CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 649 of 1
Non-Antibody Products
Page 649 of 1,297
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| 3-keto Ursolic Acid | A triterpenoid with diverse biological activities; inhibits the proliferat… | 250 mg | 37364-250 | More Info |
| 3-keto Ursolic Acid | A triterpenoid with diverse biological activities; inhibits the proliferat… | 50 mg | 37364-50 | More Info |
| Kevetrin (hydrochloride) | An activator of p53; increases levels of activated p53 and expression of p… | 10 mg | 28288-10 | More Info |
| Kevetrin (hydrochloride) | An activator of p53; increases levels of activated p53 and expression of p… | 25 mg | 28288-25 | More Info |
| Kevetrin (hydrochloride) | An activator of p53; increases levels of activated p53 and expression of p… | 5 mg | 28288-5 | More Info |
| Kevetrin (hydrochloride) | An activator of p53; increases levels of activated p53 and expression of p… | 50 mg | 28288-50 | More Info |
| KH7 | A selective inhibitor of sAC with an IC50 value between 3-10 µM; dec… | 10 mg | 13243-10 | More Info |
| KH7 | A selective inhibitor of sAC with an IC50 value between 3-10 µM; dec… | 25 mg | 13243-25 | More Info |
| KH7 | A selective inhibitor of sAC with an IC50 value between 3-10 µM; dec… | 5 mg | 13243-5 | More Info |
| KH7 | A selective inhibitor of sAC with an IC50 value between 3-10 µM; dec… | 50 mg | 13243-50 | More Info |
| Khasianine | A steroidal glycoside with diverse biological activities; reduces the prol… | 1 mg | 38762-1 | More Info |
| Khasianine | A steroidal glycoside with diverse biological activities; reduces the prol… | 10 mg | 38762-10 | More Info |
| Khasianine | A steroidal glycoside with diverse biological activities; reduces the prol… | 25 mg | 38762-25 | More Info |
| Khasianine | A steroidal glycoside with diverse biological activities; reduces the prol… | 5 mg | 38762-5 | More Info |
| KHS-101 | An Hsp60 inhibitor and inducer of neuronal differentiation; inhibits the r… | 10 mg | 37544-10 | More Info |
| KHS-101 | An Hsp60 inhibitor and inducer of neuronal differentiation; inhibits the r… | 25 mg | 37544-25 | More Info |
| KHS-101 | An Hsp60 inhibitor and inducer of neuronal differentiation; inhibits the r… | 5 mg | 37544-5 | More Info |
| 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 |
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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