5 Results for "

EGFR-driven cancer

" in MedChemExpress (MCE) Product Catalog:
Products (5)

5 Results for "EGFR-driven cancer" in MCE Product Catalog:

Cat. No.: HY-W423595
CAS No.: 2050906-40-4
Target:  

EGFR

Research Areas:  

Cancer

BEBT-109 is a potent pan-mutant-selective EGFR inhibitor. BEBT-109 has improved pharmacokinetic properties. BEBT-109 can be used for multiple mutant-EGFR-driven non-small cell lung cancer (NSCLC) research .
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Cat. No.: HY-178242
CAS No.: 2654821-07-3
Target:  

PROTACs EGFR

Research Areas:  

Cancer

PROTAC EGFR degrader 16 is a selective EGFR PROTAC degrader with a DC50 value of < 50 nM. PROTAC EGFR degrader 16 can be used for the study of EGFR-driven cancerssuch as non-small cell lung cancer .
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Cat. No.: HY-123952
CAS No.: 1423077-49-9
Purity:  99.89%
Synonyms: TRC-382
Target:  

EGFR

Research Areas:  

Cancer

RTC-5 (TRC-382) is an optimized phenothiazine with anti-cancer potency. RTC-5 demonstrates efficacy against a xenograft model of an EGFR driven cancer, its effects is attributed to concomitant negative regulation of PI3K-AKT and RAS-ERK signaling .
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Cat. No.: HY-116091
CAS No.: 220576-72-7
Target:  

EGFR Akt ERK

Research Areas:  

Cancer

EGFR-IN-451 is an EGFR inhibitor with an IC50 value of 0.02 nM. EGFR-IN-451 also inhibits mutant EGFR L858R, EGFR T790M, and EGFR L858R/T790M with IC50 values of 0.26-34 nM. EGFR-IN-451 inhibits AKT and ERK activation and inhibits proliferation of EGFR-mutant cancer cells. EGFR-IN-451 can be used for the research of EGFR-driven cancer .
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Cat. No.: HY-158969
CAS No.: 2549192-10-9
Target:  

EGFR Apoptosis Akt ERK

Research Areas:  

Cancer

EGFR-IN-113 (compound II-1) is an EGFR kinase inhibitor with an IC50 of 14.79 μM. EGFR-IN-113 can induce apoptosis and inhibit cell proliferation by downregulating Akt and Erk1/2 signaling. EGFR-IN-113 can be used for research in EGFR-driven cancers, such as lung cancer, pancreatic cancer, and breast cancer .
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