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Hydroselenation of alkynes by lithium butylselenolate: an approach in the synthesis of vinylic selenidesOrganic and inorganic forms of selenium inhibited differently fish (Rhamdia quelen) and rat (Rattus norvergicus albinus) delta-aminolevulinate dehydrataseSynthesis and biological evaluation of new nitrogen-containing diselenides.Palladium-catalyzed coupling of sp(2)-hybridized tellurides.Vinylic tellurides: from preparation to their applicability in organic synthesis.Pharmacology and toxicology of diphenyl diselenide in several biological models.Synthesis and antitumor activity of selenium-containing quinone-based triazoles possessing two redox centres, and their mechanistic insights.Hybrid compounds with two redox centres: modular synthesis of chalcogen-containing lapachones and studies on their antitumor activity.New organochalcogen multitarget drug: synthesis and antioxidant and antitumoral activities of chalcogenozidovudine derivatives.Succinobucol, a Lipid-Lowering Drug, Protects Against 3-Nitropropionic Acid-Induced Mitochondrial Dysfunction and Oxidative Stress in SH-SY5Y Cells via Upregulation of Glutathione Levels and Glutamate Cysteine Ligase Activity.Chiral organoselenium-transition-metal catalysts in asymmetric transformations.Charge-displacement analysis as a tool to study chalcogen bonded adducts and predict their association constants in solution.An efficient one-pot synthesis of symmetrical diselenides or ditellurides from halides with CuO nanopowder/Se0 or Te0/base.Selenoxides inhibit delta-aminolevulinic acid dehydratase.Enhancement of iron-catalyzed lipid peroxidation by acidosis in brain homogenate: comparative effect of diphenyl diselenide and ebselen.Antioxidant properties of new chalcogenides against lipid peroxidation in rat brain.Addition of butoxycarbonyl group to phenylalanine derived chalcogenide increases the toxic potential: importance of non-bonding nitrogen interaction.Facilitation of long-term object recognition memory by pretraining administration of diphenyl diselenide in mice.Creatine protects against the convulsive behavior and lactate production elicited by the intrastriatal injection of methylmalonate.Renal and hepatic ALA-D activity and selected oxidative stress parameters of rats exposed to inorganic mercury and organoselenium compounds.Aziridine sulfides and disulfides as catalysts for the enantioselective addition of diethylzinc to aldehydes.Effects of age on reserpine-induced orofacial dyskinesia and possible protection of diphenyl diselenide.Selenocysteine incorporation in Kinetoplastid: selenophosphate synthetase (SELD) from Leishmania major and Trypanosoma brucei.Synthesis and biological evaluation of 2-picolylamide-based diselenides with non-bonded interactions.Acceleration of arylzinc formation and its enantioselective addition to aldehydes by microwave irradiation and aziridine-2-methanol catalysts.Efficient synthesis of chiral beta-seleno amides via ring-opening reaction of 2-oxazolines and their application in the palladium-catalyzed asymmetric allylic alkylation.Evaluation of the pharmacological properties of salicylic acid-derivative organoselenium: 2-hydroxy-5-selenocyanatobenzoic acid as an anti-inflammatory and antinociceptive compound.Decreased forelimb ability in mice intracerebroventricularly injected with low dose 6-hydroxidopamine: A model on the dissociation of bradykinesia from hypokinesia.3'3-ditrifluoromethyldiphenyl diselenide: a new organoselenium compound with interesting antigenotoxic and antimutagenic activities.Direct, Metal-free C(sp2 )-H Chalcogenation of Indoles and Imidazopyridines with Dichalcogenides Catalysed by KIO3.Regioselective, Solvent- and Metal-Free Chalcogenation of Imidazo[1,2-a]pyridines by Employing I2 /DMSO as the Catalytic Oxidation System.Succinobucol versus probucol: higher efficiency of succinobucol in mitigating 3-NP-induced brain mitochondrial dysfunction and oxidative stress in vitro.Rose Bengal catalysed photo-induced selenylation of indoles, imidazoles and arenes: a metal free approach.Synthesis of Selenium-Quinone Hybrid Compounds with Potential Antitumor Activity via Rh-Catalyzed C-H Bond Activation and Click Reactions.Oxalate modulates thiobarbituric acid reactive species (TBARS) production in supernatants of homogenates from rat brain, liver and kidney: effect of diphenyl diselenide and diphenyl ditelluride.An organic selenium compound attenuates apomorphine-induced stereotypy in mice.Effect of organic forms of selenium on delta-aminolevulinate dehydratase from liver, kidney, and brain of adult rats.Diethyl 2-phenyl-2 tellurophenyl vinylphosphonate: an organotellurium compound with low toxicity.An organoselenium drug with antioxidant activity and free radical scavenging capacity in vitro.Antioxidant activity of β-selenoamines and their capacity to mimic different enzymes.
P50
Q28252457-B310DDE9-FF90-4B77-A897-DACA9B287431Q28568311-2798408A-4CFA-4928-BA1D-2309E118FF16Q30854468-94CB2B1B-0550-494B-88D6-2ADBE1A9AC31Q35563696-67235933-2576-4549-821D-6247C9D67550Q36415721-DE62CBC5-E7D8-437C-9A51-DD0A7D311EF5Q37197834-E77B057D-6CB9-4942-ABD0-B5B784976E24Q38762468-8F4D5C9E-1A31-4BBA-AD3E-F3A8CC5F930CQ38856737-FF5291EA-B4CA-484E-A4F5-E630DA995E82Q38894811-6E496C65-CC50-4C21-A074-374AF7BA1C47Q38916576-A5F877AD-75F1-4A51-821A-DE5FC9CA065AQ39709287-46A2B42D-0C66-4261-9B6F-E7F438D41825Q40360342-EB98EAC4-3C04-4B98-8D88-845C4F3247A1Q43002417-274A63B6-58F8-4CBC-A2BB-52EE9520C1FAQ43557590-9587F8AF-9F87-4299-AE35-F4F3C9405AE6Q43859796-F25AD927-5B51-4998-9941-6C0F5F10525CQ43962331-223BEABB-C5CC-4EF1-B99F-78BD4C027F1FQ43980195-A0DA249A-9EA7-417C-9878-CA64C2B30329Q44404766-71FEF516-8C39-42A9-BE43-7E7597DE5639Q44430651-3955FA55-3268-44B0-93EE-7FAB578E0C41Q44663532-AEC8401D-FF47-4986-A3B2-5F3A8586B43DQ45130442-1098C616-9C03-4A98-9B92-138FB6B6282EQ45160995-BD9158C2-16E5-4215-9528-872C2777CA2BQ46350977-052AB6E4-D1C2-4383-B6E6-BAB9954C5919Q46720119-9BA4C067-305E-43CE-BF62-F6DDE388FD11Q46722274-42BFD186-A64A-41AC-A1C7-8AF3B7DF025BQ46764972-1BC34810-60E3-4964-8048-2C01BBD6421EQ46949979-EF71F297-0CDE-494A-825B-4CECC7BE534AQ47446893-8207AB96-0E55-4D7C-AB68-3C106035A35CQ47836941-FC0C9985-2ABA-4156-9802-BF3A1BC11CF6Q48112394-043F4236-A815-4B78-B47D-EA207B589C9BQ48169760-87E7A75B-B469-4AA4-B5C2-9AAB1E4C9ECCQ48202491-62019734-533C-4CFD-B03A-891E8C123034Q48230846-DC7AABDA-9513-4FBB-BC7C-24E77ED481B6Q48309065-5B09C539-FFAA-48EB-95B4-F7DED92B6E4FQ48328024-9F5D2E64-0B35-40F3-B9D6-FB5868B7ABCFQ48392144-A22914AF-88A0-4791-AA51-02F8D3970A40Q48478348-99086D44-712B-4615-8334-85FAB5B6A609Q48523697-07A82A9E-0B29-4D5C-9AF9-81F89FE027E9Q48528917-79867A6B-F043-4850-9279-62E4357B0460Q48670277-2FE88906-8DEC-4C58-B9F2-A81F0579B599
P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Antonio L Braga
@ast
Antonio L Braga
@en
Antonio L Braga
@es
Antonio L Braga
@nl
Antonio L Braga
@sl
type
label
Antonio L Braga
@ast
Antonio L Braga
@en
Antonio L Braga
@es
Antonio L Braga
@nl
Antonio L Braga
@sl
prefLabel
Antonio L Braga
@ast
Antonio L Braga
@en
Antonio L Braga
@es
Antonio L Braga
@nl
Antonio L Braga
@sl
P1053
B-1639-2014
P106
P21
P31
P3829
P496
0000-0001-9903-6764