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

Details

Stereochemistry ABSOLUTE
Molecular Formula C43H66O15
Molecular Weight 822.9751
Optical Activity UNSPECIFIED
Defined Stereocenters 21 / 21
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of .ALPHA.-ACETYLDIGOXIN

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](OC(C)=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=HWKJSYYYURVNQU-DXJNJSHLSA-N
InChI=1S/C43H66O15/c1-20-38(49)32(55-23(4)44)18-37(52-20)58-40-22(3)54-36(17-31(40)46)57-39-21(2)53-35(16-30(39)45)56-26-9-11-41(5)25(14-26)7-8-28-29(41)15-33(47)42(6)27(10-12-43(28,42)50)24-13-34(48)51-19-24/h13,20-22,25-33,35-40,45-47,49-50H,7-12,14-19H2,1-6H3/t20-,21-,22-,25-,26+,27-,28-,29+,30+,31+,32+,33-,35+,36+,37+,38-,39-,40-,41+,42+,43+/m1/s1

HIDE SMILES / InChI
Acetyldigoxin, a cardiac glycoside that has been studied in patients with congestive heart failure.

Approval Year

PubMed

PubMed

TitleDatePubMed
[Cardiotonic and cardiotoxic properties of acetyldigoxin].
1963 Feb 5
[Acetyldigoxin. Clinical study in 25 patients].
1963 May

Sample Use Guides

For rapid digitalization in 2-3 days, the initial dose was 1.2 to 2.6mg (average 1.96mg). For medium-fast digitalization in 4 days, the loading dose was 2.0 to 3.2mg (average 2.7mg). For slow digitalization 0.1 to 0.4mg was required for 5 to 6 days without loading dose. The maintenance dose was 0.1 to 0.4mg (average 0.33mg) daily.
Route of Administration: Oral
Name Type Language
.ALPHA.-ACETYLDIGOXIN
MI  
Common Name English
ACETYLDIGOXIN
WHO-DD  
Common Name English
.ALPHA.-ACETYLDIGOXIN [MI]
Common Name English
Acetyldigoxin [WHO-DD]
Common Name English
3.BETA.-((3-O-ACETYL-2,6-DIDEOXY-.BETA.-D-RIBO-HEXOPYRANOSYL-(1->4)-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
Systematic Name English
LANATILIN
Brand Name English
DIGOXIN IMPURITY I [EP IMPURITY]
Common Name English
DIGOXIN, 3'''-ACETATE
Common Name English
SANDOLANID
Brand Name English
Classification Tree Code System Code
WHO-VATC QC01AA52
Created by admin on Sat Dec 16 01:49:50 GMT 2023 , Edited by admin on Sat Dec 16 01:49:50 GMT 2023
WHO-ATC C01AA02
Created by admin on Sat Dec 16 01:49:50 GMT 2023 , Edited by admin on Sat Dec 16 01:49:50 GMT 2023
WHO-VATC QC01AA02
Created by admin on Sat Dec 16 01:49:50 GMT 2023 , Edited by admin on Sat Dec 16 01:49:50 GMT 2023
WHO-ATC C01AA52
Created by admin on Sat Dec 16 01:49:50 GMT 2023 , Edited by admin on Sat Dec 16 01:49:50 GMT 2023
Code System Code Type Description
FDA UNII
Q28IFH7A50
Created by admin on Sat Dec 16 01:49:50 GMT 2023 , Edited by admin on Sat Dec 16 01:49:50 GMT 2023
PRIMARY
DRUG BANK
DB13691
Created by admin on Sat Dec 16 01:49:50 GMT 2023 , Edited by admin on Sat Dec 16 01:49:50 GMT 2023
PRIMARY
EVMPD
SUB12718MIG
Created by admin on Sat Dec 16 01:49:50 GMT 2023 , Edited by admin on Sat Dec 16 01:49:50 GMT 2023
PRIMARY
CAS
5511-98-8
Created by admin on Sat Dec 16 01:49:50 GMT 2023 , Edited by admin on Sat Dec 16 01:49:50 GMT 2023
PRIMARY
ECHA (EC/EINECS)
226-855-1
Created by admin on Sat Dec 16 01:49:50 GMT 2023 , Edited by admin on Sat Dec 16 01:49:50 GMT 2023
PRIMARY
DRUG CENTRAL
68
Created by admin on Sat Dec 16 01:49:50 GMT 2023 , Edited by admin on Sat Dec 16 01:49:50 GMT 2023
PRIMARY
RXCUI
199
Created by admin on Sat Dec 16 01:49:50 GMT 2023 , Edited by admin on Sat Dec 16 01:49:50 GMT 2023
PRIMARY
PUBCHEM
11765960
Created by admin on Sat Dec 16 01:49:50 GMT 2023 , Edited by admin on Sat Dec 16 01:49:50 GMT 2023
PRIMARY
EVMPD
SUB22301
Created by admin on Sat Dec 16 01:49:50 GMT 2023 , Edited by admin on Sat Dec 16 01:49:50 GMT 2023
ALTERNATIVE
SMS_ID
100000086013
Created by admin on Sat Dec 16 01:49:50 GMT 2023 , Edited by admin on Sat Dec 16 01:49:50 GMT 2023
PRIMARY
EPA CompTox
DTXSID00203630
Created by admin on Sat Dec 16 01:49:50 GMT 2023 , Edited by admin on Sat Dec 16 01:49:50 GMT 2023
PRIMARY
WIKIPEDIA
α-Acetyldigoxin
Created by admin on Sat Dec 16 01:49:50 GMT 2023 , Edited by admin on Sat Dec 16 01:49:50 GMT 2023
PRIMARY
MERCK INDEX
m4456
Created by admin on Sat Dec 16 01:49:50 GMT 2023 , Edited by admin on Sat Dec 16 01:49:50 GMT 2023
PRIMARY Merck Index