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11

抑制剂 & 化合物

2

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T11492	GSK2983559 free acid	Others; RIP kinase	Apoptosis; NF-κB; Others
	GSK2983559 free acid 是一种有效的特异性受体相互作用蛋白 2 (RIP2) 抑制剂。 GSK2983559 free acid 在阻断人类炎症性肠病外植体样品和体内的许多促炎细胞因子反应方面表现出优异的活性。
T9016	AI-10-47 1H-Benzimidazole, 2-(2-pyridinyl)-6-(trifluoromethoxy)-AI-10-47	Others	Others
	AI-10-47 (1H-Benzimidazole, 2-(2-pyridinyl)-6-(trifluoromethoxy)-AI-10-47) 是 CBFβ-RUNX 结合的小分子抑制剂(IC50:3.2 μM)。
T28072L	MLN-3897 TFA MLN-3897 TFA(1010731-97-1 Free base)	CCR	Immunology/Inflammation; Microbiology/Virology
	MLN-3897 TFA 是一种有效的CCR1 拮抗剂，对 125I-MIP-1α 与 THP-1 细胞膜的结合具有抑制作用。
T36527	IL-4-inhibitor-1	IL Receptor	Immunology/Inflammation
	IL-4-inhibitor-1 是 IL-4 的抑制剂 (EC50 = 1.81 µM)。
T60442	NLRP3/AIM2-IN-3	NOD; AIM2	Immunology/Inflammation; NF-κB
	NLRP3/AIM2-IN-3 是一种独特的分子，能以物种特异性的方式抑制 NLRP3 和 AIM2 炎性体的激活。它对细胞裂解的 IC50 值为 0.077 ± 0.008 μ M。NLRP3/AIM2-IN-3是一种 NLRP3 和 AIM2 炎症体依赖性细胞裂解的强效抑制剂，对细胞裂解的 IC50 值为 0.077 ± 0.008 μ M。NLRP3/AIM2-IN-3 可抑制 LPS/nigericin 刺激的 THP-1 巨噬细胞的细胞裂解，其 IC50 值为 0.077 ± 0.008 μM。NLRP3/AIM2-IN-3 干扰了 NLRP3 或 AIM2 与桥接蛋白 ASC 的相互作用，抑制了 ASC 的寡聚。
T28072	MLN-3897 AVE9897,AVE 9897,CCR1 antagonist 10,AVE-9897	CCR	Immunology/Inflammation; Microbiology/Virology
	MLN-3897 (CCR1 antagonist 10) 是一种具有口服活性的 CCR1 拮抗剂，对于 125I-MIP-1α 与 THP-1 细胞膜的结合，Ki 为 2.3 nM。 MLN-3897 抑制 Akt 信号转导和 MM 细胞存活和增殖。
T79352	RIPK2/3-IN-1	RIP kinase	Apoptosis; NF-κB
	RIPK2/3-IN-1 是一款RIPK2和RIPK3 kinases的高效抑制剂，其对RIPK2和RIPK3的IC50值分别为3 nM和117 nM。在C14-TriLAN-Gly/NOD1 THP-1细胞的NF-κB报告实验中，RIPK2/3-IN-1表现出对RIPK2的有效抑制效果，IC50值为14±4 nM[sup][1]。
T38160	STING Agonist 1a	Others	Others
	STING agonist 1a is an agonist of stimulator of interferon genes (STING).1It induces expression of an IRF-inducible SEAP reporter gene in a cell-based assay (EC50= 16.77 μM). STING agonist 1a (12.5-100 μM) induces expression of IFN-β, IL-6, and chemokine (C-X-C motif) ligand 10 (CXCL10) in THP-1 cells, an effect that can be reversed by STING knockout or the STING inhibitor H-151 . 1.Hou, H., Yang, R., Liu, X., et al.Discovery of triazoloquinoxaline as novel STING agonists via structure-based vir...
T36859	C16 Globotriaosylceramide (d18:1/16:0) C16 Globotriaosylceramide (d18:1/16:0)	Others	Others
	C16 globotriaosylceramide is an endogenous sphingolipid found in mammalian cell membranes that is synthesized from C16 lactosylceramide . C16 globotriaosylceramide acts as a receptor for Shiga toxin in B cell-derived Raji cells and THP-1 monocytes. It accumulates in endothelial cells, pericytes, vascular smooth muscle cells, renal epithelial cells, dorsal ganglia neuronal cells, and myocardial cells in patients with Fabry disease. C16 globotriaosylceramide is also upregulated in plasma of patien...
T35701	FSL-1 TFA
	FSL-1 TFA, a bacterial-derived toll-like receptor 2/6 (TLR2/6) agonist, enhances resistance to experimental HSV-2 infection[1]. FSL-1 TFA induces MMP-9 production through TLR2 and NF-κB/AP-1 signaling pathways in monocytic THP-1 cells[2]. FSL-1 significantly reduces HSV-2 replication in human vaginal epithelial cells (EC)[1].FSL-1 induces significant resistance to experimental genital HSV-2 infection through elaboration of a specific cytokine response profile[1].FSL-1 (50 ng/mL, 24 hours) induce...
T37439	C18 Globotriaosylceramide (d18:1/18:0)	Others	Others
	C18 globotriaosylceramide is an endogenous sphingolipid found in mammalian cell membranes that is synthesized from lactosylceramide . It inhibits aggregation of human neutrophils induced by phorbol 12-myristate 13-acetate (PMA; 10008014) when used at a concentration of 1 μM. C18 globotriaosylceramide acts as a receptor for Shiga toxin in B cell-derived Raji cells and THP-1 monocytes. It accumulates in the brain, heart, kidney, liver, lung, and spleen in a mouse model of Fabry disease, a lysosoma...

化合物

GSK2983559 free acid

Cat.No: T11492

Target: Others, RIP kinase

Cat.No: T9016

Synonym: 1H-Benzimidazole, 2-(2-pyridinyl)-6-(trifluoromethoxy)-AI-10-47

Target: Others

Cat.No: T28072L

Synonym: MLN-3897 TFA(1010731-97-1 Free base)

Target: CCR

IL-4-inhibitor-1

Cat.No: T36527

Target: IL Receptor

NLRP3/AIM2-IN-3

Cat.No: T60442

Target: NOD, AIM2

Cat.No: T28072

Synonym: AVE9897,AVE 9897,CCR1 antagonist 10,AVE-9897

Target: CCR

Cat.No: T79352

Target: RIP kinase

STING Agonist 1a

Cat.No: T38160

Target: Others

C16 Globotriaosylceramide (d18:1/16:0)

Cat.No: T36859

Synonym: C16 Globotriaosylceramide (d18:1/16:0)

Target: Others

Cat.No: T35701

C18 Globotriaosylceramide (d18:1/18:0)

Cat.No: T37439

Target: Others

Cat. No.	Product Name	Target	Signaling Pathways
TN5593	Euphohelioscopin A
	Euphohelioscopin A, an activator of protein kinase C (PKC), it inhibits proliferation and induces differentiation of the myeloid leukemia cell lines THP-1 and HL-60. Euphohelioscopin A has anti-inflammary activity, it exhibits moderate inhibitory activity
T72742	(-)-Pinocembrin (-)-乔松素	Others	Others
	(-)-Pinocembrin 对 H37Ra 结核分枝杆菌展示了抗菌活性，无论是休眠还是活跃期，其 IC50 值分别为1.11 mg/mL 和 1.21 mg/mL。作为一种抗增殖剂，(-)-Pinocembrin 对于 THP-1、A549、Panc-1、HeLa 和 MCF7 细胞系，IC50 值范围为 1.88 至 11.00 mg/mL。

天然产物

Euphohelioscopin A

Cat.No: TN5593

(-)-Pinocembrin

Cat.No: T72742

Synonym: (-)-乔松素

Target: Others

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