About: Romano Silvestri

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

Italian pharmacologist (1959-)

Attributes	Values
rdf:type	Item
description	গবেষক (bn) ഗവേഷകൻ (ml) wetenschapper (nl) дослідник (uk) հետազոտող (hy) hulumtues (sq) Italian pharmacologist (1959-) (en) farmacologo italiano (1959-) (it)
rdfs:label	Romano Silvestri (de) Romano Silvestri (en) Romano Silvestri (es) Romano Silvestri (fr) Romano Silvestri (it) Romano Silvestri (nl) Romano Silvestri (pt) Romano Silvestri (sl) Romano Silvestri (pt-br) Romano Silvestri (ast)
skos:prefLabel	Romano Silvestri (de) Romano Silvestri (en) Romano Silvestri (es) Romano Silvestri (fr) Romano Silvestri (it) Romano Silvestri (nl) Romano Silvestri (pt) Romano Silvestri (sl) Romano Silvestri (pt-br) Romano Silvestri (ast)
name	Romano Silvestri (de) Romano Silvestri (en) Romano Silvestri (es) Romano Silvestri (fr) Romano Silvestri (it) Romano Silvestri (nl) Romano Silvestri (pt) Romano Silvestri (sl) Romano Silvestri (pt-br) Romano Silvestri (ast)
Scopus author ID	wds:Q42718323-EE303A59-2E4E-401D-8503-DE61CDE47415
Scopus author ID	7005023671
given name	wds:Q42718323-96669AAB-8C7A-44D2-AEED-9727773FA06F
given name	Romano
instance of	wds:Q42718323-41D0FB86-737C-483B-9B2B-501CFA85ED8B
instance of	Homo sapiens
IRIS Sapienza author ID	wds:Q42718323-8EEBE5CD-ACD2-4024-AAD3-23B94228E374
IRIS Sapienza author ID	47926
curriculum vitae URL	wds:Q42718323-bf0f1536-49ee-8fde-ccdc-21c99d0178f5
curriculum vitae URL	https://www.unich.it/sites/default/files/allegatiparagrafo/24-03-2016/cv_silvestri.pdf
work location	wds:Q42718323-61676ECA-EED8-4835-B210-7689AEA85FCF
work location	Rome
occupation	wds:Q42718323-AE75F6D0-4E40-4F8C-9889-3313C21BE135
employer	wds:Q42718323-6038BF20-D328-425D-8140-B38AC866BA0E wds:Q42718323-9C3B16BB-0755-48EC-B135-B14213F9640B wds:Q42718323-CBF67E48-9B1D-4CAB-A4FC-9B5DA7AECA0D wds:Q42718323-EB8BC25F-3FAC-419A-B4DE-2A77BABA75A0
languages spoken, written or signed	wds:q42718323-8eb2157d-4d97-b41d-ff2f-dd3fdf017f77 wds:q42718323-c45746b1-4b1e-ccf2-abf5-745404389266
sex or gender	wds:Q42718323-91B0BB94-C4CF-49FF-AB02-CE5D317EF662
country of citizenship	wds:q42718323-90b7c1c2-478d-efd7-130f-f13e91d30e7d
date of birth	wds:Q42718323-19c01648-4905-2ef7-2c3d-947156336a02
family name	wds:Q42718323-8B14142D-C657-4B4D-918D-691065228074
occupation	pharmacologist
employer	Sapienza University of Rome Department of Statistical Sciences, Sapienza University of Rome
languages spoken, written or signed	English Italian
sex or gender	male
country of citizenship	Italy
date of birth	1959-05-24 00:00:00Z (xsd:dateTime)
family name	Silvestri
ORCID iD	wds:Q42718323-B376FE10-64B5-46CA-887B-87E15D3E469D
Dimensions author ID	wds:Q42718323-D873A125-2F99-4589-A611-DC876E6281DF
ORCID iD	https://orcid.org/0000-0003-2489-0178
ORCID iD	0000-0003-2489-0178
Dimensions author ID	01112217434.23
IRIS UNINA author ID	wds:Q42718323-F17A38AD-C156-42C6-9489-3AE48A16CB15
IRIS UNINA author ID	47515
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q42718323
is author of	Computer-aided identification, design and synthesis of a novel series of compounds with selective antiviral activity against chikungunya virus The tubulin colchicine domain: a molecular modeling perspective A screen for kinetochore-microtubule interaction inhibitors identifies novel antitubulin compounds Synthesis, structure-activity relationships and molecular modeling studies of new indole inhibitors of monoamine oxidases A and B. New pyrrole inhibitors of monoamine oxidase: synthesis, biological evaluation, and structural determinants of MAO-A and MAO-B selectivity. Toward highly potent cancer agents by modulating the C-2 group of the arylthioindole class of tubulin polymerization inhibitors Indole-2-carboxamides as allosteric modulators of the cannabinoid CB₁ receptor. Structure-based design, synthesis, and biological evaluation of novel pyrrolyl aryl sulfones: HIV-1 non-nucleoside reverse transcriptase inhibitors active at nanomolar concentrations Computer-assisted design, synthesis and biological evaluation of novel pyrrolyl heteroaryl sulfones targeted at HIV-1 reverse transcriptase as non-nucleoside inhibitors. Synthesis, biological evaluation, and binding mode of novel 1-[2-(diarylmethoxy)ethyl]-2-methyl-5-nitroimidazoles targeted at the HIV-1 reverse transcriptase. 5H-pyrrolo[1,2-b] [1,2,5]benzothiadiazepines (PBTDs): a novel class of non-nucleoside reverse transcriptase inhibitors. Structure-based lead optimization and biological evaluation of BAX direct activators as novel potential anticancer agents. New indolylarylsulfones as highly potent and broad spectrum HIV-1 non-nucleoside reverse transcriptase inhibitors New nitrogen containing substituents at the indole-2-carboxamide yield high potent and broad spectrum indolylarylsulfone HIV-1 non-nucleoside reverse transcriptase inhibitors Indolylarylsulfones bearing natural and unnatural amino acids. Discovery of potent inhibitors of HIV-1 non-nucleoside wild type and resistant mutant strains reverse transcriptase and coxsackie B4 virus Simple, short peptide derivatives of a sulfonylindolecarboxamide (L-737,126) active in vitro against HIV-1 wild type and variants carrying non-nucleoside reverse transcriptase inhibitor resistance mutations. Indolylarylsulfones as HIV-1 non-nucleoside reverse transcriptase inhibitors: new cyclic substituents at indole-2-carboxamide Docking and 3-D QSAR studies on indolyl aryl sulfones. Binding mode exploration at the HIV-1 reverse transcriptase non-nucleoside binding site and design of highly active N-(2-hydroxyethyl)carboxamide and N-(2-hydroxyethyl)carbohydrazide derivatives Design, Molecular Modeling, Synthesis, and Anti-HIV-1 Activity of New Indolyl Aryl Sulfones. Novel Derivatives of the Indole-2-carboxamide Pyrrolo[1,2-b][1,2,5]benzothiadiazepines (PBTDs): A New Class of Agents with High Apoptotic Activity in Chronic Myelogenous Leukemia K562 Cells and in Cells from Patients at Onset and Who Were Imatinib-Resistant Direct HPLC enantioseparation of chiral aptazepine derivatives on coated and immobilized polysaccharide-based chiral stationary phases

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