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Decoglurant

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Decoglurant
Clinical data
ATC code
  • none
Legal status
Legal status
  • Development terminated
Identifiers
  • 5-({7-(Trifluoromethyl)-5-[4-(trifluoromethyl)phenyl]pyrazolo[1,5-a]pyrimidin-3-yl}ethynyl)-2-pyridinamine
CAS Number
PubChemCID
ChemSpider
UNII
KEGG
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC21H11F6N5
Molar mass447.344 g·mol−1
3D model (JSmol)
  • C1=CC(=CC=C1C2=NC3=C(C=NN3C(=C2)C(F)(F)F)C#CC4=CN=C(C=C4)N)C(F)(F)F
  • InChI=1S/C21H11F6N5/c22-20(23,24)15-6-4-13(5-7-15)16-9-17(21(25,26)27)32-19(31-16)14(11-30-32)3-1-12-2-8-18(28)29-10-12/h2,4-11H,(H2,28,29)
  • Key:DMJHZVARRXJSEG-UHFFFAOYSA-N

Decoglurant (INN) (code nameRG1578,RO4995819) is anegative allosteric modulator of themGlu2 andmGlu3 receptors which was under development byRoche for theadjunctive treatment ofmajor depressive disorder.[1][2] Decoglurant progressed as far asphase IIclinical trials[1][2] but was ultimately discontinued from further development due to disappointing efficacy results.[3][4]

See also

[edit]

References

[edit]
  1. ^ab"Roche – Pipeline". 2014. Archived fromthe original on 2022-10-23. Retrieved2014-08-01.
  2. ^ab"Roche Group Development Pipeline"(PDF). 2014. Archived fromthe original(PDF) on 2014-08-08. Retrieved2014-08-01.
  3. ^"Roche – Pipeline"(PDF). 2015. Archived fromthe original(PDF) on 2015-05-01. Retrieved2015-05-14.
  4. ^Lawrence J (March 2015)."The Secret Life of ketamine".The Pharmaceutical Journal.294 (7854/5).

External links

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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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