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Drofenine

From Wikipedia, the free encyclopedia
Chemical compound
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Pharmaceutical compound
Drofenine
Identifiers
  • 2-(diethylamino)ethyl 2-cyclohexyl-2-phenylacetate
CAS Number
PubChemCID
ChemSpider
UNII
ChEBI
ChEMBL
CompTox Dashboard(EPA)
ECHA InfoCard100.114.553Edit this at Wikidata
Chemical and physical data
FormulaC20H31NO2
Molar mass317.473 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 anantimuscarinicantispasmodic 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 proteinTRPV3.[1][2][3]

References

[edit]
  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.


mAChRsTooltip Muscarinic acetylcholine receptors
Agonists
Antagonists
Precursors
(andprodrugs)


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