Stem Cell

A TNIK inhibitor

An inhibitor of Wnt and hedgehog signaling

An inhibitor of CK1δ and CK1ε

M2912 (MSC2504877) is a very potent TNKS1/TNKS2 inhibitor (IC50=0.6 nM for TNKS1) with exquisite selectivity over other PARP family enzymes and favorable compound properties. This inhibitor potently modulates the Wnt/β-catenin pathway by elevating the levels of axin2 (EC50=17 nM) and tankyrase in DLD1 cells in a dose-dependent manner resulting in reduced cellular Wnt reporter activity.

WAY-119064 is a potent glycogen synthase kinase-3β (GSK-3β) inhibitor with an IC50 value of 80.5 nM.

YAP-TEAD Inhibitor 1 (Peptide 17) is a YAP-TEAD protein-protein interaction inhibitor which has potential usage in treatment of YAP-involved cancers with IC50 of 25 nM.

CaseinKinaseIIInhibitorIV是表皮角质形成细胞分化的小分子诱导剂。

硫酸乙酰肝素 (HS) 是一种复杂的聚阴离子多糖，广泛表达于细胞表面和细胞外基质。

tCFA15为一种三甲基环己烯长链脂肪醇，侧链含有15个碳原子，能够促进神经细胞的分化，具有调控Notch信号通路的潜力。

Adavivint (SM04690,Lorecivivint) is a potent and specific inhibitor of canonical Wnt signaling with an EC50 of 19.5 nM for inhibiting the TCF/LEF reporter. It is ?150- to 500-fold more potent than the other known Wnt inhibitors across multiple cellular assays.

Ginkgetin一种从银杏叶中提取的双黄酮类天然化合物，能够抑制Wnt信号通路（IC₅₀=5.92μM）。

Methyl Vanillate, one of the ingredients in Hovenia dulcis Thunb, activates the Wnt/β-catenin pathway and induces osteoblast differentiation in vitro.

An anthelmintic and anticancer agent

An inhibitor of the β-catenin-TCF4 protein-protein interaction

GNF-6231 is a potent, orally active and selective Porcupine inhibitor with IC50 of 0.8 nM.

EMTinhibitor-1是Hippo，TGF-β和Wnt信号通路的抑制剂，并拥有抗肿瘤活性。

KY1220 is a small molecule that destabilizes both β-catenin and Ras, via targeting the Wnt/β-catenin pathway with IC50 of 2.1 μM in HEK293 reporter cells.

LEQ506 (NVP-LEQ506) 是第二代平滑 (Smo) 抑制剂，在人和小鼠中的 IC50 分别为 2 和 4 nM。

Saridegib (IPI-926) 是一种有效且特异性的 Smoothened (Smo) 抑制剂，Smoothened (Smo) 是 Hedgehog (Hh) 通路中的关键信号跨膜蛋白。

MRT-83是有效的Smo拮抗剂，其IC50值在纳摩尔级别。

Gigantol是一种来自几种药用兰花的联苄基化合物。Gigantol对癌症有潜在治疗价值。Gigantol是Wnt/β-catenin通路的抑制剂。

CaseinKinaseIIInhibitorIVHydrochloride是表皮角质形成细胞分化的小分子诱导剂。

ALLO-2 is potent antagonist of both wild-type mouse Smo and drug-resistant D473H mutant human Smo that inhibits Smo agonist inhibited Gli-Luc activity in TM3-Gli-Luc cells with IC50 of 6 nM.

CK1-IN-1 (PUN51207, Compound 1C) is an inhibitor of casein kinase 1 (CK1) with IC50 of 15 nM, 16 nM and 73 nM for CK1δ, CK1ε and p38α MAPK, respectively.