AdooQ BioScience is a supplier of biochemicals located in Irvine, CA since 2006. In the past five years, we have been a renowned name engaged in manufacturing and supplying small molecule inhibitors including kinase inhibitors on kinds of signal pathway, such as PI3K, AKT, HDAC, MARP etc.
Company WebsiteTSU-68 (SU-6668) is an inhibitor of RTKs involved in VEGF, bFGF and PDGF signaling, which inhibits endothelial cell proliferation.
More Information Supplier PageTSU-68 (SU-6668) is an inhibitor of RTKs involved in VEGF, bFGF and PDGF signaling, which inhibits endothelial cell proliferation.
More Information Supplier PageTSU-68 (SU-6668) is an inhibitor of RTKs involved in VEGF, bFGF and PDGF signaling, which inhibits endothelial cell proliferation.
More Information Supplier PageTTNPB enhances reprogramming efficiency in chemically induced pluripotent stem cells (CiPSCs).
More Information Supplier PageTTNPB enhances reprogramming efficiency in chemically induced pluripotent stem cells (CiPSCs).
More Information Supplier PageTTNPB enhances reprogramming efficiency in chemically induced pluripotent stem cells (CiPSCs).
More Information Supplier PageTTNPB enhances reprogramming efficiency in chemically induced pluripotent stem cells (CiPSCs).
More Information Supplier PageTTP 22 is a high affinity, casein kinase 2 (CK2) inhibitor (IC50= 0.1??M, Ki= 40nM). In addition, TTP 22 shows selectivity for CK2 over JNK3, ROCK1, and MET (inhibitory effects displayed at greater than 10 ??M). TTP 22 is highly conserved serine/threonine protein kinase that is also involved in cell proliferation, cell differentiation and apoptosis.
More Information Supplier PageTTP 22 is a high affinity, casein kinase 2 (CK2) inhibitor (IC50= 0.1??M, Ki= 40nM). In addition, TTP 22 shows selectivity for CK2 over JNK3, ROCK1, and MET (inhibitory effects displayed at greater than 10 ??M). TTP 22 is highly conserved serine/threonine protein kinase that is also involved in cell proliferation, cell differentiation and apoptosis.
More Information Supplier PageTTP 22 is a high affinity, casein kinase 2 (CK2) inhibitor (IC50= 0.1??M, Ki= 40nM). In addition, TTP 22 shows selectivity for CK2 over JNK3, ROCK1, and MET (inhibitory effects displayed at greater than 10 ??M). TTP 22 is highly conserved serine/threonine protein kinase that is also involved in cell proliferation, cell differentiation and apoptosis.
More Information Supplier PageTubacin (tubulin acetylation inducer) is a highly potent and selective, reversible, cell-permeable HDAC6 inhibitor with an IC50 of 4 nM.
More Information Supplier PageTubacin (tubulin acetylation inducer) is a highly potent and selective, reversible, cell-permeable HDAC6 inhibitor with an IC50 of 4 nM.
More Information Supplier PageTubacin (tubulin acetylation inducer) is a highly potent and selective, reversible, cell-permeable HDAC6 inhibitor with an IC50 of 4 nM.
More Information Supplier PageTubacin (tubulin acetylation inducer) is a highly potent and selective, reversible, cell-permeable HDAC6 inhibitor with an IC50 of 4 nM.
More Information Supplier PageTubacin (tubulin acetylation inducer) is a highly potent and selective, reversible, cell-permeable HDAC6 inhibitor with an IC50 of 4 nM.
More Information Supplier PageTubastatin A HCl is a potent HDAC inhibitor that demonstrates over more selectivity than all other HDAC isoforms (IC50s >16 uM), excluding HDAC8 (IC50 = 0.9 M).
More Information Supplier PageTubastatin A HCl is a potent HDAC inhibitor that demonstrates over more selectivity than all other HDAC isoforms (IC50s >16 uM), excluding HDAC8 (IC50 = 0.9 M).
More Information Supplier PageTubastatin A HCl is a potent HDAC inhibitor that demonstrates over more selectivity than all other HDAC isoforms (IC50s >16 uM), excluding HDAC8 (IC50 = 0.9 M).
More Information Supplier PageTubastatin A HCl is a potent HDAC inhibitor that demonstrates over more selectivity than all other HDAC isoforms (IC50s >16 uM), excluding HDAC8 (IC50 = 0.9 M).
More Information Supplier PageTubeimoside I is a triterpenoid saponin isolated from tubers of bolbostemma paniculatum. Used as anti-tumor agent, induces cell cycle arrest and apoptosis.
More Information Supplier PageTubeimoside I is a triterpenoid saponin isolated from tubers of bolbostemma paniculatum. Used as anti-tumor agent, induces cell cycle arrest and apoptosis.
More Information Supplier PageTubeimoside I is a triterpenoid saponin isolated from tubers of bolbostemma paniculatum. Used as anti-tumor agent, induces cell cycle arrest and apoptosis.
More Information Supplier PageTuberostemonine stereoisomers are natural alkaloids found in Stemona tuberosa.
More Information Supplier PageTuberostemonine stereoisomers are natural alkaloids found in Stemona tuberosa.
More Information Supplier PageTuberostemonine stereoisomers are natural alkaloids found in Stemona tuberosa.
More Information Supplier PageTulobuterol is a beta-adrenergic receptor agonist that is related structurally to Terbutaline.
More Information Supplier PageTulobuterol is a beta-adrenergic receptor agonist that is related structurally to Terbutaline.
More Information Supplier PageTW-37, a small-molecule inhibitor of Bcl-2, inhibits cell growth and induces apoptosis in pancreatic cancer mediated through a novel pathway involving inactivation of Notch-1 and Jagged-1.
More Information Supplier PageTW-37, a small-molecule inhibitor of Bcl-2, inhibits cell growth and induces apoptosis in pancreatic cancer mediated through a novel pathway involving inactivation of Notch-1 and Jagged-1.
More Information Supplier PageTW-37, a small-molecule inhibitor of Bcl-2, inhibits cell growth and induces apoptosis in pancreatic cancer mediated through a novel pathway involving inactivation of Notch-1 and Jagged-1.
More Information Supplier PageTW-37, a small-molecule inhibitor of Bcl-2, inhibits cell growth and induces apoptosis in pancreatic cancer mediated through a novel pathway involving inactivation of Notch-1 and Jagged-1.
More Information Supplier PageTW-37, a small-molecule inhibitor of Bcl-2, inhibits cell growth and induces apoptosis in pancreatic cancer mediated through a novel pathway involving inactivation of Notch-1 and Jagged-1.
More Information Supplier PageTWS119 is a 4,6 disubstituted pyrrolopyrimidine that potently inhibits GSK3?? with an IC50 value of 30 nM.1 At 400 nM.
More Information Supplier PageTWS119 is a 4,6 disubstituted pyrrolopyrimidine that potently inhibits GSK3?? with an IC50 value of 30 nM.1 At 400 nM.
More Information Supplier PageTWS119 is a 4,6 disubstituted pyrrolopyrimidine that potently inhibits GSK3?? with an IC50 value of 30 nM.1 At 400 nM.
More Information Supplier PageTWS119 is a 4,6 disubstituted pyrrolopyrimidine that potently inhibits GSK3?? with an IC50 value of 30 nM.1 At 400 nM.
More Information Supplier PageTWS119 is a 4,6 disubstituted pyrrolopyrimidine that potently inhibits GSK3?? with an IC50 value of 30 nM.1 At 400 nM.
More Information Supplier PageTyrosine-kinase inhibitor is a pharmaceutical drug that inhibits tyrosine kinases. Tyrosine kinases are enzymes responsible for the activation of many proteins by signal transduction cascades.
More Information Supplier PageTyrosine-kinase inhibitor is a pharmaceutical drug that inhibits tyrosine kinases. Tyrosine kinases are enzymes responsible for the activation of many proteins by signal transduction cascades.
More Information Supplier PageTyrphostin AG 183 inhibits EGFR (epidermal growth factor receptor) tyrosine kinase (IC50 = 800 nM).
More Information Supplier PageTyrphostin AG 183 inhibits EGFR (epidermal growth factor receptor) tyrosine kinase (IC50 = 800 nM).
More Information Supplier PageTyrphostin AG 183 inhibits EGFR (epidermal growth factor receptor) tyrosine kinase (IC50 = 800 nM).
More Information Supplier PageTyrphostin AG 183 inhibits EGFR (epidermal growth factor receptor) tyrosine kinase (IC50 = 800 nM).
More Information Supplier PageTyrphostin AG 879 is an inhibitor of the tyrosine kinase activity of nerve growth factor (NGF) TrkA.
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