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
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
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 |
DescriptionSources: https://patents.google.com/patent/US3395220
Sources: https://patents.google.com/patent/US3395220
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.
Originator
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 15:52:46 GMT 2023
by
admin
on
Sat Dec 16 15:52:46 GMT 2023
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Record UNII |
U1E84J0228
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Record Status |
Validated (UNII)
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Record Version |
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NCI_THESAURUS |
C258
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10118-85-1
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2531
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SUB08506MIG
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CHEMBL2106616
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C90684
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100000082310
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6433555
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U1E84J0228
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127473
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DTXSID40883091
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Related Record | Type | Details | ||
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ACTIVE MOIETY |