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Details

Stereochemistry ABSOLUTE
Molecular Formula C11H12Cl2N2O.ClH
Molecular Weight 295.593
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DEXLOFEXIDINE HYDROCHLORIDE

SMILES

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

InChI

InChIKey=DWWHMKBNNNZGHF-FJXQXJEOSA-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/t7-;/m0./s1

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 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
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 Sat Dec 16 11:11:38 UTC 2023
Edited
by admin
on Sat Dec 16 11:11:38 UTC 2023
Record UNII
56H4BIV8OG
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DEXLOFEXIDINE HYDROCHLORIDE
Common Name English
1H-IMIDAZOLE, 2-((1S)-1-(2,6-DICHLOROPHENOXY)ETHYL)-4,5-DIHYDRO-, HYDROCHLORIDE (1:1)
Systematic Name English
LOFEXIDINE HYDROCHLORIDE, (+)-
Common Name English
LOFEXIDINE HYDROCHLORIDE, (S)-
Common Name English
1H-IMIDAZOLE, 2-(1-(2,6-DICHLOROPHENOXY)ETHYL)-4,5-DIHYDRO-, MONOHYDROCHLORIDE, (S)-
Common Name English
Code System Code Type Description
PUBCHEM
45279768
Created by admin on Sat Dec 16 11:11:38 UTC 2023 , Edited by admin on Sat Dec 16 11:11:38 UTC 2023
PRIMARY
FDA UNII
56H4BIV8OG
Created by admin on Sat Dec 16 11:11:38 UTC 2023 , Edited by admin on Sat Dec 16 11:11:38 UTC 2023
PRIMARY
CAS
87858-98-8
Created by admin on Sat Dec 16 11:11:38 UTC 2023 , Edited by admin on Sat Dec 16 11:11:38 UTC 2023
PRIMARY
Related Record Type Details
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