Org 48762-0 structure
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Common Name | Org 48762-0 | ||
|---|---|---|---|---|
| CAS Number | 755753-89-0 | Molecular Weight | 398.41 | |
| Density | 1.3±0.1 g/cm3 | Boiling Point | 520.1±50.0 °C at 760 mmHg | |
| Molecular Formula | C24H16F2N4 | Melting Point | N/A | |
| MSDS | N/A | Flash Point | 268.3±30.1 °C | |
Use of Org 48762-0Org 48762-0 is a potent, orally active and selective p38 inhibitor with EC50 of 0.1 μM. Org 48762-0 reduces LPS-induced TNFα release and prevents bone damage in collagen-induced arthritis in mice[1]. |
| Name | Org 48762-0 |
|---|---|
| Synonym | More Synonyms |
| Description | Org 48762-0 is a potent, orally active and selective p38 inhibitor with EC50 of 0.1 μM. Org 48762-0 reduces LPS-induced TNFα release and prevents bone damage in collagen-induced arthritis in mice[1]. |
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| Related Catalog | |
| References |
| Density | 1.3±0.1 g/cm3 |
|---|---|
| Boiling Point | 520.1±50.0 °C at 760 mmHg |
| Molecular Formula | C24H16F2N4 |
| Molecular Weight | 398.41 |
| Flash Point | 268.3±30.1 °C |
| Exact Mass | 398.134308 |
| LogP | 3.62 |
| Vapour Pressure | 0.0±1.3 mmHg at 25°C |
| Index of Refraction | 1.661 |
| 2H-Pyrazolo[3,4-b]pyridine, 4,6-bis(4-fluorophenyl)-2-methyl-5-(4-pyridinyl)- |
| 4,6-Bis(4-fluorophenyl)-2-methyl-5-(4-pyridinyl)-2H-pyrazolo[3,4-b]pyridine |
| MFCD30536377 |