CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 393 of 865
Non-Antibody Products
Page 393 of 865
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| Ibogaine (hydrochloride) | An analytical reference standard categorized as an iboga alkaloid; induces… | 5 mg | 20083-5 | More Info |
| I-BOP | A potent TP receptor agonist; induces human platelet aggregation with EC50… | 1 mg | 19600-1 | More Info |
| I-BOP | A potent TP receptor agonist; induces human platelet aggregation with EC50… | 100 µg | 19600-100 | More Info |
| I-BOP | A potent TP receptor agonist; induces human platelet aggregation with EC50… | 500 µg | 19600-500 | More Info |
| Ibotenic Acid | A neuroexcitatory amino acid that functions as a NMDA and metabotropic glu… | 1 mg | 14584-1 | More Info |
| Ibotenic Acid | A neuroexcitatory amino acid that functions as a NMDA and metabotropic glu… | 10 mg | 14584-10 | More Info |
| Ibotenic Acid | A neuroexcitatory amino acid that functions as a NMDA and metabotropic glu… | 25 mg | 14584-25 | More Info |
| Ibotenic Acid | A neuroexcitatory amino acid that functions as a NMDA and metabotropic glu… | 5 mg | 14584-5 | More Info |
| 4-IBP | A σ1 receptor ligand (Ki = 1.7 nM); selective for σ1 over &sig… | 10 mg | 31518-10 | More Info |
| 4-IBP | A σ1 receptor ligand (Ki = 1.7 nM); selective for σ1 over &sig… | 25 mg | 31518-25 | More Info |
| 4-IBP | A σ1 receptor ligand (Ki = 1.7 nM); selective for σ1 over &sig… | 5 mg | 31518-5 | More Info |
| 4-IBP | A σ1 receptor ligand (Ki = 1.7 nM); selective for σ1 over &sig… | 50 mg | 31518-50 | More Info |
| I-BRD9 | A selective BRD9 bromodomain inhibitor (pIC50 = 7.3; pKd = 8.7); used to i… | 1 mg | 17749-1 | More Info |
| I-BRD9 | A selective BRD9 bromodomain inhibitor (pIC50 = 7.3; pKd = 8.7); used to i… | 10 mg | 17749-10 | More Info |
| I-BRD9 | A selective BRD9 bromodomain inhibitor (pIC50 = 7.3; pKd = 8.7); used to i… | 5 mg | 17749-5 | More Info |
| I-BRD9 | A selective BRD9 bromodomain inhibitor (pIC50 = 7.3; pKd = 8.7); used to i… | 50 mg | 17749-50 | More Info |
| Ibrutinib | An irreversible inhibitor of BTK (IC50 = 0.5 nM) that selectively blocks B… | 1 mg | 16274-1 | More Info |
| Ibrutinib | An irreversible inhibitor of BTK (IC50 = 0.5 nM) that selectively blocks B… | 10 mg | 16274-10 | More Info |
| Ibrutinib | An irreversible inhibitor of BTK (IC50 = 0.5 nM) that selectively blocks B… | 5 mg | 16274-5 | More Info |
| Ibrutinib | An irreversible inhibitor of BTK (IC50 = 0.5 nM) that selectively blocks B… | 50 mg | 16274-50 | More Info |
| Ibrutinib-d5 | An internal standard for the quantification of ibrutinib by GC- or LC-MS, | 1 mg | 22561-1 | More Info |
| Ibrutinib-d5 | An internal standard for the quantification of ibrutinib by GC- or LC-MS, | 5 mg | 22561-5 | More Info |
| Ibrutinib-d5 | An internal standard for the quantification of ibrutinib by GC- or LC-MS, | 500 µg | 22561-500 | More Info |
| IBTP (iodide) | A lipophilic cation that is accumulated in mitochondria and forms stable t… | 10 mg | 18802-10 | More Info |
| IBTP (iodide) | A lipophilic cation that is accumulated in mitochondria and forms stable t… | 25 mg | 18802-25 | More Info |
| IBTP (iodide) | A lipophilic cation that is accumulated in mitochondria and forms stable t… | 5 mg | 18802-5 | More Info |
| Ibudilast | An inhibitor of PDE4 (IC50s = 54, 65, 239, and 166 nM for PDE4A-D, respect… | 10 mg | 14832-10 | More Info |
| Ibudilast | An inhibitor of PDE4 (IC50s = 54, 65, 239, and 166 nM for PDE4A-D, respect… | 25 mg | 14832-25 | More Info |
| Ibudilast | An inhibitor of PDE4 (IC50s = 54, 65, 239, and 166 nM for PDE4A-D, respect… | 5 mg | 14832-5 | More Info |
| Ibudilast | An inhibitor of PDE4 (IC50s = 54, 65, 239, and 166 nM for PDE4A-D, respect… | 50 mg | 14832-50 | More Info |
| Ibudilast-d7 | An internal standard for the quantification of ibudilast by GC- or LC-MS | 1 mg | 28876-1 | More Info |
| Ibufenac | A NSAID that inhibits COX-1 and -2 activity with IC50 values of 17.4 and 1… | 10 mg | 17874-10 | More Info |
| Ibufenac | A NSAID that inhibits COX-1 and -2 activity with IC50 values of 17.4 and 1… | 100 mg | 17874-100 | More Info |
| Ibufenac | A NSAID that inhibits COX-1 and -2 activity with IC50 values of 17.4 and 1… | 25 mg | 17874-25 | More Info |
| Ibufenac | A NSAID that inhibits COX-1 and -2 activity with IC50 values of 17.4 and 1… | 50 mg | 17874-50 | More Info |
| Ibuprofen Carboxylic Acid | A major metabolite of ibuprofen; prevents fructose-, cyanate-, and prednis… | 1 mg | 26594-1 | More Info |
| Ibuprofen Carboxylic Acid | A major metabolite of ibuprofen; prevents fructose-, cyanate-, and prednis… | 500 µg | 26594-500 | More Info |
| Ibutamoren (mesylate) | An orally-active, non-peptidic agonist of GHSR (Kd = 0.4 nM) and, as a res… | 10 mg | 18003-10 | More Info |
| Ibutamoren (mesylate) | An orally-active, non-peptidic agonist of GHSR (Kd = 0.4 nM) and, as a res… | 25 mg | 18003-25 | More Info |
| Ibutamoren (mesylate) | An orally-active, non-peptidic agonist of GHSR (Kd = 0.4 nM) and, as a res… | 5 mg | 18003-5 | More Info |
| Ibutamoren (mesylate) | An orally-active, non-peptidic agonist of GHSR (Kd = 0.4 nM) and, as a res… | 50 mg | 18003-50 | More Info |
| IC261 | A reversible, ATP-competitive inhibitor of CK1δ and CK1? (IC50 = ~1… | 1 mg | 17260-1 | More Info |
| IC261 | A reversible, ATP-competitive inhibitor of CK1δ and CK1? (IC50 = ~1… | 10 mg | 17260-10 | More Info |
| IC261 | A reversible, ATP-competitive inhibitor of CK1δ and CK1? (IC50 = ~1… | 25 mg | 17260-25 | More Info |
| IC261 | A reversible, ATP-competitive inhibitor of CK1δ and CK1? (IC50 = ~1… | 5 mg | 17260-5 | More Info |
| IC8 | An ionizable cationic lipid; has been used in combination with other lipid… | 10 mg | 37986-10 | More Info |
| IC8 | An ionizable cationic lipid; has been used in combination with other lipid… | 25 mg | 37986-25 | More Info |
| IC8 | An ionizable cationic lipid; has been used in combination with other lipid… | 5 mg | 37986-5 | More Info |
| IC-87114 | A cell-permeable selective inhibitor of the PI3K catalytic subunit p110&de… | 1 mg | 11589-1 | More Info |
| IC-87114 | A cell-permeable selective inhibitor of the PI3K catalytic subunit p110&de… | 10 mg | 11589-10 | More Info |
| IC-87114 | A cell-permeable selective inhibitor of the PI3K catalytic subunit p110&de… | 5 mg | 11589-5 | More Info |
| IC-87114 | A cell-permeable selective inhibitor of the PI3K catalytic subunit p110&de… | 50 mg | 11589-50 | More Info |
| IC87201 | An inhibitor of the nNOS-PSD-95 protein-protein interaction; inhibits the… | 10 mg | 32973-10 | More Info |
| IC87201 | An inhibitor of the nNOS-PSD-95 protein-protein interaction; inhibits the… | 25 mg | 32973-25 | More Info |
| IC87201 | An inhibitor of the nNOS-PSD-95 protein-protein interaction; inhibits the… | 5 mg | 32973-5 | More Info |
| ICA 069673 | A Kv7 channel activator; selective for Kv7.2 / 7.3 over Kv7.3 / 7.5 (EC50s… | 10 mg | 22995-10 | More Info |
| ICA 069673 | A Kv7 channel activator; selective for Kv7.2 / 7.3 over Kv7.3 / 7.5 (EC50s… | 25 mg | 22995-25 | More Info |
| ICA 069673 | A Kv7 channel activator; selective for Kv7.2 / 7.3 over Kv7.3 / 7.5 (EC50s… | 5 mg | 22995-5 | More Info |
| ICA 069673 | A Kv7 channel activator; selective for Kv7.2 / 7.3 over Kv7.3 / 7.5 (EC50s… | 50 mg | 22995-50 | More Info |
| ICA 110381 | An activator of Kv7.2; induces rubidium efflux in an agonist-induced rubid… | 10 mg | 37294-10 | More Info |
| ICA 110381 | An activator of Kv7.2; induces rubidium efflux in an agonist-induced rubid… | 25 mg | 37294-25 | More Info |
| ICA 110381 | An activator of Kv7.2; induces rubidium efflux in an agonist-induced rubid… | 5 mg | 37294-5 | More Info |
| ICA 110381 | An activator of Kv7.2; induces rubidium efflux in an agonist-induced rubid… | 50 mg | 37294-50 | More Info |
| ICA 121431 | A selective Nav1.1 and Nav1.3 channel blocker (IC50s = 10,000 nM for Nav1.… | 1 mg | 24669-1 | More Info |
| ICA 121431 | A selective Nav1.1 and Nav1.3 channel blocker (IC50s = 10,000 nM for Nav1.… | 10 mg | 24669-10 | More Info |
| ICA 121431 | A selective Nav1.1 and Nav1.3 channel blocker (IC50s = 10,000 nM for Nav1.… | 25 mg | 24669-25 | More Info |
| ICA 121431 | A selective Nav1.1 and Nav1.3 channel blocker (IC50s = 10,000 nM for Nav1.… | 5 mg | 24669-5 | More Info |
| ICA 27243 | An activator of Kv7.2 / Kv7.3 subunit-containing channels; enhances rubidi… | 10 mg | 40827-10 | More Info |
| ICA 27243 | An activator of Kv7.2 / Kv7.3 subunit-containing channels; enhances rubidi… | 100 mg | 40827-100 | More Info |
| ICA 27243 | An activator of Kv7.2 / Kv7.3 subunit-containing channels; enhances rubidi… | 5 mg | 40827-5 | More Info |
| ICA 27243 | An activator of Kv7.2 / Kv7.3 subunit-containing channels; enhances rubidi… | 50 mg | 40827-50 | More Info |
| ICAAc | A solvatochromic fluorescent pH probe; ex / em = 466 / 553, 431 / 515, and… | 10 mg | 28564-10 | More Info |
| ICAAc | A solvatochromic fluorescent pH probe; ex / em = 466 / 553, 431 / 515, and… | 25 mg | 28564-25 | More Info |
| ICAAc | A solvatochromic fluorescent pH probe; ex / em = 466 / 553, 431 / 515, and… | 5 mg | 28564-5 | More Info |
| Icariin | A prenylated flavonoid with diverse biological activities; induces differe… | 1 g | 13624-1 | More Info |
CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
1180 East Ellsworth Road
Ann Arbor MI 48108
P: (734) 971-3335
P: (800) 364-9897 (USA & Canada only)
F: (734) 971-3640
Customer Service: custserv@caymanchem.com
Technical Support: techserv@caymanchem.com
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