BPDBA structure
|
Common Name | BPDBA | ||
|---|---|---|---|---|
| CAS Number | 312281-74-6 | Molecular Weight | 363.28 | |
| Density | N/A | Boiling Point | N/A | |
| Molecular Formula | C19H20Cl2N2O | Melting Point | N/A | |
| MSDS | N/A | Flash Point | N/A | |
Use of BPDBABPDBA is a selective and noncompetitive betaine/GABA transporter (BGT-1) inhibitor with IC50s of 20 μM and 35 μM against human BGT-1 and mouse GAT2, respectively[1]. |
| Name | BPDBA |
|---|---|
| Synonym | More Synonyms |
| Description | BPDBA is a selective and noncompetitive betaine/GABA transporter (BGT-1) inhibitor with IC50s of 20 μM and 35 μM against human BGT-1 and mouse GAT2, respectively[1]. |
|---|---|
| Related Catalog | |
| In Vivo | BPDBA 被预测具有良好的口服吸收和血脑屏障穿透性能[1]。 |
| References |
| Molecular Formula | C19H20Cl2N2O |
|---|---|
| Molecular Weight | 363.28 |
| InChIKey | OIDACLQVAGIDMT-UHFFFAOYSA-N |
| SMILES | O=C(NC1CCN(Cc2ccccc2)CC1)c1ccc(Cl)cc1Cl |
| Storage condition | -20°C |
| N-(1-benzylpiperidin-4-yl)-2,4-dichlorobenzamide |