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
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
| 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 |
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/2879913
Sources: https://www.ncbi.nlm.nih.gov/pubmed/2879913
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
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: CHEMBL2095158 Sources: https://www.ncbi.nlm.nih.gov/pubmed/2879913 |
Conditions
| Condition | Modality | Targets | Highest Phase | Product |
|---|---|---|---|---|
PubMed
| Title | Date | PubMed |
|---|---|---|
| Pharmacokinetics of lofexidine hydrochloride in healthy volunteers. | 2009-01 |
|
| Two stereoisomeric imidazoline derivatives: synthesis and optical and alpha 2-adrenoceptor activities. | 1986-07 |
|
| Interference of enantiomers of lofexidine with alpha-adrenoceptors. | 1985-01 |
Patents
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/2988468
in rats
Route of Administration:
Intravenous
| Substance Class |
Chemical
Created
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| Record UNII |
VXJ7Z24RN1
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Validated (UNII)
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NCI_THESAURUS |
C29709
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208822
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81447-79-2
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VXJ7Z24RN1
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CHEMBL2106205
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5256
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C77296
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100000083427
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DTXSID901024658
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SUB07035MIG
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| Related Record | Type | Details | ||
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SALT/SOLVATE -> PARENT | |||
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RACEMATE -> ENANTIOMER |
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ACTIVE MOIETY |