ZW4864 free base
CAS No. 2632259-92-6
ZW4864 free base( —— )
Catalog No. M37644 CAS No. 2632259-92-6
ZW4864 (free base) is an orally active and selective β-catenin/B-Cell lymphoma 9 protein-protein interaction (β-catenin/BCL9 PPI) inhibitor, with a K_i value of 0.76 μM and an IC_50 value of 0.87 μM .
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 432 | In Stock |
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| 5MG | 392 | In Stock |
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| 10MG | 587 | In Stock |
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| 25MG | 936 | In Stock |
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| 50MG | 1237 | In Stock |
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| 100MG | 1665 | In Stock |
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| 200MG | Get Quote | In Stock |
|
| 500MG | 3339 | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product NameZW4864 free base
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NoteResearch use only, not for human use.
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Brief DescriptionZW4864 (free base) is an orally active and selective β-catenin/B-Cell lymphoma 9 protein-protein interaction (β-catenin/BCL9 PPI) inhibitor, with a K_i value of 0.76 μM and an IC_50 value of 0.87 μM .
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DescriptionZW4864 (free base) is an orally active and selective β catenin/B-Cell lymphoma 9 protein protein interaction (β catenin/BCL9 PPI) inhibitor. ZW4864 (free base) inhibits β catenin/BCL9 PPI with a Ki value of 0.76 μM and an IC50 value of 0.87 μM.
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In VitroWestern Blot Analysis Cell Line:SW480 and MBA-MD-231 cells Concentration:10~40 μM Incubation Time:24 hours Result:Decreased the expression levels of Axin2 and cyclin D1 proteins.Apoptosis Analysis Cell Line:MDA-MB231, MCF10A and MDA-MB-468 cells Concentration:10~40 μM Incubation Time:72 hours Result:Selectively triggered rapid apoptosis of triple-negative breast cancer cells with hyperactive β-catenin signaling while sparing normal mammary epithelial MCF10A cells.RT-PCR Cell Line:SW480 and MBA-MD-231 cells Concentration:10~40 μ Incubation Time:24 hours Result:Suppressed the transcription of β-catenin target genes in a concentration-dependent manner without affecting the expression of HPRT, a house-keeper gene, in both SW480 and Wnt 3a-activated MDA-MB-231 cells.
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In VivoAnimal Model:C57BL/6 mice Dosage:20 mg/kg (Pharmacokinetic Analysis)Administration:P.o.Result:Exhibited good pharmacokinetic properties with an oral bioavailability (F) of 83%.Animal Model:Mice Dosage:90 mg/kg Administration:P.o.Result:Showed a variation in tumor growth in mice.
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Synonyms——
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PathwayWnt/Notch/Hedgehog
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TargetWnt/beta/catenin
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RecptorWnt/beta-catenin
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Research Area——
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Indication——
Chemical Information
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CAS Number2632259-92-6
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Formula Weight570.72
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Molecular FormulaC33H42N6O3
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 100 mg/mL (175.22 mM; Ultrasonic )
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SMILESCC(C)(Oc1cccc(c1)N1CCC[C@H](C1)C(=O)N(Cc1ccc(cc1)-c1cn[nH]c1)C1CC1)C(=O)N1CCNCC1
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1. Wang Z, et al. Discovery of an Orally Bioavailable Small-Molecule Inhibitor for the β-Catenin/B-Cell Lymphoma 9 Protein-Protein Interaction. J Med Chem. 2021;64(16):12109-12131.?
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