Compound ID | 2664

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Pentenomycin analogues

Class: Natural product antibiotic

Spectrum of activity: Gram-positive  &  Gram-negative
Details of activity: Active against Staphylococcus aureus, Enterococcus faecium, Klebsiella pneumoniae, and Acinetobacter baumannii
Description: Synthetic compound; contains a cyclopentenone core
Institute where first reported: Institute of Multidisciplinary Research for Advanced Materials, Tohoku University, 2-1-1 Katahira, Aoba-ku, Sendai, Miyagi 980-8577, Japan
Year first mentioned: 2019
Development status: Experimental
Chemical structure(s):
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Molecular weight: 374.13
Iso. SMILES: IC1=C[C@H](OC(C2=CC=CC=C2)=O)[C@@](O)(CO)C1=O
InChI Key: PATCWYWXSKRNLF-GWCFXTLKSA-N
Can. SMILES: C1=CC=C(C=C1)C(=O)O[C@H]2C=C(C(=O)[C@@]2(CO)O)I
InChI: InChI=1S/C13H11IO5/c14-9-6-10(13(18,7-15)11(9)16)19-12(17)8-4-2-1-3-5-8/h1-6,10,15,18H,7H2/t10-,13-/m0/s1
External links:
Citations:
  • https://www.jstage.jst.go.jp/article/cpb1958/22/9/22_9_2113/_pdf/-char/en
  • https://www.sciencedirect.com/science/article/pii/S0040403919303636#:~:text=Pentenomycin%20I%20(1)%20was%20isolated,especially%20interesting%20for%20its%20synthesis.

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