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Details

Stereochemistry ACHIRAL
Molecular Formula C13H18N2.ClH
Molecular Weight 238.756
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LERIMAZOLINE HYDROCHLORIDE

SMILES

Cl.CC1=CC(C)=C(CC2=NCCN2)C(C)=C1

InChI

InChIKey=PPDOMMDYAGCCGF-UHFFFAOYSA-N
InChI=1S/C13H18N2.ClH/c1-9-6-10(2)12(11(3)7-9)8-13-14-4-5-15-13;/h6-7H,4-5,8H2,1-3H3,(H,14,15);1H

HIDE SMILES / InChI
Lerimazoline is a sympathomimetic drug that belongs to the imidazoline class of compounds, and is used as a nasal decongestant. Lerimazoline displayed high affinity for the 5-HT1A receptor and for the 5-HT1D receptor. Binding affinity estimates for α1-adrenoceptor, 5-HT2A, and D2 receptors were more than ten times lower. The mechanism of vasoconstrictor action of lerimazoline encompasses both, the activation of 5-HT2A, and to a lesser degree α1 -adrenergic receptors. These results also suggest that lerimazoline is an “atypical” decongestant. It inhibits secretion of nasal mucus. Lerimazoline causes hypertension.

Approval Year

PubMed

PubMed

TitleDatePubMed
Patents

Patents

Name Type Language
LERIMAZOLINE HYDROCHLORIDE
Common Name English
1H-IMIDAZOLE, 4,5-DIHYDRO-2-((2,4,6-TRIMETHYLPHENYL)METHYL)-, HYDROCHLORIDE (1:1)
Systematic Name English
TRIMAZOLINE HYDROCHLORIDE
Systematic Name English
Lerimazoline hydrochloride [WHO-DD]
Common Name English
4,5-DIHYDRO-2-((2,4,6-TRIMETHYLPHENYL)METHYL)-1H-IMIDAZOLE MONOHYDROCHLORIDE
Systematic Name English
Code System Code Type Description
PUBCHEM
3016907
Created by admin on Sat Dec 16 12:29:22 GMT 2023 , Edited by admin on Sat Dec 16 12:29:22 GMT 2023
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EPA CompTox
DTXSID60203171
Created by admin on Sat Dec 16 12:29:22 GMT 2023 , Edited by admin on Sat Dec 16 12:29:22 GMT 2023
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SMS_ID
100000183712
Created by admin on Sat Dec 16 12:29:22 GMT 2023 , Edited by admin on Sat Dec 16 12:29:22 GMT 2023
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ECHA (EC/EINECS)
259-298-8
Created by admin on Sat Dec 16 12:29:22 GMT 2023 , Edited by admin on Sat Dec 16 12:29:22 GMT 2023
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CAS
54707-83-4
Created by admin on Sat Dec 16 12:29:22 GMT 2023 , Edited by admin on Sat Dec 16 12:29:22 GMT 2023
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FDA UNII
PG85ABA8RC
Created by admin on Sat Dec 16 12:29:22 GMT 2023 , Edited by admin on Sat Dec 16 12:29:22 GMT 2023
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