Telapristone

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Telapristone
Telapristone.svg
Systematic (IUPAC) name
[(8S,11R,13S,14S,17R)-11-[4-(Dimethylamino)phenyl]-17-(2-methoxyacetyl)-13-methyl-3-oxo-1,2,6,7,8,11,12,14,15,16-decahydrocyclopenta[a]phenanthren-17-yl] acetate
Clinical data
Legal status
  • Investigational
Identifiers
CAS Number 198414-31-2
PubChem CID: 9806190
ChemSpider 7981950 YesY
UNII 1K9EYK92PQ YesY
Synonyms CDB-4124; 17α-Acetoxy-21-methoxy-11β-[4-N,N-dimethylaminophenyl]-19-norpregna-4,9-diene-3,20-dione)
Chemical data
Formula C31H39NO5
Molecular mass 505.65 g/mol
  • O=C5\C=C3/C(=C2/[C@@H](c1ccc(N(C)C)cc1)C[C@@]4([C@@](OC(=O)C)(C(=O)COC)CC[C@H]4[C@@H]2CC3)C)CC5
  • InChI=1S/C31H39NO5/c1-19(33)37-31(28(35)18-36-5)15-14-27-25-12-8-21-16-23(34)11-13-24(21)29(25)26(17-30(27,31)2)20-6-9-22(10-7-20)32(3)4/h6-7,9-10,16,25-27H,8,11-15,17-18H2,1-5H3/t25-,26+,27-,30-,31-/m0/s1 YesY
  • Key:JVBGZFRPTRKSBB-MJBQOYBXSA-N YesY
  (verify)

Telapristone (INN), as telapristone acetate (proposed trade names Proellex, Progenta; former code name CDB-4124), is an investigational selective progesterone receptor modulator (SPRM) being studied for the treatment of certain progesterone-sensitive conditions.[1] It was originally developed by the National Institutes of Health (NIH), and as of 2012, is in phase II clinical trials for the treatment of uterine fibroids and endometriosis.[2] In addition to its actions as an SPRM, telapristone also has some antiglucocorticoid activity.[citation needed]

See also

References

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  2. ClinicalTrials.gov



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