Lirafugratinib

  Cat. No.:  DC72885   Featured
Chemical Structure
2549174-42-5
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More than 5000 active chemicals with high quality for research!
Field of application
Lirafugratinib (RLY-4008) is an orally active and selective inhibitor of FGFR2.
Cas No.: 2549174-42-5
Chemical Name: Fgfr2-IN-3
Synonyms: Lirafugratinib;Lirafugratinib [USAN];7HY6IMH87S;FGFR2-IN-3;RLY4008;2-Propenamide, N-(4-(4-amino-5-(3-fluoro-4-((4-methyl-2-pyrimidinyl)oxy)phenyl)-7-methyl-7H-pyrrolo(2,3-d)pyrimidin-6-yl)phenyl)-2-methyl-;2-Propenamide, N-[4-[4-amino-5-[3-fluoro-4-[(4-methyl-2-pyrimidinyl)oxy]phenyl]-7-methyl-7H-pyrrolo[2,3-d]pyrimidin-6-yl]phenyl]-2-methyl-;NSC842116;WHO 12482;N-(4-(4-amino-5-(3-fluoro-4-((4-methylpy;RLY-4008
SMILES: CN1C2=NC=NC(N)=C2C(C2C=CC(OC3=NC=CC(C)=N3)=C(F)C=2)=C1C1C=CC(NC(=O)C(=C)C)=CC=1
Formula: C28H24FN7O2
M.Wt: 509.534268379211
Purity: >98%
Sotrage: 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO
Description: Lirafugratinib (RLY-4008) is an orally active and selective inhibitor of FGFR2.
Target: FGFR2[1]
References: [1]. [1] Lescarbeau, Andre, et al. Preparation of substituted pyrrolopyrimidines as FGFR inhibitors and methods of making and using the same. WO2022109577.
MSDS
Cat. No. Product name Field of application
DC72885 Lirafugratinib Lirafugratinib (RLY-4008) is an orally active and selective inhibitor of FGFR2.
DC40209 ZUN97585(FGFR1/DDR2 inhibitor 1) FGFR1/DDR2 inhibitor 1 is an orally active inhibitor of fibroblast growth factor receptor 1 (FGFR1) and discoindin domain receptor 2 (DDR2), with IC50 values of 31.1 nM and 3.2 nM, respectively. Antitumor activity.
DC10641 PRN1371 PRN1371 is an irreversible covalent FGFR1-4 kinase inhibitor, with IC50s of 0.6, 1.3, 4.1, 19.3 and 8.1 nM for FGFR1, 2, 3, 4 and CSF1R, respectively.
DC10128 FGF401( Roblitinib) FGF401 is an inhibitor of human fibroblast growth factor receptor 4 (FGFR4), with potential antineoplastic activity.
DC10559 Derazantinib (ARQ 087) Derazantinib (Derazantinib) is an ATP competitive tyrosine kinase inhibitor; exhibits potent activity against FGFR1-3 chondrocytes with IC50s of 4.5, 1.8, and 4.5 nM, respectively.
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