CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 413 of 865
Non-Antibody Products
Page 413 of 865
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| Isovitexin | A C-glycosylated flavone; scavenges DPPH radicals in a cell-free assay (IC… | 10 mg | 31212-10 | More Info |
| Isovitexin | A C-glycosylated flavone; scavenges DPPH radicals in a cell-free assay (IC… | 25 mg | 31212-25 | More Info |
| Isovitexin | A C-glycosylated flavone; scavenges DPPH radicals in a cell-free assay (IC… | 5 mg | 31212-5 | More Info |
| Isoxanthohumol | A natural prenylated chalcone with diverse biological activities; has anti… | 1 mg | 23233-1 | More Info |
| Isoxanthohumol | A natural prenylated chalcone with diverse biological activities; has anti… | 5 mg | 23233-5 | More Info |
| Isoxanthohumol | A natural prenylated chalcone with diverse biological activities; has anti… | 500 µg | 23233-500 | More Info |
| Isoxanthopterin | A natural intermediate in the pteridine pathway that can be produced natur… | 10 mg | 17564-10 | More Info |
| Isoxanthopterin | A natural intermediate in the pteridine pathway that can be produced natur… | 100 mg | 17564-100 | More Info |
| Isoxanthopterin | A natural intermediate in the pteridine pathway that can be produced natur… | 50 mg | 17564-50 | More Info |
| Isoxsuprine-d6 (hydrochloride) | An internal standard for the quantification of isoxsuprine by GC- or LC-MS | 1 mg | 27847-1 | More Info |
| Isoxsuprine (hydrochloride) | An adrenergic receptor modulator; induces vasodilation of NE-precontracted… | 10 g | 20688-10 | More Info |
| Isoxsuprine (hydrochloride) | An adrenergic receptor modulator; induces vasodilation of NE-precontracted… | 5 g | 20688-5 | More Info |
| ISP-I-28 | An immunosuppressant; increases skin graft survival time in rats at 1, 3,… | 1 mg | 9004082-1 | More Info |
| ISP-I-28 | An immunosuppressant; increases skin graft survival time in rats at 1, 3,… | 10 mg | 9004082-10 | More Info |
| ISP-I-28 | An immunosuppressant; increases skin graft survival time in rats at 1, 3,… | 5 mg | 9004082-5 | More Info |
| Ispinesib | A cell-permeable, allosteric inhibitor of Eg5 (Ki app = 2.3 nM) with >10,0… | 1 mg | 18014-1 | More Info |
| Ispinesib | A cell-permeable, allosteric inhibitor of Eg5 (Ki app = 2.3 nM) with >10,0… | 10 mg | 18014-10 | More Info |
| Ispinesib | A cell-permeable, allosteric inhibitor of Eg5 (Ki app = 2.3 nM) with >10,0… | 5 mg | 18014-5 | More Info |
| Ispinesib | A cell-permeable, allosteric inhibitor of Eg5 (Ki app = 2.3 nM) with >10,0… | 50 mg | 18014-50 | More Info |
| Isradipine | A selective L-type calcium channel blocker with long-acting antihypertensi… | 10 mg | 17536-10 | More Info |
| Isradipine | A selective L-type calcium channel blocker with long-acting antihypertensi… | 25 mg | 17536-25 | More Info |
| Isradipine | A selective L-type calcium channel blocker with long-acting antihypertensi… | 5 mg | 17536-5 | More Info |
| Isradipine | A selective L-type calcium channel blocker with long-acting antihypertensi… | 50 mg | 17536-50 | More Info |
| Istradefylline | An A2A receptor antagonist (Ki = 2.2 nM in a radioligand binding assay); i… | 10 mg | 22958-10 | More Info |
| Istradefylline | An A2A receptor antagonist (Ki = 2.2 nM in a radioligand binding assay); i… | 25 mg | 22958-25 | More Info |
| Istradefylline | An A2A receptor antagonist (Ki = 2.2 nM in a radioligand binding assay); i… | 5 mg | 22958-5 | More Info |
| Istradefylline-13C-d3 | An internal standard for the quantification of istradefylline by GC- or LC… | 1 mg | 31240-1 | More Info |
| ISX-9 | A small molecule inducer of adult neural stem cell differentiation; 2.5-20… | 1 mg | 16165-1 | More Info |
| ISX-9 | A small molecule inducer of adult neural stem cell differentiation; 2.5-20… | 10 mg | 16165-10 | More Info |
| ISX-9 | A small molecule inducer of adult neural stem cell differentiation; 2.5-20… | 25 mg | 16165-25 | More Info |
| ISX-9 | A small molecule inducer of adult neural stem cell differentiation; 2.5-20… | 5 mg | 16165-5 | More Info |
| 5-IT | A positional isomer of α-methyltryptamine; intended for research and… | 1 mg | 12042-1 | More Info |
| 5-IT | A positional isomer of α-methyltryptamine; intended for research and… | 10 mg | 12042-10 | More Info |
| 5-IT | A positional isomer of α-methyltryptamine; intended for research and… | 5 mg | 12042-5 | More Info |
| 6-IT | An analytical reference standard that is structurally categorized as an am… | 1 mg | 13938-1 | More Info |
| 6-IT | An analytical reference standard that is structurally categorized as an am… | 10 mg | 13938-10 | More Info |
| 6-IT | An analytical reference standard that is structurally categorized as an am… | 5 mg | 13938-5 | More Info |
| IT-901 | An inhibitor of the NF-κB subunit c-Rel; inhibits NF-κB DNA bi… | 1 mg | 22298-1 | More Info |
| IT-901 | An inhibitor of the NF-κB subunit c-Rel; inhibits NF-κB DNA bi… | 10 mg | 22298-10 | More Info |
| IT-901 | An inhibitor of the NF-κB subunit c-Rel; inhibits NF-κB DNA bi… | 5 mg | 22298-5 | More Info |
| IT-901 | An inhibitor of the NF-κB subunit c-Rel; inhibits NF-κB DNA bi… | 50 mg | 22298-50 | More Info |
| IT-143A | A bacterial metabolite; active against the bacterium M. luteus (MIC = 6.25… | 1 mg | 30044-1 | More Info |
| IT-143A | A bacterial metabolite; active against the bacterium M. luteus (MIC = 6.25… | 5 mg | 30044-5 | More Info |
| Itacitinib | A JAK1 inhibitor; >20- and >200-fold selective for JAK1 over JAK2 and JAK3… | 1 mg | 27597-1 | More Info |
| Itacitinib | A JAK1 inhibitor; >20- and >200-fold selective for JAK1 over JAK2 and JAK3… | 10 mg | 27597-10 | More Info |
| Itacitinib | A JAK1 inhibitor; >20- and >200-fold selective for JAK1 over JAK2 and JAK3… | 25 mg | 27597-25 | More Info |
| Itacitinib | A JAK1 inhibitor; >20- and >200-fold selective for JAK1 over JAK2 and JAK3… | 5 mg | 27597-5 | More Info |
| IT-143B | A bacterial metabolite; inhibits the proliferation of OS-RC-2 and ACHN can… | 1 mg | 29960-1 | More Info |
| IT-143B | A bacterial metabolite; inhibits the proliferation of OS-RC-2 and ACHN can… | 5 mg | 29960-5 | More Info |
| ITD 1 | An inhibitor of TGF-β (IC50 = 0.85 µM); selective for TGF-&beta… | 10 mg | 23326-10 | More Info |
| ITD 1 | An inhibitor of TGF-β (IC50 = 0.85 µM); selective for TGF-&beta… | 25 mg | 23326-25 | More Info |
| ITD 1 | An inhibitor of TGF-β (IC50 = 0.85 µM); selective for TGF-&beta… | 5 mg | 23326-5 | More Info |
| ITD 1 | An inhibitor of TGF-β (IC50 = 0.85 µM); selective for TGF-&beta… | 50 mg | 23326-50 | More Info |
| ITE | An endogenous AhR agonist; binds to AhR (Kd = 65 nM) and induces AhR-depen… | 10 mg | 25355-10 | More Info |
| ITE | An endogenous AhR agonist; binds to AhR (Kd = 65 nM) and induces AhR-depen… | 25 mg | 25355-25 | More Info |
| ITE | An endogenous AhR agonist; binds to AhR (Kd = 65 nM) and induces AhR-depen… | 5 mg | 25355-5 | More Info |
| ITE | An endogenous AhR agonist; binds to AhR (Kd = 65 nM) and induces AhR-depen… | 50 mg | 25355-50 | More Info |
| ITF 2357 | Inhibits maize HDACs: HD2, HD-1B, and HD-1A (IC50s = 7.5-16 nM) and reduce… | 1 mg | 11045-1 | More Info |
| ITF 2357 | Inhibits maize HDACs: HD2, HD-1B, and HD-1A (IC50s = 7.5-16 nM) and reduce… | 10 mg | 11045-10 | More Info |
| ITF 2357 | Inhibits maize HDACs: HD2, HD-1B, and HD-1A (IC50s = 7.5-16 nM) and reduce… | 5 mg | 11045-5 | More Info |
| ITH15004 | A P2X7 receptor antagonist (IC50 = 9 µM); inhibits ATP-induced curre… | 1 mg | 33667-1 | More Info |
| ITH15004 | A P2X7 receptor antagonist (IC50 = 9 µM); inhibits ATP-induced curre… | 10 mg | 33667-10 | More Info |
| ITH15004 | A P2X7 receptor antagonist (IC50 = 9 µM); inhibits ATP-induced curre… | 25 mg | 33667-25 | More Info |
| ITH15004 | A P2X7 receptor antagonist (IC50 = 9 µM); inhibits ATP-induced curre… | 5 mg | 33667-5 | More Info |
| ITI214 | A PDE1 inhibitor (Ki = 0.058 nM); selective for PDE1 over PDE2A, -3B, -4A,… | 1 mg | 30376-1 | More Info |
| ITI214 | A PDE1 inhibitor (Ki = 0.058 nM); selective for PDE1 over PDE2A, -3B, -4A,… | 10 mg | 30376-10 | More Info |
| ITI214 | A PDE1 inhibitor (Ki = 0.058 nM); selective for PDE1 over PDE2A, -3B, -4A,… | 5 mg | 30376-5 | More Info |
| Itopride (hydrochloride) | An AChE inhibitor (IC50 = 1.6 µM for rat stomach enzyme) and a proki… | 1 mg | 31183-1 | More Info |
| Itopride (hydrochloride) | An AChE inhibitor (IC50 = 1.6 µM for rat stomach enzyme) and a proki… | 10 mg | 31183-10 | More Info |
| Itopride (hydrochloride) | An AChE inhibitor (IC50 = 1.6 µM for rat stomach enzyme) and a proki… | 25 mg | 31183-25 | More Info |
| Itopride (hydrochloride) | An AChE inhibitor (IC50 = 1.6 µM for rat stomach enzyme) and a proki… | 5 mg | 31183-5 | More Info |
| Itraconazole | An antifungal agent and hedgehog pathway inhibitor; inhibits hedgehog sign… | 100 mg | 13288-100 | More Info |
| Itraconazole | An antifungal agent and hedgehog pathway inhibitor; inhibits hedgehog sign… | 25 mg | 13288-25 | More Info |
| Itraconazole | An antifungal agent and hedgehog pathway inhibitor; inhibits hedgehog sign… | 250 mg | 13288-250 | More Info |
| Itraconazole | An antifungal agent and hedgehog pathway inhibitor; inhibits hedgehog sign… | 50 mg | 13288-50 | 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
Sales: sales@caymanchem.com
http://www.caymanchem.com
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