Ki8751 is a potent, selective VEGFR-2 tyrosine kinase inhibitor with IC50 of 0.9 nM, 40, 67, 170 nM for VEGF-2, c-Kit, PDGFRα and FGFR-2, respectively. Find all the information about Ki8751 for cell signaling research.
Supplier ki8751 | c-Kit Inhibitor | from provider selleckbio.com
Posted by komac33 (#1) 12 days ago (http://www.selleckbio.com)
PF-04691502 is a potent and selective dual PI3K/mTOR inhibitor to phosphorylation of AKT T308 and AKT S473 with IC50 of 7.5 and 3.8 nM, respectively. Find all the information about PF-04691502 for cell signaling research.
PNU-120596 | mAChRs Inhibitor | from supplier selleckbio.com
Posted by whleif76 (#1) 12 days ago (http://www.selleckbio.com)
PNU-120596 is a potent and selective positive allosteric α7 neuronal nicotinic acetylcholine receptors modulator with an EC50 of 0.2 μM. Find all the information about PNU-120596 for cell signaling research.
RAF265 (CHIR-265) is an oral, highly selective RAF and VEGFR kinase inhibitor with IC50 of of 5 to 10 μM. Find all the information about RAF265 (CHIR-265) for cell signaling research.
PRICE PKI-587 | mTOR Inhibitor | from supplier selleckbio.com
Posted by stanner99 (#1) 12 days ago (http://www.selleckbio.com)
PKI-587 is a highly potent dual PI3K/mTOR kinase inhibitor with IC50 of 0.4 nM and
PKI-402 is a selective, reversible, ATP-competitive, equipotent class I phosphatidylinositol 3-kinases (PI3K) inhibitor with IC50 of 1, 7, 16 and 14 nM for PI3Kα, PI3Kβ, PI3Kγ and PI3Kδ, respectively. Find all the information about PKI-402 for cell signaling research.
ORDER CX-4945 | PKC Inhibitor | from provider selleckbio.com
Posted by gusterling99 (#1) 12 days ago (http://www.selleckbio.com)
CX-4945 is a potent and selective ATP-competitive small molecule protein kinase CK2 inhibitor with a Ki and an IC50 of 0.38 and 1 nM for recombinant human CK2α, respectively. Find all the information about CX-4945 for cell signaling research.
CX-5461 is a potent small-molecule rRNA synthesis inhibitor with an IC50 of 0.11 μM. Find all the information about CX-5461 for cell signaling research.
TSU-68 (SU6668) is a novel multiple receptor tyrosine kinase inhibitor with IC50 of 2.1 µM, 8 nM and 1.2 µM for VEGF-R1, PDGF-Rβ and FGF-R1, respectively. Find all the information about TSU-68 (SU6668) for cell signaling research.
BUY PH-797804 | p38 MAPK Inhibitor | from provider selleckbio.com
Posted by wacary38 (#1) 12 days ago (http://www.selleckbio.com)
PH-797804 is a highly selective, potent, and ATP-competitive p38 MAP kinase inhibitor with an IC50 of 2.3 nM. Find all the information about PH-797804 for cell signaling research.
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