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Details

Stereochemistry RACEMIC
Molecular Formula C21H27NO.ClH
Molecular Weight 345.906
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DIPHENYLPIPERIDINOBUTANOL HYDROCHLORIDE

SMILES

Cl.CC(CC(O)(C1=CC=CC=C1)C2=CC=CC=C2)N3CCCCC3

InChI

InChIKey=YFROVFWOPWMFRE-UHFFFAOYSA-N
InChI=1S/C21H27NO.ClH/c1-18(22-15-9-4-10-16-22)17-21(23,19-11-5-2-6-12-19)20-13-7-3-8-14-20;/h2-3,5-8,11-14,18,23H,4,9-10,15-17H2,1H3;1H

HIDE SMILES / InChI

Molecular Formula C21H27NO
Molecular Weight 309.4452
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

Aspaminol (1,1 diphenyl-3-piperidinobutanol hydrochloride) is a nonspecific smooth muscle relaxant. It inhibits calcium uptake. The relaxation of smooth muscle induced by aspaminol may be due to a combining of aspaminol with calcium ions at the binding sites on the surface of smooth muscle, thus decreasing the supply of calcium ions to the contractile element.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

PubMed

PubMed

TitleDatePubMed
Relationship between synaptosomal calcium uptake and antinociceptive action of morphine.
1983-06
Effect of 1,1-diphenyl-3-piperidinobutanol hydrochloride (Aspaminol) on the stimuli-induced calcium uptake in rat brain synaptosomes.
1981-12
Comparison of effects of external Ca2+ on antioxytocin actions of antispasmodics in ovariectomized and estradiol-treated rat uteri.
1980-08
Calcium ions and relaxation of intestinal smooth muscle induced by papaverine and aspaminol.
1977-04

Sample Use Guides

In Vivo Use Guide
Unknown
Route of Administration: Unknown
In Vitro Use Guide
Aspaminol 1-10 uM depressed molluscan smooth muscle contraction in a dose dependent manner.
Substance Class Chemical
Created
by admin
on Mon Mar 31 21:22:40 GMT 2025
Edited
by admin
on Mon Mar 31 21:22:40 GMT 2025
Record UNII
E071P1I925
Record Status Validated (UNII)
Record Version
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Name Type Language
DIPHENYLPIPERIDINOBUTANOL HYDROCHLORIDE
JAN  
Systematic Name English
ASPAMINOL HYDROCHLORIDE
Preferred Name English
1-PIPERIDINEPROPANOL, .GAMMA.-METHYL-.ALPHA.,.ALPHA.-DIPHENYL-, HYDROCHLORIDE, (±)-
Systematic Name English
DIPHENYLPIPERIDINOBUTANOL HYDROCHLORIDE [JAN]
Common Name English
1-PIPERIDINEPROPANOL, .GAMMA.-METHYL-.ALPHA.,.ALPHA.-DIPHENYL-, HYDROCHLORIDE
Systematic Name English
1-PIPERIDINEPROPANOL, .GAMMA.-METHYL-.ALPHA.,.ALPHA.-DIPHENYL-, HYDROCHLORIDE (1:1)
Systematic Name English
1,1-DIPHENYL-3-(1- PIPERIDYL)BUTAN-1-OL HYDROCHLORIDE
Systematic Name English
Code System Code Type Description
PUBCHEM
53297477
Created by admin on Mon Mar 31 21:22:40 GMT 2025 , Edited by admin on Mon Mar 31 21:22:40 GMT 2025
PRIMARY
CAS
55701-20-7
Created by admin on Mon Mar 31 21:22:40 GMT 2025 , Edited by admin on Mon Mar 31 21:22:40 GMT 2025
PRIMARY
FDA UNII
E071P1I925
Created by admin on Mon Mar 31 21:22:40 GMT 2025 , Edited by admin on Mon Mar 31 21:22:40 GMT 2025
PRIMARY
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ACTIVE MOIETY