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Chemical Structure| 1776112-90-3 Chemical Structure| 1776112-90-3

Structure of Mavelertinib
CAS No.: 1776112-90-3

Chemical Structure| 1776112-90-3

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PF-06747775 provides potent EGFR activity against the four common mutants (exon 19 deletion (Del), L858R, and double mutants T790M/L858R and T790M/Del), selectivity over wild-type EGFR, and desirable ADME properties.

Synonyms: PF-06747775

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Product Details of Mavelertinib

CAS No. :1776112-90-3
Formula : C18H22FN9O2
M.W : 415.42
SMILES Code : C=CC(N[C@@H]1CN(C2=NC(NC3=CN(C)N=C3OC)=C4N=CN(C)C4=N2)C[C@H]1F)=O
Synonyms :
PF-06747775
MDL No. :MFCD29079007

Safety of Mavelertinib

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319
Precautionary Statements:P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330

Related Pathways of Mavelertinib

RTK
JAK-STAT

Isoform Comparison

Biological Activity

Description
Mavelertinib is a selective, orally bioavailable, irreversible inhibitor of EGFR tyrosine kinase (EGFR TKI), exhibiting IC50 values of 5, 4, 12, and 3 nM for Del, L858R, and the double mutants T790M/L858R and T790M/Del, respectively. It holds potential for research in non-small-cell lung cancer (NSCLC)[1][2][3][4].

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

2.41mL

0.48mL

0.24mL

12.04mL

2.41mL

1.20mL

24.07mL

4.81mL

2.41mL

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