21 results for "EGF Receptor Inhibitors" in Products

EGF Receptor Inhibitors

Highly potent EGFR-kinase inhibitor

Alternate Names: Tyrphostin AG 1478
Chemical Name: N-(3-Chlorophenyl)-6,7-dimethoxy-4-quinazolinanine hydrochloride
Purity: ≥98%
Highly potent EGFR-kinase inhibitor
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Orally active, selective EGFR inhibitor

Alternate Names: Gefitinib,ZD 1839
Chemical Name: N-(3-Chloro-4-fluorophenyl)-7-methoxy-6-[3-(4-morpholinyl)propoxy]-4-quinazolinamine
Purity: ≥98%
Orally active, selective EGFR inhibitor
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EGFR-kinase inhibitor. Also JAK2, JAK3 inhibitor

Alternate Names: Tyrphostin AG 490
Chemical Name: (E)-2-Cyano-3-(3,4-dihydrophenyl)-N-(phenylmethyl)-2-propenamide
Purity: ≥98%
EGFR-kinase inhibitor. Also JAK2, JAK3 inhibitor
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EGFR kinase inhibitor. Also estrogen and PPARγ ligand

Chemical Name: 5,7-Dihydroxy-3-(4-hydroxyphenyl)-4H-1-benzopyran-4-one
Purity: ≥98%
EGFR kinase inhibitor. Also estrogen and PPARγ ligand
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Potent, reversible EGFR tyrosine kinase inhibitor

Chemical Name: N-(3-Ethynylphenyl)-6,7-bis(2-methoxyethoxy)-4-quinazolinamine hydrochloride
Purity: ≥98%
Potent, reversible EGFR tyrosine kinase inhibitor
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Potent ErbB receptor family inhibitor

Chemical Name: N4-(3-Bromophenyl)-N6-methyl-pyrido[3,4-d]pyrimidine-4,6-diamine
Purity: ≥98%
Potent ErbB receptor family inhibitor
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Potent ErbB receptor family inhibitor

Chemical Name: 5E-4-Amino-6-(4-benzyloxy-3-chlorophenylamino)pyrimidine-5-carboxaldehyde N-(2-morpholin-4-ylethyl) oxime hydrochloride
Purity: ≥97%
Potent ErbB receptor family inhibitor
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Highly potent EGFR and ErbB2 inhibitor; inhibts wild type and mutated receptors

Chemical Name: (4-Fluorophenyl)methyl N-[2-[(1-methyl-1H-pyrazol-4-yl)amino]-4-pyrimidinyl]-N-[3-[(1-oxo-2-propen-1-yl)amino]phenyl]carbamate
Purity: ≥98%
Highly potent EGFR and ErbB2 inhibitor; inhibts wild type and mutated receptors
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Potent dual EGFR/ErbB2 inhibitor; orally active

Chemical Name: N-[3-Chloro-4-[(3-fluorophenyl)methoxy]phenyl]-6-[2-[[[2-(methylsulfonyl)ethyl]amino]methyl]-4-thiazolyl]-4-quinazolinamine dihydrochloride
Purity: ≥97%
Potent dual EGFR/ErbB2 inhibitor; orally active
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Potent and selective ErbB2 inhibitor

Alternate Names: Mubritinib
Chemical Name: 1-[4-[4-[[2-[(1E)-2-[4-(trifluoromethyl)phenyl]ethenyl]-4-oxazolyl]methoxy]phenyl]butyl]-1H-1,2,3-triazole
Purity: ≥98%
Potent and selective ErbB2 inhibitor
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Potent HER2 receptor tyrosine kinase and EGFR kinase inhibitor

Chemical Name: (2E)-N-[4-[[3-Chloro-4-(2-pyridinylmethoxy)phenyl]amino]-3-cyano-7-ethoxy-6-quinolinyl]-4-(dimethylamino)-2-butenamide
Purity: ≥98%
Potent HER2 receptor tyrosine kinase and EGFR kinase inhibitor
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Potent and selective ErbB2 inhibitor

Chemical Name: N6-(4,5-Dihydro-4,4-dimethyl-2-oxazolyl)-N4-[3-methyl-4-([1,2,4]triazolo[1,5-a]pyridin-7-yloxy)phenyl]-4,6-quinazolinediamine
Purity: ≥98%
Potent and selective ErbB2 inhibitor
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Potent and selective dual ErbB2 (HER-2) and EGFR inhibitor

Chemical Name: N-[3-Chloro-4-[(3-fluorophenyl)methoxy]phenyl]-6-[5-[[[2-(methylsulfonyl)ethyl]amino]methyl]-2-furanyl]-4-quinazolinamine
Purity: ≥98%
Potent and selective dual ErbB2 (HER-2) and EGFR inhibitor
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Potent EGFR and VEGFR inhibitor

Chemical Name: 6-[4-[(4-Ethyl-1-piperazinyl)methyl]phenyl]-N-[(1R)-1-phenylethyl]-7H-pyrrolo[2,3-d]pyrimidin-4-amine
Purity: ≥98%
Potent EGFR and VEGFR inhibitor
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Potent EGFR kinase inhibitor

Alternate Names: CI 1033,PD 183805
Chemical Name: N-[4-[(3-Chloro-4-fluorophenyl)amino]-7-[3-(4-morpholinyl)propoxy]-6-quinazolinyl]-2-propenamide dihydrochloride
Purity: ≥98%
Potent EGFR kinase inhibitor
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Potent mutant-selective EGFR inhibitor

Chemical Name: N-[3-[[5-Chloro-2-[[2-methoxy-4-(4-methyl-1-piperazinyl)phenyl]amino]-4-pyrimidinyl]oxy]phenyl]-2-propenamide
Purity: ≥98%
Potent mutant-selective EGFR inhibitor
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Potent irreversible pan ErbB inhibitor

Alternate Names: PF00299804
Chemical Name: (2E)-N-[4-[(3-Chloro-4-fluorophenyl)amino]-7-methoxy-6-quinazolinyl]-4-(1-piperidinyl)-2-butenamide
Purity: ≥98%
Potent irreversible pan ErbB inhibitor
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Potent dual specificity EGFR/HER2 inhibitor; active in vivo

Alternate Names: BIBW2992
Chemical Name: (2E)-N-[4-[(3-Chloro-4-fluorophenyl)amino]-7-[[(3S)-tetrahydro-3-furanyl]oxy]-6-quinazolinyl]-4-(dimethylamino)-2-butenamide dimaleate
Purity: ≥98%
Potent dual specificity EGFR/HER2 inhibitor; active in vivo
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Potent mutant-selective EGFR inhibitor

Chemical Name: N-[2-[[2-(Dimethylamino)ethyl]methylamino]-4-methoxy-5-[[4-(1-methyl-1H-indol-3-yl)-2-pyrimidinyl]amino]phenyl]-2-propenamide
Purity: ≥98%
Potent mutant-selective EGFR inhibitor
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Potent VEGFR-2 inhibitor, also inhibits EGFR and RET oncoproteins activity

Chemical Name: N-(4-Bromo-2-fluorophenyl)-6-methoxy-7-[(1-methyl-4-piperidinyl)methoxy]-4-quinazolinamine
Purity: ≥98%
Potent VEGFR-2 inhibitor, also inhibits EGFR and RET oncoproteins activity
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Negative control for PP 2 (Cat. No. 1407)

Chemical Name: 1-Phenyl-1H-pyrazolo[3,4-d]pyrimidin-4-amine
Purity: ≥98%
Negative control for PP 2 (Cat. No. 1407)
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