about
Tetrahydrohyperforin and octahydrohyperforin are two new potent inhibitors of angiogenesisPolyacetylenes from sardinian Oenanthe fistulosa: a molecular clue to risus sardonicusA small molecule glycosaminoglycan mimetic blocks Plasmodium invasion of the mosquito midgutUncovering the structure of human red hair pheomelanin: benzothiazolylthiazinodihydroisoquinolines as key building blocks.In vitro antimalarial activity of hyperforin, a prenylated acylphloroglucinol. A structure-activity study.Two new tryptophan derivatives from the seed kernels of Entada rheedei: effects on cell viability and HIV infectivity.Synthesis of a potent antimalarial agent through natural products conjugation.(+)-Usnic acid enamines with remarkable cicatrizing properties.Cycloartane and oleanane saponins from egyptian astragalus spp. as modulators of lymphocyte proliferation.Synthesis of Resveratrol Derivatives and In Vitro Screening for Potential Cancer Chemopreventive Activities.Antiproliferative effects on tumour cells and promotion of keratinocyte wound healing by different lichen compounds.Synthesis and cytotoxic evaluation of combretafurans, potential scaffolds for dual-action antitumoral agents.Hyperforin, an Anti-Inflammatory Constituent from St. John's Wort, Inhibits Microsomal Prostaglandin E(2) Synthase-1 and Suppresses Prostaglandin E(2) Formation in vivo.In vitro antiplasmodial activity of extracts of Tristaniopsis species and identification of the active constituents: ellagic acid and 3,4,5-trimethoxyphenyl-(6'-O-galloyl)-O-beta-D-glucopyranoside.Antinociceptive profile of hodgkinsine.Cycloartane saponins from Astragalus peregrinus as modulators of lymphocyte proliferation.Synthesis and biological evaluation of hyperforin analogues. Part I. Modification of the enolized cyclohexanedione moiety.In vitro studies on the mechanism of action of two compounds with antiplasmodial activity: ellagic acid and 3,4,5-trimethoxyphenyl(6'-O-aalloyl)-beta-D-glucopyranoside.Structural investigations of isomeric oxidised forms of hyperforin by HPLC-NMR and HPLC-MSn.Resveratrol derivatives and their role as potassium channels modulators.Modulation of chemoselectivity by protein additives. Remarkable effects in the oxidation of hyperforin.Nitration versus nitrosation chemistry of menthofuran: remarkable fragmentation and dimerization pathways and expeditious entry into dehydromenthofurolactone.Determination of the absolute configurations of flexible molecules: synthesis and theoretical simulation of electronic circular dichroism/optical rotation of some pyrrolo[2,3-b]indoline alkaloids--a case study.An antioxidant bioinspired phenolic polymer for efficient stabilization of polyethylene.Polyphenolic glycosides from african proteaceaeSynthesis and antimycobacterial activity of (+)-usnic acid conjugatesSynthesis and Bioactivity Profile of 5-S-Lipoylhydroxytyrosol-Based Multidefense Antioxidants with a Sizeable (Poly)sulfide Chain4-Alkyl- and 4-phenylcoumarins from Mesua ferrea as promising multidrug resistant antibacterialsA cycloartane triterpene 3β, 16β diglucoside from Astragalus trigonus and its non natural 6-hydroxy epimerIsolation, Synthesis, and Antiplatelet Aggregation Activity of Resveratrol 3-O-β-d-Glucopyranoside and Related Compounds†Cycloartane triterpene glycosides from Astragalus alexandrinusApplication of molecular modelling to natural products: a biogenetic study of (+)-spathulenol and (+)-allospathulenolSaponins from Albizzia lucidaCycloartane triterpene glycosides from EgyptianAstragalus speciesA CONVENIENT PROCEDURE FOR THE PREPARATION OFt-BUTYLDIMETHYLSILYL ETHERS OF HYDROXYAMINO ACIDSSaponins from Albizzia anthelminticaQuadranguloside, a cycloartane triterpene glycoside from Passiflora quadrangularisSeparation of natural polar substances by reversed-phase high-performance liquid chromatography, centrifugal thin-layer chromatography and droplet counter-current chromatographyThe Reaction of Hyperforin with Hydride Reducing AgentsOxidative Fragmentation of the Bridgedβ-Triketone Core of Hyperforin
P50
Q21142634-8CA8CAB8-6612-454D-8963-7E6966126532Q24657297-D91647F2-E53E-4237-8192-AE165B2B2D9EQ28535338-B020FD71-5B09-4401-A7B0-F840D9A41E8AQ34025802-50E57291-5DFD-479B-B7BF-D9DE9B122F4DQ34603600-8286A054-96C7-43EE-97ED-E43E1B46C33DQ37126728-8F7D3154-795F-4851-910A-45F647279C04Q37331448-B0C58DC1-D789-48C3-8759-33A438234DB0Q39190038-62CC7DD2-3317-47B4-8EA6-936D2701029AQ39558603-2A17E47C-1C68-4305-8264-479E437F2586Q39782976-42E7FBD5-F150-4546-A849-FF041EDB16CAQ39886649-B044D76C-4DBC-41FE-9A51-59F58F06C82CQ40242911-5A84F596-0EFB-465A-83F5-97C681761E10Q41846509-A5216AAE-F3DA-496E-B24C-06893349678DQ41919633-38174A3C-DED2-4FA4-8B9A-4857F5ED9AC7Q43528784-BDE58BF4-2973-478C-89B1-3A54F8512C50Q43814139-F13DCDF9-65BE-4AE1-A4BB-F3D883DEFE2FQ43970552-0BA5B616-22F5-4522-8936-1AD55CFBB2B5Q44354396-36661F1A-0AC3-4C24-8E2B-2A22AF585E05Q44600609-E6366EBF-F097-43CD-9C4F-9C2DFDB8116CQ44813799-237FC2AA-0F83-41E2-A36E-96DB82C303B4Q45139766-7C7EBA4C-A015-4BD6-A25D-606398388811Q46877403-0D8C5157-0F90-4914-BE36-61A17D58FE75Q51627102-84464C01-9927-4F00-A395-7BCA49F9019FQ53086482-5979F8AD-C64F-4CDC-A3D4-4D2E2AA556EFQ54321120-D2520053-537C-4DB5-88BA-ADF00CC7789BQ58574824-5951B6A6-68AD-4F61-84C1-BEA03AA1183CQ59117752-1FB63B0D-2C58-4FA2-B6EC-E3C867024859Q59391753-25D49B1A-8DEC-4638-96FA-404E5BB8CCD2Q60442740-B82A89CC-A754-4F96-8AEC-234EB64880FEQ60442748-CFC5AF2A-9C37-4CA7-9860-FF60DC5A71D0Q60442760-D02DA3DD-F54B-4BCC-9D89-AFE9D2B44B73Q60442764-8211026D-7D20-471C-91A0-F8C5C77DF643Q60442796-B09EBA8C-AB86-48CB-9510-1CCD7A49DD63Q60442809-2631FF4F-F8FB-4CBA-8BB7-DCBAF8E50DD3Q60442815-77FFE49D-B7FD-45B5-88E2-178DB223521AQ60442843-02FC57EF-4BE3-463D-A82E-362D91449999Q60442906-49E50A36-A390-4BEA-BA29-21AFEF49BEABQ60442914-AF84A8BD-6151-4E7F-B90D-8D39D5A9764BQ60684433-6EA661C4-FEAF-4F13-86DD-B02B0E736C98Q60684443-84E1B8CE-DBCB-4F47-830C-96CEF6EE0E82
P50
description
hulumtuese
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Luisella Verotta
@ast
Luisella Verotta
@en
Luisella Verotta
@es
Luisella Verotta
@nl
Luisella Verotta
@sl
type
label
Luisella Verotta
@ast
Luisella Verotta
@en
Luisella Verotta
@es
Luisella Verotta
@nl
Luisella Verotta
@sl
prefLabel
Luisella Verotta
@ast
Luisella Verotta
@en
Luisella Verotta
@es
Luisella Verotta
@nl
Luisella Verotta
@sl
P1053
O-5953-2016
P106
P1153
7004493728
P21
P31
P3829
P496
0000-0002-5739-6291