Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C28H26F4N2OS |
| Molecular Weight | 514.577 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
FC1=CC=C(C=C1)C(=O)C2CCN(CCCN3C4=CC=CC=C4SC5=CC=C(C=C35)C(F)(F)F)CC2
InChI
InChIKey=XMUZRUCADGTCPX-UHFFFAOYSA-N
InChI=1S/C28H26F4N2OS/c29-22-9-6-19(7-10-22)27(35)20-12-16-33(17-13-20)14-3-15-34-23-4-1-2-5-25(23)36-26-11-8-21(18-24(26)34)28(30,31)32/h1-2,4-11,18,20H,3,12-17H2
| Molecular Formula | C28H26F4N2OS |
| Molecular Weight | 514.577 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Duoperone is a neuroleptic agent. Duoperone blocked d-amphetamine lethality in mice under aggregated conditions when the pretreatment interval was between one hour and seven days. Conditioned avoidance responding in mice and cats was suppressed by duoperone in doses that did not impair escape behavior. Duoperone produced catalepsy in rats. The onset of this effect was delayed and the duration was prolonged when compared with that of chlorpromazine. It was a potent antiemetic agent in dogs, with a delayed onset and prolonged duration of action.
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Wed Apr 02 09:43:11 GMT 2025
by
admin
on
Wed Apr 02 09:43:11 GMT 2025
|
| Record UNII |
E84FJ4KW3B
|
| Record Status |
Validated (UNII)
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| Record Version |
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-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
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Preferred Name | English | ||
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Official Name | English | ||
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Common Name | English | ||
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Common Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
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NCI_THESAURUS |
C740
Created by
admin on Wed Apr 02 09:43:11 GMT 2025 , Edited by admin on Wed Apr 02 09:43:11 GMT 2025
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NCI_THESAURUS |
C29710
Created by
admin on Wed Apr 02 09:43:11 GMT 2025 , Edited by admin on Wed Apr 02 09:43:11 GMT 2025
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| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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CHEMBL2110736
Created by
admin on Wed Apr 02 09:43:11 GMT 2025 , Edited by admin on Wed Apr 02 09:43:11 GMT 2025
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PRIMARY | |||
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C054030
Created by
admin on Wed Apr 02 09:43:11 GMT 2025 , Edited by admin on Wed Apr 02 09:43:11 GMT 2025
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PRIMARY | |||
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E84FJ4KW3B
Created by
admin on Wed Apr 02 09:43:11 GMT 2025 , Edited by admin on Wed Apr 02 09:43:11 GMT 2025
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PRIMARY | |||
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100000080498
Created by
admin on Wed Apr 02 09:43:11 GMT 2025 , Edited by admin on Wed Apr 02 09:43:11 GMT 2025
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PRIMARY | |||
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C65499
Created by
admin on Wed Apr 02 09:43:11 GMT 2025 , Edited by admin on Wed Apr 02 09:43:11 GMT 2025
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PRIMARY | |||
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62030-88-0
Created by
admin on Wed Apr 02 09:43:11 GMT 2025 , Edited by admin on Wed Apr 02 09:43:11 GMT 2025
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PRIMARY | |||
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43876
Created by
admin on Wed Apr 02 09:43:11 GMT 2025 , Edited by admin on Wed Apr 02 09:43:11 GMT 2025
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PRIMARY | |||
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DTXSID20866903
Created by
admin on Wed Apr 02 09:43:11 GMT 2025 , Edited by admin on Wed Apr 02 09:43:11 GMT 2025
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PRIMARY | |||
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SUB06428MIG
Created by
admin on Wed Apr 02 09:43:11 GMT 2025 , Edited by admin on Wed Apr 02 09:43:11 GMT 2025
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PRIMARY | |||
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5828
Created by
admin on Wed Apr 02 09:43:11 GMT 2025 , Edited by admin on Wed Apr 02 09:43:11 GMT 2025
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PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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SALT/SOLVATE -> PARENT |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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ACTIVE MOIETY |