Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Martin Steinman"'
Autor:
Angela Alave Reyes-Furrer, Sonia De Andrade, Dominic Bachmann, Heidi Jeker, Martin Steinmann, Nathalie Accart, Andrew Dunbar, Martin Rausch, Epifania Bono, Markus Rimann, Hansjoerg Keller
Publikováno v:
Communications Biology, Vol 4, Iss 1, Pp 1-12 (2021)
Alave-Furrer et al adapted their recently-developed 3D bioprinting platform to allow microvalve-based drop-on-demand printing of cell-laden Matrigel containing primary human muscle precursor cells. Their bioprinting platform recapitulated aspects of
Externí odkaz:
https://doaj.org/article/3e8c0388474b4dcdac2c6f21af3426d5
Autor:
and George M. Love, Martin Steinman, Yee-Shing Wong, Bruce P. Shutts, Doris P. Schumacher, W. Tormos, Guang-Zhong Wu
Publikováno v:
Organic Process Research & Development. 1:359-364
A six-step practical synthesis of (6aS,13bR)-11-chloro-6,6a,7,8,9,13b-hexahydro-7-methyl-5H-benzo[d]naphtho[2,1-b]azepin-12-ol, a selective D1 dopamine receptor, is developed starting from (1S,2S)-phenyl-2-amino-1,3-propanediol. An acid-promoted ster
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::198a41ad712c9af0e31e2edd02d8083a
https://doi.org/10.1021/op970105v
https://doi.org/10.1021/op970105v
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 3:2171-2176
Novel, stereoselective syntheses of (3S, 4R, 5R)-1-(allyloxycarbonyl)methyl-3-[1-hydroxyethyl]-4-β-naphthoxy(thiocarbonyl)thio-2-azetidinone (13) and (3S, 4R, 5R, 3′S, 4′R, 5′R)-4,4′-dithio-bis-1-(allyloxy-carbonyl)methyl-3-[-1-hydroxyethyl]
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c48edea3354d8272b27f2bb58f1cf8f1
https://doi.org/10.1016/s0960-894x(01)80920-3
https://doi.org/10.1016/s0960-894x(01)80920-3
Publikováno v:
ChemInform. 25
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::26b125bb710649b460bf8c35dcd45c25
https://doi.org/10.1002/chin.199423268
https://doi.org/10.1002/chin.199423268
Autor:
Martin Steinman, G. M. Love, YeeShing Wong, W. Tormos, Bruce P. Shutts, Doris P. Schumacher, Guangzhong Wu
Publikováno v:
ChemInform. 29
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::907a1ca4707644e54e4284029241aff7
https://doi.org/10.1002/chin.199807180
https://doi.org/10.1002/chin.199807180
Publikováno v:
Synthesis. 1991:571-574
A new, efficient synthesis of 1,8-naphthyridin-2(1H)-ones as applied to the synthesis of the leukotriene release inhibitor, 1,2-dihydro-1-phenyl-3-pyrrolidinio-2-oxo-1,8-naphthyridin-4-olate inner salt (4) from methyl 2-phenylamino-3-pyridinecarboxyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1d7f288a48d71e34d760476a993a0aa8
https://doi.org/10.1055/s-1991-26519
https://doi.org/10.1055/s-1991-26519
Publikováno v:
European journal of pharmacology. 218(1)
The aim of this study was to gain further insight into the function of cortical GABAB receptors. In chloral hydrate-anaesthetized rats, microiontophoretic administration of the GABAB receptor blocker CGP 35348 induced a moderate increase in firing of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f259e4b70a856f490f531a26f6a517c
https://pubmed.ncbi.nlm.nih.gov/1327823
https://pubmed.ncbi.nlm.nih.gov/1327823
Autor:
Yee-Shing Wong, Martin Steinman
Publikováno v:
Tetrahedron Letters. 15:2087-2090
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c08e1630f730799df48e6208d693554b
https://doi.org/10.1016/s0040-4039(01)82639-3
https://doi.org/10.1016/s0040-4039(01)82639-3
Publikováno v:
Journal of Medicinal Chemistry. 21:1327-1330
The synthesis and antiallergic activity of a new series of 9H-xanthen-9-one-2-carboxylic acids are described. Antiallergic activity was evaluated in the rat passive cutaneous anaphylaxis (PCA) screen. Biological results were analyzed using regression
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc6370d01045a60b12f32133c327fa16
https://doi.org/10.1021/jm00210a034
https://doi.org/10.1021/jm00210a034
Publikováno v:
Journal of Medicinal Chemistry. 16:1354-1360
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::56461cfcbebefd2632809e22a767be0d
https://doi.org/10.1021/jm00270a008
https://doi.org/10.1021/jm00270a008