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Dynorphin B (1-13)
CAS No. 83335-41-5
Dynorphin B (1-13)( —— )
Catalog No. M30524 CAS No. 83335-41-5
Dynorphin B (1-13) acts as an agonist on opioid κ-receptor.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
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| 10MG | 506 | Get Quote |
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| 100MG | Get Quote | Get Quote |
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Biological Information
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Product NameDynorphin B (1-13)
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NoteResearch use only, not for human use.
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Brief DescriptionDynorphin B (1-13) acts as an agonist on opioid κ-receptor.
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DescriptionDynorphin B (1-13) acts as an agonist on opioid κ-receptor.(In Vitro):Dynorphin B (1-13), a 13 amino acid, is an extraordinarily potent opioid peptide. The neurophysiological actions of Dynorphin B (1-13) have been the subject of considerable research effort.
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In VitroDynorphin B (1-13), a 13 amino acid, is an extraordinarily potent opioid peptide. The neurophysiological actions of Dynorphin B (1-13) have been the subject of considerable research effort.
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In Vivo——
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Synonyms——
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PathwayEndocrinology/Hormones
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TargetOpioid Receptor
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Recptorκ-opioid receptor
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Research Area——
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Indication——
Chemical Information
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CAS Number83335-41-5
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Formula Weight1570.84
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Molecular FormulaC74H115N21O17
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Purity>98% (HPLC)
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SolubilityIn Vitro:?H2O : 50 mg/mL (31.83 mM)
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SMILES——
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Chemical NameSequence:Tyr-Gly-Gly-Phe-Leu-Arg-Arg-Gln-Phe-Lys-Val-Val-Thr
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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β-Endorphin (human)
β-Endorphin, human, a prominent endogenous peptide, existing in the hypophysis cerebri and hypothalamus, is an agonist of opioid receptor, with preferred affinity for μ-opioid receptor and δ-opioid receptor; β-Endorphin, human exhibits antinociception activity.
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[(pF)Phe4]Nociceptin...
Highly potent and selective nociceptin/orphanin FQ receptor (OP4) agonist peptide (pKi = 10.68; pEC50 = 9.80). Displays > 8000-fold selectivity over δ, κ, and μ opioid receptors and has relatively long lasting pronociceptive, hypotensive, negative inotropic and feeding stimulation effects in vivo.
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DPDPE TFA
DPDPE TFA is selective δ-opioid receptor agonist peptide. Inhibits electrically stimulated contraction of mouse vas deferens in vitro (EC50 = 5.2 nM), and is antinociceptive in vivo.
