7 Results for "

EGFR-MUT

" in MedChemExpress (MCE) Product Catalog:
Products (7)

7 Results for "EGFR-MUT" in MCE Product Catalog:

2
2 Cited Publications
Cat. No.: HY-13984
CAS No.: 1421373-62-7
Purity:  99.51%
Synonyms: EGFR MUTant-IN-3
Research Areas:  

Cancer

NT-1 (EGFR mutant-IN-3) is a potent mutant EGFR inhibitor and an analog of Osimertinib (HY-15772). This mutant EGFR inhibitor suppresses FGFR WT with an IC50 of 0.4 nM. NT-1 also inhibits EGFR L858R, EGFR Exon 19 deletion and EGFR T790M. 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 .
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Cat. No.: HY-128860
CAS No.: 2050906-97-1
Target:  

EGFR

Research Areas:  

Cancer

Mutated EGFR-IN-2 (compound 91) is a mutant-selective EGFR inhibitor extracted from patent WO2017036263A1, which potently inhibits single-mutant EGFR (T790M) and double-mutant EGFR (including L858R/T790M (IC50=<1nM) and ex19del/T790M), and can suppress activity of single gain-of-function mutant EGFR (including L858R and ex19del) as well. Mutated EGFR-IN-2 shows anti-tumor antivity .
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Cat. No.: HY-130608
CAS No.: 2375107-27-8
Target:  

EGFR

Research Areas:  

Cancer

Mutated EGFR-IN-3 (compound 3) is a potent, ATP-competitive and highly selective allosteric dibenzodiazepinone inhibitor of the EGFR(L858R/T790M) and EGFR(L858R/T790M/C797S) mutants with IC50 values of 12 nM and 13 nM, respectively .
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Cat. No.: HY-155005
CAS No.: 2770009-06-6
Purity:  ≥97.0%
Target:  

EGFR

Research Areas:  

Cancer

EGFR mutant-IN-2 (Compound D51) is an EGFR mutant inhibitor. EGFR mutant-IN-2 inhibits the EGFR L858R/T790M/C797S mutant with an IC50 value of 14 nM. EGFR mutant-IN-2 inhibits the EGFR del19/T790M/C797S mutant with an IC50 value of 62 nM. EGFR mutant-IN-2 has favorable PK parameters, safety properties, in vivo stability, and antitumor activity .
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Cat. No.: HY-125841
Target:  

EGFR

Research Areas:  

Cancer

EGFR mutant-IN-1, a 5-methylpyrimidopyridone derivative, is a potent and selective EGFR L858R/T790M/C797S mutant inhibitor with an IC50 of 27.5 nM, while being a significantly less potent for EGFR WT (IC50 >1.0 μM) .
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Cat. No.: HY-P83891
Synonyms: ERBB; HER1; mENA; ERBB1; PIG61; L858R MUTant

Host:  

Mouse

Application:  

WB, IHC-P, FC, ELISA

Reactivity:  

Human

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Cat. No.: HY-P83891A
Synonyms: ERBB; HER1; mENA; ERBB1; PIG61; L858R MUTant

Host:  

Mouse

Application:  

WB, IHC-P, FC, ELISA

Reactivity:  

Human

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