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 |
Name | Type | Language | ||
---|---|---|---|---|
|
Common Name | English | ||
|
Common Name | English | ||
|
Brand Name | English | ||
|
Code | English | ||
|
Brand Name | English | ||
|
Common Name | English | ||
|
Brand Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Code | English |
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
m7320
Created by
admin on Sat Dec 16 07:56:18 GMT 2023 , Edited by admin on Sat Dec 16 07:56:18 GMT 2023
|
PRIMARY | Merck Index | ||
|
23674496
Created by
admin on Sat Dec 16 07:56:18 GMT 2023 , Edited by admin on Sat Dec 16 07:56:18 GMT 2023
|
PRIMARY | |||
|
054NQ722GD
Created by
admin on Sat Dec 16 07:56:18 GMT 2023 , Edited by admin on Sat Dec 16 07:56:18 GMT 2023
|
PRIMARY | |||
|
DTXSID70993758
Created by
admin on Sat Dec 16 07:56:18 GMT 2023 , Edited by admin on Sat Dec 16 07:56:18 GMT 2023
|
PRIMARY | |||
|
211-985-3
Created by
admin on Sat Dec 16 07:56:18 GMT 2023 , Edited by admin on Sat Dec 16 07:56:18 GMT 2023
|
PRIMARY | |||
|
730-68-7
Created by
admin on Sat Dec 16 07:56:18 GMT 2023 , Edited by admin on Sat Dec 16 07:56:18 GMT 2023
|
PRIMARY |
SUBSTANCE RECORD