Details
Stereochemistry | RACEMIC |
Molecular Formula | C17H24N2O3 |
Molecular Weight | 304.3841 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CN1C=C(OCC(O)CNC(C)(C)C)C2=C(C=CC=C2)C1=O
InChI
InChIKey=TWVUMMQUXMYOOH-UHFFFAOYSA-N
InChI=1S/C17H24N2O3/c1-17(2,3)18-9-12(20)11-22-15-10-19(4)16(21)14-8-6-5-7-13(14)15/h5-8,10,12,18,20H,9,11H2,1-4H3
Tilisolol (, 4-[3-(tert-butylamino)- 2-hydroxyproxy]-N-methylisoeabostyril hydrochloride/N-696 ) is a non-selective beta-adrenergic blocking agent, and has a long-lasting and stable action in the clinical treatment of hypertension and angina pectoris. This antihypertensive effect of tilisolol might be largely attributable to its potent beta-adrenergic antagonistic effects. The measurement of the I-V relationship with or without tilisolol excluded the activation of ATP-sensitive K+ current (at least in cardiac muscle) under physiological conditions. However, several investigators suggested that tilisolol has a direct action on smooth muscle cells through ATP-sensitive K+ channels. The possibility that tilisolol has additional effects on the membrane ionic channels of cardiac myocytes under ischemic conditions remains to be tested. It was synthesized by Nisshin Hour Milling Co., Ltd. (Tokyo, Japan)
Originator
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
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Target ID: CHEMBL2094118 Sources: http://www.ncbi.nlm.nih.gov/pubmed/6205196 |
159.0 nM [Ki] |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
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Primary | Unknown Approved UseUnknown |
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Primary | Unknown Approved UseUnknown |
Sample Use Guides
for hypertensive humans: 20 mg once a day
on patients with angina pectoris: 10 to 30 mg/d for 2 to 6 weeks
Route of Administration:
Oral
In Vitro Use Guide
Sources: http://www.ncbi.nlm.nih.gov/pubmed/9213200
10 microM tilisolol did not affect the L-type Ca2+ current (ICa), the inwardly rectifying K+ current (IK1), or the delayed rectifying K+ current (IK). under the nonselective beta-adrenergic stimulation with 1 microM isoproterenol, 1 microM tilisolol almost completely reversed the agonist-induced increase of IK
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NCI_THESAURUS |
C29576
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CHEMBL1742457
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6063
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QUF41MF56G
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2665
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DTXSID0043846
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100000082697
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C036593
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TILISOLOL
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SUB11053MIG
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85136-71-6
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C76560
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m10865
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PRIMARY | Merck Index |
ACTIVE MOIETY
SALT/SOLVATE (PARENT)