NS 9283 |
A positive allosteric modulator of α4β2 subunit-containing nACh… |
1 mg |
29189-1 |
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NS 9283 |
A positive allosteric modulator of α4β2 subunit-containing nACh… |
10 mg |
29189-10 |
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NS 9283 |
A positive allosteric modulator of α4β2 subunit-containing nACh… |
25 mg |
29189-25 |
More Info
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NS 9283 |
A positive allosteric modulator of α4β2 subunit-containing nACh… |
5 mg |
29189-5 |
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NS 3728 |
A chloride channel inhibitor; inhibits VRAC in HEK293 cells and chloride c… |
10 mg |
39988-10 |
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NS 3728 |
A chloride channel inhibitor; inhibits VRAC in HEK293 cells and chloride c… |
25 mg |
39988-25 |
More Info
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NS 3728 |
A chloride channel inhibitor; inhibits VRAC in HEK293 cells and chloride c… |
5 mg |
39988-5 |
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NS 3728 |
A chloride channel inhibitor; inhibits VRAC in HEK293 cells and chloride c… |
50 mg |
39988-50 |
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NSC 109555 |
An inhibitor of Chk2 (IC50 = 200 nM in a cell-free kinase assay); selectiv… |
1 mg |
19811-1 |
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NSC 109555 |
An inhibitor of Chk2 (IC50 = 200 nM in a cell-free kinase assay); selectiv… |
10 mg |
19811-10 |
More Info
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NSC 109555 |
An inhibitor of Chk2 (IC50 = 200 nM in a cell-free kinase assay); selectiv… |
5 mg |
19811-5 |
More Info
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NSC 109555 |
An inhibitor of Chk2 (IC50 = 200 nM in a cell-free kinase assay); selectiv… |
50 mg |
19811-50 |
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NSC 12 |
An extracellular trap for FGF2 that binds FGF2 (Kd = 51 µM) and inte… |
1 mg |
20117-1 |
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NSC 12 |
An extracellular trap for FGF2 that binds FGF2 (Kd = 51 µM) and inte… |
10 mg |
20117-10 |
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NSC 12 |
An extracellular trap for FGF2 that binds FGF2 (Kd = 51 µM) and inte… |
25 mg |
20117-25 |
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NSC 12 |
An extracellular trap for FGF2 that binds FGF2 (Kd = 51 µM) and inte… |
5 mg |
20117-5 |
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NSC 15520 |
A small molecule inhibitor of RPA70 dsDNA binding; selectively inhibits ds… |
1 mg |
26020-1 |
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NSC 15520 |
A small molecule inhibitor of RPA70 dsDNA binding; selectively inhibits ds… |
10 mg |
26020-10 |
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NSC 15520 |
A small molecule inhibitor of RPA70 dsDNA binding; selectively inhibits ds… |
25 mg |
26020-25 |
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NSC 15520 |
A small molecule inhibitor of RPA70 dsDNA binding; selectively inhibits ds… |
5 mg |
26020-5 |
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NSC 185058 |
An inhibitor of ATG4B; inhibits ATG4B cleavage of LC3B-GST (IC50 = 51 &mic… |
1 mg |
23957-1 |
More Info
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NSC 185058 |
An inhibitor of ATG4B; inhibits ATG4B cleavage of LC3B-GST (IC50 = 51 &mic… |
5 mg |
23957-5 |
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NSC 19005 |
A potential impurity found in commercial preparations of betahistine; a de… |
100 mg |
32898-100 |
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NSC 19005 |
A potential impurity found in commercial preparations of betahistine; a de… |
25 mg |
32898-25 |
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NSC 19005 |
A potential impurity found in commercial preparations of betahistine; a de… |
250 mg |
32898-250 |
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NSC 19005 |
A potential impurity found in commercial preparations of betahistine; a de… |
50 mg |
32898-50 |
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NSC 207895 |
An inhibitor of MDMX; decreases MDMX promoter activity in a reporter assay… |
1 mg |
27949-1 |
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NSC 207895 |
An inhibitor of MDMX; decreases MDMX promoter activity in a reporter assay… |
10 mg |
27949-10 |
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NSC 207895 |
An inhibitor of MDMX; decreases MDMX promoter activity in a reporter assay… |
25 mg |
27949-25 |
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NSC 207895 |
An inhibitor of MDMX; decreases MDMX promoter activity in a reporter assay… |
5 mg |
27949-5 |
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NSC 210902 |
A selective CK2 inhibitor (IC50 = 1 µM); selective for CK2 over JNK3… |
1 mg |
10011255-1 |
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NSC 210902 |
A selective CK2 inhibitor (IC50 = 1 µM); selective for CK2 over JNK3… |
10 mg |
10011255-10 |
More Info
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NSC 210902 |
A selective CK2 inhibitor (IC50 = 1 µM); selective for CK2 over JNK3… |
5 mg |
10011255-5 |
More Info
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NSC 210902 |
A selective CK2 inhibitor (IC50 = 1 µM); selective for CK2 over JNK3… |
50 mg |
10011255-50 |
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NSC 228155 |
An activator of EGFR and an inhibitor of the interaction between the KID o… |
10 mg |
28856-10 |
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NSC 228155 |
An activator of EGFR and an inhibitor of the interaction between the KID o… |
25 mg |
28856-25 |
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NSC 228155 |
An activator of EGFR and an inhibitor of the interaction between the KID o… |
5 mg |
28856-5 |
More Info
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NSC 232003 |
An inhibitor of the UHRF1-DNMT1 protein-protein interaction (IC50 = 15 &mi… |
1 mg |
38523-1 |
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NSC 232003 |
An inhibitor of the UHRF1-DNMT1 protein-protein interaction (IC50 = 15 &mi… |
10 mg |
38523-10 |
More Info
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NSC 232003 |
An inhibitor of the UHRF1-DNMT1 protein-protein interaction (IC50 = 15 &mi… |
25 mg |
38523-25 |
More Info
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NSC 232003 |
An inhibitor of the UHRF1-DNMT1 protein-protein interaction (IC50 = 15 &mi… |
5 mg |
38523-5 |
More Info
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NSC 23925 |
An inhibitor of P-gp; selectively reverses multidrug resistance mediated b… |
1 mg |
21947-1 |
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NSC 23925 |
An inhibitor of P-gp; selectively reverses multidrug resistance mediated b… |
10 mg |
21947-10 |
More Info
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NSC 23925 |
An inhibitor of P-gp; selectively reverses multidrug resistance mediated b… |
25 mg |
21947-25 |
More Info
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NSC 23925 |
An inhibitor of P-gp; selectively reverses multidrug resistance mediated b… |
5 mg |
21947-5 |
More Info
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NSC 245214 |
A dinitrothiophene derivative |
1 mg |
9002543-1 |
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NSC 245214 |
A dinitrothiophene derivative |
10 mg |
9002543-10 |
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NSC 245214 |
A dinitrothiophene derivative |
25 mg |
9002543-25 |
More Info
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NSC 245214 |
A dinitrothiophene derivative |
5 mg |
9002543-5 |
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NSC 319726 |
A p53 reactivator; selectively inhibits growth of human tumor cell lines c… |
10 mg |
23701-10 |
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