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Details

Stereochemistry ABSOLUTE
Molecular Formula C42H64O15
Molecular Weight 808.9486
Optical Activity UNSPECIFIED
Defined Stereocenters 21 / 21
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of GITALOXIN

SMILES

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

InChI

InChIKey=GZZJHPZDXZCDDA-MBJUQXSJSA-N
InChI=1S/C42H64O15/c1-20-37(48)28(44)14-34(52-20)56-39-22(3)54-35(16-30(39)46)57-38-21(2)53-33(15-29(38)45)55-25-8-10-40(4)24(13-25)6-7-27-26(40)9-11-41(5)36(23-12-32(47)50-18-23)31(51-19-43)17-42(27,41)49/h12,19-22,24-31,33-39,44-46,48-49H,6-11,13-18H2,1-5H3/t20-,21-,22-,24-,25+,26+,27-,28+,29+,30+,31+,33+,34+,35+,36+,37-,38-,39-,40+,41-,42+/m1/s1

HIDE SMILES / InChI

Molecular Formula C42H64O15
Molecular Weight 808.9486
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 21 / 21
E/Z Centers 0
Optical Activity UNSPECIFIED

Gitaloxin or 16-formylgiloxine is a cardiotonic glycoside extracted from Digitalis purpurea. It acts as a Na, K-ATPase. Gitaloxin has been investigated in the treatment of cardiac insufficiency.

Approval Year

PubMed

PubMed

TitleDatePubMed
Gitaloxin poisoning in a child.
1996-12
Influence of 16 beta formylation on Na, K-ATPase inhibition by cardiac glycosides.
1982-11
[CLINICAL TRIALS OF A NEW DIGITALIS CARDIOTONIC: 16-FORMYLGITOXIN IN THE TREATMENT OF CARDIAC INSUFFICIENCY].
1964-02-20
Patents

Patents

Substance Class Chemical
Created
by admin
on Wed Apr 02 09:06:13 GMT 2025
Edited
by admin
on Wed Apr 02 09:06:13 GMT 2025
Record UNII
H25D0X8L90
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
16-FORMYLGITOXIN
Preferred Name English
GITALOXIN
INN   WHO-DD  
INN  
Official Name English
GITOXIN 16-FORMATE
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)-16-(FORMYLOXY)-14-HYDROXY-, (3.BETA.,5.BETA.,16.BETA.)-
Common Name English
CRISTALOXINE
Common Name English
Gitaloxin [WHO-DD]
Common Name English
gitaloxin [INN]
Common Name English
GITOXIGENIN TRIDIGITOXOSIDE 16-FORMATE
Common Name English
Code System Code Type Description
INN
4252
Created by admin on Wed Apr 02 09:06:13 GMT 2025 , Edited by admin on Wed Apr 02 09:06:13 GMT 2025
PRIMARY
ChEMBL
CHEMBL1908317
Created by admin on Wed Apr 02 09:06:13 GMT 2025 , Edited by admin on Wed Apr 02 09:06:13 GMT 2025
PRIMARY
ECHA (EC/EINECS)
221-864-7
Created by admin on Wed Apr 02 09:06:13 GMT 2025 , Edited by admin on Wed Apr 02 09:06:13 GMT 2025
PRIMARY
CHEBI
70996
Created by admin on Wed Apr 02 09:06:13 GMT 2025 , Edited by admin on Wed Apr 02 09:06:13 GMT 2025
PRIMARY
FDA UNII
H25D0X8L90
Created by admin on Wed Apr 02 09:06:13 GMT 2025 , Edited by admin on Wed Apr 02 09:06:13 GMT 2025
PRIMARY
PUBCHEM
10440404
Created by admin on Wed Apr 02 09:06:13 GMT 2025 , Edited by admin on Wed Apr 02 09:06:13 GMT 2025
PRIMARY
SMS_ID
100000080399
Created by admin on Wed Apr 02 09:06:13 GMT 2025 , Edited by admin on Wed Apr 02 09:06:13 GMT 2025
PRIMARY
NCI_THESAURUS
C170028
Created by admin on Wed Apr 02 09:06:13 GMT 2025 , Edited by admin on Wed Apr 02 09:06:13 GMT 2025
PRIMARY
EVMPD
SUB07908MIG
Created by admin on Wed Apr 02 09:06:13 GMT 2025 , Edited by admin on Wed Apr 02 09:06:13 GMT 2025
PRIMARY
MESH
C021029
Created by admin on Wed Apr 02 09:06:13 GMT 2025 , Edited by admin on Wed Apr 02 09:06:13 GMT 2025
PRIMARY
CAS
3261-53-8
Created by admin on Wed Apr 02 09:06:13 GMT 2025 , Edited by admin on Wed Apr 02 09:06:13 GMT 2025
PRIMARY
EPA CompTox
DTXSID10186304
Created by admin on Wed Apr 02 09:06:13 GMT 2025 , Edited by admin on Wed Apr 02 09:06:13 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY