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Cat. No. | Product Name | Target | Signaling Pathways |
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T23587 |
8-CSC
8 CSC,CSC |
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8-CSC is a dual agent endowed with good hMAO-B inhibitory activity (Ki: 235 nM in baboon liver mitochondria) and A2A affinity (Ki: 36 nM in rat brain striatal membranes receptor). | |||
T73995 | EGFR/CSC-IN-1 | EGFR | Angiogenesis; JAK/STAT signaling; Tyrosine Kinase/Adaptors |
EGFR/CSC-IN-1为针对三阴性乳腺癌研究的潜在EGFR(IC50为10.52 nM)及肿瘤干细胞(CSC)双重抑制剂。 | |||
T0365 |
Thioridazine hydrochloride
盐酸硫利达嗪,Mellaril,Aldazine |
Apoptosis; Potassium Channel; Dopamine Receptor; 5-HT Receptor; Antibacterial; Adrenergic Receptor; Autophagy | Apoptosis; Autophagy; GPCR/G Protein; Membrane transporter/Ion channel; Microbiology/Virology; Neuroscience |
Thioridazine hydrochloride (Mellaril) 是一种多巴胺受体D2家族蛋白的拮抗剂,有抗精神病和抗焦虑活性。它也是一种PI3K-Akt-mTOR 信号通路的抑制剂,具有抗血管生成作用。它在多种类型的癌细胞中显示出抗增殖和凋亡诱导作用,对靶向癌症干细胞具有特异性。 | |||
T33519 |
MTOB
α-keto-γ-Methylthiobutyric acid,4-甲硫基-2-氧丁酸钠,KMBA,MTOB salt,4-methylthio 2-oxobutyric acid |
Others | Others |
MTOB (α-keto-γ-Methylthiobutyric acid) 是 c 末端结合蛋白 (CtBP) 的底物,可干扰 CtBP 在细胞培养物和小鼠中的致癌活性。它还积极调节 TCF-4 信号传导,导致癌症干细胞 (CSC) 生长和自我更新。 | |||
T10904 |
CWP232228
|
Wnt/beta-catenin | Cytoskeletal Signaling; Stem Cells |
CWP232228 是一种高效的、选择性的Wnt/β-catenin 信号通路抑制剂,在细胞核中,拮抗 β-catenin 与 T 细胞因子结合。它能够抑制乳腺癌和肝癌干细胞的生长,抑制肿瘤的形成和转移,且没有毒性。 | |||
T20974 |
IR-780 Iodide
IR 780 iodide,IR-780 碘化物 |
Others | Others |
IR-780 Iodide (IR 780 iodide) 是一种近红外荧光染料,用于通过 HIF-1α/糖酵解依赖性线粒体转运蛋白 ABCB10 的活性对人类 CSC 进行独特的表征。 | |||
T74092 |
Cyanine5 alkyne
|
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Cyanine5 alkyne (Alkyne-Cy5) 是一种荧光染料,用于标记叠氮蛋白,可用于分析蛋白质的翻译后修饰,糖基化等。Cyanine5 alkyne 也可以作为线粒体OXPHOS 抑制剂,抑制癌症干细胞 (CSC) 的生长。储存方式:避光。 | |||
T24879 |
Thioxodihydroquinazolinone-19
Thioxodihydroquinazolinone19 |
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In platinum-resistant A2780cis human ovarian cancer cells, thioxodihydroquinazolinone-19 is an inducer of apoptotic cell death. It acts by exhibiting a strong inhibitory effect in ovarian CSC-LCs in combination with cisplatin. | |||
T61885 | Sulconazole | ||
Sulconazole是一种咪唑类抗真菌剂,有效阻断NF-κB/IL-8信号通路和癌症干细胞(CSC)的形成,抑制肿瘤生长,适用于乳腺癌研究。 | |||
T71998 |
673-A
|
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673-A is an aldehyde dehydrogenase (ALDH1A) inhibitor that depletes CD133+ cancer stem cells (CSC) in ovarian cancer cell lines. 673-A triggers necroptosis in ovarian CSCs and induces expression of mitochondrial uncoupling proteins (UCP). 673-A also overcomes chemotherapy resistance in vivo. | |||
T39792 | AMPC | ||
AMPC, a powerful and efficient inhibitor of TFF3, demonstrates inhibitory effects on cell proliferation, survival, oncogenicity, and CSC-like behavior in TFF3-positive CMS4 CRC cells. It acts as a promising standalone anti-cancer agent and also enhances the effects of 5-FU when used in combination, making it a valuable tool for cancer research. | |||
T21762 |
LDN-211904
|
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LDN-211904 oxalate (compound 32) 是一种有效的选择性EphB3抑制剂,IC50为 0.079 μM。LDN-211904 oxalate 在小鼠肝微粒体中具有良好的代谢稳定性。LDN-211904 oxalate 与西妥昔单抗联用可有效抑制 STAT3 激活的 CSC 干性和 CRC 中的西妥昔单抗耐药性。 | |||
T4134L |
OTS514
OTS514 HCl,OTS514 Hydrochloride,OTS-514,OTS 514 |
Apoptosis; TOPK | Apoptosis; MAPK |
OTS514 (OTS514 Hydrochloride) 是一种高效的 TOPK 抑制剂,IC50为 2.6 nM。它强效抑制 TOPK 阳性的肿瘤细胞生长,还可诱导细胞周期停滞和凋亡。 | |||
T72658 | cRIPGBM chloride | ||
cRIPGBM chloride是一种口服有效的促凋亡衍生物,针对多形性胶质母细胞瘤(GBM)中的癌症干细胞(CSC)。该化合物通过靶向受体相互作用蛋白激酶2(RIPK2),诱导caspase 1依赖的细胞凋亡,抑制RIPK2/TAK1的活性,增加RIPK2/caspase 1复合物的形成,表现出强大的体内抗肿瘤效果。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T19971 |
Cyclosporin C
CsC,Cs-C,Cyclosporin-C,环孢菌素 C |
Antiviral; Antifungal | Immunology/Inflammation; Microbiology/Virology |
Cyclosporin C (Cs-C) 是一种抗丝状植物病原真菌的真菌代谢物。 Cyclosporin C 具有抗真菌、抗病毒和免疫抑制特性。 |