CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 784 of 1
Non-Antibody Products
Page 784 of 1,288
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| MRS2179 (ammonium salt hydrate) | A competitive purinergic P2Y1 receptor antagonist (Kb = 102 nM); selective… | 1 mg | 10011450-1 | More Info |
| MRS2179 (ammonium salt hydrate) | A competitive purinergic P2Y1 receptor antagonist (Kb = 102 nM); selective… | 10 mg | 10011450-10 | More Info |
| MRS2179 (ammonium salt hydrate) | A competitive purinergic P2Y1 receptor antagonist (Kb = 102 nM); selective… | 5 mg | 10011450-5 | More Info |
| MRT10 | An antagonist of the Smo receptor (IC50 = 0.64 µM in a luciferase re… | 1 mg | 22138-1 | More Info |
| MRT10 | An antagonist of the Smo receptor (IC50 = 0.64 µM in a luciferase re… | 10 mg | 22138-10 | More Info |
| MRT10 | An antagonist of the Smo receptor (IC50 = 0.64 µM in a luciferase re… | 25 mg | 22138-25 | More Info |
| MRT10 | An antagonist of the Smo receptor (IC50 = 0.64 µM in a luciferase re… | 5 mg | 22138-5 | More Info |
| MRT68921 | An inhibitor of ULK1 and ULK2 (IC50s = 2.9 and 1.1 nM, respectively); bloc… | 1 mg | 19905-1 | More Info |
| MRT68921 | An inhibitor of ULK1 and ULK2 (IC50s = 2.9 and 1.1 nM, respectively); bloc… | 10 mg | 19905-10 | More Info |
| MRT68921 | An inhibitor of ULK1 and ULK2 (IC50s = 2.9 and 1.1 nM, respectively); bloc… | 25 mg | 19905-25 | More Info |
| MRT68921 | An inhibitor of ULK1 and ULK2 (IC50s = 2.9 and 1.1 nM, respectively); bloc… | 5 mg | 19905-5 | More Info |
| MRT67307 (hydrochloride) | A kinase inhibitor that inhibits TBK1, MARK1-4, IKKε, and NUAK1 (I… | 1 mg | 19916-1 | More Info |
| MRT67307 (hydrochloride) | A kinase inhibitor that inhibits TBK1, MARK1-4, IKKε, and NUAK1 (I… | 10 mg | 19916-10 | More Info |
| MRT67307 (hydrochloride) | A kinase inhibitor that inhibits TBK1, MARK1-4, IKKε, and NUAK1 (I… | 25 mg | 19916-25 | More Info |
| MRT67307 (hydrochloride) | A kinase inhibitor that inhibits TBK1, MARK1-4, IKKε, and NUAK1 (I… | 5 mg | 19916-5 | More Info |
| MRTX-1133 | An inhibitor of K-RasG12D; selectively reduces ERK phosphorylation in AsPC… | 1 mg | 36413-1 | More Info |
| MRTX-1133 | An inhibitor of K-RasG12D; selectively reduces ERK phosphorylation in AsPC… | 10 mg | 36413-10 | More Info |
| MRTX-1133 | An inhibitor of K-RasG12D; selectively reduces ERK phosphorylation in AsPC… | 5 mg | 36413-5 | More Info |
| MRTX-1257 | A covalent inhibitor of K-RasG12C; inhibits proliferation of NCI H358 cell… | 1 mg | 33527-1 | More Info |
| MRTX-1257 | A covalent inhibitor of K-RasG12C; inhibits proliferation of NCI H358 cell… | 10 mg | 33527-10 | More Info |
| MRTX-1257 | A covalent inhibitor of K-RasG12C; inhibits proliferation of NCI H358 cell… | 25 mg | 33527-25 | More Info |
| MRTX-1257 | A covalent inhibitor of K-RasG12C; inhibits proliferation of NCI H358 cell… | 5 mg | 33527-5 | More Info |
| MRTX-849 | A covalent inhibitor of K-RasG12C; binds to and stabilizes GDP-bound inact… | 1 mg | 31440-1 | More Info |
| MRTX-849 | A covalent inhibitor of K-RasG12C; binds to and stabilizes GDP-bound inact… | 10 mg | 31440-10 | More Info |
| MRTX-849 | A covalent inhibitor of K-RasG12C; binds to and stabilizes GDP-bound inact… | 5 mg | 31440-5 | More Info |
| MRTX-0902 | An inhibitor of the SOS1-K-RasG12C protein-protein interaction (Ki = 1.9 n… | 1 mg | 38578-1 | More Info |
| MRTX-0902 | An inhibitor of the SOS1-K-RasG12C protein-protein interaction (Ki = 1.9 n… | 10 mg | 38578-10 | More Info |
| MRTX-0902 | An inhibitor of the SOS1-K-RasG12C protein-protein interaction (Ki = 1.9 n… | 25 mg | 38578-25 | More Info |
| MRTX-0902 | An inhibitor of the SOS1-K-RasG12C protein-protein interaction (Ki = 1.9 n… | 5 mg | 38578-5 | More Info |
| MRX-2843 | A Mer and FLT3 inhibitor (IC50s = 1.3 and 1 nM, respectively); inhibits Ax… | 1 mg | 27923-1 | More Info |
| MRX-2843 | A Mer and FLT3 inhibitor (IC50s = 1.3 and 1 nM, respectively); inhibits Ax… | 10 mg | 27923-10 | More Info |
| MRX-2843 | A Mer and FLT3 inhibitor (IC50s = 1.3 and 1 nM, respectively); inhibits Ax… | 5 mg | 27923-5 | More Info |
| MS023 | An inhibitor of type I PRMTs (IC50s = 30, 119, 83, 4, and 5 nM for PRMT1,… | 10 mg | 34786-10 | More Info |
| MS023 | An inhibitor of type I PRMTs (IC50s = 30, 119, 83, 4, and 5 nM for PRMT1,… | 25 mg | 34786-25 | More Info |
| MS023 | An inhibitor of type I PRMTs (IC50s = 30, 119, 83, 4, and 5 nM for PRMT1,… | 5 mg | 34786-5 | More Info |
| MS023 | An inhibitor of type I PRMTs (IC50s = 30, 119, 83, 4, and 5 nM for PRMT1,… | 50 mg | 34786-50 | More Info |
| MS-1020 | A cell-permeable inhibitor of JAK3, strongly inhibiting constitutive autop… | 1 mg | 14273-1 | More Info |
| MS1943 | A PROTAC that drives EZH2 degradation; inhibits EZH2 (IC50 = 120 nM) and i… | 1 mg | 35466-1 | More Info |
| MS1943 | A PROTAC that drives EZH2 degradation; inhibits EZH2 (IC50 = 120 nM) and i… | 10 mg | 35466-10 | More Info |
| MS1943 | A PROTAC that drives EZH2 degradation; inhibits EZH2 (IC50 = 120 nM) and i… | 25 mg | 35466-25 | More Info |
| MS1943 | A PROTAC that drives EZH2 degradation; inhibits EZH2 (IC50 = 120 nM) and i… | 5 mg | 35466-5 | More Info |
| MS-275 | An inhibitor of HDACs that preferentially inhibits HDAC1 (IC50 = 300 nM) o… | 1 mg | 13284-1 | More Info |
| MS-275 | An inhibitor of HDACs that preferentially inhibits HDAC1 (IC50 = 300 nM) o… | 10 mg | 13284-10 | More Info |
| MS-275 | An inhibitor of HDACs that preferentially inhibits HDAC1 (IC50 = 300 nM) o… | 25 mg | 13284-25 | More Info |
| MS-275 | An inhibitor of HDACs that preferentially inhibits HDAC1 (IC50 = 300 nM) o… | 5 mg | 13284-5 | More Info |
| MS37452 | A competitive inhibitor of CBX7 chromodomain binding to H3K27me3 (Ki = 43… | 1 mg | 17533-1 | More Info |
| MS37452 | A competitive inhibitor of CBX7 chromodomain binding to H3K27me3 (Ki = 43… | 10 mg | 17533-10 | More Info |
| MS37452 | A competitive inhibitor of CBX7 chromodomain binding to H3K27me3 (Ki = 43… | 25 mg | 17533-25 | More Info |
| MS37452 | A competitive inhibitor of CBX7 chromodomain binding to H3K27me3 (Ki = 43… | 5 mg | 17533-5 | More Info |
| MSA-2 | A STING agonist; binds to wild-type and HAQ variant STING in a 3H-cGAMP fi… | 1 mg | 30140-1 | 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
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