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| Product | Description | |
|---|---|---|
| PL 017 | PL 017, a morphiceptin analog, is a selective μ opioid receptor agonist (IC50= 5.5 and > 10000 nM for inhibition of 125I-FK 33,824 and 125I-DADLE binding to μ and δ sites respectively). Although the affinity of PL017 for μ-sites is lower than that of morphine, PL 017 is more potent than morphine in all in vitro studies, suggesting a difference in the way in which peptide and alkaloid activate μ-receptors. Synonyms: Tyr-Pro-MePhe-D-Pro; PL 017; PL017; PL-017. CAS No. 83397-56-2. Molecular formula: C29H37N5O5. Mole weight: 535.64. |  |
| PL 017 | PL 017. Group: Biochemicals. Grades: Purified. CAS No. 83397-56-2. Pack Sizes: 1mg. US Biological Life Sciences. |  Worldwide |
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