DIMP (antiandrogen)

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Short description: Chemical compound
DIMP
DIMP (antiandrogen).svg
Clinical data
Other namesRo 7-8117; N-(3,5-Dimethyl-4-isoxazolylmethyl)phthalimide
Drug classNonsteroidal antiandrogen
Identifiers
CAS Number
PubChem CID
ChemSpider
UNII
ChEMBL
Chemical and physical data
FormulaC14H12N2O3
Molar mass256.261 g·mol−1
3D model (JSmol)

DIMP (developmental code name Ro 7-8117), or N-(3,5-dimethyl-4-isoxazolylmethyl)phthalimide, is a nonsteroidal antiandrogen (NSAA) structurally related to thalidomide (which also binds to and antagonizes the androgen receptor (AR))[1][2][3] that was first described in 1973 and was never marketed.[4] Along with flutamide, it was one of the earliest NSAAs to be discovered,[5] and for this reason, has been described as a "classical" NSAA.[1][2][3] The drug is a selective, competitive, silent antagonist of the AR,[4][6] although it is described as an "only relatively weak competitor".[7][8] Its relative binding affinity for the androgen receptor is about 2.6% of that of metribolone.[9] DIMP possesses no androgenic, estrogenic, progestogenic, or antigonadotropic activity,[4] but it does reverse the antigonadotropic effects of testosterone, indicating that, like other pure AR antagonists, it is progonadotropic.[4]

DIMP is the lead antiandrogen of the phthalimide group of nonsteroidal AR ligands, and a variety of AR ligands with higher affinity for the AR have been derived from DIMP and thalidomide.[10][11]

See also

References

  1. 1.0 1.1 "Thalidomide as a multitarget drug and its application as a template for drug design". Drugs of the Future 29 (4): 383. 2004. doi:10.1358/dof.2004.029.04.792298. ISSN 0377-8282. 
  2. 2.0 2.1 "Developments in nonsteroidal antiandrogens targeting the androgen receptor". ChemMedChem 5 (10): 1651–1661. October 2010. doi:10.1002/cmdc.201000259. PMID 20853390. 
  3. 3.0 3.1 "Structural development of synthetic retinoids and thalidomide-related molecules". Cancer Chemotherapy and Pharmacology 52 (Suppl 1): S16–S23. July 2003. doi:10.1007/s00280-003-0590-3. PMID 12819930. 
  4. 4.0 4.1 4.2 4.3 "Endocrine profile of a nonsteroidal antiandrogen N-(3,5-dimethyl-4-isoxazolylmethyl)phthalimide (DIMP)". Acta Endocrinologica 72 (3): 604–614. March 1973. doi:10.1530/acta.0.0720604. PMID 4739363. 
  5. Cellular Mechanisms Modulating Gonadal Action. University Park Press. 1 January 1976. p. 239. ISBN 978-0-8391-0776-7. https://books.google.com/books?id=2eNqAAAAMAAJ. 
  6. "The male genital tract and the nipples of male and female offspring of rats given the non-steroidal antiandrogens DIMP and Sch 13521, during pregnancy". Archives d'Anatomie Microscopique et de Morphologie Experimentale 64 (1): 27–44. 1975. PMID 1217898. 
  7. "Androgen binding in rat uterus cytosol. Study of the specificity". Journal of Steroid Biochemistry 7 (5): 335–343. May 1976. doi:10.1016/0022-4731(76)90092-3. PMID 180344. 
  8. "Chemical control of androgen action.". Annual Reports in Medicinal Chemistry. 21. Academic Press. January 1986. pp. 179-188 (182). ISBN 978-0-08-058365-5. https://books.google.com/books?id=qsFCGskRHZQC&pg=PA182. 
  9. "Receptor binding and biological activity of steroidal and nonsteroidal antiandrogens". Journal of Steroid Biochemistry 15: 355–359. December 1981. doi:10.1016/0022-4731(81)90297-1. PMID 7339263. 
  10. "Chemistry and structural biology of androgen receptor". Chemical Reviews 105 (9): 3352–3370. September 2005. doi:10.1021/cr020456u. PMID 16159155. 
  11. "Advancements in Non-steroidal Antiandrogens as Potential Therapeutic Agents for the Treatment of Prostate Cancer". Mini Reviews in Medicinal Chemistry 16 (7): 531–546. 2016. doi:10.2174/1389557516666160118112448. PMID 26776222. 




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