Cipamfylline
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Non-proprietary name | Cipamfylline | ||||||||||||||||||
other names |
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Molecular formula | C 13 H 17 N 5 O 2 | ||||||||||||||||||
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properties | |||||||||||||||||||
Molar mass | 275.31 g · mol -1 | ||||||||||||||||||
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As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . |
Cipamfylline is a type 4 phosphodiesterase inhibitor . As a dermatological agent, it should be used against atopic eczema .
History
Cipamfylline was synthesized in the late 1980s by the Gronau company Beecham-Wülfing (today GlaxoSmithKline ). Cipamfylline has been clinically tested since the late 1990s. In 2002, the manufacturer stopped development because the plasma levels could not be sufficiently high .
Individual evidence
- ↑ This substance has either not yet been classified with regard to its hazardousness or a reliable and citable source has not yet been found.
- ↑ Harald Maschler et al. (March 23, 1989): Great Britain Patent Application No. 8906792.0 .
- ↑ CEM Griffiths, EJM van Leent, M. Gilbert, J. Traulsen (2002): Randomized comparison of the type 4 phosphodiesterase inhibitor cipamfylline cream, cream vehicle and hydrocortisone 17-butyrate cream for the treatment of atopic dermatitis . In: British Journal of Dermatology , 147 (2): 299-307. doi : 10.1046 / j.1365-2133.2002.04894.x