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Wnt Related Products (332)
Related Products (332)
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IWR-1
0 ImagesSynonyms: endo-IWR 1; IWR-1-endoIWR-1 (IWR-1-endo) is a tankyrase inhibitor targeting Wnt/β-catenin (IC50 = 180 nM). IWR-1 compromises critical steps of the canonical Wnt signaling, namely translocation of β-catenin to the nucleus and subsequent TCF/LEF activation and expression of Wnt/β-catenin downstream targets. IWR-1 promotes β-catenin phosphorylation by promoting stability of Axin-scaffolded destruction complexes. IWR-1 can be studied in research for anti-tumor purposes, and diseases such as osteosarcoma, colorectal cancer and psoriasis. -
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Monensin sodium
0 ImagesSynonyms: Monensin A sodiumMonensin (Monensin A) sodium, an orally active antibiotic, is an ionophore that mediates Na+/H+ exchange. Monensin sodium is a potent Wnt signaling inhibitor. Monensin sodium causes a marked enlargement of the multivesicular bodies (MVBs) and regulates exosome secretion. Monensin sodium can be used for bacterial, fungal, and parasitic infections research, and shows anticancer effects. -
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- Wnt-C59
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- MSAB
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- SKL2001
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Remigromig
0 ImagesCat. No.: HY-P992126CAS No.: 3059389-31-7Synonyms: EYE-103; MK-3000Remigromig (EYE-103; MK-3000) is a humanized bispecific monoclonal antibody targeting LRP5 and FZD4, suitable for use in research related to macular degeneration. -
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FJ9
0 ImagesCat. No.: HY-182624CAS No.: 873841-43-1FJ9 is a NHERF1/PDZ inhibitor with human NHERF1 PDZ1 IC50 1540 μM, NHERF1 PDZ2 IC50 160 μM, and Frizzled-7-Dishevelled PDZ complex Ki 10 μM. FJ9 binds ligand-binding pockets of NHERF1 PDZ domains to block cognate ligand interactions, disrupts Frizzled-7-Dishevelled interactions, and down-regulates canonical Wnt signaling. FJ9 induces apoptosis in cancer cells with intact β-catenin signaling. FJ9 can be used for the research of non-small cell lung cancer, melanoma. -
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EML631
0 ImagesCat. No.: HY-121511CAS No.: 2101206-36-2EML631 is a SPIN1 inhibitor with a Kd of 3-7 μM. EML631 interacts with the second Tudor domain of SPIN1 and blocks its ability to read the H3K4me3 histone mark. EML631 inhibits the coactivator activity of SPIN1 in the Wnt signaling pathway and reduces the activity of Wnt response reporter genes. EML631 can be used in cancer-related research. -
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Echinacoside
0 ImagesEchinacoside, one of the phenylethanoids isolated from the stems of Cistanche deserticola, effectively inhibits Wnt/β-catenin signaling. Echinacoside elicits neuroprotection by activating Trk receptors and their downstream signal pathways. Antiosteoporotic activity. -
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- Pyrvinium pamoate
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- BML-284
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Salinomycin sodium salt
0 ImagesSynonyms: Salinomycin sodium; Sodium salinomycinSalinomycin sodium salt (Salinomycin sodium), an antibiotic potassium ionophore, is a potent inhibitor of Wnt/β-catenin signaling. Salinomycin sodium salt acts on the Wnt/Fzd/LRP complex, blocks Wnt-induced LRP6 phosphorylation, and causes degradation of the LRP6 protein. Salinomycin sodium salt shows selective activity against human cancer stem cells. -
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Adavivint
0 ImagesSynonyms: SM04690; Lorecivivint -
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Foscenvivint
0 ImagesSynonyms: PRI-724PRI-724 is a selective inhibitor of the CBP/β-catenin interaction. -
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- iCRT 14
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- WAY-262611
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Neohesperidin
0 ImagesSynonyms: Hesperetin 7-O-neohesperidoside -
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SKI II
0 ImagesSKI-II is an oral active and synthetic inhibitor of sphingosine kinase (SK) activity, with IC50 values of 78 μM and 45 μM for SK1 and for SK2, respectively. SKI II causes an irreversible inhibition of SK1 by inducing its lysosomal and/or proteasomal degradation. -
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Triptonide
0 ImagesSynonyms: NSC 165677; PG 492Triptonide (NSC 165677) is a natural product identified in Tripterygium wilfordii Hook F.. Triptonide is a Wnt signaling inhibitor with an IC50 of appropriately 0.3 nM. Triptonide has immunosuppression, anti-inflammatory, anti-fertility, neuroprotective and anti-lymphoma effects. -
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