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1445879-21-9

中文名稱 1445879-21-9
英文名稱 GSK2837808A
CAS 1445879-21-9
分子式 C31H25F2N5O7S
分子量 649.62
MOL 文件 1445879-21-9.mol
更新日期 2025/03/03 11:17:49
1445879-21-9 結(jié)構(gòu)式 1445879-21-9 結(jié)構(gòu)式

基本信息

中文別名
化合物GSK2837808A
乳酸脫氫酶A(LDHA)抑制劑(GSK2837808A)
英文別名
GSK2837808A
GSK 2837808A (GSK2837808A)
3-[[3-[(Cyclopropylamino)sulfonyl]-7-(2,4-dimethoxy-5-pyrimidinyl)-4-quinolinyl]amino]-5-(3,5-difluorophenoxy)benzoic acid
Benzoic acid, 3-[[3-[(cyclopropylamino)sulfonyl]-7-(2,4-dimethoxy-5-pyrimidinyl)-4-quinolinyl]amino]-5-(3,5-difluorophenoxy)-
所屬類別
有機原料:羧酸類化合物及衍生物

物理化學性質(zhì)

沸點783.5±70.0 °C(Predicted)
密度1.57±0.1 g/cm3(Predicted)
儲存條件-20°C儲存
溶解度溶于二甲基亞砜
酸度系數(shù)(pKa)3.81±0.10(Predicted)
形態(tài)結(jié)晶固體
顏色Light yellow to yellow

安全數(shù)據(jù)

危險性符號(GHS)GHS hazard pictograms
GHS07
警示詞警告
危險性描述H302-H315-H319-H335
1445879-21-9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-1006811445879-21-9
GSK2837808A
1445879-21-91 mg569元
2025/02/08HY-1006811445879-21-9
GSK2837808A
1445879-21-95mg1800元
2025/02/08HY-1006811445879-21-9
GSK2837808A
1445879-21-910mM * 1mLin DMSO2572元

常見問題列表

生物活性
GSK 2837808A 是一種選擇性的 LDHA (lactate dehydrogenase A) 的抑制劑,對hLDHA和hLDHB的IC50分別為2.6 nM和43 nM。
靶點
TargetValue
hLDHA
(Cell-free assay)
2.6 nM
hLDHB
(Cell-free assay)
43 nM
體外研究

GSK2837808A rapidly and profoundly inhibits lactate production rates in multiple cancer cell lines including hepatocellular and breast carcinomas. The potency of GSK2837808A across 30 cancer cell lines with different LDHA and LDHB expression levels ranges from 400 nM to no effect (EC 50 reported as 30 μM). GSK2837808A potency does not correlate with LDHA, LDHB, or the total LDH expression levels. GSK2837808A inhibits lactate production in hypoxia but at higher concentrations than in normoxia (EC 50 =10 μM). It also reduces ECAR with EC 50 =10 μM. LDH inhibition by GSK2837808A alters multiple metabolic pathways in Snu398 cells.

體內(nèi)研究

Clearance following IV infusion of GSK2837808A at 0.25 mg/kg is shown to be 69 mL/minute/kg in rats, which exceeds the animal liver blood flow. Oral dosing of GSK2837808A at 50 mg/kg in rats or 100 mg/kg in mice results in blood compound levels at or below the detection limit of 2.5 ng/mL.

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