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Details

Stereochemistry RACEMIC
Molecular Formula C15H21NO2.ClH
Molecular Weight 283.794
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

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

SMILES

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

InChI

InChIKey=MVDJMRCMFUAEQQ-UHFFFAOYSA-N
InChI=1S/C15H21NO2.ClH/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;1H

HIDE SMILES / InChI
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
Antiarrhythmic activity of 1-(7-indenyloxy)-3-isopropylaminopropane-2-ol hydrochloride (YB-2) and its optical isomers.
1974 Aug
[Effects of beta receptor blocking agent, 1-(7-indenyloxy)-3-isopropylaminopropane-2-ol hydrochloride (YB-2) on the circulatory system during intubation for general anesthesia].
1975 Aug
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
Name Type Language
7-(2-HYDROXY-3-ISOPROPYLAMINOPROPOXY)INDENE HYDROCHLORIDE
Systematic Name English
DL-1-(7-INDENYLOXY)-3-ISOPROPYLAMINOPROPAN-2-OL HYDROCHLORIDE
Common Name English
2-PROPANOL, 1-(1H-INDEN-7-YLOXY)-3-((1-METHYLETHYL)AMINO)-, HYDROCHLORIDE
Systematic Name English
1-(7-INDENYLOXY)-3-ISOPROPYLAMINOPROPAN-2-OL HYDROCHLORIDE
Systematic Name English
7-(2-HYDROXY-3-ISOPROPYLAMINOPROPOXY)INDENE HCL
Common Name English
2-PROPANOL, 1-(1H-INDEN-7-YLOXY)-3-((1-METHYLETHYL)AMINO)-, HYDROCHLORIDE (1:1)
Systematic Name English
2-PROPANOL, 1-(INDEN-7-YLOXY)-3-(ISOPROPYLAMINO)-, HYDROCHLORIDE
Systematic Name English
Code System Code Type Description
FDA UNII
BRV874RC9S
Created by admin on Fri Dec 15 18:57:21 GMT 2023 , Edited by admin on Fri Dec 15 18:57:21 GMT 2023
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PUBCHEM
207529
Created by admin on Fri Dec 15 18:57:21 GMT 2023 , Edited by admin on Fri Dec 15 18:57:21 GMT 2023
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CAS
30190-87-5
Created by admin on Fri Dec 15 18:57:21 GMT 2023 , Edited by admin on Fri Dec 15 18:57:21 GMT 2023
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EPA CompTox
DTXSID30952583
Created by admin on Fri Dec 15 18:57:21 GMT 2023 , Edited by admin on Fri Dec 15 18:57:21 GMT 2023
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