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 225 - 232 of 9359 hot products
| Catalog No. | Product Name |
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| BCC1724 | LY341495 |
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Highly potent and selective group II metabotropic glutamate receptor antagonist (K<sub>i</sub>/IC<sub>50</sub> values are 2.3, 1.3, 173, 990, 6800, 8200 and 22000 nM for human mGlu<sub>2</sub>, mGlu<sub>3</sub>, mGlu<sub>8</sub> , mGlu<sub>7a</sub>, mGlu<sub>1a</sub>, mGlu<sub>5a</sub> and mGlu<sub>4a</sub> receptors respectively). Readily brain penetrant and active <em>in vivo</em>. Disodium salt also available. Also available as part of the Group II mGlu Receptor, Group III mGlu Receptor and Mixed mGlu Receptor
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| BCC1730 | Maxacalcitol |
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Maxacalcitol (22-Oxacalcitriol) is non-calcemic analog of vitamin D3 and VDR ligand of VDR-like receptors.
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| BCC1733 | MC 1046 |
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MC 1046 is impurity of Calcipotriol.
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| BCC1734 | MC 976 |
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MC 976 is a derivative of Vitamin D3.
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| BCC1738 | MEK inhibitor |
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MEK inhibitor is a potent MEK inhibitor with antitumor potency.
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| BCC1749 | Mibefradil dihydrochloride |
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Ca<sup>2+</sup> channel blocker with moderate selectivity for T-type Ca<sup>2+</sup> channels displaying IC<sub>50</sub> values of 2.7 <span class='symbol'>μ</span>M and 18.6 <span class='symbol'>μ</span>M for T-type and L-type channels respectively. Antihypertensive agent.
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| BCC1770 | ML-7 hydrochloride |
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Selective MLCK inhibitor (K<sub>i </sub>= 0.3 <span class='symbol'>μ</span>M). Exhibits more potent inhibition than ML 9 hydrochloride Displays reversible, ATP-competitive inhibition of Ca<sup>2+</sup>-calmodulin-dependent and -independent smooth muscle MLCKs. Inhibits proplatelet formation and stabilization.
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| BCC1777 | MPEP Hydrochloride |
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Potent and highly selective non-competitive antagonist at the mGlu<sub>5</sub> receptor subtype (IC<sub>50</sub> = 36 nM) and a positive allosteric modulator at mGlu<sub>4</sub> receptors. Centrally active following systemic administration <em>in vivo</em>. Reverses mechanical hyperalgesia in the inflamed rat hind paw. Also available as part of the Group I mGlu Receptor.
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