Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C19H28ClN3O4 |
| Molecular Weight | 397.896 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCCOC(=O)CN1CCC(CC1)NC(=O)C2=CC(Cl)=C(N)C=C2OC
InChI
InChIKey=AQMLPMSSCWTNNN-UHFFFAOYSA-N
InChI=1S/C19H28ClN3O4/c1-3-4-9-27-18(24)12-23-7-5-13(6-8-23)22-19(25)14-10-15(20)16(21)11-17(14)26-2/h10-11,13H,3-9,12,21H2,1-2H3,(H,22,25)
| Molecular Formula | C19H28ClN3O4 |
| Molecular Weight | 397.896 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Positive modulation of alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid (AMPA) receptors in prefrontal cortical pyramidal neurons by a novel allosteric potentiator. | 2001 Jul |
|
| Survival signaling and selective neuroprotection through glutamatergic transmission. | 2002 Mar |
|
| Preliminary experience with an ampakine (CX516) as a single agent for the treatment of schizophrenia: a case series. | 2002 Oct 1 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 11:14:58 GMT 2023
by
admin
on
Sat Dec 16 11:14:58 GMT 2023
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| Record UNII |
XVR3JT7PGA
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| Record Status |
Validated (UNII)
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| Record Version |
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287399-47-7
Created by
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XVR3JT7PGA
Created by
admin on Sat Dec 16 11:14:58 GMT 2023 , Edited by admin on Sat Dec 16 11:14:58 GMT 2023
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9822171
Created by
admin on Sat Dec 16 11:14:58 GMT 2023 , Edited by admin on Sat Dec 16 11:14:58 GMT 2023
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ACTIVE MOIETY |
