Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T10721 |
CD73-IN-1
|
CD73 | Immunology/Inflammation |
CD73-IN-1 是一种具有抗癌活性的 CD73 抑制剂。 | |||
T8875 |
CD73-IN-3
EX-A4254,LY-3475070 |
CD73 | Immunology/Inflammation |
CD73-IN-3 (LY-3475070) 是一种有效的选择性 CD73 抑制剂,IC50 为 28 nM,具有癌症的研究潜力。 | |||
T9210 |
CD73-IN-4
|
CD73 | Immunology/Inflammation |
CD73-IN-4 是高选择性的亚甲基膦酸 CD73抑制剂,对人 CD73 作用的 IC50值为 2.6 nM,在癌症免疫学中具有研究潜力。 | |||
T40033 |
CD73-IN-5
CD73-IN-5 |
||
CD73-IN-5 is a highly potent and selective small molecule inhibitor of CD73, demonstrating non-nucleotide characteristics. It exerts its inhibitory effects with a remarkable IC50 value of 19 nM. | |||
T63128 | CD73-IN-2 | ||
CD73-IN-2 是一种 CD73 的有效抑制剂 (IC50: 0.09 nM)。 | |||
T61691 |
CD73-IN-6
|
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CD73-IN-6, serves as a potent inhibitor of CD73. This compound finds utility in cancer research [1]. | |||
T61053 |
CD73-IN-11
|
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CD73-IN-11 可用于肿瘤相关疾病的药物制备。CD73-IN-11 是 CD73的有效抑制剂。CD73 可以催化细胞外5'-磷酸腺苷 (5'-AMP) 产生腺苷,从而诱导免疫抑制并促进肿瘤增殖和/或转移。 | |||
T61000 |
CD73-IN-10
|
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CD73-IN-10 可用于肿瘤相关疾病药物的制备。CD73-IN-10 是 CD73的有效抑制剂, 能够催化细胞外5'-磷酸腺苷 (5'-AMP) 产生腺苷。腺苷具有诱导免疫抑制的作用,能够促进肿瘤增殖和/或转移。 | |||
T60844 |
CD73-IN-9
|
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CD73-IN-9 是 CD73 的有效抑制剂,可用于制备治疗肿瘤相关疾病的药物。CD73 可以催化细胞外5'-磷酸腺苷 (5'-AMP) 产生腺苷。腺苷能够诱导免疫抑制作用,并且促进肿瘤增殖和/或转移。 | |||
T10216 |
AB-680
|
CD73 | Immunology/Inflammation |
AB-680 是一种选择性可逆的CD73(胞外核苷酸酶) 抑制剂,具有抗肿瘤活性。它对 hCD73 的Ki 值为 4.9 pM,对其选择性是对相关胞外核苷酸酶 CD39 的 10000 多倍。 | |||
T60779 | CD73-IN-13 | ||
CD73-IN-13 可用于制备肿瘤相关疾病的药物。CD73-IN-13 是CD73的有效抑制剂,CD73 与肿瘤生长、血管生成和转移密切相关。 | |||
T61118 | CD73-IN-12 | ||
CD73-IN-12 is a highly effective CD73 inhibitor that displays strong potential in tumor suppression. CD73, an enzyme intricately linked to tumor development, angiogenesis, and metastasis, is significantly inhibited by CD73-IN-12. This compound holds promise in the formulation of therapeutic medications targeting tumor-related diseases[1]. | |||
T61090 |
CD73-IN-8
|
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CD73-IN-8, a potent CD73 inhibitor, prevents the catalytic activity of CD73, an enzyme responsible for converting extracellular 5'-phosphate adenosine (5'-AMP) to adenosine. Adenosine, once produced, can induce immunosuppressive effects and facilitate tumor proliferation and/or metastasis. Therefore, CD73-IN-8 holds promise in the development of therapeutic interventions for tumor-related diseases[1]. | |||
T60599 |
CD73-IN-7
|
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CD73-IN-7 是一种有效的CD73抑制剂,可用于制备治疗肿瘤相关疾病的药物。CD73 催化细胞外5'-磷酸腺苷 (5'-AMP) 产生腺苷,从而诱导免疫抑制作用并促进肿瘤增殖和/或转移。 | |||
T12569L |
PSB-12379 ditriethylamine salt
|
CD73 | Immunology/Inflammation |
PSB-12379 ditriethylamine salt 是一种核苷酸类似物,是一种有效的 Ecto-5'-Nucleotidase (CD73) 抑制剂,Kis 值为 9.03 nM (鼠) 和 2.21 nM (人)。 | |||
T76735 |
Mupadolimab
CPI-006 |
CD73 | Immunology/Inflammation |
Mupadolimab (CPI-006) 是一种人源化 FcγR 结合缺陷型 IgG1 抗 CD73抗体,具有潜在的抗癌活性,可激活 CD73POS B 细胞。 | |||
T22392 |
OP-5244
|
Others | Others |
OP-5244 has comparable potency to bisphosphonic acid series and targets CD73. | |||
T12008 |
MethADP
Adenosine 5'-(α,β-methylene)diphosphate |
Others | Others |
MethADP is a specific inhibitor of CD73. | |||
T12007 |
MethADP sodium salt
|
Others | Others |
MethADP is a specific CD73 inhibitor. | |||
T12569 | PSB-12379 | Others | Others |
PSB-12379 is a potent inhibitor of Ecto-5'-Nucleotidase (CD73)(Kis of 9.03 nM (rat) and 2.21 nM (human)). | |||
T76695 | Oleclumab | ||
Oleclumab (MEDI9447) 是一种人 IgG1λ 抗CD73单克隆抗体,可抑制CD73功能。Oleclumab 具有抗肿瘤活性。 | |||
T76214 | 5′-Nucleotidase | ||
5′-Nucleotidase (CD73) 是一种作为胞外酶存在的内在膜糖蛋白。5′-Nucleotidase 催化 5-核苷酸水解成相应的核苷。 | |||
T71538 | AMPCP | ||
AMPCP is an Ecto-5'-nucleotidase (CD73) inhibitor. | |||
T22411 | PSB-12489 | Others | Others |
PSB-12489 is an optimized inhibitor of CD73. | |||
T73886 | AB-680 ammonium | ||
AB-680 ammonium 是一种有效、可逆、选择性的 CD73(胞外核苷酸酶) 抑制剂,对 hCD73 的Ki 值为 4.9 pM,对其选择性是对相关胞外核苷酸酶CD39的 10000 多倍。具有抗肿瘤活性。 | |||
T80603 |
Dresbuxelimab
AK-119 |
CD73 | Immunology/Inflammation |
Dresbuxelimab (AK-119) 为靶向CD73的IgG-κ型单克隆抗体,常用CHO(中国仓鼠卵巢)细胞作为表达系统。 | |||
T77155 | Dalutrafusp alfa | ||
Dalutrafusp alfa (AGEN-1423; GS-1423) 为针对CD73与TGF-β的特异性双功能抗体,涉及免疫抑制路径。 | |||
T64019 | ZM514 | ||
ZM514 是 CD73 的有效抑制剂,能够作用于 hCD73 (IC50: 1.39 μM) 和 mCD73 (IC50: 14.65 μM)。ZM514 具有较低的细胞毒性,能够用于进行抗癌的研究。 | |||
T73628 | PSB-12379 disodium | ||
PSB-12379 disodium 是一种核苷类似物,是一种有效的 Ecto-5'-Nucleotidase(CD73) 抑制剂,Kis 值为 9.03 nM (鼠) 和 2.21 nM (人)。 | |||
T76730 | Uliledlimab | ||
Uliledlimab 是一种有效的抗 CD73人源单克隆抗体。Uliledlimab 抑制胞外单磷酸腺苷 (AMP) 向腺苷的转化。Uliledlimab 可用于癌症的研究。 | |||
T63956 | OP-5244 sodium | ||
OP-5244 sodium 是有效的、口服具有活力的 CD73 抑制剂 (IC50: 0.25 nM)。OP-5244 sodium 能够阻断腺苷的产生,进而逆转免疫抑制作用,对癌症表现出研究潜力。 | |||
T74865 | BK50164 | ||
BK50164 是一种有效的CD73抑制剂,IC50值为 13.089 µM。BK50164 与 CD99 结合KD 值为 1.5 µM。BK50164 显示抗增殖活性。BK50164 诱导细胞凋亡 (Apoptosis) 和细胞周期停滞在 Sub-G1 阶段。 | |||
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) ... |