RS-1269
Modify Date: 2024-04-11 20:18:40
RS-1269 structure
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Common Name | RS-1269 | ||
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| CAS Number | 1310462-38-4 | Molecular Weight | 562.714 | |
| Density | N/A | Boiling Point | N/A | |
| Molecular Formula | C35H38N4O3 | Melting Point | N/A | |
| MSDS | N/A | Flash Point | N/A | |
Use of RS-1269RS-1269 is a highly potent, selective CCR4 antagonist, inhibits [125I]CCL17 binding to human CCR4 with IC50 of 27.7 nM.RS-1269 also has strong affinity to displace the CCL17 binding with IC50 of 27.0 nM in CCR4-expressing CHO cells.RS-1269 displays no competitive displacement in the binding of [125I]CCL3 (MIP-1α) to CCR1 and [125I]CCL2 (MCP-1) to CCR2b.RS-1269 dose-dependently inhibited CCL17-induced migration of Th2 cells with IC50 of 5.5 nM.Orally administered RS-1269 (30 mg/kg) ameliorates ovalbumin-induced ear swelling in mice.RS-1269 also inhibited LPS-induced TNF-α production in vivo. |
| Name | RS-1269 |
|---|
| Description | RS-1269 is a highly potent, selective CCR4 antagonist, inhibits [125I]CCL17 binding to human CCR4 with IC50 of 27.7 nM.RS-1269 also has strong affinity to displace the CCL17 binding with IC50 of 27.0 nM in CCR4-expressing CHO cells.RS-1269 displays no competitive displacement in the binding of [125I]CCL3 (MIP-1α) to CCR1 and [125I]CCL2 (MCP-1) to CCR2b.RS-1269 dose-dependently inhibited CCL17-induced migration of Th2 cells with IC50 of 5.5 nM.Orally administered RS-1269 (30 mg/kg) ameliorates ovalbumin-induced ear swelling in mice.RS-1269 also inhibited LPS-induced TNF-α production in vivo. |
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| References | 1. Nakagami Y, et al. Basic Clin Pharmacol Toxicol. 2010 Oct;107(4):793-7. |
| Molecular Formula | C35H38N4O3 |
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| Molecular Weight | 562.714 |