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Details

Stereochemistry ABSOLUTE
Molecular Formula C18H21NO3.H3O4P
Molecular Weight 397.3594
Optical Activity UNSPECIFIED
Defined Stereocenters 5 / 5
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CODEINE PHOSPHATE ANHYDROUS

SMILES

OP(O)(O)=O.[H][C@@]12OC3=C4C(C[C@H]5N(C)CC[C@@]14[C@@]5([H])C=C[C@@H]2O)=CC=C3OC

InChI

InChIKey=WUXLCJZUUHIXFY-FFHNEAJVSA-N
InChI=1S/C18H21NO3.H3O4P/c1-19-8-7-18-11-4-5-13(20)17(18)22-16-14(21-2)6-3-10(15(16)18)9-12(11)19;1-5(2,3)4/h3-6,11-13,17,20H,7-9H2,1-2H3;(H3,1,2,3,4)/t11-,12+,13-,17-,18-;/m0./s1

HIDE SMILES / InChI

Molecular Formula C18H21NO3
Molecular Weight 299.3642
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 5 / 5
E/Z Centers 0
Optical Activity UNSPECIFIED

Molecular Formula H3O4P
Molecular Weight 97.9952
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Codeine is an opiate used to manage mild to moderate pain severe enough to require an opioid. Codeine is a selective agonist for the mu opioid receptor and has an affinity to delta and kappa-opioid receptors. In some countries, this drug is regulated under various narcotic control laws, because its chronic use can cause physical dependence. In others, it is available without a medical prescription in combination with paracetamol.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
6.1 µM [EC50]
Target ID: P41145
Gene ID: 4986.0
Gene Symbol: OPRK1
Target Organism: Homo sapiens (Human)
Target ID: P41143
Gene ID: 4985.0
Gene Symbol: OPRD1
Target Organism: Homo sapiens (Human)
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
CAPITAL AND CODEINE

Approved Use

Unknown
Sourcing

Sourcing

Vendor/AggregatorIDURL
PubMed

PubMed

TitleDatePubMed
Mimicking gene defects to treat drug dependence.
2000
Over-the-counter medications for acute cough in children and adults in ambulatory settings.
2001
[Guillain-Barre syndrome as a result of poisoning with a mixture of "kompot"(Polish heroin) and drugs].
2001
Chromatographic analysis of phenethylamine-antihistamine combinations using C8, C18 or cyano columns and micellar sodium dodecyl sulfate-pentanol mixtures.
2001 Apr
Angle closure risk from proprietary medicines.
2001 Apr
LC method for the analysis of acetylsalicylic acid, caffeine and codeine phosphate in pharmaceutical preparations.
2001 Apr
[Adverse cutaneous side-effect of codeine administration].
2001 Apr 15
LC method for the analysis of paracetamol, caffeine and codeine phosphate in pharmaceutical preparations.
2001 Dec
The safety of dextromethorphan in pregnancy : results of a controlled study.
2001 Feb
Dose-related effects of controlled release dihydrocodeine on oro-cecal transit and pupillary light reflex. A study in human volunteers.
2001 Jan
Successful use of propranolol in migraine associated with electroconvulsive therapy.
2001 Jan
Opiate-sensitivity: clinical characteristics and the role of skin prick testing.
2001 Jul
Contribution of dihydrocodeine and dihydromorphine to analgesia following dihydrocodeine administration in man: a PK-PD modelling analysis.
2001 Jul
Use of beta-cyclodextrin in the capillary zone electrophoretic separation of the components of clandestine heroin preparations.
2001 Jul 27
Analysis of cocaine, benzoylecgonine, codeine, and morphine in hair by supercritical fluid extraction with carbon dioxide modified with methanol.
2001 Jun 1
Opiate use to control bowel motility may induce chronic daily headache in patients with migraine.
2001 Mar
Audit of pain management at home following tonsillectomy in children.
2001 Mar
Treatment of severe pain from osteoarthritis with slow-release tramadol or dihydrocodeine in combination with NSAID's: a randomised study comparing analgesia, antinociception and gastrointestinal effects.
2001 Mar
Dihydrocodeine--drug of use or misuse?
2001 May
Effect of an enteric-release formulation of naloxone on intestinal transit in volunteers taking codeine.
2001 May
Selective antibodies to methadone enantiomers: synthesis of (R)- and (R,S)-methadone conjugates and determination by an immunoenzymatic method in human serum.
2001 May 5
Application of liquid chromatography to the simultaneous determination of acetylsalicylic acid, caffeine, codeine, paracetamol, pyridoxine, and thiamine in pharmaceutical preparations.
2001 May-Jun
Regional block and mexiletine: the effect on pain after cancer breast surgery.
2001 May-Jun
Concentration ratios of morphine to codeine in blood of impaired drivers as evidence of heroin use and not medication with codeine.
2001 Nov
Seizures with intravenous codeine phosphate.
2001 Oct
Endogenous morphine and codeine. Possible role as endogenous anticonvulsants.
2001 Oct 12
Detection of non-prescription heroin markers in urine with liquid chromatography-atmospheric pressure chemical ionization mass spectrometry.
2001 Sep
Pain control in medical abortion.
2001 Sep
Experience with urine drug testing by the Correctional Service of Canada.
2001 Sep 15
Patents

Sample Use Guides

Unknown
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Fri Dec 15 17:39:30 UTC 2023
Edited
by admin
on Fri Dec 15 17:39:30 UTC 2023
Record UNII
2X585M1M3T
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CODEINE PHOSPHATE ANHYDROUS
Common Name English
Codeine phosphate [WHO-DD]
Common Name English
MORPHINAN-6-OL, 7,8-DIDEHYDRO-4,5-EPOXY-3-METHOXY-17-METHYL-, (5.ALPHA.,6.ALPHA.)-, PHOSPHATE (1:1) (SALT)
Common Name English
CODEINE PHOSPHATE [MI]
Common Name English
7,8-DIDEHYDRO-4,5.ALPHA.-EPOXY-3-METHOXY-17-METHYLMORPHINAN-6.ALPHA.-OL PHOSPHATE (1:1) (SALT)
Common Name English
Code System Code Type Description
EPA CompTox
DTXSID0024844
Created by admin on Fri Dec 15 17:39:30 UTC 2023 , Edited by admin on Fri Dec 15 17:39:30 UTC 2023
PRIMARY
CAS
52-28-8
Created by admin on Fri Dec 15 17:39:30 UTC 2023 , Edited by admin on Fri Dec 15 17:39:30 UTC 2023
PRIMARY
DAILYMED
2X585M1M3T
Created by admin on Fri Dec 15 17:39:30 UTC 2023 , Edited by admin on Fri Dec 15 17:39:30 UTC 2023
PRIMARY
PUBCHEM
5359227
Created by admin on Fri Dec 15 17:39:30 UTC 2023 , Edited by admin on Fri Dec 15 17:39:30 UTC 2023
PRIMARY
MERCK INDEX
m3718
Created by admin on Fri Dec 15 17:39:30 UTC 2023 , Edited by admin on Fri Dec 15 17:39:30 UTC 2023
PRIMARY Merck Index
RXCUI
1652891
Created by admin on Fri Dec 15 17:39:30 UTC 2023 , Edited by admin on Fri Dec 15 17:39:30 UTC 2023
PRIMARY RxNorm
SMS_ID
100000079791
Created by admin on Fri Dec 15 17:39:30 UTC 2023 , Edited by admin on Fri Dec 15 17:39:30 UTC 2023
PRIMARY
FDA UNII
2X585M1M3T
Created by admin on Fri Dec 15 17:39:30 UTC 2023 , Edited by admin on Fri Dec 15 17:39:30 UTC 2023
PRIMARY
ECHA (EC/EINECS)
200-137-8
Created by admin on Fri Dec 15 17:39:30 UTC 2023 , Edited by admin on Fri Dec 15 17:39:30 UTC 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE
SOLVATE->ANHYDROUS
Related Record Type Details
ACTIVE MOIETY