Scopolamine (hydrobromide) |
A tropane alkaloid and muscarinic receptor antagonist that can be used to… |
1 mg |
14108-1 |
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Scopolamine (hydrobromide) |
A tropane alkaloid and muscarinic receptor antagonist that can be used to… |
5 mg |
14108-5 |
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Scopolamine N-butyl (bromide) |
An antispasmodic agent; inhibits electrically induced urinary bladder cont… |
1 g |
27223-1 |
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Scopolamine N-butyl (bromide) |
An antispasmodic agent; inhibits electrically induced urinary bladder cont… |
10 g |
27223-10 |
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Scopolamine N-butyl (bromide) |
An antispasmodic agent; inhibits electrically induced urinary bladder cont… |
5 g |
27223-5 |
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Scopoletin |
A natural coumarin that binds iron; inhibits aldose reductase activity in… |
25 mg |
20042-25 |
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Scopoletin |
A natural coumarin that binds iron; inhibits aldose reductase activity in… |
250 mg |
20042-250 |
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Scopoletin |
A natural coumarin that binds iron; inhibits aldose reductase activity in… |
50 mg |
20042-50 |
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Scopolin |
A coumarin glucoside; inhibits A23187-induced production of PGE2 and LTC4… |
1 mg |
33874-1 |
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Scopolin |
A coumarin glucoside; inhibits A23187-induced production of PGE2 and LTC4… |
10 mg |
33874-10 |
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Scopolin |
A coumarin glucoside; inhibits A23187-induced production of PGE2 and LTC4… |
5 mg |
33874-5 |
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Scopoline |
A tropane alkaloid |
100 mg |
35301-100 |
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Scopoline |
A tropane alkaloid |
250 mg |
35301-250 |
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Scopoline |
A tropane alkaloid |
50 mg |
35301-50 |
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Scoulerine |
A benzylisoquinoline alkaloid with diverse biological activities; selectiv… |
1 mg |
35140-1 |
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Scoulerine |
A benzylisoquinoline alkaloid with diverse biological activities; selectiv… |
10 mg |
35140-10 |
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Scoulerine |
A benzylisoquinoline alkaloid with diverse biological activities; selectiv… |
5 mg |
35140-5 |
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(S)-CR8 |
An inhibitor of cyclin-dependent kinases (IC50s = 0.15, 0.08, 0.06, 0.12,… |
1 mg |
29985-1 |
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(S)-CR8 |
An inhibitor of cyclin-dependent kinases (IC50s = 0.15, 0.08, 0.06, 0.12,… |
10 mg |
29985-10 |
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(S)-CR8 |
An inhibitor of cyclin-dependent kinases (IC50s = 0.15, 0.08, 0.06, 0.12,… |
25 mg |
29985-25 |
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(S)-CR8 |
An inhibitor of cyclin-dependent kinases (IC50s = 0.15, 0.08, 0.06, 0.12,… |
5 mg |
29985-5 |
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SCR130 |
An NHEJ inhibitor; selectively inhibits DNA ligase IV- over ligase I- or l… |
1 mg |
37779-1 |
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SCR130 |
An NHEJ inhibitor; selectively inhibits DNA ligase IV- over ligase I- or l… |
10 mg |
37779-10 |
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SCR130 |
An NHEJ inhibitor; selectively inhibits DNA ligase IV- over ligase I- or l… |
5 mg |
37779-5 |
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SCR7 |
A small molecule inhibitor of DNA ligase IV that prevents nonhomologous en… |
1 mg |
18015-1 |
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SCR7 |
A small molecule inhibitor of DNA ligase IV that prevents nonhomologous en… |
10 mg |
18015-10 |
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SCR7 |
A small molecule inhibitor of DNA ligase IV that prevents nonhomologous en… |
25 mg |
18015-25 |
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SCR7 |
A small molecule inhibitor of DNA ligase IV that prevents nonhomologous en… |
5 mg |
18015-5 |
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SCR-1481B1 |
A pyridone |
1 mg |
33269-1 |
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SCR-1481B1 |
A pyridone |
10 mg |
33269-10 |
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SCR-1481B1 |
A pyridone |
25 mg |
33269-25 |
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SCR-1481B1 |
A pyridone |
5 mg |
33269-5 |
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Scriptaid |
An HDAC inhibitor that has an optimal effective concentration of 6-8 &micr… |
1 mg |
10572-1 |
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Scriptaid |
An HDAC inhibitor that has an optimal effective concentration of 6-8 &micr… |
10 mg |
10572-10 |
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Scriptaid |
An HDAC inhibitor that has an optimal effective concentration of 6-8 &micr… |
5 mg |
10572-5 |
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(S)-Crizotinib |
An MTH1 inhibitor (IC50 = 72 nM); selective for MTH1 over a panel of 456 k… |
1 mg |
31114-1 |
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(S)-Crizotinib |
An MTH1 inhibitor (IC50 = 72 nM); selective for MTH1 over a panel of 456 k… |
10 mg |
31114-10 |
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(S)-Crizotinib |
An MTH1 inhibitor (IC50 = 72 nM); selective for MTH1 over a panel of 456 k… |
25 mg |
31114-25 |
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(S)-Crizotinib |
An MTH1 inhibitor (IC50 = 72 nM); selective for MTH1 over a panel of 456 k… |
5 mg |
31114-5 |
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Scutellarein |
A flavone; has antioxidant activity in a TRAP assay at 1 µg / ml; in… |
1 mg |
24977-1 |
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Scutellarein |
A flavone; has antioxidant activity in a TRAP assay at 1 µg / ml; in… |
10 mg |
24977-10 |
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Scutellarein |
A flavone; has antioxidant activity in a TRAP assay at 1 µg / ml; in… |
5 mg |
24977-5 |
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Scutellarein |
A flavone; has antioxidant activity in a TRAP assay at 1 µg / ml; in… |
50 mg |
24977-50 |
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Scutellarin |
A flavone with diverse biological activities; inhibits proliferation of PC… |
10 mg |
27461-10 |
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Scutellarin |
A flavone with diverse biological activities; inhibits proliferation of PC… |
100 mg |
27461-100 |
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Scutellarin |
A flavone with diverse biological activities; inhibits proliferation of PC… |
25 mg |
27461-25 |
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Scutellarin |
A flavone with diverse biological activities; inhibits proliferation of PC… |
50 mg |
27461-50 |
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scyllo-Inositol |
A stereoisomer of inositol; reduces Aβ40- and Aβ42-induced decre… |
10 mg |
31214-10 |
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scyllo-Inositol |
A stereoisomer of inositol; reduces Aβ40- and Aβ42-induced decre… |
100 mg |
31214-100 |
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scyllo-Inositol |
A stereoisomer of inositol; reduces Aβ40- and Aβ42-induced decre… |
5 mg |
31214-5 |
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scyllo-Inositol |
A stereoisomer of inositol; reduces Aβ40- and Aβ42-induced decre… |
50 mg |
31214-50 |
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scyllo-Inositol hexakisphosphate (sodium salt) |
A stereoisomer of IP6; identified in soil samples from Madagascar, New Zea… |
1 mg |
9002339-1 |
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scyllo-Inositol hexakisphosphate (sodium salt) |
A stereoisomer of IP6; identified in soil samples from Madagascar, New Zea… |
10 mg |
9002339-10 |
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scyllo-Inositol hexakisphosphate (sodium salt) |
A stereoisomer of IP6; identified in soil samples from Madagascar, New Zea… |
5 mg |
9002339-5 |
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scyllo-Inositol hexakisphosphate (sodium salt) |
A stereoisomer of IP6; identified in soil samples from Madagascar, New Zea… |
500 µg |
9002339-500 |
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SD 169 |
A selective inhibitor of the MAP kinases p38α (IC50 = 3.2 nM) and p3… |
10 mg |
14156-10 |
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SD 169 |
A selective inhibitor of the MAP kinases p38α (IC50 = 3.2 nM) and p3… |
25 mg |
14156-25 |
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SD 169 |
A selective inhibitor of the MAP kinases p38α (IC50 = 3.2 nM) and p3… |
5 mg |
14156-5 |
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SD 208 |
A potent inhibitor of TGF-βRI kinase (EC50 = 48 nM) that has minimal… |
1 mg |
16619-1 |
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SD 208 |
A potent inhibitor of TGF-βRI kinase (EC50 = 48 nM) that has minimal… |
10 mg |
16619-10 |
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SD 208 |
A potent inhibitor of TGF-βRI kinase (EC50 = 48 nM) that has minimal… |
25 mg |
16619-25 |
More Info
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SD 208 |
A potent inhibitor of TGF-βRI kinase (EC50 = 48 nM) that has minimal… |
5 mg |
16619-5 |
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SD-06 |
An inhibitor of p38α MAPK (IC50 = 0.016 µM); selective for p38… |
10 mg |
30686-10 |
More Info
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SD-06 |
An inhibitor of p38α MAPK (IC50 = 0.016 µM); selective for p38… |
25 mg |
30686-25 |
More Info
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SD-06 |
An inhibitor of p38α MAPK (IC50 = 0.016 µM); selective for p38… |
5 mg |
30686-5 |
More Info
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SD-06 |
An inhibitor of p38α MAPK (IC50 = 0.016 µM); selective for p38… |
50 mg |
30686-50 |
More Info
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SD-1029 |
A JAK2 inhibitor; inhibits autophosphorylation of recombinant JAK2 at 30 a… |
1 mg |
21029-1 |
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SD-1029 |
A JAK2 inhibitor; inhibits autophosphorylation of recombinant JAK2 at 30 a… |
5 mg |
21029-5 |
More Info
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SDB-005 |
An indazole analog of PB-22; intended for forensic and research applicatio… |
1 mg |
15389-1 |
More Info
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SDB-005 |
An indazole analog of PB-22; intended for forensic and research applicatio… |
10 mg |
15389-10 |
More Info
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SDB-005 |
An indazole analog of PB-22; intended for forensic and research applicatio… |
5 mg |
15389-5 |
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SDB-006 |
A cannabimimetic indole that binds CB1 and CB2 receptors with EC50 values… |
1 mg |
15156-1 |
More Info
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SDB-006 |
A cannabimimetic indole that binds CB1 and CB2 receptors with EC50 values… |
10 mg |
15156-10 |
More Info
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SDB-006 |
A cannabimimetic indole that binds CB1 and CB2 receptors with EC50 values… |
5 mg |
15156-5 |
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SDB-006 N-phenyl analog |
A cannabimimetic indole that binds the CB1 and CB2 receptors with EC50 val… |
1 mg |
16044-1 |
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