CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 323 of 644
Non-Antibody Products
Page 323 of 644
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| Kifunensine | A potent and selective inhibitor of class I α-mannosidases and serve… | 10 mg | 10009437-10 | More Info |
| Kifunensine | A potent and selective inhibitor of class I α-mannosidases and serve… | 5 mg | 10009437-5 | More Info |
| Kifunensine | A potent and selective inhibitor of class I α-mannosidases and serve… | 50 mg | 10009437-50 | More Info |
| Kigamicin C | An antitumor antibiotic; active against various strains of S. aureus, incl… | 2.5 mg | 19445-25 | More Info |
| Kigamicin C | An antitumor antibiotic; active against various strains of S. aureus, incl… | 500 µg | 19445-500 | More Info |
| Kijanimicin | An antibiotic active against a broad spectrum of microorganisms in vitro i… | 2.5 mg | 20586-25 | More Info |
| Kijanimicin | An antibiotic active against a broad spectrum of microorganisms in vitro i… | 500 µg | 20586-500 | More Info |
| KIN101 | An antiviral agent; inhibits HCV2a replication in Huh7 cells (EC50 = 0.2 &… | 10 mg | 37429-10 | More Info |
| KIN101 | An antiviral agent; inhibits HCV2a replication in Huh7 cells (EC50 = 0.2 &… | 100 mg | 37429-100 | More Info |
| KIN101 | An antiviral agent; inhibits HCV2a replication in Huh7 cells (EC50 = 0.2 &… | 5 mg | 37429-5 | More Info |
| KIN101 | An antiviral agent; inhibits HCV2a replication in Huh7 cells (EC50 = 0.2 &… | 50 mg | 37429-50 | More Info |
| KIN1148 | An IRF3 activator and adjuvant; increases the mRNA expression of the genes… | 1 mg | 38980-1 | More Info |
| KIN1148 | An IRF3 activator and adjuvant; increases the mRNA expression of the genes… | 10 mg | 38980-10 | More Info |
| KIN1148 | An IRF3 activator and adjuvant; increases the mRNA expression of the genes… | 25 mg | 38980-25 | More Info |
| KIN1148 | An IRF3 activator and adjuvant; increases the mRNA expression of the genes… | 5 mg | 38980-5 | More Info |
| KIN1400 | An activator of the RLR pathway; induces expression of the innate immune g… | 1 mg | 22441-1 | More Info |
| KIN1400 | An activator of the RLR pathway; induces expression of the innate immune g… | 10 mg | 22441-10 | More Info |
| KIN1400 | An activator of the RLR pathway; induces expression of the innate immune g… | 5 mg | 22441-5 | More Info |
| KIN1408 | An activator of the RLR pathway; induces IRF3 activation and translocation… | 10 mg | 21790-10 | More Info |
| KIN1408 | An activator of the RLR pathway; induces IRF3 activation and translocation… | 5 mg | 21790-5 | More Info |
| KIN59 | An allosteric inhibitor of TPase (IC50s = 44 and 67 µM for purified… | 10 mg | 19833-10 | More Info |
| KIN59 | An allosteric inhibitor of TPase (IC50s = 44 and 67 µM for purified… | 100 mg | 19833-100 | More Info |
| KIN59 | An allosteric inhibitor of TPase (IC50s = 44 and 67 µM for purified… | 50 mg | 19833-50 | More Info |
| Kinase Screening Library (96-Well) | For screening of a variety of kinase inhibitors; contains ~160 selective a… | 50 µL | 10505-50µL | More Info |
| Kinetensin (human) (trifluoroacetate salt) | A peptide; binds to neurotensin receptors in HT-29 cells and mouse brain (… | 1 mg | 33138-1 | More Info |
| Kinetensin (human) (trifluoroacetate salt) | A peptide; binds to neurotensin receptors in HT-29 cells and mouse brain (… | 10 mg | 33138-10 | More Info |
| Kinetensin (human) (trifluoroacetate salt) | A peptide; binds to neurotensin receptors in HT-29 cells and mouse brain (… | 25 mg | 33138-25 | More Info |
| Kinetensin (human) (trifluoroacetate salt) | A peptide; binds to neurotensin receptors in HT-29 cells and mouse brain (… | 5 mg | 33138-5 | More Info |
| Kinetin | A cytokinin and plant growth regulator; increases the percentage of tetrap… | 100 mg | 20712-100 | More Info |
| Kinetin Riboside | An anticancer nucleoside; induces ROS production, cellular ATP depletion,… | 1 g | 36570-1 | More Info |
| Kinetin Riboside | An anticancer nucleoside; induces ROS production, cellular ATP depletion,… | 5 g | 36570-5 | More Info |
| Kinsenoside | A glycoside with diverse biological activities; increases adipose triglyce… | 1 mg | 25144-1 | More Info |
| Kinsenoside | A glycoside with diverse biological activities; increases adipose triglyce… | 10 mg | 25144-10 | More Info |
| Kinsenoside | A glycoside with diverse biological activities; increases adipose triglyce… | 5 mg | 25144-5 | More Info |
| KIRA6 | An ATP-competitive, allosteric inhibitor of IRE1α RNase kinase activ… | 1 mg | 19151-1 | More Info |
| KIRA6 | An ATP-competitive, allosteric inhibitor of IRE1α RNase kinase activ… | 10 mg | 19151-10 | More Info |
| KIRA6 | An ATP-competitive, allosteric inhibitor of IRE1α RNase kinase activ… | 5 mg | 19151-5 | More Info |
| Kirenol | A diterpenoid with diverse biological activities; inhibits Gram-positive a… | 10 mg | 26212-10 | More Info |
| Kirenol | A diterpenoid with diverse biological activities; inhibits Gram-positive a… | 25 mg | 26212-25 | More Info |
| Kirenol | A diterpenoid with diverse biological activities; inhibits Gram-positive a… | 5 mg | 26212-5 | More Info |
| Kirromycin | An inhibitor of protein biosynthesis; inhibits isoleucine incorporation, p… | 1 mg | 25189-1 | More Info |
| Kisspeptin-54 (human) (trifluoroacetate salt) | A peptide ligand of GPR54 (Kis = 1.81 and 1.45 nM for rat and human recept… | 500 µg | 24477-500 | More Info |
| Kisspeptin-10 (mouse, rat) | A neuropeptide and kisspeptin receptor ligand; corresponds to amino acids… | 1 mg | 14036-1 | More Info |
| Kisspeptin-10 (mouse, rat) | A neuropeptide and kisspeptin receptor ligand; corresponds to amino acids… | 10 mg | 14036-10 | More Info |
| Kisspeptin-10 (mouse, rat) | A neuropeptide and kisspeptin receptor ligand; corresponds to amino acids… | 25 mg | 14036-25 | More Info |
| Kisspeptin-10 (mouse, rat) | A neuropeptide and kisspeptin receptor ligand; corresponds to amino acids… | 5 mg | 14036-5 | More Info |
| Kisspeptin-234 (trifluoroacetate salt) | A peptide kisspeptin receptor antagonist; inhibits kisspeptin-10-induced i… | 1 mg | 35633-1 | More Info |
| Kisspeptin-234 (trifluoroacetate salt) | A peptide kisspeptin receptor antagonist; inhibits kisspeptin-10-induced i… | 10 mg | 35633-10 | More Info |
| Kisspeptin-234 (trifluoroacetate salt) | A peptide kisspeptin receptor antagonist; inhibits kisspeptin-10-induced i… | 25 mg | 35633-25 | More Info |
| Kisspeptin-234 (trifluoroacetate salt) | A peptide kisspeptin receptor antagonist; inhibits kisspeptin-10-induced i… | 5 mg | 35633-5 | More Info |
| Kisspeptin-10 (zebrafish) (trifluoroacetate salt) | A neuropeptide; increases levels of the mRNA encoding Lh receptor, as well… | 1 mg | 35652-1 | More Info |
| Kisspeptin-10 (zebrafish) (trifluoroacetate salt) | A neuropeptide; increases levels of the mRNA encoding Lh receptor, as well… | 10 mg | 35652-10 | More Info |
| Kisspeptin-10 (zebrafish) (trifluoroacetate salt) | A neuropeptide; increases levels of the mRNA encoding Lh receptor, as well… | 25 mg | 35652-25 | More Info |
| Kisspeptin-10 (zebrafish) (trifluoroacetate salt) | A neuropeptide; increases levels of the mRNA encoding Lh receptor, as well… | 5 mg | 35652-5 | More Info |
| KJ Pyr 9 | A cell-permeable inhibitor of c-Myc (Kd = 6.5 nM) that interferes with Myc… | 1 mg | 19116-1 | More Info |
| KJ Pyr 9 | A cell-permeable inhibitor of c-Myc (Kd = 6.5 nM) that interferes with Myc… | 10 mg | 19116-10 | More Info |
| KJ Pyr 9 | A cell-permeable inhibitor of c-Myc (Kd = 6.5 nM) that interferes with Myc… | 25 mg | 19116-25 | More Info |
| KJ Pyr 9 | A cell-permeable inhibitor of c-Myc (Kd = 6.5 nM) that interferes with Myc… | 5 mg | 19116-5 | More Info |
| 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 |
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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