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321688-88-4

中文名稱 2-甲基-5-(1-甲基乙基)-2,5-環(huán)己二烯-1,4-二酮 1-[O-(2-甲基苯甲酰)肟]
英文名稱 2-Methyl-5-(1-methylethyl)-2,5-cyclohexadiene-1,4-dione 1-[O-(2-methylbenzoyl)oxime]
CAS 321688-88-4
分子式 C18H19NO3
分子量 297.35
MOL 文件 321688-88-4.mol
更新日期 2025/02/05 11:34:51
321688-88-4 結(jié)構(gòu)式 321688-88-4 結(jié)構(gòu)式

基本信息

中文別名
POLO-LIKE KINASE1(PLK1)抑制劑(POLOXIN)
2-甲基-5-(1-甲基乙基)-2,5-環(huán)己二烯-1,4-二酮 1-[O-(2-甲基苯甲酰)肟]
英文別名
Poloxin
Polo-like Kinase Inhibitor V, Poloxin
Polo-like Kinase Inhibitor V, Poloxin - CAS 321688-88-4 - Calbiochem
(Z)-2-Isopropyl-5-methyl-4-(((2-methylbenzoyl)oxy)imino)cyclohexa-2,5-dienone
2-Methyl-5-(1-methylethyl)-1-[O-(2-methylbenzoyl)oxime]-2,5-Cyclohexadiene-1,4-dione
2-Methyl-5-(1-methylethyl)-2,5-cyclohexadiene-1,4-dione 1-[O-(2-methylbenzoyl)oxime]
2,5-Cyclohexadiene-1,4-dione, 2-methyl-5-(1-methylethyl)-, 1-[O-(2-methylbenzoyl)oxime]
所屬類別
生物化工:激動劑抑制劑

物理化學性質(zhì)

沸點418.6±55.0 °C(Predicted)
密度1.11
儲存條件2-8°C
溶解度DMSO:可溶5mg/mL(透明溶液,加熱)
形態(tài)黃色固體
顏色白色至米色

安全數(shù)據(jù)

危險性符號(GHS)GHS hazard pictogramsGHS hazard pictograms
GHS07,GHS09
警示詞警告
危險性描述H317-H400
防范說明P273-P280
危險品標志Xi,N
危險類別碼43-50
安全說明36/37-61
危險品運輸編號UN 3077 9 / PGIII
WGK Germany3
2-甲基-5-(1-甲基乙基)-2,5-環(huán)己二烯-1,4-二酮 1-[O-(2-甲基苯甲酰)肟]價格(試劑級)
報價日期產(chǎn)品編號產(chǎn)品名稱CAS號包裝價格
2025/02/08HY-121342-甲基-5-(1-甲基乙基)-2,5-環(huán)己二烯-1,4-二酮 1-[O-(2-甲基苯甲酰)肟]
Poloxin
321688-88-45 mg360元
2025/02/08HY-121342-甲基-5-(1-甲基乙基)-2,5-環(huán)己二烯-1,4-二酮 1-[O-(2-甲基苯甲酰)肟]
Poloxin
321688-88-410 mg577元
2025/02/08HY-121342-甲基-5-(1-甲基乙基)-2,5-環(huán)己二烯-1,4-二酮 1-[O-(2-甲基苯甲酰)肟]
Poloxin
321688-88-410mM * 1mLin DMSO635元

常見問題列表

生物活性
Poloxin 是一種 Polo-like Kinase 1 (PLK1) 的 ATP 非競爭性抑制劑,靶作用于 polo-box 結(jié)構(gòu)域,IC50 值約為 4.8 μM。
靶點

PLK1 PBD

4.8 μM (IC 50 )

PLK2 PBD

18.7 μM (IC 50 )

PLK3 PBD

53.9 μM (IC 50 )

體外研究

Poloxin (25 μM) induces defects in centrosome integrity, spindle formation, and chromosome alignment in mitosis. Centrosomal fragmentation induced by Poloxin is partially rescued by Kiz T379E. Poloxin (25 μM) activates the mitotic checkpoint, induces apoptosis and inhibits proliferation of MDA-MB-231 cells. Poloxin inhibits proliferation in both cell lines with a comparable efficiency through 72 h period. Poloxin inhibits the polo-box domain (PBD) interaction with an apparent IC 50 of ~4.8 μM. Poloxin exhibits a loose Plk1 PBD specificity with 4-10 times higher IC 50 values for Plk2 and Plk3, and does not significantly inhibit other types of phosphopeptide-binding domains such as FHA, WW, and SH2 domains.

體內(nèi)研究

Poloxin (40 mg/kg) decreases the proliferation of MDA-MB-231 cells, and surpresses the growth of the tumor nude mice bearing established xenografts of MDA-MB-231.

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