Drofenine

Last updated
Drofenine
Drofenine structure.svg
Identifiers
  • 2-(diethylamino)ethyl 2-cyclohexyl-2-phenylacetate
CAS Number
PubChem CID
ChemSpider
UNII
ChEBI
ChEMBL
CompTox Dashboard (EPA)
ECHA InfoCard 100.114.553 OOjs UI icon edit-ltr-progressive.svg
Chemical and physical data
Formula C20H31NO2
Molar mass 317.473 g·mol−1
3D model (JSmol)
  • CCN(CC)CCOC(=O)C(C1CCCCC1)C2=CC=CC=C2
  • InChI=1S/C20H31NO2/c1-3-21(4-2)15-16-23-20(22)19(17-11-7-5-8-12-17)18-13-9-6-10-14-18/h5,7-8,11-12,18-19H,3-4,6,9-10,13-16H2,1-2H3
  • Key:AGJBLWCLQCKRJP-UHFFFAOYSA-N

Drofenine is an antimuscarinic antispasmodic drug used for relaxing smooth muscle, thereby treating conditions, such as: dysmenorrhea, and pain in the gastrointestinal tract, biliary passages, and urogenital tract. Drofenine is assumed to work by increasing the levels of the protein TRPV3. [1] [2] [3]

References

  1. ↑ Kunysz EL, Michel AD, Whiting RL (March 1988). "Functional and direct binding studies using subtype selective muscarinic receptor antagonists". British Journal of Pharmacology. 93 (3): 491–500. doi:10.1111/j.1476-5381.1988.tb10303.x. PMC   1853838 . PMID   2897216.
  2. ↑ Bodur E, Cokuğraş AN, Tezcan EF (February 2001). "Inhibition effects of benactyzine and drofenine on human serum butyrylcholinesterase". Archives of Biochemistry and Biophysics. 386 (1): 25–9. doi:10.1006/abbi.2000.2188. PMID   11360997.
  3. ↑ Deering-Rice CE, Mitchell VK, Romero EG, Abdel Aziz MH, Ryskamp DA, Križaj D, et al. (October 2014). "Drofenine: A 2-APB Analogue with Greater Selectivity for Human TRPV3". Pharmacology Research & Perspectives. 2 (5): e00062. doi:10.1002/prp2.62. PMC   4115637 . PMID   25089200.



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