Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C29H37NO4 |
| Molecular Weight | 463.6084 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCCN(CCCC)CCCOC1=C(C)C=C(C=C1C)C(=O)C2=CC(=O)C3=C(O2)C=CC=C3
InChI
InChIKey=DYGLNTZLBQBOPT-UHFFFAOYSA-N
InChI=1S/C29H37NO4/c1-5-7-14-30(15-8-6-2)16-11-17-33-29-21(3)18-23(19-22(29)4)28(32)27-20-25(31)24-12-9-10-13-26(24)34-27/h9-10,12-13,18-20H,5-8,11,14-17H2,1-4H3
| Molecular Formula | C29H37NO4 |
| Molecular Weight | 463.6084 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Bucromarone is a coronary vasodilator. It is a compound exhibiting a structural relationship with amiodarone, a widely used antiangorous and antiarrythmic drug. Bucromarone appeared promising in the treatment of cardiac arrhythmia. Bucromarone is rapidly concentrated in the tissues after intravenous administration, and mainly eliminated in the bile. Bucromarone is well absorbed through the gastrointestinal tract after per os administration, but after liver uptake through the portal vein and extensive metabolism, unchanged drug and its metabolites are mainly excreted in the bile. As compared with amiodarone, bucromarone seems more rapidly distributed in the tissues and eliminated from the organs and blood.
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/1673429
Dose: 4.4 mmol/kg body weight
Route of Administration:
Other
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:25:33 GMT 2025
by
admin
on
Mon Mar 31 18:25:33 GMT 2025
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| Record UNII |
JI688O846T
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| Record Status |
Validated (UNII)
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NCI_THESAURUS |
C47793
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JI688O846T
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DTXSID50868475
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132852
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CHEMBL2107592
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100000088435
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C72577
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5134
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X-84
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C059720
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SUB05953MIG
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| Related Record | Type | Details | ||
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ACTIVE MOIETY |