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

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
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