CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 326 of 649
Non-Antibody Products
Page 326 of 649
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| KL001 | A cryptochrome protein stabilizer; inhibits ubiquitin-induced degradation… | 10 mg | 13878-10 | More Info |
| KL001 | A cryptochrome protein stabilizer; inhibits ubiquitin-induced degradation… | 25 mg | 13878-25 | More Info |
| KL001 | A cryptochrome protein stabilizer; inhibits ubiquitin-induced degradation… | 5 mg | 13878-5 | More Info |
| KLH45 | An inhibitor of DDHD2 (IC50 = 1.3 nM); selective for DDHD2 over greater th… | 1 mg | 19889-1 | More Info |
| KLH45 | An inhibitor of DDHD2 (IC50 = 1.3 nM); selective for DDHD2 over greater th… | 10 mg | 19889-10 | More Info |
| KLH45 | An inhibitor of DDHD2 (IC50 = 1.3 nM); selective for DDHD2 over greater th… | 25 mg | 19889-25 | More Info |
| KLH45 | An inhibitor of DDHD2 (IC50 = 1.3 nM); selective for DDHD2 over greater th… | 5 mg | 19889-5 | More Info |
| Klotho-derived Peptide 1 (56-87) (human) (trifluoroacetate salt) | A TGF-β disrupting peptide; binds to ALK5 and TGFBR2 (Kds = 1.41 and… | 1 mg | 38166-1 | More Info |
| Klotho-derived Peptide 1 (56-87) (human) (trifluoroacetate salt) | A TGF-β disrupting peptide; binds to ALK5 and TGFBR2 (Kds = 1.41 and… | 10 mg | 38166-10 | More Info |
| Klotho-derived Peptide 1 (56-87) (human) (trifluoroacetate salt) | A TGF-β disrupting peptide; binds to ALK5 and TGFBR2 (Kds = 1.41 and… | 5 mg | 38166-5 | More Info |
| Klotho-derived Peptide 1 (56-87) (human) (trifluoroacetate salt) | A TGF-β disrupting peptide; binds to ALK5 and TGFBR2 (Kds = 1.41 and… | 500 µg | 38166-500 | More Info |
| KM 11060 | A F508del-CFTR corrector; increases cell surface expression and restores c… | 10 mg | 23481-10 | More Info |
| KM 11060 | A F508del-CFTR corrector; increases cell surface expression and restores c… | 25 mg | 23481-25 | More Info |
| KM 11060 | A F508del-CFTR corrector; increases cell surface expression and restores c… | 5 mg | 23481-5 | More Info |
| KM 11060 | A F508del-CFTR corrector; increases cell surface expression and restores c… | 50 mg | 23481-50 | More Info |
| KM 233 | Δ8-THC analog with 13-fold selectivity for the CB2 receptor (Kis = 1… | 1 mg | 10640-1 | More Info |
| KM 233 | Δ8-THC analog with 13-fold selectivity for the CB2 receptor (Kis = 1… | 10 mg | 10640-10 | More Info |
| KM 233 | Δ8-THC analog with 13-fold selectivity for the CB2 receptor (Kis = 1… | 25 mg | 10640-25 | More Info |
| KM 233 | Δ8-THC analog with 13-fold selectivity for the CB2 receptor (Kis = 1… | 5 mg | 10640-5 | More Info |
| KML29 | An O-hexafluoroisopropyl carbamate analog of JZL 184 that potently and sel… | 10 mg | 11777-10 | More Info |
| KML29 | An O-hexafluoroisopropyl carbamate analog of JZL 184 that potently and sel… | 100 mg | 11777-100 | More Info |
| KML29 | An O-hexafluoroisopropyl carbamate analog of JZL 184 that potently and sel… | 5 mg | 11777-5 | More Info |
| KML29 | An O-hexafluoroisopropyl carbamate analog of JZL 184 that potently and sel… | 50 mg | 11777-50 | More Info |
| KMN-80 | A selective, potent agonist of EP4 with an IC50 value of 3 nM (versus 1.4… | 1 mg | 15435-1 | More Info |
| KMN-80 | A selective, potent agonist of EP4 with an IC50 value of 3 nM (versus 1.4… | 500 µg | 15435-500 | More Info |
| KN-62 | A selective, cell permeable inhibitor of CaMKII (IC50 = 900 nM) | 1 mg | 13318-1 | More Info |
| KN-62 | A selective, cell permeable inhibitor of CaMKII (IC50 = 900 nM) | 10 mg | 13318-10 | More Info |
| KN-62 | A selective, cell permeable inhibitor of CaMKII (IC50 = 900 nM) | 25 mg | 13318-25 | More Info |
| KN-62 | A selective, cell permeable inhibitor of CaMKII (IC50 = 900 nM) | 5 mg | 13318-5 | More Info |
| KN-93 | A selective inhibitor of CaMKII, competitively blocking CaM binding to the… | 1 mg | 13319-1 | More Info |
| KN-93 | A selective inhibitor of CaMKII, competitively blocking CaM binding to the… | 10 mg | 13319-10 | More Info |
| KN-93 | A selective inhibitor of CaMKII, competitively blocking CaM binding to the… | 5 mg | 13319-5 | More Info |
| KN-92 (hydrochloride) | An inactive derivative of KN-93, the selective inhibitor of CaMKII; ineffe… | 1 mg | 9000890-1 | More Info |
| KN-92 (hydrochloride) | An inactive derivative of KN-93, the selective inhibitor of CaMKII; ineffe… | 10 mg | 9000890-10 | More Info |
| KN-92 (hydrochloride) | An inactive derivative of KN-93, the selective inhibitor of CaMKII; ineffe… | 5 mg | 9000890-5 | More Info |
| KN-93 (hydrochloride) | A selective inhibitor of CaMKII, competitively blocking CaM binding to the… | 1 mg | 13864-1 | More Info |
| KN-93 (hydrochloride) | A selective inhibitor of CaMKII, competitively blocking CaM binding to the… | 10 mg | 13864-10 | More Info |
| KN-93 (hydrochloride) | A selective inhibitor of CaMKII, competitively blocking CaM binding to the… | 5 mg | 13864-5 | More Info |
| KN-93 (phosphate) | A CaMKII inhibitor (Ki = 370 nM) that inhibits the α- and β-sub… | 1 mg | 21472-1 | More Info |
| KN-93 (phosphate) | A CaMKII inhibitor (Ki = 370 nM) that inhibits the α- and β-sub… | 10 mg | 21472-10 | More Info |
| KN-93 (phosphate) | A CaMKII inhibitor (Ki = 370 nM) that inhibits the α- and β-sub… | 25 mg | 21472-25 | More Info |
| KN-93 (phosphate) | A CaMKII inhibitor (Ki = 370 nM) that inhibits the α- and β-sub… | 5 mg | 21472-5 | More Info |
| Ko 143 | A potent and selective inhibitor of BCRP, preventing the export of mitoxan… | 10 mg | 15215-10 | More Info |
| Ko 143 | A potent and selective inhibitor of BCRP, preventing the export of mitoxan… | 25 mg | 15215-25 | More Info |
| Ko 143 | A potent and selective inhibitor of BCRP, preventing the export of mitoxan… | 5 mg | 15215-5 | More Info |
| Ko 143 | A potent and selective inhibitor of BCRP, preventing the export of mitoxan… | 50 mg | 15215-50 | More Info |
| KO947 | An ERK inhibitor (IC50 = 50-fold selective for ERK over a panel of 450 kin… | 1 mg | 29213-1 | More Info |
| KO947 | An ERK inhibitor (IC50 = 50-fold selective for ERK over a panel of 450 kin… | 10 mg | 29213-10 | More Info |
| KO947 | An ERK inhibitor (IC50 = 50-fold selective for ERK over a panel of 450 kin… | 25 mg | 29213-25 | More Info |
| KO947 | An ERK inhibitor (IC50 = 50-fold selective for ERK over a panel of 450 kin… | 5 mg | 29213-5 | More Info |
| Kobe 0065 | An orally active Ras inhibitor with selectivity for H-Ras (Ki = 46 µ… | 1 mg | 16261-1 | More Info |
| Kobe 0065 | An orally active Ras inhibitor with selectivity for H-Ras (Ki = 46 µ… | 10 mg | 16261-10 | More Info |
| Kobe 0065 | An orally active Ras inhibitor with selectivity for H-Ras (Ki = 46 µ… | 25 mg | 16261-25 | More Info |
| Kobe 0065 | An orally active Ras inhibitor with selectivity for H-Ras (Ki = 46 µ… | 5 mg | 16261-5 | More Info |
| Kobe 2602 | A selective Ras inhibitor that blocks H-Ras GTP binding to c-Raf-1 (Ki = 1… | 10 mg | 16262-10 | More Info |
| Kobe 2602 | A selective Ras inhibitor that blocks H-Ras GTP binding to c-Raf-1 (Ki = 1… | 100 mg | 16262-100 | More Info |
| Kobe 2602 | A selective Ras inhibitor that blocks H-Ras GTP binding to c-Raf-1 (Ki = 1… | 50 mg | 16262-50 | More Info |
| Kobe 2602 | A selective Ras inhibitor that blocks H-Ras GTP binding to c-Raf-1 (Ki = 1… | 500 mg | 16262-500 | More Info |
| Kocurin | A peptide antibiotic; active against MRSA (MIC = 0.25 µg / ml), as w… | 1 mg | 29125-1 | More Info |
| KOdiA-PC | Oxidized LDL (oxLDL) particles contain low molecular weight species which… | 1 mg | 62945-1 | More Info |
| KOdiA-PC | Oxidized LDL (oxLDL) particles contain low molecular weight species which… | 10 mg | 62945-10 | More Info |
| KOdiA-PC | Oxidized LDL (oxLDL) particles contain low molecular weight species which… | 5 mg | 62945-5 | More Info |
| KOdiA-PC | Oxidized LDL (oxLDL) particles contain low molecular weight species which… | 500 µg | 62945-500 | More Info |
| Kojic Acid | A tyrosinase inhibitor (IC50 = 30.6 µM); decreases growth of Leishma… | 10 g | 22712-10 | More Info |
| Kojic Acid | A tyrosinase inhibitor (IC50 = 30.6 µM); decreases growth of Leishma… | 100 g | 22712-100 | More Info |
| Kojic Acid | A tyrosinase inhibitor (IC50 = 30.6 µM); decreases growth of Leishma… | 5 g | 22712-5 | More Info |
| Kojic Acid | A tyrosinase inhibitor (IC50 = 30.6 µM); decreases growth of Leishma… | 50 g | 22712-50 | More Info |
| Kotanin A | A fungal metabolite; produced by A. glaucus (A. clavatus), A. alliaceus, a… | 2.5 mg | 24917-25 | More Info |
| Kotanin A | A fungal metabolite; produced by A. glaucus (A. clavatus), A. alliaceus, a… | 500 µg | 24917-500 | More Info |
| Koumine | An alkaloid with diverse biological activities; inhibits the proliferation… | 1 mg | 36210-1 | More Info |
| Koumine | An alkaloid with diverse biological activities; inhibits the proliferation… | 10 mg | 36210-10 | More Info |
| Koumine | An alkaloid with diverse biological activities; inhibits the proliferation… | 25 mg | 36210-25 | More Info |
| Koumine | An alkaloid with diverse biological activities; inhibits the proliferation… | 5 mg | 36210-5 | More Info |
| KP372-1 | A specific Akt inhibitor; inhibits Akt, PDK1, and FLT3 in acute myelogenou… | 1 mg | 17808-1 | More Info |
| KP372-1 | A specific Akt inhibitor; inhibits Akt, PDK1, and FLT3 in acute myelogenou… | 10 mg | 17808-10 | More Info |
| KP372-1 | A specific Akt inhibitor; inhibits Akt, PDK1, and FLT3 in acute myelogenou… | 5 mg | 17808-5 | More Info |
| K6PC-5 | An SPHK1 activator; activates SPHK1 in F9-12 cell lysates and isolated mur… | 10 mg | 34070-10 | More Info |
| K6PC-5 | An SPHK1 activator; activates SPHK1 in F9-12 cell lysates and isolated mur… | 25 mg | 34070-25 | More Info |
| K6PC-5 | An SPHK1 activator; activates SPHK1 in F9-12 cell lysates and isolated mur… | 5 mg | 34070-5 | More Info |
| KPT-185 | An inhibitor of XPO1 / CRM1; reduces proliferation in a panel of patient-d… | 10 mg | 26074-10 | More Info |
| KPT-185 | An inhibitor of XPO1 / CRM1; reduces proliferation in a panel of patient-d… | 25 mg | 26074-25 | More Info |
| KPT-185 | An inhibitor of XPO1 / CRM1; reduces proliferation in a panel of patient-d… | 5 mg | 26074-5 | More Info |
| KPT-276 | An inhibitor of XPO1 / CRM1; increases survival and reduces spleen weight… | 10 mg | 29158-10 | More Info |
| KPT-276 | An inhibitor of XPO1 / CRM1; increases survival and reduces spleen weight… | 25 mg | 29158-25 | More Info |
| KPT-276 | An inhibitor of XPO1 / CRM1; increases survival and reduces spleen weight… | 5 mg | 29158-5 | More Info |
| KPT-276 | An inhibitor of XPO1 / CRM1; increases survival and reduces spleen weight… | 50 mg | 29158-50 | More Info |
| KPT-6566 | A covalent PIN1 inhibitor ( IC50 = 0.64 µM); inhibits cell prolifera… | 10 mg | 37308-10 | More Info |
| KPT-6566 | A covalent PIN1 inhibitor ( IC50 = 0.64 µM); inhibits cell prolifera… | 25 mg | 37308-25 | More Info |
| KPT-6566 | A covalent PIN1 inhibitor ( IC50 = 0.64 µM); inhibits cell prolifera… | 5 mg | 37308-5 | More Info |
| KPT-6566 | A covalent PIN1 inhibitor ( IC50 = 0.64 µM); inhibits cell prolifera… | 50 mg | 37308-50 | More Info |
| KR-32568 | An NHE-1 inhibitor (IC50 = 230 nM); restores cardiac contractile function… | 1 mg | 23968-1 | More Info |
| KR-32568 | An NHE-1 inhibitor (IC50 = 230 nM); restores cardiac contractile function… | 5 mg | 23968-5 | More Info |
| KR-33493 | An inhibitor of FAF1; inhibits chemical hypoxia-induced apoptosis in H9c2… | 1 mg | 22071-1 | More Info |
| KR-33493 | An inhibitor of FAF1; inhibits chemical hypoxia-induced apoptosis in H9c2… | 10 mg | 22071-10 | More Info |
| KR-33493 | An inhibitor of FAF1; inhibits chemical hypoxia-induced apoptosis in H9c2… | 25 mg | 22071-25 | More Info |
| KR-33493 | An inhibitor of FAF1; inhibits chemical hypoxia-induced apoptosis in H9c2… | 5 mg | 22071-5 | More Info |
| K-Ras(G12C) Inhibitor 12 | An allosteric inhibitor of oncogenic K-Ras(G12C); decreases viability and… | 1 mg | 20118-1 | More Info |
| K-Ras(G12C) Inhibitor 12 | An allosteric inhibitor of oncogenic K-Ras(G12C); decreases viability and… | 10 mg | 20118-10 | More Info |
| K-Ras(G12C) Inhibitor 12 | An allosteric inhibitor of oncogenic K-Ras(G12C); decreases viability and… | 25 mg | 20118-25 | More Info |
| K-Ras(G12C) Inhibitor 12 | An allosteric inhibitor of oncogenic K-Ras(G12C); decreases viability and… | 5 mg | 20118-5 | 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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http://www.caymanchem.com
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