Compound ID | 3302

Update compound information

Deepoxycirramycin A1

Synonym(s): 23-Deoxy-5-O-mycaminosyltylonolide

Class: Macrolide

Spectrum of activity: Gram-positive
Details of activity: Active against Staphylococcus aureus, Streptococcus pyogenes, Streptococcus pneumoniae,
Description: Semi-synthetic compound; not effective against Streptococcus pyogenes infection in mice
Institute where first reported: Lilly Research Laboratories, Lilly Corporate Center, USA
Year first mentioned: 1987
Development status: Experimental
Chemical structure(s):
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Molecular weight: 581.74
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)N(C)C)O)CC=O)C)\C)C
InChI Key: FERSDKADYZRIAA-HISVIJAKSA-N
Can. SMILES: CC[C@@H]1[C@@H](C)/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)N(C)C)O
InChI: InChI=1S/C31H51NO9/c1-9-25-19(4)14-17(2)10-11-23(34)18(3)15-22(12-13-33)30(20(5)24(35)16-26(36)40-25)41-31-29(38)27(32(7)8)28(37)21(6)39-31/h10-11,13-14,18-22,24-25,27-31,35,37-38H,9,12,15-16H2,1-8H3/b11-10+,17-14+/t18-,19+,20+,21-,22+,24-,25-,27+,28+,29-,30-,31+/m1/s1
External links:
PubChem link: https://pubchem.ncbi.nlm.nih.gov/compound/6450888
Citation: https://www.jstage.jst.go.jp/article/antibiotics1968/40/6/40_6_823/_article/-char/en

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