Compound ID | 2671

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Platenomycin A1

Synonym(s): YL-704 A1

Class: Macrolide

Spectrum of activity: Gram-positive
Details of activity: Active against Staphylococcus aureus
Description: Natural product from Streptomyces platensis subsp. Malvinus (part of YL-704 antibiotic complex)
Institute where first reported: Microbial Chemistry Research Laboratory, Tanabe Seiyaku Co., Ltd.
Year first mentioned: 1974
Development status: Experimental
Chemical structure(s):
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Molecular weight: 842.02
Iso. SMILES: CCC(=O)O[C@@H]1CC(=O)O[C@@H](C/C=C/C=C\[C@@H]([C@@H](C[C@@H]([C@@H]([C@H]1OC)O[C@H]2[C@@H]([C@H]([C@@H]([C@H](O2)C)O[C@H]3C[C@@]([C@H]([C@@H](O3)C)OC(=O)CC(C)C)(C)O)N(C)C)O)CC=O)C)O)C
InChI Key: MGVDOYIXWZRNIN-LEHVWPSKSA-N
Can. SMILES: CCC(=O)O[C@@H]1CC(=O)O[C@H](C)C/C=C/C=C\[C@@H]([C@H](C)C[C@H](CC=O)[C@@H]([C@H]1OC)O[C@H]2[C@@H]([C@H]([C@@H]([C@@H](C)O2)O[C@H]3C[C@](C)([C@H]([C@H](C)O3)OC(=O)CC(C)C)O)N(C)C)O)O
InChI: InChI=1S/C43H71NO15/c1-12-32(47)56-31-22-34(49)53-26(5)16-14-13-15-17-30(46)25(4)21-29(18-19-45)39(40(31)52-11)59-42-37(50)36(44(9)10)38(27(6)55-42)58-35-23-43(8,51)41(28(7)54-35)57-33(48)20-24(2)3/h13-15,17,19,24-31,35-42,46,50-51H,12,16,18,20-23H2,1-11H3/b14-13+,17-15-/t25-,26-,27-,28+,29+,30+,31-,35+,36-,37-,38-,39+,40+,41+,42+,43-/m1/s1
External links:
PubChem link: https://pubchem.ncbi.nlm.nih.gov/compound/168432112
Citation: https://www.jstage.jst.go.jp/article/antibiotics1968/27/2/27_2_102/_article

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