Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C17H26ClN3O3 |
| Molecular Weight | 355.86 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCN(CC)CCNC(=O)C1=C(OC(C)C(C)=O)C=C(N)C(Cl)=C1
InChI
InChIKey=ZYOJXUNLLOBURP-UHFFFAOYSA-N
InChI=1S/C17H26ClN3O3/c1-5-21(6-2)8-7-20-17(23)13-9-14(18)15(19)10-16(13)24-12(4)11(3)22/h9-10,12H,5-8,19H2,1-4H3,(H,20,23)
Batanopride, previously known as BMY-25801, a 5-hydroxytryptamine 3 receptor antagonist, was studied against emesis for cancer patients that were treated by chemotherapy procedure. Batanopride had the dose-limiting side effects including hypotension and long QT syndrome that is why any further experiments for its medical application were discontinued.
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| BMY-25801, an antiemetic agent free of D2-dopamine receptor antagonist properties. | 1988 Mar |
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| Dose-limiting hypotension with the 5-HT3-antagonist batanopride (BMY-25801). | 1991 Feb |
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| A randomized, double-blinded study comparing six doses of batanopride (BMY-25801) with methylprednisolone in patients receiving moderately emetogenic chemotherapy. | 1991 Oct |
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NCI_THESAURUS |
C267
Created by
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DTXSID20869373
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6420
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SUB06108MIG
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BATANOPRIDE
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C060190
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100000088431
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59692
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C1021
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1AT99K728N
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CHEMBL38594
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102670-46-2
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ACTIVE MOIETY
METABOLITE (PARENT)
METABOLITE (PARENT)
SALT/SOLVATE (PARENT)
