Compound ID | 3337

Update compound information

Demycinosyltylosin 

Class: Macrolide

Agent Type: Natural product; Small molecule;
Spectrum of activity: Gram-positive
Mechanism of action: Unknown
Target Pathogen: Active against Staphylococcus aureus, Corynebacterium diphtheriae, Corynebacterium flavescens, and Mycoplasma sp.
Description: Natural product produced by mutant Streptomyces fradiae
Institute where first reported: Sanraku Inc., Central Research Laboratories
Year first mentioned: 1989
Development status: Experimental
Chemical structure(s):
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Molecular weight: 741.91
Iso. SMILES: CC[C@@H]1[C@H](/C=C(/C=C/C(=O)[C@@H](C[C@@H]([C@@H]([C@H]([C@@H](CC(=O)O1)O)C)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)O)(C)O)N(C)C)O)CC=O)C)\C)CO
InChI Key: ZVOOGERIHVAODX-QWWGUZMMSA-N
Can. SMILES: CC[C@@H]1[C@H](/C=C(\C)/C=C/C(=O)[C@H](C)C[C@H](CC=O)[C@@H]([C@@H](C)[C@@H](CC(=O)O1)O)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)O)O)N(C)C)O)CO
InChI: InChI=1S/C38H63NO13/c1-10-29-26(19-41)15-20(2)11-12-27(42)21(3)16-25(13-14-40)34(22(4)28(43)17-30(44)50-29)52-37-33(45)32(39(8)9)35(23(5)49-37)51-31-18-38(7,47)36(46)24(6)48-31/h11-12,14-15,21-26,28-29,31-37,41,43,45-47H,10,13,16-19H2,1-9H3/b12-11+,20-15+/t21-,22+,23-,24+,25+,26-,28-,29-,31+,32-,33-,34-,35+,36+,37+,38-/m1/s1
External links:
PubChem link: https://pubchem.ncbi.nlm.nih.gov/compound/6438458
Citation: https://www.jstage.jst.go.jp/article/antibiotics1968/42/11/42_11_1661/_article/-char/en

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