Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T2502 |
INH1
IBT13131 |
Apoptosis; Microtubule Associated | Apoptosis; Cytoskeletal Signaling |
INH1 (IBT13131) 通过直接结合Hec1,特异性干扰 Hec1/Nek2 的相互作用。它在体内外均表现出良好的抗肿瘤活性。 | |||
T9720 |
T3Inh-1
|
Others | Others |
T3Inh-1 是一种有效的选择性 ppGalNAc-T3 抑制剂,IC50 为 7 µM。 T3Inh-1 可预防乳腺癌细胞。 T3Inh-1 降低组织细胞和小鼠中的 FGF23 激素水平,而不会引起任何毒副作用。 | |||
T81539 | PAT1inh-B01 | ||
PAT1inh-B01为选择性SLC26A6抑制剂,抑制PAT1(Cl-/HCO3-交换器)介导的阴离子交换(IC50: 350 nM),并阻断小肠液体吸收,适用于小肠分泌不足相关疾病研究。 | |||
T74906 |
ODN 20844
|
||
ODN 20844,鸟嘌呤修饰的抑制性寡核苷酸 (INH-ODN),是一种 TLR7和TLR9(Toll-like receptor) 的抑制剂,其亲本为 INH-ODN 2088。ODN 20844 可以破坏TLR7和TLR9介导的免疫细胞免疫反应。ODN 20844 序列:5'-TCCTGGCGc7GGGAAGT-3'。 | |||
T79561 |
Mtb-IN-5
|
||
Mtb-IN-5(化合物(-)17j)是一种异恶唑类化合物,对结核分枝杆菌(Mtb)具有活性。它能够抑制宿主巨噬细胞内Mtb的呼吸及生物膜生长,且能够增强异烟肼(INH)对耐INH Mtb突变株的抑制效果。 | |||
T74912 | ODN 24991 | ||
ODN 24991,鸟嘌呤修饰的抑制性寡核苷酸 (INH-ODN),是一种 TLR3、TLR7和 TLR9(Toll-like receptor) 的抑制剂,其亲本为 INH-ODN 2088。ODN 24991 破坏了 TLR3、TLR7 和 TLR9介导的免疫细胞免疫反应。ODN 24991 序列:5'-C-C-T-G-G-C-c7rGm-G-G-G-3'。 | |||
T79559 | Mtb-IN-4 | ||
Mtb-IN-4(化合物17h)是一种异恶唑类化合物,显示出针对结核分枝杆菌(Mtb)的抗活性,其IC50值为0.70 μM。它能阻断巨噬细胞内Mtb的呼吸和生物膜形成,并可以增强抗生素异烟肼(INH)对耐INH Mtb突变体的抑制效果。 | |||
T74873 | ODN 105871 | ||
ODN 105871,一种G修饰的抑制性寡核苷酸(INH-ODN),作为选择性TLR7抑制剂,适用于炎症免疫反应的研究。 | |||
T74872 | ODN 105870 | ||
ODN 105870 是一种 G 修饰的抑制性寡核苷酸 (INH-ODN),是一种选择性 TLR7抑制剂。ODN 105870 可用于炎症免疫反应研究。 | |||
T38073 |
Thiocarlide
Isoxyl |
||
Thiocarlide (isoxyl) is a thiourea derivative that was used in the 1960s to successfully treat tuberculosis (TB). It has considerable antimycobacterial activity in vitro and is effective against multi-drug resistant strains of Mycobacterium tuberculosis in the range of 1-10 µg/ml. [1] [2] At concentrations of 10 µM, isoxyl inhibits the synthesis of M. bovis during six hours of exposure which is similar to isoniazid (INH) and ethionamide (ETH), two other predominant anti-tuberculosis drug... | |||
T35883 |
RNF5 inhibitor inh-02
RNF5 inhibitor inh-02 |
||
RNF5 inhibitor inh-02, a potent E3 ubiquitin ligase RNF5/RMA1 inhibitor, demonstrates significant efficacy in rescuing F508del-CFTR with an EC50 of 2.2 uM in bronchial epithelial cells homozygous for the F508del mutation. This compound is valuable for cystic fibrosis research[1]. | |||
T74910 | ODN 24888 | ||
ODN 24888 是一种鸟嘌呤修饰的抑制性寡核苷酸 (INH-ODN),对TLR7/TLR9介导的信号通路表现出强烈的抑制作用。ODN 24888 损害 IFN-α 水平和NF-κB 激活,抑制IL-6的释放。ODN 24888 参与免疫和炎症应答,可作为疫苗佐剂使用。 | |||
T74907 | ODN 21595 | ||
ODN 21595是一种鸟嘌呤修饰的抑制性寡核苷酸(INH-ODN)。该化合物能够抑制IFN-α和IL-6的释放,同时不具有细胞毒性。它还能降低CD86与HLA-DR的表达,显示出对于研究系统性红斑狼疮(SLE)具有潜力。 | |||
T37880 |
OPC-167832
|
||
OPC-167832 is a potent and orally active dprE1 Inhibitor with an IC50 of 0.258 μM. OPC-167832 has antituberculosis activity and can be used for the research of tuberculosis caused by Mycobacterium tuberculosis[1]. OPC-167832 exhibits very low MICs against laboratory strains of M. tuberculosis H37Rv (MIC: 0.0005 μg/ml) and Kurono (MIC: 0.0005 μg/ml) and strains with monoresistance to rifampin (RIF), isoniazid (INH), ethambutol (EMB), streptomycin (STR), and pyrazinamide (PZA) (MIC: 0.00024-0.001 ... |