CAS NO: | 1425381-60-7 |
生物活性 | Gusacitinib (ASN-002) is an orally active and potent dual inhibitor of spleen tyrosine kinase (SYK) and janus kinase (JAK) withIC50values of 5-46 nM. Gusacitinib has anti-cancer activity in both solid and hematological tumor types[1]. | ||||||||||||||||
IC50& Target | IC50: 5-46 nM (SYK, JAK)[1]. | ||||||||||||||||
体外研究 (In Vitro) | In mechanistic cell-based studies involving IgE and cytokine stimulations, Gusacitinib (ASN-002) strongly suppresses the SYK and JAK family kinase signaling pathways measured as pLAT and pSTAT levels, respectively. Gusacitinib (ASN-002) shows anti-proliferative activity in a broad panel of human cancer cell lines including DHL6, DHL4, OCI-LY10, H929, Pfeiffer, HT-1376, and Lovo, suggesting activity in both solid and hematological tumor types[1]. | ||||||||||||||||
体内研究 (In Vivo) | In a multiple myeloma (H929) xenograft model, Gusacitinib (ASN-002) exhibits significant efficacy in inhibiting tumor growth (>95%). It also significantly delays the onset of hind limb paralysis in the human erythroleukemia (HEL) mouse model. Gusacitinib (ASN-002) has good oral bioavailability, metabolic stability, is not a Pgp substrate, and shows little to no inhibition of CYP450 isozymes. Gusacitinib (ASN-002) shows a favorable safety profile in rat and dog toxicology studies[1]. | ||||||||||||||||
Clinical Trial | |||||||||||||||||
分子量 | 460.53 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C24H28N8O2 | ||||||||||||||||
CAS 号 | 1425381-60-7 | ||||||||||||||||
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 : 100 mg/mL(217.14 mM;Need ultrasonic) 配制储备液
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