CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 322 of 649
Non-Antibody Products
Page 322 of 649
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| Kasugamycin (hydrochloride) | An aminoglycoside with diverse biological activities; active against S. dy… | 100 mg | 15322-100 | More Info |
| Katacalcin (trifluoroacetate salt) | An endogenous peptide; expressed in, and secreted from, thyroid parafollic… | 1 mg | 39285-1 | More Info |
| Katacalcin (trifluoroacetate salt) | An endogenous peptide; expressed in, and secreted from, thyroid parafollic… | 10 mg | 39285-10 | More Info |
| Katacalcin (trifluoroacetate salt) | An endogenous peptide; expressed in, and secreted from, thyroid parafollic… | 25 mg | 39285-25 | More Info |
| Katacalcin (trifluoroacetate salt) | An endogenous peptide; expressed in, and secreted from, thyroid parafollic… | 5 mg | 39285-5 | More Info |
| KAT8 Inhibitor 19 | A KAT8 inhibitor; selective for KAT8 over KAT2A, KAT2B, KAT3B, KAT6A, and… | 1 mg | 38977-1 | More Info |
| KAT8 Inhibitor 19 | A KAT8 inhibitor; selective for KAT8 over KAT2A, KAT2B, KAT3B, KAT6A, and… | 10 mg | 38977-10 | More Info |
| KAT8 Inhibitor 19 | A KAT8 inhibitor; selective for KAT8 over KAT2A, KAT2B, KAT3B, KAT6A, and… | 25 mg | 38977-25 | More Info |
| KAT8 Inhibitor 19 | A KAT8 inhibitor; selective for KAT8 over KAT2A, KAT2B, KAT3B, KAT6A, and… | 5 mg | 38977-5 | More Info |
| Kaurenoic Acid | A diterpene with diverse biological activities; cytotoxic to a variety of… | 1 mg | 28957-1 | More Info |
| Kaurenoic Acid | A diterpene with diverse biological activities; cytotoxic to a variety of… | 10 mg | 28957-10 | More Info |
| Kaurenoic Acid | A diterpene with diverse biological activities; cytotoxic to a variety of… | 25 mg | 28957-25 | More Info |
| Kaurenoic Acid | A diterpene with diverse biological activities; cytotoxic to a variety of… | 5 mg | 28957-5 | More Info |
| Kavain | An analytical reference standard categorized as a kavalactone; has analges… | 1 mg | 33881-1 | More Info |
| Kavain | An analytical reference standard categorized as a kavalactone; has analges… | 5 mg | 33881-5 | More Info |
| Kavain | A kavalactone with diverse biological activities; a positive allosteric mo… | 10 mg | 26524-10 | More Info |
| Kavain | A kavalactone with diverse biological activities; a positive allosteric mo… | 100 mg | 26524-100 | More Info |
| Kavain | A kavalactone with diverse biological activities; a positive allosteric mo… | 50 mg | 26524-50 | More Info |
| Kazusamycin A | An antitumor antibiotic that inhibits nuclear export and translocation of… | 100 µg | 20137-100 | More Info |
| Kazusamycin A | An antitumor antibiotic that inhibits nuclear export and translocation of… | 500 µg | 20137-500 | More Info |
| Kazusamycin B | A bacterial metabolite; has antifungal activity against S. pombe and R. ja… | 100 µg | 28119-100 | More Info |
| Kazusamycin B | A bacterial metabolite; has antifungal activity against S. pombe and R. ja… | 500 µg | 28119-500 | More Info |
| K252b | A cell-impermeable kinase inhibitor, first described as an inhibitor of PK… | 1 mg | 11339-1 | More Info |
| K252b | A cell-impermeable kinase inhibitor, first described as an inhibitor of PK… | 500 µg | 11339-500 | More Info |
| KB-130015 | An antiarrhythmic agent; inhibits acetylcholine or adenosine-induced potas… | 1 mg | 33461-1 | More Info |
| KB-130015 | An antiarrhythmic agent; inhibits acetylcholine or adenosine-induced potas… | 10 mg | 33461-10 | More Info |
| KB-130015 | An antiarrhythmic agent; inhibits acetylcholine or adenosine-induced potas… | 25 mg | 33461-25 | More Info |
| KB-130015 | An antiarrhythmic agent; inhibits acetylcholine or adenosine-induced potas… | 5 mg | 33461-5 | More Info |
| KB2115 | A synthetic thyroid hormone mimetic that lowers total and LDL cholesterol… | 100 mg | 10011054-100 | More Info |
| KB2115 | A synthetic thyroid hormone mimetic that lowers total and LDL cholesterol… | 25 mg | 10011054-25 | More Info |
| KB2115 | A synthetic thyroid hormone mimetic that lowers total and LDL cholesterol… | 5 mg | 10011054-5 | More Info |
| KB2115 | A synthetic thyroid hormone mimetic that lowers total and LDL cholesterol… | 50 mg | 10011054-50 | More Info |
| KB-0742 (hydrochloride) | A Cdk9 inhibitor (IC50 = 6 nM); selective for Cdk9 over Cdk1-8 (IC50s = 39… | 10 mg | 39772-10 | More Info |
| KB-0742 (hydrochloride) | A Cdk9 inhibitor (IC50 = 6 nM); selective for Cdk9 over Cdk1-8 (IC50s = 39… | 25 mg | 39772-25 | More Info |
| KB-0742 (hydrochloride) | A Cdk9 inhibitor (IC50 = 6 nM); selective for Cdk9 over Cdk1-8 (IC50s = 39… | 5 mg | 39772-5 | More Info |
| KB-0742 (hydrochloride) | A Cdk9 inhibitor (IC50 = 6 nM); selective for Cdk9 over Cdk1-8 (IC50s = 39… | 50 mg | 39772-50 | More Info |
| K-Biotin-W-Histone H2B (108-125) (trifluoroacetate salt) | A biotinylated peptide fragment of histone H2B | 1 mg | 28214-1 | More Info |
| kb NB 142-70 | A selective PKD inhibitor (IC50s = 28.3, 58.7, and 53.2 nM for PKD1, 2, an… | 10 mg | 18002-10 | More Info |
| kb NB 142-70 | A selective PKD inhibitor (IC50s = 28.3, 58.7, and 53.2 nM for PKD1, 2, an… | 25 mg | 18002-25 | More Info |
| kb NB 142-70 | A selective PKD inhibitor (IC50s = 28.3, 58.7, and 53.2 nM for PKD1, 2, an… | 5 mg | 18002-5 | More Info |
| kb NB 142-70 | A selective PKD inhibitor (IC50s = 28.3, 58.7, and 53.2 nM for PKD1, 2, an… | 50 mg | 18002-50 | More Info |
| kb-NB77-78 | An inactive analog of the PKD inhibitor CID755673; does not bind PKD1 in a… | 1 mg | 21562-1 | More Info |
| kb-NB77-78 | An inactive analog of the PKD inhibitor CID755673; does not bind PKD1 in a… | 10 mg | 21562-10 | More Info |
| kb-NB77-78 | An inactive analog of the PKD inhibitor CID755673; does not bind PKD1 in a… | 25 mg | 21562-25 | More Info |
| kb-NB77-78 | An inactive analog of the PKD inhibitor CID755673; does not bind PKD1 in a… | 5 mg | 21562-5 | More Info |
| KB-R7943 (mesylate) | A selective inhibitor of the reverse mode of NCX1 (IC50 = 1.2-2.4 µM… | 10 mg | 16352-10 | More Info |
| KB-R7943 (mesylate) | A selective inhibitor of the reverse mode of NCX1 (IC50 = 1.2-2.4 µM… | 5 mg | 16352-5 | More Info |
| KB-R7943 (mesylate) | A selective inhibitor of the reverse mode of NCX1 (IC50 = 1.2-2.4 µM… | 50 mg | 16352-50 | More Info |
| K252c | A cell-permeable PKC inhibitor (IC50s = 2.45 and 25.7 µM for PKC and… | 1 mg | 13514-1 | More Info |
| K252c | A cell-permeable PKC inhibitor (IC50s = 2.45 and 25.7 µM for PKC and… | 10 mg | 13514-10 | More Info |
| K252c | A cell-permeable PKC inhibitor (IC50s = 2.45 and 25.7 µM for PKC and… | 5 mg | 13514-5 | More Info |
| KC01 | A covalent inhibitor of ABHD16A (IC50s = 90 and 520 nM for human and mouse… | 1 mg | 17364-1 | More Info |
| KC01 | A covalent inhibitor of ABHD16A (IC50s = 90 and 520 nM for human and mouse… | 500 µg | 17364-500 | More Info |
| KC02 | An inactive control probe (IC50 > 10 µM) for KC01 (Item No. 17364),… | 1 mg | 17365-1 | More Info |
| KC02 | An inactive control probe (IC50 > 10 µM) for KC01 (Item No. 17364),… | 100 µg | 17365-100 | More Info |
| KC02 | An inactive control probe (IC50 > 10 µM) for KC01 (Item No. 17364),… | 500 µg | 17365-500 | More Info |
| KC7F2 | An inhibitor of HIF-1α protein translation; suppresses phosphorylati… | 10 mg | 14123-10 | More Info |
| KC7F2 | An inhibitor of HIF-1α protein translation; suppresses phosphorylati… | 5 mg | 14123-5 | More Info |
| KC7F2 | An inhibitor of HIF-1α protein translation; suppresses phosphorylati… | 50 mg | 14123-50 | More Info |
| K252d | An indolocarbazole alkaloid found in Nocardiopsis; a PKC inhibitor; inhibi… | 1 mg | 28469-1 | More Info |
| KD 025 | A ROCK2 inhibitor (IC50 = 0.105 µM); selective for ROCK2 over ROCK1… | 10 mg | 17055-10 | More Info |
| KD 025 | A ROCK2 inhibitor (IC50 = 0.105 µM); selective for ROCK2 over ROCK1… | 100 mg | 17055-100 | More Info |
| KD 025 | A ROCK2 inhibitor (IC50 = 0.105 µM); selective for ROCK2 over ROCK1… | 25 mg | 17055-25 | More Info |
| KD 025 | A ROCK2 inhibitor (IC50 = 0.105 µM); selective for ROCK2 over ROCK1… | 50 mg | 17055-50 | More Info |
| KD 5170 | A mercaptoketone-based inhibitor of class I and II HDACs (IC50s = 20, 2,06… | 1 mg | 13214-1 | More Info |
| KD 5170 | A mercaptoketone-based inhibitor of class I and II HDACs (IC50s = 20, 2,06… | 10 mg | 13214-10 | More Info |
| KD 5170 | A mercaptoketone-based inhibitor of class I and II HDACs (IC50s = 20, 2,06… | 25 mg | 13214-25 | More Info |
| KD 5170 | A mercaptoketone-based inhibitor of class I and II HDACs (IC50s = 20, 2,06… | 5 mg | 13214-5 | More Info |
| KDdiA-PC | Oxidized LDL (oxLDL) particles contain low molecular weight species which… | 1 mg | 62935-1 | More Info |
| KDdiA-PC | Oxidized LDL (oxLDL) particles contain low molecular weight species which… | 10 mg | 62935-10 | More Info |
| KDdiA-PC | Oxidized LDL (oxLDL) particles contain low molecular weight species which… | 5 mg | 62935-5 | More Info |
| KDdiA-PC | Oxidized LDL (oxLDL) particles contain low molecular weight species which… | 500 µg | 62935-500 | More Info |
| KDM5-C70 | An inhibitor of JARID1B (IC50 = 49 nM); selective for JARID1B over KDM4C (… | 10 mg | 36817-10 | More Info |
| KDM5-C70 | An inhibitor of JARID1B (IC50 = 49 nM); selective for JARID1B over KDM4C (… | 25 mg | 36817-25 | More Info |
| KDM5-C70 | An inhibitor of JARID1B (IC50 = 49 nM); selective for JARID1B over KDM4C (… | 5 mg | 36817-5 | More Info |
| KDM5-C70 | An inhibitor of JARID1B (IC50 = 49 nM); selective for JARID1B over KDM4C (… | 50 mg | 36817-50 | More Info |
| KDM4D-IN-1 | An inhibitor of JMJD2D (IC50 = 0.41 µM); selective for JMJD2D over J… | 1 mg | 37431-1 | More Info |
| KDM4D-IN-1 | An inhibitor of JMJD2D (IC50 = 0.41 µM); selective for JMJD2D over J… | 10 mg | 37431-10 | More Info |
| KDM4D-IN-1 | An inhibitor of JMJD2D (IC50 = 0.41 µM); selective for JMJD2D over J… | 25 mg | 37431-25 | More Info |
| KDM4D-IN-1 | An inhibitor of JMJD2D (IC50 = 0.41 µM); selective for JMJD2D over J… | 5 mg | 37431-5 | More Info |
| Kdo2-Lipid A (sodium salt) | The active component of LPS; selectively induces Il-6 expression in wild-t… | 1 mg | 10860-1 | More Info |
| KDU691 | An antimalarial compound; inhibits the activity of recombinant P. vivax PI… | 1 mg | 29019-1 | More Info |
| KDU691 | An antimalarial compound; inhibits the activity of recombinant P. vivax PI… | 10 mg | 29019-10 | More Info |
| KDU691 | An antimalarial compound; inhibits the activity of recombinant P. vivax PI… | 25 mg | 29019-25 | More Info |
| KDU691 | An antimalarial compound; inhibits the activity of recombinant P. vivax PI… | 5 mg | 29019-5 | More Info |
| Keap1 (human, recombinant) | Source: Recombinant human N-terminal His-GST-tagged Keap1 expressed in ins… | 100 µg | 32035-100 | More Info |
| KEMPFPKYPVEP Peptide (bovine, ovine) (trifluoroacetate salt) | A peptide fragment of β-casein; can be produced by the protease M fro… | 10 mg | 38850-10 | More Info |
| KEMPFPKYPVEP Peptide (bovine, ovine) (trifluoroacetate salt) | A peptide fragment of β-casein; can be produced by the protease M fro… | 100 mg | 38850-100 | More Info |
| KEMPFPKYPVEP Peptide (bovine, ovine) (trifluoroacetate salt) | A peptide fragment of β-casein; can be produced by the protease M fro… | 250 mg | 38850-250 | More Info |
| KEMPFPKYPVEP Peptide (bovine, ovine) (trifluoroacetate salt) | A peptide fragment of β-casein; can be produced by the protease M fro… | 50 mg | 38850-50 | More Info |
| Kemptide | A synthetic heptapeptide that acts as a specific substrate for PKA | 1 mg | 15555-1 | More Info |
| Kemptide | A synthetic heptapeptide that acts as a specific substrate for PKA | 10 mg | 15555-10 | More Info |
| Kemptide | A synthetic heptapeptide that acts as a specific substrate for PKA | 25 mg | 15555-25 | More Info |
| Kemptide | A synthetic heptapeptide that acts as a specific substrate for PKA | 5 mg | 15555-5 | More Info |
| Kendomycin | A macrolide from Streptomyces which displays potent cytotoxicity against s… | 100 µg | 11037-100 | More Info |
| Kendomycin | A macrolide from Streptomyces which displays potent cytotoxicity against s… | 500 µg | 11037-500 | More Info |
| Kenpaullone | An ATP-competitive inhibitor of several CDKs as well as GSK3β | 1 mg | 10010239-1 | More Info |
| Kenpaullone | An ATP-competitive inhibitor of several CDKs as well as GSK3β | 10 mg | 10010239-10 | More Info |
| Kenpaullone | An ATP-competitive inhibitor of several CDKs as well as GSK3β | 25 mg | 10010239-25 | More Info |
| Kenpaullone | An ATP-competitive inhibitor of several CDKs as well as GSK3β | 5 mg | 10010239-5 | 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
Sales: sales@caymanchem.com
http://www.caymanchem.com
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