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Details

Stereochemistry ABSOLUTE
Molecular Formula C24H24N2O4
Molecular Weight 404.4584
Optical Activity UNSPECIFIED
Defined Stereocenters 5 / 5
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of NICOCODINE

SMILES

[H][C@@]12CC3=C4C(O[C@H]5[C@@H](OC(=O)C6=CN=CC=C6)C=C[C@]1([H])[C@@]45CCN2C)=C(OC)C=C3

InChI

InChIKey=RYBGRHAWFUVMST-MJFIPZRTSA-N
InChI=1S/C24H24N2O4/c1-26-11-9-24-16-6-8-19(29-23(27)15-4-3-10-25-13-15)22(24)30-21-18(28-2)7-5-14(20(21)24)12-17(16)26/h3-8,10,13,16-17,19,22H,9,11-12H2,1-2H3/t16-,17+,19-,22-,24-/m0/s1

HIDE SMILES / InChI

Description

Nicocodine is an opioid related to codeine. It is also an antitussive agent. Nicocodine exhibits at least twice the potency of codeine in clinical experiments. The study of the pharmacokinetic behaviour of nicocodine by means of blood and brain level curves of rats after i .v. application showed that the penetration of the blood brain barrier seems to be favoured for nicocodine. The detected peak concentration of nicocodine in brain after i.v. application is 4.4 times higher than the blood level values at the same time - codeine the main metabolite is detected in almost equal amounts in brain and blood. A comparative assay of codeine and nicocodine after p.o. application of equimolar doses per kg body weight revealed that predominantly codeine is found in brain and its peak value after nicocodine administration is 3-fold higher than after codeine administration. Nicocodine is hydrolysable to morphine and the WHO Expert Committee on Addiction-Producing Drugs (1962) recommended its international control as a narcotic, like other convertible drugs in the morphine series.

CNS Activity

Approval Year

PubMed

Sample Use Guides

In Vivo Use Guide
Single doses of nicocodine of 5 or 10 mg in 27 tuberculous patients who had been receiving codeine gave similar cough relief without side-effects.
Route of Administration: Oral