about
A new family of choline kinase inhibitors with antiproliferative and antitumor activity derived from natural products.Bis-pyranobenzoquinones as a new family of reversal agents of the multidrug resistance phenotype mediated by P-glycoprotein in mammalian cells and the protozoan parasite Leishmania.CM363, a novel naphthoquinone derivative which acts as multikinase modulator and overcomes imatinib resistance in chronic myelogenous leukemiaAntiproliferative and quinone reductase-inducing activities of withanolides derivatives.Inhibition of potato cyst nematode hatch by lignans fromBupleurum salicifolium (Unbelliferae).Antiproliferative and Structure Activity Relationships of Amaryllidaceae Alkaloids.Synthesis of 4,4'-Diaminotriphenylmethanes with Potential Selective Estrogen Receptor Modulator (SERM)-like Activity.5-Ethynylarylnaphthalimides as antitumor agents: Synthesis and biological evaluation.Synthesis and study of antiproliferative, antitopoisomerase II, DNA-intercalating and DNA-damaging activities of arylnaphthalimides.Synthesis and cytotoxic activity of metallic complexes of lawsone.Synthesis and anti-inflammatory activity of ent-kaurene derivatives.Evaluation of labdane derivatives as potential anti-inflammatory agents.Synthesis and induction of apoptosis signaling pathway of ent-kaurane derivatives.Structure and estrogenic activity of new lignans from Iryanthera lancifolia.Synthesis and pharmacophore modeling of naphthoquinone derivatives with cytotoxic activity in human promyelocytic leukemia HL-60 cell line.Structure and antimicrobial activity of phloroglucinol derivatives from Achyrocline satureioides.Synthesis and antiplasmodial activity of lycorine derivatives.Synthesis and anti-HIV activity of lupane and olean-18-ene derivatives. Absolute configuration of 19,20-epoxylupanes by VCD.Yeast cytotoxic sensitivity to the antitumour agent β-lapachone depends mainly on oxidative stress and is largely independent of microtubule- or topoisomerase-mediated DNA damage.Triterpenoids and a lignan from the aerial parts of Maytenus apurimacensis.A new family of densely functionalized fused-benzoquinones as potent human protein kinase CK2 inhibitors.Synthesis and Antimicrobial Activity of 4-Substituted 1,2,3-Triazole-Coumarin Derivatives.Synthesis and antibacterial activity of new symmetric polyoxygenated dibenzofurans.Metal complexes of natural product like-compounds with antitumoral activity.Synthesis and biological evaluation of naphthoquinone-coumarin conjugates as topoisomerase II inhibitors.Antiproliferative activity of withanolide derivatives from Jaborosa cabrerae and Jaborosa reflexa. Chemotaxonomic considerations.Effect of (E)-Chalcone on Potato-Cyst Nematodes (Globodera pallidaandG. rostochiensis)New terpenoids from Maytenus apurimacensis as MDR reversal agents in the parasite LeishmaniaSemisynthesis and Inhibitory Effects of Solidagenone Derivatives on TLR-Mediated Inflammatory ResponsesLight effect on the stability ofβ-lapachone in solution: pathways and kinetics of degradationPreparation, anticholinesterase activity and molecular docking of new lupane derivativesNew dammarane triterpenes from Maytenus macrocarpa.Antibiotic activity and absolute configuation of 8S-heptadeca-2(Z),9(Z)-diene-4,6-diyne-1,8-diol from Bupleurum salicifoliumSesquiterpene polyol esters from the leaves of maytenus macrocarpaBiological activities of some Argyranthemum speciesMacrocarpins A-D, new cytotoxic nor-triterpenes from Maytenus macrocarpaFriedelane triterpenoids from Maytenus macrocarpaAntiplasmodial activity of naphthoquinones related to lapachol and beta-lapachoneTerpenoids from the medicinal plant Maytenus ilicifoliaDesign and synthesis of a novel series of pyranonaphthoquinones as topoisomerase II catalytic inhibitors
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P50
description
hulumtuese
@sq
onderzoeker
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researcher
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հետազոտող
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name
Ana Estévez-Braun
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Ana Estévez-Braun
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Ana Estévez-Braun
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Ana Estévez-Braun
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type
label
Ana Estévez-Braun
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Ana Estévez-Braun
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Ana Estévez-Braun
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Ana Estévez-Braun
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Ana Estévez-Braun
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Ana Estévez-Braun
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Ana Estévez-Braun
@es
Ana Estévez-Braun
@nl
P106
P1153
6701825073
P21
P31
P496
0000-0001-5279-7099