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 2425 - 2432 of 9359 hot products
| Catalog No. | Product Name |
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| BCC6982 | BHQ |
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A selective inhibitor of endoplasmic reticulum Ca<sup>2+</sup>-ATPase.
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| BCC6983 | LY 367385 |
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A selective mGlu<sub>1a</sub> receptor antagonist, with an IC<sub>50</sub> value of 8.8 <span class='symbol'>μ</span>M for blockade of quisqualate-induced phosphoinositide hydrolysis vs. > 100 <span class='symbol'>μ</span>M for mGlu<sub>5a</sub>, and negligible action on group II and III receptors. Also available as part of the Group I mGlu Receptor.
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| BCC6984 | CCMQ |
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For use in conjunction with [<sup>3</sup>H]-homoquinolinic acid to characterize NR2B-containing NMDA receptors; selectively inhibits [<sup>3</sup>H]-homoquinolinic acid binding to non-NMDA sensitive sites.
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| BCC6985 | NF 023 |
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A subtype-selective, competitive and reversible P2X<sub>1</sub> receptor antagonist. Displays IC<sub>50</sub> values of 0.21, 28.9, > 50 and > 100 <span class='symbol'>μ</span>M for human P2X<sub>1</sub>, P2X<sub>3</sub>, P2X<sub>2</sub>, and P2X<sub>4</sub>-mediated responses respectively. Selective over adrenoceptors, histamine and P2Y receptors. Also selectively inhibits the <span class='symbol'>α</span>-subunit of G<sub>o/i</sub> (EC<sub>50</sub> ~300 nM).
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| BCC6986 | CGS 19755 |
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Potent, competitive NMDA receptor antagonist. Anticonvulsant and neuroprotective. Also available as part of the Mixed NMDA Receptor.
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| BCC6987 | SB 216641 hydrochloride |
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A selective h5-HT1B antagonist with approximately 25-fold selectivity over h5-HT1D and little or no affinity for a range of other receptor types.
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| BCC6988 | CGP 35348 |
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Selective, brain penetrant GABA<sub>B</sub> receptor antagonist (IC<sub>50</sub> = 34 <span class='symbol'>μ</span>M as measured in rat cortical membranes). Has higher affinity for postsynaptic versus presynaptic receptors.
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| BCC6989 | CGP 52432 |
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Potent, selective GABAB receptor antagonist (IC50 = 85 nM).
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