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 WebsitePD153035 is an extremely potent and specific inhibitor of the tyrosine kinase activity of EGFR.
More Information Supplier PagePD153035 is an extremely potent and specific inhibitor of the tyrosine kinase activity of EGFR.
More Information Supplier PagePD153035 is an extremely potent and specific inhibitor of the tyrosine kinase activity of EGFR.
More Information Supplier PagePD173074 is a potent, cell permeable and ATP competitive inhibitor of FGFR and VEGFR.
More Information Supplier PagePD173074 is a potent, cell permeable and ATP competitive inhibitor of FGFR and VEGFR.
More Information Supplier PagePD173074 is a potent, cell permeable and ATP competitive inhibitor of FGFR and VEGFR.
More Information Supplier PagePD173074 is a potent, cell permeable and ATP competitive inhibitor of FGFR and VEGFR.
More Information Supplier PagePD173074 is a potent, cell permeable and ATP competitive inhibitor of FGFR and VEGFR.
More Information Supplier PagePD-173955 is a src tyrosine kinase inhibitor. PD173955 inhibited Bcr-Abl-dependent cell growth. PD173955 showed cell cycle arrest in G(1). PD173955 has an IC(50) of 1-2 nM in kinase inhibition assays of Bcr-Abl, and in cellular growth assays it inhibits Bcr-Abl-dependent substrate tyrosine phosphorylation. PD173955 inhibited kit ligand-dependent c-kit autophosphorylation (IC(50) = approximately 25 nM) and […]
More Information Supplier PagePD-173955 is a src tyrosine kinase inhibitor. PD173955 inhibited Bcr-Abl-dependent cell growth. PD173955 showed cell cycle arrest in G(1). PD173955 has an IC(50) of 1-2 nM in kinase inhibition assays of Bcr-Abl, and in cellular growth assays it inhibits Bcr-Abl-dependent substrate tyrosine phosphorylation. PD173955 inhibited kit ligand-dependent c-kit autophosphorylation (IC(50) = approximately 25 nM) and […]
More Information Supplier PagePD-173955 is a src tyrosine kinase inhibitor. PD173955 inhibited Bcr-Abl-dependent cell growth. PD173955 showed cell cycle arrest in G(1). PD173955 has an IC(50) of 1-2 nM in kinase inhibition assays of Bcr-Abl, and in cellular growth assays it inhibits Bcr-Abl-dependent substrate tyrosine phosphorylation. PD173955 inhibited kit ligand-dependent c-kit autophosphorylation (IC(50) = approximately 25 nM) and […]
More Information Supplier PagePD-173955 is a src tyrosine kinase inhibitor. PD173955 inhibited Bcr-Abl-dependent cell growth. PD173955 showed cell cycle arrest in G(1). PD173955 has an IC(50) of 1-2 nM in kinase inhibition assays of Bcr-Abl, and in cellular growth assays it inhibits Bcr-Abl-dependent substrate tyrosine phosphorylation. PD173955 inhibited kit ligand-dependent c-kit autophosphorylation (IC(50) = approximately 25 nM) and […]
More Information Supplier PagePD184352 is a MEK inhibitor (IC50 = 10-100 nM), a kinase upstream in the mitogen-activated protein kinase pathway (MAPK).
More Information Supplier PagePD184352 is a MEK inhibitor (IC50 = 10-100 nM), a kinase upstream in the mitogen-activated protein kinase pathway (MAPK).
More Information Supplier PagePD184352 is a MEK inhibitor (IC50 = 10-100 nM), a kinase upstream in the mitogen-activated protein kinase pathway (MAPK).
More Information Supplier PagePD184352 is a MEK inhibitor (IC50 = 10-100 nM), a kinase upstream in the mitogen-activated protein kinase pathway (MAPK).
More Information Supplier PagePD184352 is a MEK inhibitor (IC50 = 10-100 nM), a kinase upstream in the mitogen-activated protein kinase pathway (MAPK).
More Information Supplier PagePD98059 is an equipotent antagonist of the aryl hydrocarbon receptor and inhibitor of mitogen-activated protein kinase kinase.
More Information Supplier PagePD98059 is an equipotent antagonist of the aryl hydrocarbon receptor and inhibitor of mitogen-activated protein kinase kinase.
More Information Supplier PagePD98059 is an equipotent antagonist of the aryl hydrocarbon receptor and inhibitor of mitogen-activated protein kinase kinase.
More Information Supplier PagePD98059 is an equipotent antagonist of the aryl hydrocarbon receptor and inhibitor of mitogen-activated protein kinase kinase.
More Information Supplier PagePD98059 is an equipotent antagonist of the aryl hydrocarbon receptor and inhibitor of mitogen-activated protein kinase kinase.
More Information Supplier PagePectolinarigenin is a Cirsium isolate with anti-inflammatory activity and belongs to the flavones.
More Information Supplier PagePectolinarigenin is a Cirsium isolate with anti-inflammatory activity and belongs to the flavones.
More Information Supplier PagePectolinarigenin is a Cirsium isolate with anti-inflammatory activity and belongs to the flavones.
More Information Supplier PagePectolinarin is a Cirsium isolate with anti-inflammatory activity and similar in chemical structure to linarin.
More Information Supplier PagePectolinarin is a Cirsium isolate with anti-inflammatory activity and similar in chemical structure to linarin.
More Information Supplier PagePectolinarin is a Cirsium isolate with anti-inflammatory activity and similar in chemical structure to linarin.
More Information Supplier PagePedunculoside and syringin are two bioactive compounds in herbal tea and Chinese drug Jiubiying, the dried barks of Ilex rotunda Thunb.
More Information Supplier PagePedunculoside and syringin are two bioactive compounds in herbal tea and Chinese drug Jiubiying, the dried barks of Ilex rotunda Thunb.
More Information Supplier PagePedunculoside and syringin are two bioactive compounds in herbal tea and Chinese drug Jiubiying, the dried barks of Ilex rotunda Thunb.
More Information Supplier PagePeficitinib is a novel potent JAK inhibitor, which demonstrated potent efficacy in adjuvant-induced arthritis model in rats.
More Information Supplier PagePeficitinib is a novel potent JAK inhibitor, which demonstrated potent efficacy in adjuvant-induced arthritis model in rats.
More Information Supplier PagePeficitinib is a novel potent JAK inhibitor, which demonstrated potent efficacy in adjuvant-induced arthritis model in rats.
More Information Supplier PagePefloxacin mesylate is a synthetic chemotherapeutic agent and an antibacterial agent with IC5N/A of 6.7 nM.
More Information Supplier PagePefloxacin mesylate is a synthetic chemotherapeutic agent and an antibacterial agent with IC5N/A of 6.7 nM.
More Information Supplier PagePefloxacin mesylate is a synthetic chemotherapeutic agent and an antibacterial agent with IC5N/A of 6.7 nM.
More Information Supplier PagePefloxacin mesylate is a synthetic chemotherapeutic agent and an antibacterial agent with IC5N/A of 6.7 nM.
More Information Supplier PagePefloxacin mesylate is a synthetic chemotherapeutic agent and an antibacterial agent with IC5N/A of 6.7 nM.
More Information Supplier PagePeimine is a steroidal alkaloid isolated from a variety of species of the Fritillaria plant, it exhibits anti-inflammatory activity and acts as an expectorant and anti-tussive in cough medications.
More Information Supplier PagePeimine is a steroidal alkaloid isolated from a variety of species of the Fritillaria plant, it exhibits anti-inflammatory activity and acts as an expectorant and anti-tussive in cough medications.
More Information Supplier PagePeimine is a steroidal alkaloid isolated from a variety of species of the Fritillaria plant, it exhibits anti-inflammatory activity and acts as an expectorant and anti-tussive in cough medications.
More Information Supplier Page
