首页 工具
登录
购物车

搜索结果

Search Results for " du-145 "

6

抑制剂 & 化合物

4

天然产物

如果没找到您满意的产品或者您对产品有其他要求,可以联系我们专业顾问为您提供针对性的合理建议。     QQ咨询       网站留言咨询

提交您的定制咨询

点击图片重新获取验证码
Cat. No. Product Name Target Signaling Pathways
T27998 MDK-4204

Anticancer AgentI,MDK 4204,Anticancer Agent I,MDK4204,Anticancer Agent-I

MDK-4204, an anticancer agent, shows significant anti-cancer activity with IC50 values of 8.8 µM and 9.5 µM in PC-3 and DU-145 cells, respectively.
T63391 Calpain Inhibitor-2

Calpain Inhibitor-2 是具有亲脂性的钙蛋白酶抑制剂,与黑色素瘤细胞系(A-375和B-16F1)和PC-3前列腺癌细胞相比,他们在体外具有中等到良好的抗增殖效果。Calpain Inhibitor-2 中的化合物3,在基质胶细胞侵袭测定中以2μM 浓度能够抑制了80%的DU-145细胞侵袭。
T67909 TAK1 inhibitor

compound 13a

Topoisomerase DNA Damage/DNA Repair
TAK1 inhibitor 是一种抑制剂,对MCF-7、A549 、DU-145 、MDA MB-231有抑制作用,IC50分别为 0.021、0.14、0.064 、0.19 。化合物13 具有较好的抑菌活性,麦克风范围为93.7 ~ 46.9μg / mL,麦克风范围为7.8 ~ 5.8μg / mL。
T64157 OXi8007

OXi8007 是一种水溶性磷酸盐,是 OXi8006(一种微管蛋白结合化合物)的前药。OXi8007 是一种具有潜在抗癌活性的血管破坏剂。它被发现对DU-145肿瘤细胞系具有强烈的细胞毒性,它也被证明了对肿瘤血管系统的显著干扰。
T70222 Ethonafide

Ethonafide is an anthracene-containing derivative of amonafide that belongs to the azonafide series of anticancer agents. The lack of cross-resistance in multidrug-resistant cancer cell lines and the absence of a quinone and hydroquinone moiety make ethonafide a potentially less cardiotoxic replacement for existing anthracene-containing anticancer agents. Ethonafide was cytotoxic against three human prostate cancer cell lines at nanomolar concentrations. Ethonafide was found to be better tolerat...
T71252 PC-046

PC-046 is a potent tubulin-binding agent, which was originally identified for development based on selective activity in deleted in pancreas cancer locus 4 (DPC4/SMAD4) deficient tumors. PC-046 has growth inhibitory activity in a variety of tumor types in vitro, and efficacy in SCID mice was shown in human tumor xenografts of MV-4-11 acute myeloid leukemia, MM.1S multiple myeloma, and DU-145 prostate cancer. Pharmacokinetic studies demonstrated relatively high oral bioavailability (71 %) with di...

化合物

MDK-4204
Cat.No: T27998
Synonym: Anticancer AgentI,MDK 4204,Anticancer Agent I,MDK4204,Anticancer Agent-I
Target:
Calpain Inhibitor-2
Cat.No: T63391
Synonym:
Target:
TAK1 inhibitor
Cat.No: T67909
Synonym: compound 13a
Target: Topoisomerase
OXi8007
Cat.No: T64157
Synonym:
Target:
Ethonafide
Cat.No: T70222
Synonym:
Target:
PC-046
Cat.No: T71252
Synonym:
Target:
Cat. No. Product Name Target Signaling Pathways
T2S1158 4,5-Dicaffeoylquinic acid

3,4-Dicaffeoylquinic acid,异绿原酸C(4,5),Isochlorogenic acid C

Others; HBV; Endogenous Metabolite Metabolism; Microbiology/Virology; Others
4,5-Dicaffeoylquinic acid (Isochlorogenic acid C) 是一种天然产物,有抗病毒、抗肝毒性活性。
TN4963 Scillascillin

Others Others
Scillascillin has anticancer activity, it is significantly active against human cancer cell lines MCF-7 (breast cancer) and DU-145 (prostate cancer) with inhibitory concentration (IC)50 values 9.59 and 11.32 ug/ml respectively.
TMA1841 Dihydrodaidzin

Others Others
Dihydrodaidzin shows cytotoxic activities against human stomach carcinoma (Hs 740.T, Hs 756 T), breast adenocarcinoma (Hs 578 T, Hs 742.T), and prostate carcinoma (DU 145, LNCaP-FGC) cell lines.
T1174 Topotecan hydrochloride

SKF 104864A,SKFS 104864A,NSC609699,Nogitecan HCl,NSC 609669,盐酸拓扑替康,Topotecan HCl

Apoptosis; Topoisomerase; Autophagy Apoptosis; Autophagy; DNA Damage/DNA Repair
Topotecan hydrochloride (NSC609699) 是一种具有抗癌活性的拓扑异构酶I 抑制剂。

天然产物

4,5-Dicaffeoylquinic acid
Cat.No: T2S1158
Synonym: 3,4-Dicaffeoylquinic acid,异绿原酸C(4,5),Isochlorogenic acid C
Target: Others, HBV, Endogenous Metabolite
Scillascillin
Cat.No: TN4963
Synonym:
Target: Others
Dihydrodaidzin
Cat.No: TMA1841
Synonym:
Target: Others
Topotecan hydrochloride
Cat.No: T1174
Synonym: SKF 104864A,SKFS 104864A,NSC609699,Nogitecan HCl,NSC 609669,盐酸拓扑替康,Topotecan HCl
Target: Apoptosis, Topoisomerase, Autophagy
TargetMol Loading
联系我们
400-820-0310

上海市静安区江场三路238号8楼