Výsledky vyhledávání - "M C, Schroeder"

Akademický článek

Opto-mechanical expulsion of individual micro-particles by laser-induced shockwave in air

Autor: M. C. Schroeder, U. Andral, J.-P. Wolf

Publikováno v: AIP Advances, Vol 12, Iss 9, Pp 095119-095119-6 (2022)

It was recently demonstrated that laser filamentation was able to generate an optically transparent channel through clouds and fog for free-space optical communications applications. However, no quantitative measurement of the interaction between the

Externí odkaz: https://doaj.org/article/f27086969992483c8f951c4a613bfe2b

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A non-cell-autonomous tumor suppressor role for Stat in eliminating oncogenic scribble cells

Autor: Kathleen M Gajewski, C-L Chen, M C Schroeder, Georg Halder

Publikováno v: Oncogene. 32(38)

Elucidating signaling events between tumor cells and their microenvironment is a major challenge in understanding cancer development. Drosophila melanogaster has emerged as an important tool for dissecting the genetic circuits tumors depend on becaus

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee87c1421c07ff3b275ecb7e7265a95a
https://pubmed.ncbi.nlm.nih.gov/23108407

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ChemInform Abstract: Novel 7-Substituted Quinolone Antibacterial Agents. Synthesis of 7- Alkenyl, Cycloalkenyl, and 1,2,3,6-Tetrahydro-4-pyridinyl-1,8- naphthyridines

Autor: Lawrence E. Lesheski, M. C. Schroeder, John S. Kiely, Edgardo Laborde

Publikováno v: ChemInform. 22

A convergent synthesis of 1,8-naphthyridine antibacterials bearing a carbon-carbon bonded, acyclic or cyclic vinyl substituent at the C-7 position has been achieved. The synthetic methodology is based upon the palladium-catalyzed cross coupling of a

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::8b6d06ec13eef590d5b518585a9dabb8
https://doi.org/10.1002/chin.199129189

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ChemInform Abstract: Synthesis of the Four Stereoisomers of Several 3-(1-Aminoethyl) pyrrolidines. Important Intermediates in the Preparation of Quinolone Antibacterials

Autor: André Michel, John S. Kiely, Donald R. Johnson, Edgardo Laborde, Jeffrey W. Kampf, Thomas M. Stickney, John M. Domagala, D. L. Szotek, M. C. Schroeder

Publikováno v: ChemInform. 24

The use of S-α-methylbenzyl as a chiral auxiliary at N1 allowed separation of diastereomeric 2-pyrrolidinones substituted with an ester, ketoester, ketone and oxime at the C4 position. Reduction of each diastereomer of 4-[1-(hydroxyimino)ethyl]-1-(1

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::786828ba1bf632378d90ebd12043fbbb
https://doi.org/10.1002/chin.199318200

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Synthesis of the four stereoisomers of several 3-(1-aminoethyl)pyrrolidines. Important intermediates in the preparation of quinolone antibacterials

Autor: André Michel, Thomas M. Stickney, Edgardo Laborde, Jeffrey W. Kampf, John S. Kiely, John M. Domagala, M. C. Schroeder, Donald R. Johnson, D. L. Szotek

Publikováno v: Journal of Heterocyclic Chemistry. 29:1481-1498

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::d9398c131aa60f56ad199ee6a3e65c12
https://doi.org/10.1002/jhet.5570290620

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Novel 7-substituted quinolone antibacterial agents. Synthesis of 7-alkenyl, cycloalkenyl, and 1,2,3,6-tetrahydro-4-pyridinyl-1,8-naphthyridines

Autor: John S. Kiely, M. C. Schroeder, Lawrence E. Lesheski, Edgardo Laborde

Publikováno v: Journal of Heterocyclic Chemistry. 28:191-198

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::8056ec602dadf4394205b88a8fa6d53d
https://doi.org/10.1002/jhet.5570280133

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Bioactivation and irreversible binding of the cognition activator tacrine using human and rat liver microsomal preparations. Species difference

Autor: T F, Woolf, W F, Pool, S M, Bjorge, T, Chang, O P, Goel, C F, Purchase, M C, Schroeder, K L, Kunze, W F, Trager

Publikováno v: Drug metabolism and disposition: the biological fate of chemicals. 21(5)

Tacrine's [1,2,3,4-tetrahydro-9-acridinamine monohydrochloride monohydrate, (THA)] metabolic fate was examined using human and rat liver microsomal preparations. Following 1-hr incubations with human microsomes, [14C]THA (0.4 microM) was extensively

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::72ff76f74c6cd8072ef38710bc62592e
https://pubmed.ncbi.nlm.nih.gov/7902251

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Effect of atrasentan (ABT-627, ATN) on the pharmacokinetics (PK) of fexofenadine (FEX)

Autor: T. Yanke, C. E. Klein, Robert A. Carr, Q. Wang, T. Doan, A. Allen, M. C. Schroeder, I. Facey, E. Everitt, D. Grimm

Publikováno v: Journal of Clinical Oncology. 22:4723-4723

4723 Background: ATN is an oral selective endothelin A receptor antagonist in phase 3 clinical development for treatment of hormone-refractory prostate cancer. ATN is not a p-glycoprotein (Pgp) sub...

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::6fc9af91282369a54a30816877642b93
https://doi.org/10.1200/jco.2004.22.90140.4723

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