Relevant bibliographies by topics / Dihydroergocristine

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Academic literature on the topic 'Dihydroergocristine'

Author: Grafiati
Published: 4 June 2021
Last updated: 4 February 2022

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Journal articles on the topic "Dihydroergocristine"

1

&NA;. "Dihydroergocristine." Reactions Weekly &NA;, no. 539 (1995): 7. http://dx.doi.org/10.2165/00128415-199505390-00017.

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2

&NA;. "Dihydroergocristine/dihydroergotamine mesylate/nicergoline." Reactions Weekly &NA;, no. 612 (1996): 7. http://dx.doi.org/10.2165/00128415-199606120-00020.

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3

Zvonkova, E. N., V. I. Sheichenko, G. B. Lapa, T. E. Monakhova, V. V. Anufrieva, and V. A. Bykov. "Solubility of dihydroergocristine mesylate." Pharmaceutical Chemistry Journal 32, no. 10 (1998): 567–68. http://dx.doi.org/10.1007/bf02465750.

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4

Beran, Miloš, Antonín Černý, Miroslav Kuchař, et al. "9,10-Dihydroergopeptines modified in position 6." Collection of Czechoslovak Chemical Communications 55, no. 3 (1990): 819–32. http://dx.doi.org/10.1135/cccc19900819.

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9,10-Dihydroergopeptines modified in position 6 (VII-XXIII) were prepared from 9,10-dihydroergotamine (I) and 9,10-dihydroergocristine (II) which were converted via corresponding 6-demethyl-6-cyano compounds III and IV to 6-demethyl-9,10-dihydroergotamine (V) or 6-demethyl-9,10-dihydroergocristine (VI), respectively, which were then alkylated or acylated in position 6. Methylation of 6-demethyl-6-propyl compounds VIII and IX on N1 gave 1-methyl-6-demethyl-6-propyl-9,10-dihydroergotamine (XXIV) and 1-methyl-6-demethyl-6-propyl-9,10-dihydroergocristine (XXV). In the majority of the compounds the
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5

Bicalho, Beatriz, Giovanni Guzzo, Sergio Lilla, et al. "Pharmacokinetics of Dihydroergocristine and Its Major Metabolite 8- Hydroxy-Dihydroergocristine in Human Plasma." Current Drug Metabolism 6, no. 6 (2005): 519–29. http://dx.doi.org/10.2174/138920005774832669.

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6

Pagliano, F. M., and G. C. Galbiati. "Comparison of the Efficacy and Safety of Daily Dosages of 6 mg and 20 mg Dihydroergocristine in the Treatment of Chronic Cerebro-Vascular Disease." Journal of International Medical Research 23, no. 4 (1995): 219–27. http://dx.doi.org/10.1177/030006059502300401.

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The efficacy and safety of two different regimens of dihydroergocristine, in the treatment of patients with chronic cerebro-vascular disease, were compared in this double-blind study. Forty out-patients, 11 males and 29 females, aged 55 – 80 years were randomly assigned to treatment with 6 or 20 mg dihydroergocristine, daily, for 3 months. The Sandoz Clinical Assessment for Geriatrics (SCAG) scale was used to assess the efficacy of treatment. Both doses induced a statistically significant improvement ( P < 0.01) in total SCAG scores after both 45 and 90 days of treatment. The higher dose pr
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7

Scarduelli, C., V. Cavioni, C. Galparoli, D. Spellecchia, P. G. Crosignani, and C. Ferrari. "Clinical use of an antiprolactinaemic drug: dihydroergocristine." Journal of Obstetrics and Gynaecology 7, no. 3 (1987): 225–27. http://dx.doi.org/10.3109/01443618709068524.

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8

D'Agata, Velia, Francesco Spadaro, and Filippo Drago. "Dihydroergocristine improves behavioral deficits of aged rats." Pharmacological Research Communications 20, no. 12 (1988): 1119–20. http://dx.doi.org/10.1016/s0031-6989(88)80755-0.

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9

Čejka, Jan, Bohumil Kratochvíl, Alexandr Jegorov та Ladislav Cvak. "Crystal Structures of Dihydro-α-ergokryptine and Dihydro-β-ergokryptine Mesylates". Collection of Czechoslovak Chemical Communications 65, № 8 (2000): 1329–38. http://dx.doi.org/10.1135/cccc20001329.

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The absolute crystal structures of two related ergot alkaloids dihydro-α-ergokryptine mesylate (1) monohydrate ethanol solvate and dihydro-β-ergokryptine mesylate (2) monohydrate methanol solvate have been determined by X-ray diffraction and compared with the published structures of dihydroergocristine mesylate (3) monohydrate and dihydroergotamine mesylate (4) monohydrate.
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10

Mönch, B., W. Kraus, R. Köppen, and F. Emmerling. "The different conformations and crystal structures of dihydroergocristine." Journal of Molecular Structure 1105 (February 2016): 389–95. http://dx.doi.org/10.1016/j.molstruc.2015.10.008.

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Dissertations / Theses on the topic "Dihydroergocristine"

1

Guzzo, Giovanni Carvalho. "Estudo do metabolismo, quimica e farmacocinetica do principal metabolito da diidroergocristina." [s.n.], 2009. http://repositorio.unicamp.br/jspui/handle/REPOSIP/309467.

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Abstract:
Orientador: Gilberto de Nucci<br>Tese (doutorado) - Universidade Estadual de Campinas, Faculdade de Ciencias Medicas<br>Made available in DSpace on 2018-08-14T18:13:32Z (GMT). No. of bitstreams: 1 Guzzo_GiovanniCarvalho_D.pdf: 1951061 bytes, checksum: eddc16b466ad966ac80f17737bb7d32d (MD5) Previous issue date: 2009<br>Resumo: Diidroergocristina (DHEC) é um fármaco semi-sintético, derivada do alcalóide do Ergot, principalmente utilizada para enxaqueca e estudada em distúrbios cognitivos relacionados ao envelhecimento. No presente estudo, o seu principal metabólito 8-hidroxidiidroergocristina
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Books on the topic "Dihydroergocristine"

1

(Editor), A. Volpe, F. Mailland (Editor), and Andrea R. Genazzani (Editor), eds. Dihydroergocristine. Parthenon Publishing Group, 1988.

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