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=C2C=CCC2=CC=C1
InChI
InChIKey=LQUALIUFEGJTKA-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;/h3-4,6-8,11,13,16-17H,5,9-10H2,1-2H3;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 |
Indenolol hydrochloride is a nonselective beta-adrenoceptor antagonist. It is antihypertensive, antiarrhytmic, antianginal drug. It vasodilated forearm arterioles and this effect was antagonized by beta-blockade, thus demonstrating vascular intrinsic sympathomimetic activity. Indenol is able to inhibit an exercise-induced rise in systolic pressure. Indenolol would be able to decrease myocardial O2 consumption.
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 18:58:45 GMT 2023
by
admin
on
Fri Dec 15 18:58:45 GMT 2023
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| Record UNII |
3MK6CS750V
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| Record Status |
Validated (UNII)
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| Record Version |
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-
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| Code System | Code | Type | Description | ||
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59527-63-8
Created by
admin on Fri Dec 15 18:58:45 GMT 2023 , Edited by admin on Fri Dec 15 18:58:45 GMT 2023
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118333
Created by
admin on Fri Dec 15 18:58:45 GMT 2023 , Edited by admin on Fri Dec 15 18:58:45 GMT 2023
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3MK6CS750V
Created by
admin on Fri Dec 15 18:58:45 GMT 2023 , Edited by admin on Fri Dec 15 18:58:45 GMT 2023
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PRIMARY |
| Related Record | Type | Details | ||
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PARENT -> SALT/SOLVATE |
