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197894-84-1

中文名稱 197894-84-1
英文名稱 CI-1044
CAS 197894-84-1
分子式 C23H19N5O2
分子量 397.43
MOL 文件 197894-84-1.mol
197894-84-1 結(jié)構(gòu)式 197894-84-1 結(jié)構(gòu)式

基本信息

中文別名
化合物 T14962
英文別名
CI-1044
PD-189659
CI-1044 (CI1044)
3-Pyridinecarboxamide, N-[(3R)-9-amino-3,4,6,7-tetrahydro-4-oxo-1-phenylpyrrolo[3,2,1-jk][1,4]benzodiazepin-3-yl]-

物理化學(xué)性質(zhì)

沸點(diǎn)773.2±60.0 °C(Predicted)
密度1.43±0.1 g/cm3(Predicted)
儲(chǔ)存條件-20°C儲(chǔ)存
溶解度DMSO : 125 mg/mL (314.52 mM)
酸度系數(shù)(pKa)11.27±0.40(Predicted)
形態(tài)Solid
顏色Light yellow to yellow

常見(jiàn)問(wèn)題列表

生物活性
CI-1044 是一種口服有效的 PDE4 抑制劑, 對(duì) PDE4A5,PDE4B2,PDE4C2 和 PDE4D3 的 IC50 值分別為 0.29, 0.08, 0.56, 0.09 μM。
靶點(diǎn)

PDE4A5

0.29 μM (IC 50 )

PDE4B2

0.08 μM (IC 50 )

PDE4C2

0.56 μM (IC 50 )

PDE4D3

0.09 μM (IC 50 )

體外研究

CI-1044 is an orally active PDE4 inhibitor with IC 50 s of 0.29, 0.08, 0.56, 0.09 μM for PDE4A5, PDE4B2, PDE4C2 and PDE4D3, respectively. CI-1044 selectively inhibits PDE4 crude extract from U937 cells with an IC 50 value of 0.27±0.02 μM being threefold more potent than rolipram (IC 50 =0.91±0.14) and tenfold less potent than cilomilast (IC 50 =0.026±0.007) in the same assay. In the presence of PDE4 inhibitors, the production of TNF-α is dose dependently decreased with mean IC 50 values from three separate experiments of 0.31±0.05, 0.26±0.05 and 0.11±0.01 μM, for CI-1044, cilomilast and rolipram, respectively.

體內(nèi)研究

TNF-α production is dose-dependently inhibited by CI-1044, rolipram and cilomilast with ID 50 s of 0.4, 1.4 and 1.6 mg/kg respectively following single oral administration. Following repeated administration with CI-1044, the ID 50 value represents 0.5 mg/kg p.o.. CI-1044 plasma levels increase proportionally with doses ranging between 0.1 and 40 mg/kg p.o. (R2=0.878). CI-1044 dose dependently inhibits the accumulation of eosinophils in Bronchoalveolar lavages (BAL) fluids with an ID 50 value of 3.25 mg/kg. A single dose treatment with CI-1044 (10 mg/kg, p.o.) 24, 8, 3 or 1 h before the antigen challenge induces 6, 56, 48 and 79% inhibition in the number of eosinophils in BAL.

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