Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C12H19N2O2S2.Na |
| Molecular Weight | 310.411 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 2 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
[Na+].CCCC(C)C1(CCSC)C(=O)NC(=S)[N-]C1=O
InChI
InChIKey=IPFUISOJBWATGQ-UHFFFAOYSA-M
InChI=1S/C12H20N2O2S2.Na/c1-4-5-8(2)12(6-7-18-3)9(15)13-11(17)14-10(12)16;/h8H,4-7H2,1-3H3,(H2,13,14,15,16,17);/q;+1/p-1
CNS Activity
Approval Year
Cmax
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
35 mg/L EXPERIMENT https://www.karger.com/Article/PDF/134815 |
50 mg/kg bw single, intravenous dose: 50 mg/kg bw route of administration: Intravenous experiment type: SINGLE co-administered: |
METHITURAL plasma | Homo sapiens population: UNKNOWN age: UNKNOWN sex: UNKNOWN food status: UNKNOWN |
PubMed
| Title | Date | PubMed |
|---|---|---|
| Neraval, Evipal, Pentothal, Surital: A Clinical Evaluation. | 1958-04 |
|
| Neraval (methitural sodium) (sch. 3132). | 1957-01 |
|
| Methitural sodium (neraval sodium): a new ultrashort acting intravenous anesthetic. | 1956-09-01 |
|
| Methitural, a new intravenous anesthetic: comparison with thiopental in the cat, dog and monkey. | 1956-03 |
Patents
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m7320
Created by
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23674496
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054NQ722GD
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DTXSID70993758
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211-985-3
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730-68-7
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SUBSTANCE RECORD