BG45 |
A selective inhibitor of HDAC3 (IC50 = 289 nM) that alone or in combinatio… |
25 mg |
16918-25 |
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BG45 |
A selective inhibitor of HDAC3 (IC50 = 289 nM) that alone or in combinatio… |
5 mg |
16918-5 |
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BG45 |
A selective inhibitor of HDAC3 (IC50 = 289 nM) that alone or in combinatio… |
50 mg |
16918-50 |
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BGC 20-1531 (hydrochloride) |
A potent and selective EP4 receptor antagonist (Kis = 11.7, >10,000, and >… |
1 mg |
19742-1 |
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BGC 20-1531 (hydrochloride) |
A potent and selective EP4 receptor antagonist (Kis = 11.7, >10,000, and >… |
10 mg |
19742-10 |
More Info
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BGC 20-1531 (hydrochloride) |
A potent and selective EP4 receptor antagonist (Kis = 11.7, >10,000, and >… |
5 mg |
19742-5 |
More Info
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BGC 20-1531 (hydrochloride) |
A potent and selective EP4 receptor antagonist (Kis = 11.7, >10,000, and >… |
500 µg |
19742-500 |
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BGJ398 |
A pan FGFR inhibitor (IC50s = 0.9, 1.4, and 1 nM for FGFR1, FGFR2, and FGF… |
1 mg |
19157-1 |
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BGJ398 |
A pan FGFR inhibitor (IC50s = 0.9, 1.4, and 1 nM for FGFR1, FGFR2, and FGF… |
10 mg |
19157-10 |
More Info
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BGJ398 |
A pan FGFR inhibitor (IC50s = 0.9, 1.4, and 1 nM for FGFR1, FGFR2, and FGF… |
25 mg |
19157-25 |
More Info
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BGJ398 |
A pan FGFR inhibitor (IC50s = 0.9, 1.4, and 1 nM for FGFR1, FGFR2, and FGF… |
5 mg |
19157-5 |
More Info
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BGJ398 (phosphate) |
A pan FGFR inhibitor (IC50s = 0.9, 1.4, and 1 nM for FGFR1, FGFR2, and FGF… |
1 mg |
39292-1 |
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BGJ398 (phosphate) |
A pan FGFR inhibitor (IC50s = 0.9, 1.4, and 1 nM for FGFR1, FGFR2, and FGF… |
10 mg |
39292-10 |
More Info
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BGJ398 (phosphate) |
A pan FGFR inhibitor (IC50s = 0.9, 1.4, and 1 nM for FGFR1, FGFR2, and FGF… |
25 mg |
39292-25 |
More Info
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BGJ398 (phosphate) |
A pan FGFR inhibitor (IC50s = 0.9, 1.4, and 1 nM for FGFR1, FGFR2, and FGF… |
5 mg |
39292-5 |
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BGP-15 |
A PARP inhibitor and insulin sensitizer; blocks self-ADP-ribosylation of n… |
1 mg |
17503-1 |
More Info
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BGP-15 |
A PARP inhibitor and insulin sensitizer; blocks self-ADP-ribosylation of n… |
10 mg |
17503-10 |
More Info
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BGP-15 |
A PARP inhibitor and insulin sensitizer; blocks self-ADP-ribosylation of n… |
25 mg |
17503-25 |
More Info
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BGP-15 |
A PARP inhibitor and insulin sensitizer; blocks self-ADP-ribosylation of n… |
5 mg |
17503-5 |
More Info
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BHBM |
An acylhydrazone with antifungal activity; active against C. neoformans in… |
1 mg |
29817-1 |
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BHBM |
An acylhydrazone with antifungal activity; active against C. neoformans in… |
10 mg |
29817-10 |
More Info
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BHBM |
An acylhydrazone with antifungal activity; active against C. neoformans in… |
25 mg |
29817-25 |
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BHBM |
An acylhydrazone with antifungal activity; active against C. neoformans in… |
5 mg |
29817-5 |
More Info
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B7-H3/CD276 Extracellular Domain (human, recombinant) |
Source: Recombinant C-terminal human IgG1 Fc-tagged B7-H3 expressed in HEK… |
1 mg |
31822-1 |
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B7-H3/CD276 Extracellular Domain (human, recombinant) |
Source: Recombinant C-terminal human IgG1 Fc-tagged B7-H3 expressed in HEK… |
100 µg |
31822-100 |
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BHD |
A reversible male contraceptive agent; induces spermatogenic cell apoptosi… |
1 mg |
38962-1 |
More Info
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BHD |
A reversible male contraceptive agent; induces spermatogenic cell apoptosi… |
10 mg |
38962-10 |
More Info
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BHD |
A reversible male contraceptive agent; induces spermatogenic cell apoptosi… |
5 mg |
38962-5 |
More Info
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B7-H4 (human, recombinant) |
Source: Active recombinant C-terminal human IgG1 Fc-tagged B7-H4 expressed… |
1 mg |
31823-1 |
More Info
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B7-H4 (human, recombinant) |
Source: Active recombinant C-terminal human IgG1 Fc-tagged B7-H4 expressed… |
100 µg |
31823-100 |
More Info
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BH3I-1 |
A cell permeable inhibitor that blocks the binding of BH3 peptides to Bcl-… |
1 mg |
18763-1 |
More Info
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BH3I-1 |
A cell permeable inhibitor that blocks the binding of BH3 peptides to Bcl-… |
10 mg |
18763-10 |
More Info
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BH3I-1 |
A cell permeable inhibitor that blocks the binding of BH3 peptides to Bcl-… |
25 mg |
18763-25 |
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BH3I-1 |
A cell permeable inhibitor that blocks the binding of BH3 peptides to Bcl-… |
5 mg |
18763-5 |
More Info
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Bhimanone |
An acetylated tetralone |
1 mg |
40910-1 |
More Info
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BHPI |
An antagonist of ERα that blocks 17β-estradiol-induced prolifer… |
1 mg |
17750-1 |
More Info
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BHPI |
An antagonist of ERα that blocks 17β-estradiol-induced prolifer… |
5 mg |
17750-5 |
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BHPI |
An antagonist of ERα that blocks 17β-estradiol-induced prolifer… |
500 µg |
17750-500 |
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BHT |
A synthetic antioxidant; scavenges peroxide, DPPH, superoxide, and ABTS ra… |
1 g |
89910-1 |
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BHT |
A synthetic antioxidant; scavenges peroxide, DPPH, superoxide, and ABTS ra… |
500 mg |
89910-500 |
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B-HT 920 (hydrochloride) |
A potent agonist of D2 receptors (Ki = 5.8 nM); has neuroprotective and re… |
10 mg |
14177-10 |
More Info
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B-HT 920 (hydrochloride) |
A potent agonist of D2 receptors (Ki = 5.8 nM); has neuroprotective and re… |
5 mg |
14177-5 |
More Info
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B-HT 920 (hydrochloride) |
A potent agonist of D2 receptors (Ki = 5.8 nM); has neuroprotective and re… |
50 mg |
14177-50 |
More Info
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B-HT 933 (hydrochloride) |
An α2-AR agonist (EC50 = 0.65 µM for contraction of canine sap… |
1 mg |
11941-1 |
More Info
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B-HT 933 (hydrochloride) |
An α2-AR agonist (EC50 = 0.65 µM for contraction of canine sap… |
10 mg |
11941-10 |
More Info
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B-HT 933 (hydrochloride) |
An α2-AR agonist (EC50 = 0.65 µM for contraction of canine sap… |
25 mg |
11941-25 |
More Info
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B-HT 933 (hydrochloride) |
An α2-AR agonist (EC50 = 0.65 µM for contraction of canine sap… |
5 mg |
11941-5 |
More Info
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BI-01383298 |
An NaCT inhibitor (IC50 = ~100 nM); irreversibly inhibits sodium-dependent… |
10 mg |
24482-10 |
More Info
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BI-01383298 |
An NaCT inhibitor (IC50 = ~100 nM); irreversibly inhibits sodium-dependent… |
25 mg |
24482-25 |
More Info
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BI-01383298 |
An NaCT inhibitor (IC50 = ~100 nM); irreversibly inhibits sodium-dependent… |
5 mg |
24482-5 |
More Info
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BI-01383298 |
An NaCT inhibitor (IC50 = ~100 nM); irreversibly inhibits sodium-dependent… |
50 mg |
24482-50 |
More Info
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BI-187004 |
An 11β-HSD1 inhibitor (IC50 = 31 nM) |
1 mg |
38786-1 |
More Info
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BI-187004 |
An 11β-HSD1 inhibitor (IC50 = 31 nM) |
10 mg |
38786-10 |
More Info
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BI-187004 |
An 11β-HSD1 inhibitor (IC50 = 31 nM) |
5 mg |
38786-5 |
More Info
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BI-2536 |
A selective inhibitor of Plk1 (IC50 = 0.83 nM); induces mitotic arrest and… |
1 mg |
17385-1 |
More Info
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BI-2536 |
A selective inhibitor of Plk1 (IC50 = 0.83 nM); induces mitotic arrest and… |
10 mg |
17385-10 |
More Info
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BI-2536 |
A selective inhibitor of Plk1 (IC50 = 0.83 nM); induces mitotic arrest and… |
5 mg |
17385-5 |
More Info
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BI-2536 |
A selective inhibitor of Plk1 (IC50 = 0.83 nM); induces mitotic arrest and… |
50 mg |
17385-50 |
More Info
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BI-2545 |
An inhibitor of autotaxin (IC50s = 2.2 and 3.4 for the human and rat enzym… |
10 mg |
24285-10 |
More Info
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BI-2545 |
An inhibitor of autotaxin (IC50s = 2.2 and 3.4 for the human and rat enzym… |
25 mg |
24285-25 |
More Info
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BI-2545 |
An inhibitor of autotaxin (IC50s = 2.2 and 3.4 for the human and rat enzym… |
5 mg |
24285-5 |
More Info
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BI-3406 |
An inhibitor of the K-Ras-SOS1 protein-protein interaction (IC50 = 5 nM);… |
1 mg |
35261-1 |
More Info
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BI-3406 |
An inhibitor of the K-Ras-SOS1 protein-protein interaction (IC50 = 5 nM);… |
10 mg |
35261-10 |
More Info
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BI-3406 |
An inhibitor of the K-Ras-SOS1 protein-protein interaction (IC50 = 5 nM);… |
25 mg |
35261-25 |
More Info
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BI-3406 |
An inhibitor of the K-Ras-SOS1 protein-protein interaction (IC50 = 5 nM);… |
5 mg |
35261-5 |
More Info
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BI-409306 |
A potent and selective PDE9A inhibitor (IC50s = 65 and 168 nM for the huma… |
1 mg |
30375-1 |
More Info
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BI-409306 |
A potent and selective PDE9A inhibitor (IC50s = 65 and 168 nM for the huma… |
10 mg |
30375-10 |
More Info
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BI-409306 |
A potent and selective PDE9A inhibitor (IC50s = 65 and 168 nM for the huma… |
25 mg |
30375-25 |
More Info
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BI-409306 |
A potent and selective PDE9A inhibitor (IC50s = 65 and 168 nM for the huma… |
5 mg |
30375-5 |
More Info
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BI-4394 |
An inhibitor of MMP-13 (IC50 = 0.001 µM for the recombinant human en… |
1 mg |
36855-1 |
More Info
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BI-4394 |
An inhibitor of MMP-13 (IC50 = 0.001 µM for the recombinant human en… |
10 mg |
36855-10 |
More Info
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BI-4394 |
An inhibitor of MMP-13 (IC50 = 0.001 µM for the recombinant human en… |
5 mg |
36855-5 |
More Info
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BI-6015 |
A small molecule antagonist of HNF4α that at 20 µM reduces end… |
10 mg |
12032-10 |
More Info
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BI-6015 |
A small molecule antagonist of HNF4α that at 20 µM reduces end… |
25 mg |
12032-25 |
More Info
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BI-6015 |
A small molecule antagonist of HNF4α that at 20 µM reduces end… |
5 mg |
12032-5 |
More Info
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