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Details

Stereochemistry RACEMIC
Molecular Formula C15H21NO2
Molecular Weight 247.3327
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 7-(2-HYDROXY-3-ISOPROPYLAMINOPROPOXY)INDENE

SMILES

CC(C)NCC(O)COC1=C2CC=CC2=CC=C1

InChI

InChIKey=SAWHVYHGMYAXLH-UHFFFAOYSA-N
InChI=1S/C15H21NO2/c1-11(2)16-9-13(17)10-18-15-8-4-6-12-5-3-7-14(12)15/h3-6,8,11,13,16-17H,7,9-10H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C15H21NO2
Molecular Weight 247.3327
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

7-(2-HYDROXY-3-ISOPROPYLAMINOPROPOXY)INDENE HYDROCHLORIDE (1-(7-indenyloxy)3-isopropylaminopropane-2-ol hydrochloride,YB-2) has been reported to possess a potent beta-adrenergic receptor blocking activity with a mild intrinsic beta-sympathomimetic activity and a local anesthetic effect, and to be effective against ouabain-induced and epinephrine-induced arrhythmias.1-(7-indenyloxy)3-isopropylaminopropane-2-ol hydrochloride is a component of Indenolol hydrochloride, which is a mixture of 1-(7-indenyloxy)3-isopropylaminopropane-2-ol hydrochloride and 1-(4-indenyloxy)-3-isopr opylamino-2-propanol monohydrochloride. The antihypertensive effects of indenolol were evaluated in patients with WHO grades I and II essential hypertension (range 160/95 to 200/115 mm Hg) in a double-blind, placebo-controlled study after acute (12 patients) and 2-week treatment (seven patients). Indenolol (30 to 120 mg) reduced blood pressure in a dose-dependent fashion. Maximum reduction was 26 mm Hg for systolic and 17 mm Hg for diastolic pressure. Indenolol did not alter adrenergic reflexes (standing, cold application, and hand-grip) and did not induce any side effect. It possesses an antihypertensive activity associated with reduction of vascular resistance.

Approval Year

PubMed

PubMed

TitleDatePubMed
[Effects of 1-(7-indenyloxy)-3-isopropylaminopropan-2-ol hydrochloride (YB-2) on coronary circulation and and myocardial metabolism].
1972 Nov
-adrenergic blocking and cardiovascular properties of a new compound, 1-(7-indenyloxy)-3-isopropylaminopropan-2-ol-hydrochloride (YB-2).
1972 Nov
Pharmacological studies on 1-(7-indenyloxy)-3-isopropylaminopropan-2-Ol hydrochloride (YB-2), a new -adrenergic blocking agent.
1973 Mar
Cardiovascular beta-adrenergic receptor blocking activities of 1-(7-indenyloxy)-3-isopropyl-aminopropane-2-ol hydrochloride (YB-2) and its optical isomers.
1974 Apr
Electrophysiologically determined quinidine-like actions of a beta-adrenergic blocking agent, 1-(7-indenyloxy)-3-isopropylaminopropane-2-ol hydrochloride (YB-2).
1976 Jun
Unambiguous synthesis of 1-(7-indenyloxy)-3-isopropylamino-2-propanol hydrochloride and its 4-indenyloxy isomer, potent beta-adrenergic blocking agents.
1976 Mar
Patents

Patents

Sample Use Guides

Hypertension: 60 mg twice a day
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Fri Dec 15 18:30:29 GMT 2023
Edited
by admin
on Fri Dec 15 18:30:29 GMT 2023
Record UNII
OJH4VNY008
Record Status Validated (UNII)
Record Version
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Name Type Language
7-(2-HYDROXY-3-ISOPROPYLAMINOPROPOXY)INDENE
Systematic Name English
2-PROPANOL, 1-(INDEN-7-YLOXY)-3-(ISOPROPYLAMINO)-
Systematic Name English
2-PROPANOL, 1-(1H-INDEN-7-YLOXY)-3-((1-METHYLETHYL)AMINO)-
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID101021250
Created by admin on Fri Dec 15 18:30:29 GMT 2023 , Edited by admin on Fri Dec 15 18:30:29 GMT 2023
PRIMARY
FDA UNII
OJH4VNY008
Created by admin on Fri Dec 15 18:30:29 GMT 2023 , Edited by admin on Fri Dec 15 18:30:29 GMT 2023
PRIMARY
CAS
30190-86-4
Created by admin on Fri Dec 15 18:30:29 GMT 2023 , Edited by admin on Fri Dec 15 18:30:29 GMT 2023
PRIMARY
PUBCHEM
207530
Created by admin on Fri Dec 15 18:30:29 GMT 2023 , Edited by admin on Fri Dec 15 18:30:29 GMT 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT