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Remeglurant

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Remeglurant
Clinical data
Other namesMRZ-8456
ATC code
  • None
Identifiers
  • (6-Bromopyrazolo[1,5-a]pyrimidin-2-yl)[(1R)-1-methyl-3,4-dihydro-2(1H)-isoquinolinyl]methanone
CAS Number
PubChemCID
ChemSpider
UNII
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC17H15BrN4O
Molar mass371.238 g·mol−1
3D model (JSmol)
  • C[C@@H]1c2ccccc2CCN1C(=O)c3cc4ncc(cn4n3)Br
  • InChI=1S/C17H15BrN4O/c1-11-14-5-3-2-4-12(14)6-7-21(11)17(23)15-8-16-19-9-13(18)10-22(16)20-15/h2-5,8-11H,6-7H2,1H3/t11-/m1/s1
  • Key:TUYZYSNXXSTKQX-LLVKDONJSA-N

Remeglurant (INNTooltip International Nonproprietary Name; developmental code nameMRZ-8456) is adrug which acts as aselectiveantagonist of themGlu5 receptor.[1][2][3] It is under development by Merz Pharmaceuticals for the treatment ofdrug-induced dyskinesia but no development has been reported since at least 2016.[3]

See also

[edit]

References

[edit]
  1. ^World Health Organization (2013)."International Nonproprietary Names for Pharmaceutical Substances (INN): Proposed INN: List 109"(PDF).WHO Drug Information.27 (2).World Health Organization.
  2. ^US 7985753, Danysz W, Dekundy A, Hechenberger M, Henrich M, Jatzke C, Nagel J, Parsons CG, Weil T, Fotins J, Gutcaits A, Kalvinsh I, Zemribo R, Kauss V, "Substituted pyrazolo[1,5-A]pyrimidines as metabotropic glutamate receptor modulators.", issued 4 August 2006, assigned to Merz Pharmaceuticals GmbH 
  3. ^ab"Remeglurant".Adis Insight. Springer Nature Switzerland AG.
Group I
mGluR1Tooltip Metabotropic glutamate receptor 1
mGluR5Tooltip Metabotropic glutamate receptor 5
Group II
mGluR2Tooltip Metabotropic glutamate receptor 2
mGluR3Tooltip Metabotropic glutamate receptor 3
Group III
mGluR4Tooltip Metabotropic glutamate receptor 4
mGluR6Tooltip Metabotropic glutamate receptor 6
mGluR7Tooltip Metabotropic glutamate receptor 7
mGluR8Tooltip Metabotropic glutamate receptor 8


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