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 1825 - 1832 of 9359 hot products
| Catalog No. | Product Name |
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| BCC6230 | Phenobarbital sodium salt |
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Enhances GABAergic activity. Long-acting barbiturate; slow-acting barbiturate also available.
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| BCC6231 | Pentobarbital sodium salt |
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Enhances GABAergic activity. Short-acting barbiturate; long-acting barbiturate also available.
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| BCC6232 | MLR 1023 |
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Selective allosteric activator of Lyn kinase (EC50 = 63 nM); displays no significant activity against a range of 47 other kinases, including other Src family kinases such as Fyn, Lck and Src kinase. Reduces blood glucose levels without affecting in vivo insulin secretion. Orally bioavailable.
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| BCC6233 | Deltorphin I |
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Potent <span class='symbol'>δ</span>-opioid receptor agonist (IC<sub>50</sub> = 0.5 nM in human granulocytes). Exhibits a high rate of blood-brain barrier penetrance.
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| BCC6234 | IT1t dihydrochloride |
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Potent CXCR4 antagonist (IC50 = 1.1 nM in calcium mobilization assays). Orally available. Blocks interaction with the HIV envelope protein, gp120 (IC50 = 7 nM, inhibition of X4-tropic HIV-1IIIB attachment).
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| BCC6235 | TUG 891 |
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Potent FFA4 (GPR120) agonist (pEC50 values are 7.36 and 7.77 for human and mouse GPR120 respectively). Selective for GPR120 over free fatty acid receptors (pEC50 = 4.19 for FFA1; displays no activity at FFA2 or FFA3). Cell permeable.
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| BCC6236 | LDN-27219 |
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Transglutaminase 2 (TG2) inhibitor (IC<sub>50</sub> = 0.25 <span class='symbol'>μ</span>M). Binds at GTPase site; reversible.
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| BCC6237 | LUF 5834 |
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Potent A2A and A2B adenosine receptor partial agonist ( Ki = 2.6 nM and EC50 = 12 nM respectively). Also exhibits selectivity for A1 over A3 (Ki values are 2.6 and 538 nM respectively).
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