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1-(4-Fluorophenyl)-N-[3-fluoro-4-(1H-pyrrolo[2,3-b]pyridin-4-yloxy)phenyl]-1,2-dihydro-2-oxo-3-pyridinecarboxamide

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1-(4-Fluorophenyl)-N-[3-fluoro-4-(1H-pyrrolo[2,3-b]pyridin-4-yloxy)phenyl]-1,2-dihydro-2-oxo-3-pyridinecarboxamide Basic information

Product Name:
1-(4-Fluorophenyl)-N-[3-fluoro-4-(1H-pyrrolo[2,3-b]pyridin-4-yloxy)phenyl]-1,2-dihydro-2-oxo-3-pyridinecarboxamide
Synonyms:
  • 1-(4-Fluorophenyl)-N-[3-fluoro-4-(1H-pyrrolo[2,3-b]pyridin-4-yloxy)phenyl]-1,2-dihydro-2-oxo-3-pyridinecarboxamide
  • BMS-2
  • BMS-21-(4-Fluorophenyl)-N-[3-fluoro-4-(1H-pyrrolo[2,3-b]pyridin-4-yloxy)phenyl]-1,2-dihydro-2-oxo-3-pyridinecarboxamide
  • N-(4-((1H-Pyrrolo[2,3-b]pyridin-4-yl)oxy)-3-fluorophenyl)-1-(4-fluorophenyl)-2-oxo-1,2-dihydro
  • N-(4-(1H-PYRROLO[2,3-B]PYRIDIN-4-YLOXY)-3-FLUOROPHENYL)-1-(4-FLUOROPHENYL)-2-OXO-1,2-DIHYDROPYRIDINE-3-CARBOXAMIDE
  • BMS2;BMS 2
  • 3-Pyridinecarboxamide, 1-(4-fluorophenyl)-N-[3-fluoro-4-(1H-pyrrolo[2,3-b]pyridin-4-yloxy)phenyl]-1,2-dihydro-2-oxo-
  • SYN-1022
CAS:
888719-03-7
MF:
C25H16F2N4O3
MW:
458.42
Mol File:
888719-03-7.mol
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1-(4-Fluorophenyl)-N-[3-fluoro-4-(1H-pyrrolo[2,3-b]pyridin-4-yloxy)phenyl]-1,2-dihydro-2-oxo-3-pyridinecarboxamide Chemical Properties

Melting point:
212-214℃
Density 
1.41
storage temp. 
2-8°C
solubility 
ethanol: 1mg/mL
DMSO: 10mg/mL
form 
Solid
pka
10.72±0.70(Predicted)
color 
Off-white to light yellow
InChI
1S/C25H16F2N4O3/c26-15-3-6-17(7-4-15)31-13-1-2-19(25(31)33)24(32)30-16-5-8-22(20(27)14-16)34-21-10-12-29-23-18(21)9-11-28-23/h1-14H,(H,28,29)(H,30,32)
InChIKey
OBSFXHDOLBYWRJ-UHFFFAOYSA-N
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Safety Information

WGK Germany 
WGK 2
Storage Class
11 - Combustible Solids
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1-(4-Fluorophenyl)-N-[3-fluoro-4-(1H-pyrrolo[2,3-b]pyridin-4-yloxy)phenyl]-1,2-dihydro-2-oxo-3-pyridinecarboxamide Usage And Synthesis

Uses

BMS-2 is a potent MET kinase inhibitor.

in vivo

MET kinase-IN-4 (Compound 2) (i.v., p.o.; 5, 10 mg/kg) possesses a favorable pharmacokinetic profile in mice[1].
MET kinase-IN-4 (p.o.; 6.25, 12.5, 25 and 50 mg/kg; once a day) demonstrates significant in vivo antitumor activity in the GTL-16 human gastric carcinoma xenograft model[1].

Animal Model:Mice[1]
Dosage:5, 10 mg/kg
Administration:IV, PO
Result:Showed extensive extravascular distribution and a favorable half-life.
Animal Model:Nude mice[1]
Dosage:6.25, 12.5, 25 and 50 mg/kg
Administration:PO, once a day
Result:Showed antitumor activity in dose-dependet.

1-(4-Fluorophenyl)-N-[3-fluoro-4-(1H-pyrrolo[2,3-b]pyridin-4-yloxy)phenyl]-1,2-dihydro-2-oxo-3-pyridinecarboxamideSupplier

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