PF-6422899
PF-6422899 is an inhibitor for EGFR, that it selectively binds to EGFR and SOAT1 in nanomolar levels.
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- CAS No.: 1621002-23-0
- Formule: C20H14ClFN4O2
- Masse moléculaire:396.80
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Stockage:
Please store the product under the recommended conditions in the Certificate of Analysis.
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Activité biologique
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Cell Line
|
Type | Value | Description | References |
|---|---|---|---|---|
| A549 | IC50 |
15 nM
Compound: 22
|
Inhibition of EGF-stimulated wild type EGFR autophosphorylation expressed in human A549 cells by sandwich ELISA
Inhibition of EGF-stimulated wild type EGFR autophosphorylation expressed in human A549 cells by sandwich ELISA
|
[PMID: 26756222] |
| A549 | IC50 |
>10000 nM
Compound: 4
|
Antiproliferative activity against human A549 cells harboring wild-type EGFR after 72 hrs by EZ-Cytox assay
Antiproliferative activity against human A549 cells harboring wild-type EGFR after 72 hrs by EZ-Cytox assay
|
[PMID: 30554954] |
| NCI-H1975 | IC50 |
7 nM
Compound: 22
|
Inhibition of EGFR L858R/T790M double mutant autophosphorylation in human NCI-H1975 cells after 2 hrs by sandwich ELISA
Inhibition of EGFR L858R/T790M double mutant autophosphorylation in human NCI-H1975 cells after 2 hrs by sandwich ELISA
|
[PMID: 26756222] |
| NCI-H1975 | IC50 |
1587 nM
Compound: 4
|
Antiproliferative activity against human NCI-H1975 cells harboring EGFR T790M/L858R double mutant after 72 hrs by EZ-Cytox assay
Antiproliferative activity against human NCI-H1975 cells harboring EGFR T790M/L858R double mutant after 72 hrs by EZ-Cytox assay
|
[PMID: 30554954] |
| PC-9 | IC50 |
2.9 nM
Compound: 4
|
Antiproliferative activity against human PC9 cells harboring EGFR exon-19 del mutant after 72 hrs by EZ-Cytox assay
Antiproliferative activity against human PC9 cells harboring EGFR exon-19 del mutant after 72 hrs by EZ-Cytox assay
|
[PMID: 30554954] |
| Sf21 | IC50 |
31 nM
Compound: 4
|
Inhibition of human N-terminal GST-tagged EGFR kinase domain (696 to end residues) expressed in baculovirus infected sf21 cells using poly(Glu, Tyr) 4:1 as substrate
Inhibition of human N-terminal GST-tagged EGFR kinase domain (696 to end residues) expressed in baculovirus infected sf21 cells using poly(Glu, Tyr) 4:1 as substrate
|
[PMID: 30554954] |
| Sf21 | IC50 |
55 nM
Compound: 4
|
Inhibition of human C-terminal His6-tagged ERBB2 (676 to end residues) expressed in baculovirus infected sf21 cells using poly(Glu, Tyr) 4:1 as substrate
Inhibition of human C-terminal His6-tagged ERBB2 (676 to end residues) expressed in baculovirus infected sf21 cells using poly(Glu, Tyr) 4:1 as substrate
|
[PMID: 30554954] |
| Sf21 | IC50 |
7 nM
Compound: 4
|
Inhibition of human N-terminal GST-tagged EGFR T790M/L858R double mutant (696 to end residues) expressed in baculovirus infected sf21 cells using poly(Glu, Tyr) 4:1 as substrate
Inhibition of human N-terminal GST-tagged EGFR T790M/L858R double mutant (696 to end residues) expressed in baculovirus infected sf21 cells using poly(Glu, Tyr) 4:1 as substrate
|
[PMID: 30554954] |
| SK-BR-3 | IC50 |
106 nM
Compound: 4
|
Antiproliferative activity against HER2-dependant human SKBR3 cells after 72 hrs by EZ-Cytox assay
Antiproliferative activity against HER2-dependant human SKBR3 cells after 72 hrs by EZ-Cytox assay
|
[PMID: 30554954] |
Chemical Information
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CAS No. 1621002-23-0
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Masse moléculaire 396.80
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Formule C20H14ClFN4O2
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SMILES
C=CC(NC1=CC2=C(NC3=CC=C(F)C(Cl)=C3)N=CN=C2C=C1OCC#C)=O
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Livraison
Room temperature in continental US; may vary elsewhere.
-
Stockage
Please store the product under the recommended conditions in the Certificate of Analysis.
Pureté et documentation
Références
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)