ZUN97585(FGFR1/DDR2 inhibitor 1)

  Cat. No.:  DC40209   Featured
Chemical Structure
2308497-58-5
For research use only. We do not sell to patients.
We match the best price and quality on market.
Email:order@dcchemicals.com  sales@dcchemicals.com
Tel:+86-021-58447131
We are official vendor of:
  • 20
  • 19
  • 18
  • 17
  • 16
  • 15
  • 14
  • 12
  • 11
  • 10
  • 9
  • 8
  • 13
  • 6
  • 5
  • 4
  • 3
  • 2
  • 1
More than 5000 active chemicals with high quality for research!
Field of application
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.
Cas No.: 2308497-58-5
Chemical Name: FGFR1/DDR2 inhibitor 1
Synonyms: FGFR1/DDR2 inhibitor 1;BDBM50529770;3-(3-(1-Cyclopropyl-1H-pyrazol-4-yl)-1H-indazol-6-yl)-4-methyl-N-(3-(trifluoromethyl)phenyl)benzamide;3-(3-(1-cyclopropyl-1h-pyrazol-4-yl)-1h-indazol-6-yl)-N-(3-(trifluoromethyl)phenyl)-4-methylbenzamide
SMILES: FC(C1=CC=CC(=C1)NC(C1C=CC(C)=C(C=1)C1C=CC2=C(C=1)NN=C2C1C=NN(C=1)C1CC1)=O)(F)F
Formula: C28H22F3N5O
M.Wt: 501.50239610672
Purity: >98%
Sotrage: Please store the product under the recommended conditions in the Certificate of Analysis.
Description: FGFR1/DDR2 inhibitor 1 (compound 11k) is an inhibitor of fibroblast growth factor receptor 1 (FGFR1) and discoindin domain receptor 2 (DDR2), with IC50 values of 31.1 nM, 108.4 nM and 3.2 nM for FGFR1, KG-1, and DDR2, respectively[1].
Target: IC50: 31.1 nM (FGFR1), 108.4 nM (KG-1), 3.2 nM (DDR2)[1].
References: [1]. Wang Q, et al. Discovery and optimization of a series of 3-substituted indazole derivatives as multi-target kinase inhibitors for the treatment of lung squamous cell carcinoma. Eur J Med Chem. 2019 Feb 1;163:671-689.
MSDS
COA
LOT NO. DOWNLOAD
2018-0101
2018-0101
2018-0101
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.
X