Sulfinpyrazone
Structural formula | ||||||||||||||||||||||
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Structural formula without stereochemistry - stereocenter on the sulfur atom of the S = O group | ||||||||||||||||||||||
General | ||||||||||||||||||||||
Surname | Sulfinpyrazone | |||||||||||||||||||||
other names |
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Molecular formula | C 23 H 20 N 2 O 3 S | |||||||||||||||||||||
Brief description |
White dust |
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properties | ||||||||||||||||||||||
Molar mass | 404.48 g mol −1 | |||||||||||||||||||||
Physical state |
firmly |
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safety instructions | ||||||||||||||||||||||
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Toxicological data | ||||||||||||||||||||||
As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . |
Sulfinpyrazone is a 1: 1 mixture of two stereoisomeric chemical compounds from the group of pyrazolidines .
Extraction and presentation
Sulfinpyrazone can be obtained by reacting hydrazobenzene with diethyl 2- (2-phenylmercaptoethyl) malonate.
properties
Sulfinpyrazone is a white odorless powder that is sparingly soluble in water.
use
Sulfinpyrazone is used in medicine as a platelet aggregation inhibitor from the group of uricosuric drugs . It is used against gout.
Individual evidence
- ↑ a b c d e f data sheet Sulfinpyrazon, analytical standard, for drug analysis at Sigma-Aldrich , accessed on November 4, 2016 ( PDF ).
- ↑ a b c Margitta Albinus: Hager's Handbook of Pharmaceutical Practice: Substances E - O. Springer DE, 1993, ISBN 3-540-52688-9 , p. 731–733 ( limited preview in Google Book search).
- ↑ Entry on sulfinpyrazone in Pharmawiki , accessed on January 28, 2017.