Compound ID | 3443

Update compound information

Tubelactomicin A

Class: Natural product antibiotic

Agent Type: Natural product; Small molecule;
Spectrum of activity: Antimycobacterial
Mechanism of action: Unknown
Target Pathogen: Active against Mycobacterium smegmatis including strains resistant to paromomycin, kanamycin, streptomycin, and rifampicin, Mycobacterium phlei, Mycobacterium vaccae, and Mycobacterium fortuitum
Description: Natural product from Nocardia sp.; tubelactomicin A resistant strains do not show cross-resistance to anti-tuberculotic antibiotics
Year first mentioned: 2000
Development status: Experimental
Chemical structure(s):
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Molecular weight: 486.64
Iso. SMILES: C[C@H]1CC[C@H]2[C@H]([C@@H]1O)C=C([C@H]\3[C@@]2(C(=O)O[C@@H](CCC/C=C(/[C@@H]([C@H](/C=C/C=C3)C)O)\C(=O)O)C)C)C
InChI Key: LWPAZPOZBPFAAE-WSQSGNSCSA-N
Can. SMILES: C[C@H]1/C=C/C=C/[C@H]2C(=C[C@@H]3[C@H](CC[C@H](C)[C@H]3O)[C@@]2(C)C(=O)O[C@H](C)CCC/C=C(/[C@@H]1O)\C(=O)O)C
InChI: InChI=1S/C29H42O6/c1-17-10-6-9-13-23-19(3)16-22-24(15-14-18(2)26(22)31)29(23,5)28(34)35-20(4)11-7-8-12-21(25(17)30)27(32)33/h6,9-10,12-13,16-18,20,22-26,30-31H,7-8,11,14-15H2,1-5H3,(H,32,33)/b10-6+,13-9+,21-12-/t17-,18-,20+,22+,23-,24-,25+,26+,29-/m0/s1
External links:
PubChem link: https://pubchem.ncbi.nlm.nih.gov/compound/11755172
Citation: https://www.jstage.jst.go.jp/article/antibiotics1968/53/10/53_10_1096/_article/-char/en

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