Academic literature on the topic 'Steroid enantiomers'

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Journal articles on the topic "Steroid enantiomers"

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Li, Wenjun, Douglas F. Covey, Juha-Matti Alakoskela, Paavo K. J. Kinnunen, and Joe Henry Steinbach. "Enantiomers of Neuroactive Steroids Support a Specific Interaction with the GABA-C Receptor as the Mechanism of Steroid Action." Molecular Pharmacology 69, no. 6 (2006): 1779–82. http://dx.doi.org/10.1124/mol.106.022863.

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Sheikh, Sana U., and Joseph C. Touchstone. "Effect of subambient temperatures on separation of steroid enantiomers by high-performance liquid chromatography." Analytical Chemistry 59, no. 10 (1987): 1472–73. http://dx.doi.org/10.1021/ac00137a022.

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Walle, UK, TC Fagan, MJ Topmiller, EC Conradi, and T. Walle. "The influence of gender and sex steroid hormones on the plasma binding of propranolol enantiomers." British Journal of Clinical Pharmacology 37, no. 1 (1994): 21–25. http://dx.doi.org/10.1111/j.1365-2125.1994.tb04233.x.

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Liu, Ya-Ping, Sheng-Tao Fang, Zhen-Zhen Shi, Bin-Gui Wang, Xiao-Nian Li, and Nai-Yun Ji. "Phenylhydrazone and Quinazoline Derivatives from the Cold-Seep-Derived Fungus Penicillium oxalicum." Marine Drugs 19, no. 1 (2020): 9. http://dx.doi.org/10.3390/md19010009.

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Three new phenylhydrazones, penoxahydrazones A–C (compounds 1–3), and two new quinazolines, penoxazolones A (compound 4) and B (compound 5), with unique linkages were isolated from the fungus Penicillium oxalicum obtained from the deep sea cold seep. Their structures and relative configurations were assigned by analysis of 1D/2D NMR and mass spectroscopic data, and the absolute configurations of 1, 4, and 5 were established on the basis of X-ray crystallography or ECD calculations. Compound 1 represents the first natural phenylhydrazone-bearing steroid, while compounds 2 and 3 are rarely occur
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Sneitz, Nina, Kathiresan Krishnan, Douglas F. Covey та Moshe Finel. "Glucuronidation of the steroid enantiomers ent-17β-estradiol, ent-androsterone and ent-etiocholanolone by the human UDP-glucuronosyltransferases". Journal of Steroid Biochemistry and Molecular Biology 127, № 3-5 (2011): 282–88. http://dx.doi.org/10.1016/j.jsbmb.2011.08.008.

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Audia, James E., David E. Lawhorn та Jack B. Deeter. "Synthesis of the individual enantiomers of the benzoquinolinone human type 1 steroid 5-α-reductase inhibitors LY191704 and LY266111". Tetrahedron Letters 34, № 44 (1993): 7001–4. http://dx.doi.org/10.1016/s0040-4039(00)61581-2.

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NAGAMINE, Sachiko, Eri HORISAKA, Yukari FUKUYAMA, et al. "Stereoselective Reductive Metabolism of Metyrapone and Inhibitory Activity of Metyrapone Metabolites, Metyrapol Enantiomers, on Steroid 11.BETA.-Hydroxylase in the Rat." Biological & Pharmaceutical Bulletin 20, no. 2 (1997): 188–92. http://dx.doi.org/10.1248/bpb.20.188.

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AUDIA, J. E., D. E. LAWHORN та J. B. DEETER. "ChemInform Abstract: Synthesis of the Individual Enantiomers of the Benzoquinolinone Human Type 1 Steroid 5-α-Reductase Inhibitors LY191704 and LY266111." ChemInform 25, № 4 (2010): no. http://dx.doi.org/10.1002/chin.199404178.

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Krishnan, Kathiresan, Brad D. Manion, Amanda Taylor та ін. "Neurosteroid Analogues. 17. Inverted Binding Orientations of Androsterone Enantiomers at the Steroid Potentiation Site on γ-Aminobutyric Acid Type A Receptors". Journal of Medicinal Chemistry 55, № 3 (2012): 1334–45. http://dx.doi.org/10.1021/jm2014925.

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Kravchenko, Anastasia, Ekaterina Kolobova, and Liudmila Kartsova. "Multifunction covalent coatings for separation of amino acids, biogenic amines, steroid hormones, and ketoprofen enantiomers by capillary electrophoresis and capillary electrochromatography." SEPARATION SCIENCE PLUS 3, no. 4 (2020): 102–11. http://dx.doi.org/10.1002/sscp.201900098.

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Dissertations / Theses on the topic "Steroid enantiomers"

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Kapras, Vojtěch. "Syntéza a vlastnosti neuroaktivních steroidů." Doctoral thesis, 2016. http://www.nusl.cz/ntk/nusl-347460.

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Herein is reported the synthesis of molecular probes for action of neuroactive steroids in vitro and in living organisms. In the first part, preparation of enantiomeric pregnane steroids is investigated, ultimately resulting into the total synthesis of ent-progesterone. The chirality of the target molecule is introduced by a highly effective organocatalytic asymmetric Robinson annulation. A new method for the sequential construction of five-membered carbocyclic ring is introduced as the key step. This is composed of substrate-controlled copper-catalyzed conjugate addition followed by radical o
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