MRS1845 |
An inhibitor of SOC channels (IC50 = 1.7 µM in HL-60 leukemia cells)… |
1 mg |
36814-1 |
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MRS1845 |
An inhibitor of SOC channels (IC50 = 1.7 µM in HL-60 leukemia cells)… |
10 mg |
36814-10 |
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MRS1845 |
An inhibitor of SOC channels (IC50 = 1.7 µM in HL-60 leukemia cells)… |
5 mg |
36814-5 |
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MRS1845 |
An inhibitor of SOC channels (IC50 = 1.7 µM in HL-60 leukemia cells)… |
500 µg |
36814-500 |
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MRS2578 |
A selective antagonist of the purinergic P2Y6 receptor (IC50s = 37 and 98… |
10 mg |
19704-10 |
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MRS2578 |
A selective antagonist of the purinergic P2Y6 receptor (IC50s = 37 and 98… |
25 mg |
19704-25 |
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MRS2578 |
A selective antagonist of the purinergic P2Y6 receptor (IC50s = 37 and 98… |
5 mg |
19704-5 |
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MRS2578 |
A selective antagonist of the purinergic P2Y6 receptor (IC50s = 37 and 98… |
50 mg |
19704-50 |
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MRS2179 (ammonium salt hydrate) |
A competitive purinergic P2Y1 receptor antagonist (Kb = 102 nM); selective… |
1 mg |
10011450-1 |
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MRS2179 (ammonium salt hydrate) |
A competitive purinergic P2Y1 receptor antagonist (Kb = 102 nM); selective… |
10 mg |
10011450-10 |
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MRS2179 (ammonium salt hydrate) |
A competitive purinergic P2Y1 receptor antagonist (Kb = 102 nM); selective… |
5 mg |
10011450-5 |
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MRT10 |
An antagonist of the Smo receptor (IC50 = 0.64 µM in a luciferase re… |
1 mg |
22138-1 |
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MRT10 |
An antagonist of the Smo receptor (IC50 = 0.64 µM in a luciferase re… |
10 mg |
22138-10 |
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MRT10 |
An antagonist of the Smo receptor (IC50 = 0.64 µM in a luciferase re… |
25 mg |
22138-25 |
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MRT10 |
An antagonist of the Smo receptor (IC50 = 0.64 µM in a luciferase re… |
5 mg |
22138-5 |
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MRT68921 |
An inhibitor of ULK1 and ULK2 (IC50s = 2.9 and 1.1 nM, respectively); bloc… |
1 mg |
19905-1 |
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MRT68921 |
An inhibitor of ULK1 and ULK2 (IC50s = 2.9 and 1.1 nM, respectively); bloc… |
10 mg |
19905-10 |
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MRT68921 |
An inhibitor of ULK1 and ULK2 (IC50s = 2.9 and 1.1 nM, respectively); bloc… |
25 mg |
19905-25 |
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MRT68921 |
An inhibitor of ULK1 and ULK2 (IC50s = 2.9 and 1.1 nM, respectively); bloc… |
5 mg |
19905-5 |
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MRT67307 (hydrochloride) |
A kinase inhibitor that inhibits TBK1, MARK1-4, IKKε, and NUAK1 (I… |
1 mg |
19916-1 |
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MRT67307 (hydrochloride) |
A kinase inhibitor that inhibits TBK1, MARK1-4, IKKε, and NUAK1 (I… |
10 mg |
19916-10 |
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MRT67307 (hydrochloride) |
A kinase inhibitor that inhibits TBK1, MARK1-4, IKKε, and NUAK1 (I… |
25 mg |
19916-25 |
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MRT67307 (hydrochloride) |
A kinase inhibitor that inhibits TBK1, MARK1-4, IKKε, and NUAK1 (I… |
5 mg |
19916-5 |
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MRTX-1133 |
An inhibitor of K-RasG12D; selectively reduces ERK phosphorylation in AsPC… |
1 mg |
36413-1 |
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MRTX-1133 |
An inhibitor of K-RasG12D; selectively reduces ERK phosphorylation in AsPC… |
10 mg |
36413-10 |
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MRTX-1133 |
An inhibitor of K-RasG12D; selectively reduces ERK phosphorylation in AsPC… |
5 mg |
36413-5 |
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MRTX-1257 |
A covalent inhibitor of K-RasG12C; inhibits proliferation of NCI H358 cell… |
1 mg |
33527-1 |
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MRTX-1257 |
A covalent inhibitor of K-RasG12C; inhibits proliferation of NCI H358 cell… |
10 mg |
33527-10 |
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MRTX-1257 |
A covalent inhibitor of K-RasG12C; inhibits proliferation of NCI H358 cell… |
25 mg |
33527-25 |
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MRTX-1257 |
A covalent inhibitor of K-RasG12C; inhibits proliferation of NCI H358 cell… |
5 mg |
33527-5 |
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MRTX-849 |
A covalent inhibitor of K-RasG12C; binds to and stabilizes GDP-bound inact… |
1 mg |
31440-1 |
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MRTX-849 |
A covalent inhibitor of K-RasG12C; binds to and stabilizes GDP-bound inact… |
10 mg |
31440-10 |
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MRTX-849 |
A covalent inhibitor of K-RasG12C; binds to and stabilizes GDP-bound inact… |
5 mg |
31440-5 |
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MRTX-0902 |
An inhibitor of the SOS1-K-RasG12C protein-protein interaction (Ki = 1.9 n… |
1 mg |
38578-1 |
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MRTX-0902 |
An inhibitor of the SOS1-K-RasG12C protein-protein interaction (Ki = 1.9 n… |
10 mg |
38578-10 |
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MRTX-0902 |
An inhibitor of the SOS1-K-RasG12C protein-protein interaction (Ki = 1.9 n… |
25 mg |
38578-25 |
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MRTX-0902 |
An inhibitor of the SOS1-K-RasG12C protein-protein interaction (Ki = 1.9 n… |
5 mg |
38578-5 |
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MRX-2843 |
A Mer and FLT3 inhibitor (IC50s = 1.3 and 1 nM, respectively); inhibits Ax… |
1 mg |
27923-1 |
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MRX-2843 |
A Mer and FLT3 inhibitor (IC50s = 1.3 and 1 nM, respectively); inhibits Ax… |
10 mg |
27923-10 |
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MRX-2843 |
A Mer and FLT3 inhibitor (IC50s = 1.3 and 1 nM, respectively); inhibits Ax… |
5 mg |
27923-5 |
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MS023 |
An inhibitor of type I PRMTs (IC50s = 30, 119, 83, 4, and 5 nM for PRMT1,… |
10 mg |
34786-10 |
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MS023 |
An inhibitor of type I PRMTs (IC50s = 30, 119, 83, 4, and 5 nM for PRMT1,… |
25 mg |
34786-25 |
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MS023 |
An inhibitor of type I PRMTs (IC50s = 30, 119, 83, 4, and 5 nM for PRMT1,… |
5 mg |
34786-5 |
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MS023 |
An inhibitor of type I PRMTs (IC50s = 30, 119, 83, 4, and 5 nM for PRMT1,… |
50 mg |
34786-50 |
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MS-1020 |
A cell-permeable inhibitor of JAK3, strongly inhibiting constitutive autop… |
1 mg |
14273-1 |
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MS1943 |
A PROTAC that drives EZH2 degradation; inhibits EZH2 (IC50 = 120 nM) and i… |
1 mg |
35466-1 |
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MS1943 |
A PROTAC that drives EZH2 degradation; inhibits EZH2 (IC50 = 120 nM) and i… |
10 mg |
35466-10 |
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MS1943 |
A PROTAC that drives EZH2 degradation; inhibits EZH2 (IC50 = 120 nM) and i… |
25 mg |
35466-25 |
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MS1943 |
A PROTAC that drives EZH2 degradation; inhibits EZH2 (IC50 = 120 nM) and i… |
5 mg |
35466-5 |
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MS-275 |
An inhibitor of HDACs that preferentially inhibits HDAC1 (IC50 = 300 nM) o… |
1 mg |
13284-1 |
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MS-275 |
An inhibitor of HDACs that preferentially inhibits HDAC1 (IC50 = 300 nM) o… |
10 mg |
13284-10 |
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MS-275 |
An inhibitor of HDACs that preferentially inhibits HDAC1 (IC50 = 300 nM) o… |
25 mg |
13284-25 |
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MS-275 |
An inhibitor of HDACs that preferentially inhibits HDAC1 (IC50 = 300 nM) o… |
5 mg |
13284-5 |
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MS37452 |
A competitive inhibitor of CBX7 chromodomain binding to H3K27me3 (Ki = 43… |
1 mg |
17533-1 |
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MS37452 |
A competitive inhibitor of CBX7 chromodomain binding to H3K27me3 (Ki = 43… |
10 mg |
17533-10 |
More Info
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MS37452 |
A competitive inhibitor of CBX7 chromodomain binding to H3K27me3 (Ki = 43… |
25 mg |
17533-25 |
More Info
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MS37452 |
A competitive inhibitor of CBX7 chromodomain binding to H3K27me3 (Ki = 43… |
5 mg |
17533-5 |
More Info
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MSA-2 |
A STING agonist; binds to wild-type and HAQ variant STING in a 3H-cGAMP fi… |
1 mg |
30140-1 |
More Info
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MSA-2 |
A STING agonist; binds to wild-type and HAQ variant STING in a 3H-cGAMP fi… |
10 mg |
30140-10 |
More Info
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MSA-2 |
A STING agonist; binds to wild-type and HAQ variant STING in a 3H-cGAMP fi… |
5 mg |
30140-5 |
More Info
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MSAB |
An inhibitor of Wnt/β-catenin signaling; selectively inhibits the pro… |
10 mg |
36497-10 |
More Info
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MSAB |
An inhibitor of Wnt/β-catenin signaling; selectively inhibits the pro… |
100 mg |
36497-100 |
More Info
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MSAB |
An inhibitor of Wnt/β-catenin signaling; selectively inhibits the pro… |
25 mg |
36497-25 |
More Info
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MSAB |
An inhibitor of Wnt/β-catenin signaling; selectively inhibits the pro… |
50 mg |
36497-50 |
More Info
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MSC2530818 |
A Cdk8 inhibitor (IC50 = 2.6 nM); selective for Cdk8 over a panel of 264 k… |
1 mg |
29669-1 |
More Info
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MSC2530818 |
A Cdk8 inhibitor (IC50 = 2.6 nM); selective for Cdk8 over a panel of 264 k… |
10 mg |
29669-10 |
More Info
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MSC2530818 |
A Cdk8 inhibitor (IC50 = 2.6 nM); selective for Cdk8 over a panel of 264 k… |
25 mg |
29669-25 |
More Info
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MSC2530818 |
A Cdk8 inhibitor (IC50 = 2.6 nM); selective for Cdk8 over a panel of 264 k… |
5 mg |
29669-5 |
More Info
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MSDC-0160 |
A thiazolidinedione; inactivates MPC (IC50 = 1.2 µM) without affecti… |
1 mg |
71748-1 |
More Info
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MSDC-0160 |
A thiazolidinedione; inactivates MPC (IC50 = 1.2 µM) without affecti… |
10 mg |
71748-10 |
More Info
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MSDC-0160 |
A thiazolidinedione; inactivates MPC (IC50 = 1.2 µM) without affecti… |
5 mg |
71748-5 |
More Info
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MSDC-0602 |
A PPARγ-sparing thiazolidinedione derivative; binds only weakly to P… |
10 mg |
27829-10 |
More Info
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MSDC-0602 |
A PPARγ-sparing thiazolidinedione derivative; binds only weakly to P… |
100 mg |
27829-100 |
More Info
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MSDC-0602 |
A PPARγ-sparing thiazolidinedione derivative; binds only weakly to P… |
25 mg |
27829-25 |
More Info
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MSDC-0602 |
A PPARγ-sparing thiazolidinedione derivative; binds only weakly to P… |
50 mg |
27829-50 |
More Info
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