Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Archana R. Parameswar"'
Autor:
Jacqueline A. Hawkins-Salsbury, Archana R. Parameswar, Xuntian Jiang, Paul H. Schlesinger, Ernesto Bongarzone, Daniel S. Ory, Alexei V. Demchenko, Mark S. Sands
Publikováno v:
Journal of Lipid Research, Vol 54, Iss 12, Pp 3303-3311 (2013)
Globoid cell leukodystrophy (GLD) is a neurological disease caused by deficiency of the lysosomal enzyme galactosylceramidase (GALC). In the absence of GALC, the cytotoxic glycosphingolipid, psychosine (psy), accumulates in the nervous system. Psycho
Externí odkaz:
https://doaj.org/article/516d8dd6d7a041388b68ed58eace6044
Autor:
Younghoon Oh, Peter Orlean, Erfei Bi, Jacob Gyore, Neil P. J. Price, Archana R. Parameswar, Carleigh F. F. Hebbard, Alexei V. Demchenko
Publikováno v:
The Journal of Biological Chemistry
Background: Chitin synthases are stimulated by N-acetylglucosamine (GlcNAc). Results: GlcNAc and 2-acylamido analogues of GlcNAc stimulate formation of chitin oligosaccharides by yeast chitin synthase, and GlcNAc is transferred to the 2-acylamido ana
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e64efe6a404675dc66eb6734c3d9a413
http://europepmc.org/articles/PMC4007471
http://europepmc.org/articles/PMC4007471
Autor:
Archana R. Parameswar, Alexei V. Demchenko, Paul H. Schlesinger, Jacqueline A. Hawkins-Salsbury, Xuntian Jiang, Ernesto R. Bongarzone, Mark S. Sands, Daniel S. Ory
Publikováno v:
Journal of Lipid Research, Vol 54, Iss 12, Pp 3303-3311 (2013)
Globoid cell leukodystrophy (GLD) is a neurological disease caused by deficiency of the lysosomal enzyme galactosylceramidase (GALC). In the absence of GALC, the cytotoxic glycosphingolipid, psychosine (psy), accumulates in the nervous system. Psycho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d80bc8bddad5f4ff451bb72288f7c300
https://doi.org/10.1194/jlr.m039610
https://doi.org/10.1194/jlr.m039610
Autor:
Papapida Pornsuriyasak, Yih Horng Tan, Archana R. Parameswar, Binod Pandey, Alexei V. Demchenko, Keith J. Stine
Publikováno v:
Carbohydrate Research. 373:9-17
Self-assembled monolayers (SAMs) of α-D-Gal-(1→4)-β-D-Gal-(1→4)-β-D-Glc-mercaptooctane (globotriose, Gb3-C8-SH) were prepared both as single-component SAMs and as mixed SAMs with either octanethiol (OCT) or 8-mercapto-3,6-dioxaoctanol (HO-PEG2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2babcb7755ae81e6e1ade6b444666f5a
https://doi.org/10.1016/j.carres.2012.09.021
https://doi.org/10.1016/j.carres.2012.09.021
Autor:
Manuel Temprado, Joel F. Liebman, Pilar Jiménez, Archana R. Parameswar, Carol A. Deakyne, James S. Chickos, Rafael Notario, Alexei V. Demchenko, María Victoria Roux
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
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instname
In a continuation of our investigations of the thermochemistry of heterocyclic ring systems and sulfur-containing compounds, the standard molar enthalpy of formation of tetrahydro-2H-1,3-oxazine-2-thione (CAS no. 17374-18-4) at T = 298 K has been eva
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd116cf5a94c5812721d5fbccb90057b
https://doi.org/10.1021/je200549z
https://doi.org/10.1021/je200549z
Autor:
Mark S. Sands, Archana R. Parameswar, Alexei V. Demchenko, Jacqueline Hawkins, Laurel K. Mydock
Publikováno v:
European Journal of Organic Chemistry. 2010:3269-3274
The accumulation of psychosine (galactosyl sphingosine) has been associated with the pathogenesis of Krabbe disease; however, the exact mechanism of its cytotoxicity remains unclear. Herein, we describe the synthesis of the unnatural enantiomer of er
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bace682938416e5e0917e3ed6ec04c05
https://doi.org/10.1002/ejoc.201000024
https://doi.org/10.1002/ejoc.201000024
Autor:
María Victoria Roux, Manuel Temprado, Archana R. Parameswar, Concepción Foces-Foces, Alexei V. Demchenko, Pilar Jiménez, Joel F. Liebman, Rafael Notario, Carol A. Deakyne, James S. Chickos, Alicia K. Ludden
Publikováno v:
The Journal of Physical Chemistry A. 113:10772-10778
This paper reports an experimental and a theoretical study of the structures and standard (p(o) = 0.1 MPa) molar enthalpies of formation of the synthetic reagents 1,3-thiazolidine-2-thione [CAS 96-53-7] and 1,3-oxazolidine-2-thione [CAS 5840-81-3]. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e824599cf1971bf25c957eec6fa3834
https://doi.org/10.1021/jp9034216
https://doi.org/10.1021/jp9034216
Autor:
Manuel Temprado, Archana R. Parameswar, Alexei V. Demchenko, James S. Chickos, Joel F. Liebman, María Victoria Roux
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
instname
The present study reports a DSC study of the thio-and dithiocarbamates: 3H-benzoxazole-2-thione (2-mercaptobenzoxazole), 3H-benzothiazole-2-thione (2-mercaptobenzothiazole), thiazolidine-2-thione (2-mercapto-2-thiazoline), oxazolidine-2-thione (2-mer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::42abf16df434f3899191b56720351494
https://doi.org/10.1007/s10973-007-8345-8
https://doi.org/10.1007/s10973-007-8345-8
Autor:
Alexei V. Demchenko, Gary S. Howarth, Scott J. Hasty, Larry D. Byers, Archana R. Parameswar, Elizabeth Alverson-Banks Avegno
A new, very efficient, class of thioglycoside substrates has been found for β-glucosidase. While thioglycosides are usually resistant to hydrolysis, even in the presence of acids or most glycohydrolases, the β-D-glucopyranosides of 2- mercaptobenzi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b1cfba81703b2d663dafa8b58dde3b0
https://europepmc.org/articles/PMC3755622/
https://europepmc.org/articles/PMC3755622/
Autor:
Konstantin Maslov, Alexei V. Demchenko, Archana R. Parameswar, Lihong V. Wang, Junjie Yao, Vassiliy Tsytsarev
Accurately locating epileptic foci has great importance in advancing the treatment of epilepsy. In this study, epileptic seizures were first induced by intracortical injection of 4-aminopyridine in rats. A fluorescent deoxyglucose substitute, 2-(N-(7
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29b813ef5f9220e56e3745e17eee542a
https://europepmc.org/articles/PMC3221836/
https://europepmc.org/articles/PMC3221836/