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Merck
CN

SML3681

Sigma-Aldrich

ATM-3507

≥95% (HPLC)

别名:

ATM 3507, [3-​[[2,​3-​Dimethyl-​1-​[3-​(4-​methyl-​1-​piperazinyl)​propyl]​-​1H-​indol-​5-​yl]​oxy]​phenyl]​[4-​[2-​(4-​fluorophenyl)​ethyl]​-​1-​piperazinyl]​-methanone

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About This Item

经验公式(希尔记法):
C37H46FN5O2
分子量:
611.79
MDL编号:
UNSPSC代码:
12352200
NACRES:
NA.77

质量水平

方案

≥95% (HPLC)

表单

powder

颜色

, Colorless to light brown

溶解性

DMSO: 2 mg/mL, clear

储存温度

-10 to -25°C

生化/生理作用

ATM-3507 is a potent anti-tropomyosin agent that disables Tpm3.1 containing actin filaments. It exhibits potent cytotoxic activity against multiple neuroblastoma cancer cell lines. ATM-3507 sensitizes cancer cells to anti-microtubule agents. ATM-3507 significantly prolonged mitotic arrest induced by anti-microtubule agent vinorelbine.
Potent anti-tropomyosin agent that disables Tpm3.1 containing actin filaments

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

新产品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Identification of Cancer-Targeted Tropomyosin Inhibitors and Their Synergy with Microtubule Drugs
Molecular Cancer Therapeutics, 16(8), 1555-1565 (2017)
Molecular integration of the anti-tropomyosin compound ATM-3507 into the coiled coil overlap region of the cancer-associated Tpm3.1
Scientific Reports, 9(1), 11262-11262 (2019)
Xing Xu et al.
British journal of cancer, 125(2), 265-276 (2021-05-14)
Anti-microtubule agents are widely used to treat ovarian cancers, but the efficacy is often compromised by drug resistance. We investigated co-targeting the actin/tropomyosin cytoskeleton and microtubules to increase treatment efficacy in ovarian cancers and potentially overcome resistance. The presence of

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