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Naloxone pharmacological properties

The pharmacological properties of the cloned opiate receptors are similar to the characteristics of the endogenously expressed receptors [9, 36, 45]. The binding of opiates to the cloned receptors is stereoselective and the antagonist naloxone interacts with all three of the cloned receptors, although naloxone had much lower af-... [Pg.466]

Naltrexone and nalmefene are structurally related to naloxone. Naltrexone is the /V-cyclopropy I methyl analogue of oxymorphone while nalmefene is the /V-allyl analogue. They have similar pharmacological properties to naloxone but with longer durations of action, with elimination half-lives in excess of 8 hours. They also have significant oral availability. They are used mainly in the management of addicts. [Pg.130]


See other pages where Naloxone pharmacological properties is mentioned: [Pg.522]    [Pg.267]    [Pg.267]    [Pg.148]    [Pg.93]    [Pg.477]    [Pg.112]    [Pg.17]    [Pg.18]    [Pg.38]    [Pg.148]    [Pg.691]    [Pg.3]    [Pg.350]    [Pg.398]    [Pg.407]    [Pg.468]    [Pg.148]    [Pg.532]    [Pg.552]    [Pg.532]    [Pg.552]    [Pg.1093]    [Pg.179]    [Pg.183]    [Pg.118]    [Pg.469]    [Pg.119]   
See also in sourсe #XX -- [ Pg.364 , Pg.365 ]




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Naloxon

Naloxone

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