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 2433 - 2440 of 9359 hot products
| Catalog No. | Product Name |
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| BCC6990 | CGP 46381 |
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Brain penetrant, selective GABA<sub>B</sub> receptor antagonist (IC<sub>50</sub> = 4.9 <span class='symbol'>μ</span>M).
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| BCC6991 | CY 208-243 |
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Centrally active dopamine D<sub>1</sub> receptor agonist, selective over D<sub>2</sub> receptor sites. Stimulates adenylate cyclase in rat striatal homogenates with an EC<sub>50</sub> of 125 nM. Unlike SKF 38393, it exerts antiParkinsonian activity in animal models.
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| BCC6992 | SDZ 220-040 |
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Potent competitive antagonist at the NMDA receptor (pKi = 8.5). Selective over a range of other receptor sites.
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| BCC6993 | (S)-WAY 100135 dihydrochloride |
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Potent, selective 5-HT<sub>1A</sub> receptor antagonist (IC<sub>50</sub> = 15 nM). Selective over 5-HT<sub>1B</sub>, <sub>1C</sub>, <sub>2</sub>,<span class='symbol'>α</span><sub>1</sub>, <span class='symbol'>α</span><sub>2</sub> and D<sub>2</sub> receptors (IC<sub>50</sub> > 1000 nM). Centrally active on systemic administration.
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| BCC6994 | SDZ SER 082 fumarate |
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Selective 5-HT2B/2C receptor antagonist with low affinity for 5-HT1A receptors. Inhibits [3H]-mesulergine binding to 5-HT2C receptors with a pKD of 7.8. Inhibits 5-HT2B mediated responses in the rat fundus (pKB = 7.34).
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| BCC6995 | 1-Deoxymannojirimycin hydrochloride |
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Selective inhibitor of <span class='symbol'>α</span>-mannosidase I.
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| BCC6997 | SR 95531 hydrobromide |
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Selective, competitive GABA<sub>A</sub> receptor antagonist. Displaces [<sup>3</sup>H]-GABA from rat brain membranes with a K<sub>i</sub> of 150 nM. Unlike bicuculline, selectively antagonizes GABA-induced Cl<sup>-</sup> currents with little action on pentobarbitone-induced currents. Also acts as a low affinity glycine receptor antagonist.
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| BCC6998 | GR 144053 trihydrochloride |
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A potent and selective platelet fibrinogen receptor glycoprotein IIb/IIIa (GpIIb/IIIa) antagonist (IC<sub>50</sub> = 37 nM). Orally active and highly effective at inhibiting thrombus formation <em>in vivo</em>.
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