CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 430 of 859
Non-Antibody Products
Page 430 of 859
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| KHS-101 | An Hsp60 inhibitor and inducer of neuronal differentiation; inhibits the r… | 50 mg | 37544-50 | More Info |
| K145 (hydrochloride) | A selective inhibitor of SPHK2 (Ki = 6.4 µM; IC50s = 4.3 and >10 &mi… | 1 mg | 11691-1 | More Info |
| K145 (hydrochloride) | A selective inhibitor of SPHK2 (Ki = 6.4 µM; IC50s = 4.3 and >10 &mi… | 5 mg | 11691-5 | More Info |
| K145 (hydrochloride) | A selective inhibitor of SPHK2 (Ki = 6.4 µM; IC50s = 4.3 and >10 &mi… | 500 µg | 11691-500 | More Info |
| K-7174 (hydrochloride) | A 20S proteasome inhibitor; inhibits the 20S proteasome β1, β2,… | 10 mg | 32773-10 | More Info |
| K-7174 (hydrochloride) | A 20S proteasome inhibitor; inhibits the 20S proteasome β1, β2,… | 25 mg | 32773-25 | More Info |
| K-7174 (hydrochloride) | A 20S proteasome inhibitor; inhibits the 20S proteasome β1, β2,… | 5 mg | 32773-5 | More Info |
| K-7174 (hydrochloride) | A 20S proteasome inhibitor; inhibits the 20S proteasome β1, β2,… | 50 mg | 32773-50 | More Info |
| Ki16425 | A LPA receptor antagonist with selectivity for LPA1 and LPA3; exhibits Ki… | 1 mg | 10012659-1 | More Info |
| Ki16425 | A LPA receptor antagonist with selectivity for LPA1 and LPA3; exhibits Ki… | 10 mg | 10012659-10 | More Info |
| Ki16425 | A LPA receptor antagonist with selectivity for LPA1 and LPA3; exhibits Ki… | 100 mg | 10012659-100 | More Info |
| Ki16425 | A LPA receptor antagonist with selectivity for LPA1 and LPA3; exhibits Ki… | 5 mg | 10012659-5 | More Info |
| Ki20227 | A c-Fms kinase inhibitor (IC50 = 2 nM); inhibits CSF1-dependent c-Fms phos… | 1 mg | 22258-1 | More Info |
| Ki20227 | A c-Fms kinase inhibitor (IC50 = 2 nM); inhibits CSF1-dependent c-Fms phos… | 10 mg | 22258-10 | More Info |
| Ki20227 | A c-Fms kinase inhibitor (IC50 = 2 nM); inhibits CSF1-dependent c-Fms phos… | 25 mg | 22258-25 | More Info |
| Ki20227 | A c-Fms kinase inhibitor (IC50 = 2 nM); inhibits CSF1-dependent c-Fms phos… | 5 mg | 22258-5 | More Info |
| Ki8751 | A potent, orally available inhibitor of the kinase activity of VEGFR2 (IC5… | 10 mg | 18004-10 | More Info |
| Ki8751 | A potent, orally available inhibitor of the kinase activity of VEGFR2 (IC5… | 25 mg | 18004-25 | More Info |
| Ki8751 | A potent, orally available inhibitor of the kinase activity of VEGFR2 (IC5… | 5 mg | 18004-5 | More Info |
| Ki8751 | A potent, orally available inhibitor of the kinase activity of VEGFR2 (IC5… | 50 mg | 18004-50 | More Info |
| Kibdelone A | A heterocyclic polyketide that has potent and selective cytotoxicity again… | 1 mg | 21524-1 | More Info |
| Kibdelone B | A kibdelone whose mode of action and pharmacology have not been studied | 2.5 mg | 19444-25 | More Info |
| Kibdelone B | A kibdelone whose mode of action and pharmacology have not been studied | 500 µg | 19444-500 | More Info |
| Kibdelone C | A heterocyclic polyketide that has potent and selective cytotoxicity again… | 1 mg | 21525-1 | More Info |
| Kifunensine | A potent and selective inhibitor of class I α-mannosidases and serve… | 1 mg | 10009437-1 | More Info |
| 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 |
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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