Ciproxifan hydrochloride
SIGMA/C6492 - ≥98% (HPLC), solid
Synonym: Cyclopropyl[4-
CAS Number: 1049741-81-2
Empirical Formula (Hill Notation): C16H18N2O2 · HCl
Molecular Weight: 306.79
MDL Number: MFCD08705321
Linear Formula: C16H18N2O2 · HCl
Product Type: Chemical
| assay | ≥98% (HPLC) |
| color | off-white |
| form | solid |
| InChI | 1S/C16H18N2O2.ClH/c19-16( |
| InChI key | PWAPSKMHZQQTRJ-UHFFFAOYSA |
| Quality Level | 100 ![]() |
| SMILES string | Cl.O=C(C1CC1)c2ccc(OCCCc3 |
| solubility | DMSO: 30 mg/mL |
| water, high purity: 30 mg/mL | |
| storage condition | desiccated |
| under inert gas | |
| storage temp. | 2-8°C |
| Biochem/physiol Actions: | Ciproxifan belongs to a novel chemical series of histamine H3-receptor antagonists. In vitro, it behaved as a competitive antagonist at the H3 autoreceptor controlling 3H histamine release from synaptosomes and displayed similar Ki values (0.5-1.9 nM) at the H3 receptor controlling the electrically-induced contraction of guinea pig ileum or at the brain H3 receptor labeled with 125I-iodoproxyfan. Ciproxifan appears to be an orally bioavailable, extremely potent and selective H3-receptor antagonist whose vigilance- and attention-promoting effects are promising for therapeutic applications in aging disorders. |
| Biochem/physiol Actions: | H3 histamine receptor antagonist. |
| Features and Benefits: | This compound is featured on the Histamine Receptors page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here . |
| Packaging: | 5, 25 mg in glass bottle |
| Symbol | GHS07 |
| Signal word | Warning |
| Hazard statements | H302 |
| Hazard Codes | Xn |
| Risk Statements | 22 |
| RIDADR | NONH for all modes of transport |
| WGK Germany | WGK 3 |
| Flash Point(F) | Not applicable |
| Flash Point(C) | Not applicable |
| Purity | ≥98% (HPLC) |
| Storage Temp. | 2-8°C |
| UNSPSC | 12352200 |


