Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C16H20N2OS |
| Molecular Weight | 288.408 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 3 / 3 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CSC[C@H]1CN(C)[C@@H]2CC3=CNC4=C3C(=CC=C4)[C@H]2O1
InChI
InChIKey=GYUHVILBXXBZDS-DJSGYFEHSA-N
InChI=1S/C16H20N2OS/c1-18-8-11(9-20-2)19-16-12-4-3-5-13-15(12)10(7-17-13)6-14(16)18/h3-5,7,11,14,16-17H,6,8-9H2,1-2H3/t11-,14-,16-/m1/s1
| Molecular Formula | C16H20N2OS |
| Molecular Weight | 288.408 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 3 / 3 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Voxergolide is a 9-oxoergoline derivative with dopamine D2 receptor agonist properties. It is induced a significant improvement in working memory performance of Roman high (RHA) avoidance strains of rats, which has high frontal cortex dopamine and DOPAC levels, hippocampal and striatal 5-HT and noradrenalin levels. Voxergolide failed to counteract the memory deficits induced by triazolam. It doesn’t counteracted scopolamine caused anterograde amnesia and sedative effects.
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/1684155
Single dose - 10 mg
Route of Administration:
Oral
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:14:58 GMT 2025
by
admin
on
Mon Mar 31 18:14:58 GMT 2025
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| Record UNII |
PP012U645Q
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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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NCI_THESAURUS |
C221
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6416
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PP012U645Q
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SUB00089MIG
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3086301
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100000079347
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DTXSID90869027
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CHEMBL2104920
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C66657
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89651-00-3
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| Related Record | Type | Details | ||
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ACTIVE MOIETY |