Details
Stereochemistry | RACEMIC |
Molecular Formula | C13H16N2O2S |
Molecular Weight | 264.343 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
C=CCC2(C1CCCC=C1)C(=O)NC(=S)NC2=O
InChI
InChIKey=PXLVRFQEBVNJOH-UHFFFAOYSA-N
InChI=1S/C13H16N2O2S/c1-2-8-13(9-6-4-3-5-7-9)10(16)14-12(18)15-11(13)17/h2,4,6,9H,1,3,5,7-8H2,(H2,14,15,16,17,18)
THIALBARBITAL is a barbiturate derivative with sedative effects. Barbiturates have hypnotic properties and are used as active moiety on central nervous system. Thialbarbital was synthesized in the 1960s. It was used primarily as a surgical anesthesia. Thialbarbital causes marked depression of the activity of the reticular formation and only slight depression of cortical activity. Thialbarbital is short acting and has less of a tendency to induce respiratory depression than other barbiturate derivatives such as pentobarbital.
Approval Year
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Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C67084
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467-36-7
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CHEMBL2104657
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100000082396
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14
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SUB10966MIG
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3595
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ENV72C33QD
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DTXSID90861960
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C77631
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3032306
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207-390-3
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m10714
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PRIMARY | Merck Index |
ACTIVE MOIETY
SALT/SOLVATE (PARENT)