg. (Burseraceae) leaves.Leishmanicidal and trypanocidal activities of 2-aminocyclohexanol and 1,2-cyclohexanediamine derivatives.Vasorelaxant activity of phthalazinones and related compounds.Methyl psilalate: a new antimicrobial metabolite from Psila boliviensis.Cytotoxic and antimicrobial benzophenones from the leaves of Tovomita longifolia.New pathways in transannular cyclization of germacrone [germacra-1(10),4,7(11)-trien-8-one]: evidence regarding a concerted mechanism.[1,3]Diazaheterofused isoindolol derivatives displaying anxiolytic-like effects on mice.Regioselective Synthesis of 1-Alkyl- or 1-Aryl-1H-indazoles via Copper-Catalyzed Cyclizations of 2-Haloarylcarbonylic CompoundsA new cucurbitacin glycoside from Kageneckia oblonga (Rosaceae)Synthesis and evaluation of some lipidic aminoalcohols and diamines as immunomodulatorsTotal synthesis of (+)-seco-C-oleanane via stepwise controlled radical cascade cyclizationAnti-HIV activity of stilbene-related heterocyclic compoundsTwo new alkylresorcinols from Homalomena wendlandii and their cytotoxic activityStructural diversity from the transannular cyclizations of natural germacrone and epoxy derivatives: a theoretical-experimental studyMimicking Halimane Synthases: Monitoring a Cascade of Cyclizations and Rearrangements from EpoxypolyprenesGermacrone Derivatives as new Insecticidal and Acaricidal Compounds: A Structure-Activity Relationship
P50
Q33303649-8735552C-C944-4860-8C87-1B156591BD24Q33387545-A91F648F-8E64-4E74-9164-E79CD7DA2178Q34447768-D23820BA-5E4D-43A0-97A5-DA4825AA96C1Q36060461-3BD11A11-BD5A-46E1-877F-899DB9779279Q39303248-249A9E6C-87EE-4960-A2A0-A59E1DA24104Q39346179-7A5B54CA-2C53-4CB8-B66E-B5E273638CADQ39449040-D36CBD08-62CE-4426-AA46-0C4248D8FA2FQ39469731-1AC5DFBC-301F-41EA-806F-C93F4CE5EE5BQ40129849-ACFEB83D-93F8-4BE5-9563-DED5E2E348B4Q40325450-5F5047BF-70BB-4899-8302-33DE3E1C7D1AQ40574666-1DA6472F-3EE0-4D71-97FD-84078D4F8A67Q41458532-9B2041DA-C484-4D78-8FA4-9BC65F9B012AQ43242884-35452CAB-B68B-4802-931C-F5FDCE45C11DQ43286833-BDEEAD3F-B102-4022-A5E0-6F3BB46EA788Q43713795-138D89DA-750C-4FC1-A7CD-0B991B1E6F1BQ44853039-C18E7EF5-4CE2-400F-8154-F2038F16A5C0Q45963977-DF2EB058-FFE5-4039-BCD4-0E1B51009CB2Q46390118-01E9D087-D1F5-4B2E-AF7A-D505AABEB1F1Q46400719-7EC7E6FD-1BC9-44A3-867C-6E7A6A028E03Q46505016-F2D04CE1-E2C8-4A0C-A3B7-BB589BF51EADQ46570259-4B7032E8-0FDE-48DB-945C-320552189692Q46710197-FB276F64-CC40-4500-9FC7-5CD1AD4DADD2Q46835555-A81D1690-455D-43D8-A4BC-99551AAE99E9Q46892701-5240E035-2661-4716-8FCC-061FF23E62E4Q46972717-2FB3BA94-7BC1-4DF4-8592-ABECA46897D3Q47584554-0B66D028-5FCD-438E-AD76-ED6097DB8B12Q50082662-3B5ECF40-0899-4934-8B0E-9AEC6D195D59Q50309210-3BBE927A-34A7-405B-B592-CB28A0293470Q51985724-AF31E42F-CC4F-422A-80C9-9DAFFA8BF01FQ59560259-86640CB8-F92C-42B1-981C-8307AA46885BQ73806115-39744E6E-E27A-4A07-9882-F26C803C6B68Q79135198-2F9E0CE6-1C18-41E3-86E1-A3BC1621A82AQ82807705-EAA3E605-A545-4942-B5D8-C07BF0B5E1E6Q83815902-B4F3053A-9D03-4A97-B670-BEEF38D9EC27Q84973251-4F0041E0-84D1-433E-B63F-DF21037C4B5AQ86607483-C0FD8EAE-4A66-48CD-B209-D8D77C9EB582Q90324070-E5CF621B-50A7-46F3-8726-0F472CB95E06Q92569864-133FF7F2-2AE0-4DEA-9245-52E51CE13DCB
P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
José L López-Pérez
@ast
José L López-Pérez
@en
José L López-Pérez
@es
José L López-Pérez
@nl
José L López-Pérez
@sl
type
label
José L López-Pérez
@ast
José L López-Pérez
@en
José L López-Pérez
@es
José L López-Pérez
@nl
José L López-Pérez
@sl
prefLabel
José L López-Pérez
@ast
José L López-Pérez
@en
José L López-Pérez
@es
José L López-Pérez
@nl
José L López-Pérez
@sl
P1053
M-8763-2013
P106
P1153
7004062592
P21
P31
P3829
P496
0000-0002-3728-7602