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CHZ868

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
CHZ868
Identifiers
  • N-[4-[2-(2,4-difluoroanilino)-1,4-dimethylbenzimidazol-5-yl]oxypyridin-2-yl]acetamide
CAS Number
PubChemCID
ChemSpider
ChEBI
Chemical and physical data
FormulaC22H19F2N5O2
Molar mass423.424 g·mol−1
3D model (JSmol)
  • CC1=C(C=CC2=C1N=C(N2C)NC3=C(C=C(C=C3)F)F)OC4=CC(=NC=C4)NC(=O)C
  • InChI=1S/C22H19F2N5O2/c1-12-19(31-15-8-9-25-20(11-15)26-13(2)30)7-6-18-21(12)28-22(29(18)3)27-17-5-4-14(23)10-16(17)24/h4-11H,1-3H3,(H,27,28)(H,25,26,30)
  • Key:KQQLBXFPTDVFAJ-UHFFFAOYSA-N

CHZ868 is a drug which acts as aJanus kinase inhibitor selective for theJAK2 subtype. It was one of the first Janus kinase inhibitors developed, originally for the treatment ofleukemia and related blood cancers, and while it did not get approved for clinical use, it is still used for research in the area.[1][2][3][4]

See also

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References

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  1. ^Meyer SC, Keller MD, Chiu S, Koppikar P, Guryanova OA, Rapaport F, et al. (July 2015)."CHZ868, a Type II JAK2 Inhibitor, Reverses Type I JAK Inhibitor Persistence and Demonstrates Efficacy in Myeloproliferative Neoplasms".Cancer Cell.28 (1):15–28.doi:10.1016/j.ccell.2015.06.006.PMC 4503933.PMID 26175413.
  2. ^Kong X, Sun H, Pan P, Li D, Zhu F, Chang S, et al. (August 2017)."How Does the L884P Mutation Confer Resistance to Type-II Inhibitors of JAK2 Kinase: A Comprehensive Molecular Modeling Study".Scientific Reports.7 (1) 9088.Bibcode:2017NatSR...7.9088K.doi:10.1038/s41598-017-09586-3.PMC 5567357.PMID 28831147.
  3. ^Nair PC, Piehler J, Tvorogov D, Ross DM, Lopez AF, Gotlib J, Thomas D (September 2023)."Next-Generation JAK2 Inhibitors for the Treatment of Myeloproliferative Neoplasms: Lessons from Structure-Based Drug Discovery Approaches".Blood Cancer Discovery.4 (5):352–364.doi:10.1158/2643-3230.BCD-22-0189.PMC 10472187.PMID 37498362.
  4. ^Codilupi T, Szybinski J, Arunasalam S, Jungius S, Dunbar AC, Stivala S, et al. (February 2024)."Development of Resistance to Type II JAK2 Inhibitors in MPN Depends on AXL Kinase and Is Targetable".Clinical Cancer Research.30 (3):586–599.doi:10.1158/1078-0432.CCR-23-0163.PMC 10831334.PMID 37992313.
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