貨號(hào)	規(guī)格	價(jià)格	上海	北京	武漢	南京
S82582-5mg	99.8%	￥1020.00 S82582-5mg ￥1020.00 現(xiàn)貨	5 5	-	-	-
S82582-10mg	99.8%	￥1700.00 S82582-10mg ￥1700.00 現(xiàn)貨	5 5	-	-	-
S82582-25mg	99.8%	￥3400.00 S82582-25mg ￥3400.00 現(xiàn)貨	5 5	-	-	-
S82582-100mg	≥98%	￥10200.00 S82582-100mg ￥10200.00 2-3天	0 貨期：2-3天	-	-	-

產(chǎn)品介紹

ETP-46321 is an effective and orally bioavailable PI3Kα/PI3Kδ inhibitor (Ki: 2.3/14.2 nM).

產(chǎn)品描述：

ETP-46321 is an effective and orally bioavailable PI3Kα/PI3Kδ inhibitor (Ki: 2.3/14.2 nM).

靶點(diǎn)：

PI3K

體外研究：

ETP-4632 has been profiled and shown to be a potent PI3K α and δ inhibitor, highly selective versus mTOR and 288 representative kinases. ETP-46321 is also tested against three of the p110α mutant enzymes detected in human cancers (E542K, E545K, and H1047R), being equipotent against these mutants when compared to the wild type protein (Kiapp=2.33, 1.77 and 1.89 nM for PI3Kα-H1047R, PI3Kα-E545K and PI3Kα-E542K, respectively). ETP-46321 inhibits the phosphorylation of AKT in the U2OS cell line (IC50: 8.3 nM).

體內(nèi)研究：

ETP-46321, is selected for in vivo studies based on its appealing pharmacokinetic profile in BALB-C mice, low in vivo Clearance (0.6 L/h/Kg) and good oral bioavailability (90%). ETP-46321 demonstrates a good pharmacokinetic profile in mice and is selected for preliminary in vivo evaluation in a lung tumor mouse model driven by a K-RasG12V oncogenic mutation, showing significant tumor growth inhibition

動(dòng)物實(shí)驗(yàn)：

BALB/C mice are treated daily with ETP-46321 (50 mg/kg, p.o.) for three weeks. Tumor volumes of four mice in each treatment group are measured and compared to the starting volume at the beginning of the treatment.

參考文獻(xiàn)：

1. Mart?-nez Gonz??lez S, Hern??ndez AI, Varela C, Rodr?-guez-Ar?-stegui S, Lorenzo M, Rodr?-guez A, Rivero V, Mart?-n JI, Saluste CG, Ramos-Lima F, Cend?3n E, Cebri??n D, Aguirre E, Gomez-Casero E, Albarr??n M, Alfonso P, Garc?-a-Serelde B, Oyarzabal J, Rabal O, Mulero F, Gonzalez-Granda T, Link W, Fominaya J, Barbacid M, Bischoff JR, Pizcueta P, Pastor J. Identification of ETP-46321, a potent and orally bioavailable PI3K α, δ inhibitor. Bioorg Med Chem Lett. 2012 May 15;22(10):3460-6.

溶解性：

Soluble in DMSO

保存條件：

-20℃

配置溶液濃度參考：

	1mg	5mg	10mg
1 mM	2.112 ml	10.559 ml	21.117 ml
5 mM	0.422 ml	2.112 ml	4.223 ml
10 mM	0.211 ml	1.056 ml	2.112 ml
50 mM	0.042 ml	0.211 ml	0.422 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權(quán)威性，僅供客戶參考交流研究之用。

參考文獻(xiàn)

質(zhì)檢證書(COA)

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