About: Emanuele Amata

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

Italian chemist

Attributes	Values
rdf:type	Item
description	Itaalia keemik (et) Italian chemist (en-ca) Italian chemist (en-gb) chimist italian (ro) chimiste italien (fr) italiensk kemiker (da) italiensk kemist (sv) kimiko italiano (pap) kimist italian (sq) químic italià (ca) químico italiano (es) químico italiano (gl) כימאי איטלקי (he) كيميائي إيطالي (ar) ইতালীয় রসায়নবিদ (bn) Italian chemist (en) ceimiceoir Iodálach (ga) chimico italiano (it) italienischer Chemiker (de) italiensk kjemikar (nn) químicu italianu (ast) شیمیدان ایتالیایی (fa) İtalyan araştırmacı (tr) Italiaans onderzoeker (nl)
rdfs:label	Emanuele Amata (ca) Emanuele Amata (en) Emanuele Amata (es) Emanuele Amata (fr) Emanuele Amata (ga) Emanuele Amata (it) Emanuele Amata (nl) Emanuele Amata (sl) Emanuele Amata (sq) Emanuele Amata (ast) Emanuele Amata (pap)
skos:prefLabel	Emanuele Amata (ca) Emanuele Amata (en) Emanuele Amata (es) Emanuele Amata (fr) Emanuele Amata (ga) Emanuele Amata (it) Emanuele Amata (nl) Emanuele Amata (sl) Emanuele Amata (sq) Emanuele Amata (ast) Emanuele Amata (pap)
name	Emanuele Amata (ca) Emanuele Amata (en) Emanuele Amata (es) Emanuele Amata (fr) Emanuele Amata (ga) Emanuele Amata (it) Emanuele Amata (nl) Emanuele Amata (sl) Emanuele Amata (sq) Emanuele Amata (ast) Emanuele Amata (pap)
Scopus author ID	wds:Q47478912-39E3DD7C-1D26-44F7-856D-E0D3A511B270
Scopus author ID	36902617700
given name	wds:Q47478912-37136265-FA33-4995-9798-72ABA819FCF4
given name	Emanuele
instance of	wds:Q47478912-cb61b384-445f-653d-ce7f-8ed83043b87f
instance of	Homo sapiens
work location	wds:Q47478912-22703C79-00E9-48E7-A872-3A53D4DE0951
work location	Catania
occupation	wds:Q47478912-22BB9150-6419-4545-8038-8F8D38B4E248
employer	wds:Q47478912-81551548-F0C5-45C2-86CC-7879564CB1F4
languages spoken, written or signed	wds:Q47478912-95DF96C9-1679-4B92-8EB0-CA85EC41F59C
sex or gender	wds:Q47478912-08c6f81f-47ff-3891-8319-e2e0b784eba8
country of citizenship	wds:Q47478912-2245f609-4fbe-79d6-9812-7aadc4d705a4
family name	wds:Q47478912-D8B04FF5-CCCC-4CE6-8817-882B487CE85C
occupation	chemist
employer	University of Catania
languages spoken, written or signed	Italian
sex or gender	male
country of citizenship	Italy
family name	Amata
ORCID iD	wds:Q47478912-c015444f-41ab-c56f-1053-4b9df702edcc
ORCID iD	https://orcid.org/0000-0002-4750-3479
ORCID iD	0000-0002-4750-3479
IRIS UNICT author ID	wds:Q47478912-656EB9BE-CCBC-4824-9EDE-2CFA6E2810A2
IRIS UNICT author ID	00883
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q47478912
is author of	Antitrypanosomal Lead Discovery: Identification of a Ligand-Efficient Inhibitor of Trypanosoma cruzi CYP51 and Parasite Growth Identification and characterization of hundreds of potent and selective inhibitors of Trypanosoma brucei growth from a kinase-targeted library screening campaign S2RSLDB: a comprehensive manually curated, internet-accessible database of the sigma-2 receptor selective ligands (+)-Methyl (1R,2S)-2-{[4-(4-Chlorophenyl)-4-hydroxypiperidin-1-yl]methyl}-1-phenylcyclopropanecarboxylate [(+)-MR200] Derivatives as Potent and Selective Sigma Receptor Ligands: Stereochemistry and Pharmacological Properties. Evaluation of N-substitution in 6,7-benzomorphan compounds. Development of a Sigma-2 Receptor affinity filter through a Monte Carlo based QSAR analysis. 4-Nitro-2,1,3-benzoxadiazole derivatives as potential fluorescent sigma receptor probes (+)-and (-)-Phenazocine enantiomers: Evaluation of their dual opioid agonist/σ1 antagonist properties and antinociceptive effects Repurposing of Human Kinase Inhibitors in Neglected Protozoan Diseases. Evaluation of pyrrolidine and pyrazolone derivatives as inhibitors of trypanosomal phosphodiesterase B1 (TbrPDEB1) Protozoan Parasite Growth Inhibitors Discovered by Cross-Screening Yield Potent Scaffolds for Lead Discovery. Synthesis and Structure-Activity Relationships of (-)-cis-N-Normetazocine-Based LP1 Derivatives. Heme Oxygenase Database (HemeOxDB) and QSAR Analysis of Isoform 1 Inhibitors. Recent advances in drug discovery of phototherapeutic non-porphyrinic anticancer agents. Identification of potentially potent Heme Oxygenase-1 inhibitors through 3D-QSAR coupled to scaffold hopping analysis. A Structure- and Ligand-Based Virtual Screening of a Database of "Small" Marine Natural Products for the Identification of "Blue" Sigma-2 Receptor Ligands

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