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 2121 - 2128 of 9359 hot products
| Catalog No. | Product Name |
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| BCC6672 | Dimaprit dihydrochloride |
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Selective H<sub>2</sub> agonist with central effects upon systemic administration. Also inhibits nNOS (IC<sub>50</sub> = 49 <span class='symbol'>μ</span>M).
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| BCC6673 | Dantrolene, sodium salt |
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Inhibits release of Ca2+ from sarcoplasmic reticulum via inhibition of ryanodine receptor (RYR) channels. Displays selectivity for RYR1 and RYR3 over RYR2. Protective against the effects of a variety of conditions and agents, including excitatory amino acids. Skeletal muscle relaxant and neuroprotectant.
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| BCC6674 | BD 1008 dihydrobromide |
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Potent and selective <span class='symbol'>σ</span>-ligand (K<sub>i</sub> against [<sup>3</sup>H]-(+)-3-PPP = 0.34 nM).
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| BCC6675 | SKF 91488 dihydrochloride |
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Homolog of dimaprit; strong inhibitor of histamine N-methyltransferase. Exhibits no histamine agonist activity.
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| BCC6676 | GBR 12783 dihydrochloride |
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A very potent and selective inhibitor of dopamine uptake (IC50 for inhibition of [3H]-dopamine uptake in rat striatal synaptosomes is 1.8 nM).
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| BCC6677 | EBPC |
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Potent aldose reductase inhibitor. Improves the cytotoxicity of anticancer reagents such as cisplatin and doxorubicin in HeLa cervical carcinoma cells through an increase in ERK activity.
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| BCC6678 | 4F 4PP oxalate |
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A selective 5-HT2A antagonist with almost as high affinity (Ki = 5.3 nM) as ketanserin but with a much lower affinity for 5-HT2C sites (Ki = 620 nM).
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| BCC6679 | AMI-193 |
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Selective 5-HT antagonist, which binds to 5-HT2 sites as potently as spiperone but has lower affinity for 5-HT2C receptors. Also a high affinity D2 receptor antagonist (Ki = 3 nM). Lacks the disruptive effect of spiperone on animal behavior.
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