Pawhuskin A (original) (raw)

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Pawhuskin A is a naturally occurring prenylated stilbene isolated from Dalea purpurea which acts as a competitive silent antagonist of the κ-, μ-, and δ-opioid receptors (Ke = 203 nM, 570 nM, and 2900 nM, respectively). The compound was named after Pawhuska, Oklahoma, a place near where the samples of Dalea purpurea that led to its discovery were taken from. Other isolates of the plant with affinity for opioid receptors include and , though these compounds produce comparatively weak opioid receptor displacement (4.2–11.4 μM) relative to Pawhuskin A. Dalea purpurea was used in traditional Native American medicine to treat various ailments, and pawhuskin A and related isolates may be some of the constituents of the plant which underlay this use.

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dbo:abstract Pawhuskin A is a naturally occurring prenylated stilbene isolated from Dalea purpurea which acts as a competitive silent antagonist of the κ-, μ-, and δ-opioid receptors (Ke = 203 nM, 570 nM, and 2900 nM, respectively). The compound was named after Pawhuska, Oklahoma, a place near where the samples of Dalea purpurea that led to its discovery were taken from. Other isolates of the plant with affinity for opioid receptors include and , though these compounds produce comparatively weak opioid receptor displacement (4.2–11.4 μM) relative to Pawhuskin A. Dalea purpurea was used in traditional Native American medicine to treat various ailments, and pawhuskin A and related isolates may be some of the constituents of the plant which underlay this use. (en)
dbo:iupacName 4-[(E)-2-{2-[(2E)-3,7-Dimethylocta-2,6-dien-1-yl]-3,5-dihydroxyphenyl}ethen-1-yl]-3-(3-methylbut-2-en-1-yl)benzene-1,2-diol (en)
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dbo:wikiPageWikiLink dbr:Catechin dbr:Salvinorin_A dbr:Hyperoside dbr:Pawhuska,_Oklahoma dbr:Δ-opioid_receptor dbc:Stilbenoids dbr:Competitive_antagonist dbr:Natural_product dbr:Opioid_receptor dbc:Mu-opioid_receptor_antagonists dbr:Receptor_antagonist dbr:Prenylation dbr:Amentoflavone dbc:Kappa-opioid_receptor_antagonists dbr:Dalea_purpurea dbr:Μ-opioid_receptor dbc:Delta-opioid_receptor_antagonists dbr:Affinity_(pharmacology) dbr:Κ-opioid_receptor dbr:Native_American_ethnobotany dbr:Stilbene dbr:Silent_antagonist dbr:Pawhuskin_B dbr:Pawhuskin_C
dbp:imagealt Skeletal formula (en) Ball-and-stick model of pawhuskin A (en)
dbp:imagefile Pawhuskin A molecule ball.png (en) pawhuskin A.svg (en)
dbp:imagesize 220 (xsd:integer)
dbp:pin 4 (xsd:integer)
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dcterms:subject dbc:Stilbenoids dbc:Mu-opioid_receptor_antagonists dbc:Kappa-opioid_receptor_antagonists dbc:Delta-opioid_receptor_antagonists
gold:hypernym dbr:Stilbene
rdf:type owl:Thing dul:ChemicalObject dbo:ChemicalSubstance wikidata:Q11173 dbo:ChemicalCompound
rdfs:comment Pawhuskin A is a naturally occurring prenylated stilbene isolated from Dalea purpurea which acts as a competitive silent antagonist of the κ-, μ-, and δ-opioid receptors (Ke = 203 nM, 570 nM, and 2900 nM, respectively). The compound was named after Pawhuska, Oklahoma, a place near where the samples of Dalea purpurea that led to its discovery were taken from. Other isolates of the plant with affinity for opioid receptors include and , though these compounds produce comparatively weak opioid receptor displacement (4.2–11.4 μM) relative to Pawhuskin A. Dalea purpurea was used in traditional Native American medicine to treat various ailments, and pawhuskin A and related isolates may be some of the constituents of the plant which underlay this use. (en)
rdfs:label Pawhuskin A (en)
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