CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 1 of 1
Non-Antibody Products
Page 1,289 of 1,304
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| Y-27632 (hydrochloride) | A potent, ATP-competitive inhibitor of ROCKs including p160ROCK (Ki = 140… | 50 mg | 10005583-50 | More Info |
| Y-33075 (hydrochloride) | An inhibitor of ROCK2 (IC50 = 3.6 nM); selective for ROCK2 over PKC and Ca… | 1 mg | 36216-1 | More Info |
| Y-33075 (hydrochloride) | An inhibitor of ROCK2 (IC50 = 3.6 nM); selective for ROCK2 over PKC and Ca… | 10 mg | 36216-10 | More Info |
| Y-33075 (hydrochloride) | An inhibitor of ROCK2 (IC50 = 3.6 nM); selective for ROCK2 over PKC and Ca… | 25 mg | 36216-25 | More Info |
| Y-33075 (hydrochloride) | An inhibitor of ROCK2 (IC50 = 3.6 nM); selective for ROCK2 over PKC and Ca… | 5 mg | 36216-5 | More Info |
| YIL 781 (hydrochloride) | An antagonist of GHS-R1a (Ki = 0.017 µM); selective for GHS-R1a over… | 1 mg | 29217-1 | More Info |
| YIL 781 (hydrochloride) | An antagonist of GHS-R1a (Ki = 0.017 µM); selective for GHS-R1a over… | 10 mg | 29217-10 | More Info |
| YIL 781 (hydrochloride) | An antagonist of GHS-R1a (Ki = 0.017 µM); selective for GHS-R1a over… | 25 mg | 29217-25 | More Info |
| YIL 781 (hydrochloride) | An antagonist of GHS-R1a (Ki = 0.017 µM); selective for GHS-R1a over… | 5 mg | 29217-5 | More Info |
| YK-009 | An ionizable cationic lipid (pKa = 6.512); administration of SARS-CoV-2 Om… | 1 mg | 38282-1 | More Info |
| YK-009 | An ionizable cationic lipid (pKa = 6.512); administration of SARS-CoV-2 Om… | 10 mg | 38282-10 | More Info |
| YK-009 | An ionizable cationic lipid (pKa = 6.512); administration of SARS-CoV-2 Om… | 5 mg | 38282-5 | More Info |
| YK-11 | A partial agonist of the androgen receptor; activates androgen receptor tr… | 10 mg | 9003137-10 | More Info |
| YK-11 | A partial agonist of the androgen receptor; activates androgen receptor tr… | 100 mg | 9003137-100 | More Info |
| YK-11 | A partial agonist of the androgen receptor; activates androgen receptor tr… | 50 mg | 9003137-50 | More Info |
| YK-3-237 | An inhibitor of tubulin polymerization and an activator of SIRT1; inhibits… | 1 mg | 21516-1 | More Info |
| YK-3-237 | An inhibitor of tubulin polymerization and an activator of SIRT1; inhibits… | 10 mg | 21516-10 | More Info |
| YK-3-237 | An inhibitor of tubulin polymerization and an activator of SIRT1; inhibits… | 25 mg | 21516-25 | More Info |
| YK-3-237 | An inhibitor of tubulin polymerization and an activator of SIRT1; inhibits… | 5 mg | 21516-5 | More Info |
| YKL-05-099 | An inhibitor of SIK2 (IC50 = 0.04 µM for the human enzyme); selectiv… | 10 mg | 36116-10 | More Info |
| YKL-05-099 | An inhibitor of SIK2 (IC50 = 0.04 µM for the human enzyme); selectiv… | 25 mg | 36116-25 | More Info |
| YKL-05-099 | An inhibitor of SIK2 (IC50 = 0.04 µM for the human enzyme); selectiv… | 5 mg | 36116-5 | More Info |
| YKL-05-099 | An inhibitor of SIK2 (IC50 = 0.04 µM for the human enzyme); selectiv… | 50 mg | 36116-50 | More Info |
| YL-109 | An anticancer agent; inhibits the proliferation of MCF-7 and MDA-MB-231 ce… | 10 mg | 30290-10 | More Info |
| YL-109 | An anticancer agent; inhibits the proliferation of MCF-7 and MDA-MB-231 ce… | 25 mg | 30290-25 | More Info |
| YL-109 | An anticancer agent; inhibits the proliferation of MCF-7 and MDA-MB-231 ce… | 5 mg | 30290-5 | More Info |
| YL-109 | An anticancer agent; inhibits the proliferation of MCF-7 and MDA-MB-231 ce… | 50 mg | 30290-50 | More Info |
| YLF-466D | An AMPK activator at a concentration of 150 µM in platelets; inhibit… | 1 mg | 19475-1 | More Info |
| YLF-466D | An AMPK activator at a concentration of 150 µM in platelets; inhibit… | 10 mg | 19475-10 | More Info |
| YLF-466D | An AMPK activator at a concentration of 150 µM in platelets; inhibit… | 5 mg | 19475-5 | More Info |
| YM-155 | A small molecule that suppresses transactivation of survivin through direc… | 1 mg | 11490-1 | More Info |
| YM-155 | A small molecule that suppresses transactivation of survivin through direc… | 10 mg | 11490-10 | More Info |
| YM-155 | A small molecule that suppresses transactivation of survivin through direc… | 25 mg | 11490-25 | More Info |
| YM-155 | A small molecule that suppresses transactivation of survivin through direc… | 5 mg | 11490-5 | More Info |
| YM-201636 | A cell-permeable and selective inhibitor of PIKfyve (IC50 = 33 nM); revers… | 1 mg | 13576-1 | More Info |
| YM-201636 | A cell-permeable and selective inhibitor of PIKfyve (IC50 = 33 nM); revers… | 10 mg | 13576-10 | More Info |
| YM-201636 | A cell-permeable and selective inhibitor of PIKfyve (IC50 = 33 nM); revers… | 5 mg | 13576-5 | More Info |
| YM-254890 | A cyclic depsipeptide Gαq / 11 inhibitor; inhibits Gαq / 11-me… | 1 mg | 29735-1 | More Info |
| YM-26734 | A competitive sPLA2-IIA inhibitor with IC50 values of 80, 30, 120, 110, 52… | 1 mg | 17631-1 | More Info |
| YM-26734 | A competitive sPLA2-IIA inhibitor with IC50 values of 80, 30, 120, 110, 52… | 10 mg | 17631-10 | More Info |
| YM-26734 | A competitive sPLA2-IIA inhibitor with IC50 values of 80, 30, 120, 110, 52… | 25 mg | 17631-25 | More Info |
| YM-26734 | A competitive sPLA2-IIA inhibitor with IC50 values of 80, 30, 120, 110, 52… | 5 mg | 17631-5 | More Info |
| YM-53601 | A squalene synthase inhibitor (IC50s = 79 and 90 nM in HepG2 cells and rat… | 1 mg | 18113-1 | More Info |
| YM-53601 | A squalene synthase inhibitor (IC50s = 79 and 90 nM in HepG2 cells and rat… | 5 mg | 18113-5 | More Info |
| YM-53601 | A squalene synthase inhibitor (IC50s = 79 and 90 nM in HepG2 cells and rat… | 500 µg | 18113-500 | More Info |
| YM-58483 | A potent inhibitor of calcium release-activated calcium channels in lympho… | 1 mg | 13246-1 | More Info |
| YM-58483 | A potent inhibitor of calcium release-activated calcium channels in lympho… | 10 mg | 13246-10 | More Info |
| YM-58483 | A potent inhibitor of calcium release-activated calcium channels in lympho… | 25 mg | 13246-25 | More Info |
| YM-58483 | A potent inhibitor of calcium release-activated calcium channels in lympho… | 5 mg | 13246-5 | More Info |
| YM-90709 | An IL-5 receptor antagonist (IC50s = 1 and 0.57 µM for peripheral hu… | 10 mg | 23448-10 | 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
http://www.caymanchem.com
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