Adaphostin

Discontinued Product

3716 has been discontinued.

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说明: p210bcr/abl kinase inhibitor
别名: NSC 680410
化学名: 4-[[(2,5-Dihydroxyphenyl)methyl]amino]benzoic acid tricyclo[3.3.1.13,7]dec-1-yl ester
纯度: ≥98% (HPLC)
说明书
引用文献 (1)
评论

生物活性 for Adaphostin

p210bcr/abl tyrosine kinase inhibitor (IC50 = 14 μM). Induces apoptosis in T-lymphoblastic human leukemia cell lines (IC50 values range from 16.8 to 216.3 nM) in vitro. Displays selectivity for chronic myelogenous leukemia (CML) myeloid progenitors in vitro.

技术数据 for Adaphostin

分子量 393.48
公式 C24H27NO4
储存 Desiccate at +4°C
纯度 ≥98% (HPLC)
CAS Number 241127-58-2
PubChem ID 387042
InChI Key YJZSUCFGHXQWDM-UHFFFAOYSA-N
Smiles O=C(C4=CC=C(NCC5=C(O)C=CC(O)=C5)C=C4)OC12CC(C3)CC(CC3C2)C1

上方提供的技术数据仅供参考。批次相关数据请参见分析证书。

Tocris products are intended for laboratory research use only, unless stated otherwise.

参考文献 for Adaphostin

参考文献是支持产品生物活性的出版物。

Svingen et al (2000) Effects of the bcl/abl kinase inhibitors AG957 and NSC 680410 on chronic myelogenous leukemia cells in vitro. Clin.Cancer Res. 6 237 PMID: 10656455

Avramis et al (2002) In vitro and in vivo evaluations of the tyrosine kinase inhibitor NSC 680410 against human leukemia and glioblastoma cell lines. Cancer Chemother.Pharmacol. 50 479 PMID: 12451475

Mow et al (2002) Effects of bcr/abl kinase inhibitors STI571 and adaphostin (NSC 680410) on chronic myelogenous leukemia cells in vitro. Blood 99 664 PMID: 11781252

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关键词: Adaphostin, Adaphostin supplier, p210bcr/abl, kinases, inhibitors, inhibits, chronic, myelogenous, leukaemia, leukemia, CML, NSC680410, NSC, 680410, Abl, Kinase, 3716, Tocris Bioscience

1 篇 Adaphostin 的引用文献

引用文献是使用了 Tocris 产品的出版物。 Adaphostin 的部分引用包括:

Xia et al (2014) EZH2 silencing with RNA interference induces G2/M arrest in human lung cancer cells in vitro. Biomed Res Int 2014 348728 PMID: 24745014


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