ChemicalBook > CAS DataBase List > JNJ-38877605

JNJ-38877605

Product Name
JNJ-38877605
CAS No.
943540-74-7
Chemical Name
JNJ-38877605
Synonyms
JNJ;OMO-1);JNJ-38877618;JNJ-38877618 (OMO1;Venadaparib Impurity 21;JNJ-38877618,Inhibitor,c-Met/HGFR,JNJ 38877618,JNJ38877618,inhibit;6-[Difluoro[6-(4-pyridinyl)-1,2,4-triazolo[4,3-b]pyridazin-3-yl]methyl]quinoline;6-(difluoro(6-(pyridin-4-yl)-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methyl)quinoline;Quinoline, 6-[difluoro[6-(4-pyridinyl)-1,2,4-triazolo[4,3-b]pyridazin-3-yl]methyl]-
CBNumber
CB24660859
Molecular Formula
C20H12F2N6
Formula Weight
374.35
MOL File
943540-74-7.mol
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JNJ-38877605 Property

storage temp. 
Store at -20°C
solubility 
DMSO : 5 mg/mL (13.36 mM)
form 
Solid
color 
White to off-white
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

ChemScene
Product number
CS-0034063
Product name
JNJ-38877618
Purity
99.01%
Packaging
5mg
Price
$210
Updated
2021/12/16
ChemScene
Product number
CS-0034063
Product name
JNJ-38877618
Purity
99.01%
Packaging
10mg
Price
$310
Updated
2021/12/16
ChemScene
Product number
CS-0034063
Product name
JNJ-38877618
Purity
99.01%
Packaging
50mg
Price
$910
Updated
2021/12/16
ChemScene
Product number
CS-0034063
Product name
JNJ-38877618
Purity
99.01%
Packaging
100mg
Price
$1300
Updated
2021/12/16
DC Chemicals
Product number
DC21440
Product name
JNJ-38877618
Purity
>98%
Packaging
100mg
Price
$800
Updated
2021/12/16
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JNJ-38877605 Chemical Properties,Usage,Production

Biological Activity

JNJ-38877618 (OMO-1) is a potent, highly selective, and orally bioavailable Met (c-Met) kinase inhibitor with a Kd of 1.4 nM. Its IC50 values for wild-type Met (c-Met) and mutant Met (c-Met) (M1268T) were 2 nM and 3 nM, respectively.

in vivo

In vivo, JNJ-38877618(OMO-1) completely inhibited tumor growth in 3 tumor models: SNU5 MET amp gastric cancer model, U87-MG HGF autocrine glioblastoma model, and exon 14 skipping deletion mutation Hs746T gastric cancer model of MET gene. Administration of OMO-1 in combination with other drugs is well tolerated and can improve and enhance the effect of EGFR-targeted therapy. Although single-agent OMO-1 has no effect on NSCLC HCC827 EGFR, its combination with erlotinib can delay tumor recurrence.

target

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JNJ-38877605 Preparation Products And Raw materials

Raw materials

Preparation Products

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JNJ-38877605 Suppliers

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943540-74-7, JNJ-38877605Related Search:


  • JNJ-38877618
  • JNJ-38877618 (OMO1
  • OMO-1)
  • 6-(difluoro(6-(pyridin-4-yl)-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methyl)quinoline
  • Quinoline, 6-[difluoro[6-(4-pyridinyl)-1,2,4-triazolo[4,3-b]pyridazin-3-yl]methyl]-
  • 6-[Difluoro[6-(4-pyridinyl)-1,2,4-triazolo[4,3-b]pyridazin-3-yl]methyl]quinoline
  • JNJ-38877618,Inhibitor,c-Met/HGFR,JNJ 38877618,JNJ38877618,inhibit
  • JNJ
  • Venadaparib Impurity 21
  • 943540-74-7
  • TargetValue
    Met
    (Cell-free assay)
    2 nM
    MET (M1268T)
    (Cell-free assay)
    3 nM