| Name | desloratadine |
|---|---|
| Synonyms |
Desloratadine Citrate Disodium //BP
Rupatadine Impurity B (Loratadine Impurity D) (Desloratadine) DESLORATADINE IMPURITY-D, 8-CHLORO-6,11-DIHYDRO-11-(4-PIPERDINYLIDENE)- 5H-BENZO[5,6]CYCLOHTA[1,2-B]PYRIDINE 8-chloro-11-piperidin-4-ylidene-6,11-dihydro-5H-benzo[5,6]cyclohta[1,2-b]pyridine Desloratadine for system suitability Desloratadine> UNII-FVF865388R Desloratadine [USAN] DESLORATIDINE MFCD00871949 Sch-34117, 8-Chloro-6,11-dihydro-11-(4-piperidinylidene)-5H- benzo[5,6]cyclohta[1,2-β]pyridine, Clairinex, Aerius Loratadine Impurity D (Desloratadine) SCH-34117 Loratadine Impurity D (Desloratadine) (Rupatadine Impurity B) Desalex Deslloratadine Loratadine Impurity D/ Rupatadine Impurity B 8-CHLORO-6,11-DIHYDRO-11-(4-PIPERIDINYLIDENE)-5H-BENZO[5,6]CYCLOHTA[1,2-B]PYRIDINE Clinex RediTabs descarboethoxyloratadine Loratadine Related CoMpound A Loratadine Impurity 4(Loratadine Impurity D) 8-chloro-6,11-dihydro-11-(4-piperdinylidene)-5h-benzo[5,6]cyclohta[1,2-b]pyridine Clarinex 8-Chloro-6,11-dihydro-11-(4-piperidinylidene)-5H-benzo[5,6]cyclohepta[1,2-b]pyridine Clinex(R), 8-Chloro-6,11-dihydro-11-(4-piperidinylidene)-5H- benzo[5,6]cyclohta[1,2,b]pyridine Loratadine Related Compound A (15 mg) (8-Chloro-6,11-dihydro-11(4-piperidinylidene)-5H-benzo[5,6]cyclohta[1,2-b] pyridine) Desloratadine(Clinex) Loratadine IMpurity D Rupatadine Impurity B Opulis Rupatadine Impurity D Descboethoxyoratidine 8-Chloro-6,11-dihydro-11-(4-piperidylidene)-5H-benzo[5,6]cyclohta[1,2-b] pyridine Allex Descarboethoxyoratidine Denosin Desloratadine Citrate Disodium DesL Desloratadine CRS descboethoxyloratadine Desloratadine for system suitability CRS Loratadine impurity-D Loratadine Related Compound A (15 mg) (8-chloro-6,11-dihydro-11(4-piperidylidene)-5H-benzo[5,6]cyclohta[1,2-b] pyridine) 13-chloro-2-(piperidin-4-ylidene)-4-azatricyclo[9.4.0.0^{3,8}]pentadeca-1,3,5,7,11,13-hexaene 8-chloro-11-piperidin-4-ylidene-5,6-dihydrobenzo[1,2]cyclohta[2,4-b]pyridine Dis-loratadine Neoclarityn Loratidine Impurity D/ Loratidine Related Compound A (Desloratadine) Clinex Desloratadine (Sch34117) desloratadine intermediate oratadine 8-Chlor-11-piperidin-4-yliden-6,11-dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyridin AzoMyr Sch-34117, 8-Chloro-6,11-dihydro-11-(4-piperidinylidene)-5H- benzo[5,6]cyclohta[1,2-b]pyridine, Clairinex, Aerius 5H-Benzo[5,6]cyclohta[1,2-b]pyridine, 8-chloro-6,11-dihydro- 11-(4-piperidinylidene) Desloratadine (USAN) 8-Chloro-11-(4-piperidinylidene)-6,11-dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyridine Neoclityn Aerius Sch34117 Desloratadine //BP 8-chloro-11-(piperidin-4-ylidene)-6,11-dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyridine Clinex (TN) esloratadine |
| Description | Desloratadine(Sch34117) is a potent antagonist for human histamine H1 receptor used to treat allergies.Target: Histamine H1 ReceptorDesloratadine binds to the human H1 receptor with Ki value of 0.87 nM in displacing tritiated mepyramine. Desloratadine (100 nM to 10 μM) inhibits both IgE-mediated and non-IgE-mediated generation of the cytokines IL-4 and IL-13 by human basophils. Desloratadine (300 nM to 100 μM) inhibits both IgE and non-IgE-mediated histamine release from human peripheral blood basophils. Desloratadine (0.1 μM to 10 μM) is also shown to inhibit platelet-activating factor-induced eosinophil chemotaxis and TNF-α-induced eosinophil adhesion in eosinophils obtained from patients with allergic rhinitis or allergic asthma [1]. Desloratadine (1 μM-10 μM) dose-dependently inhibits the release of histamine and LTC4 from human basophils. Desloratadine (0.1 μM-10 μM) dose-dependently inhibits IL-13 secretion from basophils activated with IL-3 and PMA from human basophils. Desloratadine (10 μM) pretreatment results in a substantial decrease of the induced cytokine message in cultured basophils. Desloratadine (10 μM) pretreatment causes approximately an 80% reduction in the IL-4 message accumulated with anti-IgE activation in cultured basophils. Desloratadine (10 μM) also inhibits the histamine and IL-4 protein secreted into the supernatants of cultured basophils [2]. [3H]Desloratadine binds to the human histamine H1 receptor expressed in CHO cells with Kd of 1.1 nM. Desloratadine is 52, 57, 194, and 153 times more potent than cetirizine, ebastine, fexofenadine, and loratadine, respectively, in competition-binding studies [3]. |
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| Related Catalog | |
| References |
| Density | 1.2±0.1 g/cm3 |
|---|---|
| Boiling Point | 467.9±45.0 °C at 760 mmHg |
| Melting Point | 150-151°C |
| Molecular Formula | C19H19ClN2 |
| Molecular Weight | 310.821 |
| Flash Point | 236.8±28.7 °C |
| Exact Mass | 310.123688 |
| PSA | 24.92000 |
| LogP | 6.77 |
| Vapour Pressure | 0.0±1.2 mmHg at 25°C |
| Index of Refraction | 1.626 |
| Storage condition | 2-8°C |
| Hazard Codes | Xi |
|---|---|
| Risk Phrases | R11:Highly Flammable. |
| Safety Phrases | S16-S23-S36/37/39 |
| RIDADR | 1993 |
| Precursor 9 | |
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| DownStream 2 | |