Details
| Stereochemistry | MIXED |
| Molecular Formula | C18H29NO4.ClH |
| Molecular Weight | 359.888 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 0 / 2 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.CC(C)(C)NCC(O)COC1=C(OCC2CCCO2)C=CC=C1
InChI
InChIKey=DTAWWMIEZBHDDH-UHFFFAOYSA-N
InChI=1S/C18H29NO4.ClH/c1-18(2,3)19-11-14(20)12-22-16-8-4-5-9-17(16)23-13-15-7-6-10-21-15;/h4-5,8-9,14-15,19-20H,6-7,10-13H2,1-3H3;1H
DescriptionSources: http://www.ncbi.nlm.nih.gov/pubmed/9502Curator's Comment: Description was created based on several sources, including https://www.drugs.com/international/adobiol.html and https://www.jstage.jst.go.jp/article/circj/80/3/80_CJ-66-0122/_pdf
Sources: http://www.ncbi.nlm.nih.gov/pubmed/9502
Curator's Comment: Description was created based on several sources, including https://www.drugs.com/international/adobiol.html and https://www.jstage.jst.go.jp/article/circj/80/3/80_CJ-66-0122/_pdf
Bufetolol is a β-adrenergic blocking agent. Bufetolol hydrochloride (a derivative of Bufetolol) is reported as an ingredient of Adobiol in Japan. It is used for the treatment of hypertension and hypertrophic cardiomyopathy.
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Effects of beta-adrenoceptor blocking agents of N-tertiary butyl derivatives on maximum upstroke velocity of action potential in guinea-pig papillary muscles. | 1983-09 |
|
| Possible significance of the pharmacological differentiation of beta-blocking agents in hemodynamic effects in essential hypertension. | 1983-03 |
Patents
Sample Use Guides
Daily dose approved in Japan for the treatment of hypertrophic cardiomyopathy - 15mg/day
Route of Administration:
Oral
In Vitro Use Guide
Sources: http://www.ncbi.nlm.nih.gov/pubmed/18384
Bufetolol (10(-4) M) additionally prolonged the time for 90% repolarization of the dog Purkinje fibres.
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ACTIVE MOIETY
SUBSTANCE RECORD