ENX-105

Chemical compound From Wikipedia, the free encyclopedia

ENX-105 is an investigational new drug being developed by Engrail Therapeutics for the treatment of post-traumatic stress disorder (PTSD).[2][3][4][5] It is currently in the preclinical stage, trailing behind a closely related Engrail compound, ENX-104,[1] which is focused on depression and anhedonia.[3]

Other namesENX105; Deuterated nemonapride enantiomer[1]
CAS Number
FormulaC21H21ClD5N3O2
Quick facts Clinical data, Other names ...
ENX-105
Clinical data
Other namesENX105; Deuterated nemonapride enantiomer[1]
Identifiers
  • 5-chloro-2-methoxy-N-((2R,3R)-2-methyl-1-(phenylmethyl-d2)pyrrolidin-3-yl)-4-((methyl-d3)amino)benzamide
CAS Number
PubChem CID
Chemical and physical data
FormulaC21H21ClD5N3O2
Molar mass392.94 g·mol−1
3D model (JSmol)
  • C(N[C@H]1[C@@H](C)N(C(C2=CC=CC=C2)([2H])[2H])CC1)(=O)C3=C(OC)C=C(NC([2H])([2H])[2H])C(Cl)=C3
  • InChI=1S/C21H26ClN3O2/c1-14-18(9-10-25(14)13-15-7-5-4-6-8-15)24-21(26)16-11-17(22)19(23-2)12-20(16)27-3/h4-8,11-12,14,18,23H,9-10,13H2,1-3H3,(H,24,26)/t14-,18-/m1/s1/i2D3,13D2
  • Key:KRVOJOCLBAAKSJ-RUFGIDIBSA-N
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The drug is described as a dopamine D2 and D3 receptor antagonist and serotonin 5-HT1A and 5-HT2A receptor agonist.[2][1][4] Its antagonistic potencies (IC50Tooltip half-maximal inhibitory concentration) are 0.08 nM at the dopamine D2L receptor, 0.8 nM at the dopamine D2S receptor, and 3.8 nM at the dopamine D3 receptor, whereas its activational potencies (EC50Tooltip half-maximal effective concentration) are 5 nM at the serotonin 5-HT2A receptor and 16 nM at the serotonin 5-HT1A receptor.[2]

ENX-105 does not produce the head-twitch response, a behavioral proxy of psychedelic effects, in rodents, and hence is putatively non-hallucinogenic.[2][1] The drug has shown anxiolytic-, antipsychotic-, anti-anhedonic-, and pro-cognitive-like effects in rodents.[2] It has also been found to increase dopamine levels in the nucleus accumbens in rodents.[2]

As with ENX-104, ENX-105 is a deuterated enantiomer of nemonapride.[1]

See also

References

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