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Details

Stereochemistry ABSOLUTE
Molecular Formula C10H14N2O3S
Molecular Weight 242.295
Optical Activity UNSPECIFIED
Defined Stereocenters 3 / 3
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of Lydimycin

SMILES

[H][C@]12CS[C@@]([H])(CC\C=C\C(O)=O)[C@@]1([H])NC(=O)N2

InChI

InChIKey=NZERRTYPTPRCIR-ARSLAPBQSA-N
InChI=1S/C10H14N2O3S/c13-8(14)4-2-1-3-7-9-6(5-16-7)11-10(15)12-9/h2,4,6-7,9H,1,3,5H2,(H,13,14)(H2,11,12,15)/b4-2+/t6-,7-,9-/m0/s1

HIDE SMILES / InChI

Molecular Formula C10H14N2O3S
Molecular Weight 242.295
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 3 / 3
E/Z Centers 1
Optical Activity UNSPECIFIED

Lydimycin is a biosynthetic product obtained by culturing a lydimycin-producing actinomycete in a suitable aqueous nutrient medium under aerobic conditions. Lydimycin inhibits the growth of Nocardia asteroides, Blastomyces dermatitidis, Geotrichum sp., Phlalophora varrucosa, Cryptococcus neoformans, H Histoplasma capsulatum, and Trichophyton mentagrophytes. Thus, lydimycin is useful alone or in combination with other antifungal or antibiotic agents to prevent the growth of, or reduce the number of, susceptible organisms present in various environments.

Approval Year

Patents

Patents

Substance Class Chemical
Created
by admin
on Sat Dec 16 15:52:46 GMT 2023
Edited
by admin
on Sat Dec 16 15:52:46 GMT 2023
Record UNII
U1E84J0228
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
Lydimycin
USAN  
USAN  
Official Name English
U-15965
Code English
LYDIMYCIN [USAN]
Common Name English
LIDIMYCIN
INN  
INN  
Official Name English
2-PENTENOIC ACID, 5-(HEXAHYDRO-2-OXO-1H-THIENO(3,4-D)IMIDAZOL-4-YL)-, (3AS(3A.ALPHA.,4.BETA.,6A.ALPHA.))-
Common Name English
lidimycin [INN]
Common Name English
U-15,965
Code English
NSC-127473
Code English
Classification Tree Code System Code
NCI_THESAURUS C258
Created by admin on Sat Dec 16 15:52:46 GMT 2023 , Edited by admin on Sat Dec 16 15:52:46 GMT 2023
Code System Code Type Description
CAS
10118-85-1
Created by admin on Sat Dec 16 15:52:46 GMT 2023 , Edited by admin on Sat Dec 16 15:52:46 GMT 2023
PRIMARY
INN
2531
Created by admin on Sat Dec 16 15:52:46 GMT 2023 , Edited by admin on Sat Dec 16 15:52:46 GMT 2023
PRIMARY
EVMPD
SUB08506MIG
Created by admin on Sat Dec 16 15:52:46 GMT 2023 , Edited by admin on Sat Dec 16 15:52:46 GMT 2023
PRIMARY
ChEMBL
CHEMBL2106616
Created by admin on Sat Dec 16 15:52:46 GMT 2023 , Edited by admin on Sat Dec 16 15:52:46 GMT 2023
PRIMARY
NCI_THESAURUS
C90684
Created by admin on Sat Dec 16 15:52:46 GMT 2023 , Edited by admin on Sat Dec 16 15:52:46 GMT 2023
PRIMARY
SMS_ID
100000082310
Created by admin on Sat Dec 16 15:52:46 GMT 2023 , Edited by admin on Sat Dec 16 15:52:46 GMT 2023
PRIMARY
PUBCHEM
6433555
Created by admin on Sat Dec 16 15:52:46 GMT 2023 , Edited by admin on Sat Dec 16 15:52:46 GMT 2023
PRIMARY
FDA UNII
U1E84J0228
Created by admin on Sat Dec 16 15:52:46 GMT 2023 , Edited by admin on Sat Dec 16 15:52:46 GMT 2023
PRIMARY
NSC
127473
Created by admin on Sat Dec 16 15:52:46 GMT 2023 , Edited by admin on Sat Dec 16 15:52:46 GMT 2023
PRIMARY
EPA CompTox
DTXSID40883091
Created by admin on Sat Dec 16 15:52:46 GMT 2023 , Edited by admin on Sat Dec 16 15:52:46 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY