BIMU-1 is an agonist of 5-HT4 receptor.

Bindarit displays specific inhibition against monocyte chemotactic proteins MCP-1/CCL2, MCP-3/CCL7 and MCP-2/CCL8.

Bindarit displays specific inhibition against monocyte chemotactic proteins MCP-1/CCL2, MCP-3/CCL7 and MCP-2/CCL8.

Bindarit displays specific inhibition against monocyte chemotactic proteins MCP-1/CCL2, MCP-3/CCL7 and MCP-2/CCL8.

Binedaline is a selective norepinephrine reuptake inhibitor with Ki value of 25 nM.

Binedaline is a selective norepinephrine reuptake inhibitor with Ki value of 25 nM.

Binedaline is a selective norepinephrine reuptake inhibitor with Ki value of 25 nM.

Binfloxacin is a bio-active chemical.

Binifibrate is a hyperlipemiant drug used for the treatment of hyperlipidemia.

Binifibrate is a hyperlipemiant drug used for the treatment of hyperlipidemia.

Binifibrate is a hyperlipemiant drug used for the treatment of hyperlipidemia.

Binimetinib (MEK162, ARRY-162, ARRY-438162) is an orally available inhibitor of MEK1/2 (IC50: 12 nM) in a cell-free assay.

Binodenoson is a potent and selective A2A adenosine receptor agonist (KD=270 nM). Binodenoson is being developed as a short-acting coronary vasodilator as an adjunct to radiotracers for use in myocardial stress imaging[1].

Binodenoson is a potent and selective A2A adenosine receptor agonist (KD=270 nM). Binodenoson is being developed as a short-acting coronary vasodilator as an adjunct to radiotracers for use in myocardial stress imaging[1].

Binodenoson is a potent and selective A2A adenosine receptor agonist (KD=270 nM). Binodenoson is being developed as a short-acting coronary vasodilator as an adjunct to radiotracers for use in myocardial stress imaging[1].

Binodenoson is a potent and selective A2A adenosine receptor agonist (KD=270 nM). Binodenoson is being developed as a short-acting coronary vasodilator as an adjunct to radiotracers for use in myocardial stress imaging[1].

Binodenoson is a potent and selective A2A adenosine receptor agonist (KD=270 nM). Binodenoson is being developed as a short-acting coronary vasodilator as an adjunct to radiotracers for use in myocardial stress imaging[1].

Binodenoson is a potent and selective A2A adenosine receptor agonist (KD=270 nM). Binodenoson is being developed as a short-acting coronary vasodilator as an adjunct to radiotracers for use in myocardial stress imaging[1].

Binodenoson is a potent and selective A2A adenosine receptor agonist (KD=270 nM). Binodenoson is being developed as a short-acting coronary vasodilator as an adjunct to radiotracers for use in myocardial stress imaging[1].

Binospirone mesylate is a putative 5-HT(1A) receptor antagonist.

Binospirone mesylate is a putative 5-HT(1A) receptor antagonist.

Binospirone mesylate is a putative 5-HT(1A) receptor antagonist.

Binucleine 2 is an isoform-specific and ATP-competitive inhibitor of Drosophila Aurora B kinase (Ki = 0.36 μM), a kinase involved in cell division. It is specific for Drosophila Aurora B kinase, inhibiting it in a dose-dependent manner, with minimal inhibition of human or X. laevis Aurora B kinases at concentrations up to 100 μM. Binucleine […]

Binucleine 2 is an isoform-specific and ATP-competitive inhibitor of Drosophila Aurora B kinase (Ki = 0.36 μM), a kinase involved in cell division. It is specific for Drosophila Aurora B kinase, inhibiting it in a dose-dependent manner, with minimal inhibition of human or X. laevis Aurora B kinases at concentrations up to 100 μM. Binucleine […]

Binucleine 2 is an isoform-specific and ATP-competitive inhibitor of Drosophila Aurora B kinase (Ki = 0.36 μM), a kinase involved in cell division. It is specific for Drosophila Aurora B kinase, inhibiting it in a dose-dependent manner, with minimal inhibition of human or X. laevis Aurora B kinases at concentrations up to 100 μM. Binucleine […]

BIO-013077-01 is a potent TGFbeta family type I receptors antagonist.

BIO-013077-01 is a potent TGFbeta family type I receptors antagonist.

BIO-013077-01 is a potent TGFbeta family type I receptors antagonist.

BIO-013077-01 is a potent TGFbeta family type I receptors antagonist.

BIO-013077-01 is a potent TGFbeta family type I receptors antagonist.

BIO-013077-01 is a potent TGFbeta family type I receptors antagonist.

BIO-013077-01 is a potent TGFbeta family type I receptors antagonist.

BIO-11006 acetate salt is a polyglycosylated alanine rich C kinase substrate (MARCKS) inhibitor similar to MANS peptides.

BIO-11006 acetate salt is a polyglycosylated alanine rich C kinase substrate (MARCKS) inhibitor similar to MANS peptides.

BIO-11006 acetate salt is a polyglycosylated alanine rich C kinase substrate (MARCKS) inhibitor similar to MANS peptides.

BIO-11006 acetate salt is a polyglycosylated alanine rich C kinase substrate (MARCKS) inhibitor similar to MANS peptides.

BIO-11006 acetate salt is a polyglycosylated alanine rich C kinase substrate (MARCKS) inhibitor similar to MANS peptides.

BIO-11006 acetate salt is a polyglycosylated alanine rich C kinase substrate (MARCKS) inhibitor similar to MANS peptides.