上海源葉生物科技有限公司

主營產(chǎn)品: S30260異硫氰酸胍,30259鹽酸胍,嗜熱菌蛋白酶

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15921386130

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聯(lián)人:
何小姐
話:
86-021-61559134
機:
15921386130
真:
86-021-55068248
址:
上海市松江區(qū)長塔路465號6幢
編:
200433
網(wǎng)址:
www.shyuanye.com
鋪:
http://true-witness.com/st191837/
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S80040
S80040
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更新時間:2024-07-02 20:14:56瀏覽次數(shù):145

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【簡單介紹】
提示:詳情請下載說明書
  • 提示:詳情請下載說明書。
  • 靶點: Apitolisib (GDC-0980; GNE 390; RG 7422) is a selective, potent, orally bioavailable Class I PI3 kinase and mTOR kinase (TORC1/2)
  • 體外研究: Apitolisib (GDC-0980) is remarkably selective for several other members of the closely related PIKK family kinases: C2alpha IC50=1300 nM; C2beta IC50=7 94 nM; VPS34 IC50=2000 nM; PI4Kalpha >10 μM; PI4Kbeta >10 μM; DNA-PK Kiapp=623 nM, respectively. A recent study shows that Apitolisib (GDC-0980) reduces cancer cell viability by inhibiting cell-cycle procession and inducing apoptosis with most potency in prostate (IC50 < 200="" nm="" 50%),=""><500 nm="" 100%),="" breast="" (ic50=""><200 nm="" 37%,=""><500 nm="" 78%)="" and="" nsclc="" lines="" (ic50=""><200 nm="" 29%,=""><500 nm="" 88%)="" and="" less="" potency="" in="" pancreatic="" (ic50=""><200 nm="" 13%,=""><500 nm="" 67%)="" and="" melanoma="" cell="" lines="" (ic50=""><200 nm="" 0%,=""><500 nm="" 33%).="">
  • 體內(nèi)研究: Apitolisib (GDC-0980) (1 mg/kg, p.o.) demonstrats significant efficacy in mouse xenografts and is currently in phase I clinical trials for cancer. Clearance and PPB are low, and Apitolisib (GDC-0980) shows dose-proportional exposure from 5 mg/kg dosed in PEG to 50 mg/kg dosed in suspension in MCT, a finding attributed partially to the compound’s good solubility. Apitolisib (GDC-0980) (5 mg/kg, p.o.) results in greater than 50% TGI in 15 of the 20 xenograft models. The difference in tumor response to Apitolisib (GDC-0980) treatment correlates with the duration of knockdown of pAkt/tAkt.
  • 參考文獻:
    [1]. Sutherlin DP, et al. Discovery of a potent, selective, and orally available class I phosphatidylinositol 3-kinase (PI3K)/mammalian target of rapamycin (mTOR) kinase inhibitor (GDC-0980) for the treatment of cancer. J Med Chem, 2011, 54(21), 7579-7587.

    [2]. Wallin JJ, et al. GDC-0980 is a novel class I PI3K/mTOR kinase inhibitor with robust activity in cancer models driven by the PI3K pathway. Mol Cancer Ther, 2011, 10(12), 2426-2436.
  • 溶解度: soluble  in  DMSO
  • 保存條件: -20℃
  • 配置溶液濃度參考:
    1mg 5mg 10mg
    1 mM 2.006 ml 10.028 ml 20.056 ml
    5 mM 0.401 ml 2.006 ml 4.011 ml
    10 mM 0.201 ml 1.003 ml 2.006 ml
    50 mM 0.04 ml 0.201 ml 0.401 ml
  • 注意:部分產(chǎn)品我司僅能提供部分信息,我司不保證所提供信息的性,僅供客戶參考交流研究之用。
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