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The anti-inflammatory sesquiterpene lactone helenalin inhibits the transcription factor NF-kappaB by directly targeting p65Potential of 2-hydroxy-3-phenylsulfanylmethyl-[1,4]-naphthoquinones against Leishmania (L.) infantum: biological activity and structure-activity relationshipsExtract from Rumex acetosa L. for prophylaxis of periodontitis: inhibition of bacterial in vitro adhesion and of gingipains of Porphyromonas gingivalis by epicatechin-3-O-(4β→8)-epicatechin-3-O-gallate (procyanidin-B2-Di-gallate)Antitrypanosomal and antileishmanial activities of flavonoids and their analogues: in vitro, in vivo, structure-activity relationship, and quantitative structure-activity relationship studies(+)-Pinoresinol/(-)-lariciresinol reductase from Linum perenne Himmelszelt involved in the biosynthesis of justicidin B.Reactivity of dimethyl fumarate and methylhydrogen fumarate towards glutathione and N-acetyl-L-cysteine--preparation of S-substituted thiosuccinic acid esters.In Silico prediction and experimental evaluation of furanoheliangolide sesquiterpene lactones as potent agents against Trypanosoma brucei rhodesiense.Secondary metabolites from Vietnamese marine invertebrates with activity against Trypanosoma brucei and T. cruzi.3-O-galloylated procyanidins from Rumex acetosa L. inhibit the attachment of influenza A virus.Kruppel-like factor KLF4 facilitates cutaneous wound healing by promoting fibrocyte generation from myeloid-derived suppressor cells.Targeting acute myeloid leukemia with a small molecule inhibitor of the Myb/p300 interaction.Search for Antiprotozoal Activity in Herbal Medicinal Preparations; New Natural Leads against Neglected Tropical Diseases.Anti-Protozoal Activities of Cembrane-Type Diterpenes from Vietnamese Soft Corals.Antiprotozoal activity of Achillea ptarmica (Asteraceae) and its main alkamide constituents.Antiprotozoal activity of Buxus sempervirens and activity-guided isolation of O-tigloylcyclovirobuxeine-B as the main constituent active against Plasmodium falciparum.PLS-Prediction and Confirmation of Hydrojuglone Glucoside as the Antitrypanosomal Constituent of Juglans Spp.In Silico Identification and in Vitro Activity of Novel Natural Inhibitors of Trypanosoma brucei Glyceraldehyde-3-phosphate-dehydrogenase.Natural sesquiterpene lactones as inhibitors of Myb-dependent gene expression: structure-activity relationships.Evaluation of ethnomedical claim III: anti-hyperglycemic activities of Gongronema latifolium root and stem.9β-hydroxyparthenolide esters from Inula montbretiana and their antiprotozoal activity.Inhibition of Myb-dependent gene expression by the sesquiterpene lactone mexicanin-I.A New Alkamide with an Endoperoxide Structure from Acmella ciliata (Asteraceae) and Its in Vitro Antiplasmodial Activity.Phenolic Constituents of Medicinal Plants with Activity against Trypanosoma brucei.Encecalol angelate, an unstable chromene from Ageratum conyzoides L.: total synthesis and investigation of its antiprotozoal activity.Hologram QSAR studies of antiprotozoal activities of sesquiterpene lactones.Tirucallic acids are novel pleckstrin homology domain-dependent Akt inhibitors inducing apoptosis in prostate cancer cells.Quantitative structure--antiprotozoal activity relationships of sesquiterpene lactones.Pharmacological properties of the extract and some isolated compounds of Clausena lansium stem bark: anti-trichomonal, antidiabetic, anti-inflammatory, hepatoprotective and antioxidant effects.Engineering of a monomeric fluorescent protein AsGFP499 and its applications in a dual translocation and transcription assay.Antileishmanial activity, cytotoxicity and QSAR analysis of synthetic dihydrobenzofuran lignans and related benzofurans.Structure-cytotoxicity relationships of some helenanolide-type sesquiterpene lactones.Cytotoxicity of flavonoids and sesquiterpene lactones from Arnica species against the GLC4 and the COLO 320 cell lines.Natural product derived antiprotozoal agents: synthesis, biological evaluation, and structure-activity relationships of novel chromene and chromane derivatives.Enantioselective synthesis of encecaline-derived potent antimalarial agents.An unusual dimeric guaianolide with antiprotozoal activity and further sesquiterpene lactones from Eupatoriumperfoliatum.Lignans in flowering aerial parts of Linum species--chemodiversity in the light of systematics and phylogeny.Pinoresinol-lariciresinol reductases with opposite enantiospecificity determine the enantiomeric composition of lignans in the different organs of Linum usitatissimum L.The antiprotozoal activity of methylated flavonoids from Ageratum conyzoides L.6-methoxypodophyllotoxin-7-O-n-hexanoate, a new aryltetralin lignan ester from seeds of Linum flavum.New allo-cedrane type sesquiterpene hemiketals and further sesquiterpene lactones from fruits of Illicium floridanum.
P50
Q28290401-3BF6ADE7-7312-437B-A605-606A4C45A263Q28542652-569D54EE-D3D3-4D7A-8434-0D1CB73DC2F5Q28544970-F0C97A7E-ED63-49EA-9B05-B6112EF069AAQ34510572-B80BC7A7-C310-4157-9DC4-0384CD2DE73DQ34574421-7A4DF3D9-04B2-4833-938E-78AE6675F3D5Q34574881-BA2D8481-9E80-4A54-B893-19E3E37DAC1BQ35027306-372530C2-B8C0-4FE8-8AF9-4653743588FFQ35194400-E76C3740-14F1-4D3B-A188-1CB0F0079DE7Q35321520-FBDFA61F-5B45-4985-82E7-2D25AB5DA2C0Q35470164-FF1920BC-38DF-41E1-B90B-DB0A9588D5A6Q35859473-07A9EF0B-2131-4474-A9A2-6A7B5FCD63D4Q38845902-449A75D2-8991-4399-80A1-E3A59E050E2EQ38852010-D69E54E6-DE7E-415A-AC3F-501B6F89AE0EQ38871004-BC72165F-08FA-4000-A633-657B98F48224Q38871008-F7BEC07D-7704-4F38-9818-35D0F1C76B6DQ38991626-960AFA87-0491-43D4-A601-E06EB482F28DQ39065699-72F92835-E40D-4307-8978-FD20AAD959ABQ39179794-370841D0-D57C-4DEB-B01D-0CCA69644134Q39231595-4EAB5F55-B90F-421E-84C4-9F3D4811A972Q39438483-2F3196B4-431B-46D9-9D37-D2A8C4F5651CQ39460430-7B3D520E-5DF6-4797-9A9E-9A485834A937Q39463761-01F05D08-7836-4821-8F1D-52BFBCCDC0ACQ39498814-405DE985-9C8F-47DA-BF8F-2FFFDC27CDA5Q39517135-AF239B6D-2CE0-4206-9410-671B523633B2Q39534582-8D6D9BE9-EF00-4205-8270-D49977A4F7CFQ39761901-6F3E194D-A3E7-4914-A498-9B344B6C4332Q39840361-12BAE443-47EA-4139-B226-EAA94371EE22Q39903696-D3171E04-B571-475D-9A55-16431FADA71EQ39954317-ABBB403A-5CDE-42BD-8C08-A4510A17728EQ40470382-32B74804-DA84-4052-B213-AE5126319D1DQ41123677-DD8B1B8D-CB0F-4E36-96C7-E4E9843D4BB6Q41437369-0873A790-3350-49E5-AE47-620F44E1DD22Q41924537-D88DAFA7-FF1D-4750-95E2-DC146E183377Q42709244-66662753-5E71-4973-8327-6E91013976D3Q42750134-87C9352E-4979-4ED9-988A-B319069D34D1Q42959708-3CE032CA-0F31-4407-891E-1E518816EC05Q43049391-F5CC1566-818A-4E80-8470-AEDFE824DF91Q43134897-07144580-5CCC-44D6-AB92-B0385955EC09Q43230067-50393A2E-B36E-41B4-A01E-C300EB6C3578Q43589948-28103DFA-3EF9-4809-9682-7977B88D24AD
P50
description
hulumtues
@sq
researcher
@en
ricercatore
@it
հետազոտող
@hy
name
Thomas J Schmidt
@ast
Thomas J Schmidt
@en
Thomas J Schmidt
@es
Thomas J Schmidt
@nl
Thomas J Schmidt
@sl
type
label
Thomas J Schmidt
@ast
Thomas J Schmidt
@en
Thomas J Schmidt
@es
Thomas J Schmidt
@nl
Thomas J Schmidt
@sl
prefLabel
Thomas J Schmidt
@ast
Thomas J Schmidt
@en
Thomas J Schmidt
@es
Thomas J Schmidt
@nl
Thomas J Schmidt
@sl
P1053
M-1678-2016
P106
P21
P214
1875145856887422920250
P31
P3829
P496
0000-0003-2634-9705
P734
P735
P7859
viaf-1875145856887422920250