Compound ID | 3340

Update compound information

SF2487

Synonym(s): tetromadurin

Class: Natural product antibiotic

Agent Type: Natural product; Small molecule;
Spectrum of activity: Gram-positive
Mechanism of action: Unknown
Target Pathogen: Active against Staphylococcus aureus, Enterococcus faecalis, and Bacillus anthracis
Description: Natural product from Actinomadura sp.; also shows anti-influenza virus activity; a polyether
Institute where first reported: Meiji Seika Kaisha, Ltd.
Year first mentioned: 1990
Development status: Experimental
Chemical structure(s):
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Molecular weight: 783.94
Iso. SMILES: CC[C@H]([C@@H]1CC[C@@H](O1)[C@@]2(C[C@H]([C@@H](O2)C/C=C(\C)/[C@@H]3[C@H](CC[C@@H](O3)/C(=C/[C@H]4C[C@H]([C@H]([C@H]([C@@H]4[C@@H](C(=O)C5C(=O)C(=C)OC5=O)OC)CO)O)C)/CO)C)C)C)O.[Na]
InChI Key: JINRBYOWHJLDLT-FYJCAEPUSA-N
Can. SMILES: CC[C@H]([C@@H]1CC[C@H]([C@]2(C)C[C@@H](C)[C@H](C/C=C(\C)/[C@@H]3[C@@H](C)CC[C@H](/C(=C/[C@H]4C[C@@H](C)[C@H]([C@@H](CO)[C@@H]4[C@@H](C(=O)C5C(=O)C(=C)OC5=O)OC)O)/CO)O3)O2)O1)O.[Na]
InChI: InChI=1S/C42H64O12.Na/c1-9-29(45)32-14-15-33(52-32)42(7)18-24(5)30(54-42)12-10-21(2)39-22(3)11-13-31(53-39)27(19-43)17-26-16-23(4)36(46)28(20-44)34(26)40(50-8)38(48)35-37(47)25(6)51-41(35)49;/h10,17,22-24,26,28-36,39-40,43-46H,6,9,11-16,18-20H2,1-5,7-8H3;/b21-10+,27-17+;/t22-,23+,24+,26+,28-,29+,30-,31+,32-,33+,34+,35?,36+,39+,40-,42-;/m0./s1
External links:
PubChem link: https://pubchem.ncbi.nlm.nih.gov/compound/6440092
Citation: https://www.jstage.jst.go.jp/article/antibiotics1968/43/3/43_3_259/_article/-char/en

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