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  • DC Chemicals Limited
  • China
  • Product Name: XMD8-87
  • Price: $550.0/100mg $1000.0/250mg $2100.0/1g
  • Purity: 98.0%
  • Stocking Period: 3 Day
  • Contact: Tony Cao

1234480-46-6

1234480-46-6 structure
1234480-46-6 structure
  • Name: XMD 8-87
  • Chemical Name: 2-{[2-Methoxy-4-(4-methyl-1-piperazinyl)phenyl]amino}-11-methyl-5,11-dihydro-6H-pyrimido[4,5-b][1,4]benzodiazepin-6-one
  • CAS Number: 1234480-46-6
  • Molecular Formula: C24H27N7O2
  • Molecular Weight: 445.517
  • Catalog: Signaling Pathways Metabolic Enzyme/Protease Tyrosinase
  • Create Date: 2018-05-30 07:14:48
  • Modify Date: 2024-01-09 11:23:09
  • XMD8-87 is a potent TNK2 inhibitor with IC50 values of 38 and 113 nM for the D163E and R806Q mutations, respectively.

Name 2-{[2-Methoxy-4-(4-methyl-1-piperazinyl)phenyl]amino}-11-methyl-5,11-dihydro-6H-pyrimido[4,5-b][1,4]benzodiazepin-6-one
Synonyms 6H-Pyrimido[4,5-b][1,4]benzodiazepin-6-one, 5,11-dihydro-2-[[2-methoxy-4-(4-methyl-1-piperazinyl)phenyl]amino]-11-methyl-
2-{[2-Methoxy-4-(4-methyl-1-piperazinyl)phenyl]amino}-11-methyl-5,11-dihydro-6H-pyrimido[4,5-b][1,4]benzodiazepin-6-one
XMD8-87
Description XMD8-87 is a potent TNK2 inhibitor with IC50 values of 38 and 113 nM for the D163E and R806Q mutations, respectively.
Related Catalog
Target

IC50: 38 nM (TNK2, D163E mutation), 113 nM (TNK2, R806Q mutation)[1]

In Vitro XMD8-87 potently inhibits the growth of the TNK2 mutant expressing cell lines while having little or no effect on the control cells out to the highest tested concentrations (1,000 nM). XMD8-87 has IC50s of 38 nM and 113 nM for the D163E and R806Q mutations. The effects of XMD8-87 on TNK2 cell lines are largely due to on-target effects on TNK2. Auto-phosphorylation of overexpressed TNK2 mutants could be blocked with TNK2 inhibitor XMD8-87[1].
Kinase Assay Kinase targets are tested with biochemical enzymatic kinase assays using the SelectScreen Kinase Profiling Service to determine IC50 values. The compounds (XMD8-87) are assayed at 10 concentrations (3-fold serial dilutions starting from 1 μM) at an ATP concentration equal to the ATP Km[1].
Cell Assay Cells are treated with the following inhibitors for 72 hours: dasatinib, AIM-100, XMD8-87 and XMD16-5. Cell viability is measured using a methanethiosulfonate (MTS)-based assay and absorbance (490 nm) is read at 1 and 3 hours after adding reagent[1].
References

[1]. Maxson JE, et al. Identification and Characterization of Tyrosine Kinase Nonreceptor 2 Mutations in Leukemia through Integration of Kinase Inhibitor Screening and Genomic Analysis.

Density 1.3±0.1 g/cm3
Molecular Formula C24H27N7O2
Molecular Weight 445.517
Exact Mass 445.222626
LogP 1.23
Index of Refraction 1.648
Storage condition -20℃
Hazard Codes N