CAS NO: | 1229208-44-9 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
5mg | 电议 |
10mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
500mg | 电议 |
生物活性 | Entospletinib (GS-9973) is an orally bioavailable, selectiveSykinhibitor with anIC50of 7.7 nM. | ||||||||||||||||
IC50& Target | IC50: 7.7 nM (Syk) | ||||||||||||||||
体外研究 (In Vitro) | Entospletinib (GS-9973) shows good bidirectional permeability across Caco-2 cell monolayers in vitro. In cells, Entospletinib (GS-9973) also shows excellent selectivity for Syk, and potently inhibits BCR-mediated activation and proliferation of B-cells as well as immune-complex-stimulated cytokine production in monocytes[1]. The combination of idelalisib and Entospletinib (GS-9973) synergistically inhibits CLL cell viability and further disrupts chemokine signaling[2]. | ||||||||||||||||
体内研究 (In Vivo) | Entospletinib (GS-9973) (1 mg/kg, p.o.) shows moderate to high bioavailability in rat and dog. In a rat collagen-induced arthritis model, Entospletinib (GS-9973) (1-10 mg/kg, p.o.) significantly inhibits ankle inflammation. Moreover, Entospletinib (GS-9973) also shows disease-modifying activity in multiple histological measurements, including inhibition of pannus formation, cartilage damage, bone resorption, and peritosteal bone formation with ED50ranging from 1.2 to 3.9 mg/kg[1]. | ||||||||||||||||
Clinical Trial | |||||||||||||||||
分子量 | 411.46 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C23H21N7O | ||||||||||||||||
CAS 号 | 1229208-44-9 | ||||||||||||||||
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 : ≥ 43 mg/mL(104.51 mM) *"≥" means soluble, but saturation unknown. 配制储备液
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