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 2745 - 2752 of 9359 hot products
| Catalog No. | Product Name |
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| BCC7308 | PMPA (NMDA antagonist) |
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Competitive NMDA receptor antagonist. Displays K<sub>i</sub> values of 0.84, 2.74, 3.53 and 4.16 <span class='symbol'>μ</span>M at NR2A, NR2B, NR2C and NR2D subunit-containing receptors respectively. Selective over AMPA receptors.
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| BCC7309 | PPPA |
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Competitive NMDA receptor antagonist that displays moderate selectivity for NR2A-containing receptors (K<sub>i</sub> values are 0.13, 0.47, 1.10 and 3.86 <span class='symbol'>μ</span>M for NR2A, NR2B, NR2C and NR2D subunits respectively).
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| BCC7310 | FPL 55712 |
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Leukotriene receptor antagonist; inhibits contraction of guinea pig trachealis induced by leukotrienes C4, D4, E4 and F4.
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| BCC7311 | 2'-MeCCPA |
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Potent and highly selective agonist at A1 adenosine receptors (Ki values are 3.3, 9580, 37600 and 1150 nM for human recombinant A1, A2A, A2B and A3 receptors respectively). Acts as a full agonist; inhibits forskolin-stimulated adenylyl cyclase activity in rat cortical membranes with an IC50 value of 13.1 nM.
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| BCC7312 | SEW 2871 |
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Novel, potent and selective sphingosine-1-phosphate 1 (S1P<sub>1</sub>) receptor agonist. Activates S1P<sub>1</sub> receptor with an EC<sub>50</sub> of 13 nM, but does not activate S1P<sub>2</sub>, S1P<sub>3</sub>, S1P<sub>4</sub> or S1P<sub>5</sub> receptors at concentrations up to 10 <span class='symbol'>μ</span>M. Cell-permeable and active <em>in vivo</em>.
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| BCC7313 | O-1918 |
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Selective, silent antagonist of a putative endothelial anandamide receptor distinct from CB1 or CB2 receptors. Inhibits vasodilation and cell migration induced by abnormal-cannabidiol (abn-CBD).
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| BCC7314 | AQ-RA 741 |
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High affinity, selective muscarinic M2 receptor antagonist (pKi values are 8.3, 7.7 and 6.82 for M2, M1 and M3 receptors, respectively). Displays cardioselectivity in vivo, over intestinal, tracheal and bladder muscarinic receptors; inhibits vagally and agonist-induced bradycardia.
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| BCC7315 | (±)-Cloprostenol sodium salt |
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Water-soluble prostaglandin F<sub>2<span class='symbol'>α</span></sub> (PGF<sub>2<span class='symbol'>α</span></sub>) analog; acts as a potent FP receptor agonist (EC<sub>50</sub> = 0.84 nM). Potently inhibits differentiation of adipocyte precursor cells. Luteolytic agent <em>in vivo</em>.
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