CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 768 of 1

Non-Antibody Products
Page 768 of 1,288
  • Records 38,351 - 38,400 of 64,374
Name Description Size Catalog #
ML-226 An inhibitor of ABHD11 (IC50s = 15 and 0.68 nM, respectively, in vitro and… 5 mg 25681-5 More Info
ML-228 An activator of the HIF signaling pathway, as demonstrated by HRE reporter… 1 mg 14568-1 More Info
ML-228 An activator of the HIF signaling pathway, as demonstrated by HRE reporter… 10 mg 14568-10 More Info
ML-228 An activator of the HIF signaling pathway, as demonstrated by HRE reporter… 5 mg 14568-5 More Info
ML-228 An activator of the HIF signaling pathway, as demonstrated by HRE reporter… 50 mg 14568-50 More Info
ML-230 An inhibitor of ABCG2; selectively inhibits JC-1 efflux in Ig-MXP3 cells o… 1 mg 32552-1 More Info
ML-230 An inhibitor of ABCG2; selectively inhibits JC-1 efflux in Ig-MXP3 cells o… 10 mg 32552-10 More Info
ML-230 An inhibitor of ABCG2; selectively inhibits JC-1 efflux in Ig-MXP3 cells o… 5 mg 32552-5 More Info
ML-233 A novel apelin receptor agonist (EC50 = 3.7 µM) that is >21-fold sel… 1 mg 15187-1 More Info
ML-233 A novel apelin receptor agonist (EC50 = 3.7 µM) that is >21-fold sel… 10 mg 15187-10 More Info
ML-233 A novel apelin receptor agonist (EC50 = 3.7 µM) that is >21-fold sel… 25 mg 15187-25 More Info
ML-233 A novel apelin receptor agonist (EC50 = 3.7 µM) that is >21-fold sel… 5 mg 15187-5 More Info
ML-239 An inhibitor of cancer stem cells, displaying greater than 23-fold selecti… 1 mg 15188-1 More Info
ML-239 An inhibitor of cancer stem cells, displaying greater than 23-fold selecti… 10 mg 15188-10 More Info
ML-239 An inhibitor of cancer stem cells, displaying greater than 23-fold selecti… 25 mg 15188-25 More Info
ML-239 An inhibitor of cancer stem cells, displaying greater than 23-fold selecti… 5 mg 15188-5 More Info
ML-240 An ATP-competitive inhibitor of the D2 domain of the p97 ATPase (IC50 = 0.… 1 mg 17373-1 More Info
ML-240 An ATP-competitive inhibitor of the D2 domain of the p97 ATPase (IC50 = 0.… 10 mg 17373-10 More Info
ML-240 An ATP-competitive inhibitor of the D2 domain of the p97 ATPase (IC50 = 0.… 25 mg 17373-25 More Info
ML-240 An ATP-competitive inhibitor of the D2 domain of the p97 ATPase (IC50 = 0.… 5 mg 17373-5 More Info
ML-243 An inhibitor of cancer stem cells, displaying 32-fold selective inhibition… 1 mg 15189-1 More Info
ML-243 An inhibitor of cancer stem cells, displaying 32-fold selective inhibition… 10 mg 15189-10 More Info
ML-243 An inhibitor of cancer stem cells, displaying 32-fold selective inhibition… 25 mg 15189-25 More Info
ML-243 An inhibitor of cancer stem cells, displaying 32-fold selective inhibition… 5 mg 15189-5 More Info
ML-261 A thienopyrrole-5-carboxamide; inhibits lipid droplet formation in murine… 1 mg 15192-1 More Info
ML-261 A thienopyrrole-5-carboxamide; inhibits lipid droplet formation in murine… 10 mg 15192-10 More Info
ML-261 A thienopyrrole-5-carboxamide; inhibits lipid droplet formation in murine… 25 mg 15192-25 More Info
ML-261 A thienopyrrole-5-carboxamide; inhibits lipid droplet formation in murine… 5 mg 15192-5 More Info
ML-262 An inhibitor of lipid droplet formation (IC50 = 6.4 nM in murine AML-12 ce… 1 mg 21902-1 More Info
ML-262 An inhibitor of lipid droplet formation (IC50 = 6.4 nM in murine AML-12 ce… 10 mg 21902-10 More Info
ML-262 An inhibitor of lipid droplet formation (IC50 = 6.4 nM in murine AML-12 ce… 5 mg 21902-5 More Info
ML-264 A selective inhibitor of KLF5 (IC50 = 29 nM in a cell-based assay for prol… 1 mg 18880-1 More Info
ML-264 A selective inhibitor of KLF5 (IC50 = 29 nM in a cell-based assay for prol… 10 mg 18880-10 More Info
ML-264 A selective inhibitor of KLF5 (IC50 = 29 nM in a cell-based assay for prol… 25 mg 18880-25 More Info
ML-264 A selective inhibitor of KLF5 (IC50 = 29 nM in a cell-based assay for prol… 5 mg 18880-5 More Info
ML-265 A selective activator of tumor-specific PKM2 (EC50 = 92 nM) that binds to… 1 mg 13942-1 More Info
ML-265 A selective activator of tumor-specific PKM2 (EC50 = 92 nM) that binds to… 10 mg 13942-10 More Info
ML-265 A selective activator of tumor-specific PKM2 (EC50 = 92 nM) that binds to… 25 mg 13942-25 More Info
ML-265 A selective activator of tumor-specific PKM2 (EC50 = 92 nM) that binds to… 5 mg 13942-5 More Info
ML-277 A potent activator of KCNQ1 (Kv7.1) channels (EC50 = 260 nM); EC50 > 30 &m… 1 mg 15193-1 More Info
ML-277 A potent activator of KCNQ1 (Kv7.1) channels (EC50 = 260 nM); EC50 > 30 &m… 10 mg 15193-10 More Info
ML-277 A potent activator of KCNQ1 (Kv7.1) channels (EC50 = 260 nM); EC50 > 30 &m… 25 mg 15193-25 More Info
ML-277 A potent activator of KCNQ1 (Kv7.1) channels (EC50 = 260 nM); EC50 > 30 &m… 5 mg 15193-5 More Info
ML-281 An inhibitor of STK33 (IC50 = 14 nM); has 700- and 550-fold selectivity fo… 1 mg 20116-1 More Info
ML-281 An inhibitor of STK33 (IC50 = 14 nM); has 700- and 550-fold selectivity fo… 10 mg 20116-10 More Info
ML-281 An inhibitor of STK33 (IC50 = 14 nM); has 700- and 550-fold selectivity fo… 25 mg 20116-25 More Info
ML-281 An inhibitor of STK33 (IC50 = 14 nM); has 700- and 550-fold selectivity fo… 5 mg 20116-5 More Info
ML-289 A negative allosteric modulator of mGlu3 (IC50 = 0.66 µM) that displ… 1 mg 15195-1 More Info
ML-289 A negative allosteric modulator of mGlu3 (IC50 = 0.66 µM) that displ… 10 mg 15195-10 More Info
ML-289 A negative allosteric modulator of mGlu3 (IC50 = 0.66 µM) that displ… 25 mg 15195-25 More Info
CAYMAN CHEMICAL COMPANY
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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