1421373-62-7
Chemical Structure
NT-1
Synonym(s): EGFR mutant-IN-3
- CAS No.: 1421373-62-7
- Formula:C27H30ClN7O2
- Molecular Weight:520.03
IUPAC Name: N-(5-((5-chloro-4-(1H-indol-3-yl)pyrimidin-2-yl)amino)-2-((2-(dimethylamino)ethyl)(methyl)amino)-4-methoxyphenyl)acrylamide
InChIKey: SUPQPCQJBYPRPC-UHFFFAOYSA-N
SMILES: C=CC(NC1=CC(NC2=NC=C(Cl)C(C3=CNC4=C3C=CC=C4)=N2)=C(OC)C=C1N(CCN(C)C)C)=O
Biological Activity: NT-1 (EGFR mutant-IN-3) is a potent mutant EGFR inhibitor and an analog of Osimertinib (HY-15772). This mutant EGFR inhibitor suppresses FGFRWT with an IC50 of 0.4 nM. NT-1 also inhibits EGFRL858R, EGFRExon 19 deletion and EGFRT790M. NT-1 exerts deeper inhibition on p-EGFR and p-ERK, and induces tumor cell apoptosis. NT-1 can be used in colorectal cancer research[1].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
NT-1 | 99.40% | NT-1 (EGFR mutant-IN-3) is a potent mutant EGFR inhibitor and an analog of Osimertinib (HY-15772). This mutant EGFR inhibitor suppresses FGFRWT with an IC50 of 0.4 nM. NT-1 also inhibits EGFRL858R, EGFRExon 19 deletion and EGFRT790M. NT-1 exerts deeper inhibition on p-EGFR and p-ERK, and induces tumor cell apoptosis. NT-1 can be used in colorectal cancer research. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
