Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C14H16N2O4 |
| Molecular Weight | 276.2878 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 5 / 5 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
O=C1[C@H]2[C@H]3CC[C@H](C3)[C@H]2C(=O)N1[C@@H]4CCC(=O)NC4=O
InChI
InChIKey=URPJPYAYMWPUPR-BEBVASNESA-N
InChI=1S/C14H16N2O4/c17-9-4-3-8(12(18)15-9)16-13(19)10-6-1-2-7(5-6)11(10)14(16)20/h6-8,10-11H,1-5H2,(H,15,17,18)/t6-,7+,8-,10-,11+/m1/s1
| Molecular Formula | C14H16N2O4 |
| Molecular Weight | 276.2878 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 5 / 5 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Taglutimide is a norbornane derivative patented by Kwizda, F. Joh., Chemische Fabrik as the sedative-hypnotic compound. In preclinical studies, Taglutimide did not produce any toxic effects when administered orally to mice even at a very high dosage. Central-nervous depression was demonstrated by a reduction in spontaneous motor activity, potentiation of the central-depressant effect of pentobarbital, antagonism of the central-stimulant effect of amphetamine after oral administration and by narcotic activity after i.v. administration of the drug. Furthermore, oral administration of Taglutimide potentiated the analgesic action of morphine without being effective on its own.
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/971049
200 mg
Route of Administration:
Oral
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 17:55:13 GMT 2025
by
admin
on
Mon Mar 31 17:55:13 GMT 2025
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| Record UNII |
X94T930W1C
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| Record Status |
Validated (UNII)
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| Record Version |
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Official Name | English | ||
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Preferred Name | English |
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NCI_THESAURUS |
C29756
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4486
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CHEMBL2104485
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C006161
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SUB10798MIG
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X94T930W1C
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100000083014
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C152491
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14166-26-8
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76958691
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DTXSID301043080
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PRIMARY |
| Related Record | Type | Details | ||
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ACTIVE MOIETY |