CAS NO: | 897657-95-3 |
生物活性 | MSX-122 is an orally active partial antagonist ofCXCR4, inhibitingCXCR4/CXCL12actions, with anIC50of ~10 nM. MSX-122 has anti-inflammatory and anti-metastatic activity. | ||||||||||||||||
IC50& Target[1] |
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体外研究 (In Vitro) | MSX-122 is a partial antagonist of CXCR4, inhibiting CXCR4/CXCL12 actions, with an IC50of ~10 nM. MSX-122 shows no inhibition on cAMP reduction mediated by their corresponding ligands CCR3/CCL5 and CCR5/CCL5. MSX-122 (100 nM) potently blocks invasion of 78% MDA-MB-231 cells. However, MSX-122 does not suppress T-tropic HIV infection and is inactive in calcium flux assay[1]. | ||||||||||||||||
体内研究 (In Vivo) | MSX-122 (10 mg/kg, i.p.) blocks inflammation induced by carrageenan and lung fibrosis induced by bleomycin in mice. MSX-122 (4 mg/kg, i.p., daily) blocks metastasis in an experimental animal model of breast cancer metastasis. Furthermore, MSX-122 (10 mg/kg i.p., daily) significantly decreases the numbers of hepatic micrometastases[1]. | ||||||||||||||||
Clinical Trial | |||||||||||||||||
分子量 | 292.34 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C16H16N6 | ||||||||||||||||
CAS 号 | 897657-95-3 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 |
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溶解性数据 | In Vitro: DMSO : 4 mg/mL(13.68 mM;Need ultrasonic) 配制储备液
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以下溶剂前显示的百
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