Arturo San Feliciano

ORCID: 0000-0002-0578-0611
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Research Areas
  • Plant-derived Lignans Synthesis and Bioactivity
  • Biological Activity of Diterpenoids and Biflavonoids
  • Phytochemistry and Biological Activities
  • Bioactive Compounds and Antitumor Agents
  • Natural product bioactivities and synthesis
  • Traditional and Medicinal Uses of Annonaceae
  • Synthesis and biological activity
  • Sesquiterpenes and Asteraceae Studies
  • Phytochemical compounds biological activities
  • Synthetic Organic Chemistry Methods
  • Synthesis and Biological Evaluation
  • Plant biochemistry and biosynthesis
  • Synthesis and Reactions of Organic Compounds
  • Research on Leishmaniasis Studies
  • Carbohydrate Chemistry and Synthesis
  • Asymmetric Synthesis and Catalysis
  • Synthesis of heterocyclic compounds
  • Synthesis and Reactivity of Heterocycles
  • Synthesis and Characterization of Heterocyclic Compounds
  • Phytochemistry and Bioactive Compounds
  • Cancer therapeutics and mechanisms
  • Magnolia and Illicium research
  • Trypanosoma species research and implications
  • Synthesis of Organic Compounds
  • Organic Chemistry Cycloaddition Reactions

Universidad de Salamanca
2015-2024

Instituto de Investigación Biomédica de Salamanca
2015-2024

Universidade do Vale do Itajaí
2020-2024

Pontificia Universidad Católica de Valparaíso
2001-2015

Universidade de Sorocaba
2014

Universidad de Antioquia
2014

University of Valparaíso
1998-2010

Instituto Superior Técnico
1997-2006

University of Lisbon
2000-2006

Universidad de Panamá
2005

We confirmed the ability of triterpenoid betulin to protect against neurotoxicity caused by Bothrops jararacussu snake venom in vitro mouse isolated phrenic nerve-diaphragm (PND) preparations and examined its capability vivo protection using rat external popliteal/sciatic nerve-tibialis anterior (EPSTA) preparation. Venom complete, irreversible blockade PND (40 μ g/mL), but only partial (~30%) EPSTA (3.6 mg/kg, i.m.) after 120 min. In PND, preincubation with commercial bothropic antivenom...

10.1155/2015/939523 article EN cc-by Evidence-based Complementary and Alternative Medicine 2015-01-01

A general method for the one-step regioselective synthesis of 1-alkyl- or 1-aryl-1H-indazoles from ortho-halogenated alkanoylphenones, benzophenones, and arylcarboxylic acids, via copper-catalyzed amination, was developed by using 0.2% mol CuO in presence K2CO3. The reaction involves amination followed intramolecular dehydration. Different functionalized alkyl aryl ketones, diaryl benzoic acid derivatives were efficiently coupled with several hydrazines. Ligands commonly employed as...

10.1021/ol062890e article EN Organic Letters 2007-01-10

Several pinacol derivatives of podophyllotoxins bearing different side chains and functions at C-7 were synthesized through reductive cross-coupling podophyllotoxone several aldehydes ketones. While possessing a hydroxylated chain C-7, the compounds retained their respective hydroxyl group with either 7α (podo) or 7β (epipodo) configuration. Along pinacols, some alkylidene alkyl also prepared. Cytotoxicities against neoplastic cells followed by cell cycle arrest cellular microtubule...

10.1021/jm2017573 article EN Journal of Medicinal Chemistry 2012-05-21

We have synthesized fourteen 3-phenylcoumarin derivatives and evaluated their anti-HIV activity. Antiviral activity was assessed on MT-2 cells infected with viral clones carrying the luciferase gene as reporter. Inhibition of HIV transcription Tat function were tested stably transfected HIV-LTR protein. Six compounds displayed NF-κB inhibition, four resulted antagonists three them showed both activities. Three inhibited replication IC₅₀ values < 25 µM. The antiviral effect 4-hydroxycoumarin...

10.3390/molecules17089245 article EN cc-by Molecules 2012-08-02

The effect of four sub-extracts prepared from the lyophilized hydroalcoholic bark Dipteryx alata (Leguminosae-Papilionoideae) dissolved in a methanol-water (80:20) mixture through liquid-liquid partition procedure has been investigated against neuromuscular blockade venom snake Bothrops jararacussu. active CH2Cl2 sub-extract extensively analyzed for its chemical constituents, resulting isolation lupane-type triterpenoids: lupeol (1), lupenone (2), 28-hydroxylup-20(29)-en-3-one (3), betulin...

10.3390/molecules15118193 article EN cc-by Molecules 2010-11-12

The immunosuppressive activity of several lactonic, nonlactonic, and heterocycle-fused cyclolignans has been demonstrated for the first time by use a T-cell-mediated immune response. Of compounds tested, 4'-demethyldeoxypodophyllotoxin (8), β-apopicropodophyllin (6), isoxazoline-fused cyclolignan 15 are most potent with respect to their suppression activated splenocytes.

10.1021/jm960023h article EN Journal of Medicinal Chemistry 1996-01-01

Bioassay-guided fractionation of the chloroform and ethanol extracts Tovomita longifolia leaves using cytotoxic antimicrobial assays resulted in isolation four new benzophenones, (E)-3-(2-hydroxy-7-methyl-3-methyleneoct-6-enyl)-2,4,6-trihydroxybenzophenone (1), (E)-3-(6-hydroxy-3,7-dimethylocta-2,7-dienyl)-2,4,6-trihydroxybenzophenone (2), 8-benzoyl-2-(4-methylpenten-3-yl)chromane-3,5,7-triol (3), 5-benzoyl-1,1,4a-trimethyl-2,3,4,4a,9,9a-hexahydro-1H-xanthene-6,8-diol (4), two known...

10.1021/np050338c article EN Journal of Natural Products 2006-02-25

Certain members of the genus Eugenia are used as foods. One these species is umbelliflora, which for its fruits. The aim study was to isolate constituents CH2Cl2 fraction obtained from E. umbelliflora O. Berg (Myrtaceae) and also evaluate antimicrobial properties. Two new meroterpenoids, eugenial C (3) D (4) were isolated unripe fruits their structures established mainly by extensive NMR spectroscopy. In previous studies, extract showed significant antibacterial activity, can be attributed...

10.1021/acs.jafc.5b03562 article EN Journal of Agricultural and Food Chemistry 2015-08-26

Quinones are secondary metabolites of higher plants associated with many biological activities, including antiviral effects and cytotoxicity. In this study, the anti-herpetic anti-dengue evaluation 27 terpenyl-1,4-naphthoquinone (NQ), 1,4-anthraquinone (AQ) heterocycle-fused quinone (HetQ) derivatives was done in vitro against Human Herpesvirus (HHV) type 1 2, Dengue virus serotype 2 (DENV-2). The cytotoxicity on HeLa Jurkat tumor cell lines also tested. Using plaque forming unit assays,...

10.3390/molecules24071279 article EN cc-by Molecules 2019-04-02

Abstract 28 cyclolignans, most of them derived from podophyllotoxin, have been evaluated for their antineoplastic and antiviral activities. They were subjected to screening against P‐388 murine leukemia, A‐549 human lung carcinoma, HT‐29 colon while assays performed on herpes simplex virus type I infecting fibroblasts monkey kidney (HSV/CV‐1) vesicular stomatitis hamster (VSV/BHK). A number substances active in both groups at concentrations below 1μM; deoxypodophyllotoxin ( 1 ) being the...

10.1002/ardp.19943270309 article EN Archiv der Pharmazie 1994-01-01

Nineteen cyclolignans of varied structures, most them isolated from Juniperus sabina leaves, were evaluated for their antineoplastic and anti-viral activities. They subjected to screening against P-388 murine leukemia, A-549 human lung carcinoma, HT-29 colon while the antiviral assays performed on herpes simplex virus type 1 infecting fibroblasts monkey kidney (HSV-1/CV-1) vesicular stomatitis hamster (VSV/BHK). A number substances active in both types at concentrations below µg/ml;...

10.1055/s-2006-959660 article EN Planta Medica 1993-06-01
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