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Details

Stereochemistry MIXED
Molecular Formula C22H30N2O2.2ClH
Molecular Weight 427.408
Optical Activity UNSPECIFIED
Defined Stereocenters 0 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of EPROZINOL HYDROCHLORIDE

SMILES

Cl.Cl.COC(CN1CCN(CCC(O)C2=CC=CC=C2)CC1)C3=CC=CC=C3

InChI

InChIKey=KVKUGOLSESPAPP-UHFFFAOYSA-N
InChI=1S/C22H30N2O2.2ClH/c1-26-22(20-10-6-3-7-11-20)18-24-16-14-23(15-17-24)13-12-21(25)19-8-4-2-5-9-19;;/h2-11,21-22,25H,12-18H2,1H3;2*1H

HIDE SMILES / InChI

Molecular Formula C22H30N2O2
Molecular Weight 354.4858
Charge 0
Count
Stereochemistry MIXED
Additional Stereochemistry No
Defined Stereocenters 0 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

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

Eprozinol inhibits bronchoconstriction by an action on histamine H1 receptors and has been used in the treatment of asthma and bronchitis. No significant changes in cAMP and cGMP levels are observed in guinea pig trachea, with eprozinol or isoprenaline, at doses capable of inducing relaxation. Eprozinol is only a very weak phosphodiesterase inhibitor, at large concentrations. The anti-bronchoconstrictor activities of eprozinol and isoprenaline with regard to histamine are directly additive and show absolutely no interference with one another. Propranolol is without effect on in vivo anti-bronchoconstrictor activity of eprozinol on tracheal musculature. It is concluded, that the mechanisms brought into play by eprozinol to exert anti-bronchoconstrictor and bronchorelaxant activity, are completely independent of the adrenergic system. In a retrospective study of 199 cases of accidental or intentional acute poisoning with eprozinol, eprazinone and zipeprol, collected at the Poison Control Center were seven cases of seizures, all after ingestion of eight times the therapeutic dose. They resolved rapidly and without recurrence with symptomatic treatment.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 17:47:16 GMT 2023
Edited
by admin
on Fri Dec 15 17:47:16 GMT 2023
Record UNII
X9AMI360PI
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
EPROZINOL HYDROCHLORIDE
MART.   WHO-DD  
Common Name English
3-(4-(.BETA.-METHOXYPHENETHYL)PIPERAZIN-1-YL)-1-PHENYLPROPAN-1-OL DIHYDROCHLORIDE
Systematic Name English
Eprozinol hydrochloride [WHO-DD]
Common Name English
EPROZINOL HYDROCHLORIDE [MART.]
Common Name English
1-PIPERAZINEPROPANOL, 4-(2-METHOXY-2-PHENYLETHYL)-.ALPHA.-PHENYL-, HYDROCHLORIDE (1:2)
Systematic Name English
EPROZINOL HCL
Common Name English
EPROZINOL DIHYDROCHLORIDE [MI]
Common Name English
EPROZINOL DIHYDROCHLORIDE
MI  
Common Name English
Code System Code Type Description
RXCUI
402567
Created by admin on Fri Dec 15 17:47:16 GMT 2023 , Edited by admin on Fri Dec 15 17:47:16 GMT 2023
PRIMARY RxNorm
EVMPD
SUB01921MIG
Created by admin on Fri Dec 15 17:47:16 GMT 2023 , Edited by admin on Fri Dec 15 17:47:16 GMT 2023
PRIMARY
CAS
27588-43-8
Created by admin on Fri Dec 15 17:47:16 GMT 2023 , Edited by admin on Fri Dec 15 17:47:16 GMT 2023
PRIMARY
MESH
C015853
Created by admin on Fri Dec 15 17:47:16 GMT 2023 , Edited by admin on Fri Dec 15 17:47:16 GMT 2023
PRIMARY
MERCK INDEX
m4963
Created by admin on Fri Dec 15 17:47:16 GMT 2023 , Edited by admin on Fri Dec 15 17:47:16 GMT 2023
PRIMARY Merck Index
FDA UNII
X9AMI360PI
Created by admin on Fri Dec 15 17:47:16 GMT 2023 , Edited by admin on Fri Dec 15 17:47:16 GMT 2023
PRIMARY
EPA CompTox
DTXSID00950258
Created by admin on Fri Dec 15 17:47:16 GMT 2023 , Edited by admin on Fri Dec 15 17:47:16 GMT 2023
PRIMARY
ECHA (EC/EINECS)
248-548-1
Created by admin on Fri Dec 15 17:47:16 GMT 2023 , Edited by admin on Fri Dec 15 17:47:16 GMT 2023
PRIMARY
SMS_ID
100000087247
Created by admin on Fri Dec 15 17:47:16 GMT 2023 , Edited by admin on Fri Dec 15 17:47:16 GMT 2023
PRIMARY
PUBCHEM
161574
Created by admin on Fri Dec 15 17:47:16 GMT 2023 , Edited by admin on Fri Dec 15 17:47:16 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY