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 2185 - 2192 of 9359 hot products
| Catalog No. | Product Name |
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| BCC6737 | (±)-Vesamicol hydrochloride |
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Inhibitor of acetylcholine transport (K<sub>i</sub> = 2 nM). Centrally active following systemic administration <em>in vivo</em>.
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| BCC6738 | FGIN-1-27 |
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Binds specifically and with high affinity to the peptide DBI receptor (benzodiazepine receptor) on mitochondrial membranes, inducing production of neurosteroids, which modulate GABA receptors (EC50 = 3 nM for increase in production of pregnenolone in glial cells). Thus it reduces anxiety without causing sedation.
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| BCC6739 | FGIN-1-43 |
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Most active of the 2-aryl-3-indoleacetamides; a new class of potent and specific ligands as probes for the mitochondial DBI receptor (peripheral benzodiazepine receptor).
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| BCC6740 | Mepyramine maleate |
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Selective inverse agonist for the H1 receptor. Inhibits histamine induced inositol phosphate (InsP) production (log EC50 = -7.94) and intracellular calcium mobilization. Sequesters Gq/11 protein, reducing its availability for other receptors associated with the same signaling pathway.
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| BCC6741 | 2-MPMDQ |
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Potent and selective <span class='symbol'>α</span><sub>1</sub>-adrenoceptor antagonist; hypotensive.
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| BCC6742 | trans-Triprolidine hydrochloride |
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Potent H<sub>1</sub> receptor antagonist.
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| BCC6743 | 3-AQC |
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A competitive 5-HT3 antagonist, almost 100 times more potent than tropisetron, but with widely differing activity in various tissues.
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| BCC6744 | Amthamine dihydrobromide |
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Highly selective H2 agonist, slightly more potent than histamine itself. Only a weak antagonist at H3 and has no activity at H1 receptors. Induces vasodilation of cerebral arteries and decreases myogenic tone in vitro.
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