CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 431 of 649
Non-Antibody Products
Page 431 of 649
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| NS 11394 | A positive allosteric modulator of the GABAA receptor (Ki = 0.423 nM); sel… | 5 mg | 23872-5 | More Info |
| NS 13001 | A positive allosteric modulator of KCa2.2 / SK2 and KCa2.3 / SK3; increase… | 1 mg | 37317-1 | More Info |
| NS 13001 | A positive allosteric modulator of KCa2.2 / SK2 and KCa2.3 / SK3; increase… | 10 mg | 37317-10 | More Info |
| NS 13001 | A positive allosteric modulator of KCa2.2 / SK2 and KCa2.3 / SK3; increase… | 25 mg | 37317-25 | More Info |
| NS 13001 | A positive allosteric modulator of KCa2.2 / SK2 and KCa2.3 / SK3; increase… | 5 mg | 37317-5 | More Info |
| NS 1619 | A calcium-dependent activator of BKCa channels that is typically used at a… | 1 mg | 18876-1 | More Info |
| NS 1619 | A calcium-dependent activator of BKCa channels that is typically used at a… | 10 mg | 18876-10 | More Info |
| NS 1619 | A calcium-dependent activator of BKCa channels that is typically used at a… | 25 mg | 18876-25 | More Info |
| NS 1619 | A calcium-dependent activator of BKCa channels that is typically used at a… | 5 mg | 18876-5 | More Info |
| NS 1643 | An activator of ERG1 (KV11.1, KCNH2, hERG; EC50 = 10.5 µM); also act… | 10 mg | 20343-10 | More Info |
| NS 1643 | An activator of ERG1 (KV11.1, KCNH2, hERG; EC50 = 10.5 µM); also act… | 25 mg | 20343-25 | More Info |
| NS 1643 | An activator of ERG1 (KV11.1, KCNH2, hERG; EC50 = 10.5 µM); also act… | 5 mg | 20343-5 | More Info |
| NS 1643 | An activator of ERG1 (KV11.1, KCNH2, hERG; EC50 = 10.5 µM); also act… | 50 mg | 20343-50 | More Info |
| NS 1738 | A positive allosteric modulator of the α7-containing nAChRs, increas… | 1 mg | 21018-1 | More Info |
| NS 1738 | A positive allosteric modulator of the α7-containing nAChRs, increas… | 10 mg | 21018-10 | More Info |
| NS 1738 | A positive allosteric modulator of the α7-containing nAChRs, increas… | 5 mg | 21018-5 | More Info |
| NS 2028 | NS 2028 is a specific inhibitor of soluble guanylyl cyclase. It inhibits p… | 1 mg | 81600-1 | More Info |
| NS 2028 | NS 2028 is a specific inhibitor of soluble guanylyl cyclase. It inhibits p… | 10 mg | 81600-10 | More Info |
| NS 2028 | NS 2028 is a specific inhibitor of soluble guanylyl cyclase. It inhibits p… | 25 mg | 81600-25 | More Info |
| NS 2028 | NS 2028 is a specific inhibitor of soluble guanylyl cyclase. It inhibits p… | 5 mg | 81600-5 | More Info |
| NS 304 | An IP receptor agonist prodrug; a long-lasting prodrug of the active form… | 1 mg | 10010411-1 | More Info |
| NS 304 | An IP receptor agonist prodrug; a long-lasting prodrug of the active form… | 10 mg | 10010411-10 | More Info |
| NS 304 | An IP receptor agonist prodrug; a long-lasting prodrug of the active form… | 5 mg | 10010411-5 | More Info |
| NS 304 | An IP receptor agonist prodrug; a long-lasting prodrug of the active form… | 50 mg | 10010411-50 | More Info |
| NS 309 | A nonselective activator of SK / KCa2 and IK / KCa3.1 channels (EC50s rang… | 10 mg | 18889-10 | More Info |
| NS 309 | A nonselective activator of SK / KCa2 and IK / KCa3.1 channels (EC50s rang… | 5 mg | 18889-5 | More Info |
| NS 309 | A nonselective activator of SK / KCa2 and IK / KCa3.1 channels (EC50s rang… | 50 mg | 18889-50 | More Info |
| NS 3623 | An ion channel modulator; inhibits the VRAC in HEK293 cells and chloride c… | 10 mg | 34992-10 | More Info |
| NS 3623 | An ion channel modulator; inhibits the VRAC in HEK293 cells and chloride c… | 100 mg | 34992-100 | More Info |
| NS 3623 | An ion channel modulator; inhibits the VRAC in HEK293 cells and chloride c… | 5 mg | 34992-5 | More Info |
| NS 3623 | An ion channel modulator; inhibits the VRAC in HEK293 cells and chloride c… | 50 mg | 34992-50 | More Info |
| NS 3694 | A cell-permeable diarylurea compound that inhibits apoptosome formation an… | 10 mg | 19190-10 | More Info |
| NS 3694 | A cell-permeable diarylurea compound that inhibits apoptosome formation an… | 25 mg | 19190-25 | More Info |
| NS 3694 | A cell-permeable diarylurea compound that inhibits apoptosome formation an… | 5 mg | 19190-5 | More Info |
| NS 3694 | A cell-permeable diarylurea compound that inhibits apoptosome formation an… | 50 mg | 19190-50 | More Info |
| NS 3861 | A neuronal nAChR agonist; induces inward currents in patch-clamp assays us… | 10 mg | 37406-10 | More Info |
| NS 3861 | A neuronal nAChR agonist; induces inward currents in patch-clamp assays us… | 25 mg | 37406-25 | More Info |
| NS 3861 | A neuronal nAChR agonist; induces inward currents in patch-clamp assays us… | 5 mg | 37406-5 | More Info |
| NS 398 | NS 398 is a selective inhibitor of COX-2. The IC50 values for human recomb… | 10 mg | 70590-10 | More Info |
| NS 398 | NS 398 is a selective inhibitor of COX-2. The IC50 values for human recomb… | 25 mg | 70590-25 | More Info |
| NS 398 | NS 398 is a selective inhibitor of COX-2. The IC50 values for human recomb… | 5 mg | 70590-5 | More Info |
| NS 398 | NS 398 is a selective inhibitor of COX-2. The IC50 values for human recomb… | 50 mg | 70590-50 | More Info |
| NS 5806 | An Ito current activator; increases Kv4.3-mediated Ito current amplitudes… | 1 mg | 33226-1 | More Info |
| NS 5806 | An Ito current activator; increases Kv4.3-mediated Ito current amplitudes… | 10 mg | 33226-10 | More Info |
| NS 5806 | An Ito current activator; increases Kv4.3-mediated Ito current amplitudes… | 25 mg | 33226-25 | More Info |
| NS 5806 | An Ito current activator; increases Kv4.3-mediated Ito current amplitudes… | 5 mg | 33226-5 | More Info |
| NS 6180 | An inhibitor of IKCa1 / KCa3.1 channels (IC50 = 9.4 nM); inhibits A23187-i… | 10 mg | 14664-10 | More Info |
| NS 6180 | An inhibitor of IKCa1 / KCa3.1 channels (IC50 = 9.4 nM); inhibits A23187-i… | 25 mg | 14664-25 | More Info |
| NS 6180 | An inhibitor of IKCa1 / KCa3.1 channels (IC50 = 9.4 nM); inhibits A23187-i… | 5 mg | 14664-5 | More Info |
| NS 6180 | An inhibitor of IKCa1 / KCa3.1 channels (IC50 = 9.4 nM); inhibits A23187-i… | 50 mg | 14664-50 | More Info |
| NS 638 | An N- and L-type calcium channel inhibitor; inhibits potassium-induced cal… | 10 mg | 37193-10 | More Info |
| NS 638 | An N- and L-type calcium channel inhibitor; inhibits potassium-induced cal… | 100 mg | 37193-100 | More Info |
| NS 638 | An N- and L-type calcium channel inhibitor; inhibits potassium-induced cal… | 50 mg | 37193-50 | More Info |
| NS 9283 | A positive allosteric modulator of α4β2 subunit-containing nACh… | 1 mg | 29189-1 | More Info |
| NS 9283 | A positive allosteric modulator of α4β2 subunit-containing nACh… | 10 mg | 29189-10 | More Info |
| NS 9283 | A positive allosteric modulator of α4β2 subunit-containing nACh… | 25 mg | 29189-25 | More Info |
| NS 9283 | A positive allosteric modulator of α4β2 subunit-containing nACh… | 5 mg | 29189-5 | More Info |
| NS 3728 | A chloride channel inhibitor; inhibits VRAC in HEK293 cells and chloride c… | 10 mg | 39988-10 | More Info |
| NS 3728 | A chloride channel inhibitor; inhibits VRAC in HEK293 cells and chloride c… | 25 mg | 39988-25 | More Info |
| NS 3728 | A chloride channel inhibitor; inhibits VRAC in HEK293 cells and chloride c… | 5 mg | 39988-5 | More Info |
| NS 3728 | A chloride channel inhibitor; inhibits VRAC in HEK293 cells and chloride c… | 50 mg | 39988-50 | More Info |
| NSC 109555 | An inhibitor of Chk2 (IC50 = 200 nM in a cell-free kinase assay); selectiv… | 1 mg | 19811-1 | More Info |
| NSC 109555 | An inhibitor of Chk2 (IC50 = 200 nM in a cell-free kinase assay); selectiv… | 10 mg | 19811-10 | More Info |
| NSC 109555 | An inhibitor of Chk2 (IC50 = 200 nM in a cell-free kinase assay); selectiv… | 5 mg | 19811-5 | More Info |
| NSC 109555 | An inhibitor of Chk2 (IC50 = 200 nM in a cell-free kinase assay); selectiv… | 50 mg | 19811-50 | More Info |
| NSC 12 | An extracellular trap for FGF2 that binds FGF2 (Kd = 51 µM) and inte… | 1 mg | 20117-1 | More Info |
| NSC 12 | An extracellular trap for FGF2 that binds FGF2 (Kd = 51 µM) and inte… | 10 mg | 20117-10 | More Info |
| NSC 12 | An extracellular trap for FGF2 that binds FGF2 (Kd = 51 µM) and inte… | 25 mg | 20117-25 | More Info |
| NSC 12 | An extracellular trap for FGF2 that binds FGF2 (Kd = 51 µM) and inte… | 5 mg | 20117-5 | More Info |
| NSC 15520 | A small molecule inhibitor of RPA70 dsDNA binding; selectively inhibits ds… | 1 mg | 26020-1 | More Info |
| NSC 15520 | A small molecule inhibitor of RPA70 dsDNA binding; selectively inhibits ds… | 10 mg | 26020-10 | More Info |
| NSC 15520 | A small molecule inhibitor of RPA70 dsDNA binding; selectively inhibits ds… | 25 mg | 26020-25 | More Info |
| NSC 15520 | A small molecule inhibitor of RPA70 dsDNA binding; selectively inhibits ds… | 5 mg | 26020-5 | More Info |
| NSC 185058 | An inhibitor of ATG4B; inhibits ATG4B cleavage of LC3B-GST (IC50 = 51 &mic… | 1 mg | 23957-1 | More Info |
| NSC 185058 | An inhibitor of ATG4B; inhibits ATG4B cleavage of LC3B-GST (IC50 = 51 &mic… | 5 mg | 23957-5 | More Info |
| NSC 19005 | A potential impurity found in commercial preparations of betahistine; a de… | 100 mg | 32898-100 | More Info |
| NSC 19005 | A potential impurity found in commercial preparations of betahistine; a de… | 25 mg | 32898-25 | More Info |
| NSC 19005 | A potential impurity found in commercial preparations of betahistine; a de… | 250 mg | 32898-250 | More Info |
| NSC 19005 | A potential impurity found in commercial preparations of betahistine; a de… | 50 mg | 32898-50 | More Info |
| NSC 207895 | An inhibitor of MDMX; decreases MDMX promoter activity in a reporter assay… | 1 mg | 27949-1 | More Info |
| NSC 207895 | An inhibitor of MDMX; decreases MDMX promoter activity in a reporter assay… | 10 mg | 27949-10 | More Info |
| NSC 207895 | An inhibitor of MDMX; decreases MDMX promoter activity in a reporter assay… | 25 mg | 27949-25 | More Info |
| NSC 207895 | An inhibitor of MDMX; decreases MDMX promoter activity in a reporter assay… | 5 mg | 27949-5 | More Info |
| NSC 210902 | A selective CK2 inhibitor (IC50 = 1 µM); selective for CK2 over JNK3… | 1 mg | 10011255-1 | More Info |
| NSC 210902 | A selective CK2 inhibitor (IC50 = 1 µM); selective for CK2 over JNK3… | 10 mg | 10011255-10 | More Info |
| NSC 210902 | A selective CK2 inhibitor (IC50 = 1 µM); selective for CK2 over JNK3… | 5 mg | 10011255-5 | More Info |
| NSC 210902 | A selective CK2 inhibitor (IC50 = 1 µM); selective for CK2 over JNK3… | 50 mg | 10011255-50 | More Info |
| NSC 228155 | An activator of EGFR and an inhibitor of the interaction between the KID o… | 10 mg | 28856-10 | More Info |
| NSC 228155 | An activator of EGFR and an inhibitor of the interaction between the KID o… | 25 mg | 28856-25 | More Info |
| NSC 228155 | An activator of EGFR and an inhibitor of the interaction between the KID o… | 5 mg | 28856-5 | More Info |
| NSC 232003 | An inhibitor of the UHRF1-DNMT1 protein-protein interaction (IC50 = 15 &mi… | 1 mg | 38523-1 | More Info |
| NSC 232003 | An inhibitor of the UHRF1-DNMT1 protein-protein interaction (IC50 = 15 &mi… | 10 mg | 38523-10 | More Info |
| NSC 232003 | An inhibitor of the UHRF1-DNMT1 protein-protein interaction (IC50 = 15 &mi… | 25 mg | 38523-25 | More Info |
| NSC 232003 | An inhibitor of the UHRF1-DNMT1 protein-protein interaction (IC50 = 15 &mi… | 5 mg | 38523-5 | More Info |
| NSC 23925 | An inhibitor of P-gp; selectively reverses multidrug resistance mediated b… | 1 mg | 21947-1 | More Info |
| NSC 23925 | An inhibitor of P-gp; selectively reverses multidrug resistance mediated b… | 10 mg | 21947-10 | More Info |
| NSC 23925 | An inhibitor of P-gp; selectively reverses multidrug resistance mediated b… | 25 mg | 21947-25 | More Info |
| NSC 23925 | An inhibitor of P-gp; selectively reverses multidrug resistance mediated b… | 5 mg | 21947-5 | More Info |
| NSC 245214 | A dinitrothiophene derivative | 1 mg | 9002543-1 | More Info |
| NSC 245214 | A dinitrothiophene derivative | 10 mg | 9002543-10 | More Info |
CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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Ann Arbor MI 48108
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