Name | azd-5069 |
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Synonyms |
1-Azetidinesulfonamide, N-[2-[[(2,3-difluorophenyl)methyl]thio]-6-[(1R,2S)-2,3-dihydroxy-1-methylpropoxy]-4-pyrimidinyl]-
N-(2-[(2,3-Difluorobenzyl)sulfanyl]-6-{[(2R,3S)-3,4-dihydroxy-2-butanyl]oxy}-4-pyrimidinyl)-1-azetidinesulfonamide |
Description | AZD-5069 is a potent CXCR2 chemokine receptor antagonist, used for caner treatment. |
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Related Catalog | |
Target |
125I-IL-8-CXCR2 |
In Vitro | AZD-5069 (Compound 2) acts as CXCR2 antagonist by inhibition of [125I]-IL-8 binding to human CXCR2 receptors and as inhibitor of GROα-induced Ca2+ flux in human neutrophils loaded with fluo-3 dye[1]. |
References |
Density | 1.6±0.1 g/cm3 |
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Boiling Point | 680.5±65.0 °C at 760 mmHg |
Molecular Formula | C18H22F2N4O5S2 |
Molecular Weight | 476.518 |
Flash Point | 365.4±34.3 °C |
Exact Mass | 476.099976 |
LogP | 2.43 |
Vapour Pressure | 0.0±2.2 mmHg at 25°C |
Index of Refraction | 1.651 |
Storage condition | 2-8℃ |