CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 708 of 1
Non-Antibody Products
Page 708 of 1,304
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| LY2562175 | An FXR agonist (EC50 = 193 nM in a reporter assay); selective for FXR over… | 10 mg | 28912-10 | More Info |
| LY2562175 | An FXR agonist (EC50 = 193 nM in a reporter assay); selective for FXR over… | 25 mg | 28912-25 | More Info |
| LY2562175 | An FXR agonist (EC50 = 193 nM in a reporter assay); selective for FXR over… | 5 mg | 28912-5 | More Info |
| LY2603618 | A Chk1 inhibitor (IC50 = 7 nM) that prevents the repair of DNA caused by D… | 10 mg | 20351-10 | More Info |
| LY2603618 | A Chk1 inhibitor (IC50 = 7 nM) that prevents the repair of DNA caused by D… | 25 mg | 20351-25 | More Info |
| LY2603618 | A Chk1 inhibitor (IC50 = 7 nM) that prevents the repair of DNA caused by D… | 5 mg | 20351-5 | More Info |
| LY2603618 | A Chk1 inhibitor (IC50 = 7 nM) that prevents the repair of DNA caused by D… | 50 mg | 20351-50 | More Info |
| LY2606368 | A Chk1 inhibitor (Ki = 0.9 nM); IC50 values of 2 / M checkpoint in HeLa ce… | 1 mg | 21490-1 | More Info |
| LY2606368 | A Chk1 inhibitor (Ki = 0.9 nM); IC50 values of 2 / M checkpoint in HeLa ce… | 10 mg | 21490-10 | More Info |
| LY2606368 | A Chk1 inhibitor (Ki = 0.9 nM); IC50 values of 2 / M checkpoint in HeLa ce… | 25 mg | 21490-25 | More Info |
| LY2606368 | A Chk1 inhibitor (Ki = 0.9 nM); IC50 values of 2 / M checkpoint in HeLa ce… | 5 mg | 21490-5 | More Info |
| LY2608204 | An activator of glucokinase (EC50 = 42 nM); stimulates glucose metabolism… | 1 mg | 22914-1 | More Info |
| LY2608204 | An activator of glucokinase (EC50 = 42 nM); stimulates glucose metabolism… | 10 mg | 22914-10 | More Info |
| LY2608204 | An activator of glucokinase (EC50 = 42 nM); stimulates glucose metabolism… | 25 mg | 22914-25 | More Info |
| LY2608204 | An activator of glucokinase (EC50 = 42 nM); stimulates glucose metabolism… | 5 mg | 22914-5 | More Info |
| LY272015 | A 5-HT2B receptor antagonist; binds to 5-HT2B receptors in isolated rat fu… | 1 mg | 31471-1 | More Info |
| LY272015 | A 5-HT2B receptor antagonist; binds to 5-HT2B receptors in isolated rat fu… | 5 mg | 31471-5 | More Info |
| LY2784544 | A potent, ATP-competitive inhibitor of JAK2 that less effectively inhibits… | 1 mg | 16705-1 | More Info |
| LY2784544 | A potent, ATP-competitive inhibitor of JAK2 that less effectively inhibits… | 10 mg | 16705-10 | More Info |
| LY2784544 | A potent, ATP-competitive inhibitor of JAK2 that less effectively inhibits… | 25 mg | 16705-25 | More Info |
| LY2784544 | A potent, ATP-competitive inhibitor of JAK2 that less effectively inhibits… | 5 mg | 16705-5 | More Info |
| 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 |
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
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