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MIBE

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
MIBE
Identifiers
  • Ethyl 3-[5-(2-ethoxycarbonyl-1-methylvinyloxy)-1-methyl-1H-indol-3-yl]but-2-enoate
CAS Number
Chemical and physical data
FormulaC21H25NO5
Molar mass371.433 g·mol−1
3D model (JSmol)
  • C(OC(/C=C(/OC1=CC=C2C(C(/C(/C)=C/C(OCC)=O)=CN2C)=C1)\C)=O)C
  • InChI=1S/C21H25NO5/c1-6-25-20(23)10-14(3)18-13-22(5)19-9-8-16(12-17(18)19)27-15(4)11-21(24)26-7-2/h8-13H,6-7H2,1-5H3/b14-10+,15-11+
  • Key:VFEAHZYKQWLUSD-WFYKWJGLSA-N

MIBE is asynthetic,nonsteroidalantiestrogen that acts as a dualantagonist of theERα and theGPER.[1][2] It was found to preventestradiol-inducedproliferation ofMCF-7breast cancercells, an action that was mediated via inhibition of both receptors.[1][2] The drug wassynthesized in 2012.[1] It has been suggested that drugs like MIBE might be superior agents in the treatment of breast cancer compared to current antiestrogens liketamoxifen andfulvestrant, which are antagonistic at the ERα but were found in 2005 to be GPER agonists.[1][2]

References

[edit]
  1. ^abcdLappano R, Santolla MF, Pupo M, Sinicropi MS, Caruso A, Rosano C, Maggiolini M (2012)."MIBE acts as antagonist ligand of both estrogen receptor α and GPER in breast cancer cells".Breast Cancer Res.14 (1): R12.doi:10.1186/bcr3096.PMC 3496129.PMID 22251451.
  2. ^abcRosano C, Lappano R, Santolla MF, Ponassi M, Donadini A, Maggiolini M (2012). "Recent advances in the rationale design of GPER ligands".Curr. Med. Chem.19 (36):6199–206.doi:10.2174/092986712804485755.PMID 23116143.


ERTooltip Estrogen receptor
Agonists
Mixed
(SERMsTooltip Selective estrogen receptor modulators)
Antagonists
GPERTooltip G protein-coupled estrogen receptor
Agonists
Antagonists
Unknown


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