首页 工具
登录
购物车

搜索结果

Search Results for " hct-8 "

8

抑制剂 & 化合物

8

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
T69172 Acetomycin

Acetomycin is a γ-lactone microbial metabolite originally isolated from S. ramulosus that has anticancer activity. It inhibits proliferation of HCT-8 human colon and L1210 mouse leukemia cancer cells.
T63470 PI3K/mTOR Inhibitor-8

PI3K/mTOR Inhibitor-8 是 PI3K (PI3Kα IC50: 0.46 nM) 和 mTOR (mTOR IC50: 12 nM) 双重抑制剂。PI3K/mTOR Inhibitor-8 能够将 HCT-116 细胞的细胞周期阻滞在G1/S 期,并诱导其凋亡 (apoptosis)。
T60727 B-Raf IN 8

B-Raf IN 8 (compound 7g) 是 B-Raf 的有效抑制剂 (IC50 = 70.65 nM)。B-Raf IN 8 显示出抗肿瘤活性,其对肝细胞癌 (HEPG-2)、结肠癌 (HCT-116),乳腺癌 (MCF-7) 和人前列腺癌 (PC-3) 细胞的 IC50值分别为9.78、13.78、18.52 和 29.85 μM。
T74627 Angiogenesis inhibitor 3

Angiogenesis inhibitor 3 (compound 8) 是一种有效的血管生成(angiogenesis)抑制剂,能够抑制HUVEC和HCT-15细胞增殖,其IC50值分别为1.00和0.71 μM。此外,此化合物还能诱导这两种细胞的凋亡(apoptosis)并具有抑制癌细胞侵袭的抗癌活性。Angiogenesis inhibitor 3还能够抑制斑马鱼胚胎的血管生成。
T83887 SLU-10482

SLU-10482是一种抗寄生虫化合物,能减少HCT-8细胞中C. parvum寄生虫的数量(EC50 = 0.07 µM)。相较于另一种抗寄生虫化合物SLU-2633,SLU-10482与人类ether-a-go-go (hERG; Kd = 43 µM)的结合能力较弱。在体内,SLU-10482以5和15 mg/kg的剂量,每天两次给药,能减少C. parvum感染小鼠模型中粪便中卵囊的数量。
T81446 PKM2 activator 6

PKM2 activator 6 (Compound Z10) 作为一种PKM2激活剂同时抑制PDK1,其KD值分别为121 μM和19.6 μM。该化合物诱导结直肠细胞发生凋亡,并显著抑制细胞增殖与迁移。通过抑制糖酵解作用,PKM2 activator 6降低DLD-1、HCT-8、HT-29、MCF-10A细胞的增殖,IC50值分别为10.04、2.16、3.57、66.39 μM。
T78780 Anticancer agent 139

Anticanceragent 139(Compound 6h)展现了针对多种癌细胞株的抗癌效能。该化合物能够与Tubulin的Lys352残基发生π-阳离子相互作用。在对SNB-19、OVCAR-8和NCI-H460细胞株的测试中,Anticanceragent 139展现出较高的生长抑制率(PGI),数值分别为86.61、85.26和75.99。同时,该化合物对于HOP-62、SNB-75、ACHN、NCI/ADR-RES、786-O、A549/ATCC、HCT-116以及MDA-MB-231细胞株亦表现出中等的生长抑制作用,其PGI值分别为67.55、65.46、59.09、59.02、57.88、56.88、56.53和56.4、51.88
T35696 Olomoucine II

Olomoucine II is an inhibitor of cyclin-dependent kinases (CDKs; IC50s = 7.6, 0.1, 19.8, 0.45, and 0.06 μM for Cdk1, -2, -4, -7, and -9, respectively).1It is selective for CDKs over 10 additional kinases (IC50s = >100 μM for all) but does inhibit ERK2 (IC50= 32 μM) and the ATP-binding cassette transporter B1 (ABCB1; IC50= 6.4 μM).1,2Olomoucine II inhibits proliferation of a variety of cancer cells, including those expressing wild-type p53 or mutant p53 (mean IC50s = 7.4 and 10.1 μM, respectively...

化合物

Acetomycin
Cat.No: T69172
Synonym:
Target:
PI3K/mTOR Inhibitor-8
Cat.No: T63470
Synonym:
Target:
B-Raf IN 8
Cat.No: T60727
Synonym:
Target:
Angiogenesis inhibitor 3
Cat.No: T74627
Synonym:
Target:
SLU-10482
Cat.No: T83887
Synonym:
Target:
PKM2 activator 6
Cat.No: T81446
Synonym:
Target:
Anticancer agent 139
Cat.No: T78780
Synonym:
Target:
Olomoucine II
Cat.No: T35696
Synonym:
Target:
Cat. No. Product Name Target Signaling Pathways
TN2054 Periplocymarin

Calcium Channel Membrane transporter/Ion channel; Metabolism
Periplocymarin 是一种强心苷,从 Periploca sepium 和 Periploca graeca 中分离得到,具有抗癌潜力。
TN1146 8-​Prenylnaringenin

8-Prenylnaringenin,8-异戊烯基柚皮素

Apoptosis; ROS Apoptosis; Immunology/Inflammation
8-prenylnaringenin 是一种从啤酒花穗中分离到的异戊烯类黄酮,具有细胞毒性。它能通过激活小鼠 Akt 磷酸化途径,使其从静止诱导的停用性肌肉萎缩中恢复。它能通过诱导内源性和外源性通路介导的凋亡,对 HCT-116 结肠癌细胞产生抗增殖活性。
TN2590 11alpha,12alpha-Oxidotaraxerol palmitate

Others Others
11alpha,12alpha-Oxidotaraxerol palmitate shows selective cytotoxicity against HCT-8, Bel-7402, BGC-823, A549 and A2780.
TN4352 Jatamanvaltrate B

Others Others
Jatamanvaltrate B shows cytotoxicity against lung adenocarcinoma (A549), metastatic prostate cancer (PC-3M), colon cancer (HCT-8),and hepatoma (Bel7402) cell lines.
TN3646 Chlorovaltrate K

Others Others
Chlorovaltrate K shows moderate cytotoxicity against lung adenocarcinoma (A 549), metastatic prostate cancer (PC-3M), colon cancer (HCT-8) and hepatoma (Bel 7402) cell lines with IC50 values of 0.89-9.76 uM.
TN5249 Volvaltrate B

Others Others
Volvaltrate B shows cytotoxic activity against the lung adenocarcinoma (A549), metastatic prostate cancer (PC-3M), colon cancer (HCT-8), and hepatoma (Bel7402) cell lines, with IC50 values of 8.5, 2.0, 3.2, and 6.1 uM, respectively.
TN1728 Hellebrigenin

PARP; Akt; CDK Cell Cycle/Checkpoint; Chromatin/Epigenetic; Cytoskeletal Signaling; DNA Damage/DNA Repair; PI3K/Akt/mTOR signaling
Hellebrigenin has anti-hepatoma activities, it induces cell cycle arrest and apoptosis in human hepatocellular carcinoma HepG2 cells through inhibition of Akt. Hellebrigenin exhibites moderate to strong activity against human HL-60, SF-295, MDA-MB-435, and HCT-8 cancer cell strains without hemolysis of mouse erythrocytes.
TN1646 Flemiphilippinin A

Others Others
Flemiphilippin A has antioxidant activity, it shows DPPH radical scavenging activity with effective half maximal concentration (EC50) of 18.36 ug/mL. Flemiphilippinin A (5 ug/mL) exhibits some level of antitumor activity against human hepatocellular carci

天然产物

Periplocymarin
Cat.No: TN2054
Synonym:
Target: Calcium Channel
8-​Prenylnaringenin
Cat.No: TN1146
Synonym: 8-Prenylnaringenin,8-异戊烯基柚皮素
Target: Apoptosis, ROS
11alpha,12alpha-Oxidotaraxerol palmitate
Cat.No: TN2590
Synonym:
Target: Others
Jatamanvaltrate B
Cat.No: TN4352
Synonym:
Target: Others
Chlorovaltrate K
Cat.No: TN3646
Synonym:
Target: Others
Volvaltrate B
Cat.No: TN5249
Synonym:
Target: Others
Hellebrigenin
Cat.No: TN1728
Synonym:
Target: PARP, Akt, CDK
Flemiphilippinin A
Cat.No: TN1646
Synonym:
Target: Others
TargetMol Loading
联系我们
400-820-0310

上海市静安区江场三路238号8楼