CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 211 of 1

Non-Antibody Products
Page 211 of 1,297
  • Records 10,501 - 10,550 of 64,815
Name Description Size Catalog #
CAY10597 A potent CRTH2 / DP2 receptor antagonist that binds to the human receptor… 5 mg 10012539-5 More Info
CAY10598 A very potent agonist of EP4, binding with a Ki value of 1.2 nM; does not… 1 mg 13281-1 More Info
CAY10598 A very potent agonist of EP4, binding with a Ki value of 1.2 nM; does not… 10 mg 13281-10 More Info
CAY10598 A very potent agonist of EP4, binding with a Ki value of 1.2 nM; does not… 5 mg 13281-5 More Info
CAY10598 A very potent agonist of EP4, binding with a Ki value of 1.2 nM; does not… 500 µg 13281-500 More Info
CAY10599 An agonist of PPARγ (EC50 = 0.05 µM); selective for PPAR&gamma… 1 mg 13282-1 More Info
CAY10599 An agonist of PPARγ (EC50 = 0.05 µM); selective for PPAR&gamma… 10 mg 13282-10 More Info
CAY10599 An agonist of PPARγ (EC50 = 0.05 µM); selective for PPAR&gamma… 5 mg 13282-5 More Info
CAY10599 An agonist of PPARγ (EC50 = 0.05 µM); selective for PPAR&gamma… 500 µg 13282-500 More Info
CAY10602 A SIRT1 activator; inhibits LPS-induced TNF-α release in THP-1 cells… 10 mg 10009796-10 More Info
CAY10602 A SIRT1 activator; inhibits LPS-induced TNF-α release in THP-1 cells… 100 mg 10009796-100 More Info
CAY10602 A SIRT1 activator; inhibits LPS-induced TNF-α release in THP-1 cells… 5 mg 10009796-5 More Info
CAY10602 A SIRT1 activator; inhibits LPS-induced TNF-α release in THP-1 cells… 50 mg 10009796-50 More Info
CAY10603 A potent and selective inhibitor of HDAC6 (IC50 = 0.002 nM, as compared wi… 1 mg 13146-1 More Info
CAY10603 A potent and selective inhibitor of HDAC6 (IC50 = 0.002 nM, as compared wi… 10 mg 13146-10 More Info
CAY10603 A potent and selective inhibitor of HDAC6 (IC50 = 0.002 nM, as compared wi… 25 mg 13146-25 More Info
CAY10603 A potent and selective inhibitor of HDAC6 (IC50 = 0.002 nM, as compared wi… 5 mg 13146-5 More Info
CAY10606 A potent, reversible inhibitor of 5-LO, in cell-free assays (IC50 = 86 nM)… 1 mg 13381-1 More Info
CAY10606 A potent, reversible inhibitor of 5-LO, in cell-free assays (IC50 = 86 nM)… 5 mg 13381-5 More Info
CAY10608 A propanolamine that potently, selectively, and non-competitively antagoni… 1 mg 13358-1 More Info
CAY10608 A propanolamine that potently, selectively, and non-competitively antagoni… 10 mg 13358-10 More Info
CAY10608 A propanolamine that potently, selectively, and non-competitively antagoni… 25 mg 13358-25 More Info
CAY10608 A propanolamine that potently, selectively, and non-competitively antagoni… 5 mg 13358-5 More Info
CAY10614 An antagonist of lipid A activation of TLR4 (IC50 =1.68 µM), in a ce… 1 mg 13615-1 More Info
CAY10614 An antagonist of lipid A activation of TLR4 (IC50 =1.68 µM), in a ce… 10 mg 13615-10 More Info
CAY10614 An antagonist of lipid A activation of TLR4 (IC50 =1.68 µM), in a ce… 25 mg 13615-25 More Info
CAY10614 An antagonist of lipid A activation of TLR4 (IC50 =1.68 µM), in a ce… 5 mg 13615-5 More Info
CAY10616 An analog of resveratrol which potently induces apoptosis in HL-60 cells (… 1 mg 13291-1 More Info
CAY10616 An analog of resveratrol which potently induces apoptosis in HL-60 cells (… 10 mg 13291-10 More Info
CAY10616 An analog of resveratrol which potently induces apoptosis in HL-60 cells (… 25 mg 13291-25 More Info
CAY10616 An analog of resveratrol which potently induces apoptosis in HL-60 cells (… 5 mg 13291-5 More Info
CAY10621 A selective inhibitor of SPHK1 1 mg 13371-1 More Info
CAY10621 A selective inhibitor of SPHK1 10 mg 13371-10 More Info
CAY10621 A selective inhibitor of SPHK1 25 mg 13371-25 More Info
CAY10621 A selective inhibitor of SPHK1 5 mg 13371-5 More Info
CAY10622 A potent inhibitor of ROCK1 and ROCK2 (IC50s = 6 and 4 nM, respectively) 1 mg 13687-1 More Info
CAY10622 A potent inhibitor of ROCK1 and ROCK2 (IC50s = 6 and 4 nM, respectively) 10 mg 13687-10 More Info
CAY10622 A potent inhibitor of ROCK1 and ROCK2 (IC50s = 6 and 4 nM, respectively) 5 mg 13687-5 More Info
CAY10625 An antagonist of the interaction between survivin and the apoptosis-promot… 1 mg 13836-1 More Info
CAY10625 An antagonist of the interaction between survivin and the apoptosis-promot… 10 mg 13836-10 More Info
CAY10625 An antagonist of the interaction between survivin and the apoptosis-promot… 5 mg 13836-5 More Info
CAY10626 A potent, dual PI3Kα/mTOR inhibitor (IC50s = 0.9 and 0.6 nM, respect… 1 mg 13838-1 More Info
CAY10626 A potent, dual PI3Kα/mTOR inhibitor (IC50s = 0.9 and 0.6 nM, respect… 10 mg 13838-10 More Info
CAY10626 A potent, dual PI3Kα/mTOR inhibitor (IC50s = 0.9 and 0.6 nM, respect… 25 mg 13838-25 More Info
CAY10626 A potent, dual PI3Kα/mTOR inhibitor (IC50s = 0.9 and 0.6 nM, respect… 5 mg 13838-5 More Info
CAY10631 An alcohol related to a C32:6 very long chain fatty acid found in the reti… 1 mg 10562-1 More Info
CAY10631 An alcohol related to a C32:6 very long chain fatty acid found in the reti… 10 mg 10562-10 More Info
CAY10631 An alcohol related to a C32:6 very long chain fatty acid found in the reti… 5 mg 10562-5 More Info
CAY10631 An alcohol related to a C32:6 very long chain fatty acid found in the reti… 500 µg 10562-500 More Info
CAY10632 A C32:6 VLCPUFA whose specific biological actions are largely unknown, but… 1 mg 10497-1 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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