About: Pascal Marchand

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

researcher

Attributes	Values
rdf:type	Item
description	researcher (en) 연구원 (ko) 研究者 (ja) araştırmacı (tr) wetenschapper (nl) дослідник (uk) वैज्ञानिक (hi) изилдөөчү (ky) 研究者 (zh)
rdfs:label	Pascal Marchand (en) Pascal Marchand (nl)
skos:prefLabel	Pascal Marchand (en) Pascal Marchand (nl)
name	Pascal Marchand (en) Pascal Marchand (nl)
Scopus author ID	wds:Q73233307-A70BD4FF-8DFD-46B5-A530-501E5EB7CDDA
Scopus author ID	7101914669
given name	wds:Q73233307-A49BE07C-A56E-4308-8467-F495929E65A8
given name	Pascal
instance of	wds:Q73233307-E7595F8C-5364-4797-ACA3-2822B8596352
instance of	Homo sapiens
occupation	wds:Q73233307-06E7C3DB-2297-48FD-A9FC-9433A1EF3F8C
employer	wds:Q73233307-77F8A5E1-1EDE-4D75-9F64-D2C8F86FCFA7
sex or gender	wds:Q73233307-0947E466-799C-4841-B7C7-94AAFEAF12C5
ISNI	wds:Q73233307-46DA3529-2F60-4F2D-99BC-C61AB616966A
VIAF ID	wds:Q73233307-11076025-4B8B-4804-9F2B-A7F447CAC073
IdRef ID	wds:Q73233307-62387089-5037-40E1-954E-8C1E949525D5
date of birth	wds:Q73233307-F5B7A9E4-9A45-41B1-99B9-38081F8DDD50
educated at	wds:Q73233307-9F92774E-4CEB-49D2-8C52-50D771008233 wds:Q73233307-BC9F1622-56FC-415C-87CE-BC0633D7F424
VIAF ID	http://viaf.org/viaf/207200217
IdRef ID	http://www.idref.fr/121424480/id
occupation	researcher
employer	University of Nantes
sex or gender	male
ISNI	0000000432051873
VIAF ID	207200217
IdRef ID	121424480
date of birth	1970-01-01 00:00:00Z (xsd:dateTime)
educated at	University of Nantes
ORCID iD	wds:Q73233307-DE7C92EE-A89B-488A-BB0C-E7D6FB3C379B
ORCID iD	https://orcid.org/0000-0001-7773-8642
ORCID iD	0000-0001-7773-8642
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q73233307
is author of	Retinoic acid metabolism inhibition by 3-azolylmethyl-1H-indoles and 2, 3 or 5-(alpha-azolylbenzyl)-1H-indoles Synthesis and biological evaluation of N-aryl-7-methoxybenzo[b]furo[3,2-d]pyrimidin-4-amines and their N-arylbenzo[b]thieno[3,2-d]pyrimidin-4-amine analogues as dual inhibitors of CLK1 and DYRK1A kinases. Synthesis and structure-activity relationships of N-aryl(indol-3-yl)glyoxamides as antitumor agents. Synthesis and biological evaluation of 3-(azolylmethyl)-1H-indoles and 3-(alpha-azolylbenzyl)-1H-indoles as selective aromatase inhibitors. Three-dimensional model of cytochrome P450 human aromatase. 2- and 3-[(aryl)(azolyl)methyl]indoles as potential non-steroidal aromatase inhibitors. Preparation and pharmacological profile of 7-(alpha-azolylbenzyl)-1H-indoles and indolines as new aromatase inhibitors Synthesis and in vitro evaluation of 3-(1-azolylmethyl)-1H-indoles and 3-(1-azolyl-1-phenylmethyl)-1H-indoles as inhibitors of P450 arom New selective nonsteroidal aromatase inhibitors: synthesis and inhibitory activity of 2,3 or 5-(alpha-azolylbenzyl)-1H-indoles Synthesis of novel 7-substituted pyrido[2',3':4,5]furo[3,2-d]pyrimidin-4-amines and their N-aryl analogues and evaluation of their inhibitory activity against Ser/Thr kinases. A Decade of Antifungal Leads from Natural Products: 2010-2019 Characterization of the biochemical, physiological, and medicinal properties of Streptomyces hygroscopicus ACTMS-9H isolated from the Amazon (Brazil). Synthesis and antileishmanial activity of 3-(alpha-azolylbenzyl)indoles Benzofuro[3,2-d]pyrimidines inspired from cercosporamide CaPkc1 inhibitor: Synthesis and evaluation of fluconazole susceptibility restoration. Antileishmanial activities and mechanisms of action of indole-based azoles A novel indole-3-propanamide exerts its immunosuppressive activity by inhibiting JAK3 in T cells. 26th Annual GP2A Medicinal Chemistry Conference & 32nd Journées Franco-Belges de Pharmacochimie In vitro activity of a new antifungal azolyl-substituted indole against Aspergillus fumigatus Synthesis, antileishmanial activity and cytotoxicity of 2,3-diaryl- and 2,3,8-trisubstituted imidazo[1,2-a]pyrazines. Synthesis and antiproliferative activity of benzofuran-based analogs of cercosporamide against non-small cell lung cancer cell lines. Discovery of 7-aryl-substituted (1,5-naphthyridin-4-yl)ureas as aurora kinase inhibitors. Discovery of (7-aryl-1,5-naphthyridin-2-yl)ureas as dual inhibitors of ERK2 and Aurora B kinases with antiproliferative activity against cancer cells. 27th Annual GP2A Medicinal Chemistry Conference Side chain modifications of (indol-3-yl)glyoxamides as antitumor agents Synthesis and anticancer activity of novel bisindolylhydroxymaleimide derivatives with potent GSK-3 kinase inhibition Microwave-Assisted Synthesis of Potential Bioactive Benzo-, Pyrido- or Pyrazino-thieno[3,2-d]pyrimidin-4-amine Analogs of MPC-6827
is author of	wds:Q30732753-714E1314-3543-476A-A7BF-B2E2227B5B35 wds:Q46884372-4AFF9803-3BCA-4A23-8594-5B270D015B33 wds:Q44406418-B089393B-3507-4848-A44E-E5D03C1EAEC6 wds:Q74635037-35558A37-2830-4888-883D-BD7C9E603FF1 wds:Q92011714-3D9B4CCF-DEF5-4BE8-8353-0A70F5477015 wds:Q38739752-AB2D27CD-BA97-455C-80F3-2CDE57E84E85 wds:Q54977508-C246FFA1-2E26-426F-84AD-BE840AC7596A wds:Q92119126-1C7299F7-623F-4C53-9E8D-25A94519971E wds:Q44395556-314E2813-D9EB-47F3-B55A-D7B5C7B73941 wds:Q54399933-A526F0B9-8F32-40D7-854D-727D69519A5C wds:Q80136503-6761169D-6D74-4193-BCE3-5E676392A792 wds:Q39812380-93A04E25-09CB-47E7-8A71-77BFDEF477F8 wds:Q44395536-B489BE78-5B4B-446A-8BFD-39FDC26B5F27 wds:Q38834476-BBD72E80-4F24-4352-BED6-BC24AE9F9436 wds:Q39055807-F9E5EA97-A253-4050-81E2-93B10F1EEBA9 wds:Q39079857-ECAE9EE3-ECF0-4CF7-8DDC-19D32F3D4727 wds:Q38975540-F15B5803-F375-4E44-A2DB-49E1C524D3C1 wds:Q73545001-2BCAE393-E418-4FBD-883D-94B4E047BA88 wds:Q91814095-583A7E71-DE36-46DC-8FB0-D750E79804D4 wds:Q45232715-71A9533F-CFD1-49AB-A5B3-68B164CB232B wds:Q43285291-0F5E6134-4ABE-49F1-A335-B58582ACE4BE wds:Q82095814-9E0859B6-628B-4F24-9F26-C12899B4EC6B wds:Q46891612-8898C721-3577-4A3F-BE6C-E81448657CCC wds:Q44579955-FB5E2C1F-F018-446C-9AFB-073E79509B9E wds:Q57170358-68421746-29B5-401A-A4C4-703128C83CEA wds:Q98619514-8107FB45-8047-4DDB-A671-95DD2C85131A

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