INT107330

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Context Info
Confidence 0.01
First Reported 2003
Last Reported 2003
Negated 0
Speculated 0
Reported most in Abstract
Documents 1
Total Number 1
Disease Relevance 0
Pain Relevance 0.65

This is a graph with borders and nodes. Maybe there is an Imagemap used so the nodes may be linking to some Pages.

nucleus (Adarb1, Trh) nucleoplasm (Adarb1) intracellular (Adarb1)
cytoplasm (Trh) extracellular region (Trh) RNA binding (Adarb1)
Adarb1 (Rattus norvegicus)
Trh (Rattus norvegicus)
Pain Link Frequency Relevance Heat
antagonist 9 100.00 Very High Very High Very High
opioid receptor 3 100.00 Very High Very High Very High
Antinociceptive 4 82.96 Quite High
agonist 6 75.00 Quite High
antinociception 1 75.00 Quite High
Potency 1 75.00 Quite High
MU agonist 1 74.72 Quite High
withdrawal 1 62.16 Quite High
Morphine 2 58.24 Quite High
Buprenorphine 1 56.16 Quite High

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Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
D-Phe-Cys-Tyr-D-Trp-Arg-Thr-Pen-Thr-NH2 (CTAP) is a peptide antagonist that demonstrates potent and selective affinity for micro-opioid receptors in radioligand binding assays and in vitro bioassays.
receptors Binding (affinity) of D-Phe-Cys-Tyr-D-Trp-Arg-Thr-Pen-Thr-NH2 associated with antagonist and opioid receptor
1) Confidence 0.01 Published 2003 Journal J. Pharmacol. Exp. Ther. Section Abstract Doc Link 12490605 Disease Relevance 0 Pain Relevance 0.65

General Comments

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