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 3129 - 3136 of 9359 hot products
| Catalog No. | Product Name |
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| BCC7697 | BMS 493 |
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Pan-retinoic acid receptor (pan-RAR) inverse agonist. Enhances nuclear corepressor (NCoR) interaction with RARs. Binding induces analogous conformational changes in all RAR types (RAR<span class='symbol'>α</span>, RAR<span class='symbol'>β</span> and RAR<span class='symbol'>γ</span>).
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| BCC7698 | NPE-caged-proton |
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1-(2-nitrophenyl)ethyl caged proton that releases a proton and a sulfate ion upon photolysis. Generates rapid acidifications down to pH 2 (pH jumps).
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| BCC7699 | Tunicamycin |
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Antibiotic; inhibits GlcNAc phosphotransferase (GPT). Blocks the formation of N-glycosidic linkages by inhibiting the first step in glycoprotein synthesis. Activity induces ER stress and causes G1 arrest; can be used to induce autophagy. Tunicamycin contains four main components as follows: Homolog A, n=8, C37H60N4O16, molecular weight = 816.90 Homolog B, n=9, C38H62N4O16, molecular weight = 830.93 Homolog C, n=10, C39H64N4O16, molecular weight = 844.95 Homolog D, n=11, C40H66N4O16, molecular weight = 858.99 The composition of this product will vary from batch to batch and can be found on the relevant certificate of analysis.
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| BCC7700 | S 24795 |
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Partial agonist of <span class='symbol'>α</span>7 nAChR. Improves mnemonic function in aged mice for the treatment of aging-related memory disturbances. Displays more efficient memory-enhancing effects than memantine in Alzheimer's disease mouse models.
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| BCC7701 | FERb 033 |
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Potent and selective ER<span class='symbol'>β</span> receptor agonist (K<sub>i</sub> = 7.1 nM, EC<sub>50</sub> = 4.8 nM). Displays 62-fold selectivity over ER<span class='symbol'>α</span>.
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| BCC7702 | PD 168568 dihydrochloride |
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Potent and selective dopamine D4 receptor antagonist (Ki values are 8.8 and 1842 nM at D4 and D2 receptors respectively). Reverses amphetamine-stimulated locomotion in vivo and is orally active.
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| BCC7703 | HQL 79 |
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Orally active and specific inhibitor of human hematopoietic prostaglandin D synthase (H-PGDS) (IC<sub>50</sub> = 6 <span class='symbol'>μ</span>M). Antiallergic and anti-inflammatory; displays antiasthmatic activity and potent antihistaminic properties <em>in vivo</em>.
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| BCC7704 | PNU 74654 |
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Binds to <span class='symbol'>β</span>-catenin (K<sub>D</sub> = 450 nM). Inhibits the interaction between <span class='symbol'>β</span>-catenin and T cell factor 4 (Tcf4) and disrupts the Wnt signaling pathway.
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