U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C13H14N2S.ClH
Molecular Weight 266.79
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of METIZOLINE HYDROCHLORIDE

SMILES

Cl.CC1=C(CC2=NCCN2)C3=C(S1)C=CC=C3

InChI

InChIKey=FPTJVMYMFXHIFO-UHFFFAOYSA-N
InChI=1S/C13H14N2S.ClH/c1-9-11(8-13-14-6-7-15-13)10-4-2-3-5-12(10)16-9;/h2-5H,6-8H2,1H3,(H,14,15);1H

HIDE SMILES / InChI

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

Molecular Formula C13H14N2S
Molecular Weight 230.329
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Metizoline is an adrenergic agent with vasoconstrictor properties. It has been used as the active component of nasal decongestant spray (Ellsyl).

Approval Year

Patents

Patents

Substance Class Chemical
Created
by admin
on Fri Dec 15 16:51:18 GMT 2023
Edited
by admin
on Fri Dec 15 16:51:18 GMT 2023
Record UNII
PU364U720Z
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
METIZOLINE HYDROCHLORIDE
MART.   MI   USAN   WHO-DD  
USAN  
Official Name English
EX 10-781
Code English
RMI 10,482A
Code English
METIZOLINE HYDROCHLORIDE [USAN]
Common Name English
METIZOLINE HCL
Common Name English
RMI-10482A
Code English
2-[(2-Methylbenzo[b]thien-3-yl)methyl]-2-imidazoline monohydrochloride
Systematic Name English
METIZOLINE HYDROCHLORIDE [MI]
Common Name English
ELLSYL
Brand Name English
1H-IMIDAZOLE, 4,5-DIHYDRO-2-((2-METHYLBENZO(B)THIEN-3-YL)METHYL)-, MONOHYDROCHLORIDE
Common Name English
EX-10-781
Code English
Metizoline hydrochloride [WHO-DD]
Common Name English
METIZOLINE HYDROCHLORIDE [MART.]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C29709
Created by admin on Fri Dec 15 16:51:18 GMT 2023 , Edited by admin on Fri Dec 15 16:51:18 GMT 2023
Code System Code Type Description
ChEMBL
CHEMBL1370446
Created by admin on Fri Dec 15 16:51:18 GMT 2023 , Edited by admin on Fri Dec 15 16:51:18 GMT 2023
PRIMARY
FDA UNII
PU364U720Z
Created by admin on Fri Dec 15 16:51:18 GMT 2023 , Edited by admin on Fri Dec 15 16:51:18 GMT 2023
PRIMARY
PUBCHEM
68629
Created by admin on Fri Dec 15 16:51:18 GMT 2023 , Edited by admin on Fri Dec 15 16:51:18 GMT 2023
PRIMARY
ECHA (EC/EINECS)
225-811-9
Created by admin on Fri Dec 15 16:51:18 GMT 2023 , Edited by admin on Fri Dec 15 16:51:18 GMT 2023
PRIMARY
NCI_THESAURUS
C90632
Created by admin on Fri Dec 15 16:51:18 GMT 2023 , Edited by admin on Fri Dec 15 16:51:18 GMT 2023
PRIMARY
CAS
5090-37-9
Created by admin on Fri Dec 15 16:51:18 GMT 2023 , Edited by admin on Fri Dec 15 16:51:18 GMT 2023
PRIMARY
MERCK INDEX
m347
Created by admin on Fri Dec 15 16:51:18 GMT 2023 , Edited by admin on Fri Dec 15 16:51:18 GMT 2023
PRIMARY Merck Index
EPA CompTox
DTXSID00198931
Created by admin on Fri Dec 15 16:51:18 GMT 2023 , Edited by admin on Fri Dec 15 16:51:18 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE
Related Record Type Details
ACTIVE MOIETY