AER-271 structure
|
Common Name | AER-271 | ||
|---|---|---|---|---|
| CAS Number | 634913-39-6 | Molecular Weight | 463.653 | |
| Density | N/A | Boiling Point | N/A | |
| Molecular Formula | C15H9ClF6NO5P | Melting Point | N/A | |
| MSDS | N/A | Flash Point | N/A | |
Use of AER-271AER-271, a phosphonate prodrug derivative of AER-270, is an aquaporin-4 (AQP4) inhibitor for the research of acute ischemic stroke[1]. |
| Name | AER-271 |
|---|---|
| Synonym | More Synonyms |
| Description | AER-271, a phosphonate prodrug derivative of AER-270, is an aquaporin-4 (AQP4) inhibitor for the research of acute ischemic stroke[1]. |
|---|---|
| Related Catalog | |
| Target |
Aquaporin-4 (AQP4)[1] |
| In Vivo | AER-271 is converted in vivo to AER-270 by endogenous phosphatases. AER-271 blocks acute cerebral edema and improves early outcome in a pediatric model of asphyxial cardiac arrest[1]. AER-271 reduces cerebral edema and improves neurological outcomes in rodent ischemic stroke models. Mice treated with AER-271 (5 mg/kg; i.p. injection) show improved outcomes and reduced cerebral edema in a model of ischemic stroke[2]. Animal Model: Male mice (C57BL/6J, 8-12 week-old, 25-30 g)[2] Dosage: 5 mg/kg Administration: Treated by i.p. injection Result: Had better outcomes with an average neurological score of 0.89±0.31 compared with control mice receiving vehicle had an average neurological score of 2.50±0.62. |
| References |
| Molecular Formula | C15H9ClF6NO5P |
|---|---|
| Molecular Weight | 463.653 |
| InChIKey | WSHXPHFIHYXZKC-UHFFFAOYSA-N |
| SMILES | O=C(Nc1cc(C(F)(F)F)cc(C(F)(F)F)c1)c1cc(Cl)ccc1OP(=O)(O)O |
| Storage condition | -20°C 12 Months; 4°C 6 Months |
| 2-{[3,5-Bis(trifluoromethyl) phenyl]carbamoyl}-4-chlorophenyl dihydrogen phosphate |