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Details

Stereochemistry ABSOLUTE
Molecular Formula C18H23NO3
Molecular Weight 301.3801
Optical Activity UNSPECIFIED
Defined Stereocenters 5 / 5
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DIHYDROCODEINE

SMILES

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

InChI

InChIKey=RBOXVHNMENFORY-DNJOTXNNSA-N
InChI=1S/C18H23NO3/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/h3,6,11-13,17,20H,4-5,7-9H2,1-2H3/t11-,12+,13-,17-,18-/m0/s1

HIDE SMILES / InChI

Approval Year

Unknown
86413
Name Type Language
DIHYDROCODEINE
INN   MART.   MI   VANDF   WHO-DD  
INN  
Official Name English
HYDROCODONE HYDROGEN TARTRATE 2.5-HYDRATE IMPURITY B [EP IMPURITY]
Common Name English
DIHYDROCODEINE [MI]
Common Name English
DH-CODEINE
Common Name English
.ALPHA.-HYDROCODOL
Common Name English
DEHACODIN
Common Name English
Dihydrocodeine [WHO-DD]
Common Name English
RAPACODIN
Common Name English
IDS-ND-008(SECT.2)
Code English
NOVICONDIN
Common Name English
3-METHOXY-12-METHYL-5,6,7,7A,8,9-HEXAHYDRO-4AH-8,9C-IMINOETHANOPHENANTHRO(4,5-BCD)FURAN-5-OL
Systematic Name English
dihydrocodeine [INN]
Common Name English
DIHYDROCODEINE [MART.]
Common Name English
REMEDACEN
Brand Name English
4,5.ALPHA.-EPOXY-3-METHOXY-17-METHYLMORPHINAN-6.ALPHA.-OL
Systematic Name English
CODHYDRINE
Common Name English
NSC-231319
Code English
MORPHINAN-6-OL, 4,5-EPOXY-3-METHOXY-17-METHYL-
Systematic Name English
DIHYDROCODEINE [VANDF]
Common Name English
DIHYDRONEOPINE
Common Name English
8,14-DIHYDRONEOPINE
Common Name English
Classification Tree Code System Code
WHO-VATC QN02AA58
Created by admin on Fri Dec 15 16:29:26 UTC 2023 , Edited by admin on Fri Dec 15 16:29:26 UTC 2023
WHO-ATC N02AA08
Created by admin on Fri Dec 15 16:29:26 UTC 2023 , Edited by admin on Fri Dec 15 16:29:26 UTC 2023
WHO-VATC QN02AA08
Created by admin on Fri Dec 15 16:29:26 UTC 2023 , Edited by admin on Fri Dec 15 16:29:26 UTC 2023
WHO-ATC N02AJ02
Created by admin on Fri Dec 15 16:29:26 UTC 2023 , Edited by admin on Fri Dec 15 16:29:26 UTC 2023
LIVERTOX 308
Created by admin on Fri Dec 15 16:29:26 UTC 2023 , Edited by admin on Fri Dec 15 16:29:26 UTC 2023
NDF-RT N0000175684
Created by admin on Fri Dec 15 16:29:26 UTC 2023 , Edited by admin on Fri Dec 15 16:29:26 UTC 2023
DEA NO. 9120
Created by admin on Fri Dec 15 16:29:26 UTC 2023 , Edited by admin on Fri Dec 15 16:29:26 UTC 2023
NCI_THESAURUS C1506
Created by admin on Fri Dec 15 16:29:26 UTC 2023 , Edited by admin on Fri Dec 15 16:29:26 UTC 2023
NCI_THESAURUS C67413
Created by admin on Fri Dec 15 16:29:26 UTC 2023 , Edited by admin on Fri Dec 15 16:29:26 UTC 2023
WHO-ATC N02AA58
Created by admin on Fri Dec 15 16:29:26 UTC 2023 , Edited by admin on Fri Dec 15 16:29:26 UTC 2023
WHO-ATC N02AJ01
Created by admin on Fri Dec 15 16:29:26 UTC 2023 , Edited by admin on Fri Dec 15 16:29:26 UTC 2023
WHO-ATC N02AJ03
Created by admin on Fri Dec 15 16:29:26 UTC 2023 , Edited by admin on Fri Dec 15 16:29:26 UTC 2023
NDF-RT N0000175690
Created by admin on Fri Dec 15 16:29:26 UTC 2023 , Edited by admin on Fri Dec 15 16:29:26 UTC 2023
Code System Code Type Description
DAILYMED
N9I9HDB855
Created by admin on Fri Dec 15 16:29:26 UTC 2023 , Edited by admin on Fri Dec 15 16:29:26 UTC 2023
PRIMARY
MERCK INDEX
m4459
Created by admin on Fri Dec 15 16:29:26 UTC 2023 , Edited by admin on Fri Dec 15 16:29:26 UTC 2023
PRIMARY Merck Index
ECHA (EC/EINECS)
204-732-3
Created by admin on Fri Dec 15 16:29:26 UTC 2023 , Edited by admin on Fri Dec 15 16:29:26 UTC 2023
PRIMARY
NSC
231319
Created by admin on Fri Dec 15 16:29:26 UTC 2023 , Edited by admin on Fri Dec 15 16:29:26 UTC 2023
PRIMARY
DRUG CENTRAL
886
Created by admin on Fri Dec 15 16:29:26 UTC 2023 , Edited by admin on Fri Dec 15 16:29:26 UTC 2023
PRIMARY
WIKIPEDIA
DIHYDROCODEINE
Created by admin on Fri Dec 15 16:29:26 UTC 2023 , Edited by admin on Fri Dec 15 16:29:26 UTC 2023
PRIMARY
RXCUI
23088
Created by admin on Fri Dec 15 16:29:26 UTC 2023 , Edited by admin on Fri Dec 15 16:29:26 UTC 2023
PRIMARY RxNorm
NCI_THESAURUS
C84508
Created by admin on Fri Dec 15 16:29:26 UTC 2023 , Edited by admin on Fri Dec 15 16:29:26 UTC 2023
PRIMARY
IUPHAR
7594
Created by admin on Fri Dec 15 16:29:26 UTC 2023 , Edited by admin on Fri Dec 15 16:29:26 UTC 2023
PRIMARY
ChEMBL
CHEMBL1595
Created by admin on Fri Dec 15 16:29:26 UTC 2023 , Edited by admin on Fri Dec 15 16:29:26 UTC 2023
PRIMARY
CAS
125-28-0
Created by admin on Fri Dec 15 16:29:26 UTC 2023 , Edited by admin on Fri Dec 15 16:29:26 UTC 2023
PRIMARY
FDA UNII
N9I9HDB855
Created by admin on Fri Dec 15 16:29:26 UTC 2023 , Edited by admin on Fri Dec 15 16:29:26 UTC 2023
PRIMARY
PUBCHEM
5284543
Created by admin on Fri Dec 15 16:29:26 UTC 2023 , Edited by admin on Fri Dec 15 16:29:26 UTC 2023
PRIMARY
SMS_ID
100000092218
Created by admin on Fri Dec 15 16:29:26 UTC 2023 , Edited by admin on Fri Dec 15 16:29:26 UTC 2023
PRIMARY
DRUG BANK
DB01551
Created by admin on Fri Dec 15 16:29:26 UTC 2023 , Edited by admin on Fri Dec 15 16:29:26 UTC 2023
PRIMARY
LACTMED
Dihydrocodeine
Created by admin on Fri Dec 15 16:29:26 UTC 2023 , Edited by admin on Fri Dec 15 16:29:26 UTC 2023
PRIMARY
EVMPD
SUB07138MIG
Created by admin on Fri Dec 15 16:29:26 UTC 2023 , Edited by admin on Fri Dec 15 16:29:26 UTC 2023
PRIMARY
INN
728
Created by admin on Fri Dec 15 16:29:26 UTC 2023 , Edited by admin on Fri Dec 15 16:29:26 UTC 2023
PRIMARY
EPA CompTox
DTXSID5022936
Created by admin on Fri Dec 15 16:29:26 UTC 2023 , Edited by admin on Fri Dec 15 16:29:26 UTC 2023
PRIMARY
MESH
C014481
Created by admin on Fri Dec 15 16:29:26 UTC 2023 , Edited by admin on Fri Dec 15 16:29:26 UTC 2023
PRIMARY
ACTIVE MOIETY
Structure of DIHYDROCODEINE
METABOLITE ACTIVE (PARENT)
Structure of DIHYDROMORPHINE
PARENT (SALT/SOLVATE)
Structure of DIHYDROCODEINE THIOCYANATE
SALT/SOLVATE (PARENT)
Structure of DIHYDROCODEINE BITARTRATE
SALT/SOLVATE (PARENT)
Structure of DIHYDROCODEINE PHOSPHATE
NIH
NCATS
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