Chemistry of Myrtaceous Phloroglucinols

NO Compound Information Name MF MW Optical Value Source Structure Biosynthetic Precursor Reference
1 syncarpic acid C10H14O3 182.22 Syncarpia laurifolia Simple monomeric triketone
https://www.publish.csiro.au/CH/CH9600385
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2 flavesone C14H20O4 252.31 Leptospermum flavescens Simple monomeric triketone
https://doi.org/10.1039/JR9650003690
/2020/0629/c23337a493627/page.psp
3 baeckenone H C13H18O5 254.28 −52 Baeckea frutescens Simple monomeric triketone
https://www.sciencedirect.com/science/article/abs/pii/S0040402017300297
/2020/0629/c23337a493629/page.psp
4 baeckenone A C10H14O3 182.22 Baeckea frutescens Simple monomeric triketone
https://www.sciencedirect.com/science/article/abs/pii/S1874390015301178
/2020/0629/c23337a493633/page.psp
5 agglomerone C13H18O4 238.28 Eucalyptus agglomerata Simple monomeric triketone
https://www.publish.csiro.au/CH/CH9641418
/2020/0629/c23337a493635/page.psp
6 callistenone K C14H20O4 252.31 0 Callistemon viminalis Simple monomeric triketone
https://www.sciencedirect.com/science/article/abs/pii/S0367326X16302076
/2020/0629/c23337a493639/page.psp
7 tasmanone C14H20O4 252.31 Eucalyptus risdoni Simple monomeric triketone
https://www.publish.csiro.au/CH/CH9560095
/2020/0629/c23337a493641/page.psp
8 norflavesone C13H18O4 238.28 +1.3 Leptospermum scoparium Simple monomeric triketone
https://pubs.acs.org/doi/10.1021/acs.jnatprod.5b00968
/2020/0629/c23337a493643/page.psp
9 norleptospermone C14H20O4 252.31 +1.5 Leptospermum scoparium Simple monomeric triketone
https://pubs.acs.org/doi/10.1021/acs.jnatprod.5b00968
/2020/0629/c23337a493647/page.psp
10 norisoleptospermone C14H20O4 252.31 −8.5 Leptospermum scoparium Simple monomeric triketone
https://pubs.acs.org/doi/10.1021/acs.jnatprod.5b00968
/2020/0629/c23337a493649/page.psp
11 myrigalone A C18H20O4 300.35 +1.0 Leptospermum scoparium Simple monomeric triketone
https://pubs.acs.org/doi/10.1021/acs.jnatprod.5b00968
/2020/0629/c23337a493695/page.psp
12 syzygiol C18H18O5 314.33 Syzygium polycephaloides Simple monomeric triketone
https://www.sciencedirect.com/science/article/pii/0040403991808573
/2020/0629/c23337a493697/page.psp
13 grandiflorone C19H22O4 314.38 Leptospermum scoparium Simple monomeric triketone
https://doi.org/10.1039/J39660001496
/2020/0629/c23337a493699/page.psp
14 champanone B C18H18O4 298.34 Xanthostemon chrysanthus Simple monomeric triketone
https://pubs.acs.org/doi/10.1021/acs.joc.9b02373
/2020/0629/c23337a493701/page.psp
15 baeckenone F C14H22O4 254.32 −44.0 Baeckea frutescens Simple monomeric triketone
https://www.sciencedirect.com/science/article/pii/S0367326X16300156
/2020/0629/c23337a493703/page.psp
16 triumphalone C15H26O4 270.36 Melaleuca triumphalis Simple monomeric triketone
https://www.sciencedirect.com/science/article/abs/pii/0031942295006591
/2020/0629/c23337a493705/page.psp
17 leptospermone 266.33 Leptospermum flavescens Simple monomeric triketone
https://doi.org/10.1039/JR9650003690
/2020/0629/c23337a493707/page.psp
18 isoleptospermone C15H22O4 266.33 Leptospermum scoparium Simple monomeric triketone
https://pubs.acs.org/doi/10.1021/np980350n
/2020/0629/c23337a493709/page.psp
19 papuanone C16H24O4 280.36 Corymbia dallachiana Simple monomeric triketone
https://pubs.acs.org/doi/10.1021/np980350n
/2020/0629/c23337a493711/page.psp
20 2,5-diacetoxy-2-benzyl-4,4,6,6-tetramethyl-1,3-cyclohexanedione C21H26O6 374.43 Syzygium lineare Simple monomeric triketone
https://www.sciencedirect.com/science/article/pii/S1319562X11000040
/2020/0629/c23337a493713/page.psp
21 woodsianone B C15H22O4 266.33 Angophora woodsiana Simple monomeric triketone
https://www.sciencedirect.com/science/article/pii/S0960894X1730313X
/2020/0629/c23337a493721/page.psp
22 (+)-tomentodione N C15H22O4 266.33 +16.3 Rhodomyrtus tomentosa Simple monomeric triketone
https://www.sciencedirect.com/science/article/pii/S0960894X1730313X
/2020/0629/c23337a493723/page.psp
23 (−)-tomentodione N C15H22O4 266.33 −15.9 Rhodomyrtus tomentosa Simple monomeric triketone
https://www.sciencedirect.com/science/article/pii/S0960894X1730313X
/2020/0629/c23337a493725/page.psp
24 baeckenone I C15H22O4 266.33 −16.0 Baeckea frutescens Simple monomeric triketone
https://www.sciencedirect.com/science/article/abs/pii/S0040402017300297
/2020/0629/c23337a493727/page.psp
25 baeckenone J C14H20O4 252.31 +7.5 Baeckea frutescens Simple monomeric triketone
https://www.sciencedirect.com/science/article/abs/pii/S0040402017300297
/2020/0629/c23337a493729/page.psp
26 baeckenone K C15H22O4 266.34 −12.0 Baeckea frutescens Simple monomeric triketone
https://www.sciencedirect.com/science/article/abs/pii/S0040402017300297
/2020/0629/c23337a493731/page.psp
27 (R)-8a-hydroxy-7-methoxy-3,3,6,8,8-pentamethyl-8,8a-dihydrobenzo[c][1,2]dioxin-5(3H)-one C14H20O5 268.31 0 Baeckea frutescens Simple monomeric triketone
https://www.sciencedirect.com/science/article/abs/pii/0040402096005108
/2020/0629/c23337a493733/page.psp
28 baeckenone D C15H22O5 282.33 0 Baeckea frutescens Simple monomeric triketone
https://www.sciencedirect.com/science/article/pii/S0367326X16300156
/2020/0629/c23337a493735/page.psp
29 baeckenone E C15H22O5 282.33 0 Baeckea frutescens Simple monomeric triketone
https://www.sciencedirect.com/science/article/pii/S0367326X16300156
/2020/0629/c23337a493737/page.psp
30 baeckenone G C13H18O6 270.28 +48 Baeckea frutescens Simple monomeric triketone
https://www.sciencedirect.com/science/article/abs/pii/S0040402017300297
/2020/0629/c23337a493739/page.psp
31 endoperoxide G3 C14H20O5 268.31 0 Eucalyptus grandis Simple monomeric triketone
https://www.sciencedirect.com/science/article/pii/S0040403901967085
/2020/0629/c23337a493741/page.psp
32 inhibitor G2 C15H22O5 282.33 0 Eucalyptus grandis Simple monomeric triketone
https://www.sciencedirect.com/science/article/pii/S0040403901967085
/2020/0629/c23337a493743/page.psp
33 inhibitor G1 C15H22O5 282.33 0 Eucalyptus grandis Simple monomeric triketone
https://www.sciencedirect.com/science/article/pii/S0040403901967085
/2020/0629/c23337a493745/page.psp
34 callistemonol B C13H20O4 240.3 0 Callistemon viminalis Simple monomeric triketone
https://pubs.acs.org/doi/abs/10.1021/acs.jnatprod.9b00064
/2020/0629/c23337a493747/page.psp
35 (+)-xanchryone E C18H18O5 314.34 +39.6 Xanthostemon chrysanthus Simple monomeric triketone
https://pubs.acs.org/doi/10.1021/acs.joc.9b02373
/2020/0629/c23337a493749/page.psp
36 (−)-xanchryone E C18H18O5 314.34 –45.2 Xanthostemon chrysanthus Simple monomeric triketone
https://pubs.acs.org/doi/10.1021/acs.joc.9b02373
/2020/0629/c23337a493751/page.psp
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