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Details

Stereochemistry ABSOLUTE
Molecular Formula C11H12Cl2N2O
Molecular Weight 259.132
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DEXLOFEXIDINE

SMILES

C[C@H](OC1=C(Cl)C=CC=C1Cl)C2=NCCN2

InChI

InChIKey=KSMAGQUYOIHWFS-ZETCQYMHSA-N
InChI=1S/C11H12Cl2N2O/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)/t7-/m0/s1

HIDE SMILES / InChI

Molecular Formula C11H12Cl2N2O
Molecular Weight 259.132
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Dexlofexidine is an isomer “+“ of lofexidine, which is agonist of alpha 2-adrenoceptor, but in 10 times less potent than the other isomer, levlofexidine.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
PubMed

PubMed

TitleDatePubMed
Interference of enantiomers of lofexidine with alpha-adrenoceptors.
1985 Jan
Two stereoisomeric imidazoline derivatives: synthesis and optical and alpha 2-adrenoceptor activities.
1986 Jul
Pharmacokinetics of lofexidine hydrochloride in healthy volunteers.
2009 Jan
Patents

Sample Use Guides

in rats
Route of Administration: Intravenous
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:07:52 UTC 2023
Edited
by admin
on Fri Dec 15 16:07:52 UTC 2023
Record UNII
VXJ7Z24RN1
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DEXLOFEXIDINE
INN  
INN  
Official Name English
(+)-(S)-2-(1-(2,6-DICHLOROPHENOXY)ETHYL)-2-IMIDAZOLINE
Systematic Name English
LOFEXIDINE, (S)-
Common Name English
dexlofexidine [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C29709
Created by admin on Fri Dec 15 16:07:53 UTC 2023 , Edited by admin on Fri Dec 15 16:07:53 UTC 2023
Code System Code Type Description
PUBCHEM
208822
Created by admin on Fri Dec 15 16:07:53 UTC 2023 , Edited by admin on Fri Dec 15 16:07:53 UTC 2023
PRIMARY
CAS
81447-79-2
Created by admin on Fri Dec 15 16:07:53 UTC 2023 , Edited by admin on Fri Dec 15 16:07:53 UTC 2023
PRIMARY
FDA UNII
VXJ7Z24RN1
Created by admin on Fri Dec 15 16:07:53 UTC 2023 , Edited by admin on Fri Dec 15 16:07:53 UTC 2023
PRIMARY
ChEMBL
CHEMBL2106205
Created by admin on Fri Dec 15 16:07:53 UTC 2023 , Edited by admin on Fri Dec 15 16:07:53 UTC 2023
PRIMARY
INN
5256
Created by admin on Fri Dec 15 16:07:53 UTC 2023 , Edited by admin on Fri Dec 15 16:07:53 UTC 2023
PRIMARY
NCI_THESAURUS
C77296
Created by admin on Fri Dec 15 16:07:53 UTC 2023 , Edited by admin on Fri Dec 15 16:07:53 UTC 2023
PRIMARY
SMS_ID
100000083427
Created by admin on Fri Dec 15 16:07:53 UTC 2023 , Edited by admin on Fri Dec 15 16:07:53 UTC 2023
PRIMARY
EPA CompTox
DTXSID901024658
Created by admin on Fri Dec 15 16:07:53 UTC 2023 , Edited by admin on Fri Dec 15 16:07:53 UTC 2023
PRIMARY
EVMPD
SUB07035MIG
Created by admin on Fri Dec 15 16:07:53 UTC 2023 , Edited by admin on Fri Dec 15 16:07:53 UTC 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
RACEMATE -> ENANTIOMER
Related Record Type Details
ACTIVE MOIETY