Compound ID | 3252

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Aldgamycin G

Class: Macrolide

Agent Type: Natural product; Small molecule;
Spectrum of activity: Gram-positive
Mechanism of action: Unknown
Target Pathogen: Active against Staphylococcus aureus and Streptococcus pyogenes
Description: Natural product from Streptomyces avidinii
Institute where first reported: Applied Bioscience Laboratory, Kirin Brewery Co., Ltd.
Year first mentioned: 1986
Development status: Experimental
Chemical structure(s):
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Molecular weight: 740.83
Iso. SMILES: C[C@H]1C[C@H](C(=O)/C=C/[C@H]2[C@@H](O2)[C@@H]([C@H](OC(=O)/C=C/[C@@H]([C@H]1O[C@H]3[C@@H](C4(C[C@H](O3)C)[C@@H](OC(=O)O4)C)O)C)C)CO[C@H]5[C@@H]([C@@H]([C@@H]([C@H](O5)C)O)OC)OC)C
InChI Key: PNKWSYXWMPOOOF-SJCYFYBXSA-N
Can. SMILES: C[C@H]1/C=C/C(=O)O[C@H](C)[C@@H](CO[C@H]2[C@@H]([C@@H]([C@@H]([C@@H](C)O2)O)OC)OC)[C@H]3[C@H](/C=C/C(=O)[C@H](C)C[C@H](C)[C@@H]1O[C@H]4[C@@H](C5(C[C@@H](C)O4)[C@H](C)OC(=O)O5)O)O3
InChI: InChI=1S/C37H56O15/c1-17-10-13-27(39)47-21(5)24(16-45-34-32(44-9)31(43-8)28(40)22(6)48-34)30-26(50-30)12-11-25(38)18(2)14-19(3)29(17)51-35-33(41)37(15-20(4)46-35)23(7)49-36(42)52-37/h10-13,17-24,26,28-35,40-41H,14-16H2,1-9H3/b12-11+,13-10+/t17-,18+,19-,20+,21+,22+,23-,24+,26-,28+,29+,30-,31+,32+,33-,34+,35-,37?/m0/s1
External links:
PubChem link: https://pubchem.ncbi.nlm.nih.gov/compound/6442105
Citation: https://www.jstage.jst.go.jp/article/antibiotics1968/39/12/39_12_1776/_article/-char/en

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