CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 859 of 870
Non-Antibody Products
Page 859 of 870
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| 1-(2,6-Xylyl)-2-thiourea | An analytical reference standard categorized as an anesthetic metabolite;… | 10 mg | 39373-10 | More Info |
| 1-(2,6-Xylyl)-2-thiourea | An analytical reference standard categorized as an anesthetic metabolite;… | 50 mg | 39373-50 | More Info |
| Y11 | Inhibits FAK1 autophosphorylation by blocking phosphorylation of Y397; dec… | 1 mg | 18521-1 | More Info |
| Y11 | Inhibits FAK1 autophosphorylation by blocking phosphorylation of Y397; dec… | 10 mg | 18521-10 | More Info |
| Y11 | Inhibits FAK1 autophosphorylation by blocking phosphorylation of Y397; dec… | 25 mg | 18521-25 | More Info |
| Y11 | Inhibits FAK1 autophosphorylation by blocking phosphorylation of Y397; dec… | 5 mg | 18521-5 | More Info |
| Y-26763 | An activator of KATP channels; increases the frequency of KATP channel ope… | 1 mg | 21459-1 | More Info |
| Y-26763 | An activator of KATP channels; increases the frequency of KATP channel ope… | 10 mg | 21459-10 | More Info |
| Y-26763 | An activator of KATP channels; increases the frequency of KATP channel ope… | 5 mg | 21459-5 | More Info |
| Y320 | An inhibitor of the release of IL-17 by CD4 T cells stimulated with IL-15,… | 1 mg | 16314-1 | More Info |
| Y320 | An inhibitor of the release of IL-17 by CD4 T cells stimulated with IL-15,… | 10 mg | 16314-10 | More Info |
| Y320 | An inhibitor of the release of IL-17 by CD4 T cells stimulated with IL-15,… | 25 mg | 16314-25 | More Info |
| Y320 | An inhibitor of the release of IL-17 by CD4 T cells stimulated with IL-15,… | 5 mg | 16314-5 | More Info |
| Y-33075 | An inhibitor of ROCK2 (IC50 = 3.6 nM); selective for ROCK2 over PKC and Ca… | 1 mg | 35108-1 | More Info |
| Y-33075 | An inhibitor of ROCK2 (IC50 = 3.6 nM); selective for ROCK2 over PKC and Ca… | 10 mg | 35108-10 | More Info |
| Y-33075 | An inhibitor of ROCK2 (IC50 = 3.6 nM); selective for ROCK2 over PKC and Ca… | 5 mg | 35108-5 | More Info |
| Yamogenin | A steroidal sapogenin with diverse biological activities; inhibits T090131… | 1 mg | 36008-1 | More Info |
| Yamogenin | A steroidal sapogenin with diverse biological activities; inhibits T090131… | 10 mg | 36008-10 | More Info |
| Yamogenin | A steroidal sapogenin with diverse biological activities; inhibits T090131… | 25 mg | 36008-25 | More Info |
| Yamogenin | A steroidal sapogenin with diverse biological activities; inhibits T090131… | 5 mg | 36008-5 | More Info |
| Yangonin | A natural kavalactone that enhances the binding of bicuculline at the GABA… | 1 mg | 14351-1 | More Info |
| Yangonin | A natural kavalactone that enhances the binding of bicuculline at the GABA… | 10 mg | 14351-10 | More Info |
| Yangonin | A natural kavalactone that enhances the binding of bicuculline at the GABA… | 25 mg | 14351-25 | More Info |
| Yangonin | A natural kavalactone that enhances the binding of bicuculline at the GABA… | 5 mg | 14351-5 | More Info |
| Yangonin | An analytical reference standard categorized as a kavalactone; intended fo… | 1 mg | 33883-1 | More Info |
| Yangonin | An analytical reference standard categorized as a kavalactone; intended fo… | 5 mg | 33883-5 | More Info |
| Yatein | A lignan with diverse biological activities; inhibits CYP3A4 (IC50 = 1 &mi… | 1 mg | 29766-1 | More Info |
| Yatein | A lignan with diverse biological activities; inhibits CYP3A4 (IC50 = 1 &mi… | 500 µg | 29766-500 | More Info |
| YC-1 | YC-1 is an NO-independent activator of soluble guanylyl cyclase. It inhibi… | 1 mg | 81560-1 | More Info |
| YC-1 | YC-1 is an NO-independent activator of soluble guanylyl cyclase. It inhibi… | 10 mg | 81560-10 | More Info |
| YC-1 | YC-1 is an NO-independent activator of soluble guanylyl cyclase. It inhibi… | 5 mg | 81560-5 | More Info |
| YC-1 | YC-1 is an NO-independent activator of soluble guanylyl cyclase. It inhibi… | 50 mg | 81560-50 | More Info |
| YCH1899 | A PARP1 and PARP2 inhibitor (IC50s = 50s = 1-14.1 nM); inhibits the prolif… | 1 mg | 39737-1 | More Info |
| YCH1899 | A PARP1 and PARP2 inhibitor (IC50s = 50s = 1-14.1 nM); inhibits the prolif… | 10 mg | 39737-10 | More Info |
| YCH1899 | A PARP1 and PARP2 inhibitor (IC50s = 50s = 1-14.1 nM); inhibits the prolif… | 5 mg | 39737-5 | More Info |
| YCT529 | A RARα antagonist (IC50 = 6.8 nM); selective for RARα over RAR… | 1 mg | 39995-1 | More Info |
| YCT529 | A RARα antagonist (IC50 = 6.8 nM); selective for RARα over RAR… | 5 mg | 39995-5 | More Info |
| YE 120 | An agonist of GPR35 (EC50 = 32 nM in a DMR assay using HT-29 cells); induc… | 1 mg | 29720-1 | More Info |
| YE 120 | An agonist of GPR35 (EC50 = 32 nM in a DMR assay using HT-29 cells); induc… | 5 mg | 29720-5 | More Info |
| YF-2 | A HAT activator; inhibits proliferation of CCRF-CEM, Hs 578T, A549, U251,… | 1 mg | 31230-1 | More Info |
| YF-2 | A HAT activator; inhibits proliferation of CCRF-CEM, Hs 578T, A549, U251,… | 10 mg | 31230-10 | More Info |
| YF-2 | A HAT activator; inhibits proliferation of CCRF-CEM, Hs 578T, A549, U251,… | 25 mg | 31230-25 | More Info |
| YF-2 | A HAT activator; inhibits proliferation of CCRF-CEM, Hs 578T, A549, U251,… | 5 mg | 31230-5 | More Info |
| YH 239-EE | A prodrug form of YH 239; inhibits the growth of OCI-AML-3 cells and halts… | 10 mg | 27678-10 | More Info |
| YH 239-EE | A prodrug form of YH 239; inhibits the growth of OCI-AML-3 cells and halts… | 25 mg | 27678-25 | More Info |
| YH 239-EE | A prodrug form of YH 239; inhibits the growth of OCI-AML-3 cells and halts… | 5 mg | 27678-5 | More Info |
| YH 239-EE | A prodrug form of YH 239; inhibits the growth of OCI-AML-3 cells and halts… | 50 mg | 27678-50 | More Info |
| Y-27632 (hydrochloride) | A potent, ATP-competitive inhibitor of ROCKs including p160ROCK (Ki = 140… | 1 mg | 10005583-1 | More Info |
| Y-27632 (hydrochloride) | A potent, ATP-competitive inhibitor of ROCKs including p160ROCK (Ki = 140… | 10 mg | 10005583-10 | More Info |
| Y-27632 (hydrochloride) | A potent, ATP-competitive inhibitor of ROCKs including p160ROCK (Ki = 140… | 5 mg | 10005583-5 | More Info |
| 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 |
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
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