| Identification | Back Directory | [Name]
WZ8040 | [CAS]
1214265-57-2 | [Synonyms]
WZ8040
CS-471
WZ-8040;WZ 8040
WZ8040 USP/EP/BP
N-(3-(5-chloro-2-(4-(4-methylpiperazin-1-yl)phenylamino)pyrimidin-4-ylthio)phenyl)acrylamide
N-(3-((5-Chloro-2-((4-(4-methylpiperazin-1-yl)phenyl)amino)pyrimidin-4-yl)thio)phenyl)acrylami
N-[3-[[5-Chloro-2-[[4-(4-methyl-1-piperazinyl)phenyl]amino]-4-pyrimidinyl]thio]phenyl]-2-propenamide
2-Propenamide, N-[3-[[5-chloro-2-[[4-(4-methyl-1-piperazinyl)phenyl]amino]-4-pyrimidinyl]thio]phenyl]-
N-[3-[[5-Chloro-2-[[4-(4-methyl-1-piperazinyl)phenyl]amino]-4-pyrimidinyl]thio]phenyl]-2-propenamide WZ8040 | [Molecular Formula]
C24H25ClN6OS | [MDL Number]
MFCD18074511 | [MOL File]
1214265-57-2.mol | [Molecular Weight]
481.02 |
| Chemical Properties | Back Directory | [density ]
1.37 | [storage temp. ]
Store at -20°C | [solubility ]
≥24.05 mg/mL in DMSO; insoluble in H2O; ≥2.61 mg/mL in EtOH with gentle warming and ultrasonic | [form ]
solid | [pka]
12.94±0.70(Predicted) | [color ]
Light yellow to green yellow |
| Hazard Information | Back Directory | [Description]
WZ8040 is an inhibitor of mutant EGF receptors (EGFRs) with IC50 values ranging from 2 to 306 nM in Ba/F3 cells.1 It is selective for EGFR mutants, including the EGFRDel E746_A750 and EGFRL858R mutations conferring gefitinib sensitivity and the EGFRDel E746_A750/T790M mutation conferring gefitinib resistance (IC50s = 2, 6, and 6 nM in Ba/F3 cells), over wild-type EGFR (IC50 = 1,820 nM in HN11 cells) but also inhibits ERBB2Ins G776V,C and wild-type ERBB2 (IC50s = 20 and 32 nM, respectively, in Ba/F3 cells). WZ8040 inhibits proliferation of PC-9 cells harboring the EGFRDel E746_A750 mutation and gefitinib-resistant PC-9 GR cells harboring the EGFRT790M resistant allele (EC50s = 6 and 8 nM, respectively).2 | [Uses]
WZ8040 is an irreversiblely EGFR T790M inhibitor (IC50<10nM). | [target]
EGFR T790M | [IC 50]
EGFR Del E746_A750: 1 nM (IC50, in HCC827 cells); EGFR Del E746_A750: 6 nM (IC50, in PC9 cells); EGFR L858R: 66 nM (IC50, in H3255 cells
); EGFR L858R/T790M: 9 nM (IC50, in H1975 cells); EGFR Del E746_A750/T790M: 8 nM (IC50, in PC9 GR cells); EGFR E746_A750/MET amp: >3.3 μM (IC50, in HCC827 GR cells); ERBB2 amp: 738 nM (IC50, in H1819 cells); ERBB2 amp: 915 nM (IC50, in Calu-3 cells); ERBB2 Ins G776V, C: 744 nM (IC50, in H1781 cells); EGFR & ERBB2 WT: 1.82 μM (IC50, in HN11 cells) | [storage]
Store at -20°C | [References]
[1] zhou w1, ercan d, chen l, yun ch, li d, capelletti m, cortot ab, chirieac l, iacob re, padera r, engen jr, wong kk, eck mj, gray ns, j?nne pa. novel mutant-selective egfr kinase inhibitors against egfr t790m. nature. 2009 dec 24;462(7276):1070-4. doi: 10.1038/nature08622. |
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| Company Name: |
China Langchem Inc.
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| Telephone: |
0086-21-58956006 |
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www.chemicalbook.com/ShowSupplierProductsList19141/0_EN.htm |
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NCE Biomedical Co.,Ltd.
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4000-027-021 |24 +86-13986109188 | +86-15623472865 | +81-08033611988 |
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www.chemicalbook.com/ShowSupplierProductsList15748/0_EN.htm |
| Company Name: |
LETOPHARM LIMITED
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+86-21-5821 5861 |
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www.letopharm.com |
| Company Name: |
SPIRO PHARMA
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www.spiropharma.com.cn |
| Company Name: |
Twochem Co.Ltd
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021-021-58111628 15800915896 |
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www.twochem.com |
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