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CSNpharm
SJG-136 is a rationally designed DNA minor groove interstrand cross-linking agent with potent and broad spectrum antitumor activity.
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CSNpharm
SJG-136 is a rationally designed DNA minor groove interstrand cross-linking agent with potent and broad spectrum antitumor activity.
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CSNpharm
SJG-136 is a rationally designed DNA minor groove interstrand cross-linking agent with potent and broad spectrum antitumor activity.
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CSNpharm
SJG-136 is a rationally designed DNA minor groove interstrand cross-linking agent with potent and broad spectrum antitumor activity.
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CSNpharm
Skatole (3-Methylindole) is a mildly toxic white crystalline organic compound that occurs naturally in feces. It has a fairly broad bacteriostatic effect.
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CSNpharm
SKF-34288 HCl is a PEPCK inhibitor which could inhibit glucose synthesis through inhibition of PEPCK in the gluconeogenesis pathway.
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CSNpharm
SKF-34288 HCl is a PEPCK inhibitor which could inhibit glucose synthesis through inhibition of PEPCK in the gluconeogenesis pathway.
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CSNpharm
SKF-34288 HCl is a PEPCK inhibitor which could inhibit glucose synthesis through inhibition of PEPCK in the gluconeogenesis pathway.
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CSNpharm
SKF-38393 HCl is an agonist of dopamine D1 receptor (the IC50 value is 110 nM). It has anorectic and stimulant effects.
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CSNpharm
SKF-38393 HCl is an agonist of dopamine D1 receptor (the IC50 value is 110 nM). It has anorectic and stimulant effects.
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CSNpharm
SKF-38393 HCl is an agonist of dopamine D1 receptor (the IC50 value is 110 nM). It has anorectic and stimulant effects.
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CSNpharm
SKF-38393 HCl is an agonist of dopamine D1 receptor (the IC50 value is 110 nM). It has anorectic and stimulant effects.
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CSNpharm
CSNpharm
CSNpharm
CSNpharm
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CSNpharm
SKF-86002 is a potent inhibitor of p38 MAP kinase with IC50 of 0.5-1 μM and inhibits LPS-induced IL-1 and TNF-α production in human monocytes (IC50 = 1 μM).
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CSNpharm
SKF-86002 is a potent inhibitor of p38 MAP kinase with IC50 of 0.5-1 μM and inhibits LPS-induced IL-1 and TNF-α production in human monocytes (IC50 = 1 μM).
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CSNpharm
SKF-86002 is a potent inhibitor of p38 MAP kinase with IC50 of 0.5-1 μM and inhibits LPS-induced IL-1 and TNF-α production in human monocytes (IC50 = 1 μM).
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CSNpharm
SKF-86002 is a potent inhibitor of p38 MAP kinase with IC50 of 0.5-1 μM and inhibits LPS-induced IL-1 and TNF-α production in human monocytes (IC50 = 1 μM).
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CSNpharm
SKF-89976A HCl is a selective GABA transporter (GAT-1) inhibitor with IC50s of 0.28 μM, 137.34 μM and 202.8 μM for GAT-1, GAT-2 and GAT-3 in CHO cells, respectively.
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CSNpharm
SKF-89976A HCl is a selective GABA transporter (GAT-1) inhibitor with IC50s of 0.28 μM, 137.34 μM and 202.8 μM for GAT-1, GAT-2 and GAT-3 in CHO cells, respectively.
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CSNpharm
SKF-89976A HCl is a selective GABA transporter (GAT-1) inhibitor with IC50s of 0.28 μM, 137.34 μM and 202.8 μM for GAT-1, GAT-2 and GAT-3 in CHO cells, respectively.
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CSNpharm
SKF-89976A HCl is a selective GABA transporter (GAT-1) inhibitor with IC50s of 0.28 μM, 137.34 μM and 202.8 μM for GAT-1, GAT-2 and GAT-3 in CHO cells, respectively.
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CSNpharm
SKF-96365 HCl is a transient receptor potential canonical type (TRPC) channel blocker, also bolcks voltage-gated Ca2+ channels and potassium channels.
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CSNpharm
SKF-96365 HCl is a transient receptor potential canonical type (TRPC) channel blocker, also bolcks voltage-gated Ca2+ channels and potassium channels.
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CSNpharm
SKF-96365 HCl is a transient receptor potential canonical type (TRPC) channel blocker, also bolcks voltage-gated Ca2+ channels and potassium channels.
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CSNpharm
SKF-96365 HCl is a transient receptor potential canonical type (TRPC) channel blocker, also bolcks voltage-gated Ca2+ channels and potassium channels.
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CSNpharm
SKF-96365 HCl is a transient receptor potential canonical type (TRPC) channel blocker, also bolcks voltage-gated Ca2+ channels and potassium channels.
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CSNpharm
SKF-96365 HCl is a transient receptor potential canonical type (TRPC) channel blocker, also bolcks voltage-gated Ca2+ channels and potassium channels.
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SKI V
1mg
| ≥98%
CSNpharm
for hPI3k. SKI V decreases formation of the mitogenic second messenger sphingosine-1-phosphate (S1P). SKI V induces apoptosis and has antitumor activity[1][2].
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SKI V
10mg
| ≥98%
CSNpharm
for hPI3k. SKI V decreases formation of the mitogenic second messenger sphingosine-1-phosphate (S1P). SKI V induces apoptosis and has antitumor activity[1][2].
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SKI V
5mg
| ≥98%
CSNpharm
for hPI3k. SKI V decreases formation of the mitogenic second messenger sphingosine-1-phosphate (S1P). SKI V induces apoptosis and has antitumor activity[1][2].
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CSNpharm
Skimmin, a natural product isolated and purified from the herbs of Hydrangea paniculata with anti-inflammatory activity, can significantly improve renal function and suppress the IgG deposition as well as the development of glomerular lesions in a rat model of membranous glomerulonephritis, suppress diabetic nephropathy in rats effectively, and may slow down the renal fibrosis by […]
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CSNpharm
Skullcapflavone I, a natural product isolated and purified from the roots of Scutellaria baicalensis Georgi, selectively induces apoptosis in T-HSC/Cl-6 cells via caspase-3 and caspase-9 activation.
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CSNpharm
Skullcapflavone I, a natural product isolated and purified from the roots of Scutellaria baicalensis Georgi, selectively induces apoptosis in T-HSC/Cl-6 cells via caspase-3 and caspase-9 activation.
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CSNpharm
Skyrin is a fungal bisanthroquinone. It exhibits functional glucagon antagonism by uncoupling the glucagon receptor from adenylate cyclase activation in rat liver membranes.
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CSNpharm
SL0101 is a selective inhibitor of ribosomal S6 kinase (RSK) (IC50 = 89 nM for RSK2) which does not inhibit upstream kinases such as MEK, Raf and PKC. SL0101 Inhibits the growth of MCF-7 human breast cancer cells with no effect on the normal breast cell line.
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CSNpharm
SL0101 is a selective inhibitor of ribosomal S6 kinase (RSK) (IC50 = 89 nM for RSK2) which does not inhibit upstream kinases such as MEK, Raf and PKC. SL0101 Inhibits the growth of MCF-7 human breast cancer cells with no effect on the normal breast cell line.
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