Details
Stereochemistry | RACEMIC |
Molecular Formula | C17H26ClN3O3.ClH |
Molecular Weight | 392.321 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.CCN(CC)CCNC(=O)C1=C(OC(C)C(C)=O)C=C(N)C(Cl)=C1
InChI
InChIKey=CUTCEGXKJDBAFQ-UHFFFAOYSA-N
InChI=1S/C17H26ClN3O3.ClH/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);1H
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.
Originator
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/1742224
six patient groups each received a single intravenous dose of batanopride ranging from 0.2 to 6.0 mg/kg
Route of Administration:
Intravenous
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NCI_THESAURUS |
C66885
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102670-59-7
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59691
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C72717
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00L331RFEC
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C060190
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AA-77
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DTXSID30907977
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CHEMBL38594
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ACTIVE MOIETY
SUBSTANCE RECORD