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Search Results for " egfr tyrosine kinase "

20

Compounds

Cat No. Product Name Synonyms Targets
T41099 EGFR Protein Tyrosine Kinase Substrate
EGFR Protein Tyrosine Kinase Substrate is a EGFR protein tyrosine kinase substrate.
T9865 Almonertinib mesylate EGFR
Almonertinib mesylate is an irreversible inhibitor of EGFR tyrosine kinase with high selectivity for EGFR-sensitizing and T790M resistance mutations. Almonertinib mesylate can be used in the non-small cell lung cancer st...
T4015 HG-14-10-04 ALK
HG-14-10-04 is a potent and specific ALK inhibitor.
T1181 Gefitinib ZD1839 EGFR , Tyrosine Kinases , Autophagy
Gefitinib (ZD1839) is an EGFR first-generation inhibitor with oral activity that inhibits the EGFR 19 Del and L858R mutations. Gefitinib has antitumor activity and is used for the treatment of EGFR-mutated non-small-cell...
T3024 Avitinib AC0010 EGFR , JAK , BTK
Avitinib (AC0010), also known as AC0010 or AC0010MA, is an orally available, irreversible, epidermal growth factor receptor (EGFR) mutant-selective inhibitor, with potential antineoplastic activity. Upon oral administrat...
T39275 Befotertinib D-0316,Befotertinib EGFR
Befotertinib (D-0316) is an inhibitor of EGFR tyrosine kinase and can be used for studies about EGFR T790M-positive non-small cell lung cancer.
T6712 Tyrphostin AG 879 AG 879 Apoptosis , EGFR , Trk receptor , HER , PDGFR
Tyrphostin AG 879 (AG 879) effectively inhibits HER2/ErbB2 (IC50: 1 μM), 100- and 500-fold higher selective to ErbB2 than EGFR and PDGFR.
T4185 Lavendustin C HDBA,NSC 666251 CaMK , EGFR , Tyrosinase , Src
lavendustin C (NSC 666251) is a potent inhibitor of epidermal growth factor (EGF) receptor-associated tyrosine kinase.
T9304 (S)-Sunvozertinib N-[5-[[4-[5-Chloro-4-fluoro-2-(2-hydroxypropan-2-yl)anilino]pyrimidin-2-yl]amino]-2-[(3S)-3-(dimethylamino)pyrrolidin-1-yl]-4-methoxyphenyl]prop-2-enamide,DZD9008 EGFR , HER
(S)-Sunvozertinib (DZD9008) is a rationally designed selective, irreversible EGFR/HER2 inhibitor.
T77746 Tyrosine kinase-IN-7 EGFR , Antiviral
Tyrosine kinase-IN-7 is a potent inhibitor of the tyrosine kinase EGFR, inhibiting EGFR(WT) and EGFR(T790M) and showing anti-cancer and anti-tumor activity in a variety of cancer cell lines. Tyrosine kinase-IN-7 has pote...
T60108 PDGFR Tyrosine Kinase Inhibitor III PDGF Receptor Tyrosine Kinase Inhibitor III PDGFR
PDGFR Tyrosine Kinase Inhibitor III (PDGF Receptor Tyrosine Kinase Inhibitor III) (PDGF Receptor Tyrosine Kinase Inhibitor III) is a multikinase inhibitor that inhibits PDGFR, EGFR, FGFR, PKA, and PKC, respectively. PDGF...
T2307 Icotinib Hydrochloride BPI-2009H EGFR
Icotinib Hydrochloride (BPI-2009H) is the hydrochloride salt form of icotinib, an orally available quinazoline-based inhibitor of EGFR, with potential antineoplastic activity. Icotinib selectively inhibits the wild-type ...
T4326 AG 555 Tyrphostin B46,Tyrphostin AG 555 EGFR , Reverse Transcriptase
AG 555 (Tyrphostin B46) is an EGFR tyrosine kinase inhibitor.
T7175 Alflutinib mesylate AST2818 mesylate EGFR
Alflutinib mesylate (AST2818 mesylate) ,is an irreversible tyrosine kinase inhibitor that selectively inhibits EGFR mutations, especially T790M.
T4694 AG-1557 hydrochloride (189290-58-2(free base)) EGFR , HER
AG-1557 hydrochloride is an inhibitor of the epidermal growth factor receptor (EGFR) tyrosine kinase (pIC50: 8.194).
T2034 AG1557 AG-1557,AG 1557 EGFR , HER
AG1557 (AG-1557) is an inhibitor of the epidermal growth factor receptor (EGFR) tyrosine kinase (pIC50: 8.194).
T21322 Mavelertinib PF 06747775,PFE-X775,PF-06747775,PF-7775,PF 6747775,PF6747775 EGFR
Mavelertinib (PF-06747775) is an orally available, selective and potent EGFR tyrosine kinase (EGFR TKI) inhibitor with inhibitory effects on T790M/L858R and T790M/Del, and can be used in the study of oncology and respira...
T4183 Lavendustin A RG-14355,NSC 678027 EGFR , Tyrosinase
lavendustin A (RG-14355) is a potent, cell-permeable inhibitor of epidermal growth factor receptor (EGFR) tyrosine kinase.
T14692 BMX-IN-1 BMX kinase inhibitor BTK
BMX-IN-1 (BMX kinase inhibitor) is a selective inhibitor of bone marrow tyrosine kinase on chromosome X (BMX, IC50 = 8 nM) and the related Bruton’s tyrosine kinase (BTK, IC50 = 10.4 nM), but BMX-IN-1 is more than 47-656 ...
T7649 Tyrphostin A1 AG9,Tyrphostin 1 EGFR , Interleukin
Tyrphostin A1 (Tyrphostin 1) is an inhibitor of EGFR tyrosine kinase .

Compounds

EGFR Protein Tyrosine Kinase Substrate
T41099
Synonym:
Target:
Almonertinib mesylate
T9865
Synonym:
Target: EGFR
HG-14-10-04
T4015
Synonym:
Target: ALK
Gefitinib
T1181
Synonym: ZD1839
Target: EGFR, Tyrosine Kinases, Autophagy
Avitinib
T3024
Synonym: AC0010
Target: EGFR, JAK, BTK
Befotertinib
T39275
Synonym: D-0316,Befotertinib
Target: EGFR
Tyrphostin AG 879
T6712
Synonym: AG 879
Target: Apoptosis, EGFR, Trk receptor, HER, PDGFR
lavendustin C
T4185
Synonym: HDBA,NSC 666251
Target: CaMK, EGFR, Tyrosinase, Src
(S)-Sunvozertinib
T9304
Synonym: N-[5-[[4-[5-Chloro-4-fluoro-2-(2-hydroxypropan-2-yl)anilino]pyrimidin-2-yl]amino]-2-[(3S)-3-(dimethylamino)pyrrolidin-1-yl]-4-methoxyphenyl]prop-2-enamide,DZD9008
Target: EGFR, HER
Tyrosine kinase-IN-7
T77746
Synonym:
Target: EGFR, Antiviral
PDGFR Tyrosine Kinase Inhibitor III
T60108
Synonym: PDGF Receptor Tyrosine Kinase Inhibitor III
Target: PDGFR
Icotinib Hydrochloride
T2307
Synonym: BPI-2009H
Target: EGFR
AG 555
T4326
Synonym: Tyrphostin B46,Tyrphostin AG 555
Target: EGFR, Reverse Transcriptase
Alflutinib mesylate
T7175
Synonym: AST2818 mesylate
Target: EGFR
AG-1557 hydrochloride (189290-58-2(free base))
T4694
Synonym:
Target: EGFR, HER
AG1557
T2034
Synonym: AG-1557,AG 1557
Target: EGFR, HER
Mavelertinib
T21322
Synonym: PF 06747775,PFE-X775,PF-06747775,PF-7775,PF 6747775,PF6747775
Target: EGFR
lavendustin A
T4183
Synonym: RG-14355,NSC 678027
Target: EGFR, Tyrosinase
BMX-IN-1
T14692
Synonym: BMX kinase inhibitor
Target: BTK
Tyrphostin A1
T7649
Synonym: AG9,Tyrphostin 1
Target: EGFR, Interleukin
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TargetMol