Lividomycin

Lividomycin

Identifiers
IUPAC name (1R,2R,3S,4R,6S)-4,6-Diamino-3-hydroxy-2-{[α-D-mannopyranosyl-(1->4)-2,6-diamino-2,6-dideoxy-β-L-idopyranosyl-(1->3)-β-D-ribofuranosyl]oxy}cyclohexyl 2-amino-2,3-dideoxy-α-D-ribo-hexopyranoside
CAS Number	36441-41-5 Y
PubChem CID	72394
DrugBank	DB04728
ChemSpider	65327
UNII	A606AJ494W
ChEBI	CHEBI:71961 Y
ChEMBL	ChEMBL389029
CompTox Dashboard (EPA)	DTXSID8023218
Chemical and physical data
Formula	C29H55N5O19
Molar mass	777.775 g·mol−1
3D model (JSmol)	Interactive image
SMILES O([C@H]4[C@H](O[C@@H]3O[C@H](CO)[C@@H](O[C@H]2O[C@@H](CN)[C@@H](O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]1O)[C@H](O)[C@H]2N)[C@H]3O)[C@@H](O)[C@H](N)C[C@@H]4N)[C@H]5O[C@@H]([C@@H](O)C[C@H]5N)CO
InChI InChI=1S/C29H55N5O18/c30-3-11-23(51-28-20(43)19(42)17(40)13(5-36)47-28)18(41)15(34)27(45-11)50-24-14(6-37)48-29(21(24)44)52-25-16(39)7(31)1-8(32)22(25)49-26-9(33)2-10(38)12(4-35)46-26/h7-29,35-44H,1-6,30-34H2/t7-,8+,9-,10+,11+,12-,13-,14-,15-,16+,17-,18-,19+,20+,21-,22-,23-,24-,25-,26-,27-,28-,29+/m1/s1 Key:DBLVDAUGBTYDFR-SWMBIRFSSA-N

Lividomycin is a broad-spectrum aminoglycoside antibiotic. It is effective against most gram positive and gram negative bacteria including Mycobacterial tuberculosis (the causative agent of tuberculosis) and Pseudomonas aeruginosa.