CSNpharm
CSNpharm
CSNpharm
CSNpharm
CSNpharm
Pyridostatin Trifluoroacetate stabilizes and binds G-quadruplexe with Kd of 490 nM (cell-free assay), which targets the proto-oncogene c-kit, K-ras and Bcl-2.
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CSNpharm
Pyridostatin Trifluoroacetate stabilizes and binds G-quadruplexe with Kd of 490 nM (cell-free assay), which targets the proto-oncogene c-kit, K-ras and Bcl-2.
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CSNpharm
Pyridostatin Trifluoroacetate stabilizes and binds G-quadruplexe with Kd of 490 nM (cell-free assay), which targets the proto-oncogene c-kit, K-ras and Bcl-2.
More Information
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CSNpharm
Pyridostatin Trifluoroacetate stabilizes and binds G-quadruplexe with Kd of 490 nM (cell-free assay), which targets the proto-oncogene c-kit, K-ras and Bcl-2.
More Information
Supplier Page
CSNpharm
Pyridostatin Trifluoroacetate stabilizes and binds G-quadruplexe with Kd of 490 nM (cell-free assay), which targets the proto-oncogene c-kit, K-ras and Bcl-2.
More Information
Supplier Page
CSNpharm
Pyridostatin Trifluoroacetate stabilizes and binds G-quadruplexe with Kd of 490 nM (cell-free assay), which targets the proto-oncogene c-kit, K-ras and Bcl-2.
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CSNpharm
CSNpharm
CSNpharm
CSNpharm
Pyridoxal 5-phosphate monohydrate is an active vitamin B6 metabolite, which is a cofactor in many reactions of amino acid metabolism.
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CSNpharm
CSNpharm
CSNpharm
CSNpharm
Pyridoxal phosphate is the active form of vitamin B6, acts as an inhibitor of reverse transcriptases, and is used for the treatment of tardive dyskinesia.
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CSNpharm
Pyridoxine, 4-methanol form of vitamin B6, can be converted to pyridoxal 5-phosphate in body. It is used as a vitamin B6 dietary supplement.
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CSNpharm
Pyridoxine, 4-methanol form of vitamin B6, can be converted to pyridoxal 5-phosphate in body. It is used as a vitamin B6 dietary supplement.
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CSNpharm
Pyridoxine, 4-methanol form of vitamin B6, can be converted to pyridoxal 5-phosphate in body. It is used as a vitamin B6 dietary supplement.
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CSNpharm
Pyridoxine, 4-methanol form of vitamin B6, can be converted to pyridoxal 5-phosphate in body. It is used as a vitamin B6 dietary supplement.
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CSNpharm
Pyridoxine, 4-methanol form of vitamin B6, can be converted to pyridoxal 5-phosphate in body. It is used as a vitamin B6 dietary supplement.
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CSNpharm
CSNpharm
CSNpharm
CSNpharm
CSNpharm
Pyrimethamine inhibits multidrug and toxin extrusion (MATE) transporter potently, it also inhibits dihydrofolate reductase (DHFR), used for protozoal infections and interferes with tetrahydrofolic acid synthesis from folic acid.
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CSNpharm
Pyrimethamine inhibits multidrug and toxin extrusion (MATE) transporter potently, it also inhibits dihydrofolate reductase (DHFR), used for protozoal infections and interferes with tetrahydrofolic acid synthesis from folic acid.
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CSNpharm
CSNpharm
CSNpharm
Pyrithioxin 2HCl is a neurodynamic compound, combined with a short period of hyperventilation (HV) was applied in cerebral infarct patients with Hemiplegia.
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CSNpharm
Pyrithioxin 2HCl is a neurodynamic compound, combined with a short period of hyperventilation (HV) was applied in cerebral infarct patients with Hemiplegia.
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CSNpharm
Pyrogallol, a natural product isolated and purified from the stem of Cotinus coggygria Scop, is carcinogenic in female mice and may have caused tumors in male mice.
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CSNpharm
Pyrogallol, a natural product isolated and purified from the stem of Cotinus coggygria Scop, is carcinogenic in female mice and may have caused tumors in male mice.
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CSNpharm
Pyrrole-2-carboxylic acid is a degradation product of sialic acids and a derivative of the oxidation of the D-hydroxyproline isomers by mammalian D-amino acid oxidase.
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CSNpharm
Pyrrole-2-carboxylic acid is a degradation product of sialic acids and a derivative of the oxidation of the D-hydroxyproline isomers by mammalian D-amino acid oxidase.
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CSNpharm
Pyruvic acid is an intermediate compound in body metabolism. It reacts with N-acetyl mannosamine to form sialic acid. Pyruvic acid is also a component of commercial red seaweed polysaccharide.
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CSNpharm
CSNpharm
CSNpharm
QS11
5mg
| ≥99%
CSNpharm
QS11 is a GTPase activating protein of ADP-ribosylation factor 1 (ARFGAP1) inhibitor that increases activity of ARFs in NIH3T3 cells at concentration of 1 μM, it also modulates Wnt/β-catenin signaling.
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QS11
10mg
| ≥99%
CSNpharm
QS11 is a GTPase activating protein of ADP-ribosylation factor 1 (ARFGAP1) inhibitor that increases activity of ARFs in NIH3T3 cells at concentration of 1 μM, it also modulates Wnt/β-catenin signaling.
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QS11
25mg
| ≥99%
CSNpharm
QS11 is a GTPase activating protein of ADP-ribosylation factor 1 (ARFGAP1) inhibitor that increases activity of ARFs in NIH3T3 cells at concentration of 1 μM, it also modulates Wnt/β-catenin signaling.
More Information
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QS11
1mg
| ≥99%
CSNpharm
QS11 is a GTPase activating protein of ADP-ribosylation factor 1 (ARFGAP1) inhibitor that increases activity of ARFs in NIH3T3 cells at concentration of 1 μM, it also modulates Wnt/β-catenin signaling.
More Information
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QS11
50mg
| ≥99%
CSNpharm
QS11 is a GTPase activating protein of ADP-ribosylation factor 1 (ARFGAP1) inhibitor that increases activity of ARFs in NIH3T3 cells at concentration of 1 μM, it also modulates Wnt/β-catenin signaling.
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CSNpharm
Quercetin is a flavonoid isolated and purified from the flower bud of Sophora flavescens Ait., with anticancer activity. It is also a mitochondrial ATPase and phosphodiesterase inhibitor and Inhibits PI3-kinase activity and slightly inhibits PIP kinase activity.
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CSNpharm
Quercetin is a flavonoid isolated and purified from the flower bud of Sophora flavescens Ait., with anticancer activity. It is also a mitochondrial ATPase and phosphodiesterase inhibitor and Inhibits PI3-kinase activity and slightly inhibits PIP kinase activity.
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CSNpharm
Quercetin-3-O-robinobioside, a natural quercetin-derived flavonol isolated and purified from the herbs of Callicarpa bodinieri Levl. with antioxidant activity, exhibits in-vitro inhibitory activities against leukemia K562 cells.
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CSNpharm
Quercetin-3-O-robinobioside, a natural quercetin-derived flavonol isolated and purified from the herbs of Callicarpa bodinieri Levl. with antioxidant activity, exhibits in-vitro inhibitory activities against leukemia K562 cells.
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