U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

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
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.

Approval Year

PubMed

PubMed

TitleDatePubMed
[Comparative actions of morphine, codeine and nicocodine on respiration and external pancreatic and biliary secretions in the rat].
1967 May
Reinforcing properties of nicocodine in the rhesus monkey.
1979

Sample Use Guides

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
Name Type Language
NICOCODINE
INN   MART.   WHO-DD  
INN  
Official Name English
Nicocodine [WHO-DD]
Common Name English
NICOCODEINE
Common Name English
NICOCODINE [MART.]
Common Name English
6-NICOTINOYLCODEINE
Common Name English
IDS-NN-001(SECT.2)
Code English
RC 146
Code English
nicocodine [INN]
Common Name English
DEA NO. 9309
Code English
LYOPECT
Common Name English
MORPHINAN-6-OL, 7,8-DIDEHYDRO-4,5-EPOXY-3-METHOXY-17-METHYL-, 6-(3-PYRIDINECARBOXYLATE), (5.ALPHA.,6.ALPHA.)-
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C66917
Created by admin on Fri Dec 15 16:18:54 GMT 2023 , Edited by admin on Fri Dec 15 16:18:54 GMT 2023
DEA NO. 9309
Created by admin on Fri Dec 15 16:18:54 GMT 2023 , Edited by admin on Fri Dec 15 16:18:54 GMT 2023
Code System Code Type Description
PUBCHEM
5463872
Created by admin on Fri Dec 15 16:18:54 GMT 2023 , Edited by admin on Fri Dec 15 16:18:54 GMT 2023
PRIMARY
EPA CompTox
DTXSID10190360
Created by admin on Fri Dec 15 16:18:54 GMT 2023 , Edited by admin on Fri Dec 15 16:18:54 GMT 2023
PRIMARY
ECHA (EC/EINECS)
222-990-5
Created by admin on Fri Dec 15 16:18:54 GMT 2023 , Edited by admin on Fri Dec 15 16:18:54 GMT 2023
PRIMARY
DRUG CENTRAL
1914
Created by admin on Fri Dec 15 16:18:54 GMT 2023 , Edited by admin on Fri Dec 15 16:18:54 GMT 2023
PRIMARY
SMS_ID
100000084189
Created by admin on Fri Dec 15 16:18:54 GMT 2023 , Edited by admin on Fri Dec 15 16:18:54 GMT 2023
PRIMARY
CAS
3688-66-2
Created by admin on Fri Dec 15 16:18:54 GMT 2023 , Edited by admin on Fri Dec 15 16:18:54 GMT 2023
PRIMARY
INN
1249
Created by admin on Fri Dec 15 16:18:54 GMT 2023 , Edited by admin on Fri Dec 15 16:18:54 GMT 2023
PRIMARY
MESH
C021063
Created by admin on Fri Dec 15 16:18:54 GMT 2023 , Edited by admin on Fri Dec 15 16:18:54 GMT 2023
PRIMARY
NCI_THESAURUS
C84008
Created by admin on Fri Dec 15 16:18:54 GMT 2023 , Edited by admin on Fri Dec 15 16:18:54 GMT 2023
PRIMARY
FDA UNII
DYX391P13E
Created by admin on Fri Dec 15 16:18:54 GMT 2023 , Edited by admin on Fri Dec 15 16:18:54 GMT 2023
PRIMARY
WIKIPEDIA
Nicocodeine
Created by admin on Fri Dec 15 16:18:54 GMT 2023 , Edited by admin on Fri Dec 15 16:18:54 GMT 2023
PRIMARY
EVMPD
SUB09233MIG
Created by admin on Fri Dec 15 16:18:54 GMT 2023 , Edited by admin on Fri Dec 15 16:18:54 GMT 2023
PRIMARY
ChEMBL
CHEMBL2105136
Created by admin on Fri Dec 15 16:18:54 GMT 2023 , Edited by admin on Fri Dec 15 16:18:54 GMT 2023
PRIMARY