Scientific name	Authority	First published in
Moronobea exserens	Endl. ex Walp.	Repert. Bot. Syst. 1: 394 (1842)
Symphonia gabonensis	Pierre	Bull. Mens. Soc. Linn. Paris 2: 1228 (1896)
Actinostigma speciosum	Welw.	Apont. : 560 (1859)
Aneuriscus aubletii	C.Presl	Symb. Bot. 1: 71 (1832)
Aneuriscus exserens	C.Presl	Symb. Bot. 1: 71 (1832)
Symphonia globulifera var. gabonensis	Vesque	Monogr. Phan. 8: 231 1893
Symphonia utilissima	R.E.Schult.	Bot. Mus. Leafl. 17: 22, tab. 10. 1955
Moronobea globulifera	Schltdl.	Linnaea 8: 190 (1833)

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- East Tropical Africa
  - Tanzania
  - Uganda
- Northeast Tropical Africa
  - Chad
- South Tropical Africa
  - Angola
  - Zambia
- West Tropical Africa
  - Ghana
  - Ivory Coast
  - Liberia
  - Nigeria
  - Sierra Leone
- West-central Tropical Africa
  - Burundi
  - Cabinda
  - Cameroon
  - Central African Republic
  - Congo
  - Equatorial Guinea
  - Gabon
  - Gulf Of Guinea Islands
  - Rwanda
  - Zaïre

Northern America click to expand
- Mexico
  - Mexico Gulf
  - Mexico Southeast
  - Mexico Southwest

Southern America click to expand
- Brazil
  - Brazil North
  - Brazil Northeast
  - Brazil Southeast
  - Brazil West-central
- Caribbean
  - Haiti
  - Jamaica
  - Leeward Islands
  - Trinidad-Tobago
  - Windward Islands
- Central America
  - Belize
  - Costa Rica
  - Guatemala
  - Nicaragua
  - Panamá
- Northern South America
  - French Guiana
  - Guyana
  - Suriname
  - Venezuela
- Western South America
  - Bolivia
  - Colombia
  - Ecuador
  - Peru

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000438147
Tropicos	7800762
INPN	630762
KEW	urn:lsid:ipni.org:names:429281-1
The Plant List	kew-2484835
Open Tree Of Life	978306
NCBI Taxonomy	156483
IUCN Red List	63072
IPNI	429281-1
iNaturalist	316836
GBIF	7330061
Freebase	/m/0274hq5
EOL	5711937
USDA GRIN	36005
Wikipedia	Symphonia_globulifera
CMAUP	NPO8408
PaleoBotany	117490

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.

Title

Authors

Publication

Released

IDs

Anti-Leishmania compounds can be screened using Leishmania spp. expressing red fluorescence (tdTomato)

Cruz MG, Santi AM, de Morais-Teixeira E, Caldeira AS, de Siqueira EP, Oliveira E, Alves TM, Murta SM

Antimicrob Agents Chemother

08-Dec-2023

PMCID:	PMC10777850
doi:	10.1128/aac.00509-23
PMID:	38063403

Brazilian Amazon Red Propolis: Leishmanicidal Activity and Chemical Composition of a New Variety of Red Propolis

Dutra RP, de Sousa MM Jr, Mignoni MS, de Oliveira KG, Pereira EB, Figueredo AS, da Costa AA, Dias TG, Vasconcelos CC, Silva LA, Reis AS, Lopes AJ

Metabolites

21-Sep-2023

PMCID:	PMC10535413
doi:	10.3390/metabo13091027
PMID:	37755307

First estimates of fine root production in tropical peat swamp and terra firme forests of the central Congo Basin

Sciumbata M, Wenina YE, Mbemba M, Dargie GC, Baird AJ, Morris PJ, Ifo SA, Aerts R, Lewis SL

Sci Rep

29-Jul-2023

PMCID:	PMC10387053
doi:	10.1038/s41598-023-38409-x
PMID:	37516765

Different routes for the construction of biologically active diversely functionalized bicyclo[3.3.1]nonanes: an exploration of new perspectives for anticancer chemotherapeutics

Roy N, Das R, Paira R, Paira P

RSC Adv

25-Jul-2023

PMCID:	PMC10369265
doi:	10.1039/d3ra02003g
PMID:	37501776

Allometric equation for Raphia laurentii De Wild, the commonest palm in the central Congo peatlands

Bocko YE, Panzou GJ, Dargie GC, Mampouya YE, Mbemba M, Loumeto JJ, Lewis SL

PLoS One

14-Apr-2023

PMCID:	PMC10104305
doi:	10.1371/journal.pone.0273591
PMID:	37058461

Improvement of the In Vitro Cytotoxic Effect on HT-29 Colon Cancer Cells by Combining 5-Fluorouacil and Fluphenazine with Green, Red or Brown Propolis

Falcão SI, Duarte D, Diallo M, Santos J, Ribeiro E, Vale N, Vilas-Boas M

Molecules

12-Apr-2023

PMCID:	PMC10145548
doi:	10.3390/molecules28083393
PMID:	37110626

Brazilian Brown Propolis: an Overview About Its Chemical Composition, Botanical Sources, Quality Control, and Pharmacological Properties

Ribeiro VP, Mejia JA, Rodrigues DM, Alves GR, de Freitas Pinheiro AM, Tanimoto MH, Bastos JK, Ambrósio SR

Rev Bras Farmacogn

24-Feb-2023

PMCID:	PMC9955532
doi:	10.1007/s43450-023-00374-x
PMID:	36908300

Xanthones: Biosynthesis and Trafficking in Plants, Fungi and Lichens

Badiali C, Petruccelli V, Brasili E, Pasqua G

Plants (Basel)

04-Feb-2023

PMCID:	PMC9967055
doi:	10.3390/plants12040694
PMID:	36840041

Genome-wide characterization leading to simple sequence repeat (SSR) markers development in Shorea robusta

Mishra G, Meena RK, Kant R, Pandey S, Ginwal HS, Bhandari MS

Funct Integr Genomics

28-Jan-2023

PMCID:	PMC9883139
doi:	10.1007/s10142-023-00975-8
PMID:	36707443

The Role of Propolis as a Natural Product with Potential Gastric Cancer Treatment Properties: A Systematic Review

Rivera-Yañez N, Ruiz-Hurtado PA, Rivera-Yañez CR, Arciniega-Martínez IM, Yepez-Ortega M, Mendoza-Arroyo B, Rebollar-Ruíz XA, Méndez-Cruz AR, Reséndiz-Albor AA, Nieto-Yañez O

Foods

16-Jan-2023

PMCID:	PMC9858610
doi:	10.3390/foods12020415
PMID:	36673507

Potential in vitro anti-periodontopathogenic, anti-Chikungunya activities and in vivo toxicity of Brazilian red propolis

Silva NB, de Souza JH, Santiago MB, da Silva Aguiar JR, Martins DO, da Silva RA, de Andrade Santos I, Aldana-Mejía JA, Jardim AC, dos Santos Pedroso R, Ambrósio SR, Veneziani RC, Bastos JK, Pires RH, Martins CH

Sci Rep

07-Dec-2022

PMCID:	PMC9729292
doi:	10.1038/s41598-022-24776-4
PMID:	36477635

Floristic composition and turnover analysis in Dahomey Gap and the surrounding sub‐humid Togolese mountain minor forest refuges: Importance for biogeography and biodiversity conservation in sub‐Saharan Africa

Adjossou K, Kokou K, Deconchat M

Ecol Evol

04-Oct-2022

PMCID:	PMC9532220
doi:	10.1002/ece3.9304
PMID:	36225837

Phytochemical profile and antimicrobial activity of the leaves and stem bark of Symphonia globulifera L.f. and Allophylus abyssinicus (Hochst.) Radlk

Lukubye B, Ajayi CO, Wangalwa R, Kagoro-Rugunda G

BMC Complement Med Ther

23-Aug-2022

PMCID:	PMC9396842
doi:	10.1186/s12906-022-03692-0
PMID:	35999537

Red propolis exhibits chemopreventive effect associated with antiproliferative and anti-inflammatory activities

de Freitas KS, da Silva LH, Squarisi IS, de Souza Oliveira LT, Ribeiro AB, Alves BS, Esperandim TR, de Melo MR, Ozelin SD, Lemes DC, Bastos JK, Veneziani RC, Tavares DC

Toxicol Res (Camb)

23-Aug-2022

PMCID:	PMC9618114
doi:	10.1093/toxres/tfac049
PMID:	36337250

Cytochemical and comparative transcriptome analyses elucidate the formation and ecological adaptation of three types of pollen coat in Zingiberaceae

Lu GH, Xu JL, Zhong MX, Li DL, Chen M, Li KT, Wang YQ

BMC Plant Biol

20-Aug-2022

PMCID:	PMC9392269
doi:	10.1186/s12870-022-03796-2
PMID:	35987603

Phytochemical Profile Top

Add a new one!

Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.

Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Benzenoids / Phenanthrenes and derivatives
6-Oxopristimerol	11754914	Click to see CC1=C2C(=CC(=C1O)O)C3(CCC4(C5CC(CCC5(CCC4(C3=CC2=O)C)C)(C)C(=O)OC)C)C	480.60	unknown	via CMAUP database
Zeylasterone	13945472	Click to see CC12CCC(CC1C3(CCC4(C5=CC(=C(C(=C5C(=O)C=C4C3(CC2)C)C(=O)O)O)O)C)C)(C)C(=O)OC	510.60	unknown	via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
CID 596370	596370	Click to see CC=CC1=CC(=C(C=C1)OC)O	164.20	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.03.008
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans
Anhydrosecoisolariciresinol	9974771	Click to see COC1=C(C=CC(=C1)CC2COCC2CC3=CC(=C(C=C3)O)OC)O	344.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
Roseoside	9930064	Click to see CC1=CC(=O)CC(C1(C=CC(C)OC2C(C(C(C(O2)CO)O)O)O)O)(C)C	386.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.11.004
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
Vierol	101297703	Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(C4)(C)O)C)CO	306.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
(+)-Isoxanthochymol	14282765	Click to see CC(=CCC1CC23CC(C(OC2=C(C(=O)C(C3=O)(C1(C)C)CC=C(C)C)C(=O)C4=CC(=C(C=C4)O)O)(C)C)CC=C(C)C)C	602.80	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.03.008
(1S,3R,8S,10S)-6-(3,4-dihydroxybenzoyl)-3-(2-hydroxypropan-2-yl)-11,11-dimethyl-10-(3-methylbut-2-enyl)-8-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-4-oxatricyclo[6.3.1.01,5]dodec-5-ene-7,12-dione	162857093	Click to see CC(=CCC1CC2(C(=O)C(=C3C(C2=O)(C1(C)C)CC(O3)C(C)(C)O)C(=O)C4=CC(=C(C=C4)O)O)CC(CC=C(C)C)C(=C)C)C	618.80	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.03.008
(1S,3R,9R,11S)-7-(3,4-dihydroxybenzoyl)-3-[(2S)-2,3-dihydroxy-3-methylbutyl]-4,4,10,10-tetramethyl-9,11-bis(3-methylbut-2-enyl)-5-oxatricyclo[7.3.1.01,6]tridec-6-ene-8,13-dione	101514310	Click to see CC(=CCC1CC23CC(C(OC2=C(C(=O)C(C3=O)(C1(C)C)CC=C(C)C)C(=O)C4=CC(=C(C=C4)O)O)(C)C)CC(C(C)(C)O)O)C	636.80	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.03.008
(1S,3R,9R,11S)-7-(3,4-dihydroxybenzoyl)-3-[(E)-3-hydroxy-3-methylbut-1-enyl]-4,4,10,10-tetramethyl-9,11-bis(3-methylbut-2-enyl)-5-oxatricyclo[7.3.1.01,6]tridec-6-ene-8,13-dione	46849358	Click to see CC(=CCC1CC23CC(C(OC2=C(C(=O)C(C3=O)(C1(C)C)CC=C(C)C)C(=O)C4=CC(=C(C=C4)O)O)(C)C)C=CC(C)(C)O)C	618.80	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.03.008
(1S,3S,8S,10S)-6-(3,4-dihydroxybenzoyl)-3-(2-hydroxypropan-2-yl)-11,11-dimethyl-10-(3-methylbut-2-enyl)-8-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-4-oxatricyclo[6.3.1.01,5]dodec-5-ene-7,12-dione	162857094	Click to see CC(=CCC1CC2(C(=O)C(=C3C(C2=O)(C1(C)C)CC(O3)C(C)(C)O)C(=O)C4=CC(=C(C=C4)O)O)CC(CC=C(C)C)C(=C)C)C	618.80	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.03.008
(1S,3S,9R,11R)-7-(3,4-dihydroxybenzoyl)-11-[(E)-3-hydroxy-3-methylbut-1-enyl]-4,4,10,10-tetramethyl-3,9-bis(3-methylbut-2-enyl)-5-oxatricyclo[7.3.1.01,6]tridec-6-ene-8,13-dione	46849357	Click to see CC(=CCC1CC23CC(C(C(C2=O)(C(=O)C(=C3OC1(C)C)C(=O)C4=CC(=C(C=C4)O)O)CC=C(C)C)(C)C)C=CC(C)(C)O)C	618.80	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.03.008
(1S,3S,9R,11R)-7-(3,4-dihydroxybenzoyl)-4,4,10,10-tetramethyl-11-[(1E)-3-methylbuta-1,3-dienyl]-3,9-bis(3-methylbut-2-enyl)-5-oxatricyclo[7.3.1.01,6]tridec-6-ene-8,13-dione	46849195	Click to see CC(=CCC1CC23CC(C(C(C2=O)(C(=O)C(=C3OC1(C)C)C(=O)C4=CC(=C(C=C4)O)O)CC=C(C)C)(C)C)C=CC(=C)C)C	600.80	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.03.008
(1S,3S,9R,11S)-7-(3-hydroxybenzoyl)-4,4,10,10-tetramethyl-3,9,11-tris(3-methylbut-2-enyl)-5-oxatricyclo[7.3.1.01,6]tridec-6-ene-8,13-dione	46849194	Click to see CC(=CCC1CC23CC(C(OC2=C(C(=O)C(C3=O)(C1(C)C)CC=C(C)C)C(=O)C4=CC(=CC=C4)O)(C)C)CC=C(C)C)C	586.80	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.03.008
6-(3,4-Dihydroxybenzoyl)-3-(2-hydroxypropan-2-yl)-11,11-dimethyl-10-(3-methylbut-2-enyl)-8-(5-methyl-2-prop-1-en-2-ylhex-4-enyl)-4-oxatricyclo[6.3.1.01,5]dodec-5-ene-7,12-dione	75220982	Click to see CC(=CCC1CC2(C(=O)C(=C3C(C2=O)(C1(C)C)CC(O3)C(C)(C)O)C(=O)C4=CC(=C(C=C4)O)O)CC(CC=C(C)C)C(=C)C)C	618.80	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.03.008
7-(3-Hydroxybenzoyl)-4,4,10,10-tetramethyl-3,9,11-tris(3-methylbut-2-enyl)-5-oxatricyclo[7.3.1.01,6]tridec-6-ene-8,13-dione	75220832	Click to see CC(=CCC1CC23CC(C(OC2=C(C(=O)C(C3=O)(C1(C)C)CC=C(C)C)C(=O)C4=CC(=CC=C4)O)(C)C)CC=C(C)C)C	586.80	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.03.008
7-(3,4-Dihydroxybenzoyl)-11-(3-hydroxy-3-methylbut-1-enyl)-4,4,10,10-tetramethyl-3,9-bis(3-methylbut-2-enyl)-5-oxatricyclo[7.3.1.01,6]tridec-6-ene-8,13-dione	75220909	Click to see CC(=CCC1CC23CC(C(C(C2=O)(C(=O)C(=C3OC1(C)C)C(=O)C4=CC(=C(C=C4)O)O)CC=C(C)C)(C)C)C=CC(C)(C)O)C	618.80	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.03.008
7-(3,4-Dihydroxybenzoyl)-3-(2,3-dihydroxy-3-methylbutyl)-4,4,10,10-tetramethyl-9,11-bis(3-methylbut-2-enyl)-5-oxatricyclo[7.3.1.01,6]tridec-6-ene-8,13-dione	75220910	Click to see CC(=CCC1CC23CC(C(OC2=C(C(=O)C(C3=O)(C1(C)C)CC=C(C)C)C(=O)C4=CC(=C(C=C4)O)O)(C)C)CC(C(C)(C)O)O)C	636.80	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.03.008
7-(3,4-Dihydroxybenzoyl)-3-(3-hydroxy-3-methylbut-1-enyl)-4,4,10,10-tetramethyl-9,11-bis(3-methylbut-2-enyl)-5-oxatricyclo[7.3.1.01,6]tridec-6-ene-8,13-dione	74412776	Click to see CC(=CCC1CC23CC(C(OC2=C(C(=O)C(C3=O)(C1(C)C)CC=C(C)C)C(=O)C4=CC(=C(C=C4)O)O)(C)C)C=CC(C)(C)O)C	618.80	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.03.008
7-(3,4-Dihydroxybenzoyl)-4,4,10,10-tetramethyl-11-(3-methylbuta-1,3-dienyl)-3,9-bis(3-methylbut-2-enyl)-5-oxatricyclo[7.3.1.01,6]tridec-6-ene-8,13-dione	75220833	Click to see CC(=CCC1CC23CC(C(C(C2=O)(C(=O)C(=C3OC1(C)C)C(=O)C4=CC(=C(C=C4)O)O)CC=C(C)C)(C)C)C=CC(=C)C)C	600.80	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.03.008
7-Epi-Isogarcinol	25242772	Click to see CC(=CCC1CC23CC(C(OC2=C(C(=O)C(C3=O)(C1(C)C)CC=C(C)C)C(=O)C4=CC(=C(C=C4)O)O)(C)C)CC=C(C)C)C	602.80	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.03.008
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(1R,5R,7R,8S)-3-(3,4-Dihydroxybenzoyl)-4-hydroxy-8-methyl-1,5,7-tris(3-methyl-2-butenyl)-8-(4-methyl-3-pentenyl)bicyclo[3.3.1]non-3-ene-2,9-dione	139071568	Click to see CC(=CCCC1(C(CC2(C(=O)C(=C(C3=CC(=C(C=C3)O)O)O)C(=O)C1(C2=O)CC=C(C)C)CC=C(C)C)CC=C(C)C)C)C	602.80	unknown	https://doi.org/10.1016/S0040-4020(01)89039-6 https://doi.org/10.4314/BCSE.V18I2.61439
Guttiferone A	5352090	Click to see CC(=CCCC1(C(CC2(C(=O)C(=C(C3=CC(=C(C=C3)O)O)O)C(=O)C1(C2=O)CC=C(C)C)CC=C(C)C)CC=C(C)C)C)C	602.80	unknown	https://doi.org/10.1016/S0040-4020(01)89039-6 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149078/
Guttiferone C	5469793	Click to see CC(=CCCC1(C(CC2(C(=O)C(=C(C3=CC(=C(C=C3)O)O)O)C(=O)C1(C2=O)CC=C(C)C)CC(CCC(=C)C)C(=C)C)CC=C(C)C)C)C	670.90	unknown	https://doi.org/10.1016/S0040-4020(01)89039-6
Guttiferone D	5469794	Click to see CC(=CCCC1(C(CC2(C(=O)C(=C(C3=CC(=C(C=C3)O)O)O)C(=O)C1(C2=O)CC=C(C)C)CC(CC=C(C)C)C(=C)C)CC=C(C)C)C)C	670.90	unknown	https://doi.org/10.1016/S0040-4020(01)89039-6
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,5S,7R)-3-[(3,4-dihydroxyphenyl)-hydroxymethylidene]-1,7-bis[(2E)-3,7-dimethylocta-2,6-dienyl]-6,6-dimethyl-5-(3-methylbut-2-enyl)bicyclo[3.3.1]nonane-2,4,9-trione	101180770	Click to see CC(=CCCC(=CCC1CC2(C(=O)C(=C(C3=CC(=C(C=C3)O)O)O)C(=O)C(C2=O)(C1(C)C)CC=C(C)C)CC=C(C)CCC=C(C)C)C)C	670.90	unknown	https://doi.org/10.1016/S0040-4020(01)89039-6
(1S,3S,9R,11S)-7-(3,4-dihydroxybenzoyl)-11-[(2E)-3,7-dimethylocta-2,6-dienyl]-4,4,10,10-tetramethyl-3,9-bis(3-methylbut-2-enyl)-5-oxatricyclo[7.3.1.01,6]tridec-6-ene-8,13-dione	46849196	Click to see CC(=CCCC(=CCC1CC23CC(C(OC2=C(C(=O)C(C3=O)(C1(C)C)CC=C(C)C)C(=O)C4=CC(=C(C=C4)O)O)(C)C)CC=C(C)C)C)C	670.90	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.03.008
7-(3,4-Dihydroxybenzoyl)-11-(3,7-dimethylocta-2,6-dienyl)-4,4,10,10-tetramethyl-3,9-bis(3-methylbut-2-enyl)-5-oxatricyclo[7.3.1.01,6]tridec-6-ene-8,13-dione	75220834	Click to see CC(=CCCC(=CCC1CC23CC(C(OC2=C(C(=O)C(C3=O)(C1(C)C)CC=C(C)C)C(=O)C4=CC(=C(C=C4)O)O)(C)C)CC=C(C)C)C)C	670.90	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.03.008
Guttiferone B	5469792	Click to see CC(=CCCC(=CCC1CC2(C(=O)C(=C(C3=CC(=C(C=C3)O)O)O)C(=O)C(C2=O)(C1(C)C)CC=C(C)C)CC=C(C)CCC=C(C)C)C)C	670.90	unknown	https://doi.org/10.1016/S0040-4020(01)89039-6
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-D:B-Friedoolean-5-ene-3beta,29-diol	13918509	Click to see CC1(C(CCC2C1=CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)CO)C)C)C)C)O)C	442.70	unknown	via CMAUP database
(1S,2S,4S,5R,6S,9S,10R,11R,14R,15S,18S,23R)-9-[(2S,3R,4S,5S)-4,5-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-10-(hydroxymethyl)-6,10,14,15,21,21-hexamethyl-3,24-dioxaheptacyclo[16.5.2.01,15.02,4.05,14.06,11.018,23]pentacosan-25-one	45270111	Click to see CC1(CCC23CCC4(C5(CCC6C(C5C7C(C4(C2C1)OC3=O)O7)(CCC(C6(C)CO)OC8C(C(C(CO8)O)O)OC9C(C(C(C(O9)CO)O)O)O)C)C)C)C	780.90	unknown	https://doi.org/10.1016/S0040-4020(01)89039-6
(4aS,6aS,6aS,6bR,8aS,10S,12aR,14bR)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	51892422	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C	456.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.11.004
20(29)-Lupene-1beta,3beta-diol	488250	Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(C(CC(C5(C)C)O)O)C)C)C	442.70	unknown	via CMAUP database
3-Hydroxyolean-12-en-28-oic acid	619166	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C	456.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.11.004
3alpha,16beta-Dihydroxylupa-12-ene	44179020	Click to see CC(C)C1CCC2(C1C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)O)C)C	442.70	unknown	via CMAUP database
3alpha,16beta,28-Trihydroxylupa-20(29)-ene	44178931	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)O)C)CO	458.70	unknown	via CMAUP database
3beta-Hydroperoxy-7beta,25-epoxy-D:B-friedooleanane-5-ene	101481671	Click to see CC1(CCC2(CCC3(C4C5C=C6C(C4(CCC3(C2C1)C)CO5)CCC(C6(C)C)OO)C)C)C	456.70	unknown	via CMAUP database
3beta,16beta-Dihydroxylupa-12-ene	44178932	Click to see CC(C)C1CCC2(C1C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)O)C)C	442.70	unknown	via CMAUP database
Calenduladiol	461835	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)O)C)C	442.70	unknown	via CMAUP database
Friedelin	91472	Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C	426.70	unknown	via CMAUP database
Glochidiol	13969554	Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(C(CC(C5(C)C)O)O)C)C)C	442.70	unknown	via CMAUP database
Lupeol	259846	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C	426.70	unknown	via CMAUP database
Oleanolic Acid	10494	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C	456.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.11.004 https://doi.org/10.4314/BCSE.V18I2.61439
Paniculatadiol	101286253	Click to see CC1(C2CCC3(C(C2(CCC1O)C)CC=C4C3(CCC5(C4CC(CC5)(C)CO)C)C)C)C	442.70	unknown	via CMAUP database
Pristimerin	159516	Click to see CC1=C(C(=O)C=C2C1=CC=C3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C(=O)OC)C)C)C)C)O	464.60	unknown	via CMAUP database
Resinone	101316848	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2O)C)C)(C)C)C)C	440.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids
Salignarine F	11154961	Click to see CC=C(C)C(=O)NC1CCC2(C3CCC4(C(C3CC=C2C1O)CCC4C(C)N(C)C)C)C	442.70	unknown	https://doi.org/10.1016/S0040-4020(01)89039-6
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid acids
16beta-Hydroxy-3,4-secolupane-20(29)-ene-3-oic acid	44179021	Click to see CC(C)C1CCC2(C(C1(C)CCC(=O)O)CCC3C2(CC(C4(C3C(CC4)C(=C)C)C)O)C)C	458.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Bufanolides and derivatives
5-[3-[5-[3,4-dihydroxy-6-(hydroxymethyl)-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxy-6-methyloxan-2-yl]oxy-8,14-dihydroxy-10,13-dimethyl-2,3,6,7,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]pyran-2-one	162934223	Click to see CC1C(C(C(C(O1)OC2CCC3(C4CCC5(C(CCC5(C4(CCC3=C2)O)O)C6=COC(=O)C=C6)C)C)O)O)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)O)O)O)O	870.90	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.11.004
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins / Cucurbitacin glycosides
[(2R,3S,4S,5R,6R)-6-[[(1S,3R,6S,8R,9S,11S,12S,14S,15R,16R)-9,14-dihydroxy-15-[(2R,5S)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-7,7,12,16-tetramethyl-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]oxy]-4,5-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]methyl acetate	162964060	Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OC3CCC45CC46CCC7(C(C(CC7(C6CC(C5C3(C)C)O)C)O)C8(CCC(O8)C(C)(C)O)C)C)COC(=O)C)O)O)O	841.00	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.03.008
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	122544	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	https://doi.org/10.1021/NP010478W
Beta-Sitosterol	222284	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	via CMAUP database
Stigmasterol	5280794	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	https://doi.org/10.1021/NP010478W
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
2-(Hydroxymethyl)-6-[(3-hydroxy-1,5,9,9-tetramethyl-10-oxatricyclo[6.2.2.02,6]dodecan-12-yl)oxy]oxane-3,4,5-triol	162906174	Click to see CC1CC(C2C1CC3C(CC2(OC3(C)C)C)OC4C(C(C(C(O4)CO)O)O)O)O	416.50	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149078/
> Organoheterocyclic compounds / Benzofurans
Isololiolide	11019783	Click to see CC1(CC(CC2(C1=CC(=O)O2)C)O)C	196.24	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
(1S,13S,15S)-5,6-dihydroxy-16,16-dimethyl-1,15-bis(3-methylbut-2-enyl)-13-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-3-oxatetracyclo[11.3.1.02,11.04,9]heptadeca-2(11),4(9),5,7-tetraene-10,12,17-trione	162875992	Click to see CC(=CCC1CC2(C(=O)C3=C(C(C2=O)(C1(C)C)CC=C(C)C)OC4=C(C3=O)C=CC(=C4O)O)CC(CC=C(C)C)C(=C)C)C	600.80	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.03.008
(1S,3S,6S,17S,19S)-6,12,13-trihydroxy-18,18-dimethyl-3,17,19-tris(3-methylbut-2-enyl)-4-methylidene-15-oxapentacyclo[15.3.1.01,6.07,16.09,14]henicosa-7(16),9(14),10,12-tetraene-8,21-dione	163042865	Click to see CC(=CCC1CC23CC(C(C(C2=O)(C4=C(C3(CC1=C)O)C(=O)C5=C(O4)C(=C(C=C5)O)O)CC=C(C)C)(C)C)CC=C(C)C)C	600.80	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.03.008
1,2,5,6-Tetrahydroxy-4-(2-methylbut-3-EN-2-YL)xanthen-9-one	15292820	Click to see CC(C)(C=C)C1=CC(=C(C2=C1OC3=C(C2=O)C=CC(=C3O)O)O)O	328.30	unknown	via CMAUP database
1,6-Dihydroxy-5-methoxy-7-(3-methylbuta-1,3-dienyl)xanthen-9-one	78385682	Click to see CC(=C)C=CC1=CC2=C(C(=C1O)OC)OC3=CC=CC(=C3C2=O)O	324.30	unknown	https://doi.org/10.1021/NP010478W
5,6-Dihydroxy-16,16-dimethyl-1,15-bis(3-methylbut-2-enyl)-13-(5-methyl-2-prop-1-en-2-ylhex-4-enyl)-3-oxatetracyclo[11.3.1.02,11.04,9]heptadeca-2(11),4(9),5,7-tetraene-10,12,17-trione	162875991	Click to see CC(=CCC1CC2(C(=O)C3=C(C(C2=O)(C1(C)C)CC=C(C)C)OC4=C(C3=O)C=CC(=C4O)O)CC(CC=C(C)C)C(=C)C)C	600.80	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.03.008
6,12,13-Trihydroxy-18,18-dimethyl-3,17,19-tris(3-methylbut-2-enyl)-4-methylidene-15-oxapentacyclo[15.3.1.01,6.07,16.09,14]henicosa-7(16),9(14),10,12-tetraene-8,21-dione	163042864	Click to see CC(=CCC1CC23CC(C(C(C2=O)(C4=C(C3(CC1=C)O)C(=O)C5=C(O4)C(=C(C=C5)O)O)CC=C(C)C)(C)C)CC=C(C)C)C	600.80	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2010.03.008
Globulixanthone A	5323527	Click to see CC(=C)C=CC1=CC2=C(C(=C1O)OC)OC3=CC=CC(=C3C2=O)O	324.30	unknown	https://doi.org/10.1021/NP010478W
Globuxanthone	60148490	Click to see CC(C)(C=C)C1=CC(=C(C2=C1OC3=C(C2=O)C=CC=C3O)O)O	312.30	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 2-prenylated xanthones
6,11-Dihydroxy-3,3-dimethyl-5-(3-methylbut-2-enyl)pyrano[2,3-c]xanthen-7-one	493305	Click to see CC(=CCC1=C2C(=C3C(=C1O)C(=O)C4=C(O3)C(=CC=C4)O)C=CC(O2)(C)C)C	378.40	unknown	https://doi.org/10.1016/S0031-9422(98)00085-5
6,11-Dihydroxy-9,10-dimethoxy-3,3-dimethyl-5-(3-methylbut-2-enyl)pyrano[2,3-c]xanthen-7-one	11561211	Click to see CC(=CCC1=C2C(=C3C(=C1O)C(=O)C4=CC(=C(C(=C4O3)O)OC)OC)C=CC(O2)(C)C)C	438.50	unknown	https://doi.org/10.4314/BCSE.V18I2.61439 https://doi.org/10.1016/J.PHYTOCHEM.2005.11.004
Globuxanthone D	5317658	Click to see CC(=CCC1=CC2=C(C(=C1O)OC)OC3=CC=CC(=C3C2=O)O)C	326.30	unknown	https://doi.org/10.1016/S0031-9422(02)00222-4 https://doi.org/10.1021/NP010478W
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 4-prenylated xanthones
1,3,5-Trihydroxy-6,7-dimethoxy-2,4-bis(3-methylbut-2-enyl)xanthen-9-one	132989344	Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C3=CC(=C(C(=C3O2)O)OC)OC)CC=C(C)C)O)C	440.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.11.004
5,9,10-Trihydroxy-2,2-dimethyl-12-(3-methylbut-2-enyl)pyrano[3,2-b]xanthen-6-one	11859087	Click to see CC(=CCC1=C2C(=C(C3=C1OC4=C(C3=O)C=CC(=C4O)O)O)C=CC(O2)(C)C)C	394.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149078/
Gaboxanthone	11704807	Click to see CC(=CCC1=C2C(=C(C3=C1OC4=C(C(=C(C=C4C3=O)OC)OC)O)O)C=CC(O2)(C)C)C	438.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.11.004
Globuxanthone E	5317659	Click to see CC(=CCC1=C2C(=C(C=C1)C3=C4C(=C(C(=C3OC)O)O)C(=O)C5=C(C=CC=C5O4)O)C(=O)C6=C(O2)C=C7C=CC(OC7=C6)(C)C)C	618.60	unknown	https://doi.org/10.1021/NP010478W https://doi.org/10.1016/S0031-9422(02)00222-4
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / Pyranoxanthones
(3R)-6,11-dihydroxy-3-methyl-3-(4-methylpent-3-enyl)pyrano[3,2-a]xanthen-12-one	162866813	Click to see CC(=CCCC1(C=CC2=C(O1)C=C(C3=C2C(=O)C4=C(C=CC=C4O3)O)O)C)C	378.40	unknown	https://doi.org/10.1021/NP010478W
Globulixanthone B	10452251	Click to see CC(=CCCC1(C=CC2=C(O1)C=C(C3=C2C(=O)C4=C(C=CC=C4O3)O)O)C)C	378.40	unknown	https://doi.org/10.1021/NP010478W
Globulixanthone C	5317656	Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC4=C(C3=O)C(=C(C=C4)O)O)O)C	326.30	unknown	https://doi.org/10.1016/S0031-9422(02)00222-4 https://doi.org/10.1021/NP010478W https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149078/
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
3-[(1R)-1-(3,4-dihydroxyphenyl)ethyl]-7-hydroxy-6,8-dimethoxychromen-2-one	162851267	Click to see CC(C1=CC(=C(C=C1)O)O)C2=CC3=CC(=C(C(=C3OC2=O)OC)O)OC	358.30	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149078/ https://doi.org/10.1016/S0040-4020(01)89039-6
> Phenylpropanoids and polyketides / Macrolides and analogues
Aigialomycin E	11727360	Click to see CC1CC=CC(C(CCC=CC2=C(C(=CC(=C2)O)O)C(=O)O1)O)O	334.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.11.004

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Symphonia globulifera

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