Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T15573 |
Inarigivir soproxil
SB9200 |
HCV Protease | Microbiology/Virology; Proteases/Proteasome |
Inarigivir soproxil (SB9200) 是一种先天免疫激动剂。 它还显示出针对耐药丙型肝炎病毒 (HCV) 变体的有效抗病毒活性。在基因型 1 HCV 复制子系统细胞中, HCV 1a/1b 的 EC50 为 2.2 和 1.0 μM。 | |||
T5128 |
RGX-104 hydrochloride
SB742881,RGX-104 HCl,盐酸RGX-104 |
Liver X Receptor | Metabolism |
RGX-104 hydrochloride (SB742881) 是小分子LXR 激动剂,利用 ApoE 基因的转录激活,调节先天免疫。 | |||
T19508 |
Peroxidase
|
Others | Others |
Peroxidase 来自辣根,在先天免疫、氧化活性氧、激素生物合成和多种疾病的发病机制等方面具有重要作用。 | |||
T9518 |
Inarigivir ammonium
ORI-9020 ammonium,SB-9200 ammonium,Inarigivir铵 |
HBV | Microbiology/Virology |
Inarigivir ammonium (SB-9200 ammonium) 是一种二核苷酸抗病毒化合物,可显着降低表达乙型肝炎病毒的转基因小鼠的 HBV DNA。它是一种激活细胞内先天免疫的视黄酸诱导基因-I 激动剂。 | |||
T67883 |
EZH2-IN-15
SHR2554 |
Histone Methyltransferase | Chromatin/Epigenetic |
EZH2-IN-15 是zeste 2组蛋白修饰增强子(EZH2)的特异性抑制剂。EZH2在许多人类癌症中异常过表达,通过调节Treg 活性来控制适应性反应。肿瘤内EZH2的表达也被证明可以控制先天免疫 | |||
T41086 |
IDR-1
|
||
IDR-1 is an antimicrobial peptide with activity against both Gram-positive and Gram-negative bacteria. This compound modulates innate immunity to counter infections while avoiding evident toxicities. Additionally, IDR-1 exhibits anti-inflammatory and anti-infective properties, increases the levels of monocyte chemokines, and reduces the release of pro-inflammatory cytokines. | |||
T76933 | Botensilimab | ||
Botensilimab (AGEN 1181),一种针对细胞毒性T淋巴细胞抗原4 (CTLA-4) 的人源化单克隆抗体,既能激活先天性免疫也能激活适应性免疫,主要应用于癌症研究领域。 | |||
T71325 |
ANA-773
|
||
ANA773 is a Toll-like Receptor 7 (TLR7) agonist prodrug with potential immunostimulating activity. Upon oral administration, ANA773 is metabolized into its active form that binds to and activates TLR7, thereby stimulating dendritic cells (DCs) and enhancing natural killer cell (NK) cytotoxicity. This activation results in the production of proinflammatory cytokines, including interferon alpha, and enhanced antibody-dependent cellular cytotoxicity (ADCC). TLR7 is a member of the TLR family, which... | |||
T78325 |
Orilanolimab
SYNT001 |
||
Orilanolimab (SYNT001) 是一种人源化、去免疫化的单克隆抗体,具有阻断FcRn功能。它可以干预FcRn与IgG分子的 Fc 部分之间的相互作用,并妨碍IgGIC 通过激活FcRn介导的免疫反应,影响与IgG相关的稳态以及先天性和适应性免疫功能。 | |||
T79133 |
UC-764864
|
E1/E2/E3 Enzyme | Ubiquitination |
UC-764864是一种UBE2N抑制剂,能够抑制其酶活性,并对白血病细胞中的UBE2N依赖性信号传导具有细胞毒性作用。此外,UC-764864还能阻断人AML细胞系中先天免疫和炎症相关底物的泛素化。 | |||
T10065 |
2',3'-cGAMP
2'-3'-cyclic GMP-AMP |
STING; cGAS | Immunology/Inflammation |
2',3'-cGAMP (2'-3'-cyclic GMP-AMP) 是细胞天然免疫中第二信使,在DNA结合条件下由 cGAMP 合成酶 (cGAS) 催化形成。2',3'-cGAMP 可与 STING 结合形成二聚体,诱导干扰素-β(IFN-β)及其他细胞因子的产生和表达。 | |||
T74067 | Poly (I:C):Kanamycin (1:1) (sodium) | ||
Poly (I:C):Kanamycin (1:1) sodium 是 Poly (I:C) 和 Kanamycin 的等比例复合物。Poly(I:C) sodium 是双链 RNA 的合成类似物,是一种TLR3和视黄酸诱导型基因 I 受体 (RIG-I 和MDA5) 的激动剂。Poly(I:C) sodium 可以用作疫苗佐剂,增强先天性和适应性免疫反应,并诱导癌细胞凋亡。Kanamycin 是一种具有口服活性的抗菌剂(革兰氏阴性/阳性细菌),可抑制易位并通过与 70 S 核糖体亚基结合引起错误编码。Kanamycin 对结核分枝杆菌(敏感和耐药)和肺炎克雷伯菌均表现出良好的抑制活性,可用于结核病和肺炎的研究。 | |||
T36985 |
Cyclic di-UMP (sodium salt)
|
||
Cyclic di-UMP is a pyrimidine-containing cyclic dinucleotide (CDN).1It is produced by bacterial cGAS/DncV-like nucleotidyltransferases (CD-NTases), such as LpCdnE02 fromL. pneumophila, and binds to cGAS, in the apo or dsDNA-bound forms, with reduced affinity compared to 2'3'-cGAMP or 3'3'-cGAMP .1,2Cyclic di-UMP is intended for use as a negative control for cyclic di-GMP signaling. 1.Whiteley, A.T., Eaglesham, J.B., de Oliveira Mann, C.C., et al.Bacterial cGAS-like enzymes synthesize diverse nuc... |