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BAY 2666605
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
BAY 2666605图片
CAS NO:2275774-60-0
包装与价格:
包装价格(元)
1 mg询价
5 mg询价
10 mg询价
25 mg询价
50 mg询价
100 mg询价
1 mL*10 mM(in DMSO)询价

BAY 2666605 是一种具有口服活性的 PDE3A 和 PDE3B 抑制剂,IC50 分别为 87 nM 和 50 nM。 BAY 2666605 具有抗癌作用。

产品描述

BAY 2666605 is an orally active inhibitor of PDE3A and PDE3B with IC50s of 87 nM and 50 nM, respectively. BAY 2666605 has anticancer effects.

体外活性

BAY 2666605 inhibits brain cancer(glioma, more specifically glioblastoma, astrocytoma), breast cancer (ductal carcinoma and adenocarcinoma), cervical cancer, AML(erythroleukemia), lung cancer(NSCLC adenocarcinoma and SCLC), skin cancer(melanoma), esophagus cancer (squamous cell carcinoma), ovarian cancer, (teratocarcinoma, adenocarcinoma), pancreas cancer and prostatic cancer[1].

体内活性

In murine xenotransplantation models of human cancer, BAY 2666605 (5 mg/kg; p.o) exhibits anti-tumor efficacy[1].

Cas No.

2275774-60-0

分子式

C17H12F4N2O2

分子量

352.28

储存和溶解度

DMSO:245 mg/mL (695.47 mM),Need ultrasonic
Powder: -20°C for 3 years
In solvent: -80°C for 2 years
 
 
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