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
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
| 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 | ( + / - ) |
| 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 |
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
| Title | Date | PubMed |
|---|---|---|
| Electrophysiologically determined quinidine-like actions of a beta-adrenergic blocking agent, 1-(7-indenyloxy)-3-isopropylaminopropane-2-ol hydrochloride (YB-2). | 1976-06 |
|
| Unambiguous synthesis of 1-(7-indenyloxy)-3-isopropylamino-2-propanol hydrochloride and its 4-indenyloxy isomer, potent beta-adrenergic blocking agents. | 1976-03 |
|
| [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]. | 1975-08 |
|
| Antiarrhythmic activity of 1-(7-indenyloxy)-3-isopropylaminopropane-2-ol hydrochloride (YB-2) and its optical isomers. | 1974-08 |
|
| Cardiovascular beta-adrenergic receptor blocking activities of 1-(7-indenyloxy)-3-isopropyl-aminopropane-2-ol hydrochloride (YB-2) and its optical isomers. | 1974-04 |
|
| Pharmacological studies on 1-(7-indenyloxy)-3-isopropylaminopropan-2-Ol hydrochloride (YB-2), a new -adrenergic blocking agent. | 1973-03 |
|
| [Effects of 1-(7-indenyloxy)-3-isopropylaminopropan-2-ol hydrochloride (YB-2) on coronary circulation and and myocardial metabolism]. | 1972-11 |
|
| -adrenergic blocking and cardiovascular properties of a new compound, 1-(7-indenyloxy)-3-isopropylaminopropan-2-ol-hydrochloride (YB-2). | 1972-11 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:27:52 GMT 2025
by
admin
on
Mon Mar 31 19:27:52 GMT 2025
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| Record UNII |
BRV874RC9S
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| Record Status |
Validated (UNII)
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| Record Version |
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207529
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30190-87-5
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DTXSID30952583
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