| Cat. No. |
Product Name |
Information |
| PC-23843 |
Canertinib
pan-ErbB inhibitor
|
Canertinib (CI-1033, PD183805) is a potent, irreversible, orally available pan-ErbB inhibitor for EGFR and ErbB2 with IC50 of 7.5 nM and 9.0 nM in autophosphorylation assay. |
| PC-23647 |
BBT-176
EGFR C797S inhibitor
|
BBT-176 is a potent, mutant-selective fourth-generation inhibitor of EGFR C797S mutations with IC50 of 4.36, 1.79, and 5.35 nM for EGFR 19Del/C797S, EGFR 19Del/T790M/C797S, and EGFR L858R/C797S, respectively. |
| PC-23646 |
EGFR triple mutant inhibitor 31
EGFR inhibitor
|
EGFR triple mutant inhibitor 31 is a potent, mutant-selective inhibitor of EGFR L858R/T790M/C797S with Ki of 2.1 nM, inhibits EGFR del19/T790M/C797S in a Ba/F3 cellular assay with IC50 of 56.9 nM. |
| PC-22888 |
DS06652923
EGFR C797S inhibitor
|
DS06652923 is a potent, and orally available EGFR-triple-mutant inhibitor with IC50 of 2.0 nM, 0.89 nM and 6.0 nM for del19/T790M/C797S, L858R/T790M/C797S and WT EGFR resceptively. |
| PC-22843 |
Arglabin
EGFR inhibitor
|
Arglabin is a sesquiterpene lactone from the Chinese herb Artemisia myriantha Wall. (Asteraceae), shows anti-inflammatory and antitumor activities, inhibits the EGFR downstream signaling pathways mTORC1 and mTORC2. |
| PC-22389 |
AZ14133346
EGFR Ex20Ins inhibitor
|
AZ14133346 is a potent and selective inhibitor of EGFR Ex20Ins with enzyme IC50 of <3 nM and cell IC50 of 85 nM, 14-fold selective over wild-type EGFR (cell IC50=1200 nM). |
| PC-22088 |
Icotinib hydrochloride
EGFR inhibitor
|
Icotinib hydrochloride (BPI-2009H) is a potent and specific EGFR inhibitor with IC50 of 5 nM, also inhibits mutant EGFRL858R, EGFR L858R/T790M, EGFR T790M and EGFR L861Q. |
| PC-22087 |
Icotinib
EGFR inhibitor
|
Icotinib (BPI-2009) is a potent and specific EGFR inhibitor with IC50 of 5 nM, also inhibits mutant EGFRL858R, EGFR L858R/T790M, EGFR T790M and EGFR L861Q. |
| PC-21851 |
DDC4002
mutant EGFR inhibitor
|
DDC4002 is a potent, selective and allosteric EGFR inhibitor, shows selectivity against L858R/T790M/C797S EGFR mutants with IC50 of 39-50 nM, does not inhibit WT EGFR. |
| PC-21850 |
EAI001
mutant EGFR inhibitor
|
EAI001 is a potent, mutant-selectiveepidermal growth factor receptor (EGFR) allosteric inhibitor with IC50 value of 24 nM for EGFRL858R/T790M. |
| PC-21841 |
AG1478
EGFR inhibitor
|
AG1478 (Tyrphostin AG-1478) is a potent, selective EGFR tyrosine kinase inhibitor with IC50 of 3 nM. |
| PC-21465 |
BI-8128
EGFR inhibitor
|
BI-8128 is a potent, selective, reversible and orally bioavailable fourth generation EGFR inhibitor, potently inhibits oncogenic EGFR variants del19 and L858R as well as the acquired EGFR resistance mutations T790M and C797S. |
