Details
Stereochemistry | RACEMIC |
Molecular Formula | C10H15N2O2S.Na |
Molecular Weight | 250.293 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 2 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[Na+].CCC(C)C1(CC)C(=O)NC(=S)[N-]C1=O
InChI
InChIKey=SLZHLQUFNFXTHB-UHFFFAOYSA-M
InChI=1S/C10H16N2O2S.Na/c1-4-6(3)10(5-2)7(13)11-9(15)12-8(10)14;/h6H,4-5H2,1-3H3,(H2,11,12,13,14,15);/q;+1/p-1
Molecular Formula | C10H16N2O2S |
Molecular Weight | 228.311 |
Charge | 0 |
Count |
|
Stereochemistry | RACEMIC |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Optical Activity | ( + / - ) |
Molecular Formula | Na |
Molecular Weight | 22.9898 |
Charge | 1 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Thiobutabarbital is a barbiturate derivative invented in the 1950s. It has sedative, anticonvulsant and hypnotic effects, it is used in veterinary medicine for induction in surgical anaesthesia. Thiobutabarbital was formerly used as anesthetic Inactin. ‘Inactin’ (sodium thiobutabarbital) produces smooth induction of anaesthesia after intravenous administration and has a prolonged duration of action. It has variable analgesic activity.
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: GO:0008645 Sources: https://www.ncbi.nlm.nih.gov/pubmed/7819247 |
1.0 mM [IC50] | ||
Target ID: GO:0008645 Sources: https://www.ncbi.nlm.nih.gov/pubmed/7819247 |
1.0 mM [IC50] |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Primary | Inactin Approved UseUnknown |
PubMed
Title | Date | PubMed |
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Enhanced intestinal motility influences absorption in anaesthetized rat. | 2001 Jun |
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Renal interstitial fluid concentrations of angiotensins I and II in anesthetized rats. | 2002 Jan |
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Chemoprophylaxis of transfusion-transmitted agents in labile blood components. | 2002 Jul-Aug |
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Brevenal is a natural inhibitor of brevetoxin action in sodium channel receptor binding assays. | 2004 Aug |
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Glucose-induced time-dependent potentiation of insulin release, but not islet blood perfusion, in anesthetized rats. | 2008 |
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Antenatal Corticosteroids and Postnatal Fluid Restriction Produce Differential Effects on AQP3 Expression, Water Handling, and Barrier Function in Perinatal Rat Epidermis. | 2010 |
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Gastric emptying of enterally administered liquid meal in conscious rats and during sustained anaesthesia. | 2010 Feb |
Patents
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/19881310
Male Wistar rats (8 to 10 weeks old) were anesthetized with thiobutabarbital (120 mg/kg, intraperitoneally (i.p.)).
Route of Administration:
Intraperitoneal
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/7819247
Thiobutabarbital inhibits hexose transport in cultured 3T3-C2 cells with IC50 value of 1.0 mM.
Substance Class |
Chemical
Created
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admin
on
Edited
Fri Dec 15 15:09:56 GMT 2023
by
admin
on
Fri Dec 15 15:09:56 GMT 2023
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Record UNII |
VE5XWZ299Q
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Record Status |
Validated (UNII)
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Record Version |
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NCI_THESAURUS |
C67084
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