Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Emilie David"'
Publikováno v:
PLoS ONE, Vol 18, Iss 1, p e0280380 (2023)
Protection from the toxicity of nerve agents is achieved by pretreatment with human butyrylcholinesterase (BChE). Current methods for purifying large quantities of BChE from frozen Cohn fraction IV-4 produce 99% pure enzyme, but the yield is low (21%
Externí odkaz:
https://doaj.org/article/276bc035f5dc4e2db13f98512aa3fbd3
Publikováno v:
PLoS ONE, Vol 14, Iss 1, p e0209795 (2019)
Human butyrylcholinesterase (HuBChE) is being developed as a therapeutic for protection from the toxicity of nerve agents. An enriched source of HuBChE is Cohn fraction IV-4 from pooled human plasma. For the past 40 years, purification of HuBChE has
Externí odkaz:
https://doaj.org/article/affc078c1bbb4040bab862cd9ed54a21
Publikováno v:
Frontiers in Pharmacology, Vol 8 (2017)
Hupresin is a new affinity resin that binds butyrylcholinesterase (BChE) in human plasma and acetylcholinesterase (AChE) solubilized from red blood cells (RBC). Hupresin is available from the CHEMFORASE company. BChE in human plasma binds to Hupresin
Externí odkaz:
https://doaj.org/article/306a5261570548f0ae06ec4dc404d69d
Publikováno v:
Journal of Organic Chemistry
Journal of Organic Chemistry, American Chemical Society, 2020, 85 (21), pp.14055-14067. ⟨10.1021/acs.joc.0c02081⟩
Journal of Organic Chemistry, American Chemical Society, 2020, 85 (21), pp.14055-14067. ⟨10.1021/acs.joc.0c02081⟩
International audience; In this manuscript, a simple and efficient sulfa-Michael addition reaction of aryl thiols to trisubstituted α-fluoro-α,β-unsaturated esters both in racemic and, for the first time, in enantioselective version is reported. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::28e78eb796d74c0853e1c61279e93c0b
https://hal.archives-ouvertes.fr/hal-03004699/document
https://hal.archives-ouvertes.fr/hal-03004699/document
Autor:
Florian Nachon, Emilie David, Xavier Brazzolotto, Patrick Masson, Oksana Lockridge, Lawrence M. Schopfer
Publikováno v:
Journal of Chromatography B. :109-115
Affinity chromatography on procainamide-Sepharose has been an important step in the purification of butyrylcholinesterase (BChE) and acetylcholinesterase (AChE) since its introduction in 1978. The procainamide affinity gel has limitations. In the pre
Autor:
Emilie David, Florian Nachon, Oksana Lockridge, Xavier Brazzolotto, Lawrence M. Schopfer, Patrick Masson
Affinity chromatography on procainamide-Sepharose has been an important step in the purification of butyrylcholinesterase (BChE) and acetylcholinesterase (AChE) since its introduction in 1978. The procainamide affinity gel has limitations. In the pre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::60512228c0f94e7ec3f2bf9810f93163
https://doi.org/10.20944/preprints201806.0443.v1
https://doi.org/10.20944/preprints201806.0443.v1
Publikováno v:
PLoS ONE, Vol 14, Iss 1, p e0209795 (2019)
Human butyrylcholinesterase (HuBChE) is being developed as a therapeutic for protection from the toxicity of nerve agents. An enriched source of HuBChE is Cohn fraction IV-4 from pooled human plasma. For the past 40 years, purification of HuBChE has
Publikováno v:
Tetrahedron
Tetrahedron, Elsevier, 2013, 69 (52), pp.11039-11055. ⟨10.1016/j.tet.2013.10.048⟩
Tetrahedron, Elsevier, 2013, 69 (52), pp.11039-11055. ⟨10.1016/j.tet.2013.10.048⟩
International audience
Autor:
Ying Zheng, Katherine H. Shiavoni, Albena T. Dinkova-Kostova, Dale F. Mierke, Tadashi Honda, Y. R. Santosh Laxmi, W. Christian Wigley, Ronald Bumeister, Yanqing Ren, Isaac Trevino, Emilie David, Suqing Zheng, James B. Bliska, Iwao Ojima
Publikováno v:
Journal of Medicinal Chemistry. 55:4837-4846
Novel monocyclic cyanoenones examined to date display unique features regarding chemical reactivity as Michael acceptors and biological potency. Remarkably, in some biological assays, the simple structure is more potent than pentacyclic triterpenoids
Autor:
Marc Lemaire, Emilie David, Guillaume Pilet, Maurice Médebielle, Etsuji Okada, Sandrine Lassara, Jerome Molette, Jean-Florent Lamarque, Dai Shibata, Christophe Lamarque, Stéphane Pellet-Rostaing
Publikováno v:
Journal of Fluorine Chemistry. 129:788-798
The synthesis of N -(2-trifluoroacetylaryl)propargylamines 10 – 14 and 17 is presented. The copper(I) catalyzed cycloaddition reaction of these propargylamines (dipolarophiles) with a series of azides (1,3-dipoles) 18 – 20 , 21 and 24 was found t