AZD 1678 structure
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Common Name | AZD 1678 | ||
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CAS Number | 942137-41-9 | Molecular Weight | 352.169 | |
Density | 1.6±0.1 g/cm3 | Boiling Point | 469.8±55.0 °C at 760 mmHg | |
Molecular Formula | C11H8Cl2FN3O3S | Melting Point | N/A | |
MSDS | N/A | Flash Point | 237.9±31.5 °C |
Use of AZD 1678AZD 1678 is a potent, selective orally bioavailable CCR4 receptor antagonist with pIC50 of 8.6 for hCCR4, pIC50 of 9.0 for rCCR4; shows no significant activity against a panel of chemokine receptors (CXCR1, CXCR2, CCR1, CCR2b, CCR5, CCR7, CCR8; inactive at 10 uM); inhibits Th2 cell CCL22 driven chemotaxis in 0.3% HSA with pIC50 of 6.8. Asthma Phase 1 Clinical |
Name | 2,3-Dichloro-N-(5-fluoro-3-methoxy-2-pyrazinyl)benzenesulfonamide |
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Synonym | More Synonyms |
Description | AZD 1678 is a potent, selective orally bioavailable CCR4 receptor antagonist with pIC50 of 8.6 for hCCR4, pIC50 of 9.0 for rCCR4; shows no significant activity against a panel of chemokine receptors (CXCR1, CXCR2, CCR1, CCR2b, CCR5, CCR7, CCR8; inactive at 10 uM); inhibits Th2 cell CCL22 driven chemotaxis in 0.3% HSA with pIC50 of 6.8. Asthma Phase 1 Clinical |
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References | References 1. Kindon N, et al. ACS Med Chem Lett. 2017 Sep 1;8(9):981-986. View Related Products by Target Chemokine Receptor (CCR and CXCR) Asthma |
Density | 1.6±0.1 g/cm3 |
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Boiling Point | 469.8±55.0 °C at 760 mmHg |
Molecular Formula | C11H8Cl2FN3O3S |
Molecular Weight | 352.169 |
Flash Point | 237.9±31.5 °C |
Exact Mass | 350.964752 |
LogP | 3.86 |
Vapour Pressure | 0.0±1.2 mmHg at 25°C |
Index of Refraction | 1.614 |
2,3-Dichloro-N-(5-fluoro-3-methoxy-2-pyrazinyl)benzenesulfonamide |
MFCD28975034 |
Benzenesulfonamide, 2,3-dichloro-N-(5-fluoro-3-methoxy-2-pyrazinyl)- |