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 HY-13020 GSK1838705A的機(jī)制（別名GSK1838705A）：ALK

技術(shù)參數(shù)：價(jià)格和可用性

M.Wt：532.57

分子式：C27H29FN8O3

純度：> 98％

貯存：貯存在-20℃2年

CAS號(hào)：1116235-97-2

溶解性：DMSO≥107mg/mL;水濃度為1mg/mL;乙醇濃度為1mg/mL

生物活性的：

     是一種有效的小分子IGF-IR，胰島素受體和間變性淋巴瘤激酶（ALK）抑制劑的IC50分別為2.0，1.6和0.5海里。 防止來(lái)自固體和惡性血液病，包括多發(fā)性骨髓瘤，尤因氏肉瘤，并阻礙在體內(nèi)生長(zhǎng)的人類(lèi)腫瘤異種移植的細(xì)胞系在體外增殖。盡管胰島素受體的抑制作用，對(duì)葡萄糖穩(wěn)態(tài)的影響zui小，得到在有效劑量。在0.1和0.3毫克/公斤口服單劑量的導(dǎo)致到35％和65％的預(yù)防，IGF-IR的磷酸化，分別，而劑量≥1毫克/公斤，導(dǎo)致完成的配體誘導(dǎo)的IGF-IR的磷酸化的抑制。同時(shí)，在30毫克/公斤的劑量，預(yù)防持續(xù)？化合物注射后的24小時(shí)。 也抑制了間變性淋巴瘤激酶（ALK），介導(dǎo)的異常??增長(zhǎng)的間變性大細(xì)胞淋巴瘤，神經(jīng)母細(xì)胞瘤，非小細(xì)胞肺癌的一個(gè)子集。由于其抑制ALK中，提供了良好的耐受劑量在體內(nèi)引起的ALK-依賴(lài)性腫瘤*消退。

HY-13020   (Synonyms  GSK 1838705A)  Mechanisms:ALK 
Technical Data: Price and Availability of   
M.Wt: 532.57
Formula: C27H29FN8O3
Purity: >98%
Storage: at -20℃ 2 years
CAS No.: 1116235-97-2
Solubility: DMSO ≥107mg/mL; Water <1mg/mL; Ethanol <1mg/mL     
5mg
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200mg
Biological Activity of : 
is a potent small-molecule IGF-IR, the insulin receptor and anaplastic lymphoma kinase (ALK) inhibitor with IC50 of 2.0, 1.6 and 0.5 nM, respectively. prevents the in vitro proliferation of cell lines derived from solid and hematologic malignancies, including multiple myeloma and Ewing’s sarcoma, and retards the growth of human tumor xenografts in vivo. Despite the inhibitory effect of on insulin receptor, minimal effects on glucose homeostasis were obtained at efficacious doses. A single oral dose of at 0.1 and 0.3 mg/kg led to 35% and 65% prevention of IGF-IR phosphorylation, respectively, whereas doses ≥1 mg/kg led to complete inhibition of ligand-induced IGF-IR phosphorylation. Meanwhile, at a dose of 30 mg/kg, prevention was lasted for ?24 hours after compound injection. also suppresses the anaplastic lymphoma kinase (ALK), which mediates the aberrant growth of anaplastic large-cell lymphomas, some neuroblastomas, and a subset of non–small cell lung cancers. Due to its inhibition of ALK, gives rise to complete regression of ALK-dependent tumors in vivo at well-tolerated doses