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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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 |
More Info
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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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BI-6015 |
A small molecule antagonist of HNF4α that at 20 µM reduces end… |
50 mg |
12032-50 |
More Info
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BI-605906 |
An IKKβ inhibitor (IC50 = 380 nM); selective for IKKβ over insul… |
1 mg |
19184-1 |
More Info
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BI-605906 |
An IKKβ inhibitor (IC50 = 380 nM); selective for IKKβ over insul… |
10 mg |
19184-10 |
More Info
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BI-605906 |
An IKKβ inhibitor (IC50 = 380 nM); selective for IKKβ over insul… |
5 mg |
19184-5 |
More Info
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BI-671800 |
An antagonist of CRTH2 / DP2 (IC50 = 42 nM in a radioligand binding assay)… |
1 mg |
27638-1 |
More Info
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BI-671800 |
An antagonist of CRTH2 / DP2 (IC50 = 42 nM in a radioligand binding assay)… |
10 mg |
27638-10 |
More Info
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BI-671800 |
An antagonist of CRTH2 / DP2 (IC50 = 42 nM in a radioligand binding assay)… |
5 mg |
27638-5 |
More Info
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BI-6727 |
A dihydropteridinone that inhibits Plk1, Plk2, and Plk3 (IC50s = 0.87, 5,… |
1 mg |
18193-1 |
More Info
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BI-6727 |
A dihydropteridinone that inhibits Plk1, Plk2, and Plk3 (IC50s = 0.87, 5,… |
10 mg |
18193-10 |
More Info
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BI-6727 |
A dihydropteridinone that inhibits Plk1, Plk2, and Plk3 (IC50s = 0.87, 5,… |
25 mg |
18193-25 |
More Info
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BI-6727 |
A dihydropteridinone that inhibits Plk1, Plk2, and Plk3 (IC50s = 0.87, 5,… |
5 mg |
18193-5 |
More Info
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BI-7273 |
A potent and selective BRD9 bromodomain inhibitor (Kd = 15.4 nM; IC50 = 19… |
1 mg |
20311-1 |
More Info
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BI-7273 |
A potent and selective BRD9 bromodomain inhibitor (Kd = 15.4 nM; IC50 = 19… |
10 mg |
20311-10 |
More Info
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BI-7273 |
A potent and selective BRD9 bromodomain inhibitor (Kd = 15.4 nM; IC50 = 19… |
25 mg |
20311-25 |
More Info
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BI-7273 |
A potent and selective BRD9 bromodomain inhibitor (Kd = 15.4 nM; IC50 = 19… |
5 mg |
20311-5 |
More Info
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BI-847325 |
A selective dual MEK / Aurora kinase inhibitor (IC50s = 3, 25, 15, 25, and… |
1 mg |
18301-1 |
More Info
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BI-847325 |
A selective dual MEK / Aurora kinase inhibitor (IC50s = 3, 25, 15, 25, and… |
5 mg |
18301-5 |
More Info
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BI-882370 |
A RAF inhibitor (IC50s = 0.8, 0.8, and 0.6 nM for B-RAFV600E, wild-type B-… |
1 mg |
24273-1 |
More Info
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BI-882370 |
A RAF inhibitor (IC50s = 0.8, 0.8, and 0.6 nM for B-RAFV600E, wild-type B-… |
10 mg |
24273-10 |
More Info
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BI-882370 |
A RAF inhibitor (IC50s = 0.8, 0.8, and 0.6 nM for B-RAFV600E, wild-type B-… |
25 mg |
24273-25 |
More Info
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BI-882370 |
A RAF inhibitor (IC50s = 0.8, 0.8, and 0.6 nM for B-RAFV600E, wild-type B-… |
5 mg |
24273-5 |
More Info
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BI-9564 |
A selective inhibitor of BRD9 and BRD7 bromodomains (Kds = 14.1 and 239 nM… |
1 mg |
17897-1 |
More Info
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BI-9564 |
A selective inhibitor of BRD9 and BRD7 bromodomains (Kds = 14.1 and 239 nM… |
10 mg |
17897-10 |
More Info
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BI-9564 |
A selective inhibitor of BRD9 and BRD7 bromodomains (Kds = 14.1 and 239 nM… |
500 µg |
17897-500 |
More Info
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BI-9627 |
An NHE1 inhibitor (IC50s = 6 and 31 nM in pHi and human platelet swelling… |
1 mg |
27640-1 |
More Info
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BI-9627 |
An NHE1 inhibitor (IC50s = 6 and 31 nM in pHi and human platelet swelling… |
10 mg |
27640-10 |
More Info
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BI-9627 |
An NHE1 inhibitor (IC50s = 6 and 31 nM in pHi and human platelet swelling… |
5 mg |
27640-5 |
More Info
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BI-1467335 |
An inhibitor of VAP-1 (IC50 = 50s = >1,000 and >10,000 nM, respectively);… |
1 mg |
30672-1 |
More Info
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BI-1467335 |
An inhibitor of VAP-1 (IC50 = 50s = >1,000 and >10,000 nM, respectively);… |
10 mg |
30672-10 |
More Info
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BI-1467335 |
An inhibitor of VAP-1 (IC50 = 50s = >1,000 and >10,000 nM, respectively);… |
25 mg |
30672-25 |
More Info
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BI-1467335 |
An inhibitor of VAP-1 (IC50 = 50s = >1,000 and >10,000 nM, respectively);… |
5 mg |
30672-5 |
More Info
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BIA 10-2474 |
An inhibitor of FAAH (IC50 = 4.9 nM in HEK293T cells expressing the human… |
10 mg |
23157-10 |
More Info
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BIA 10-2474 |
An inhibitor of FAAH (IC50 = 4.9 nM in HEK293T cells expressing the human… |
25 mg |
23157-25 |
More Info
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BIA 10-2474 |
An inhibitor of FAAH (IC50 = 4.9 nM in HEK293T cells expressing the human… |
5 mg |
23157-5 |
More Info
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