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Details

Stereochemistry ABSOLUTE
Molecular Formula C29H44O6
Molecular Weight 488.6561
Optical Activity UNSPECIFIED
Defined Stereocenters 11 / 11
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of RAMNODIGIN

SMILES

[H][C@@]1(CC[C@@H](O)[C@H](C)O1)O[C@H]2CC[C@@]3(C)[C@]([H])(CC[C@]4([H])[C@]3([H])CC[C@]5(C)[C@H](CC[C@]45O)C6=CC(=O)OC6)C2

InChI

InChIKey=LDZRENBZALBYIS-XZUAUHNRSA-N
InChI=1S/C29H44O6/c1-17-24(30)6-7-26(34-17)35-20-8-11-27(2)19(15-20)4-5-23-22(27)9-12-28(3)21(10-13-29(23,28)32)18-14-25(31)33-16-18/h14,17,19-24,26,30,32H,4-13,15-16H2,1-3H3/t17-,19+,20-,21+,22-,23+,24+,26-,27-,28+,29-/m0/s1

HIDE SMILES / InChI

Molecular Formula C29H44O6
Molecular Weight 488.6561
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 11 / 11
E/Z Centers 0
Optical Activity UNSPECIFIED

Ramnodigin is a cardenolide derivative patented by Farbwerke Hoechst A.-G. as cardiotonic, diuretic, and antidiarrheic compound. In in vitro studies, Ramnodigin shows cytotoxicity against nonsmall cell human lung cancer cells.

Approval Year

PubMed

PubMed

TitleDatePubMed
C5'-Alkyl Substitution Effects on Digitoxigenin α-l-Glycoside Cancer Cytotoxicity.
2011 Apr 14
Patents

Patents

Substance Class Chemical
Created
by admin
on Fri Dec 15 16:35:21 GMT 2023
Edited
by admin
on Fri Dec 15 16:35:21 GMT 2023
Record UNII
Z8SRY7BR30
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
RAMNODIGIN
INN  
INN  
Official Name English
ramnodigin [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C78322
Created by admin on Fri Dec 15 16:35:21 GMT 2023 , Edited by admin on Fri Dec 15 16:35:21 GMT 2023
Code System Code Type Description
CAS
33156-28-4
Created by admin on Fri Dec 15 16:35:21 GMT 2023 , Edited by admin on Fri Dec 15 16:35:21 GMT 2023
PRIMARY
EVMPD
SUB10251MIG
Created by admin on Fri Dec 15 16:35:21 GMT 2023 , Edited by admin on Fri Dec 15 16:35:21 GMT 2023
PRIMARY
EPA CompTox
DTXSID301043347
Created by admin on Fri Dec 15 16:35:21 GMT 2023 , Edited by admin on Fri Dec 15 16:35:21 GMT 2023
PRIMARY
FDA UNII
Z8SRY7BR30
Created by admin on Fri Dec 15 16:35:21 GMT 2023 , Edited by admin on Fri Dec 15 16:35:21 GMT 2023
PRIMARY
PUBCHEM
20055386
Created by admin on Fri Dec 15 16:35:21 GMT 2023 , Edited by admin on Fri Dec 15 16:35:21 GMT 2023
PRIMARY
NCI_THESAURUS
C76589
Created by admin on Fri Dec 15 16:35:21 GMT 2023 , Edited by admin on Fri Dec 15 16:35:21 GMT 2023
PRIMARY
INN
4348
Created by admin on Fri Dec 15 16:35:21 GMT 2023 , Edited by admin on Fri Dec 15 16:35:21 GMT 2023
PRIMARY
ChEMBL
CHEMBL2106911
Created by admin on Fri Dec 15 16:35:21 GMT 2023 , Edited by admin on Fri Dec 15 16:35:21 GMT 2023
PRIMARY
SMS_ID
100000080314
Created by admin on Fri Dec 15 16:35:21 GMT 2023 , Edited by admin on Fri Dec 15 16:35:21 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY