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Details

Stereochemistry RACEMIC
Molecular Formula C11H12Cl2N2O.ClH
Molecular Weight 295.593
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LOFEXIDINE HYDROCHLORIDE

SMILES

Cl.CC(OC1=C(Cl)C=CC=C1Cl)C2=NCCN2

InChI

InChIKey=DWWHMKBNNNZGHF-UHFFFAOYSA-N
InChI=1S/C11H12Cl2N2O.ClH/c1-7(11-14-5-6-15-11)16-10-8(12)3-2-4-9(10)13;/h2-4,7H,5-6H2,1H3,(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 C11H12Cl2N2O
Molecular Weight 259.132
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

Unknown
86413
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:24:50 UTC 2023
Edited
by admin
on Fri Dec 15 15:24:50 UTC 2023
Record UNII
V47G1SDI1B
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
LOFEXIDINE HYDROCHLORIDE
MART.   MI   USAN   VANDF   WHO-DD  
USAN  
Official Name English
2-(1-(2,6-DICHLOROPHENOXY)ETHYL)-4,5-DIHYDRO-1H-IMIDAZOLE HYDROCHLORIDE
Systematic Name English
LOFEXIDINE HYDROCHLORIDE [USAN]
Common Name English
MDL-14042
Code English
2-[1-(2,6-Dichlorophenoxy)ethyl]-2-imidazoline monohydrochloride
Systematic Name English
LOFEXIDINE HYDROCHLORIDE [VANDF]
Common Name English
Lofexidine hydrochloride [WHO-DD]
Common Name English
MDL 14,042
Code English
1H-IMIDAZOLE, 2-(1-(2,6-DICHLOROPHENOXY)ETHYL)-4,5-DIHYDRO-, MONOHYDROCHLORIDE
Common Name English
LUCEMYRA
Brand Name English
NSC-759654
Code English
LOFEXIDINE HCL
Common Name English
LOFEXIDINE HYDROCHLORIDE [MART.]
Common Name English
LOFEXIDINE HYDROCHLORIDE [ORANGE BOOK]
Common Name English
LOFEXIDINE HYDROCHLORIDE [MI]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C29709
Created by admin on Fri Dec 15 15:24:50 UTC 2023 , Edited by admin on Fri Dec 15 15:24:50 UTC 2023
Code System Code Type Description
NSC
759654
Created by admin on Fri Dec 15 15:24:50 UTC 2023 , Edited by admin on Fri Dec 15 15:24:50 UTC 2023
PRIMARY
FDA UNII
V47G1SDI1B
Created by admin on Fri Dec 15 15:24:50 UTC 2023 , Edited by admin on Fri Dec 15 15:24:50 UTC 2023
PRIMARY
MESH
C025655
Created by admin on Fri Dec 15 15:24:50 UTC 2023 , Edited by admin on Fri Dec 15 15:24:50 UTC 2023
PRIMARY
CAS
21498-08-8
Created by admin on Fri Dec 15 15:24:50 UTC 2023 , Edited by admin on Fri Dec 15 15:24:50 UTC 2023
PRIMARY
DAILYMED
V47G1SDI1B
Created by admin on Fri Dec 15 15:24:50 UTC 2023 , Edited by admin on Fri Dec 15 15:24:50 UTC 2023
PRIMARY
PUBCHEM
30667
Created by admin on Fri Dec 15 15:24:50 UTC 2023 , Edited by admin on Fri Dec 15 15:24:50 UTC 2023
PRIMARY
MERCK INDEX
m6885
Created by admin on Fri Dec 15 15:24:50 UTC 2023 , Edited by admin on Fri Dec 15 15:24:50 UTC 2023
PRIMARY Merck Index
EPA CompTox
DTXSID0020781
Created by admin on Fri Dec 15 15:24:50 UTC 2023 , Edited by admin on Fri Dec 15 15:24:50 UTC 2023
PRIMARY
SMS_ID
100000086132
Created by admin on Fri Dec 15 15:24:50 UTC 2023 , Edited by admin on Fri Dec 15 15:24:50 UTC 2023
PRIMARY
RXCUI
235853
Created by admin on Fri Dec 15 15:24:50 UTC 2023 , Edited by admin on Fri Dec 15 15:24:50 UTC 2023
PRIMARY RxNorm
DRUG BANK
DBSALT000829
Created by admin on Fri Dec 15 15:24:50 UTC 2023 , Edited by admin on Fri Dec 15 15:24:50 UTC 2023
PRIMARY
USAN
X-75
Created by admin on Fri Dec 15 15:24:50 UTC 2023 , Edited by admin on Fri Dec 15 15:24:50 UTC 2023
PRIMARY
EVMPD
SUB02966MIG
Created by admin on Fri Dec 15 15:24:50 UTC 2023 , Edited by admin on Fri Dec 15 15:24:50 UTC 2023
PRIMARY
ChEMBL
CHEMBL17860
Created by admin on Fri Dec 15 15:24:50 UTC 2023 , Edited by admin on Fri Dec 15 15:24:50 UTC 2023
PRIMARY
NCI_THESAURUS
C87581
Created by admin on Fri Dec 15 15:24:50 UTC 2023 , Edited by admin on Fri Dec 15 15:24:50 UTC 2023
PRIMARY
Related Record Type Details
Structure of DEXLOFEXIDINE HYDROCHLORIDE
ENANTIOMER -> RACEMATE
Structure of LEVLOFEXIDINE HYDROCHLORIDE
ENANTIOMER -> RACEMATE
Structure of LOFEXIDINE
PARENT -> SALT/SOLVATE
Related Record Type Details
Structure of LOFEXIDINE
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