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Merck
CN

S1697

Sigma-Aldrich

SPD304

≥98% (HPLC), solid

别名:

6,7-二甲基-3-[[甲基[2- [甲基[[1-[3-(三氟甲基)苯基]-1H-吲哚-3-基]甲基]氨基]乙基]氨基]甲基]-(4H-1-苯并吡喃-4-酮 二盐酸盐, SPD00000304

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About This Item

经验公式(希尔记法):
C32H32F3N3O2 · 2HCl
分子量:
620.53
MDL编号:
UNSPSC代码:
51111800
PubChem化学物质编号:
NACRES:
NA.77

质量水平

方案

≥98% (HPLC)

表单

solid

颜色

white

溶解性

H2O: >5 mg/mL

储存温度

2-8°C

SMILES字符串

Cl.Cl.CN(CCN(C)Cc1cn(-c2cccc(c2)C(F)(F)F)c3ccccc13)CC4=COc5cc(C)c(C)cc5C4=O

InChI

1S/C32H32F3N3O2.2ClH/c1-21-14-28-30(15-22(21)2)40-20-24(31(28)39)18-37(4)13-12-36(3)17-23-19-38(29-11-6-5-10-27(23)29)26-9-7-8-25(16-26)32(33,34)35;;/h5-11,14-16,19-20H,12-13,17-18H2,1-4H3;2*1H

InChI key

GOZMBJCYMQQACI-UHFFFAOYSA-N

基因信息

human ... TNF(7124)
mouse ... TNF(21926)
rat ... TNF(24835)

应用

SPD304可用于TNF-α介导的细胞信号传导研究。
SPD304已用于抑制背根神经节细胞元中的肿瘤坏死因子受体1(TNFR1)以及结肠上皮细胞系中的肿瘤坏死因子受体α。

生化/生理作用

SPD304是一种具有全新作用机制的TNF-a活性小分子抑制剂。它可干扰三聚体TNF-a亚基的接触表面上的蛋白-蛋白相互作用、置换三聚体单元之一、导致三聚体的解离以及受体TNFR1的活性丧失。SPD304可抑制TNFR1受体与TNF-a结合,其体外IC50为22μM,并在HeLa细胞中抑制TNF-a介导的IkB降解刺激,其IC50为4.6 μM。
TNF-α的三聚化对其生物活性至关重要。SPD304通过与甘氨酸122残基的相互作用而抑制三聚化。它还可通过类似的相互作用抑制核因子-κB配体(RANKL)的受体活化剂的活性。

储存分类代码

11 - Combustible Solids

WGK

WGK 3

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

法规信息

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分析证书(COA)

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访问文档库

Anthi Mettou et al.
SLAS discovery : advancing life sciences R & D, 23(1), 84-93 (2017-06-07)
The aim of this study is to improve the aqueous solubility of a group of compounds without interfering with their bioassay as well as to create a relevant prediction model. A series of 55 potential small-molecule inhibitors of tumor necrosis
Dysregulated Up-Frameshift Protein 1 Promotes Ulcerative Colitis Pathogenesis Through the TNFR1-NF-kappaB/MAPKs Pathway
Zhu H, et al.
Digestive Diseases and Sciences, 63(10), 2593-2603 (2018)
Molly M He et al.
Science (New York, N.Y.), 310(5750), 1022-1025 (2005-11-15)
We have identified a small-molecule inhibitor of tumor necrosis factor alpha (TNF-alpha) that promotes subunit disassembly of this trimeric cytokine family member. The compound inhibits TNF-alpha activity in biochemical and cell-based assays with median inhibitory concentrations of 22 and 4.6
Cannabinoid WIN-55,212-2 mesylate inhibits tumor necrosis factor-alpha-induced expression of nitric oxide synthase in dorsal root ganglion neurons
Tan R and Cao L
International Journal of Molecular Medicine, 42(2), 919-925 (2018)
Yan Zhang et al.
Molecular cancer research : MCR, 12(8), 1181-1191 (2014-05-14)
The relationship between tumor-associated macrophages (TAM) and epithelial-to-mesenchymal transition (EMT) during the initiation and progression of metastasis is still unclear. Here, a role for the vitamin D receptor (VDR) in metastasis was identified, as well as a role in the

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