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Other protein kinase inhibitors and protein inhibitors.
1,1'-(4,4'-(4,4'-(5-chloropyrimidine-2,4-diyl)bis(azanediyl)bis(3-methoxy-4,1-phenylene))bis(piperazine-4,1-diyl))diethanone KRCA 0008 is s potent and selective dual ALK (anaplastic lymphoma kinase ) and ACK1 inhibitor.
(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
N-[2-[(1S,4R)-6-[[4-(cyclobutylamino)-5-(trifluoromethyl)-2-pyrimidinyl]amino]-1,2,3,4-tetrahydronaphthalen-1,4-imin-9-yl]-2-oxoethyl]-acetamide PF 03814735 is a potent, orally bioavailable, ATP-competitive and reversible inhibitor of aurora kinase A and aurora kinase B
4-(2-(4-(2-(4-acetylpiperazin-1-yl)-2-oxoethyl)phenylamino)-5-fluoropyrimidin-4-ylamino)-N-(2-chlorophenyl)benzamide Aurora A inhibitor II is a potent and selective inhibitor of Aurora A kinase (AurA)
CGK 733 is a selective inhibitor of ATM and ATR kinases, 2,2-di(phenyl)-N-[2,2,2-trichloro-1-[(4-fluoro-3-nitrophenyl)carbamothioylamino]ethyl]acetamide Synonyms: CGK733inhibitor of ATM and ATR kinases, CAS number: 905973-89-9
2-hydroxy-5-((4-(N-pyridin-2-ylsulfamoyl)phenyl)diazenyl)benzoic acid Sulfasalazine (SSZ) is a inhibitor of NF-κB activation via its ability to block the activity of the inhibitor of κB (IκB) kinases α and β (IKKα and IKKβ).
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