Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C24H28N2O2.ClH |
| Molecular Weight | 412.952 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.CC1=CC=C(CN2CCC(CC2)C3(CCC(=O)NC3=O)C4=CC=CC=C4)C=C1
InChI
InChIKey=OQKFLYMKNMISTR-UHFFFAOYSA-N
InChI=1S/C24H28N2O2.ClH/c1-18-7-9-19(10-8-18)17-26-15-12-21(13-16-26)24(20-5-3-2-4-6-20)14-11-22(27)25-23(24)28;/h2-10,21H,11-17H2,1H3,(H,25,27,28);1H
CNS Activity
Sources: https://www.ncbi.nlm.nih.gov/pubmed/6055523
Curator's Comment: Meletimide exerts central anticholinergic properties in rats.
Approval Year
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17108-99-5
Created by
admin on Mon Mar 31 23:07:22 GMT 2025 , Edited by admin on Mon Mar 31 23:07:22 GMT 2025
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KSR8X3XZW3
Created by
admin on Mon Mar 31 23:07:22 GMT 2025 , Edited by admin on Mon Mar 31 23:07:22 GMT 2025
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PRIMARY | |||
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129718719
Created by
admin on Mon Mar 31 23:07:22 GMT 2025 , Edited by admin on Mon Mar 31 23:07:22 GMT 2025
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PRIMARY |
ACTIVE MOIETY
SUBSTANCE RECORD