Compound ID | 1679

Update compound information

Elloramycin

Class: Natural product antibiotic

Agent Type: Natural product; Small molecule; Direct acting;
Spectrum of activity: Gram-positive
Mechanism of action: Protein synthesis inhibitor. Binds to the large ribosomal subunit within the polypeptide exit tunnel
Description: Natural product from Streptomyces olivaceus; a tetracenomycin-type antibiotic
Institute where first reported: Universitat Gottingen, Germany
Year first mentioned: 1990
Development status: Experimental
Chemical structure(s):
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Molecular weight: 660.62
Iso. SMILES: C[C@H]1[C@@H]([C@H]([C@H]([C@@H](O1)OC2=CC3=CC4=C(C(=C3C(=C2C(=O)OC)C)O)C(=O)[C@@]5(C(=O)C=C([C@H]([C@@]5(C4=O)O)O)OC)OC)OC)OC)OC
InChI Key: OYEXGNNKRQPUBW-FJYHMNRNSA-N
Can. SMILES: CC1=C(C(=CC2=C1C(=C3C(=C2)C(=O)[C@]4([C@@H](C(=CC(=O)[C@]4(C3=O)OC)OC)O)O)O)O[C@H]5[C@@H]([C@@H]([C@H]([C@H](C)O5)OC)OC)OC)C(=O)OC
InChI: InChI=1S/C32H36O15/c1-12-19-14(10-16(20(12)29(38)44-7)47-30-25(43-6)24(42-5)23(41-4)13(2)46-30)9-15-21(22(19)34)28(37)32(45-8)18(33)11-17(40-3)27(36)31(32,39)26(15)35/h9-11,13,23-25,27,30,34,36,39H,1-8H3/t13-,23-,24+,25+,27+,30-,31+,32+/m0/s1
External links:
PubChem link: https://pubchem.ncbi.nlm.nih.gov/compound/10009567
Citation: https://www.jstage.jst.go.jp/article/antibiotics1968/43/9/43_9_1169/_article

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