- WZ4003
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- $43.00 / 5mg
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2026-04-22
- CAS:1214265-58-3
- Min. Order:
- Purity: 99.65%
- Supply Ability: 10g
- WZ4003
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- $0.10 / 1g
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2020-01-13
- CAS:1214265-58-3
- Min. Order: 1g
- Purity: 98%min
- Supply Ability: 1g,10g,1kg
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| Product Name: | WZ4003 | | Synonyms: | Propanamide, N-[3-[[5-chloro-2-[[2-methoxy-4-(4-methyl-1-piperazinyl)phenyl]amino]-4-pyrimidinyl]oxy]phenyl]-;WZ4003;N-[3-[[5-Chloro-2-[[2-methoxy-4-(4-methyl-1-piperazinyl)phenyl]amino]-4-pyrimidinyl]oxy]phenyl]propanamide;N-(3-((5-chloro-2-((2-methoxy-4-(4-methylpiperazin-1-yl)phenyl)amino)pyrimidin-4-yl)oxy)phenyl)propionamide;N-[3-[5-chloro-2-[2-methoxy-4-(4-methylpiperazin-1-yl)anilino]pyrimidin-4-yl]oxyphenyl]propanamide;WZ 4003;WZ4003;CS-1174;WZ 4003, NUAK kinase inhibitor | | CAS: | 1214265-58-3 | | MF: | C25H29ClN6O3 | | MW: | 496.99 | | EINECS: | | | Product Categories: | Inhibitors | | Mol File: | 1214265-58-3.mol |  |
| | WZ4003 Chemical Properties |
| density | 1.303±0.06 g/cm3(Predicted) | | storage temp. | -20°C | | solubility | insoluble in H2O; ≥2.68 mg/mL in EtOH with gentle warming and ultrasonic; ≥7.85 mg/mL in DMSO with gentle warming | | pka | 14.27±0.70(Predicted) | | form | powder | | color | white to beige | | InChIKey | SDGJBAUIGHSMRI-UHFFFAOYSA-N | | SMILES | ClC1=CN=C(NC2=C(OC)C=C(N3CCN(C)CC3)C=C2)N=C1OC4=CC(NC(CC)=O)=CC=C4 |
| WGK Germany | WGK 3 | | Storage Class | 11 - Combustible Solids | | Hazard Classifications | Acute Tox. 4 Oral |
| | WZ4003 Usage And Synthesis |
| Uses | WZ4003 is a highly specific protein kinase inhibitor of NUAK kinases. | | Biological Activity | wz4003 is a potent and selective inhibitor of nuak1 and nuak2 with ic50 values of 20 and 100 nm, respectively [1].nuak family snf1-like kinase-1 (nuak1) and the related nuak2 belong to the amp-activated protein kinase (ampk) family and are activated by liver kinase b1 (lkb1) tumour suppressor protein kinase [1].wz4003 is a potent and selective nuak1/2 inhibitor. in hek-293 cells, wz4003 inhibited the phosphorylation of myosin phosphate-targeting subunit 1 (mypt1), which was phosphorylated by nuak1 at ser445. in hek-293 cells overexpressing inhibitor-resistant nuak1[a195t], wz4003 didn’t inhibit the phosphorylation of mypt1 at ser445. in mouse embryonic fibroblasts (mefs), wz4003 significantly inhibited migration in a wound-healing assay and inhibited mefs proliferation. in a cell invasion assay, wz4003 inhibited the invasive potential of u2os cells [1]. in u2os cells, wz4003 (10 μm) inhibited phosphorylation of mypt1 and reduced the cells in s-phase by 50%. also, wz4003 prevented cells from entering into mitosis [2]. | | Biochem/physiol Actions | WZ4003 helps to repress the migration of cells. It also prevents cell proliferation. | | IC 50 | NUAK1: 20 nM (IC50); NUAK2: 100 nM (IC50) | | storage | Store at -20°C | | references | [1]. banerjee s, buhrlage sj, huang ht, et al. characterization of wz4003 and hth-01-015 as selective inhibitors of the lkb1-tumour-suppressor-activated nuak kinases. biochem j, 2014, 457(1): 215-225.
[2]. banerjee s, zagórska a, deak m, et al. interplay between polo kinase, lkb1-activated nuak1 kinase, pp1βmypt1 phosphatase complex and the scfβtrcp e3 ubiquitin ligase. biochem j, 2014, 461(2): 233-245. |
| | WZ4003 Preparation Products And Raw materials |
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