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Details

Stereochemistry ABSOLUTE
Molecular Formula C41H64O14
Molecular Weight 780.9385
Optical Activity UNSPECIFIED
Defined Stereocenters 21 / 21
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Digoxin

SMILES

[H][C@@]1(C[C@H](O)[C@H](O[C@@]2([H])C[C@H](O)[C@H](O[C@@]3([H])C[C@H](O)[C@H](O)[C@@H](C)O3)[C@@H](C)O2)[C@@H](C)O1)O[C@H]4CC[C@@]5(C)[C@]([H])(CC[C@]6([H])[C@]5([H])C[C@@H](O)[C@]7(C)[C@H](CC[C@]67O)C8=CC(=O)OC8)C4

InChI

InChIKey=LTMHDMANZUZIPE-PUGKRICDSA-N
InChI=1S/C41H64O14/c1-19-36(47)28(42)15-34(50-19)54-38-21(3)52-35(17-30(38)44)55-37-20(2)51-33(16-29(37)43)53-24-8-10-39(4)23(13-24)6-7-26-27(39)14-31(45)40(5)25(9-11-41(26,40)48)22-12-32(46)49-18-22/h12,19-21,23-31,33-38,42-45,47-48H,6-11,13-18H2,1-5H3/t19-,20-,21-,23-,24+,25-,26-,27+,28+,29+,30+,31-,33+,34+,35+,36-,37-,38-,39+,40+,41+/m1/s1

HIDE SMILES / InChI

Approval Year

Unknown
86413
Name Type Language
Digoxin
EP   HSDB   INN   MART.   MI   ORANGE BOOK   USP   USP-RS   VANDF   WHO-DD   WHO-IP  
INN  
Official Name English
DYNAMOS
Common Name English
DIGOXIN [IARC]
Common Name English
STILLACOR-
Common Name English
LANOCARDIN
Common Name English
DIGOXIN [WHO-IP]
Common Name English
DIGOXIN [MI]
Common Name English
Digoxin [WHO-DD]
Common Name English
TOLOXIN
Common Name English
MAPLUXIN
Common Name English
DIGOXIN [VANDF]
Common Name English
DIGOXIN [EP MONOGRAPH]
Common Name English
DIGOXIN [HSDB]
Common Name English
3.BETA.-((O-2,6-DIDEOXY-.BETA.-D-RIBO-HEXOPYRANOSYL-(1->4)-O-2,6-DIDEOXY-.BETA.-D-RIBO-HEXOPYRANOSYL-(1->4)-2,6-DIDEOXY-.BETA.-D-RIBO-HEXOPYRANOSYL)OXY)-12.BETA.,14-DIHYDROXY-5.BETA.-CARD-20(22)-ENOLIDE
Common Name English
DIGOXINUM [WHO-IP LATIN]
Common Name English
NATIGOXIN
Common Name English
digoxin [INN]
Common Name English
DIGOXIN [USP-RS]
Common Name English
DIGOXIN [MART.]
Common Name English
DIGOXIN [JAN]
Common Name English
DIGOXIN [USP MONOGRAPH]
Common Name English
VANOXIN
Common Name English
CARD-20(22)-ENOLIDE, 3-((O-2,6-DIDEOXY-.BETA.-D-RIBO-HEXOPYRANOSYL-(1->4)-O-2,6-DIDEOXY-.BETA.-D-RIBO-HEXOPYRANOSYL-(1->4)-2,6-DIDEOXY-.BETA.-D-RIBO-HEXOPYRANOSYL)OXY)-12,14-DIHYDROXY-,(3.BETA.,5.BETA.,12.BETA.)-
Common Name English
NSC-95100
Code English
DIGOXIN [ORANGE BOOK]
Common Name English
LANOXIN
Brand Name English
ROUGOXIN
Common Name English
FARGOXIN
Common Name English
Classification Tree Code System Code
NDF-RT N0000175568
Created by admin on Fri Dec 15 15:07:22 UTC 2023 , Edited by admin on Fri Dec 15 15:07:22 UTC 2023
WHO-VATC QC01AA05
Created by admin on Fri Dec 15 15:07:22 UTC 2023 , Edited by admin on Fri Dec 15 15:07:22 UTC 2023
WHO-ESSENTIAL MEDICINES LIST 12.2
Created by admin on Fri Dec 15 15:07:22 UTC 2023 , Edited by admin on Fri Dec 15 15:07:22 UTC 2023
NCI_THESAURUS C823
Created by admin on Fri Dec 15 15:07:22 UTC 2023 , Edited by admin on Fri Dec 15 15:07:22 UTC 2023
LIVERTOX 307
Created by admin on Fri Dec 15 15:07:22 UTC 2023 , Edited by admin on Fri Dec 15 15:07:22 UTC 2023
NDF-RT N0000008157
Created by admin on Fri Dec 15 15:07:22 UTC 2023 , Edited by admin on Fri Dec 15 15:07:22 UTC 2023
NDF-RT N0000008157
Created by admin on Fri Dec 15 15:07:22 UTC 2023 , Edited by admin on Fri Dec 15 15:07:22 UTC 2023
CFR 21 CFR 862.3320
Created by admin on Fri Dec 15 15:07:22 UTC 2023 , Edited by admin on Fri Dec 15 15:07:22 UTC 2023
WHO-ESSENTIAL MEDICINES LIST 12.4
Created by admin on Fri Dec 15 15:07:22 UTC 2023 , Edited by admin on Fri Dec 15 15:07:22 UTC 2023
NCI_THESAURUS C78322
Created by admin on Fri Dec 15 15:07:22 UTC 2023 , Edited by admin on Fri Dec 15 15:07:22 UTC 2023
WHO-ATC C01AA05
Created by admin on Fri Dec 15 15:07:22 UTC 2023 , Edited by admin on Fri Dec 15 15:07:22 UTC 2023
Code System Code Type Description
ECHA (EC/EINECS)
244-068-1
Created by admin on Fri Dec 15 15:07:22 UTC 2023 , Edited by admin on Fri Dec 15 15:07:22 UTC 2023
PRIMARY
HSDB
214
Created by admin on Fri Dec 15 15:07:22 UTC 2023 , Edited by admin on Fri Dec 15 15:07:22 UTC 2023
PRIMARY
MERCK INDEX
m4456
Created by admin on Fri Dec 15 15:07:22 UTC 2023 , Edited by admin on Fri Dec 15 15:07:22 UTC 2023
PRIMARY Merck Index
EPA CompTox
DTXSID5022934
Created by admin on Fri Dec 15 15:07:22 UTC 2023 , Edited by admin on Fri Dec 15 15:07:22 UTC 2023
PRIMARY
CAS
20830-75-5
Created by admin on Fri Dec 15 15:07:22 UTC 2023 , Edited by admin on Fri Dec 15 15:07:22 UTC 2023
PRIMARY
SMS_ID
100000091378
Created by admin on Fri Dec 15 15:07:22 UTC 2023 , Edited by admin on Fri Dec 15 15:07:22 UTC 2023
PRIMARY
EVMPD
SUB07135MIG
Created by admin on Fri Dec 15 15:07:22 UTC 2023 , Edited by admin on Fri Dec 15 15:07:22 UTC 2023
PRIMARY
RXCUI
3407
Created by admin on Fri Dec 15 15:07:22 UTC 2023 , Edited by admin on Fri Dec 15 15:07:22 UTC 2023
PRIMARY RxNorm
CHEBI
145795
Created by admin on Fri Dec 15 15:07:22 UTC 2023 , Edited by admin on Fri Dec 15 15:07:22 UTC 2023
PRIMARY
ChEMBL
CHEMBL1751
Created by admin on Fri Dec 15 15:07:22 UTC 2023 , Edited by admin on Fri Dec 15 15:07:22 UTC 2023
PRIMARY
INN
389
Created by admin on Fri Dec 15 15:07:22 UTC 2023 , Edited by admin on Fri Dec 15 15:07:22 UTC 2023
PRIMARY
WIKIPEDIA
DIGOXIN
Created by admin on Fri Dec 15 15:07:22 UTC 2023 , Edited by admin on Fri Dec 15 15:07:22 UTC 2023
PRIMARY
NSC
95100
Created by admin on Fri Dec 15 15:07:22 UTC 2023 , Edited by admin on Fri Dec 15 15:07:22 UTC 2023
PRIMARY
LACTMED
Digoxin
Created by admin on Fri Dec 15 15:07:22 UTC 2023 , Edited by admin on Fri Dec 15 15:07:22 UTC 2023
PRIMARY
DRUG CENTRAL
882
Created by admin on Fri Dec 15 15:07:22 UTC 2023 , Edited by admin on Fri Dec 15 15:07:22 UTC 2023
PRIMARY
DRUG BANK
DB00390
Created by admin on Fri Dec 15 15:07:22 UTC 2023 , Edited by admin on Fri Dec 15 15:07:22 UTC 2023
PRIMARY
NCI_THESAURUS
C28990
Created by admin on Fri Dec 15 15:07:22 UTC 2023 , Edited by admin on Fri Dec 15 15:07:22 UTC 2023
PRIMARY
IUPHAR
4726
Created by admin on Fri Dec 15 15:07:22 UTC 2023 , Edited by admin on Fri Dec 15 15:07:22 UTC 2023
PRIMARY
CHEBI
4551
Created by admin on Fri Dec 15 15:07:22 UTC 2023 , Edited by admin on Fri Dec 15 15:07:22 UTC 2023
PRIMARY
FDA UNII
73K4184T59
Created by admin on Fri Dec 15 15:07:22 UTC 2023 , Edited by admin on Fri Dec 15 15:07:22 UTC 2023
PRIMARY
MESH
D004077
Created by admin on Fri Dec 15 15:07:22 UTC 2023 , Edited by admin on Fri Dec 15 15:07:22 UTC 2023
PRIMARY
RS_ITEM_NUM
1200000
Created by admin on Fri Dec 15 15:07:22 UTC 2023 , Edited by admin on Fri Dec 15 15:07:22 UTC 2023
PRIMARY
DAILYMED
73K4184T59
Created by admin on Fri Dec 15 15:07:22 UTC 2023 , Edited by admin on Fri Dec 15 15:07:22 UTC 2023
PRIMARY
PUBCHEM
2724385
Created by admin on Fri Dec 15 15:07:22 UTC 2023 , Edited by admin on Fri Dec 15 15:07:22 UTC 2023
PRIMARY
WHO INTERNATIONAL PHARMACOPEIA
DIGOXIN
Created by admin on Fri Dec 15 15:07:22 UTC 2023 , Edited by admin on Fri Dec 15 15:07:22 UTC 2023
PRIMARY Description: Colourless crystals or a white or almost white, crystalline powder; odourless.Solubility: Practically insoluble in water and ether R; freely soluble in pyridine R; slightly soluble in ethanol (~750 g/l) TS.Category: Cardiotonic.Storage: Digoxin should be kept in a well-closed container, protected from light.Additional information: CAUTION: Digoxin is extremely poisonous and should be handled with care.Requirements : Definition. Digoxin contains not less than 95.0% and not more than 103.0% of C41H64O14, calculated with reference to the driedsubstance.
ACTIVE MOIETY
Structure of Digoxin
METABOLITE (PARENT)
Structure of DIGOXIGENIN 3-O-SULFATE
METABOLITE (PARENT)
Structure of DIHYDRODIGOXIN
METABOLITE (PARENT)
Structure of 3-OXODIGOXIGENIN
METABOLITE (PARENT)
Structure of DIGOXIGENIN
PARENT (METABOLITE)
Structure of METILDIGOXIN
NIH
NCATS
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