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1-[4-(3-ethyl-7-morpholin-4-yltriazolo[4,5-d]pyrimidin-5-yl)phenyl]-3-[4-(4-methylpiperazine-1-carbonyl)phenyl]urea

1-[4-(3-ethyl-7-morpholin-4-yltriazolo[4,5-d]pyrimidin-5-yl)phenyl]-3-[4-(4-methylpiperazine-1-carbonyl)phenyl]urea

CAS號(hào) 1173204-81-3
規(guī)格 5mg10mg
純度 98%
貨號(hào) HY-10683
貨期 3天
品牌 Medchemexpress
庫(kù)存 ---
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參考價(jià): ¥1534.00 元/5mg
貨號(hào) 品牌 純度 規(guī)格 參考價(jià) 貨期
HY-10683 Medchemexpress 98% 5mg10mg ¥1534.00元/5mg 3天

產(chǎn)品詳情

詳細(xì)信息(中文):
PKI-402是PI3K/mTOR雙重抑制劑,對(duì)于PI3Kα、β、γ、δ和mTOR的IC50分別為2 nM、7 nM、16 nM、14 nM和3 nM。同時(shí)對(duì)PI3Kα的突變型E545K和H1047R也有一定的抑制性。
詳細(xì)信息(英文):
產(chǎn)品描述:PKI-402PKI-402 is a potent dual pan-PI3K/mTOR inhibitor targeting PI3Kα/β/γ/δ and mTOR with IC50 of 2 nM/7 nM/16 nM/14 nM and 3 nM, respectively; also potent to PI3Kα mutants E545K and H1047R._x000D_ IC50 value: 2 nM/7 nM/16 nM/14 nM(PI3Kα/β/γ/δ); 3 nM (mTOR) [1]_x000D_ Target: pan-PI3K/mTOR_x000D_ in vitro: PKI-402 inhibits E545K and H1047R PI3Kα mutants with IC50 of 3 nM. In a panel of 236 human protein kinases, PKI-402 only displays inhibitory activity against C-Raf and B-Raf with IC50 of 7 μM, and displays little activity against all other kinases with IC50 of > 10 μM. PKI-402 inhibits the growth of human tumor cell lines with IC50 of 6-349 nM. Consistently, PKI-402 inhibits phosphorylation of PI3K and mTOR effector proteins, particularly phosphorylated Akt (p-Akt) at T308 and S473 with IC50 of

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英文名 1-[4-(3-ethyl-7-morpholin-4-yltriazolo[4,5-d]pyrimidin-5-yl)phenyl]-3-[4-(4-methylpiperazine-1-carbonyl)phenyl]urea
中文名 1-[4-(3-ethyl-7-morpholin-4-yltriazolo[4,5-d]pyrimidin-5-yl)phenyl]-3-[4-(4-methylpiperazine-1-carbonyl)phenyl]urea
CAS號(hào) 1173204-81-3 溶解性 ---
分子量 570.64500 熔點(diǎn) ---
密度 --- 沸點(diǎn) ---

商家信息

上海皓元生物醫(yī)藥科技有限公司

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  • 公司類型:研發(fā)型
  • 成立時(shí)間:2009-03-17
  • 所在地區(qū):上海市市轄區(qū)
  • 注冊(cè)資本:300萬(wàn)元
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產(chǎn)品:1-[4-(3-ethyl-7-morpholin-4-yltriazolo[4,5-d]pyrimidin-5-yl)phenyl]-3-[4-(4-methylpiperazine-1-carbonyl)phenyl]urea