Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C21H24F2N2O3 |
| Molecular Weight | 390.4237 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OC(=O)COCCN1CCN(CC1)C(C2=CC=C(F)C=C2)C3=CC=C(F)C=C3
InChI
InChIKey=BAWMMJAUVBLLEE-UHFFFAOYSA-N
InChI=1S/C21H24F2N2O3/c22-18-5-1-16(2-6-18)21(17-3-7-19(23)8-4-17)25-11-9-24(10-12-25)13-14-28-15-20(26)27/h1-8,21H,9-15H2,(H,26,27)
| Molecular Formula | C21H24F2N2O3 |
| Molecular Weight | 390.4237 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/11829715Curator's Comment: description was created based on several sources, including:
http://www.pharmacodia.com/yaodu/html/v1/chemicals/9c3368c58b7c3569a3e83048cfc8d023.html
Sources: https://www.ncbi.nlm.nih.gov/pubmed/11829715
Curator's Comment: description was created based on several sources, including:
http://www.pharmacodia.com/yaodu/html/v1/chemicals/9c3368c58b7c3569a3e83048cfc8d023.html
Efletirizine is histamine H1 receptor antagonist. Restricted to topical use. It was under investigation in Phase III (in Europe) clinical studies for the treatment of allergic rhinitis and chronic idiopathic urticarial. Research was discontinued in 2005 due to limited clinical efficacy and safety data. Efletirizine also reduced ocular itching.
Originator
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: CHEMBL231 Sources: https://www.ncbi.nlm.nih.gov/pubmed/11829715 |
Conditions
| Condition | Modality | Targets | Highest Phase | Product |
|---|---|---|---|---|
| Palliative | Unknown Approved UseUnknown |
|||
| Palliative | Unknown Approved UseUnknown |
PubMed
| Title | Date | PubMed |
|---|---|---|
| Cetirizine and loratadine-based antihistamines with 5-lipoxygenase inhibitory activity. | 2004-11-15 |
|
| Antihistamines in late-phase clinical development for allergic disease. | 2002-02 |
|
| Quantitation of efletirizine in human plasma and urine using automated solid-phase extraction and column-switching high-performance liquid chromatography. | 1999-07-09 |
Patents
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/11829715
15, 30 and 60 ug/100 ul (0.15%, 0.3% or 0.6%) twice-daily for two weeks
Route of Administration:
Topical
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:25:04 GMT 2025
by
admin
on
Mon Mar 31 18:25:04 GMT 2025
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| Record UNII |
B6C301298G
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| Record Status |
Validated (UNII)
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NCI_THESAURUS |
C29578
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150756-35-7
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SUB06467MIG
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C73048
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| Related Record | Type | Details | ||
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TARGET -> INHIBITOR |
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SALT/SOLVATE -> PARENT |
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ACTIVE MOIETY |
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