About: Vincenza Andrisano

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Italian pharmacologist (1958-)

Attributes	Values
rdf:type	Item
description	연구원 (ko) 研究者 (ja) wetenschapper (nl) дослідниця (uk) 研究者 (zh) հետազոտող (hy) hulumtuese (sq) Italian pharmacologist (1958-) (en) farmacologa italiana (1958-) (it)
rdfs:label	Vincenza Andrisano (de) Vincenza Andrisano (en) Vincenza Andrisano (es) Vincenza Andrisano (fr) Vincenza Andrisano (it) Vincenza Andrisano (nl) Vincenza Andrisano (pt) Vincenza Andrisano (pt-br) Vincenza Andrisano (ast)
skos:prefLabel	Vincenza Andrisano (de) Vincenza Andrisano (en) Vincenza Andrisano (es) Vincenza Andrisano (fr) Vincenza Andrisano (it) Vincenza Andrisano (nl) Vincenza Andrisano (pt) Vincenza Andrisano (pt-br) Vincenza Andrisano (ast)
name	Vincenza Andrisano (de) Vincenza Andrisano (en) Vincenza Andrisano (es) Vincenza Andrisano (fr) Vincenza Andrisano (it) Vincenza Andrisano (nl) Vincenza Andrisano (pt) Vincenza Andrisano (pt-br) Vincenza Andrisano (ast)
Scopus author ID	wds:Q56441574-A7584C9E-8EDE-479C-8252-2CC8B83C75B6
Scopus author ID	7006871746
given name	wds:Q56441574-EC36F9FC-E9A3-46DF-8DCB-AF03E86716FC
given name	Vincenza
instance of	wds:Q56441574-3AB3A0CB-0B01-4085-AF97-444C5E9F7914
instance of	Homo sapiens
CONOR.AL ID	wds:Q56441574-60DF67B5-1F28-46DA-8D89-2398181A986E
CONOR.AL ID	6215014
skos:altLabel	V. Andrisano (en) V. Andrisano (it)
occupation	wds:Q56441574-D6D8B7AF-9F1C-4F11-A9B1-ED8E74DE9E91 wds:q56441574-661e8a38-480f-1d7d-e8ce-0877023a64d1
employer	wds:q56441574-3aeebfa0-48be-7da8-ecf4-4debfb6392fd
languages spoken, written or signed	wds:q56441574-1f4dce45-4e81-27e3-64b7-1b4bdff4b39b wds:q56441574-b7c887a6-4e0d-c4b6-44df-1540734009cc
sex or gender	wds:Q56441574-2da2b838-4052-ad75-9dd2-43fdb1a8cc2c
VIAF ID	wds:Q56441574-B29B1102-1818-4EBF-9402-7FFC612AA79F
country of citizenship	wds:q56441574-f2c523dd-4bd6-3eaa-eb5f-e3e6cbca40a6
SBN author ID	wds:Q56441574-95277D27-F031-45C8-905A-D2540812BEC1
SHARE Catalogue author ID	wds:Q56441574-28EA8BB2-A12F-4269-B44D-2F55FD164147 wds:Q56441574-85117D0A-1277-4846-AF22-6DFCE44783E0
date of birth	wds:Q56441574-67e83a98-40d4-5761-78b4-ea19caaec174
family name	wds:q56441574-6b9529fb-42a4-3c09-3097-80073fbdd2df
VIAF ID	http://viaf.org/viaf/17167759945713571457
occupation	university teacher pharmacologist
employer	University of Bologna
languages spoken, written or signed	English Italian
sex or gender	female organism
VIAF ID	17167759945713571457
country of citizenship	Italy
SBN author ID	UBOV891215
SHARE Catalogue author ID	291079 553816
date of birth	1958-05-17 00:00:00Z (xsd:dateTime)
family name	Andrisano
ORCID iD	wds:Q56441574-4D12C21D-7597-48B0-81CB-4D8A656E654A
Dimensions author ID	wds:Q56441574-29B6DCDE-2D62-4070-B315-4B6C3D785FD4
ORCID iD	https://orcid.org/0000-0003-4396-1904
ORCID iD	0000-0003-4396-1904
Dimensions author ID	01134715142.70
IRIS UNIBO author ID	wds:Q56441574-59A02ACA-7EC0-4709-AB9E-2EBE051E6A60
IRIS UNIBO author ID	07720
IRIS UNIFE author ID	wds:Q56441574-3EEECA1C-72F6-4AC8-934B-D348A6579432
IRIS UNIFE author ID	14056
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q56441574
is author of	Strategies for the inhibition of protein aggregation in human diseases Multitarget drug design strategy: quinone-tacrine hybrids designed to block amyloid-β aggregation and to exert anticholinesterase and antioxidant effects Novel tacrine-grafted Ugi adducts as multipotent anti-Alzheimer drugs: a synthetic renewal in tacrine-ferulic acid hybrids. Novel huprine derivatives with inhibitory activity toward β-amyloid aggregation and formation as disease-modifying anti-Alzheimer drug candidates beta-Amyloid aggregation induced by human acetylcholinesterase: inhibition studies Cholinesterase inhibitors: xanthostigmine derivatives blocking the acetylcholinesterase-induced beta-amyloid aggregation Multi-target-directed coumarin derivatives: hAChE and BACE1 inhibitors as potential anti-Alzheimer compounds. Pyrano[3,2-c]quinoline-6-chlorotacrine hybrids as a novel family of acetylcholinesterase- and beta-amyloid-directed anti-Alzheimer compounds. Targeting Alzheimer's disease: Novel indanone hybrids bearing a pharmacophoric fragment of AP2238. 3-(4-[[Benzyl(methyl)amino]methyl]phenyl)-6,7-dimethoxy-2H-2-chromenone (AP2238) inhibits both acetylcholinesterase and acetylcholinesterase-induced beta-amyloid aggregation: a dual function lead for Alzheimer's disease therapy Benzofuran-based hybrid compounds for the inhibition of cholinesterase activity, beta amyloid aggregation, and abeta neurotoxicity Application of high-performance liquid chromatography with diode-array detection and on-line post-column photochemical derivatization to the determination of analgesics Acetylcholinesterase inhibitors: synthesis and structure-activity relationships of omega-[N-methyl-N-(3-alkylcarbamoyloxyphenyl)- methyl]aminoalkoxyheteroaryl derivatives. Synthesis of monomeric derivatives to probe memoquin's bivalent interactions. Novel donepezil-based inhibitors of acetyl- and butyrylcholinesterase and acetylcholinesterase-induced beta-amyloid aggregation. Multi-target-directed drug design strategy: from a dual binding site acetylcholinesterase inhibitor to a trifunctional compound against Alzheimer's disease.

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