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Details

Stereochemistry ACHIRAL
Molecular Formula C9H17NO
Molecular Weight 155.2374
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of VALDETAMIDE

SMILES

CCC(CC)(CC=C)C(N)=O

InChI

InChIKey=LOMDVEFCNVDZMZ-UHFFFAOYSA-N
InChI=1S/C9H17NO/c1-4-7-9(5-2,6-3)8(10)11/h4H,1,5-7H2,2-3H3,(H2,10,11)

HIDE SMILES / InChI
Valdetamide (Novonal), a sedative/hypnotic dispensed without medical prescription in West Germany. It is quickly absorbed after oral intake, with a blood half-life of 6-11 hours, most of it being excreted by the kidneys after metabolic degradation. Analysis of 23 cases of Novonal intoxication revealed that cardiac arrhythmias, hypotension and respiratory depression may occur with 6 g Novonal (contained in a pocket of 20 tablets) and must thus be rated as potentially lethal.

Approval Year

PubMed

PubMed

TitleDatePubMed
Patents

Sample Use Guides

In Vivo Use Guide
The application of 0.15 and 0.3% of diethylallylacetamide (Valdetamide, DA) in the drinking water to rats during 10 days increased the relative liver weight, the yield of hepatic microsomes, and cytochromes P-450 and b5. Single s.c. doses of 400 mg DA per kg reduced cytochrome P-450 concentrations in the hepatic endoplasmic reticulum of rats.
Route of Administration: Other
In Vitro Use Guide
The aerobic incubation of 0.1 mM Valdetamide with rabbit hepatic microsomes in the presence of NADPH produced 50% destruction of cytochrome P-450 within 1 h.
Name Type Language
VALDETAMIDE
INN   MI   WHO-DD  
INN  
Official Name English
Valdetamide [WHO-DD]
Common Name English
valdetamide [INN]
Common Name English
VALDETAMIDE [MI]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C29756
Created by admin on Fri Dec 15 15:57:36 GMT 2023 , Edited by admin on Fri Dec 15 15:57:36 GMT 2023
Code System Code Type Description
INN
5542
Created by admin on Fri Dec 15 15:57:36 GMT 2023 , Edited by admin on Fri Dec 15 15:57:36 GMT 2023
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FDA UNII
1X50HHA8FY
Created by admin on Fri Dec 15 15:57:36 GMT 2023 , Edited by admin on Fri Dec 15 15:57:36 GMT 2023
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SMS_ID
100000079121
Created by admin on Fri Dec 15 15:57:36 GMT 2023 , Edited by admin on Fri Dec 15 15:57:36 GMT 2023
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EPA CompTox
DTXSID90199210
Created by admin on Fri Dec 15 15:57:36 GMT 2023 , Edited by admin on Fri Dec 15 15:57:36 GMT 2023
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ChEMBL
CHEMBL2107706
Created by admin on Fri Dec 15 15:57:36 GMT 2023 , Edited by admin on Fri Dec 15 15:57:36 GMT 2023
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DRUG CENTRAL
3640
Created by admin on Fri Dec 15 15:57:36 GMT 2023 , Edited by admin on Fri Dec 15 15:57:36 GMT 2023
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CAS
512-48-1
Created by admin on Fri Dec 15 15:57:36 GMT 2023 , Edited by admin on Fri Dec 15 15:57:36 GMT 2023
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PUBCHEM
68845
Created by admin on Fri Dec 15 15:57:36 GMT 2023 , Edited by admin on Fri Dec 15 15:57:36 GMT 2023
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NCI_THESAURUS
C74376
Created by admin on Fri Dec 15 15:57:36 GMT 2023 , Edited by admin on Fri Dec 15 15:57:36 GMT 2023
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ECHA (EC/EINECS)
208-143-2
Created by admin on Fri Dec 15 15:57:36 GMT 2023 , Edited by admin on Fri Dec 15 15:57:36 GMT 2023
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MERCK INDEX
m11357
Created by admin on Fri Dec 15 15:57:36 GMT 2023 , Edited by admin on Fri Dec 15 15:57:36 GMT 2023
PRIMARY Merck Index
EVMPD
SUB00005MIG
Created by admin on Fri Dec 15 15:57:36 GMT 2023 , Edited by admin on Fri Dec 15 15:57:36 GMT 2023
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