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35773-42-3

35773-42-3 structure
35773-42-3 structure
  • Name: EMI1
  • Chemical Name: 3-(2-benzoxazolyl)-7-(diethylamino)-2H-1-benzopyran-2-one
  • CAS Number: 35773-42-3
  • Molecular Formula: C20H18N2O3
  • Molecular Weight: 334.36900
  • Catalog: Signaling Pathways JAK/STAT Signaling EGFR
  • Create Date: 2016-08-02 03:48:19
  • Modify Date: 2024-01-11 09:37:34
  • EMI1 is an EGFR ex19del/T790M/C797S and EGFR L858R/T790M/C797S inhibitor[1].

Name 3-(2-benzoxazolyl)-7-(diethylamino)-2H-1-benzopyran-2-one
Synonyms 3-benzooxazol-2-yl-7-diethylamino-chromen-2-one
3-(1,3-BENZOXAZOL-2-YL)-7-(DIETHYLAMINO)-2H-CHROMEN-2-ONE
Description EMI1 is an EGFR ex19del/T790M/C797S and EGFR L858R/T790M/C797S inhibitor[1].
Related Catalog
Target

EGFRdel19 T790M C797S

EGFRL858R/T790M/C797S

In Vitro EMI1 inhibits PC9 EGFR ex19del/T790M/C797S organoid growth with the EC50 of 131 nM[1]. EMI1 (1 nM-10 μM) potently reduces the interaction of EGFR triple mutant with Shc1[1]. EMI1 (1 nM-100μM) strongly inhibits the viability and increase the caspase 3/7 activity of PC9 EGFR ex19del/T790M/C797S triple-mutant cells than noncancerous human bronchial epithelial (HBE) cells[1]. Cell Viability Assay[1] Cell Line: PC9 EGFR ex19del/T790M/C797S and HBE bronchial epithelial lung EGFR-WT control cells. Concentration: 0.001, 0.01, 0.1, 1, 10, 100 μM Incubation Time: 72 hours Result: Strongly inhibited the viability.
References

[1]. Punit Saraon, et al. A drug discovery platform to identify compounds that inhibit EGFR triple mutants. Nat Chem Biol. 2020 May;16(5):577-586.

Molecular Formula C20H18N2O3
Molecular Weight 334.36900
Exact Mass 334.13200
PSA 59.48000
LogP 4.44740
HS Code 2934999090
HS Code 2934999090
Summary 2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%