托法替尼 Tofacitinib

交易须知
tofacitinib产品活性:tofacitinib是 jak1/2/3 抑制剂,ic50 分别为1,20 和 112 nm。
研究领域:epigenetics  |  stem cell/wnt  |  jak/stat signaling
作用靶点:jak
in vitro: tofacitinib (cp-690550) citrate binds potentially at jak3 and jak2 as 2.2 nm and 5 nm (kd). the report includes additional binding for tofacitinib at camk1 (kd of 5,000 nm), dcamkl3 (kd of 4.5 nm), mst2 (kd of 4,300 nm), pkn1 (kd of 200 nm), rps6ka2 (kin.dom.2-c-terminal) (kd of 1,400 nm), rps6ka6 (kin.dom.2-c-terminal) (kd of 1,200 nm), snark (kd of 420 nm), tnk1 (kd of 640 nm) and tyk2 (kd of 620 nm).
in vivo: animals that are treated with tofacitinib show a significantly lower production of anti-drug antibodies (adas) compare with peg-treated control mice (for five weeks after initial immunization, p<0.01, n=8). moreover adas become detectable earliest on day 28. a difference of 1000- to 200-fold in titers to ss1p is apparent from days 21 through 35, respectively. compare to ss1p, mice injected with keyhole limpet hemocyanin (klh) generate a more rapid antibody response. yet, the administration of tofacitinib reduces anti-klh titers compare to controls (p<0.05 on day 21, p4 hours.
相关产品:fda-approved drug library plus  |  drug repurposing compound library  |  fda-approved drug library mini  |  kinase inhibitor library  |  jak/stat compound library  |  stem cell signaling compound library  |  fda-approved drug library  |  drug repurposing compound library plus  |  epigenetics compound library  |  bioactive compound library plus  |  ruxolitinib  |  baricitinib  |  upadacitinib  |  tofacitinib citrate  |  momelotinib  |  pacritinib  |  chz868  |  azd-1480  |  at9283  |  filgotinib  |  wp1066  |  itacitinib  |  sb1317  |  cerdulatinib  |  tyk2-in-4  |  gandotinib  |  cucurbitacin i  |  pyridone 6  |  peficitinib  |  delgocitinib  |  solcitinib  |  rgb-286638 free base  |  atractylenolide i  |  pf-06651600  |  cep-33779  |  decernotinib  |  tg101209  |  az960

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托法替尼 Tofacitinib
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