Details
Stereochemistry | MIXED |
Molecular Formula | C18H29NO4 |
Molecular Weight | 323.4272 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 0 / 2 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)(C)NCC(O)COC1=C(OCC2CCCO2)C=CC=C1
InChI
InChIKey=AKLNLVOZXMQGSI-UHFFFAOYSA-N
InChI=1S/C18H29NO4/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
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 |
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Possible significance of the pharmacological differentiation of beta-blocking agents in hemodynamic effects in essential hypertension. | 1983 Mar |
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Effects of beta-adrenoceptor blocking agents of N-tertiary butyl derivatives on maximum upstroke velocity of action potential in guinea-pig papillary muscles. | 1983 Sep |
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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NCI_THESAURUS |
C29576
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3046
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WS1467RT9Z
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Bufetolol
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3412
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m1045
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C72612
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100000076885
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SUB13131MIG
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DTXSID9057763
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53684-49-4
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C100228
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CHEMBL347830
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2465
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ACTIVE MOIETY
SALT/SOLVATE (PARENT)