CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 704 of 1

Non-Antibody Products
Page 704 of 1,297
  • Records 35,151 - 35,200 of 64,815
Name Description Size Catalog #
LY2795050 A κ-opioid receptor antagonist (Ki = 0.722 nM); selective for the KO… 1 mg 33604-1 More Info
LY2795050 A κ-opioid receptor antagonist (Ki = 0.722 nM); selective for the KO… 10 mg 33604-10 More Info
LY2795050 A κ-opioid receptor antagonist (Ki = 0.722 nM); selective for the KO… 25 mg 33604-25 More Info
LY2795050 A κ-opioid receptor antagonist (Ki = 0.722 nM); selective for the KO… 5 mg 33604-5 More Info
LY2801653 A MET kinase inhibitor (Ki = 2 nM); inhibits MST1R, Axl, MNK1 / 2, FLT3, D… 1 mg 25978-1 More Info
LY2801653 A MET kinase inhibitor (Ki = 2 nM); inhibits MST1R, Axl, MNK1 / 2, FLT3, D… 10 mg 25978-10 More Info
LY2801653 A MET kinase inhibitor (Ki = 2 nM); inhibits MST1R, Axl, MNK1 / 2, FLT3, D… 5 mg 25978-5 More Info
LY2801653 A MET kinase inhibitor (Ki = 2 nM); inhibits MST1R, Axl, MNK1 / 2, FLT3, D… 50 mg 25978-50 More Info
LY2811376 A non-peptide inhibitor of BACE1 (IC50 = 239 nM) that demonstrates ~10-fol… 1 mg 16712-1 More Info
LY2811376 A non-peptide inhibitor of BACE1 (IC50 = 239 nM) that demonstrates ~10-fol… 10 mg 16712-10 More Info
LY2811376 A non-peptide inhibitor of BACE1 (IC50 = 239 nM) that demonstrates ~10-fol… 5 mg 16712-5 More Info
LY2811376 A non-peptide inhibitor of BACE1 (IC50 = 239 nM) that demonstrates ~10-fol… 50 mg 16712-50 More Info
LY2828360 A CB2 agonist (Ki = 40.3 nM) selectively activates CB2 over CB1 in a GTP&g… 1 mg 26791-1 More Info
LY2828360 A CB2 agonist (Ki = 40.3 nM) selectively activates CB2 over CB1 in a GTP&g… 10 mg 26791-10 More Info
LY2828360 A CB2 agonist (Ki = 40.3 nM) selectively activates CB2 over CB1 in a GTP&g… 25 mg 26791-25 More Info
LY2828360 A CB2 agonist (Ki = 40.3 nM) selectively activates CB2 over CB1 in a GTP&g… 5 mg 26791-5 More Info
LY2835219 An orally bioavailable dual inhibitor of Cdk4 and Cdk6 (IC50s = 2 and 10 n… 1 mg 21560-1 More Info
LY2835219 An orally bioavailable dual inhibitor of Cdk4 and Cdk6 (IC50s = 2 and 10 n… 10 mg 21560-10 More Info
LY2835219 An orally bioavailable dual inhibitor of Cdk4 and Cdk6 (IC50s = 2 and 10 n… 25 mg 21560-25 More Info
LY2835219 An orally bioavailable dual inhibitor of Cdk4 and Cdk6 (IC50s = 2 and 10 n… 5 mg 21560-5 More Info
LY2857785 A Cdk9 inhibitor (IC50 = 0.011 µM); inhibits Cdk8 and Cdk7 (IC50s =… 1 mg 34880-1 More Info
LY2857785 A Cdk9 inhibitor (IC50 = 0.011 µM); inhibits Cdk8 and Cdk7 (IC50s =… 10 mg 34880-10 More Info
LY2857785 A Cdk9 inhibitor (IC50 = 0.011 µM); inhibits Cdk8 and Cdk7 (IC50s =… 25 mg 34880-25 More Info
LY2857785 A Cdk9 inhibitor (IC50 = 0.011 µM); inhibits Cdk8 and Cdk7 (IC50s =… 5 mg 34880-5 More Info
LY2874455 A pan-FGFR inhibitor (IC50s = 2.8, 2.6, 6.4, 6, and 7 nM for FGFR1, FGFR2,… 1 mg 20843-1 More Info
LY2874455 A pan-FGFR inhibitor (IC50s = 2.8, 2.6, 6.4, 6, and 7 nM for FGFR1, FGFR2,… 10 mg 20843-10 More Info
LY2874455 A pan-FGFR inhibitor (IC50s = 2.8, 2.6, 6.4, 6, and 7 nM for FGFR1, FGFR2,… 25 mg 20843-25 More Info
LY2874455 A pan-FGFR inhibitor (IC50s = 2.8, 2.6, 6.4, 6, and 7 nM for FGFR1, FGFR2,… 5 mg 20843-5 More Info
LY2886721 Selective inhibitor of BACE (IC50 = 20 nM for recombinant hBACE1) 1 mg 21599-1 More Info
LY2886721 Selective inhibitor of BACE (IC50 = 20 nM for recombinant hBACE1) 10 mg 21599-10 More Info
LY2886721 Selective inhibitor of BACE (IC50 = 20 nM for recombinant hBACE1) 25 mg 21599-25 More Info
LY2886721 Selective inhibitor of BACE (IC50 = 20 nM for recombinant hBACE1) 5 mg 21599-5 More Info
LY293111 A potent antagonist of the LTB4 receptor, BLT1, that inhibits the specific… 1 mg 10009768-1 More Info
LY293111 A potent antagonist of the LTB4 receptor, BLT1, that inhibits the specific… 10 mg 10009768-10 More Info
LY293111 A potent antagonist of the LTB4 receptor, BLT1, that inhibits the specific… 5 mg 10009768-5 More Info
LY293111 A potent antagonist of the LTB4 receptor, BLT1, that inhibits the specific… 500 µg 10009768-500 More Info
LY294002 A selective PI3K inhibitor with an IC50 value of 1.4 µM 10 mg 70920-10 More Info
LY294002 A selective PI3K inhibitor with an IC50 value of 1.4 µM 25 mg 70920-25 More Info
LY294002 A selective PI3K inhibitor with an IC50 value of 1.4 µM 5 mg 70920-5 More Info
LY294002 A selective PI3K inhibitor with an IC50 value of 1.4 µM 50 mg 70920-50 More Info
LY2940680 A Smo antagonist; inhibits [35S]GTPγS binding in CHO cells expressin… 1 mg 16264-1 More Info
LY2940680 A Smo antagonist; inhibits [35S]GTPγS binding in CHO cells expressin… 10 mg 16264-10 More Info
LY2940680 A Smo antagonist; inhibits [35S]GTPγS binding in CHO cells expressin… 5 mg 16264-5 More Info
LY2955303 A potent RARγ antagonist (Ki = 1.1 nM); selective for RARγ ove… 1 mg 25833-1 More Info
LY2955303 A potent RARγ antagonist (Ki = 1.1 nM); selective for RARγ ove… 10 mg 25833-10 More Info
LY2955303 A potent RARγ antagonist (Ki = 1.1 nM); selective for RARγ ove… 25 mg 25833-25 More Info
LY2955303 A potent RARγ antagonist (Ki = 1.1 nM); selective for RARγ ove… 5 mg 25833-5 More Info
LY3000328 A potent cathepsin S inhibitor (IC50 = 7.7 nM for the human enzyme); selec… 1 mg 29729-1 More Info
LY3000328 A potent cathepsin S inhibitor (IC50 = 7.7 nM for the human enzyme); selec… 10 mg 29729-10 More Info
LY3000328 A potent cathepsin S inhibitor (IC50 = 7.7 nM for the human enzyme); selec… 5 mg 29729-5 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

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