Hot Natural Products & Bioactive Compounds
BioCrick offers high-purity natural products and bioactive compounds for scientific research. Our natural product collection includes compounds derived from plants, microorganisms and other biological sources and is widely used in pharmacological, biochemical and drug discovery research.
Natural products remain an important source of bioactive molecules and drug leads. BioCrick provides researchers with high-quality natural product compounds together with catalog numbers, product information and biological activity data.
Hot Products from BioCrick
Showing 2377 - 2384 of 9359 hot products
| Catalog No. | Product Name |
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| BCC6934 | CGP 54626 hydrochloride |
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A potent, selective GABAB receptor antagonist (IC50 = 4 nM).
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| BCC6935 | 8-Bromo-cGMP, sodium salt |
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Membrane permeable cGMP analog that activates protein kinase G (PKG). 4.3-fold more potent than cGMP in activating PKG1<span class='symbol'>α</span> and promotes relaxation of tracheal and vascular smooth muscle tissue <em>in vitro</em>.
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| BCC6936 | BU 226 hydrochloride |
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A high affinity ligand for I<sub>2</sub> imidazoline sites (K<sub>i</sub> = 2.7 nM) with very high selectivity (> 2000-fold) over <span class='symbol'>α</span><sub>2</sub>-adrenoceptors (K<sub>i</sub> = 6700 nM).
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| BCC6937 | Procaterol hydrochloride |
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Specific and very potent <span class='symbol'>β</span><sub>2</sub> agonist.
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| BCC6938 | 2-Cl-IB-MECA |
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High affinity and extremely selective A3 adenosine receptor agonist (Ki = 0.33 nM). Displays 2500- and 1400-fold selectivity over A1 and A2A receptors respectively. Exhibits high selectivity over the Na+-independent adenosine transporter.
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| BCC6939 | AF-DX 116 |
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Selective M<sub>2</sub> muscarinic receptor antagonist. K<sub>i</sub> values are 64, 417, 786, 211 and 5130 nM for human recombinant M<sub>2</sub>, M<sub>1</sub>, M<sub>3</sub>, M<sub>4</sub> and M<sub>5</sub> muscarinic receptors, respectively.
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| BCC6940 | ATPA |
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A selective and potent GluR5 kainate receptor agonist (K<sub>i</sub> = 4.3 nM), inactive at GluR6 (K<sub>i</sub> > 1 mM) and only weakly active at AMPA receptors (GluR1-4) and the kainate receptors KA-2 and GluR7 (K<sub>i</sub> values of 6 - 14 <span class='symbol'>μ</span>M). Also available as part of the Kainate Receptor.
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| BCC6941 | GR 103691 |
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A potent and selective dopamine D3 receptor antagonist, with a Ki value of 0.3 nM and > 100- fold selectivity over D2 and D4 sites.
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