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Details

Stereochemistry ABSOLUTE
Molecular Formula C41H67NO16
Molecular Weight 829.9678
Optical Activity UNSPECIFIED
Defined Stereocenters 18 / 18
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MARIDOMYCIN

SMILES

[H][C@@]12C[C@@H](C)OC(=O)C[C@@H](OC(=O)CC)[C@H](OC)[C@@H](O[C@@H]3O[C@H](C)[C@@H](O[C@H]4C[C@@](C)(O)[C@@H](OC(=O)CC)[C@H](C)O4)[C@@H]([C@H]3O)N(C)C)[C@@H](CC=O)C[C@@H](C)[C@@H](O)\C=C\[C@]1([H])O2

InChI

InChIKey=FFXJTOKFQATYBI-UEANCSDJSA-N
InChI=1S/C41H67NO16/c1-11-30(45)55-29-19-32(47)51-22(4)18-28-27(54-28)14-13-26(44)21(3)17-25(15-16-43)37(38(29)50-10)58-40-35(48)34(42(8)9)36(23(5)53-40)57-33-20-41(7,49)39(24(6)52-33)56-31(46)12-2/h13-14,16,21-29,33-40,44,48-49H,11-12,15,17-20H2,1-10H3/b14-13+/t21-,22-,23-,24+,25+,26+,27+,28-,29-,33+,34-,35-,36-,37+,38+,39+,40+,41-/m1/s1

HIDE SMILES / InChI
Maridomycin is a macrolide antibiotic. Sreptomyces sp. No. B-5050 was found to produce maridomycin. Maridomycin was found to be composed of six components, maridomycins I, II, III, IV, V and VI. Their structures are different from each other in acyl moieties at C3 and C4" positions. Maridomycins I, II, III, IV, V and VI showed similar antibacterial spectra against Gram-positive bacteria including acid-fast bacteria. Maridomycin has bacteriostatic activity rather than bactericidal activity. Prominent therapeutic effect was observed against certain Gram-positive bacterial infection in mice.

Approval Year

PubMed

PubMed

TitleDatePubMed
Maridomycin, a new macrolide antibiotic. I. Taxonomy and fermentation.
1973 Apr
Maridomycin, a new macrolide antibiotic. 3. In vitro and in vivo antibacterial activity.
1973 Apr
Microbial transformation of antibiotics II. Additional transformation products of maridomycin III.
1976 Aug
Name Type Language
MARIDOMYCIN
INN  
INN  
Official Name English
TURIMYCIN EP3
Common Name English
10-(FORMYLMETHYL)-7,13-DIHYDROXY-8-METHOXY-3,12-DIMETHYL-5-OXO-4,17-DIOXABICYCLO(14.1.0)HEPTADEC-14-EN-9-YL-3,6-DIDEOXY-4-O-(2,6-DIDEOXY-3-C-METHYL-.ALPHA.-L-RIBO-HEXOPYRANOSYL)-3-(DIMETHYLAMINO)-.BETA.-D-GLUCOPYRANOSIDE 4'',7'-DIPROPIONATE (ESTER)
Common Name English
MARIDOMYCIN III
Common Name English
ANTIBIOTIC YL 704C1
Code English
ANTIBIOTIC B 5050C
Code English
maridomycin [INN]
Common Name English
LEUCOMYCIN V, 12,13-EPOXY-12,13-DIHYDRO-, 3,4B-DIPROPANOATE, (12S,13S)-
Common Name English
MARIDOMYCIN [JAN]
Common Name English
Code System Code Type Description
INN
3650
Created by admin on Fri Dec 15 18:08:07 GMT 2023 , Edited by admin on Fri Dec 15 18:08:07 GMT 2023
PRIMARY
EVMPD
SUB08649MIG
Created by admin on Fri Dec 15 18:08:07 GMT 2023 , Edited by admin on Fri Dec 15 18:08:07 GMT 2023
PRIMARY
EPA CompTox
DTXSID301023452
Created by admin on Fri Dec 15 18:08:07 GMT 2023 , Edited by admin on Fri Dec 15 18:08:07 GMT 2023
PRIMARY
MESH
C010602
Created by admin on Fri Dec 15 18:08:07 GMT 2023 , Edited by admin on Fri Dec 15 18:08:07 GMT 2023
PRIMARY
PUBCHEM
154925908
Created by admin on Fri Dec 15 18:08:07 GMT 2023 , Edited by admin on Fri Dec 15 18:08:07 GMT 2023
PRIMARY
SMS_ID
100000081724
Created by admin on Fri Dec 15 18:08:07 GMT 2023 , Edited by admin on Fri Dec 15 18:08:07 GMT 2023
PRIMARY
NCI_THESAURUS
C170151
Created by admin on Fri Dec 15 18:08:07 GMT 2023 , Edited by admin on Fri Dec 15 18:08:07 GMT 2023
PRIMARY
CAS
39378-35-3
Created by admin on Fri Dec 15 18:08:07 GMT 2023 , Edited by admin on Fri Dec 15 18:08:07 GMT 2023
ALTERNATIVE
CAS
35775-82-7
Created by admin on Fri Dec 15 18:08:07 GMT 2023 , Edited by admin on Fri Dec 15 18:08:07 GMT 2023
PRIMARY
FDA UNII
J9XX668K4U
Created by admin on Fri Dec 15 18:08:07 GMT 2023 , Edited by admin on Fri Dec 15 18:08:07 GMT 2023
PRIMARY
ChEMBL
CHEMBL2105819
Created by admin on Fri Dec 15 18:08:07 GMT 2023 , Edited by admin on Fri Dec 15 18:08:07 GMT 2023
PRIMARY