UU-T01

目录号：SY-110267

UU-T01 是 β-Catenin/T-cell factor 4 蛋白互作 (β-catenin/Tcf PPI) 的选择性抑制剂，Ki 值为 3.14 µM。UU-T01 与β-catenin 直接结合，KD 值为 0.531 µM。

¥1725.00

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16,16-Dimethyl prostaglandin E2

目录号：SY-110268

16,16-Dimethyl prostaglandin E2 is an orally active vertebrate Hematopoietic stem cells homeostasis critical regulator. It can act through EP2/EP4 and has an interaction with the Wnt pathway.

¥3036.00

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A3334

目录号：SY-110269

A3051, is a robust and orally active inhibitor of CXXC5-DVL with an IC 50 of 63.06 nM. Its applications include research into phenotypes associated with obesity, diabetes, and NASH that are induced by high fat diet (HFD) and methionine-choline deficient diet (MCD).

¥1828.00

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TWS-119

目录号：SY-110270

TWS-119是一种强效 GSK-3β 抑制剂，可激活 Wnt/β-catenin 信号通路。它能诱导神经元分化，增强 T 细胞抗肿瘤活性，并在缺血性卒中模型中保护血脑屏障。

¥920.00

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GNF-1331

目录号：SY-110271

GNF-1331 is a potent, selective, and orally bioavailable porcupine inhibitor (IC50 = 12 nM). Blocking abnormal Wnt signaling is an attractive treatment for a variety of cancers.

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FZD7 antagonist 1

目录号：SY-110272

FZD7 antagonist 1 (peptide 34), a dFz7-21 analogue, inhibits wnt3a with an IC50 of 9.2 nM and blocks TcdB−FZD interaction by targeting FZD receptors [1].

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PTK7/β-catenin-IN-6

目录号：SY-110273

PTK7/β-catenin-IN-6 (Compound 03653) 作为一类抑制PTK7/β-catenin相互作用的化合物，能有效地抑制Wnt信号通路，对结直肠癌 (CRC) 具有抗癌效果。

¥4278.00

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β-catenin-IN-6

目录号：SY-110274

β-catenin-IN-6是一种针对Wnt/β-catenin(典型的wingless相关整合位点)通路的抑制剂，能够抑制人类结直肠癌细胞的增殖，并在β-catenin/RK3E小鼠模型上展现出效果。

¥4257.00

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8-Prenylkaempferol

目录号：SY-110275

8-Prenylkaempferol is an effective agent for attenuating pro-inflammatory NO induction, it may be an anti-inflammatory agent for suppressing influenza A virus-induced RANTES production acts by blocking PI3K-mediated transcriptional activation of NF-κB and

¥5814.00

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