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MK 1775

 - AZD 1775  - Adavosertib
Axon 1494
CAS:  955365-80-7
Purity:  99%
  • Soluble in 0.1N HCl(aq) and DMSO
  • MF:  C27H32N8O2
  • MW:  500.6

Description

A potent and selective Wee1 kinase inhibitor in vitro and in vivo. MK 1775 abolishes cyclin-dependent kinase 1 (CDC2) activity by phosphorylation of the Tyr15 residue. It abrogates a DNA damage checkpoint (G2-phase), leading to apoptosis in combination with several DNA-damaging agents selectively in p53-deficient tumor cell lines. It is under clinical trial for advanced solid tumors.

More Information

Certificate of Analysis

Material Safety Data Sheet

Parent CAS No. 955365-80-7
Chemical Name 2-Allyl-1-[6-(1-hydroxy-1-methyl-ethyl)-pyridin-2-yl]-6-[4-(4-methyl-piperazin-1-yl)-phenylamino]-1,2-dihydro-pyrazolo[3,4-d]pyrimidin-3-one
SMILES C1(NC2C=CC(N3CCN(C)CC3)=CC=2)=NC2N(C3C=CC=C(C(O)(C)C)N=3)N(CC=C)C(=O)C=2C=N1
MFCD MFCD17215200
InChi InChI=1S/C27H32N8O2/c1-5-13-34-25(36)21-18-28-26(29-19-9-11-20(12-10-19)33-16-14-32(4)15-17-33)31-24(21)35(34)23-8-6-7-22(30-23)27(2,3)37/h5-12,18,37H,1,13-17H2,2-4H3,(H,28,29,31)
InChiKey BKWJAKQVGHWELA-UHFFFAOYSA-N
CID 24856436
Short Description Wee1 inhibitor

References

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