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Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T7611 |
ODM-203
|
VEGFR; FGFR | Angiogenesis; Tyrosine Kinase/Adaptors |
ODM-203 是 FGFR 和 VEGFR 家族的抑制剂,具有显著的抗肿瘤活性,能够诱导抗肿瘤免疫。 | |||
T77401 |
Bavituximab
Anti-PS MAb 3G4 |
Others | Others |
Bavituximab (Anti-Human Phosphatidylserine Recombinant Antibody) 是一种针对磷脂酰丝氨酸 (PS) 的单克隆抗体,具有血管靶向和免疫调节特性,能够重新激活抗肿瘤免疫来抑制肿瘤生长。Bavituximab 具有抗癌活性,常联合Paclitaxel 和 Carboplatin 来研究非小细胞肺癌。 | |||
T61248 | HDAC-IN-32 | ||
HDAC-IN-32 is a highly effective HDAC inhibitor presenting IC50 values of 5.2, 11, and 28 nM for HDAC1, HDAC2, and HDAC6, respectively. This compound demonstrates notable anti-proliferative properties against tumor cells, as well as significant in vivo antitumor efficacy, which can elicit antitumor immunity [1]. | |||
T82043 | Iso5-2DC18 | ||
Iso5-2DC18是用于合成含胺脂质的化合物。该脂质适用于mRNA传递、激活STING通路及表达抗肿瘤免疫效应。 | |||
T63329 | PD-1/PD-L1-IN-25 | ||
PD-1/PD-L1-IN-25 是一种 PD-1/PD-L1 互作的抑制剂 (IC50: 16.17 nM),可有效激活 PBMCs 中 T 细胞的抗肿瘤免疫。PD-1/PD-L1-IN-25 能够用于研究癌症。 | |||
T79635 |
LYP-IN-4
|
Phosphatase | Metabolism |
LYP-IN-4(compound D14)是一种针对淋巴酪氨酸磷酸酶(LYP)的可逆且特异性抑制剂,具有Ki值1.34 μM和IC50值3.52 μM。该化合物通过抑制LYP来调控TCR信号传递,并上调PD-1/PD-L1的表达,以此增强抗肿瘤免疫反应。此外,LYP-IN-4能够激活T细胞、抑制M2型巨噬细胞的极化,并在MC38同基因小鼠模型中抑制肿瘤生长。 | |||
T63553 |
HPK1-IN-28
|
||
HPK1-IN-28 是 HPK1 的有效抑制剂。其中造血祖细胞激酶 1 (HPK1) 是一种树突状细胞 (DC)、T 细胞和 B 细胞活化反应的负调节剂。HPK1-IN-28 能够有效提高人体的抗肿瘤免疫力,对免疫相关疾病,尤其是肿瘤表现出研究潜力。 | |||
T63270 |
HPK1-IN-29
|
||
HPK1-IN-29 是 HPK1 有效的抑制剂,其中造血祖细胞激酶 1 (HPK1) 是一种树突状细胞 (DC)、T 细胞和 B 细胞活化反应的负调节剂。HPK1-IN-29 能够提高人体的抗肿瘤免疫力,表现出研究免疫相关疾病,尤其是肿瘤的潜力。 | |||
T77052 | Latikafusp | ||
Latikafusp (AMG 256)是一种靶向PD-1+细胞的双功能融合蛋白,整合了针对PD-1的抗体及IL-21突变蛋白,用于提供IL-21通路的刺激。通过启动和延长细胞毒性及记忆T细胞的活性,该蛋白质能够诱导抗肿瘤免疫反应,显示出对实体瘤研究的应用潜力。 | |||
T35573 | Adenosine 5’-methylenediphosphate (hydrate) | ||
Adenosine 5’-methylenediphosphate is an inhibitor of ecto-5’-nucleotidase, also known as CD73, with a Kivalue of 37 nM.1It inhibits cAMP accumulation induced by adenosine 5’-monophosphate , adenosine 5’-diphosphate , or adenosine 5’-triphosphate but not adenosine in VA-13 human fibroblasts when used at a concentration of 100 μM. Adenosine 5’-methylenediphosphate reduces proliferation of U138MG glioma cells, as well as inhibits the invasion and migration of MHCC97H hepatocellular carcinoma (HCC) ... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T3S1513 |
(20R)-Protopanaxadiol
Protopanaxadiol,20R-Protopanaxadiol,(20R)-原人参二醇,(20R)-Protopanaxdiol |
Others; Antibacterial | Microbiology/Virology; Others |
(20R)-Protopanaxadiol ((20R)-Protopanaxdiol) 是黑参中20(R)-人参皂甙 Rg3的一种三萜皂苷代谢物。它抑制幽门螺杆菌的生长,有抗肿瘤活性和细胞毒性。 |