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 1593 - 1600 of 9359 hot products
| Catalog No. | Product Name |
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| BCC5994 | [Lys5,MeLeu9,Nle10]-NKA(4-10) |
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Highy selective and potent NK<sub>2</sub> receptor agonist (IC<sub>50</sub> = 6.1 nM). Induces contraction of the rat fundus and bladder (EC<sub>50</sub> values are 117 and 10 nM respectively).
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| BCC5995 | [Phe8Ψ(CH-NH)-Arg9]-Bradykinin |
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Selective bradykinin B<sub>2</sub> receptor agonist that is resistant to carboxypeptidase cleavage. 5-fold more potent and exhibits a more prolonged duration of action than bradykinin</a> (Cat No. 3004) <em>in vivo</em>.
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| BCC5996 | Sar-[D-Phe8]-des-Arg9-Bradykinin |
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Potent and selective bradykinin B<sub>1</sub> receptor agonist (EC<sub>50</sub> = 9.02 nM in rabbit aorta) that is resistant to aminopeptidase, kininase I and II (ACE) and neutral endopeptidase cleavage. Exhibits hypotensive and angiogenic activity <em>in vivo</em>.
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| BCC5997 | Ac9-25 |
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N-terminal peptide of Annexin I (AI/Lipocortin I) that inhibits leukocyte extravasation. Acts as a formyl peptide receptor 1 (FPR1) ligand and stimulates neutrophil NADPH oxidase activation.
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| BCC5998 | BIM 23042 |
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Selective neuromedin B receptor (NMB-R, BB<sub>1</sub>) antagonist (K<sub>i</sub> values are 216 and 18,264 nM for BB<sub>1</sub> and BB<sub>2</sub> receptors respectively). Displays no activity at a range of other receptors.
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| BCC5999 | TCS PrP Inhibitor 13 |
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Antiprion agent. Potently inhibits protease-resistant prion protein (PrP-res) accumulation in two types of prion-infected mouse neuroblastoma (N2a) cell lines (IC<sub>50</sub> = 3 nM).
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| BCC6000 | Fentanyl citrate |
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Potent and selective <span class='symbol'>μ</span>-opioid receptor agonist (K<sub>i</sub> values are 7.0, 151 and 470 nM for <span class='symbol'>μ</span>-, <span class='symbol'>δ</span>- and <span class='symbol'>κ</span>-opioid receptors respectively). Displays antinociceptive activity <em>in vivo</em>.
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| BCC6001 | GLP-1 (9-36) amide |
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N-terminal truncated metabolite of glucagon-like peptide GLP-1-(7-36) formed by dipeptidyl peptidase-IV cleavage. Acts as an antagonist at the human GLP-1 receptor. Inhibits hepatic glucose production <em>in vivo</em> and is a weak insulinotropic agent.
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