Compound ID | 3352

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Tetrazomine

Class: Natural product antibiotic

Spectrum of activity: Gram-positive  &  Gram-negative
Details of activity: Active against Staphylococcus aureus, Streptococcus pyogenes, Enterococcus faecalis, Enterococcus faecium, Mycobacterium smegmatis, Escherichia coli, Klebsiella pneumoniae, Pseudomonas aeruginosa, and Proteus vulgaris
Description: Natural product from Saccharothrix mutabilis subsp. chichijimaensis; also shows anti-tumour acitivity
Institute where first reported: Yamanouchi Pharmaceutical Co., Ltd.
Year first mentioned: 1991
Development status: Experimental
Chemical structure(s):
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Molecular weight: 458.55
Iso. SMILES: CN1[C@@H]2C[C@H]([C@H]1[C@@H]3CC4=C([C@H]5N3[C@@H]2OC5)C(=C(C=C4)NC(=O)C6[C@@H](CCCN6)O)OC)CO
InChI Key: WXZSUBHBYQYTNM-WMDJANBXSA-N
Can. SMILES: CN1[C@@H]2C[C@@H](CO)[C@H]1[C@@H]3CC4=CC=C(C(=C4[C@@H]5CO[C@H]2N35)OC)NC(=O)C6[C@@H](CCCN6)O
InChI: InChI=1S/C24H34N4O5/c1-27-16-9-13(10-29)21(27)15-8-12-5-6-14(26-23(31)20-18(30)4-3-7-25-20)22(32-2)19(12)17-11-33-24(16)28(15)17/h5-6,13,15-18,20-21,24-25,29-30H,3-4,7-11H2,1-2H3,(H,26,31)/t13-,15-,16+,17-,18+,20?,21-,24+/m0/s1
External links:
PubChem link: https://pubchem.ncbi.nlm.nih.gov/compound/188405
Citation: https://www.jstage.jst.go.jp/article/antibiotics1968/44/5/44_5_479/_article/-char/en

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