U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry RACEMIC
Molecular Formula C17H24N2O3.ClH
Molecular Weight 340.845
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TILISOLOL HYDROCHLORIDE

SMILES

Cl.CN1C=C(OCC(O)CNC(C)(C)C)C2=C(C=CC=C2)C1=O

InChI

InChIKey=SGPGESCZOCHFCL-UHFFFAOYSA-N
InChI=1S/C17H24N2O3.ClH/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;1H

HIDE SMILES / InChI

Molecular Formula C17H24N2O3
Molecular Weight 304.3841
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

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)

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
159.0 nM [Ki]
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
Primary
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Effective plasma concentrations of antiarrhythmic drugs against sustained halothane-adrenaline arrhythmia in dogs.
1983 Jul-Aug
Biodistribution and pharmacokinetics of O-palmitoyl tilisolol, a lipophilic prodrug of tilisolol, after intravenous administration in rats.
2002 Aug
One-side-coated insert as a unique ophthalmic drug delivery system.
2003 Oct 30
Transport of timolol and tilisolol in rabbit corneal epithelium.
2006 Oct
Patents

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
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
Substance Class Chemical
Created
by admin
on Sat Dec 16 05:58:03 GMT 2023
Edited
by admin
on Sat Dec 16 05:58:03 GMT 2023
Record UNII
JW02T8UTIN
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TILISOLOL HYDROCHLORIDE
JAN   MI   WHO-DD  
Common Name English
TILISOLOL HYDROCHLORIDE [MI]
Common Name English
TILISOLOL HYDROCHLORIDE, (±)-
Common Name English
Tilisolol hydrochloride [WHO-DD]
Common Name English
TILISOLOL MONOHYDROCHLORIDE
Common Name English
N-696
Code English
1(2H)-ISOQUINOLINONE, 4-(3-((1,1-DIMETHYLETHYL)AMINO)-2-HYDROXYPROPOXY)-2-METHYL-, HYDROCHLORIDE (1:1)
Systematic Name English
TILISOLOL HYDROCHLORIDE [JAN]
Common Name English
(±)-TILISOLOL HYDROCHLORIDE
Common Name English
SELECAL
Brand Name English
Code System Code Type Description
MERCK INDEX
m10865
Created by admin on Sat Dec 16 05:58:03 GMT 2023 , Edited by admin on Sat Dec 16 05:58:03 GMT 2023
PRIMARY Merck Index
EPA CompTox
DTXSID3021350
Created by admin on Sat Dec 16 05:58:03 GMT 2023 , Edited by admin on Sat Dec 16 05:58:03 GMT 2023
PRIMARY
EVMPD
SUB04871MIG
Created by admin on Sat Dec 16 05:58:03 GMT 2023 , Edited by admin on Sat Dec 16 05:58:03 GMT 2023
PRIMARY
PUBCHEM
44155
Created by admin on Sat Dec 16 05:58:03 GMT 2023 , Edited by admin on Sat Dec 16 05:58:03 GMT 2023
PRIMARY
FDA UNII
JW02T8UTIN
Created by admin on Sat Dec 16 05:58:03 GMT 2023 , Edited by admin on Sat Dec 16 05:58:03 GMT 2023
PRIMARY
CAS
62774-96-3
Created by admin on Sat Dec 16 05:58:03 GMT 2023 , Edited by admin on Sat Dec 16 05:58:03 GMT 2023
PRIMARY
SMS_ID
100000084626
Created by admin on Sat Dec 16 05:58:03 GMT 2023 , Edited by admin on Sat Dec 16 05:58:03 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE
Related Record Type Details
ACTIVE MOIETY