Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Lukasz Koroniak"'
Autor:
B. Gabriel Gugiu, Kevin Mouillesseaux, Victoria Duong, Tabitha Herzog, Avetis Hekimian, Lukasz Koroniak, Thomas M. Vondriska, Andrew D. Watson
Publikováno v:
Journal of Lipid Research, Vol 49, Iss 3, Pp 510-520 (2008)
Oxidation products of 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphatidylcholine (Ox-PAPC) are found in atherosclerotic lesions, apoptotic cells, and oxidized LDL and stimulate human aortic endothelial cells (HAECs) to produce inflammatory cytokines
Externí odkaz:
https://doaj.org/article/c4f3ec94463e49738273537f4c769ae3
Autor:
B. Gabriel Gugiu, Rongsong Li, Judith A. Berliner, Jinluo Cheng, Lukasz Koroniak, Xinmin Yan, Sangderk Lee, Michael E. Jung
Publikováno v:
Biochemical and Biophysical Research Communications. 444:69-74
Atherosclerosis is the main underlying cause of major cardiovascular diseases such as stroke and heart attack. Oxidized phospholipids such as oxidized 1-palmitoyl-2-arachidonoyl-sn-Glycero-3-phosphorylcholine (OxPAPC) accumulate in lesions of and pro
Autor:
Martin Dun, Dennis Montoya, Lukasz Koroniak, Judith A. Berliner, Kevin Mouillesseaux, Rongsong Li, Navid Gharavi, Daniel Cruz
Publikováno v:
Circulation Research. 98:642-650
Oxidized 1-palmitoyl-2-arachidonoyl- sn -glycero-3-phosphorylcholine (OxPAPC), which has been shown to accumulate in atherosclerotic lesions and other sites of chronic inflammation, activates endothelial cells (EC) to bind monocytes by activation of
Publikováno v:
Organic Letters. 5:2033-2036
[structure: see text] The synthesis of N-acylsulfonamide 6, which is an analogue of beta-aspartyl-AMP, is described. This compound appears to be the first and only potent inhibitor of human asparagine synthetase that has been described to date. The N
Autor:
Judith A. Berliner, Daniela Angst, Lukasz Koroniak, Rongsong Li, Dawei Yue, and Andrew D. Watson, Michael E. Jung
Publikováno v:
Organic Letters. 7:3933-3935
A total synthesis of the naturally occurring hydroxy ketone PEIPC 1, a compound that plays a role in endothelial activation in atherosclerosis, has been completed via a triply convergent preparation of a protected EI derivative 13 from 3,5-diacetoxyc
Publikováno v:
Tetrahedron Letters. 42:1241-1243
Several conduritol derivatives protected as allyl and cinnamyl ethers were subjected to electrochemical reduction at a mercury cathode, resulting in selective removal of the cinnamyl group.
Autor:
Christopher D. Claeboe, Larry E. Brammer, Ion Ghiviriga, Gabor Butora, Lukasz Koroniak, Tomas Hudlicky
Publikováno v:
ChemInform. 30
Several vinyl halides previously used in inositol syntheses were subjected to electrochemical reduction. The unreactivity of allylic alcohols or allylic ethers at the applied potentials allowed the...
Publikováno v:
ChemInform. 32
Publikováno v:
ChemInform. 40
An improved synthesis of the naturally occurring hydroxy ketone 1-palmitoyl-2-(5,6)-epoxyisoprostane E2-sn-glycero-3-phosphocholine (PEIPC) 1, a compound that plays a role in endothelial activation...
Publikováno v:
Green Chemistry. 1:57-59
Several synthetic pathways to cyclohex-5-ene-1R,2S,3R,4R-tetrol (conduritol C) and cyclohex-5-ene-1S,2R,3R,4R-tetrol (conduritol F) are compared; each is analyzed for effectiveness of waste minimization. The latest synthesis, reported in this manuscr