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 2601 - 2608 of 9359 hot products
| Catalog No. | Product Name |
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| BCC7160 | N6-Cyclopentyladenosine |
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Potent and selective adenosine A1 receptor agonist (Ki values are 2.3, 790 and 43 nM for human A1, A2A and A3 receptors respectively; EC50 = 18600 nM for hA2B). Centrally active following systemic administration in vivo.
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| BCC7161 | 2-Chloro-N6-cyclopentyladenosine |
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Potent and selective adenosine A1 receptor agonist (Ki values are 0.8, 2300 and 42 nM for human A1, A2A and A3 receptors respectively; EC50 = 18800 nM for hA2B). Centrally active following systemic administration in vivo.
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| BCC7162 | CL 218872 |
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Benzodiazepine agonist displaying selectivity for <span class='symbol'>α</span>1 subunit-containing GABA<sub>A</sub> receptors (K<sub>i</sub> values are 130, 1820, 1530, > 10000, 490 and > 10000 nM for <span class='symbol'>α</span>1, <span class='symbol'>α</span>2, <span class='symbol'>α</span>3, <span class='symbol'>α</span>4, <span class='symbol'>α</span>5 and <span class='symbol'>α</span>6-subunit containing receptors respectively). Orally active anxiolytic and anticonvulsant <em>in vivo</em>.
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| BCC7163 | CV 1808 |
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Adenosine A2 receptor agonist. Coronary vasodilator, antihypertensive and antipsychotic following systemic administration in vivo.
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| BCC7164 | R-96544 hydrochloride |
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Potent, selective 5-HT<sub>2</sub> receptor antagonist; displays some selectivity for 5-HT<sub>2A</sub> receptors (K<sub>i</sub> = 1.6 nM). IC<sub>50</sub> values are 2.2, 310, 2400, 3700, > 5000 and > 5000 nM for 5-HT<sub>2</sub>, <span class='symbol'>α</span><sub>1</sub>-adrenergic, D<sub>2</sub> dopamine, 5-HT<sub>1</sub>, 5-HT<sub>3</sub> and <span class='symbol'>β</span>-adrenergic receptors respectively. Inhibits 5-HT-induced platelet aggregation and pressor responses <em>in vivo</em>.
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| BCC7165 | Nemonapride |
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Highly potent dopamine D2-like receptor antagonist; selective over D1-like receptors (Ki values are 0.1 and 740 nM for D2-like and D1-like receptors respectively). Also potent 5-HT1A receptor agonist (IC50 = 34 nM) and has affinity for sigma receptors.
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| BCC7166 | HexylHIBO |
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Group I mGlu receptor antagonist (K<sub>i</sub> values are 140 and 110 <span class='symbol'>μ</span>M at mGlu<sub>1a</sub> and mGlu<sub>5a</sub> receptors respectively). Decreases sEPSCs in rat pyramidal neurons <em>in vitro</em>.
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| BCC7167 | (S)-HexylHIBO |
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Group I mGlu receptor antagonist (K<sub>b</sub> values are 30 and 61 <span class='symbol'>μ</span>M at mGlu<sub>1a</sub> and mGlu<sub>5a</sub> receptors respectively). Enantiomer of hexylHIBO.
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