Chemistry of Myrtaceous Phloroglucinols

NO Compound Information Name MF MW Optical Value Source Structure Biosynthetic Precursor Reference
1 callviminol C C22H32O5 376.49 0 Callistemon viminalis Phloroglucinol-monoterpene adduct 1-1.png
https://www.sciencedirect.com/science/article/pii/S0367326X16302611
/2020/0701/c23343a496139/page.psp
2 callviminol D C21H30O5 362.47 0 Callistemon viminalis Phloroglucinol-monoterpene adduct 2-1.png
https://www.sciencedirect.com/science/article/pii/S0367326X16302611
/2020/0701/c23343a496143/page.psp
3 eucalrobusone F C23H28O5 384.47 Eucalyptus robusta Phloroglucinol-monoterpene adduct 3-1.png
https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/chem.201601732
/2020/0701/c23343a496151/page.psp
4 eucalrobusone Z C23H30O6 402.49 –3.7 Eucalyptus robusta Phloroglucinol-monoterpene adduct 4-1.png
https://www.sciencedirect.com/science/article/abs/pii/S0031942218304709
/2020/0701/c23343a496157/page.psp
5 (+)-eucalrobusone X C23H26O5 382.45 +16.0 Eucalyptus robusta Phloroglucinol-monoterpene adduct 5-1.png
https://www.sciencedirect.com/science/article/abs/pii/S0031942218304709
/2020/0701/c23343a496165/page.psp
6 (−)-eucalrobusone X C23H26O5 382.45 –16.8 Eucalyptus robusta Phloroglucinol-monoterpene adduct 6-1.png
https://www.sciencedirect.com/science/article/abs/pii/S0031942218304709
/2020/0701/c23343a496171/page.psp
7 (+)-7'α-eucalrobusone X C23H26O5 382.45 +14.2 Eucalyptus robusta Phloroglucinol-monoterpene adduct 7-1.png
https://www.sciencedirect.com/science/article/abs/pii/S0031942218304709
/2020/0701/c23343a496177/page.psp
8 (−)-7'α-eucalrobusone X C23H26O5 382.45 –14.8 Eucalyptus robusta Phloroglucinol-monoterpene adduct 8-1.png
https://www.sciencedirect.com/science/article/abs/pii/S0031942218304709
/2020/0701/c23343a496183/page.psp
9 eucalyptin C C23H30O6 402.49 −42.7 Eucalyptus globulus Phloroglucinol-monoterpene adduct 9-1.png
https://pubs.acs.org/doi/10.1021/acs.jnatprod.8b00920
/2020/0701/c23343a496189/page.psp
10 eucalyptin D C23H30O6 402.49 −30.3 Eucalyptus globulus Phloroglucinol-monoterpene adduct 10-1.png
https://pubs.acs.org/doi/10.1021/acs.jnatprod.8b00920
/2020/0701/c23343a496195/page.psp
11 eugenial A C22H28O5 372.45 Eugenia multiflora Phloroglucinol-monoterpene adduct 11-1.png
https://www.tandfonline.com/doi/full/10.1080/14786419.2012.656113
/2020/0701/c23343a496199/page.psp
12 eugenial B C22H28O5 372.45 Eugenia multiflora Phloroglucinol-monoterpene adduct 12-1.png
https://www.tandfonline.com/doi/full/10.1080/14786419.2012.656113
/2020/0701/c23343a496203/page.psp
13 euglobal T1 C23H30O5 386.49 −143.7 Eucalyptus tereticornis Phloroglucinol-monoterpene adduct 13-1.png
https://pubs.acs.org/doi/10.1021/np50076a025
/2020/0701/c23343a496209/page.psp
14 euglobal IIc C23H30O5 386.49 −144 Eucalyptus globulus Phloroglucinol-monoterpene adduct 14-1.png
https://www.jstage.jst.go.jp/article/cpb1958/30/6/30_6_1952/_article/-char/ja/
/2020/0701/c23343a496215/page.psp
15 eucalypglobulusal J C23H30O6 402.48 −51.7 Eucalyptus globulus Phloroglucinol-monoterpene adduct 15-1.png
https://pubs.acs.org/doi/10.1021/acs.jnatprod.8b00430
/2020/0701/c23343a496223/page.psp
16 euglobal G6 C23H30O5 386.49 0 Eucalyptus grandis Phloroglucinol-monoterpene adduct 16-1.png
https://www.sciencedirect.com/science/article/pii/S0031942298800915
/2020/0701/c23343a496229/page.psp
17 euglobal G7 C23H30O5 386.49 0 Eucalyptus grandis Phloroglucinol-monoterpene adduct 17-1.png
https://www.sciencedirect.com/science/article/pii/S0031942298800915
/2020/0701/c23343a496237/page.psp
18 euglobal G9 C23H30O5 386.49 0 Eucalyptus grandis Phloroglucinol-monoterpene adduct 18-1.png
https://www.sciencedirect.com/science/article/pii/S0031942298002891
/2020/0701/c23343a496243/page.psp
19 euglobal G10 C23H30O5 386.49 0 Eucalyptus grandis Phloroglucinol-monoterpene adduct 19-1.png
https://www.sciencedirect.com/science/article/pii/S0031942298002891
/2020/0701/c23343a496247/page.psp
20 euglobal G11 C23H30O5 386.49 0 Eucalyptus grandis Phloroglucinol-monoterpene adduct 20-1.png
https://www.sciencedirect.com/science/article/pii/S0031942298002891
/2020/0701/c23343a496253/page.psp
21 euglobal G8 C23H30O5 386.49 0 Eucalyptus grandis Phloroglucinol-monoterpene adduct 21-1.png
https://www.sciencedirect.com/science/article/pii/S0031942298002891
/2020/0701/c23343a496261/page.psp
22 euglobal Ia1 C23H30O5 386.49 −216.7 Eucalyptus globulus Phloroglucinol-monoterpene adduct 22-1.png
https://www.jstage.jst.go.jp/article/cpb1958/30/6/30_6_1952/_article/-char/ja/
/2020/0701/c23343a496265/page.psp
23 euglobal Ia2 C23H30O5 386.49 +31.8 Eucalyptus globulus Phloroglucinol-monoterpene adduct 23-1.png
https://www.jstage.jst.go.jp/article/cpb1958/30/6/30_6_1952/_article/-char/ja/
/2020/0701/c23343a496273/page.psp
24 eucalypglobulusal I C23H30O7 418.49 +70.7 Eucalyptus globulus Phloroglucinol-monoterpene adduct 24-1.png
https://pubs.acs.org/doi/10.1021/acs.jnatprod.8b00430
/2020/0701/c23343a496277/page.psp
25 euglobal IIb C23H30O5 386.49 +12.2 Eucalyptus globulus Phloroglucinol-monoterpene adduct 25-1.png
https://www.jstage.jst.go.jp/article/cpb1958/30/6/30_6_1952/_article/-char/ja/
/2020/0701/c23343a496281/page.psp
26 guajavadial A C25H26O5 406.48 −70.8 Psidium guajava Phloroglucinol-monoterpene adduct 26-1.png
https://www.nature.com/articles/srep32748
/2020/0701/c23343a496293/page.psp
27 euglobal G2 C23H30O5 386.49 +103 Eucalyptus grandis Phloroglucinol-monoterpene adduct 27-1.png
https://www.jstage.jst.go.jp/article/cpb1958/38/5/38_5_1444/_article/-char/ja/
/2020/0701/c23343a496301/page.psp
28 euglobal G1 C23H30O5 386.49 +116 Eucalyptus grandis Phloroglucinol-monoterpene adduct 28-1.png
https://www.jstage.jst.go.jp/article/cpb1958/38/5/38_5_1444/_article/-char/ja/
/2020/0701/c23343a496307/page.psp
29 guadial B C25H26O5 406.48 Psidium guajava Phloroglucinol-monoterpene adduct 29-1.png
https://www.ncbi.nlm.nih.gov/pubmed/25965842
/2020/0701/c23343a496311/page.psp
30 operculatol A C28H32O4 432.55 −33.0 Cleistocalyx operculatus Phloroglucinol-monoterpene adduct 30-1.png
https://pubs.acs.org/doi/10.1021/acs.joc.8b01050
/2020/0701/c23343a496315/page.psp
31 operculatol B C28H32O4 432.55 +69.0 Cleistocalyx operculatus Phloroglucinol-monoterpene adduct 31-1.png
https://pubs.acs.org/doi/10.1021/acs.joc.8b01050
/2020/0701/c23343a496323/page.psp
32 euglobal-G12 C23H30O5 386.49 0 Eucalyptus grandis Phloroglucinol-monoterpene adduct 32-1.png
https://www.sciencedirect.com/science/article/pii/S0031942298002891
/2020/0701/c23343a496331/page.psp
33 euglobal R2 C23H30O5 386.49 0 Eucalyptus robusta Phloroglucinol-monoterpene adduct 33-1.png
https://www.tandfonline.com/doi/full/10.1080/10286020.2012.697457
/2020/0701/c23343a496341/page.psp
34 euglobal R1 C23H30O5 386.49 0 Eucalyptus robusta Phloroglucinol-monoterpene adduct 34-1.png
https://www.tandfonline.com/doi/full/10.1080/10286020.2012.697457
/2020/0701/c23343a496347/page.psp
35 euglobal IIa C23H30O5 386.49 +9.24 Eucalyptus globulus Phloroglucinol-monoterpene adduct 35-1.png
https://www.jstage.jst.go.jp/article/cpb1958/30/6/30_6_1952/_article/-char/ja/
/2020/0701/c23343a496353/page.psp
36 euglobal Ic C23H30O5 386.49 −3.12 Eucalyptus globulus Phloroglucinol-monoterpene adduct 36-1.png
https://www.jstage.jst.go.jp/article/cpb1958/30/6/30_6_1952/_article/-char/ja/
/2020/0701/c23343a496359/page.psp
37 psiguajavadial A C25H26O5 406.48 + 115.3 Psidium guajava Phloroglucinol-monoterpene adduct 37-1.png
https://pubs.acs.org/doi/abs/10.1021/acs.jafc.7b01762
/2020/0701/c23343a496369/page.psp
38 euglobal-BI-1 C23H30O5 386.49 +11.3 Eucalyptus blakelyi Phloroglucinol-monoterpene adduct 38-1.png
https://www.jstage.jst.go.jp/article/cpb1958/42/10/42_10_2177/_article/-char/ja/
/2020/0701/c23343a496373/page.psp
39 euglobal-Ib C23H30O5 386.49 −1.94 Eucalyptus globulus Phloroglucinol-monoterpene adduct 39-1.png
https://www.jstage.jst.go.jp/article/cpb1958/30/6/30_6_1952/_article/-char/ja/
/2020/0701/c23343a496379/page.psp
40 psiguajadial K C25H26O5 406.48 +147.6 Psidium guajava Phloroglucinol-monoterpene adduct 40-1.png
https://www.ncbi.nlm.nih.gov/pubmed/28432317
/2020/0701/c23343a496383/page.psp
41 guadial A C25H26O5 406.48 Psidium guajava Phloroglucinol-monoterpene adduct 41-1.png
https://pubs.acs.org/doi/abs/10.1021/ol302423b
/2020/0701/c23343a496393/page.psp
42 euglobal-G3 C23H30O5 386.49 +11 Eucalyptus grandis Phloroglucinol-monoterpene adduct 42-1.png
https://www.jstage.jst.go.jp/article/cpb1958/38/5/38_5_1444/_article/-char/ja/
/2020/0701/c23343a496401/page.psp
43 euglobal-G4 C23H30O5 386.49 +14.1 Eucalyptus grandis Phloroglucinol-monoterpene adduct 43-1.png
https://www.jstage.jst.go.jp/article/cpb1958/42/12/42_12_2591/_article/-char/ja/
/2020/0701/c23343a496407/page.psp
44 robustadial A C23H30O5 386.49 Eucalyptus robusta Phloroglucinol-monoterpene adduct 44-1.png
https://pubs.acs.org/doi/10.1021/ja00315a047
/2020/0701/c23343a496413/page.psp
45 robustadial B C23H30O5 386.49 Eucalyptus robusta Phloroglucinol-monoterpene adduct 45-1.png
https://pubs.acs.org/doi/10.1021/ja00315a047
/2020/0701/c23343a496419/page.psp
46 guadial C C25H26O5 406.48 Psidium guajava Phloroglucinol-monoterpene adduct 46-1.png
https://www.ncbi.nlm.nih.gov/pubmed/25965842
/2020/0701/c23343a496425/page.psp
47 viminalin A/callviminol A C22H30O5 374.47 −34.9 Callistemon viminalis Phloroglucinol-monoterpene adduct 47-1.png
https://www.sciencedirect.com/science/article/abs/pii/S0040402016313825 https://pubs.rsc.org/en/content/articlelanding/2019/ob/c9ob01426h/unauth
/2020/0701/c23343a496435/page.psp
48 viminalin B/callviminol B C21H28O5 360.44 −26.3 Callistemon viminalis Phloroglucinol-monoterpene adduct 48-1.png
https://www.sciencedirect.com/science/article/abs/pii/S0040402016313825 https://pubs.rsc.org/en/content/articlelanding/2019/ob/c9ob01426h/unauth
/2020/0701/c23343a496445/page.psp
49 viminalin C C22H30O5 374.47 −12.4 Callistemon viminalis Phloroglucinol-monoterpene adduct 49-1.png
https://www.sciencedirect.com/science/article/abs/pii/S0040402016313825
/2020/0701/c23343a496451/page.psp
50 viminalin D C22H30O5 374.47 −30 Callistemon viminalis Phloroglucinol-monoterpene adduct 50-1.png
https://www.sciencedirect.com/science/article/abs/pii/S0040402016313825
/2020/0701/c23343a496457/page.psp
51 viminalin H C22H30O4 358.48 −44.5 Callistemon viminalis Phloroglucinol-monoterpene adduct 51-1.png
https://www.sciencedirect.com/science/article/abs/pii/S0040402016313825 https://pubs.rsc.org/en/content/articlelanding/2019/ob/c9ob01426h/unauth
/2020/0701/c23343a496589/page.psp
52 viminalin I C21H28O4 344.44 −30.7 Callistemon viminalis Phloroglucinol-monoterpene adduct 52-1.png
https://www.sciencedirect.com/science/article/abs/pii/S0040402016313825 https://pubs.rsc.org/en/content/articlelanding/2019/ob/c9ob01426h/unauth
/2020/0701/c23343a496591/page.psp
53 viminalin J C22H30O4 358.47 −28.0 Callistemon viminalis Phloroglucinol-monoterpene adduct 53-1.png
https://www.sciencedirect.com/science/article/abs/pii/S004040201730087X
/2020/0701/c23343a496593/page.psp
54 viminalin K C22H30O4 358.47 −61.3 Callistemon viminalis Phloroglucinol-monoterpene adduct 54-1.png
https://www.sciencedirect.com/science/article/abs/pii/S0040402016313825
/2020/0701/c23343a496595/page.psp
55 callviminol E C22H30O4 358.48 −6.0 Callistemon viminalis Phloroglucinol-monoterpene adduct 55-1.png
https://www.sciencedirect.com/science/article/abs/pii/S0367326X1830649X
/2020/0701/c23343a496597/page.psp
56 viminalin L C22H30O4 358.47 −17.4 Callistemon viminalis Phloroglucinol-monoterpene adduct 56-1.png
https://www.sciencedirect.com/science/article/abs/pii/S0040402016313825
/2020/0701/c23343a496599/page.psp
57 callisalignene C C22H30O4 358.47 −131.0 Callistemon salignus Phloroglucinol-monoterpene adduct 57-1.png
https://www.sciencedirect.com/science/article/abs/pii/S004040201730087X
/2020/0701/c23343a496601/page.psp
58 viminalin M C22H30O4 358.47 −46.8 Callistemon viminalis Phloroglucinol-monoterpene adduct 58-1.png
https://www.sciencedirect.com/science/article/abs/pii/S0040402016313825 https://pubs.rsc.org/en/content/articlelanding/2019/ob/c9ob01426h/unauth
/2020/0701/c23343a496603/page.psp
59 viminalin O C22H30O4 358.47 −25.0 Callistemon viminalis Phloroglucinol-monoterpene adduct 59-1.png
https://www.sciencedirect.com/science/article/abs/pii/S0040402016313825
/2020/0701/c23343a496605/page.psp
60 viminalin N C21H28O4 344.44 −39.0 Callistemon viminalis Phloroglucinol-monoterpene adduct 60-1.png
https://www.sciencedirect.com/science/article/abs/pii/S0040402016313825 https://pubs.rsc.org/en/content/articlelanding/2019/ob/c9ob01426h/unauth
/2020/0701/c23343a496607/page.psp
61 viminalin E C22H30O5 374.47 −85.2 Callistemon viminalis Phloroglucinol-monoterpene adduct 61-1.png
https://www.sciencedirect.com/science/article/abs/pii/S0040402016313825
/2020/0701/c23343a496609/page.psp
62 viminalin F C21H28O5 360.44 −57.8 Callistemon viminalis Phloroglucinol-monoterpene adduct 62-1.png
https://www.sciencedirect.com/science/article/abs/pii/S0040402016313825
/2020/0701/c23343a496611/page.psp
63 viminalin G C22H30O5 374.47 −67.2 Callistemon viminalis Phloroglucinol-monoterpene adduct 63-1.png
https://www.sciencedirect.com/science/article/abs/pii/S0040402016313825
/2020/0701/c23343a496613/page.psp
64 callisretone A C22H30O5 374.48 +28 Callistemon rigidus Phloroglucinol-monoterpene adduct 64-1.png
https://pubs.acs.org/doi/10.1021/acs.jnatprod.7b00606
/2020/0701/c23343a496615/page.psp
65 callisretone B C21H28O5 360.45 +98 Callistemon rigidus Phloroglucinol-monoterpene adduct 65-1.png
https://pubs.acs.org/doi/10.1021/acs.jnatprod.7b00606
/2020/0701/c23343a496617/page.psp
66 eucalrobusone Y C23H28O5 384.47 +8.7 Eucalyptus robusta Phloroglucinol-monoterpene adduct 66-1.png
https://www.sciencedirect.com/science/article/abs/pii/S0031942218304709
/2020/0701/c23343a496619/page.psp
67 melaleucadine A C25H30O3 378.5 Melaleuca leucadendron Phloroglucinol-monoterpene adduct 67-1.png
https://www.sciencedirect.com/science/article/pii/S0040403919302230
/2020/0701/c23343a496621/page.psp
68 euglobal G5 C23H30O5 386.49 +213.8 Eucalyptus grandis Phloroglucinol-monoterpene adduct 68-1.png
https://www.jstage.jst.go.jp/article/cpb1958/42/12/42_12_2591/_article/-char/ja/
/2020/0701/c23343a496623/page.psp
69 tomentosenol A C25H38O3 386.57 −12.6 Rhodomyrtus tomentosa Phloroglucinol-monoterpene adduct 69-1.png
https://pubs.rsc.org/--/content/articlehtml/2016/ra/c6ra01594h
/2020/0701/c23343a496625/page.psp
70 (+)-cleistocaltones B C28H34O5 450.58 +61.0 Cleistocalyx operculatus Phloroglucinol-monoterpene adduct 70-1.png
https://pubs.acs.org/doi/10.1021/acs.orglett.9b03743
/2020/0701/c23343a496627/page.psp
71 (−)-cleistocaltones B C28H34O5 450.58 −60.3 Cleistocalyx operculatus Phloroglucinol-monoterpene adduct 71-1.png
https://pubs.acs.org/doi/10.1021/acs.orglett.9b03743
/2020/0701/c23343a496629/page.psp
72 calliviminone C C24H36O3 372.55 0 Callistemon viminalis Phloroglucinol-monoterpene adduct 72-1.png
https://pubs.rsc.org/en/content/articlelanding/2015/ra/c5ra19651e
/2020/0701/c23343a496631/page.psp
73 (+)-tomentodione H C25H38O3 386.58 +36.0 Rhodomyrtus tomentosa Phloroglucinol-monoterpene adduct 73-1.png
https://pubs.acs.org/doi/10.1021/acs.jnatprod.6b01005
/2020/0701/c23343a496633/page.psp
74 (−)-tomentodione H C25H38O3 386.58 −36.0 Rhodomyrtus tomentosa Phloroglucinol-monoterpene adduct 74-1.png
https://pubs.acs.org/doi/10.1021/acs.jnatprod.6b01005
/2020/0701/c23343a496635/page.psp
75 (+)-tomentodione I C25H38O3 386.58 +92.0 Rhodomyrtus tomentosa Phloroglucinol-monoterpene adduct 75-1.png
https://pubs.acs.org/doi/10.1021/acs.jnatprod.6b01005
/2020/0701/c23343a496637/page.psp
76 (–)-tomentodione I C25H38O3 386.58 −92.0 Rhodomyrtus tomentosa Phloroglucinol-monoterpene adduct 76-1.png
https://pubs.acs.org/doi/10.1021/acs.jnatprod.6b01005
/2020/0701/c23343a496639/page.psp
77 calliviminone D C24H36O3 372.55 0 Callistemon viminalis Phloroglucinol-monoterpene adduct 77-1.png
https://pubs.rsc.org/en/content/articlelanding/2015/ra/c5ra19651e
/2020/0701/c23343a496641/page.psp
78 callistiviminene M C24H36O3 372.55 +35.8 Callistemon viminalis Phloroglucinol-monoterpene adduct 78-1.png
https://www.sciencedirect.com/science/article/abs/pii/S0031942216301832
/2020/0701/c23343a496643/page.psp
79 callistiviminene N C24H36O3 372.55 −82.5 Callistemon viminalis Phloroglucinol-monoterpene adduct 79-1.png
https://www.sciencedirect.com/science/article/abs/pii/S0031942216301832
/2020/0701/c23343a496645/page.psp
80 callisalignene G C25H38O3 386.58 +188.3 Callistemon salignus Phloroglucinol-monoterpene adduct 80-1.png
https://www.ncbi.nlm.nih.gov/pubmed/28620873
/2020/0701/c23343a496647/page.psp
81 callisalignene D C25H38O3 386.58 +120.0 Callistemon salignus Phloroglucinol-monoterpene adduct 81-1.png
https://www.sciencedirect.com/science/article/abs/pii/S004040201730087X
/2020/0701/c23343a496649/page.psp
82 callisalignene H C25H38O3 386.58 −221.4 Callistemon salignus Phloroglucinol-monoterpene adduct 82-1.png
https://www.ncbi.nlm.nih.gov/pubmed/28620873
/2020/0701/c23343a496651/page.psp
83 viminadione A C25H38O3 386.58 +120.3 Callistemon viminalis Phloroglucinol-monoterpene adduct 83-1.png
https://pubs.acs.org/doi/10.1021/np990056a
/2020/0701/c23343a496653/page.psp
84 viminadione B C25H38O3 386.58 −25.5 Callistemon viminalis Phloroglucinol-monoterpene adduct 84-1.png
https://pubs.acs.org/doi/10.1021/np990056a
/2020/0701/c23343a496655/page.psp
85 callistiviminene O C24H36O3 372.55 −100.1 Callistemon viminalis Phloroglucinol-monoterpene adduct 85-1.png
https://www.sciencedirect.com/science/article/abs/pii/S0031942216301832
/2020/0701/c23343a496657/page.psp
86 rtomentone F C25H39O3 386.58 +59 Rhodomyrtus tomentosa Phloroglucinol-monoterpene adduct 86-1.png
https://www.sciencedirect.com/science/article/pii/S0367326X20301672
/2020/0701/c23343a496659/page.psp
87 intermedione D C27H34O3 406.57 Corymbia intermedia Phloroglucinol-monoterpene adduct 87-1.png
https://pubs.acs.org/doi/10.1021/acs.jnatprod.8b00494
/2020/0701/c23343a496661/page.psp
88 rtomentone G C25H38O3 386.58 −43 Rhodomyrtus tomentosa Phloroglucinol-monoterpene adduct 88-1.png
https://www.sciencedirect.com/science/article/pii/S0367326X20301672
/2020/0701/c23343a496663/page.psp
89 rtomentone H C25H38O3 386.58 +94 Rhodomyrtus tomentosa Phloroglucinol-monoterpene adduct 89-1.png
https://www.sciencedirect.com/science/article/pii/S0367326X20301672
/2020/0701/c23343a496665/page.psp
90 baeckfrutone A C24H36O3 372.55 +133.3 Baeckea frutescens Phloroglucinol-monoterpene adduct 90-1.png
https://www.sciencedirect.com/science/article/abs/pii/S0040402018311463
/2020/0701/c23343a496667/page.psp
91 baeckfrutone H C23H34O3 358.52 −95.6 Baeckea frutescens Phloroglucinol-monoterpene adduct 91-1.png
https://www.sciencedirect.com/science/article/abs/pii/S0040402018311463
/2020/0701/c23343a496669/page.psp
92 baeckfrutone E C24H36O3 372.55 −93.9 Baeckea frutescens Phloroglucinol-monoterpene adduct 92-1.png
https://www.sciencedirect.com/science/article/abs/pii/S0040402018311463
/2020/0701/c23343a496671/page.psp
93 BF-2 C24H36O3 372.55 +166.5 Baeckea frutescens Phloroglucinol-monoterpene adduct 93-1.png
https://www.sciencedirect.com/science/article/abs/pii/0031942295006591
/2020/0701/c23343a496673/page.psp
94 baeckfrutone M C24H36O3 372.55 +29.3 Baeckea frutescens Phloroglucinol-monoterpene adduct 94-1.png
https://www.ncbi.nlm.nih.gov/pubmed/30374905 https://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/chem.202001111
/2020/0701/c23343a496675/page.psp
95 baeckone D C23H34O3 358.52 –60.8 Baeckea frutescens Phloroglucinol-monoterpene adduct 95-1.png
https://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/chem.202001111
/2020/0701/c23343a496677/page.psp
96 baeckone E C23H34O3 358.52 –11.1 Baeckea frutescens Phloroglucinol-monoterpene adduct 96-1.png
https://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/chem.202001111
/2020/0701/c23343a496679/page.psp
97 baeckone F C24H36O3 372.55 –183.4 Baeckea frutescens Phloroglucinol-monoterpene adduct 97-1.png
https://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/chem.202001111
/2020/0701/c23343a496681/page.psp
98 baeckone G C24H36O3 372.55 +10.5 Baeckea frutescens Phloroglucinol-monoterpene adduct 98-1.png
https://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/chem.202001111
/2020/0701/c23343a496683/page.psp
99 baeckone H C23H34O3 372.55 –113.7 Baeckea frutescens Phloroglucinol-monoterpene adduct 99-1.png
https://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/chem.202001111
/2020/0701/c23343a496685/page.psp
100 (+)-baeckfrutone B C24H36O3 372.55 +117.7 Baeckea frutescens Phloroglucinol-monoterpene adduct 100-1.png
https://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/chem.202001111 https://www.sciencedirect.com/science/article/abs/pii/S0040402018311463
/2020/0701/c23343a496689/page.psp
101 (–)-baeckfrutone B C24H36O3 372.55 − 120.6 Baeckea frutescens Phloroglucinol-monoterpene adduct 101-1.png
https://www.sciencedirect.com/science/article/abs/pii/S0040402018311463
/2020/0701/c23343a496691/page.psp
102 baeckfrutone D C24H36O3 372.55 −191.0 Baeckea frutescens 102-1.png
https://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/chem.202001111 https://www.sciencedirect.com/science/article/abs/pii/S0040402018311463
/2020/0701/c23343a496693/page.psp
103 baeckfrutone F C23H34O3 358.52 +62.3 Baeckea frutescens Phloroglucinol-monoterpene adduct 103-1.png
https://www.sciencedirect.com/science/article/abs/pii/S0040402018311463
/2020/0701/c23343a496695/page.psp
104 (+)-baeckfrutone C C24H36O3 372.55 +96.2 Baeckea frutescens Phloroglucinol-monoterpene adduct 104-1.png
https://www.sciencedirect.com/science/article/abs/pii/S0040402018311463 https://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/chem.202001111
/2020/0701/c23343a496697/page.psp
105 (–)-baeckfrutone C C24H36O3 372.55 −97.6 Baeckea frutescens Phloroglucinol-monoterpene adduct 105-1.png
https://www.sciencedirect.com/science/article/abs/pii/S0040402018311463 https://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/chem.202001111
/2020/0701/c23343a496699/page.psp
106 baeckfrutone G C23H34O3 358.52 −171.7 Baeckea frutescens Phloroglucinol-monoterpene adduct 106-1.png
https://www.sciencedirect.com/science/article/abs/pii/S0040402018311463
/2020/0701/c23343a496701/page.psp
107 (+)-baeckfrutone N C24H36O3 372.54 +60.8 Baeckea frutescens Phloroglucinol-monoterpene adduct 107-1.png
https://www.ncbi.nlm.nih.gov/pubmed/30374905
/2020/0701/c23343a496703/page.psp
108 (–)-baeckfrutone N C24H36O3 372.54 −58.2 Baeckea frutescens Phloroglucinol-monoterpene adduct 108-1.png
https://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/chem.202001111 https://www.ncbi.nlm.nih.gov/pubmed/30374905
/2020/0701/c23343a496705/page.psp
109 (+)-baeckfrutone I C23H34O3 358.52 +46.8 Baeckea frutescens Phloroglucinol-monoterpene adduct 109-1.png
https://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/chem.202001111 https://www.sciencedirect.com/science/article/abs/pii/S0040402018311463
/2020/0701/c23343a496711/page.psp
110 (−)-baeckfrutone I C23H34O3 358.52 –46.2 Baeckea frutescens Phloroglucinol-monoterpene adduct 110-1.png
https://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/chem.202001111 https://www.sciencedirect.com/science/article/abs/pii/S0040402018311463
/2020/0701/c23343a496713/page.psp
111 frutescone O C24H36O3 372.55 −21 Baeckea frutescens Phloroglucinol-monoterpene adduct 111-1.png
https://pubs.acs.org/doi/10.1021/acs.jnatprod.7b00042
/2020/0701/c23343a496715/page.psp
112 baeckfrutone K C24H36O3 372.55 −58.1 Baeckea frutescens Phloroglucinol-monoterpene adduct 112-1.png
https://www.sciencedirect.com/science/article/abs/pii/S0040402018311463
/2020/0701/c23343a496719/page.psp
113 baeckfrutone R C24H36O3 372.55 +20.6 Baeckea frutescens Phloroglucinol-monoterpene adduct 113-1.png
https://www.ncbi.nlm.nih.gov/pubmed/30374905
/2020/0701/c23343a496721/page.psp
114 (+)-baeckfrutone Q C23H34O3 358.52 +21.1 Baeckea frutescens Phloroglucinol-monoterpene adduct 114-1.png
https://www.ncbi.nlm.nih.gov/pubmed/30374905 https://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/chem.202001111
/2020/0701/c23343a496723/page.psp
115 (–)-baeckfrutone Q C23H34O3 358.52 –56.0 Baeckea frutescens Phloroglucinol-monoterpene adduct 115-1.png
https://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/chem.202001111
/2020/0701/c23343a496725/page.psp
116 (+)-baeckone A C23H34O3 358.52 +40.0 Baeckea frutescens Phloroglucinol-monoterpene adduct 116-1.png
https://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/chem.202001111
/2020/0701/c23343a496729/page.psp
117 (–)-baeckone A C23H34O3 358.52 –41.0 Baeckea frutescens Phloroglucinol-monoterpene adduct 117-1.png
https://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/chem.202001111
/2020/0701/c23343a496731/page.psp
118 baeckone B C23H34O3 358.52 +44.0 Baeckea frutescens Phloroglucinol-monoterpene adduct 118-1.png
https://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/chem.202001111
/2020/0701/c23343a496733/page.psp
119 (+)-baeckone C C24H36O3 372.55 +149.3 Baeckea frutescens Phloroglucinol-monoterpene adduct 119-1.png
https://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/chem.202001111
/2020/0701/c23343a496735/page.psp
120 (–)-baeckone C C24H36O3 372.55 –148.5 Baeckea frutescens Phloroglucinol-monoterpene adduct 120-1.png
https://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/chem.202001111
/2020/0701/c23343a496737/page.psp
121 (+)-baeckfrutone J C24H36O3 372.55 +36.3 Baeckea frutescens Phloroglucinol-monoterpene adduct 121-1.png
https://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/chem.202001111
/2020/0701/c23343a496739/page.psp
122 (+)-baeckfrutone J C24H36O3 372.55 +36.3 Baeckea frutescens Phloroglucinol-monoterpene adduct 122-1.png
https://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/chem.202001111
/2020/0701/c23343a496741/page.psp
123 baeckfrutone L C24H36O3 372.55 57.8 Baeckea frutescens Phloroglucinol-monoterpene adduct 123-1.png
https://www.sciencedirect.com/science/article/abs/pii/S0040402018311463
/2020/0701/c23343a496745/page.psp
124 frutescone P C24H36O3 372.55 +272 Baeckea frutescens Phloroglucinol-monoterpene adduct 124-1.png
https://pubs.acs.org/doi/10.1021/acs.jnatprod.7b00042
/2020/0701/c23343a496753/page.psp
125 callisalignene E C24H36O3 372.55 −29.0 Callistemon salignus Phloroglucinol-monoterpene adduct 125-1.png
https://www.sciencedirect.com/science/article/abs/pii/S004040201730087X
/2020/0701/c23343a496755/page.psp
126 callisalignene F C24H36O3 372.55 +29.0 Callistemon salignus Phloroglucinol-monoterpene adduct 126-1.png
https://www.sciencedirect.com/science/article/abs/pii/S004040201730087X
/2020/0701/c23343a496757/page.psp
127 callistiviminene K C24H36O3 372.55 0 Callistemon viminalis Phloroglucinol-monoterpene adduct 127-1.png
https://www.sciencedirect.com/science/article/abs/pii/S0031942216301832
/2020/0701/c23343a496759/page.psp
128 callistiviminene L C24H36O3 372.55 −18.6 Callistemon viminalis Phloroglucinol-monoterpene adduct 128-1.png
https://www.sciencedirect.com/science/article/abs/pii/S0031942216301832
/2020/0701/c23343a496763/page.psp
129 baeckfrutone O C23H34O4 374.52 −18.5 Baeckea frutescens Phloroglucinol-monoterpene adduct 129-1.png
https://www.ncbi.nlm.nih.gov/pubmed/30374905
/2020/0701/c23343a496767/page.psp
130 myrtucommulone L C24H36O3 372.55 0 Myrtus communis Phloroglucinol-monoterpene adduct 130-1.png
https://pubs.acs.org/doi/10.1021/np2009219
/2020/0701/c23343a496769/page.psp
131 baeckfrutone P C23H34O4 374.52 +43.3 Baeckea frutescens Phloroglucinol-monoterpene adduct 131-1.png
https://www.ncbi.nlm.nih.gov/pubmed/30374905
/2020/0701/c23343a496771/page.psp
132 callistiviminene F C24H36O3 372.55 +30.4 Callistemon viminalis Phloroglucinol-monoterpene adduct 132-1.png
https://www.sciencedirect.com/science/article/abs/pii/S0031942216301832
/2020/0701/c23343a496773/page.psp
133 tomentodione L C25H38O3 386.58 −9 Rhodomyrtus tomentosa Phloroglucinol-monoterpene adduct 133-1.png
https://pubs.acs.org/doi/10.1021/acs.jnatprod.6b01005
/2020/0701/c23343a496777/page.psp
134 tomentodione M C25H38O3 386.58 +94 Rhodomyrtus tomentosa Phloroglucinol-monoterpene adduct 134-1.png
https://pubs.acs.org/doi/10.1021/acs.jnatprod.6b01005
/2020/0701/c23343a496781/page.psp
135 callistiviminene G C24H36O3 372.55 +9.0 Callistemon viminalis Phloroglucinol-monoterpene adduct 135-1.png
https://www.sciencedirect.com/science/article/abs/pii/S0031942216301832
/2020/0701/c23343a496785/page.psp
136 callistiviminene H C24H36O3 372.55 −22.1 Callistemon viminalis Phloroglucinol-monoterpene adduct 136-1.png
https://www.sciencedirect.com/science/article/abs/pii/S0031942216301832
/2020/0701/c23343a496787/page.psp
137 tomentodione J C25H38O3 386.58 −43 Rhodomyrtus tomentosa Phloroglucinol-monoterpene adduct 137-1.png
https://pubs.acs.org/doi/10.1021/acs.jnatprod.6b01005
/2020/0701/c23343a496789/page.psp
138 tomentodione K C25H38O3 386.58 −24 Rhodomyrtus tomentosa Phloroglucinol-monoterpene adduct 138-1.png
https://pubs.acs.org/doi/10.1021/acs.jnatprod.6b01005
/2020/0701/c23343a496793/page.psp
139 ficifolidione C25H38O3 386.58 +64.2 Eucalyptus ficifolia Phloroglucinol-monoterpene adduct 139-1.png
https://www.sciencedirect.com/science/article/abs/pii/S0040402003010950
/2020/0701/c23343a496795/page.psp
140 4R-focifolidione C25H38O3 386.58 −78 Rhodomyrtus tomentosa Phloroglucinol-monoterpene adduct 140-1.png
https://pubs.rsc.org/--/content/articlehtml/2016/ra/c6ra01594h
/2020/0701/c23343a496797/page.psp
141 intermedione A C27H34O3 406.57 Corymbia intermedia Phloroglucinol-monoterpene adduct 141-1.png
https://pubs.acs.org/doi/10.1021/acs.jnatprod.8b00494
/2020/0701/c23343a496799/page.psp
142 intermedione B C27H34O3 406.57 Corymbia intermedia Phloroglucinol-monoterpene adduct 142-1.png
https://pubs.acs.org/doi/10.1021/acs.jnatprod.8b00494
/2020/0701/c23343a496801/page.psp
143 callistiviminene J C24H36O3 372.55 −60.6 Callistemon viminalis Phloroglucinol-monoterpene adduct 143-1.png
https://www.sciencedirect.com/science/article/abs/pii/S0031942216301832
/2020/0701/c23343a496803/page.psp
144 callisalignene I C24H38O3 386.57 +164.7 Callistemon salignus Phloroglucinol-monoterpene adduct 144-1.png
https://www.ncbi.nlm.nih.gov/pubmed/28620873
/2020/0701/c23343a496805/page.psp
145 (+)-callistiviminene I C24H36O3 372.55 +10.8 Callistemon viminalis Phloroglucinol-monoterpene adduct 145-1.png
https://www.sciencedirect.com/science/article/abs/pii/S0031942216301832
/2020/0701/c23343a496807/page.psp
146 (–)-callistiviminene I C24H36O3 372.55 −8.9 Callistemon viminalis Phloroglucinol-monoterpene adduct 146-1.png
https://www.sciencedirect.com/science/article/abs/pii/S0031942216301832
/2020/0701/c23343a496809/page.psp
147 intermedione C C27H34O3 406.57 Corymbia intermedia Phloroglucinol-monoterpene adduct 147-1.png
https://pubs.acs.org/doi/10.1021/acs.jnatprod.8b00494
/2020/0701/c23343a496811/page.psp
148 (+)-frutescone Q C24H36O3 372.55 +133 Baeckea frutescens Phloroglucinol-monoterpene adduct 148-1.png
https://pubs.acs.org/doi/10.1021/acs.jnatprod.7b00042
/2020/0701/c23343a496813/page.psp
149 (–)-frutescone Q C24H36O3 372.55 −147 Baeckea frutescens Phloroglucinol-monoterpene adduct 149-1.png
https://pubs.acs.org/doi/10.1021/acs.jnatprod.7b00042 https://pubs.acs.org/doi/10.1021/acs.jnatprod.7b00042
/2020/0701/c23343a496815/page.psp
150 (+)-frutescone R C24H36O3 372.55 +85 Baeckea frutescens Phloroglucinol-monoterpene adduct 150-1.png
https://pubs.acs.org/doi/10.1021/acs.jnatprod.7b00042 https://pubs.acs.org/doi/10.1021/acs.jnatprod.7b00042
/2020/0701/c23343a496817/page.psp
151 (−)-frutescone R C24H36O3 372.55 −90 Baeckea frutescens Phloroglucinol-monoterpene adduct 151-1.png
https://pubs.acs.org/doi/10.1021/acs.jnatprod.7b00042
/2020/0701/c23343a496821/page.psp
152 calliviminone A C24H36O3 372.55 Callistemon viminalis Phloroglucinol-monoterpene adduct 152-1.png
https://www.sciencedirect.com/science/article/pii/S0040403914019686
/2020/0701/c23343a496823/page.psp
153 calliviminone E C25H38O3 386.57 0 Callistemon viminalis Phloroglucinol-monoterpene adduct 153-1.png
https://pubs.rsc.org/en/content/articlelanding/2015/ra/c5ra19651e
/2020/0701/c23343a496825/page.psp
154 calliviminone G C25H38O3 386.57 −13.8 Callistemon viminalis Phloroglucinol-monoterpene adduct 154-1.png
https://pubs.rsc.org/en/content/articlelanding/2015/ra/c5ra19651e
/2020/0701/c23343a496827/page.psp
155 calliviminone I C25H38O3 386.58 Syncarpia glomulifera Phloroglucinol-monoterpene adduct 155-1.png
https://www.sciencedirect.com/science/article/pii/S0968089617304066
/2020/0701/c23343a496829/page.psp
156 calliviminone B C24H36O3 372.55 Callistemon viminalis Phloroglucinol-monoterpene adduct 156-1.png
https://www.sciencedirect.com/science/article/pii/S0040403914019686
/2020/0701/c23343a496833/page.psp
157 calliviminone F C25H38O3 386.57 0 Callistemon viminalis Phloroglucinol-monoterpene adduct 157-1.png
https://pubs.rsc.org/en/content/articlelanding/2015/ra/c5ra19651e
/2020/0701/c23343a496837/page.psp
158 calliviminone H C25H38O3 386.57 +14.7 Callistemon viminalis Phloroglucinol-monoterpene adduct 158-1.png
https://pubs.rsc.org/en/content/articlelanding/2015/ra/c5ra19651e
/2020/0701/c23343a496843/page.psp
159 (+)-cleistocaltones A C28H32O5 448.55 +66.5 Cleistocalyx operculatus Phloroglucinol-monoterpene adduct 159-1.png
https://pubs.acs.org/doi/10.1021/acs.orglett.9b03743
/2020/0701/c23343a496847/page.psp
160 (–)-cleistocaltones A C28H32O5 448.55 –67.2 Cleistocalyx operculatus Phloroglucinol-monoterpene adduct 160-1.png
https://pubs.acs.org/doi/10.1021/acs.orglett.9b03743
/2020/0701/c23343a496849/page.psp
161 baefrutone A C35H48O7 580.76 −178.8 Baeckea frutescens Phloroglucinol-monoterpene adduct 161-1.png
https://www.ncbi.nlm.nih.gov/pubmed/30357224
/2020/0701/c23343a496851/page.psp
162 baefrutone B C35H48O7 580.76 −39.8 Baeckea frutescens Phloroglucinol-monoterpene adduct 162-1.png
https://www.ncbi.nlm.nih.gov/pubmed/30357224
/2020/0701/c23343a496853/page.psp
163 baefrutone C C35H48O7 580.76 −11.5 Baeckea frutescens Phloroglucinol-monoterpene adduct 163-1.png
https://www.ncbi.nlm.nih.gov/pubmed/30357224
/2020/0701/c23343a496855/page.psp
164 baefrutone D C35H48O7 580.76 −27.8 Baeckea frutescens Phloroglucinol-monoterpene adduct 164-1.png
https://www.ncbi.nlm.nih.gov/pubmed/30357224
/2020/0701/c23343a496859/page.psp
165 eucalyptusdimer A C44H58O8 714.94 −56.2 Eucalyptus robusta Phloroglucinol-monoterpene adduct 165-1.png
https://www.ncbi.nlm.nih.gov/pubmed/30088934
/2020/0701/c23343a496867/page.psp
166 eucalyptusdimer B C44H58O8 714.94 +45.4 Eucalyptus robusta Phloroglucinol-monoterpene adduct 166-1.png
https://www.ncbi.nlm.nih.gov/pubmed/30088934
/2020/0701/c23343a496871/page.psp
167 eucalyptusdimer C C45H60O8 728.97 –100.6 Eucalyptus robusta Phloroglucinol-monoterpene adduct 167-1.png
https://www.ncbi.nlm.nih.gov/pubmed/30088934
/2020/0701/c23343a496873/page.psp
168 callistrilone E C34H46O7 566.72 Callistemon rigidus Phloroglucinol-monoterpene adduct 168-1.png
https://pubs.rsc.org/en/content/articlehtml/2017/sc/c7sc04672c
/2020/0701/c23343a496881/page.psp
169 callistrilone F C35H48O8 596.75 +95.3 Callistemon rigidus Phloroglucinol-monoterpene adduct 169-1.png
https://pubs.rsc.org/en/content/articlehtml/2017/sc/c7sc04672c
/2020/0701/c23343a496883/page.psp
170 callistrilone C C34H44O7 564.71 Callistemon rigidus Phloroglucinol-monoterpene adduct 170-1.png
https://pubs.rsc.org/en/content/articlehtml/2017/sc/c7sc04672c
/2020/0701/c23343a496885/page.psp
171 callistrilone K C35H46O7 578.74 −76.3 Callistemon rigidus Phloroglucinol-monoterpene adduct 171-1.png
https://onlinelibrary.wiley.com/doi/10.1002/cbdv.201800172
/2020/0701/c23343a496889/page.psp
172 callistrilone G C35H48O7 580.75 +101.9 Callistemon rigidus Phloroglucinol-monoterpene adduct 172-1.png
https://onlinelibrary.wiley.com/doi/10.1002/cbdv.201800172
/2020/0701/c23343a496891/page.psp
173 callistrilone H C36H50O7 580.75 +103.2 Callistemon rigidus Phloroglucinol-monoterpene adduct 173-1.png
https://onlinelibrary.wiley.com/doi/10.1002/cbdv.201800172
/2020/0701/c23343a496895/page.psp
174 callistrilone I C36H50O7 594.78 +85.5 Callistemon rigidus Phloroglucinol-monoterpene adduct 174-1.png
https://onlinelibrary.wiley.com/doi/10.1002/cbdv.201800172
/2020/0701/c23343a496897/page.psp
175 callistrilone D C34H44O6 548.71 Callistemon rigidus Phloroglucinol-monoterpene adduct 175-1.png
https://pubs.rsc.org/en/content/articlehtml/2017/sc/c7sc04672c
/2020/0701/c23343a496901/page.psp
176 callistrilone A C34H44O7 564.71 +17.5 Callistemon rigidus Phloroglucinol-monoterpene adduct 176-1.png
https://pubs.acs.org/doi/abs/10.1021/acs.orglett.5b03360
/2020/0701/c23343a496903/page.psp
177 callistrilone J C35H46O6 562.75 −54.4 Callistemon rigidus Phloroglucinol-monoterpene adduct 177-1.png
https://onlinelibrary.wiley.com/doi/10.1002/cbdv.201800172
/2020/0701/c23343a496905/page.psp
178 callistrilone B C35H46O6 562.74 +22.6 Callistemon rigidus Phloroglucinol-monoterpene adduct 178-1.png
https://pubs.acs.org/doi/abs/10.1021/acs.orglett.5b03360
/2020/0701/c23343a496909/page.psp
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