| Title:  Fluocortin Butyl CAS Registry Number:  41767-29-7 CAS Name:  (6a,11b,16a)-6-Fluoro-11-hydroxy-16-methyl-3,20-dioxopregna-1,4-dien-21-oic acid butyl ester Additional Names:  butyl 6a-fluoro-11b-hydroxy-16a-methyl-3,20-dioxopregna-1,4-dien-21-oate Manufacturers' Codes:  SH K 203 Trademarks:  Varlane (Schering AG);  Vaspit (Schering AG) Molecular Formula:  C26H35FO5 Molecular Weight:  446.55 Percent Composition:  C 69.93%, H 7.90%, F 4.25%, O 17.91% Literature References:  The butyl ester deriv of fluocortolone-21-acid, a metabolite of fluocortolone, q.v., in humans.  Prepn:  H. Laurent et al., DE 2150268, DE 2150270; eidem, US 3824260 (1973, 1973, 1974, all to Schering AG); H. Laurent et al., Angew. Chem. 87, 70 (1975).  Description of this new corticoid structure type, the pregnan-21-oic esters, their activity and methods for synthesis:  H. Laurent et al., J. Steroid Biochem. 6, 185 (1975).  Toxicity data:  P. Günzel et al., Arzneim.-Forsch. 27, 2217 (1977).  Series of articles on synthesis, pharmacology and clinical trials:  ibid. 2185-2246. Properties:  Crystals from acetone/hexane, mp 195.1°.  [a]D25 +136° (c = 0.5 in chloroform).  uv max (methanol):  242 nm (e 16800).  Soluble in chloroform, ethanol; poorly sol in ethyl ether.  Insol in water.  LD50 in mice, rats (g/kg):  >4 orally and s.c. (Günzel). Melting point:  mp 195.1° Optical Rotation:  [a]D25 +136° (c = 0.5 in chloroform) Absorption maximum:  uv max (methanol):  242 nm (e 16800) Toxicity data:  LD50 in mice, rats (g/kg):  >4 orally and s.c. (Günzel) Therap-Cat:  Anti-inflammatory. Keywords:  Glucocorticoid.  |