VIOMYCIN SULFATE

Search structure
Trade Names:
Synonyms:
Status: Approved (1982)
Entry Type: Protein
Molecule Category: UNKNOWN
UNII: LKO141R05V

Structure
InChI Key AQONYROJHRNYQQ-QMAPKBLTSA-N
Smile NCCC[C@H](N)CC(=O)N[C@H]1CNC(=O)[C@H]([C@H]2C[C@H](O)NC(N)=N2)NC(=O)/C(=C/NC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@H](CO)NC1=O.O=S(=O)(O)O
InChI
InChI=1S/C25H43N13O10.H2O4S/c26-3-1-2-10(27)4-16(41)32-12-6-30-23(47)18(11-5-17(42)37-24(28)36-11)38-20(44)13(7-31-25(29)48)33-21(45)14(8-39)35-22(46)15(9-40)34-19(12)43;1-5(2,3)4/h7,10-12,14-15,17-18,39-40,42H,1-6,8-9,26-27H2,(H,30,47)(H,32,41)(H,33,45)(H,34,43)(H,35,46)(H,38,44)(H3,28,36,37)(H3,29,31,48);(H2,1,2,3,4)/b13-7-;/t10-,11+,12-,14-,15-,17-,18-;/m0./s1

Physicochemical Descriptors

Property Name Value
Molecular Formula C25H45N13O14S
Molecular Weight 783.78
AlogP -8.88
Hydrogen Bond Acceptor 15.0
Hydrogen Bond Donor 15.0
Number of Rotational Bond 10.0
Polar Surface Area 392.86
Molecular species BASE
Aromatic Rings 0.0
Heavy Atoms 48.0

Pharmacology

Action Mechanism of Action Reference
INHIBITOR 70S ribosome inhibitor PubMed

Cross References

Resources Reference
ChEMBL CHEMBL3989823
EPA CompTox DTXSID60872306
FDA SRS LKO141R05V
PubChem 5282488
SureChEMBL SCHEMBL1235403
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