Zobrazeno 1 - 10
of 38
pro vyhledávání: '"Marcelle Hauteville"'
Autor:
Claire Delehouzé, Arnaud Comte, Stephen Adonai Leon-Icaza, Céline Cougoule, Marcelle Hauteville, Peter Goekjian, Jeannette Chloë Bulinski, Marie-Thérèse Dimanche-Boitrel, Etienne Meunier, Morgane Rousselot, Stéphane Bach
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-10 (2022)
Abstract Nigratine (also known as 6E11), a flavanone derivative of a plant natural product, was characterized as highly specific non-ATP competitive inhibitor of RIPK1 kinase, one of the key components of necroptotic cell death signaling. We show her
Externí odkaz:
https://doaj.org/article/bec49c3acc7b48aa983463f7fc23bb1f
Autor:
Claire Delehouzé, Arnaud Comte, Stephen Adonai Leon-Icaza, Céline Cougoule, Marcelle Hauteville, Peter Goekjian, Jeannette Chloë Bulinski, Marie-Thérèse Dimanche-Boitrel, Etienne Meunier, Morgane Rousselot, Stéphane Bach
Publikováno v:
Scientific Reports
Scientific Reports, 2022, 12, pp.5118. ⟨10.1038/s41598-022-09019-w⟩
Scientific Reports, 2022, 12, pp.5118. ⟨10.1038/s41598-022-09019-w⟩
Nigratine (also known as 6E11), a flavanone derivative of a plant natural product, was characterized as highly specific non-ATP competitive inhibitor of RIPK1 kinase, one of the key components of necroptotic cell death signaling. We show here that ni
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1672ff9764b8c8fdbf5c1f99abc1e1ed
https://pubmed.ncbi.nlm.nih.gov/35332201
https://pubmed.ncbi.nlm.nih.gov/35332201
Autor:
Marcelle Hauteville, Morgane Rousselot, Stéphane Bach, Marie-Thérèse Dimanche-Boitrel, Claire Delehouzé, Arnaud Comte, Peter G. Goekjian
Nigratine (also known as 6E11), a natural flavanone derivative, was characterized as highly specific non-ATP competitive inhibitor of RIPK1 kinase, one of the key component of necroptotic cell death signaling. We show here that nigratine inhibited bo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::abd472b0de2dedce4e5d73bc4e8078dc
https://doi.org/10.1101/2020.12.15.422885
https://doi.org/10.1101/2020.12.15.422885
Publikováno v:
Liebigs Annalen. 1996:1217-1222
If the Baker-Venkataraman rearrangement of C-methylphloracetophenone triaroyl esters is carried out in DMSO with powdered NaOH, the result greatly depends on the substitution pattern both of the phloracetophenone moiety possessing either one or two C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ea5d68e168c4888f3beb8ed13facefcf
https://doi.org/10.1002/jlac.199619960724
https://doi.org/10.1002/jlac.199619960724
Publikováno v:
Biochimie. 87:223-230
A series of 6-amino-2-phenyl-4H-3,1-benzoxazin-4-one aminoacyl and dipeptidyl derivatives, in which aminoacids and dipeptides are linked to the benzoxazinone moiety via an amide bond, were synthesized and tested in vitro for their inhibitory activity
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94ab73150055a60e0cf33b3c81a90d5a
https://doi.org/10.1016/j.biochi.2004.10.015
https://doi.org/10.1016/j.biochi.2004.10.015
Publikováno v:
Journal of Chemical Crystallography. 29:681-685
Benzylation of 3-methylphloracetophenone [1-(2,4,6-trihydroxy-3-methylphenyl)ethanone] (3) with benzyl chloride gave 4-acetyl-2,6-dibenzyl-1,5-dihydroxy-2-methylcyclohexa-4,6-dien-3-one (5). Compound 5 crystallizes in the orthorhombic space group Fdd
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::01ba5ef0bf9acd791f6a78507d768416
https://doi.org/10.1023/a:1009523804263
https://doi.org/10.1023/a:1009523804263
Publikováno v:
Phytochemistry. 48:547-553
Ultraviolet spectra of fifteen natural of synthetic 6- and 8-methylflavones, with hydroxy group at C-5 and hydroxy or methoxy groups at C-7, were recorded in methanol and in presence of neutral or acidic aluminium chloride. Several spectral character
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3bc0ef430e2b0b29af5a2c0d42acde59
https://doi.org/10.1016/s0031-9422(97)00919-9
https://doi.org/10.1016/s0031-9422(97)00919-9
Publikováno v:
Acta Crystallographica Section E Structure Reports Online. 58:o1116-o1118
The crystal structure of the title compound, C20H22O6, an intermediate in the synthesis of the flavone 2-(4-methoxy-phenyl)-5,7-dimethoxy-3,8-dimethyl-4H-1-benzopyran-4-one, has been determined. The molecules are held together by van der Waals forces
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::391fccb8372c8939d33dbf72b0d67c0b
https://doi.org/10.1107/s1600536802016136
https://doi.org/10.1107/s1600536802016136
Publikováno v:
Acta Crystallographica Section E Structure Reports Online. 58:o506-o508
The crystal structure of 2-(3,4-dimethoxyphenyl)-5,7-dimethoxy-3,8-dimethyl-4H-1-benzopyran-4-one (alternatively 3′,4′-dimethoxyphenyl-5,7-dimethoxy-3,8-dimethylflavone),C21H22O6, known to be a potent and selective inhibitor o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5602d7f7ac5eb35d921ca35227f4602b
https://doi.org/10.1107/s1600536802006074
https://doi.org/10.1107/s1600536802006074
Autor:
Pascale Gaillard, Annie-France Prigent, Marcelle Hauteville, Madeleine Picq, Marie-Christine Duclos, Madeleine Dubois
Publikováno v:
ChemInform. 28
A series of eight methoxylated C-methyl-2-phenyl-4H-1-benzopyran-4-ones 3, 6, 10-15 was evaluated as inhibitors of rat heart cytosolic cyclic nucleotide phosphodiesterase (PDE). The 2-(3, 4-dimethoxyphenyl)-5, 7-dimethoxy-3, 8-dimethyl-4H-1-benzopyra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d240d2cf2b90de47ea433f58ec0fb05f
https://doi.org/10.1002/chin.199711114
https://doi.org/10.1002/chin.199711114