Results 81 to 90 of about 342 (115)

Association between Disgust Sensitivity during Pregnancy and Endogenous Steroids: A Longitudinal Study. [PDF]

open access: yesInt J Mol Sci
Kaňková Š   +5 more
europepmc   +1 more source

A Case of Rocuronium-Induced Anaphylactic Shock in an Asthmatic Child. [PDF]

open access: yesAnesth Prog, 2018
Tanoue R   +3 more
europepmc   +1 more source

Influence of 11-trimethylsilyloxy- or 11-hydroxy-substituents on the electron-impact-induced fragmentation of trimethylsilyl derivatives of some androstanols

open access: closedJournal of the Chemical Society, Perkin Transactions 1, 1973
The mass spectra of the trimethylsilyl derivatives of some androstanes containing an 11-hydroxy-substituent exhibit several prominent and characteristic ions containing the trimethylsilyl group. The mechanisms of formation of these ions have been investigated with the aid of high-resolution mass spectrometry and deuterium, 18O, and ...
Paul Vouros, David Harvey
semanticscholar   +5 more sources

Rheometry of an androstanol steroid derivative paramagnetic organogel. Methodology for a comparison with a fatty acid organogel

open access: closedTetrahedron, 2007
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
Séverine Friol, Pierre Terech
semanticscholar   +6 more sources

Orientation and vertical fluctuations of spin-labeled analogues of cholesterol and androstanol in phospholipid bilayers

open access: closedBiochimica et Biophysica Acta (BBA) - Biomembranes, 1987
We have used ESR and NMR linewidth broadening by spin-labels to determine the overall orientation of spin-labeled analogues of cholesterol and androstanol in egg lecithin bilayers. While the cholesterol analogues were found to have a single orientation in each monolayer, with the acyl chain pointing towards the center of the bilayer, the androstanol ...
Philippe F. Devaux   +5 more
openaire   +4 more sources

ChemInform Abstract: STEROIDE 28. MITT. DARST. VON STEROIDHORMON‐ANALOGEN AUS 2,3BETA‐IMINO‐5ALPHA‐ANDROSTANOL‐(17BETA) UND 3ALPHA‐CHLOR‐2BETA‐AMINO‐5ALPHA‐ANDROSTANOL‐(17BETA)

open access: closedChemischer Informationsdienst. Organische Chemie, 1971
AbstractDas Epoxid (I) gibt bei der Umsetzung mit Na‐azid in Äthylenglykol das Hydroxyazid (IIa) (92% Ausbeute), dessen Tosylat (IIb) durch Reaktion mit Naboranat in das Androstandiol‐Derivat (III) (90%) übergeführt wird.
Kurt Ponsold, Wolfgang Preibsch
openaire   +3 more sources

Steroide, 28. Darstellung von Steroidhormon‐Analogen aus 2.3 β‐Imino‐5α‐androstanol‐(17β) und 3α‐Chlor‐2 β‐amino‐5α‐androstanol‐(17 β)

open access: closedChemische Berichte, 1971
Abstract2.3β‐Imino‐5α‐androstanol‐(17β) (2a) wurde aus 2.3α‐Epoxy‐5α‐androstanon‐(17) über den entsprechenden Azidoalkoholsulfonsäureester synthetisiert und zu 3α‐Chlor‐2β‐amino‐5α‐androstanol‐(17β) (3) umgesetzt. Aus diesen beiden Verbindungen wurden Oxazoline, Thioxothiazolidine, Aminoalkohole und Aminothiole dargestellt.
Wolfgang Preibsch, Kurt Ponsold
openaire   +4 more sources

Home - About - Disclaimer - Privacy