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 WebsiteFluo-3 is a fluorescent indicator for calcium used in flow cytometry. Fluorescence intensity increases about 40-fold after calcium binding.
More Information Supplier PageFluocinonide is a potent glucocorticoid steroid used topically as an anti-inflammatory agent for the treatment of skin disorders.
More Information Supplier PageFluocinonide is a potent glucocorticoid steroid used topically as an anti-inflammatory agent for the treatment of skin disorders.
More Information Supplier PageFluocinonide is a potent glucocorticoid steroid used topically as an anti-inflammatory agent for the treatment of skin disorders.
More Information Supplier PageFluocinonide is a potent glucocorticoid steroid used topically as an anti-inflammatory agent for the treatment of skin disorders.
More Information Supplier PageGBR 12935 dihydrochloride inhibits DAT (dopamine transporter) (Ki = 21.5 nM) and SLC6A2 (norepinephrine transporter) (Ki = 225 nM).
More Information Supplier PageGBR 12935 dihydrochloride inhibits DAT (dopamine transporter) (Ki = 21.5 nM) and SLC6A2 (norepinephrine transporter) (Ki = 225 nM).
More Information Supplier PageGBR 12935 dihydrochloride inhibits DAT (dopamine transporter) (Ki = 21.5 nM) and SLC6A2 (norepinephrine transporter) (Ki = 225 nM).
More Information Supplier PageFluorocurarine chloride is a short-acting selective sympathetic ganglioblocker with weak antagonist activity on the nicotinic receptor at the neuromuscular junction.
More Information Supplier PageFluorocurarine chloride is a short-acting selective sympathetic ganglioblocker with weak antagonist activity on the nicotinic receptor at the neuromuscular junction.
More Information Supplier PageFluorocurarine chloride is a short-acting selective sympathetic ganglioblocker with weak antagonist activity on the nicotinic receptor at the neuromuscular junction.
More Information Supplier PageFluorouracil (Adrucil) is a suicide inhibitor and works through irreversible inhibition of thymidylate synthase.
More Information Supplier PageFluorouracil (Adrucil) is a suicide inhibitor and works through irreversible inhibition of thymidylate synthase.
More Information Supplier PageFluorouracil (Adrucil) is a suicide inhibitor and works through irreversible inhibition of thymidylate synthase.
More Information Supplier PageFluorouracil (Adrucil) is a suicide inhibitor and works through irreversible inhibition of thymidylate synthase.
More Information Supplier PageFlurazepam possesses anxiolytic, anticonvulsant, sedative and skeletal muscle relaxant properties.
More Information Supplier PageFlurazepam possesses anxiolytic, anticonvulsant, sedative and skeletal muscle relaxant properties.
More Information Supplier PageFlurizan is a nonsteroidal anti-inflammatory drug (NSAID) that inhibits ??-secretase activity.
More Information Supplier PageFlurizan is a nonsteroidal anti-inflammatory drug (NSAID) that inhibits ??-secretase activity.
More Information Supplier PageFlurizan is a nonsteroidal anti-inflammatory drug (NSAID) that inhibits ??-secretase activity.
More Information Supplier PageFlurizan is a nonsteroidal anti-inflammatory drug (NSAID) that inhibits ??-secretase activity.
More Information Supplier PageFluticasone propionate is a high affinity, selective glucocorticoid receptor agonist (Kd = 0.5 nM).
More Information Supplier PageFluticasone propionate is a high affinity, selective glucocorticoid receptor agonist (Kd = 0.5 nM).
More Information Supplier PageFluticasone propionate is a high affinity, selective glucocorticoid receptor agonist (Kd = 0.5 nM).
More Information Supplier PageFluticasone propionate is a high affinity, selective glucocorticoid receptor agonist (Kd = 0.5 nM).
More Information Supplier PageFluticasone propionate is a high affinity, selective glucocorticoid receptor agonist (Kd = 0.5 nM).
More Information Supplier PageFM19G11 is an inhibitor of Hypoxia Inducible Factors ?? (HIF??), which are transcription factors that respond to changes in available oxygen in the cellular environment.
More Information Supplier PageFM19G11 is an inhibitor of Hypoxia Inducible Factors ?? (HIF??), which are transcription factors that respond to changes in available oxygen in the cellular environment.
More Information Supplier PageFM19G11 is an inhibitor of Hypoxia Inducible Factors ?? (HIF??), which are transcription factors that respond to changes in available oxygen in the cellular environment.
More Information Supplier PageFM19G11 is an inhibitor of Hypoxia Inducible Factors ?? (HIF??), which are transcription factors that respond to changes in available oxygen in the cellular environment.
More Information Supplier PageFMK is potent, highly specific and irreversible inhibitor of p90 ribosomal protein S6 kinase RSK1 and RSK2; Fmk binds in the CTKD ATP-binding site and inhibits RSK autophosphorylation at Ser386. Fmk induces significant apoptosis in human FGFR3-expressing, t(4;14)-positive multiple myeloma cells.
More Information Supplier PageFMK is potent, highly specific and irreversible inhibitor of p90 ribosomal protein S6 kinase RSK1 and RSK2; Fmk binds in the CTKD ATP-binding site and inhibits RSK autophosphorylation at Ser386. Fmk induces significant apoptosis in human FGFR3-expressing, t(4;14)-positive multiple myeloma cells.
More Information Supplier PageFMK is potent, highly specific and irreversible inhibitor of p90 ribosomal protein S6 kinase RSK1 and RSK2; Fmk binds in the CTKD ATP-binding site and inhibits RSK autophosphorylation at Ser386. Fmk induces significant apoptosis in human FGFR3-expressing, t(4;14)-positive multiple myeloma cells.
More Information Supplier PageFMK is potent, highly specific and irreversible inhibitor of p90 ribosomal protein S6 kinase RSK1 and RSK2; Fmk binds in the CTKD ATP-binding site and inhibits RSK autophosphorylation at Ser386. Fmk induces significant apoptosis in human FGFR3-expressing, t(4;14)-positive multiple myeloma cells.
More Information Supplier PageFmoc-Lys(Boc, Me)-OH is a novel derivative for the introduction of monomethyl-lysine during Fmoc SPPS.
More Information Supplier PageFmoc-Lys(Boc, Me)-OH is a novel derivative for the introduction of monomethyl-lysine during Fmoc SPPS.
More Information Supplier PageFmoc-L-Lys(Me2)-OH HCl is a modified Lysine used to study histone modifications.
More Information Supplier PageFmoc-L-Lys(Me2)-OH HCl is a modified Lysine used to study histone modifications.
More Information Supplier PageFolinic Acid Calcium Salt (Leucovorin) is the active form of the B complex vitamin Folate is used as an antidote to cancer treatment drugs (i.e. methotrexate) to reduce toxicity of residual drugs.
More Information Supplier PageFolinic Acid Calcium Salt (Leucovorin) is the active form of the B complex vitamin Folate is used as an antidote to cancer treatment drugs (i.e. methotrexate) to reduce toxicity of residual drugs.
More Information Supplier PageFolinic Acid Calcium Salt (Leucovorin) is the active form of the B complex vitamin Folate is used as an antidote to cancer treatment drugs (i.e. methotrexate) to reduce toxicity of residual drugs.
More Information Supplier PageFolinic Acid Calcium Salt (Leucovorin) is the active form of the B complex vitamin Folate is used as an antidote to cancer treatment drugs (i.e. methotrexate) to reduce toxicity of residual drugs.
More Information Supplier PageForetinib (GSK1363089), a multikinase inhibitor of c-Met and VEGFR-2, blocks proliferation, induces Anoikis, and impairs ovarian cancer metastasis.
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