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Sulprostone
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| Systematic (IUPAC) name | |
| (Z)-7-[(1R,3R)-3-Hydroxy-2-[(E,3R)-3-hydroxy-4-
(phenoxy)but-1-enyl]-5-oxocyclopentyl]-N-methylsulfonylhept-5-enamide |
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| Identifiers | |
| CAS number | |
| ATC code | G02 |
| PubChem | |
| Chemical data | |
| Formula | C23H31NO7S |
| Mol. mass | 465.56 g/mol |
| Pharmacokinetic data | |
| Bioavailability | ? |
| Metabolism | ? |
| Half life | ? |
| Excretion | ? |
| Therapeutic considerations | |
| Pregnancy cat. |
? |
| Legal status | |
| Routes | ? |
Sulprostone is an oxytocic.
It is an analogue of prostaglandin E2.[1]
References
- ^ Tamma G, Wiesner B, Furkert J, et al. (August 2003). "The prostaglandin E2 analogue sulprostone antagonizes vasopressin-induced antidiuresis through activation of Rho". Journal of cell science 116 (Pt 16): 3285–94. doi:. PMID 12829746. http://jcs.biologists.org/cgi/pmidlookup?view=long&pmid=12829746.
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