943540-74-7

JNJ-38877618 Chemical Structure
943540-74-7

Chemical Structure

JNJ-38877618

  • CAS. Nr.: 943540-74-7
  • Formula:C20H12F2N6
  • Molecular Weight:374.35

IUPAC Name: 6-(difluoro(6-(pyridin-4-yl)-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methyl)quinoline

InChIKey: KOAWAWHSMVKCON-UHFFFAOYSA-N

SMILES: FC(C1=CC=C2N=CC=CC2=C1)(F)C3=NN=C4C=CC(C5=CC=NC=C5)=NN43

Biological Activity: JNJ-38877618 is a potent, highly selective, orally bioavailable Met kinase inhibitor with IC50s of 2 and 3 nM for wild type and mutant Met, respectively.

Art. -Nr. Produktname Reinheit Beschreibung Pricing
HY-111050
JNJ-38877618 98.85% JNJ-38877618 is a potent, highly selective, orally bioavailable Met kinase inhibitor with IC50s of 2 and 3 nM for wild type and mutant Met, respectively.
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This compound is listed in the SVHC (Substances of Very High Concern) candidate list of ECHA (European Chemicals Agency).

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HY-111050R
JNJ-38877618 (Standard) ≥98% JNJ-38877618 (Standard) is the analytical standard of JNJ-38877618 (HY-111050). This product is intended for research and analytical applications. JNJ-38877618 is a potent, highly selective, orally bioavailable Met Kinase inhibitor with IC50s of 2 and 3 nM for wild type and mutant Met, respectively.
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loading...
Size Price
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In-stock
(Estimated to ship on )
(Estimated to ship TODAY)
Estimated to ship on
(Estimated to ship TODAY)

Amount:

USD 0.00

This product is a controlled substance and not for sale in your territory.

This product is not for sale in your territory.

This compound is listed in the SVHC (Substances of Very High Concern) candidate list of ECHA (European Chemicals Agency).

Pricing 
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