Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T37356 |
Cbl-b-IN-1
|
Others | Others |
Cbl-b-IN-1 是一种有效的 Cbl-b 抑制剂(IC50 <100 nM),具有潜在的抗癌活性,可用于研究肠道炎症。 | |||
T63790 |
Cbl-b-IN-3
|
E1/E2/E3 Enzyme | Ubiquitination |
Cbl-b-IN-3是一种有效的casitas b 系淋巴瘤原癌基因-b (Cbl-b)抑制剂(ic50 < 1 nM)。Cbl-b 是一种环型E3泛素蛋白连接酶,与T 淋巴细胞激活阈值的设定有关。Cbl-b 以不依赖于蛋白水解的方式负调控p85,通过其E3泛素连接酶活性,参与了p85向CD28和T 细胞抗原受体ζ的募集,抑制PI3K 抑制了Cblb-/- t 细胞活化的增强。 | |||
T79893 |
Cbl-b-IN-6
|
E1/E2/E3 Enzyme | Ubiquitination |
Cbl-b-IN-6 (Compound 246),作为casitas B系淋巴瘤(Cbl-b)和c-Cbl的抑制剂,其IC50值分别为5.8 nM和4.4 nM。 | |||
T79895 |
Cbl-b-IN-8
|
E1/E2/E3 Enzyme | Ubiquitination |
Cbl-b-IN-8 (Compound 293),一种casitas B系淋巴瘤(Cbl-b)及c-Cbl的抑制剂,其IC50值分别为5.5 nM和7.8 nM。 | |||
T79894 |
Cbl-b-IN-7
|
E1/E2/E3 Enzyme | Ubiquitination |
Cbl-b-IN-7 (Compound 248)作为针对casitas B系淋巴瘤(Cbl-b)和c-Cbl的抑制剂,其IC50值分别为6.7 nM与5.2 nM。 | |||
T79897 |
Cbl-b-IN-10
|
E1/E2/E3 Enzyme | Ubiquitination |
Cbl-b-IN-10(Compound 463)为针对casitas B系淋巴瘤(Cbl-b)和c-Cbl的抑制剂,其IC50值分别为6.0 nM和3.5 nM。 | |||
T79898 |
Cbl-b-IN-11
|
E1/E2/E3 Enzyme | Ubiquitination |
Cbl-b-IN-11 (Compound 466)作为casitas B系淋巴瘤 (Cbl-b) 及c-Cbl的抑制剂,显示出对Cbl-b和c-Cbl的高度选择性,其IC50值分别为6.4 nM 和6.1 nM。 | |||
T79899 |
Cbl-b-IN-12
|
E1/E2/E3 Enzyme | Ubiquitination |
Cbl-b-IN-12 (Example 10)为casitas B系淋巴瘤(CBL-B)抑制剂,IC50值<100 nM。 | |||
T79896 |
Cbl-b-IN-9
|
E1/E2/E3 Enzyme | Ubiquitination |
Cbl-b-IN-9(Compound 300)为针对casitas B系淋巴瘤(Cbl-b)及c-Cbl的抑制剂,其IC50值分别为5.6 nM与4.7 nM。 | |||
T79900 |
Cbl-b-IN-13
|
E1/E2/E3 Enzyme | Ubiquitination |
Cbl-b-IN-13 (Example 520)是一种有效的Cbl-b抑制剂,显示出<100 nM的IC50值,并能够激活T细胞。 | |||
T37468 |
Siamycin I
|
||
Siamycin I is a tricyclic peptide originally isolated from Streptomyces and has antiviral and antibacterial activities. It is active against laboratory strains and clinical isolates of HIV-1 (ED50s = 0.05-0.45 and 0.89-5.7 μM, respectively), as well as the CBL-20 strain of HIV-2 (ED50 = 0.45 μM), in vitro. Siamycin I inhibits HIV-induced fusion of C8166 T cells with HIV-1-infected CEM-SS cells with an ED50 value of 0.08 μM. It is also active against B. subtilis, M. luteus, and S. aureus (MICs = ... |