Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C17H18BrNO |
| Molecular Weight | 332.235 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CN1CCC2=CC(Br)=C(O)C=C2C(C1)C3=CC=CC=C3
InChI
InChIKey=XFTVOHWWEQGXLS-UHFFFAOYSA-N
InChI=1S/C17H18BrNO/c1-19-8-7-13-9-16(18)17(20)10-14(13)15(11-19)12-5-3-2-4-6-12/h2-6,9-10,15,20H,7-8,11H2,1H3
| Molecular Formula | C17H18BrNO |
| Molecular Weight | 332.235 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Nanomolar propofol stimulates glutamate transmission to dopamine neurons: a possible mechanism of abuse potential? | 2008-04 |
|
| Evidence for the sensitivity of operant timing behaviour to stimulation of D1 dopamine receptors. | 2007-12 |
|
| Effects of d-amphetamine and DOI (2,5-dimethoxy-4-iodoamphetamine) on timing behavior: interaction between D1 and 5-HT2A receptors. | 2006-12 |
|
| Effects of dopamine receptor antagonists on ongoing maternal behavior in rats. | 2001-03 |
|
| Mutual inhibitory effects between dopamine and carbachol on the excitatory synaptic transmission in the rat neostriatum. | 1996-10-01 |
|
| Cloning of the gene for a human dopamine D5 receptor with higher affinity for dopamine than D1. | 1991-04-18 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 22:01:28 GMT 2025
by
admin
on
Mon Mar 31 22:01:28 GMT 2025
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| Record UNII |
D203LR7XUS
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| Record Status |
Validated (UNII)
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| Record Version |
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D203LR7XUS
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99295-33-7
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1243
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DTXSID8043816
Created by
admin on Mon Mar 31 22:01:28 GMT 2025 , Edited by admin on Mon Mar 31 22:01:28 GMT 2025
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