Propylnorapomorphine
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Systematic (IUPAC) name | |
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(6aS)-6-propyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline-10,11-diol
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Clinical data | |
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Routes of administration |
Oral |
Identifiers | |
CAS Number | 57559-68-9 |
ATC code | none |
PubChem | CID: 5311191 |
ChemSpider | 4470712 |
Chemical data | |
Formula | C19H21NO2 |
Molecular mass | 295.38 g/mol |
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N-n-Propylnorapomorphine (NPA) is an aporphine derivative dopamine agonist closely related to apomorphine.[1][2] In rodents it has been shown to produce hyperactivity, stereotypy, hypothermia, antinociception, and penile erection, among other effects.[3][4][5][6] Notably, its effects on locomotion are biphasic, with low doses producing inhibition and catalepsy and high doses resulting in enhancement of activity.[7] This is likely due to preferential activation of D2/D3 autoreceptors versus postsynaptic receptors,[8] the latter of which overcomes the former to increase postsynaptic dopaminergic signaling only with high doses.
See also
References
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- Dopamine agonists
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