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 2177 - 2184 of 9359 hot products
| Catalog No. | Product Name |
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| BCC6729 | D-erythro-Sphingosine (synthetic) |
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Inhibitor of protein kinase C and calmodulin-dependent enzymes, but may stimulate mast cells by activation of protein kinase C.
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| BCC6730 | Synthalin sulfate |
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An effective non-competitive NMDA receptor antagonist in vivo and in vitro; may bind to more than one site, one of which is the polyamine site.
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| BCC6731 | Salsolinol-1-carboxylic acid |
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An amino acid that occurs naturally in the CNS.
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| BCC6732 | CGS 12066B dimaleate |
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5-HT<sub>1B</sub> full agonist, 10-fold selective over 5-HT<sub>1A</sub> and 1000-fold selective over 5-HT<sub>2C</sub> receptors. Centrally active following systemic administration.
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| BCC6733 | MDL 72222 |
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5-HT3 antagonist.
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| BCC6734 | Thioperamide |
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Potent histamine H<sub>3</sub> and H<sub>4</sub> antagonist/inverse agonist. K<sub>i</sub> values are 25 and 27 nM for human recombinant H<sub>3</sub> and H<sub>4</sub> receptors respectively. Blocks eosinophil shape change (IC<sub>50</sub> = 1.4 <span class='symbol'>μ</span>M) and chemotaxis (IC<sub>50</sub> = 519 nM) induced by histamine. Freely crosses the blood-brain barrier. Also available as part of the Histamine H<sub>3</sub> Receptor.
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| BCC6735 | 2-TEDC |
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Potent inhibitor of 5-, 12-, and 15-lipoxygenase (IC<sub>50</sub> values are 0.09, 0.013 and 0.5 <span class='symbol'>μ</span>M respectively).
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| BCC6736 | HTMT dimaleate |
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H1 and H2 receptor agonist. 4x104 times more active than histamine in H2-mediated effects in natural suppressor cells. Increases intracellular Ca2+ and IP3 in lymphocytes through a binding site other than H1, H2 or H3.
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