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 2281 - 2288 of 9359 hot products
| Catalog No. | Product Name |
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| BCC6836 | GR 135531 |
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Binds with high affinity to MT3 melatonin sites in hamster brain, and low affinity (and no efficacy) at MT1 and MT2 melatonin receptors and thus can be used to discriminate between the melatonin receptor subtypes.
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| BCC6837 | S-Isopropylisothiourea hydrobromide |
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Potent inhibitor of NO synthase, with selectivity for the inducible form.
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| BCC6838 | BNTX maleate |
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Standard selective <span class='symbol'>δ</span><sub>1</sub> opioid receptor antagonist. Also inhibits neurogenic ion transport mediated by a putative novel opioid receptor in porcine ileal mucosa.
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| BCC6839 | 5-Nonyloxytryptamine oxalate |
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5-HT1B selective agonist, several times more potent than sumatriptan and inactive as a 5-HT1A agonist (Ki at 5-HT1B = 1 nM, selectivity over 5-HT1A > 300-fold). Mimics polysialic acid activity, stimulates neuritogenesis, myelination and Schwann cell migration in vitro.
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| BCC6840 | SYM 2081 |
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Potent and highly selective kainate receptor agonist, with an IC<sub>50</sub> for inhibition of [<sup>3</sup>H]-kainate binding of 35 nM and almost 3,000- and 200-fold selectivity for kainate receptors over AMPA and NMDA receptors respectively. Also selectively inhibits the cloned excitatory amino acid transporter EAAT2 at higher concentrations. Also available as part of the Excitatory Amino Acid Transporter Inhibitor and Kainate Receptor.
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| BCC6841 | AIDA |
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A relatively potent and selective antagonist of group I metabotropic glutamate receptors (mGlu1a), having no effect on group II (mGlu2) or group III (mGlu4) receptors expressed individually in baby hamster kidney cells. Has no effect on ionotropic glutamate receptors. Centrally active following systemic administration in vivo.
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| BCC6842 | L-701,324 |
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An orally active and long acting anticonvulsant with high affinity and selectivity for the glycine site on the NMDA receptor.
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| BCC6843 | Cilostamide |
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Selective inhibitor of type III phosphodiesterase (PDE3). Displays moderate selectivity for PDE3A isozyme vs. PDE3B (IC<sub>50</sub> values are 0.027 and 0.050 <span class='symbol'>μ</span>M for PDE3A and PDE3B respectively). Inhibits ADP-induced platelet aggregation (IC<sub>50</sub> = 16.8 <span class='symbol'>μ</span>M); antithrombotic. Also available as part of the Phosphodiesterase Inhibitor.
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