For research use only. Not for therapeutic Use.
Trilostane is an inhibitor of 3β-hydroxysteroid dehydrogenase used in the treatment of Cushing/’s syndrome. It was withdrawn from the United States market in April 1994. However, it was recently approved in 2008 for the treatment of Cushing/’s disease (hyperandrenocorticism) in dogs. It is also the first drug approved to treat both pituitary- and adrenal-dependent Cushing/’s in dogs. This prescription drug works by stopping the production of cortisol in the adrenal glands.
CAS Number | 13647-35-3 |
Synonyms | 13647-35-3; Vetoryl; Trilostanum; Desopan; Trilostano |
Molecular Formula | C20H27NO3 |
Purity | ≥95% |
Target | Dehydrogenase |
Solubility | >16.4mg/mL in DMSO |
Storage | -20°C |
InChI | 1S/C20H27NO3/c1-18-7-6-14-12(13(18)3-4-15(18)22)5-8-20-17(24-20)16(23)11(10-21)9-19(14,20)2/h12-15,17,22-23H,3-9H2,1-2H3/t12-,13-,14-,15-,17+,18-,19+,20+/m0/s1 |
InChIKey | KVJXBPDAXMEYOA-CXANFOAXSA-N |
SMILES | CC12CCC3C(C1CCC2O)CCC45C3(CC(=C(C4O5)O)C#N)C |
Reference | 1: Crosby J, Brown S. Stability of compounded trilostane suspension in cod liver 2: Sieber-Ruckstuhl N, Salesov E, Quante S, Riond B, Rentsch K, Hofmann-Lehmann 3: Nagata N, Kojima K, Yuki M. Comparison of Survival Times for Dogs with <br> 5: Boretti FS, Holzthüm J, Reusch CE, Sieber-Ruckstuhl NS. Lack of association <br> 7: Oda H, Mori A, Shono S, Onozawa E, Sako T. The effect of 1 year of trilostane <br> 9: Fracassi F, Corradini S, Floriano D, Boari A, Aste G, Pietra M, Bergamini PF, <br> |
Chemistry Calculators | Dilution Calculator In vivo Formulation Calculator Molarity Calculator Molecular Weight Calculator Reconstitution Calculator |