Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C21H29N |
| Molecular Weight | 295.4617 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)N(CCC(C1=CC=CC=C1)C2=CC=CC=C2)C(C)C
InChI
InChIKey=YBJKOPHEJOMRMN-UHFFFAOYSA-N
InChI=1S/C21H29N/c1-17(2)22(18(3)4)16-15-21(19-11-7-5-8-12-19)20-13-9-6-10-14-20/h5-14,17-18,21H,15-16H2,1-4H3
| Molecular Formula | C21H29N |
| Molecular Weight | 295.4617 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Diisopromine, a spasmolytic and a choleretic, in combination with sorbitol was marketed under the brand name Agofell. Agofell is prescribed for the biliary stasis and biliary insufficiency, hypotonia of the gall bladder, spasm of the biliary duct and of the sphincter of Oddi, cholecystitis, cholelithiasis, post cholecystotomy syndrome.
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: http://home.intekom.com/pharm/janssen/agofell.html
One 5 mL measure of syrup (Diisopromine hydrochloride and sorbitol) to be taken 15 minutes before the principal meals.
Route of Administration:
Oral
| Substance Class |
Chemical
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NCI_THESAURUS |
C29696
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WHO-VATC |
QA03AX02
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A03AX02
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C80978
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SUB07143MIG
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m694
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100000082608
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227-752-4
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236206
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Diisopromine
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5966-41-6
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| Related Record | Type | Details | ||
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SALT/SOLVATE -> PARENT |
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ACTIVE MOIETY |