1378872-36-6
中文名稱
(2,4,6-Trichloro-phenoxy)-acetic acid (1H-pyrrol-2-ylmethylene)-hydrazide
英文名稱
(2,4,6-Trichloro-phenoxy)-acetic acid (1H-pyrrol-2-ylmethylene)-hydrazide
CAS
1378872-36-6
分子式
C13H10Cl3N3O2
分子量
346.6
MOL 文件
1378872-36-6.mol
更新日期
2023/03/20 15:41:19
1378872-36-6 結(jié)構(gòu)式
基本信息
中文別名
化合物ML239(E)-N'-((1H-吡咯-2-基)亞甲基)-2-(2,4,6-三氯苯氧基)乙酰肼
英文別名
ML239CID49843203
CID 49843203
CID-49843203
CID-49843203
ML 239
NVEDPFICKAIHKD-NGYBGAFCSA-N
CID-49843203
CID 49843203
CID49843203
ML-239
ML 239
ML239
1378872-36-6
(2,4,6-Trichloro-phenoxy)-acetic acid (1H-pyrrol-2-ylmethylene)-hydrazide
N'-[(E)-1H-Pyrrol-2-ylmethylene]-2-(2,4,6-trichlorophenoxy)acetoh ydrazide
(E)-N'-((1H-pyrrol-2-yl)methylene)-2-(2,4,6-trichlorophenoxy)acetohydrazide
物理化學(xué)性質(zhì)
密度1.50±0.1 g/cm3(Predicted)
儲(chǔ)存條件Inert atmosphere,2-8°C
溶解度在DMSO中的溶解度為15mg/mL(澄清溶液)
酸度系數(shù)(pKa)11.95±0.46(Predicted)
形態(tài)粉末
顏色白色至米色
穩(wěn)定性DMSO、DMF或乙醇中的溶液可在-20°下穩(wěn)定儲(chǔ)存3個(gè)月。
安全數(shù)據(jù)
警示詞警告
危險(xiǎn)性描述H302+H312+H332-H315-H319-H335-H400
危險(xiǎn)品標(biāo)志Xn
危險(xiǎn)類別碼20/21/22-36/37/38
安全說明26
危險(xiǎn)品運(yùn)輸編號(hào)UN 3077 9 / PGIII
WGK Germany3
ML239價(jià)格(試劑級(jí))
報(bào)價(jià)日期 | 產(chǎn)品編號(hào) | 產(chǎn)品名稱 | CAS號(hào) | 包裝 | 價(jià)格 |
2024/11/08 | HY-19971 | (2,4,6-Trichloro-phenoxy)-acetic acid (1H-pyrrol-2-ylmethylene)-hydrazide ML239 | 1378872-36-6 | 5mg | 550元 |
2024/11/08 | HY-19971 | (2,4,6-Trichloro-phenoxy)-acetic acid (1H-pyrrol-2-ylmethylene)-hydrazide ML239 | 1378872-36-6 | 10mM * 1mLin DMSO | 620元 |
2024/11/08 | HY-19971 | (2,4,6-Trichloro-phenoxy)-acetic acid (1H-pyrrol-2-ylmethylene)-hydrazide ML239 | 1378872-36-6 | 10mg | 900元 |
常見問題列表
生物活性
ML239 是一種有效的選擇性的乳腺癌腫瘤干細(xì)胞抑制劑,C50 值為 1.16 μM。體外研究
ML239 (Compound 7j) is a potent and selective inhibitor of breast cancer stem cells, with an IC 50 of 1.16 μM, with ~24-fold selectivity against the control cell line. ML239 inhibits breast cancer stem-like cells, most likely through activation of fatty acid desaturase 2 (FADS2). ML239 is cytotoxic to NCIH661 cells, and FADS2 knockdown reduces ML239 cytotoxicity, and furthermore, FADS2 inhibitor SC-26196 also reduces ML239 cytotoxicity in cancer cell lines (CCLs).