CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 769 of 1

Non-Antibody Products
Page 769 of 1,297
  • Records 38,401 - 38,450 of 64,815
Name Description Size Catalog #
MK-1903 An HCA2 receptor agonist (EC50 = 12.9 nM in an HTRF assay); selective for… 5 mg 34304-5 More Info
MK-2461 A c-MET inhibitor (IC50s = 0.4-2 nM for wild-type and mutant forms); selec… 1 mg 32964-1 More Info
MK-2461 A c-MET inhibitor (IC50s = 0.4-2 nM for wild-type and mutant forms); selec… 10 mg 32964-10 More Info
MK-2461 A c-MET inhibitor (IC50s = 0.4-2 nM for wild-type and mutant forms); selec… 5 mg 32964-5 More Info
MK-3102 A DPP-4 inhibitor (IC50 = 1.6 nM); selective for DPP-4 over several protea… 1 mg 21454-1 More Info
MK-3102 A DPP-4 inhibitor (IC50 = 1.6 nM); selective for DPP-4 over several protea… 10 mg 21454-10 More Info
MK-3102 A DPP-4 inhibitor (IC50 = 1.6 nM); selective for DPP-4 over several protea… 25 mg 21454-25 More Info
MK-3102 A DPP-4 inhibitor (IC50 = 1.6 nM); selective for DPP-4 over several protea… 5 mg 21454-5 More Info
MK-3697 An orexin receptor 2 antagonist (Ki = 1.1 nM); selective for OX2R over OX1… 10 mg 34718-10 More Info
MK-3697 An orexin receptor 2 antagonist (Ki = 1.1 nM); selective for OX2R over OX1… 25 mg 34718-25 More Info
MK-3697 An orexin receptor 2 antagonist (Ki = 1.1 nM); selective for OX2R over OX1… 5 mg 34718-5 More Info
MK-3697 An orexin receptor 2 antagonist (Ki = 1.1 nM); selective for OX2R over OX1… 50 mg 34718-50 More Info
MK-3903 An AMPK activator (EC50 = 9 nM); selective for AMPK over a kinase panel at… 1 mg 29661-1 More Info
MK-3903 An AMPK activator (EC50 = 9 nM); selective for AMPK over a kinase panel at… 10 mg 29661-10 More Info
MK-3903 An AMPK activator (EC50 = 9 nM); selective for AMPK over a kinase panel at… 25 mg 29661-25 More Info
MK-3903 An AMPK activator (EC50 = 9 nM); selective for AMPK over a kinase panel at… 5 mg 29661-5 More Info
MK-4101 A Smoothened receptor antagonist; binds to human recombinant Smo expressed… 1 mg 29159-1 More Info
MK-4101 A Smoothened receptor antagonist; binds to human recombinant Smo expressed… 10 mg 29159-10 More Info
MK-4101 A Smoothened receptor antagonist; binds to human recombinant Smo expressed… 25 mg 29159-25 More Info
MK-4101 A Smoothened receptor antagonist; binds to human recombinant Smo expressed… 5 mg 29159-5 More Info
MK-5108 A potent inhibitor of Aurora A (IC50 = 0.064 nM) that less potently inhibi… 1 mg 19167-1 More Info
MK-5108 A potent inhibitor of Aurora A (IC50 = 0.064 nM) that less potently inhibi… 10 mg 19167-10 More Info
MK-5108 A potent inhibitor of Aurora A (IC50 = 0.064 nM) that less potently inhibi… 5 mg 19167-5 More Info
MK-571 A CysLT1 receptor antagonist (Ki = 2.1 nM in a radioligand binding assay u… 1 mg 10029-1 More Info
MK-571 A CysLT1 receptor antagonist (Ki = 2.1 nM in a radioligand binding assay u… 10 mg 10029-10 More Info
MK-571 A CysLT1 receptor antagonist (Ki = 2.1 nM in a radioligand binding assay u… 5 mg 10029-5 More Info
MK-571 A CysLT1 receptor antagonist (Ki = 2.1 nM in a radioligand binding assay u… 50 mg 10029-50 More Info
MK6-83 A TRPML1 activator (EC50s = 110, 100, and 1,230 nM in wild type, F465L, an… 1 mg 21944-1 More Info
MK6-83 A TRPML1 activator (EC50s = 110, 100, and 1,230 nM in wild type, F465L, an… 10 mg 21944-10 More Info
MK6-83 A TRPML1 activator (EC50s = 110, 100, and 1,230 nM in wild type, F465L, an… 25 mg 21944-25 More Info
MK6-83 A TRPML1 activator (EC50s = 110, 100, and 1,230 nM in wild type, F465L, an… 5 mg 21944-5 More Info
MK-7246 A CRTH2 / DP2 receptor antagonist (Ki = 2.5 nM); selective for CRTH2 / DP2… 1 mg 34208-1 More Info
MK-7246 A CRTH2 / DP2 receptor antagonist (Ki = 2.5 nM); selective for CRTH2 / DP2… 10 mg 34208-10 More Info
MK-7246 A CRTH2 / DP2 receptor antagonist (Ki = 2.5 nM); selective for CRTH2 / DP2… 25 mg 34208-25 More Info
MK-7246 A CRTH2 / DP2 receptor antagonist (Ki = 2.5 nM); selective for CRTH2 / DP2… 5 mg 34208-5 More Info
MK-7622 A positive allosteric modulator of M1 mAChRs; increases ACh-induced calciu… 10 mg 34407-10 More Info
MK-7622 A positive allosteric modulator of M1 mAChRs; increases ACh-induced calciu… 25 mg 34407-25 More Info
MK-7622 A positive allosteric modulator of M1 mAChRs; increases ACh-induced calciu… 5 mg 34407-5 More Info
MK-7622 A positive allosteric modulator of M1 mAChRs; increases ACh-induced calciu… 50 mg 34407-50 More Info
MK-7655 A β-lactamase inhibitor; inhibits hydrolysis of nitrocefin by KPC-2 &… 1 mg 23890-1 More Info
MK-7655 A β-lactamase inhibitor; inhibits hydrolysis of nitrocefin by KPC-2 &… 10 mg 23890-10 More Info
MK-7655 A β-lactamase inhibitor; inhibits hydrolysis of nitrocefin by KPC-2 &… 25 mg 23890-25 More Info
MK-7655 A β-lactamase inhibitor; inhibits hydrolysis of nitrocefin by KPC-2 &… 5 mg 23890-5 More Info
MK-8245 A stearoyl-CoA desaturase inhibitor (IC50s = 3, 3, and 1 nM for rat , mous… 1 mg 29421-1 More Info
MK-8245 A stearoyl-CoA desaturase inhibitor (IC50s = 3, 3, and 1 nM for rat , mous… 10 mg 29421-10 More Info
MK-8245 A stearoyl-CoA desaturase inhibitor (IC50s = 3, 3, and 1 nM for rat , mous… 25 mg 29421-25 More Info
MK-8245 A stearoyl-CoA desaturase inhibitor (IC50s = 3, 3, and 1 nM for rat , mous… 5 mg 29421-5 More Info
MK-8617 A HIF-PH1, -2, and -3 inhibitor (IC50s = 1, 1, and 14 nM, respectively); s… 100 mg 33790-100 More Info
MK-8617 A HIF-PH1, -2, and -3 inhibitor (IC50s = 1, 1, and 14 nM, respectively); s… 25 mg 33790-25 More Info
MK-8617 A HIF-PH1, -2, and -3 inhibitor (IC50s = 1, 1, and 14 nM, respectively); s… 5 mg 33790-5 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

Facebook

Twitter


Return to Profile

© 1980 - 2024 Linscott's Directory, Linscott's USA. All rights reserved.