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New products

• PI3 kinase inhibitor D 106669, 2 mg

  1-ethyl-3-(3-(p-tolylamino)pyrido[2,3-b]pyrazin-6-yl)urea D 106669 is a highly potent and selective PI3K inhibitor, selectively inhibiting class I PI3K

  144,50 €
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• LCK protein kinase inhibitor A 770041, 5 mg

  N-(4-(1-(4-(4-acetylpiperazin-1-yl)cyclohexyl)-4-amino-1H-pyrazolo[3,4-d]pyrimidin-3-yl)-2-methoxyphenyl)-1-methyl-1H-indole-2-carboxamide A 770041 is a selective and orally active Src-family Lck inhibitor

  202,50 €
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• ALK / ROS1 protein kinase inhibitor PF 06463922, 5 mg

  (10R)-7-amino-12-fluoro-10,15,16,17-tetrahydro-2,10,16-trimethyl-15-oxo-2H-4,8-methenopyrazolo[4,3-h][2,5,11]benzoxadiazacyclotetradecine-3-carbonitrile PF 06463922 is a potent, orally available and brain-penetrant ALK/ROS1 selective inhibitorSynonyms: Lorlatinib

  157,50 €
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• AKT protein kinase inhibitor VIII, 5 mg

  1-(1-(phenyl-1H-imidazo[4,5-g]quinoxalin-6-yl)benzyl)piperidin-4-yl)-1H-benzo[d]imidazol-2(3H)-one Akt Inhibitor VIII is a non-ATP competitive inhibitor of Akt isoforms 1 and 2

  187,50 €
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• AKT protein kinase activator SC 79, 5 mg

  ethyl 2-amino-6-chloro-4-(1-cyano-2-ethoxy-2-oxoethyl)-4H-chromene-3-carboxylate SC 79 is a unique specific activator of cytosolic Akt (PKB)

  127,50 €
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• B-RAF protein kinase inhibitor SB 590885, 5 mg

  5-(2-(4-(2-(dimethylamino)ethoxy)phenyl)-5-(pyridin-4-yl)-1H-imidazol-4-yl)-2,3-dihydro-1H-inden-1-one oxime SB 590885 is a selective inhibitor of B-Raf kinase.

  161,50 €
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• AKT protein kinase inhibitor GSK 2110183 hydrochloride, 5 mg

  N-((S)-1-amino-3-(3-fluorophenyl)propan-2-yl)-5-chloro-4-(4-chloro-1-methyl-1H-pyrazol-5-yl)thiophene-2-carboxamide hydrochloride GSK 2110183 hydrochloride is a potent, reversible, selective, and orally bioavailable inhibitor of the Akt kinasesSynonyms: Afuresertib hydrochloride

  157,50 €
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• ATR protein kinase inhibitor VE 822, 10 mg

  5-(4-(isopropylsulfonyl)phenyl)-3-(3-(4-((methylamino)methyl)phenyl)isoxazol-5-yl)pyrazin-2-amine VE 822 is a selective ATR inhibitor

  165,00 €
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• ATR protein kinase inhibitor AZ 20, 5 mg

  (R)-4-(2-(1H-indol-4-yl)-6-(1-(methylsulfonyl)cyclopropyl)pyrimidin-4-yl)-3-methylmorpholine AZ 20 is a potent, orally active and selective inhibitor of ATR protein kinase with monotherapy in vivo antitumor activity

  157,50 €
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• ALK5 protein kinase inhibitor SB 525334, 10 mg

  6-(2-tert-butyl-5-(6-methylpyridin-2-yl)-1H-imidazol-4-yl)quinoxaline SB 525334 is a potent and selective inhibitor of the ALK5 receptor

  157,50 €
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• IGF1R protein kinase inhibitor NT 157, 2 mg

  (E)-3-(3-bromo-4,5-dihydroxyphenyl)-N-(3,4,5-trihydroxybenzyl)prop-2-enethioamide NT 157 is a unique allosteric inhibitor of IGF1R

  157,50 €
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• ALK5 protein kinase inhibitor IN 1130, 5 mg

  3-((5-(6-methylpyridin-2-yl)-4-(quinoxalin-6-yl)-1H-imidazol-2-yl)methyl)benzamide IN 1130 is a highly selective small molecule ALK5 inhibitor

  187,50 €
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• ALK protein kinase inhibitor LDK 378, 5 mg

  5-chloro-N2-(2-isopropoxy-5-methyl-4-(piperidin-4-yl)phenyl)-N4-(2-(isopropylsulfonyl)phenyl)pyrimidine-2,4-diamine LDK 378 is a potent, bioavailable, and selective anaplastic lymphoma kinase (ALK) inhibitor.Synonyms: Ceritinib

  161,50 €
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• ALK4 and ALK5 protein kinase inhibitor SB 505124, 5 mg

  2-(4-(benzo[d][1,3]dioxol-5-yl)-2-tert-butyl-1H-imidazol-5-yl)-6-methylpyridine SB 505124 is a selective inhibitor of TGF-β type I receptors ALK4 and ALK5

  161,50 €
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• Multi AGC protein kinase inhibitor AT 13148 dihydrochloride, 2 mg

  (S)-1-(4-(1H-pyrazol-4-yl)phenyl)-2-amino-1-(4-chlorophenyl)ethanol dihydrochloride AT 13148 dihydrochloride is an oral, ATP-competitive inhibitor of multi-AGC kinases with potent pharmacodynamic and antitumor activity

  144,50 €
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