Scientific name	Authority	First published in
Coumarouna odorata	Aubl.	Hist. Pl. Guiane2: 740 (1775)
Baryosma tongo	Gaertn.	Fruct. Sem. Pl.2: 73, t. 93 (1790)
Heinzia peregrina	J.F.Gmel.	Syst. Nat. ed. 13[bis]: 609 (1791)

Common names Top

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Filter by language:

Language	Common/alternative name
English	tonka bean
English	cumaru
Spanish	cumbaru
Spanish	cumaru
Spanish	coumarouna tetraphylla
Spanish	cumarú
Spanish	cumaruna
Spanish	cumbarú
Spanish	haba tonca
Spanish	haba tonka
Arabic	tonka bean
Catalan	cumaru
Catalan	fava tonka
Catalan	kumaru
Catalan	fava tonca
Czech	silovoň obecný
Danish	tonkabønne
German	tonkabohnenbaum
Esperanto	tonka fabo
Persian	لوبیای تونکا
French	feve tonka
French	fève tonka
Hebrew	טונקה
Icelandic	tonkabaunir
Japanese	トンカビーンズ
Korean	쿠마루
Korean	통카콩
Dutch	tonkabonen
Polish	tonkowiec wonny
Polish	ziarno tonka
Polish	bób tonka
Portuguese	cumaru
Russian	Диптерикс душистый
Slovenian	tonko
Ukrainian	Диптерикс пахучий
Chinese	香豆樹
Chinese	香二翅豆
Chinese	零陵香豆
Chinese	香豆树

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

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

Suggest a correction or add new data!

No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Pacific click to expand
- Southwestern Pacific
  - Nauru

Southern America click to expand
- Brazil
  - Brazil North
  - Brazil Northeast
  - Brazil West-central
- Northern South America
  - French Guiana
  - Guyana
  - Suriname
  - Venezuela
- Western South America
  - Colombia
  - Peru

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000170550
UNII	5Q2L03JZ8B
USDA Plants	DIOD2
Tropicos	13018739
INPN	629575
KEW	urn:lsid:ipni.org:names:492769-1
The Plant List	ild-16819
Open Tree Of Life	908610
NCBI Taxonomy	53873
IUCN Red List	62024955
IPNI	492769-1
iNaturalist	479410
GBIF	2947137
Freebase	/m/075m6b
EPPO	DPXOD
EOL	639810
USDA GRIN	14393
Wikipedia	Dipteryx_odorata
CMAUP	NPO5140

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

Electrophilic Compounds in the Human Diet and Their Role in the Induction of the Transcription Factor NRF2

Andrés CM, Pérez de la Lastra JM, Bustamante Munguira E, Juan CA, Plou FJ, Pérez Lebeña E

Int J Mol Sci

20-Mar-2024

PMCID:	PMC10971185
doi:	10.3390/ijms25063521
PMID:	38542492

Diversity of Wickerhamomyces (Wickerhamomycetaceae, Saccharomycetales) in China with the description of four new species

Chai CY, Ke T, Niu QH, Hui FL

Front Microbiol

08-Feb-2024

PMCID:	PMC10881795
doi:	10.3389/fmicb.2024.1338231
PMID:	38389540

Synthesis of anthraquinone-connected coumarin derivatives via grindstone method and their evaluation of antibacterial, antioxidant, tyrosinase inhibitory activities with molecular docking, and DFT calculation studies

Loganathan V, Ahamed A, Radhakrishnan S, Z. Gaafar AR, Gurusamy R, Akbar I

Heliyon

29-Jan-2024

PMCID:	PMC10864903
doi:	10.1016/j.heliyon.2024.e25168
PMID:	38356501

Factors Influencing Venous Remodeling in the Development of Varicose Veins of the Lower Limbs

Gwozdzinski L, Pieniazek A, Gwozdzinski K

Int J Mol Sci

26-Jan-2024

PMCID:	PMC10855638
doi:	10.3390/ijms25031560
PMID:	38338837

Pest categorisation of Pratylenchus loosi

Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Migheli Q, Vloutoglou I, Gobbi A, Maiorano A, Pautasso M, Reignault PL

EFSA J

16-Jan-2024

PMCID:	PMC10790189
doi:	10.2903/j.efsa.2024.8548
PMID:	38229874

Chemical Composition of Methanol Extracts from Leaves and Flowers of Anemonopsis macrophylla (Ranunculaceae)

Kostikova VA, Petrova NV, Chernonosov AA, Koval VV, Kovaleva ER, Wang W, Erst AS

Int J Mol Sci

12-Jan-2024

PMCID:	PMC10816090
doi:	10.3390/ijms25020989
PMID:	38256067

Bioactivity and toxicity of coumarins from African medicinal plants

Anywar G, Muhumuza E

Front Pharmacol

10-Jan-2024

PMCID:	PMC10809390
doi:	10.3389/fphar.2023.1231006
PMID:	38273831

Plant Polyphenols and Their Potential Benefits on Cardiovascular Health: A Review

Iqbal I, Wilairatana P, Saqib F, Nasir B, Wahid M, Latif MF, Iqbal A, Naz R, Mubarak MS

Molecules

01-Sep-2023

PMCID:	PMC10490098
doi:	10.3390/molecules28176403
PMID:	37687232

Synthesis, characterization and crystal structure of methyl 2-(2-oxo-2H-chromen-4-ylamino)benzoate

Hollauer HV, Vilas Novas RC, Guedes GP, Buarque CD, Escobar LB

Acta Crystallogr E Crystallogr Commun

29-Aug-2023

PMCID:	PMC10483563
doi:	10.1107/S2056989023007351
PMID:	37693666

Hunting practices in southwestern Amazonia: a comparative study of techniques, modalities, and baits among urban and rural hunters

Oliveira MA, Braga-Pereira F, El Bizri HR, Morcatty TQ, Doria CR, Messias MR

J Ethnobiol Ethnomed

03-Jul-2023

PMCID:	PMC10318826
doi:	10.1186/s13002-023-00599-z
PMID:	37400859

Conformation of the Ester Group Governs the Photophysics of Highly Polarized Benzo[g]coumarins

Szychta K, Koszarna B, Banasiewicz M, Sobolewski A, O’Mari O, Clark JA, Vullev VI, Barboza CA, Gryko DT

JACS Au

26-Jun-2023

PMCID:	PMC10369411
doi:	10.1021/jacsau.3c00169
PMID:	37502148

Kinetics of maize cob and bean straw pyrolysis and combustion

Okot DK, Bilsborrow PE, Phan AN, Manning DA

Heliyon

13-Jun-2023

PMCID:	PMC10300327
doi:	10.1016/j.heliyon.2023.e17236
PMID:	37389069

Natural Coumarin Derivatives Activating Nrf2 Signaling Pathway as Lead Compounds for the Design and Synthesis of Intestinal Anti-Inflammatory Drugs

Di Stasi LC

Pharmaceuticals (Basel)

30-Mar-2023

PMCID:	PMC10142712
doi:	10.3390/ph16040511
PMID:	37111267

Phenolic Compounds in Bacterial Inactivation: A Perspective from Brazil

Kauffmann AC, Castro VS

Antibiotics (Basel)

24-Mar-2023

PMCID:	PMC10135396
doi:	10.3390/antibiotics12040645
PMID:	37107007

Caryopteris odorata and its metabolite coumarin attenuate characteristic features of cardiometabolic syndrome in high-refined carbohydrate-high fat-cholesterol-loaded feed-fed diet rats

Ahmed MG, Mehmood MH, Mehdi S, Farrukh M

Front Pharmacol

23-Mar-2023

PMCID:	PMC10076573
doi:	10.3389/fphar.2023.1097407
PMID:	37033655

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 / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid	135	Click to see C1=CC(=CC=C1C(=O)O)O	138.12	unknown	https://doi.org/10.1021/JF00111A051
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Salicylic acid and derivatives / Salicylic acids
Salicylic Acid	338	Click to see C1=CC=C(C(=C1)C(=O)O)O	138.12	unknown	https://doi.org/10.1021/JF00111A051
> Lignans, neolignans and related compounds
(2R)-3-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-2-[4-(3-hydroxypropyl)-2-methoxyphenoxy]propan-1-one	15690603	Click to see COC1=CC(=CC(=C1O)OC)C(=O)C(CO)OC2=C(C=C(C=C2)CCCO)OC	406.40	unknown	via CMAUP database
(2S)-3-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-2-[4-(3-hydroxypropyl)-2-methoxyphenoxy]propan-1-one	92466671	Click to see COC1=CC(=CC(=C1O)OC)C(=O)C(CO)OC2=C(C=C(C=C2)CCCO)OC	406.40	unknown	via CMAUP database
2-Methoxy-4-[(1R,2S)-1,3-dihydroxy-2-[2-methoxy-4-(3-hydroxypropyl)phenoxy]propyl]phenol	13893597	Click to see COC1=C(C=CC(=C1)CCCO)OC(CO)C(C2=CC(=C(C=C2)O)OC)O	378.40	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Aryltetralin lignans / 9,9p-dihydroxyaryltetralin lignans
Isoolivil	5316262	Click to see COC1=C(C=C2C(C(C(CC2=C1)(CO)O)CO)C3=CC(=C(C=C3)O)OC)O	376.40	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Flavonolignans
(inverted exclamation markA)-Hydnocarpin	11213425	Click to see COC1=C(C=CC(=C1)C2C(OC3=C(O2)C=CC(=C3)C4=CC(=O)C5=C(C=C(C=C5O4)O)O)CO)O	464.40	unknown	via CMAUP database
2-[3beta-(Hydroxymethyl)-2alpha-(4-hydroxy-3,5-dimethoxyphenyl)-2,3-dihydro-1,4-benzodioxin-6-yl]-5,7-dihydroxy-4H-1-benzopyran-4-one	10791345	Click to see COC1=CC(=CC(=C1O)OC)C2C(OC3=C(O2)C=CC(=C3)C4=CC(=O)C5=C(C=C(C=C5O4)O)O)CO	494.40	unknown	via CMAUP database
5'-Methoxyhydnocarpin	5281879	Click to see COC1=CC(=CC2=C1OC(C(O2)C3=CC(=C(C=C3)O)OC)CO)C4=CC(=O)C5=C(C=C(C=C5O4)O)O	494.40	unknown	via CMAUP database
Hydnocarpin D	11431204	Click to see COC1=C(C=CC(=C1)C2C(OC3=C(O2)C=C(C=C3)C4=CC(=O)C5=C(C=C(C=C5O4)O)O)CO)O	464.40	unknown	via CMAUP database
Palstatin	5323578	Click to see COC1=CC(=CC(=C1O)OC)C2C(OC3=C(O2)C=C(C=C3OC)C4=CC(=O)C5=C(C=C(C=C5O4)O)O)CO	524.50	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,7-epoxylignans
2beta,5alpha-Bis(4-hydroxy-3,5-dimethoxyphenyl)tetrahydro-3alpha,4beta-furandimethanol	25136967	Click to see COC1=CC(=CC(=C1O)OC)C2C(C(C(O2)C3=CC(=C(C(=C3)OC)O)OC)CO)CO	436.50	unknown	via CMAUP database
Huazhongilexin	15690604	Click to see COC1=CC(=CC(=C1O)OC)C2C(C(C(O2)C3=CC(=C(C(=C3)OC)O)OC)CO)CO	436.50	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
(-)-Lariciresinol	23815394	Click to see COC1=C(C=CC(=C1)CC2COC(C2CO)C3=CC(=C(C=C3)O)OC)O	360.40	unknown	https://doi.org/10.1021/NP020522N
Olivil	5273570	Click to see COC1=C(C=CC(=C1)CC2(COC(C2CO)C3=CC(=C(C=C3)O)OC)O)O	376.40	unknown	via CMAUP database
Tetrahydro-2-(4-hydroxy-3-methoxyphenyl)-4-((4-hydroxy-3-methoxyphenyl)methyl)-3-furanmethanol	134203	Click to see COC1=C(C=CC(=C1)CC2COC(C2CO)C3=CC(=C(C=C3)O)OC)O	360.40	unknown	https://doi.org/10.1021/NP020522N
> Lignans, neolignans and related compounds / Lignan glycosides
(2R,3S)-3-(4-Hydroxy-3,5-dimethoxyphenyl)-2-[[4-[3-(alpha-L-rhamnopyranosyloxy)propyl]-2-methoxyphenyl]oxy]propane-1,3-diol	101606109	Click to see CC1C(C(C(C(O1)OCCCC2=CC(=C(C=C2)OC(CO)C(C3=CC(=C(C(=C3)OC)O)OC)O)OC)O)O)O	554.60	unknown	via CMAUP database
(2S,3R,4S,5S,6R)-2-[4-[(3S,3aR,6S,6aR)-3-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2-methoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	486614	Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC5C(C(C(C(O5)CO)O)O)O)OC)O	520.50	unknown	via CMAUP database
(2S,3R)-3-(4-Hydroxy-3,5-dimethoxyphenyl)-2-[[4-[3-(alpha-L-rhamnopyranosyloxy)propyl]-2-methoxyphenyl]oxy]propane-1,3-diol	15690602	Click to see CC1C(C(C(C(O1)OCCCC2=CC(=C(C=C2)OC(CO)C(C3=CC(=C(C(=C3)OC)O)OC)O)OC)O)O)O	554.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Oleic Acid	445639	Click to see CCCCCCCCC=CCCCCCCCC(=O)O	282.50	unknown	https://doi.org/10.1021/JF00111A051
Palmitic Acid	985	Click to see CCCCCCCCCCCCCCCC(=O)O	256.42	unknown	https://doi.org/10.1021/JF00111A051
Stearic Acid	5281	Click to see CCCCCCCCCCCCCCCCCC(=O)O	284.50	unknown	https://doi.org/10.1021/JF00111A051
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(2R,3R,4S,5S,6R)-2-[(Z)-hex-3-enoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	5318045	Click to see CCC=CCCOC1C(C(C(C(O1)CO)O)O)O	262.30	unknown	via CMAUP database
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[(E)-3-(2,3,4-trimethoxyphenyl)prop-2-enoxy]oxane-3,4,5-triol	11972373	Click to see COC1=C(C(=C(C=C1)C=CCOC2C(C(C(C(O2)CO)O)O)O)OC)OC	386.40	unknown	via CMAUP database
(4S)-3,5,5-trimethyl-4-[(3R)-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]cyclohex-2-en-1-one	38346955	Click to see CC1=CC(=O)CC(C1CCC(C)OC2C(C(C(C(O2)CO)O)O)O)(C)C	372.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Hexacosanol	68171	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCO	382.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid	5280450	Click to see CCCCCC=CCC=CCCCCCCCC(=O)O	280.40	unknown	https://doi.org/10.1021/JF00111A051
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(+)-Vouacapenic acid	73350581	Click to see CC1C2CCC3C(C2CC4=C1C=CO4)(CCCC3(C)C(=O)O)C	316.40	unknown	https://doi.org/10.1016/0031-9422(89)80073-1
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(1R)-3,3,5-Trimethyl-4-(3-oxobutyl)-4-cyclohexen-1beta-yl beta-D-glucopyranoside	101606458	Click to see CC1=C(C(CC(C1)OC2C(C(C(C(O2)CO)O)O)O)(C)C)CCC(=O)C	372.50	unknown	via CMAUP database
CID 11968607	11968607	Click to see CC1=C(C(C(CC1)OC2C(C(C(C(O2)CO)O)O)O)(C)C)CCC(=O)C	372.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Betulin	72326	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO	442.70	unknown	https://doi.org/10.1021/JF00111A051
Lupeol	259846	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C	426.70	unknown	https://doi.org/10.1021/JF00111A051
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1S,3R,4R,5R)-3-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxy-cyclohexanecarboxylic acid	9476	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	354.31	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Icariside B2	10385469	Click to see CC(=O)C=CC12C(CC(CC1(O2)C)OC3C(C(C(C(O3)CO)O)O)O)(C)C	386.40	unknown	via CMAUP database
Phenylethyl beta-D-glucopyranoside	11289099	Click to see C1=CC=C(C=C1)CCOC2C(C(C(C(O2)CO)O)O)O	284.30	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[(3,5,6,7-tetramethoxy-9,10-dihydrophenanthren-2-yl)oxy]oxane-3,4,5-triol	15690608	Click to see COC1=C(C(=C2C(=C1)CCC3=CC(=C(C=C32)OC)OC4C(C(C(C(O4)CO)O)O)O)OC)OC	478.50	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
7-Hydroxy-4-benzopyrone	5409279	Click to see C1=CC2=C(C=C1O)OC=CC2=O	162.14	unknown	https://doi.org/10.1021/NP020522N
> Organoheterocyclic compounds / Naphthofurans
(4S,4aS,6aR,7S,10aS,11aR,11bS)-10a-hydroxy-4,7,11b-trimethyl-9-oxo-1,2,3,4a,5,6,6a,7,11,11a-decahydronaphtho[2,1-f][1]benzofuran-4-carboxylic acid	163050290	Click to see CC1C2CCC3C(C2CC4(C1=CC(=O)O4)O)(CCCC3(C)C(=O)O)C	348.40	unknown	https://doi.org/10.1021/NP020522N
10a-Hydroxy-4,7,11b-trimethyl-9-oxo-1,2,3,4a,5,6,6a,7,11,11a-decahydronaphtho[2,1-f][1]benzofuran-4-carboxylic acid	85305304	Click to see CC1C2CCC3C(C2CC4(C1=CC(=O)O4)O)(CCCC3(C)C(=O)O)C	348.40	unknown	https://doi.org/10.1021/NP020522N
Dipteryxic acid	10893432	Click to see CC1C2CCC3C(C2CC4(C1=CC(=O)O4)O)(CCCC3(C)C(=O)O)C	348.40	unknown	https://doi.org/10.1021/NP020522N
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(+)-Balanophonin	23252258	Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)C=CC=O	356.40	unknown	https://doi.org/10.1021/NP020522N
(+/-)-Balanophonin	72729357	Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)C=CC=O	356.40	unknown	https://doi.org/10.1021/NP020522N
(2R)-2beta-[3-Methoxy-4-(beta-D-glucopyranosyloxy)phenyl]-5-(3-hydroxypropyl)-7-methoxy-2,3-dihydrobenzofuran-3alpha-methanol	10625848	Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC)CCCO	522.50	unknown	via CMAUP database
Balaphonin	14274764	Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)C=CC=O	356.40	unknown	https://doi.org/10.1021/NP020522N
Dihydrodehydrodiconiferyl alcohol	384679	Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)CCCO	360.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Aurone flavonoids
(2Z)-6-hydroxy-2-[(4-hydroxy-3-methoxyphenyl)methylidene]-1-benzofuran-3-one	16376440	Click to see COC1=C(C=CC(=C1)C=C2C(=O)C3=C(O2)C=C(C=C3)O)O	284.26	unknown	https://doi.org/10.1021/NP020522N
2-(3,4-Dihydroxybenzylidene)-6-hydroxybenzofuran-3(2H)-one	5321560	Click to see C1=CC(=C(C=C1C=C2C(=O)C3=C(O2)C=C(C=C3)O)O)O	270.24	unknown	https://doi.org/10.1021/NP020522N
6-Hydroxy-2-(4'-hydroxy-3'-methoxybenzylidene)benzofuran-3(2h)-one	625109	Click to see COC1=C(C=CC(=C1)C=C2C(=O)C3=C(O2)C=C(C=C3)O)O	284.26	unknown	https://doi.org/10.1021/NP020522N
6,3',4'-Trihydroxyaurone	67111	Click to see C1=CC(=C(C=C1C=C2C(=O)C3=C(O2)C=C(C=C3)O)O)O	270.24	unknown	https://doi.org/10.1021/NP020522N
Coumaran-6-ol-3-one, 2-[4-hydroxy-3-methoxybenzylidene]-	5378222	Click to see COC1=C(C=CC(=C1)C=C2C(=O)C3=C(O2)C=C(C=C3)O)O	284.26	unknown	https://doi.org/10.1021/NP020522N
Sulfuretin	5281295	Click to see C1=CC(=C(C=C1C=C2C(=O)C3=C(O2)C=C(C=C3)O)O)O	270.24	unknown	https://doi.org/10.1021/NP020522N
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
2,4-Dihydroxycinnamic acid	446611	Click to see C1=CC(=C(C=C1O)O)C=CC(=O)O	180.16	unknown	https://doi.org/10.1021/JF00111A051
4-Hydroxycinnamic acid	322	Click to see C1=CC(=CC=C1C=CC(=O)O)O	164.16	unknown	via CMAUP database
Ferulic acid	445858	Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O	194.18	unknown	https://doi.org/10.1021/JF00111A051
> Phenylpropanoids and polyketides / Coumarins and derivatives
6-Demethoxycapillarisin	5316511	Click to see C1=CC(=CC=C1O)OC2=CC(=O)C3=C(C=C(C=C3O2)O)O	286.24	unknown	via CMAUP database
Coumarin	323	Click to see C1=CC=C2C(=C1)C=CC(=O)O2	146.14	unknown	https://doi.org/10.1021/JF00111A051 https://doi.org/10.1021/NP020563J https://doi.org/10.1007/BF02859345
Demethoxy-7-O-methylcapillarisin	71391689	Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)OC3=CC=C(C=C3)O)O	300.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Umbelliferone	5281426	Click to see C1=CC(=CC2=C1C=CC(=O)O2)O	162.14	unknown	https://doi.org/10.1021/JF00111A051
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2R)-2-(3,4-dihydroxyphenyl)-6,8-dihydroxy-2,3-dihydrochromen-4-one	57486024	Click to see C1C(OC2=C(C1=O)C=C(C=C2O)O)C3=CC(=C(C=C3)O)O	288.25	unknown	https://doi.org/10.1021/NP020522N
2-(3,4-Dihydroxyphenyl)-6,8-dihydroxy-2,3-dihydrochromen-4-one	76542175	Click to see C1C(OC2=C(C1=O)C=C(C=C2O)O)C3=CC(=C(C=C3)O)O	288.25	unknown	https://doi.org/10.1021/NP020522N
3',4',7-Trihydroxyflavanone	3496769	Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC(=C(C=C3)O)O	272.25	unknown	https://doi.org/10.1021/NP020522N
Butin	92775	Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC(=C(C=C3)O)O	272.25	unknown	https://doi.org/10.1021/NP020522N
Eriodictyol	440735	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O	288.25	unknown	https://doi.org/10.1021/NP020522N
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin	5280443	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	270.24	unknown	via CMAUP database
Luteolin	5280445	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol	5280863	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	via CMAUP database
Quercetin	5280343	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O	302.23	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2''-O-alpha-L-Rhamnopyranostylquercitrin	10698716	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)C)O)O)O)O)O	594.50	unknown	via CMAUP database
2'',4''-Di-O-(E-p-Coumaroyl)afzelin	11765457	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)OC(=O)C=CC5=CC=C(C=C5)O)O)OC(=O)C=CC6=CC=C(C=C6)O	724.70	unknown	via CMAUP database
3-[2-O-(4-Hydroxy-cis-cinnamoyl)-4-O-(4-hydroxy-trans-cinnamoyl)-alpha-L-rhamnopyranosyloxy]-5,7,4'-trihydroxyflavone	11700461	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)OC(=O)C=CC5=CC=C(C=C5)O)O)OC(=O)C=CC6=CC=C(C=C6)O	724.70	unknown	via CMAUP database
3-[2-O-(4-Hydroxy-trans-cinnamoyl)-4-O-(4-hydroxy-cis-cinnamoyl)-alpha-L-rhamnopyranosyloxy]-5,7,4'-trihydroxyflavone	49822437	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)OC(=O)C=CC5=CC=C(C=C5)O)O)OC(=O)C=CC6=CC=C(C=C6)O	724.70	unknown	via CMAUP database
3-[3-O-(4-Hydroxy-cis-cinnamoyl)-4-O-(4-hydroxy-trans-cinnamoyl)-alpha-L-rhamnopyranosyloxy]-5,7,4'-trihydroxyflavone	45783016	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)OC(=O)C=CC5=CC=C(C=C5)O)OC(=O)C=CC6=CC=C(C=C6)O	724.70	unknown	via CMAUP database
3'',4''-Di-O-p-coumaroylafzelin	51136469	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)OC(=O)C=CC5=CC=C(C=C5)O)OC(=O)C=CC6=CC=C(C=C6)O	724.70	unknown	via CMAUP database
Afzelin	5316673	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O	432.40	unknown	via CMAUP database
Baohuoside I	5488822	Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C(=CC(=C3C2=O)O)O)CC=C(C)C)C4=CC=C(C=C4)OC)O)O)O	514.50	unknown	via CMAUP database
Baohuoside II	5481982	Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C(=CC(=C3C2=O)O)O)CC=C(C)C)C4=CC=C(C=C4)O)O)O)O	500.50	unknown	via CMAUP database
Hyperoside	5281643	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O	464.40	unknown	via CMAUP database
Kaempferol 3-(2-rhamnopyranosylrhamnopyranoside)	10721917	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)C)O)O)O)O)O	578.50	unknown	via CMAUP database
Quercitrin	5280459	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O	448.40	unknown	via CMAUP database
Trifolin	5282149	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O	448.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Baohuoside V	25087702	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=C(C3=O)C(=CC(=C4CC=C(C)C)OC5C(C(C(C(O5)CO)O)O)O)O)C6=CC=C(C=C6)O)C)O)O)O)O)O	808.80	unknown	via CMAUP database
Epimedin A	13916051	Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C2=O)C(=CC(=C3CC=C(C)C)OC4C(C(C(C(O4)CO)O)O)O)O)C5=CC=C(C=C5)OC)OC6C(C(C(C(O6)CO)O)O)O)O)O	838.80	unknown	via CMAUP database
Epimedin A1	92043273	Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C2=O)C(=CC(=C3CC=C(C)C)OC4C(C(C(C(O4)CO)O)O)O)O)C5=CC=C(C=C5)OC)O)OC6C(C(C(C(O6)CO)O)O)O)O	838.80	unknown	via CMAUP database
Epimedin B	5748393	Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C2=O)C(=CC(=C3CC=C(C)C)OC4C(C(C(C(O4)CO)O)O)O)O)C5=CC=C(C=C5)OC)OC6C(C(C(CO6)O)O)O)O)O	808.80	unknown	via CMAUP database
Epimedin C	5748394	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=C(C3=O)C(=CC(=C4CC=C(C)C)OC5C(C(C(C(O5)CO)O)O)O)O)C6=CC=C(C=C6)OC)C)O)O)O)O)O	822.80	unknown	via CMAUP database
Epimedokoreanoside I	87759921	Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C2=O)C(=CC(=C3CC=C(C)C)OC4C(C(C(C(O4)CO)O)O)O)O)C5=CC=C(C=C5)OC)O)OC6C(C(C(C(O6)COC(=O)C)O)O)O)OC(=O)C	922.90	unknown	via CMAUP database
Epimedoside A	5317093	Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C2=O)C(=CC(=C3CC=C(C)C)OC4C(C(C(C(O4)CO)O)O)O)O)C5=CC=C(C=C5)O)O)O)O	662.60	unknown	via CMAUP database
Icariin	5318997	Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C2=O)C(=CC(=C3CC=C(C)C)OC4C(C(C(C(O4)CO)O)O)O)O)C5=CC=C(C=C5)OC)O)O)O	676.70	unknown	via CMAUP database
Icariside I	5745470	Click to see CC(=CCC1=C(C=C(C2=C1OC(=C(C2=O)O)C3=CC=C(C=C3)OC)O)OC4C(C(C(C(O4)CO)O)O)O)C	530.50	unknown	via CMAUP database
Sagittasine B	101437361	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=C(C3=O)C(=CC(=C4CC=C(C)C)OC5C(C(C(C(O5)CO)O)O)O)O)C6=CC(=C(C=C6)OC)O)C)O)O)O)O)O	838.80	unknown	via CMAUP database
Sagittasine C	101437362	Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C2=O)C(=CC(=C3CC=C(C)C)OC4C(C(C(C(O4)CO)O)O)O)O)C5=CC(=C(C=C5)OC)O)O)O)O	692.70	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
3'-O-methyltricetin	11267045	Click to see COC1=CC(=CC(=C1O)O)C2=CC(=O)C3=C(C=C(C=C3O2)O)O	316.26	unknown	via CMAUP database
4',5-Dihydroxy-3'-methoxyflavon-7-olate(1-)	25203524	Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)[O-]	299.25	unknown	via CMAUP database
Tricin	5281702	Click to see COC1=CC(=CC(=C1O)OC)C2=CC(=O)C3=C(C=C(C=C3O2)O)O	330.29	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
2-(1,3-Benzodioxol-5-yl)-5-hydroxy-6,7-dimethoxychromen-4-one	5321057	Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC4=C(C=C3)OCO4)O)OC	342.30	unknown	via CMAUP database
Retusin	5352005	Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)OC)OC	358.30	unknown	https://doi.org/10.1021/JF00111A051
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
7-Hydroxy-5,6-dimethoxy-3',4'-methylenedioxyisoflavone	14353466	Click to see COC1=C(C2=C(C=C1O)OC=C(C2=O)C3=CC4=C(C=C3)OCO4)OC	342.30	unknown	https://doi.org/10.1039/P19790002107
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 3-hydroxy,4-methoxyisoflavonoids
(2R,3S)-3-(4-hydroxy-3,5-dimethoxyphenyl)-8-(3-hydroxy-4-methoxyphenyl)-2-(hydroxymethyl)-5-methoxy-2,3-dihydropyrano[3,2-h][1,4]benzodioxin-7-one	154496044	Click to see COC1=C(C=C(C=C1)C2=COC3=C4C(=C(C=C3C2=O)OC)OC(C(O4)CO)C5=CC(=C(C(=C5)OC)O)OC)O	538.50	unknown	https://doi.org/10.1021/NP020522N
3-(4-Hydroxy-3,5-dimethoxyphenyl)-8-(3-hydroxy-4-methoxyphenyl)-2-(hydroxymethyl)-5-methoxy-2,3-dihydropyrano[3,2-h][1,4]benzodioxin-7-one	162960986	Click to see COC1=C(C=C(C=C1)C2=COC3=C4C(=C(C=C3C2=O)OC)OC(C(O4)CO)C5=CC(=C(C(=C5)OC)O)OC)O	538.50	unknown	https://doi.org/10.1021/NP020522N
3'-Hydroxy-8-O-methylretusin	44257262	Click to see COC1=C(C=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3OC)O)O	314.29	unknown	https://doi.org/10.1021/NP020522N
5-MethoxyanthocercinA	10886024	Click to see COC1=C(C=C(C=C1)C2=COC3=C4C(=C(C=C3C2=O)OC)OC(C(O4)CO)C5=CC(=C(C(=C5)OC)O)OC)O	538.50	unknown	https://doi.org/10.1021/NP020522N
Odoratin	13965473	Click to see COC1=C(C=C(C=C1)C2=COC3=CC(=C(C=C3C2=O)OC)O)O	314.29	unknown	https://doi.org/10.1248/CPB.53.740 https://doi.org/10.1002/CHIN.200552195
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
Afrormosin	5281704	Click to see COC1=CC=C(C=C1)C2=COC3=CC(=C(C=C3C2=O)OC)O	298.29	unknown	https://doi.org/10.1248/CPB.53.740
Dipteryxin	44257265	Click to see COC1=CC=C(C=C1)C2=COC3=C(C(=C(C=C3C2=O)OC)O)O	314.29	unknown	https://doi.org/10.1021/JF00111A051
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 7-O-methylated isoflavonoids / 7-O-methylisoflavones
5,6,7-Trimethoxy-3',4'-methylenedioxyisoflavone	21723648	Click to see COC1=C(C(=C2C(=C1)OC=C(C2=O)C3=CC4=C(C=C3)OCO4)OC)OC	356.30	unknown	https://doi.org/10.1039/P19790002107
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
GU17;ISL;Isoliquiritigen	425	Click to see C1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2)O)O)O	256.25	unknown	https://doi.org/10.1021/NP020522N
Trihydroxychalcone	638278	Click to see C1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2)O)O)O	256.25	unknown	https://doi.org/10.1021/NP020522N
> Phenylpropanoids and polyketides / Phenylpropanoic acids
2-Hydroxybenzenepropanoic acid	873	Click to see C1=CC=C(C(=C1)CCC(=O)O)O	166.17	unknown	https://doi.org/10.1021/JF00111A051

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Dipteryx odorata

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