Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C12H20N2O3 |
| Molecular Weight | 240.2988 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCC1(C(C)CC(C)C)C(=O)NC(=O)NC1=O
InChI
InChIKey=KXHLANWWTKSOMW-UHFFFAOYSA-N
InChI=1S/C12H20N2O3/c1-5-12(8(4)6-7(2)3)9(15)13-11(17)14-10(12)16/h7-8H,5-6H2,1-4H3,(H2,13,14,15,16,17)
| Molecular Formula | C12H20N2O3 |
| Molecular Weight | 240.2988 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Facilitation of recurrent inhibition in rat hippocampus by barbiturate and related nonbarbiturate depressant drugs. | 1986-08 |
|
| Characterization of barbiturate-stimulated chloride efflux from rat brain synaptoneurosomes. | 1985-11 |
|
| Regulation of [35S]t-butylbicyclophosphorothionate binding sites in rat brain by GABA, pyrethroid and barbiturate. | 1985-09-24 |
|
| The effects of barbiturates on the metabolism of phosphatidic acid and phosphatidylinositol in rat brain synaptosomes. | 1979-01-15 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 23:00:45 GMT 2025
by
admin
on
Mon Mar 31 23:00:45 GMT 2025
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| Record UNII |
31E1HC8I46
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| Record Status |
Validated (UNII)
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| Record Version |
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DTXSID301031188
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31E1HC8I46
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31256
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18079
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2964-06-9
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admin on Mon Mar 31 23:00:45 GMT 2025 , Edited by admin on Mon Mar 31 23:00:45 GMT 2025
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| Related Record | Type | Details | ||
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ENANTIOMER -> RACEMATE |
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ENANTIOMER -> RACEMATE |
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| Related Record | Type | Details | ||
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PARENT -> IMPURITY |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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PARENT -> IMPURITY |
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
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PARENT -> IMPURITY |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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PARENT -> IMPURITY |
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
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