1173900-37-2
中文名稱
AZD6482(s)
英文名稱
AZD6482(s)
CAS
1173900-37-2
分子式
C22H24N4O4
分子量
408.45
MOL 文件
1173900-37-2.mol
更新日期
2026/06/18 15:39:41
1173900-37-2 結(jié)構(gòu)式
基本信息
中文別名
化合物 T30261 英文別名
AZD6482(s)AZD6482 (S-isomer)
AZD6482 (S-ISOMER)
AZD6482 (S)
AZD6482
AZD-6482
AZD 6482.
2-((S)-1-(7-Methyl-2-morpholino-4-oxo-4h-pyrido[1,2-a]pyrimidin-9-yl)ethylamino)benzoic acid
物理化學(xué)性質(zhì)
沸點635.5±65.0 °C(Predicted)
密度1.36±0.1 g/cm3(Predicted)
儲存條件Store at 0-8 °C
酸度系數(shù)(pKa)3.90±0.50(Predicted)
應(yīng)用領(lǐng)域
用途一
AZD6482 (S-isomer), CAS#1173900-37-2, is an isomer of AZD6482 (MedKoo Cat#406268) with S-configuration. AZD6482 is a potent, selective and ATP competitive PI3Kβ inhibitor (IC(50) 0.01 μm). AZD6482 inhibited insulin-induced human adipocyte glucose uptake in vitro (IC(50) of 4.4 μm). This is the first human target validation for PI3Kβ inhibition as anti-platelet therapy showing a mild and generalized antiplatelet effect attenuating but not completely inhibiting multiple signaling pathways with an impressive separation towards primary hemostasis. AZD6482 at 'supratherapeutic' plasma concentrations may attenuate insulin signaling, most likely through PI3Kα inhibition.