CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 786 of 1

Non-Antibody Products
Page 786 of 1,326
  • Records 39,251 - 39,300 of 66,261
Name Description Size Catalog #
Mizolastine A histamine H1 receptor antagonist (Ki = 0.001 µM); selective for hi… 5 g 9000566-5 More Info
Mizolastine A histamine H1 receptor antagonist (Ki = 0.001 µM); selective for hi… 500 mg 9000566-500 More Info
Mizoribine An imidazole nucleoside with immunosuppressive properties; inhibits T cell… 10 mg 23128-10 More Info
Mizoribine An imidazole nucleoside with immunosuppressive properties; inhibits T cell… 100 mg 23128-100 More Info
Mizoribine An imidazole nucleoside with immunosuppressive properties; inhibits T cell… 25 mg 23128-25 More Info
Mizoribine An imidazole nucleoside with immunosuppressive properties; inhibits T cell… 50 mg 23128-50 More Info
MJ15 A potent CB1 receptor antagonist (IC50 = 118.9 pM; Ki = 27.2 pM for rat CB… 1 mg 11956-1 More Info
MJ15 A potent CB1 receptor antagonist (IC50 = 118.9 pM; Ki = 27.2 pM for rat CB… 10 mg 11956-10 More Info
MJ15 A potent CB1 receptor antagonist (IC50 = 118.9 pM; Ki = 27.2 pM for rat CB… 25 mg 11956-25 More Info
MJ15 A potent CB1 receptor antagonist (IC50 = 118.9 pM; Ki = 27.2 pM for rat CB… 5 mg 11956-5 More Info
MJ33 (lithium salt) A selective, reversible inhibitor of the acidic, calcium-independent (ai)P… 1 mg 90001844-1 More Info
MJ33 (lithium salt) A selective, reversible inhibitor of the acidic, calcium-independent (ai)P… 10 mg 90001844-10 More Info
MJ33 (lithium salt) A selective, reversible inhibitor of the acidic, calcium-independent (ai)P… 25 mg 90001844-25 More Info
MJ33 (lithium salt) A selective, reversible inhibitor of the acidic, calcium-independent (ai)P… 5 mg 90001844-5 More Info
MJN110 An inhibitor of MAGL (IC50 = 9.1 nM) and to a lesser extent ABHD6 with pot… 10 mg 17583-10 More Info
MJN110 An inhibitor of MAGL (IC50 = 9.1 nM) and to a lesser extent ABHD6 with pot… 100 mg 17583-100 More Info
MJN110 An inhibitor of MAGL (IC50 = 9.1 nM) and to a lesser extent ABHD6 with pot… 25 mg 17583-25 More Info
MJN110 An inhibitor of MAGL (IC50 = 9.1 nM) and to a lesser extent ABHD6 with pot… 5 mg 17583-5 More Info
MJN228 A selective ligand for the lipid-binding protein NUCB1, blocking binding o… 1 mg 18275-1 More Info
MJN228 A selective ligand for the lipid-binding protein NUCB1, blocking binding o… 10 mg 18275-10 More Info
MJN228 A selective ligand for the lipid-binding protein NUCB1, blocking binding o… 25 mg 18275-25 More Info
MJN228 A selective ligand for the lipid-binding protein NUCB1, blocking binding o… 5 mg 18275-5 More Info
MK-0457 A potent pan-Aurora kinase inhibitor that favors Aurora A (Ki = 0.6 nM) ov… 100 mg 13600-100 More Info
MK-0457 A potent pan-Aurora kinase inhibitor that favors Aurora A (Ki = 0.6 nM) ov… 25 mg 13600-25 More Info
MK-0457 A potent pan-Aurora kinase inhibitor that favors Aurora A (Ki = 0.6 nM) ov… 250 mg 13600-250 More Info
MK-0457 A potent pan-Aurora kinase inhibitor that favors Aurora A (Ki = 0.6 nM) ov… 50 mg 13600-50 More Info
MK-0524 A potent, selective DP1 receptor antagonist that binds DP1 and DP2 recepto… 1 mg 10009835-1 More Info
MK-0524 A potent, selective DP1 receptor antagonist that binds DP1 and DP2 recepto… 10 mg 10009835-10 More Info
MK-0524 A potent, selective DP1 receptor antagonist that binds DP1 and DP2 recepto… 25 mg 10009835-25 More Info
MK-0524 A potent, selective DP1 receptor antagonist that binds DP1 and DP2 recepto… 5 mg 10009835-5 More Info
MK-0557 A potent antagonist of NPY receptor Y5 (Kis = 1.3, 0.79, 0.74, and 1.4 nM… 1 mg 22134-1 More Info
MK-0557 A potent antagonist of NPY receptor Y5 (Kis = 1.3, 0.79, 0.74, and 1.4 nM… 10 mg 22134-10 More Info
MK-0557 A potent antagonist of NPY receptor Y5 (Kis = 1.3, 0.79, 0.74, and 1.4 nM… 25 mg 22134-25 More Info
MK-0557 A potent antagonist of NPY receptor Y5 (Kis = 1.3, 0.79, 0.74, and 1.4 nM… 5 mg 22134-5 More Info
MK-0591 An inhibitor of FLAP (IC50 = 1.6 nM for the human enzyme); inhibits LTB4 b… 1 mg 37322-1 More Info
MK-0591 An inhibitor of FLAP (IC50 = 1.6 nM for the human enzyme); inhibits LTB4 b… 10 mg 37322-10 More Info
MK-0591 An inhibitor of FLAP (IC50 = 1.6 nM for the human enzyme); inhibits LTB4 b… 25 mg 37322-25 More Info
MK-0591 An inhibitor of FLAP (IC50 = 1.6 nM for the human enzyme); inhibits LTB4 b… 5 mg 37322-5 More Info
MK-0752 A potent, reversible inhibitor of γ-secretase, reducing the cleavage… 1 mg 16706-1 More Info
MK-0752 A potent, reversible inhibitor of γ-secretase, reducing the cleavage… 10 mg 16706-10 More Info
MK-0752 A potent, reversible inhibitor of γ-secretase, reducing the cleavage… 5 mg 16706-5 More Info
MK-0812 A CCR2 antagonist (IC50 = 5 nM for the human receptor); inhibits mammosphe… 1 mg 21803-1 More Info
MK-0812 A CCR2 antagonist (IC50 = 5 nM for the human receptor); inhibits mammosphe… 10 mg 21803-10 More Info
MK-0812 A CCR2 antagonist (IC50 = 5 nM for the human receptor); inhibits mammosphe… 5 mg 21803-5 More Info
MK-0941 A glucokinase activator (EC50s = 0.24 and 0.065 µM at low (2.5 mM) a… 1 mg 25642-1 More Info
MK-0941 A glucokinase activator (EC50s = 0.24 and 0.065 µM at low (2.5 mM) a… 10 mg 25642-10 More Info
MK-0941 A glucokinase activator (EC50s = 0.24 and 0.065 µM at low (2.5 mM) a… 25 mg 25642-25 More Info
MK-0941 A glucokinase activator (EC50s = 0.24 and 0.065 µM at low (2.5 mM) a… 5 mg 25642-5 More Info
MK-0974 A CGRP receptor antagonist (Ki = 0.77 µM); binds selectively to the… 1 mg 23960-1 More Info
MK-0974 A CGRP receptor antagonist (Ki = 0.77 µM); binds selectively to the… 10 mg 23960-10 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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