Sterculia foetida is a tall, soft wooded tree with various common names such as bastard poon tree, java olive tree, and skunk tree. It has smooth gray bark and palmately compound leaves with a foul smell coming from the petioles. The tree is dioecious, with male and female flowers found on different trees. Its fruit consists of four to five follicles with scarlet seeds. This species is found in many areas including India, Taiwan, and the United States. The oil from its seeds has potential use as a biofuel and contains cyclopropene fatty acids. While the seeds are edible, they should be roasted before consumption. However, some evidence suggests that these fatty acids may have negative effects on human health. In Vietnam, the tree's sap is used to make a soft drink called "Mủ Trôm".

Synonyms Top

Scientific name	Authority	First published in
Sterculia polyphylla	R.Br.	Pterocymbium : 227 (1844)
Clompanus foetida	(L.) Kuntze	Revis. Gen. Pl. 1: 77 (1891)
Sterculia mexicana var. guianensis	Sagot	Ann. Sci. Nat., Bot. , sér. 6, 11: 153 (1881)

Common names Top

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Language	Common/alternative name
English	bastard poon tree
English	wild almond tree
English	hazel sterculia
ace	geulumpang
ban	kepuh
Bengali	জংলিবাদাম
Bengali	বাক্সবাদাম
French	arbre caca
French	tabac de femme
French	sterculier fétide
French	olivier putois
French	olivier de java
French	arbre moufette
French	arbre à merde
Indonesian	kepuh
jv	jangkang
jv	kepuh
Kannada	ಭಟಲ ಪಿನಾರಿ
mad	jhângkang
Malayalam	മലമ്പരത്തി
mnw	ခပြုင်
Malay	kelumpang jari
Malay	pokok kelumpang jari
Burmese	လက်ခုပ်
Dutch	kepuh
Polish	zatwar cuchnący
Portuguese	xixá-fedorento
Portuguese	chichá-fedorento
su	kepoh
Tamil	பீநாறி
Thai	สำโรง
Vietnamese	trôm
Chinese	香蘋婆
Chinese	掌葉蘋婆
Chinese	香苹婆

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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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
- West-central Tropical Africa
  - Gulf Of Guinea Islands
- Western Indian Ocean
  - Comoros

Asia-temperate click to expand
- China
  - China Southeast
  - Hainan

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
  - India
  - Pakistan
  - Sri Lanka
- Indo-China
  - Cambodia
  - Laos
  - Myanmar
  - Thailand
  - Vietnam
- Malesia
  - Lesser Sunda Islands
  - Malaya
  - Philippines
  - Sumatera

Southern America click to expand
- Caribbean
  - Cuba
  - Jamaica
  - Leeward Islands
  - Puerto Rico
  - Trinidad-Tobago
  - Windward Islands

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000491589
USDA Plants	STFO2
Tropicos	30401497
INPN	447629
KEW	urn:lsid:ipni.org:names:825227-1
The Plant List	kew-2579743
Open Tree Of Life	298691
Observations.org	336436
NCBI Taxonomy	195802
IPNI	825227-1
iNaturalist	346407
GBIF	5406675
Freebase	/m/0zmy_v1
EPPO	SRLFO
EOL	483667
Elurikkus	210639
USDA GRIN	101996
Wikipedia	Sterculia_foetida
CMAUP	NPO22636

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

Pest categorisation of Pyrrhoderma noxium

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, Golic D, Gobbi A, Maiorano A, Pautasso M, Reignault PL

EFSA J

19-Mar-2024

PMCID:	PMC10949325
doi:	10.2903/j.efsa.2024.8667
PMID:	38505477

Anticancer Property of Digera muricata Leaf Extract: An In Vitro Study

Varadarajan PS, Roy A, Jagadeswaran D

Cureus

23-Nov-2023

PMCID:	PMC10746918
doi:	10.7759/cureus.49276
PMID:	38143601

Evaluating criteria weights of street tree selection between residents and experts

Wang CW, Tu HM

12-Jun-2023

PMCID:	PMC10258739
doi:	10.1007/s11355-023-00568-4

Green synthesis of silver nanoparticles mediated Diospyros kaki L. (Persimmon): determination of chemical composition and evaluation of their antimicrobials and anticancer activities

Keskin C, Ölçekçi A, Baran A, Baran MF, Eftekhari A, Omarova S, Khalilov R, Aliyev E, Sufianov A, Beilerli A, Gareev I

Front Chem

30-May-2023

PMCID:	PMC10265676
doi:	10.3389/fchem.2023.1187808
PMID:	37324556

Microbial Lipid Based Biorefinery Concepts: A Review of Status and Prospects

Silva JD, Martins LH, Moreira DK, Silva LD, Barbosa PD, Komesu A, Ferreira NR, de Oliveira JA

Foods

22-May-2023

PMCID:	PMC10217607
doi:	10.3390/foods12102074
PMID:	37238892

Identification of 7-Ketocholesterol-Modulated Pathways and Sterculic Acid Protective Effect in Retinal Pigmented Epithelium Cells by Using Genome-Wide Transcriptomic Analysis

Pariente A, Pérez-Sala Á, Ochoa R, Bobadilla M, Villanueva-Martínez Á, Peláez R, Larráyoz IM

Int J Mol Sci

18-Apr-2023

PMCID:	PMC10144535
doi:	10.3390/ijms24087459
PMID:	37108627

Co-developing an international TLS network for the 3D ecological understanding of global trees: System architecture, remote sensing models, and functional prospects

Lin Y, Filin S, Billen R, Mizoue N

Environ Sci Ecotechnol

21-Feb-2023

PMCID:	PMC10024182
doi:	10.1016/j.ese.2023.100257
PMID:	36941885

Phenolic Composition, Wound Healing, Antinociceptive, and Anticancer Effects of Caralluma europaea Extracts

Amrati FE, Chebaibi M, Galvão de Azevedo R, Conte R, Slighoua M, Mssillou I, Kiokias S, de Freitas Gomes A, Soares Pontes G, Bousta D

Molecules

13-Feb-2023

PMCID:	PMC9961855
doi:	10.3390/molecules28041780
PMID:	36838767

Biodegradable Guar-Gum-Based Super-Porous Matrices for Gastroretentive Controlled Drug Release in the Treatment of Helicobacter pylori: A Proof of Concept

Grosso R, Benito E, Carbajo-Gordillo AI, García-Martín MG, Perez-Puyana V, Sánchez-Cid P, de-Paz MV

Int J Mol Sci

23-Jan-2023

PMCID:	PMC9917163
doi:	10.3390/ijms24032281
PMID:	36768604

Pretreatment of human retinal pigment epithelial cells with sterculic acid forestalls fenretinide-induced apoptosis

William S, Duncan T, Redmond TM

Sci Rep

23-Dec-2022

PMCID:	PMC9794835
doi:	10.1038/s41598-022-26383-9
PMID:	36575190

A toolkit for plant lipid engineering: Surveying the efficacies of lipogenic factors for accumulating specialty lipids

Cai Y, Yu XH, Shanklin J

Front Plant Sci

14-Dec-2022

PMCID:	PMC9795026
doi:	10.3389/fpls.2022.1064176
PMID:	36589075

Live‐Cell Imaging of Sterculic Acid—a Naturally Occurring 1,2‐Cyclopropene Fatty Acid—by Bioorthogonal Reaction with Turn‐On Tetrazine‐Fluorophore Conjugates

Bertheussen K, van de Plassche M, Bakkum T, Gagestein B, Ttofi I, Sarris AJ, Overkleeft HS, van der Stelt M, van Kasteren SI

Angew Chem Int Ed Engl

08-Aug-2022

PMCID:	PMC9546306
doi:	10.1002/anie.202207640
PMID:	35838324

Scope and Limitations of Current Antibiotic Therapies against Helicobacter pylori: Reviewing Amoxicillin Gastroretentive Formulations

Grosso R, de-Paz MV

Pharmaceutics

24-Jun-2022

PMCID:	PMC9320814
doi:	10.3390/pharmaceutics14071340
PMID:	35890236

Can omic tools help generate alternative newer sources of edible seed oil?

Rangan P, Maurya R, Singh S

Plant Direct

07-Jun-2022

PMCID:	PMC9219012
doi:	10.1002/pld3.399
PMID:	35774621

Seeds as Potential Sources of Phenolic Compounds and Minerals for the Indian Population

Sahu PK, Cervera-Mata A, Chakradhari S, Singh Patel K, Towett EK, Quesada-Granados JJ, Martín-Ramos P, Rufián-Henares JA

Molecules

17-May-2022

PMCID:	PMC9144825
doi:	10.3390/molecules27103184
PMID:	35630662

Phytochemical Profile Top

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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
3,4-Dihydroxybenzoic acid	72	Click to see C1=CC(=C(C=C1C(=O)O)O)O	154.12	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid	8468	Click to see COC1=C(C=CC(=C1)C(=O)O)O	168.15	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Phenylacetic acids / 2(hydroxyphenyl)acetic acids
2-Hydroxy-5-butoxyphenylacetic acid	15108711	Click to see CCCCOC1=CC(=C(C=C1)O)CC(=O)O	224.25	unknown	via CMAUP database
> Benzenoids / Phenols / Benzenediols / Hydroquinones
2,5-Dihydroxyphenylacetic acid butyl ester	44217017	Click to see CCCCOC(=O)CC1=C(C=CC(=C1)O)O	224.25	unknown	via CMAUP database
Ethyl 2,5-dihydroxyphenylacetate	297396	Click to see CCOC(=O)CC1=C(C=CC(=C1)O)O	196.20	unknown	via CMAUP database
Methyl 2-(2,5-dihydroxyphenyl)acetate	13790504	Click to see COC(=O)CC1=C(C=CC(=C1)O)O	182.17	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Malvalic acid	10416	Click to see CCCCCCCCC1=C(C1)CCCCCCC(=O)O	280.40	unknown	https://doi.org/10.1007/BF02663950
Palmitoleic Acid	445638	Click to see CCCCCCC=CCCCCCCCC(=O)O	254.41	unknown	https://doi.org/10.1007/BF02663950
Stearic Acid	5281	Click to see CCCCCCCCCCCCCCCCCC(=O)O	284.50	unknown	https://doi.org/10.1007/BF02663950
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Sterculic acid	12921	Click to see CCCCCCCCC1=C(C1)CCCCCCCC(=O)O	294.50	unknown	https://doi.org/10.1002/JCTB.5000600705 https://doi.org/10.1007/BF02663950
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
Entadamide-A-beta-D-glucopyranoside	101616680	Click to see CSC=CC(=O)NCCOC1C(C(C(C(O1)CO)O)O)O	323.36	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
[(2S,3R,4S,5S,6R)-3-[(2S,3R,4R)-4-[[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4-dihydroxyoxolan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl] (4aR,5S,6R,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2R,3R,4R,5S,6R)-3-acetamido-6-[[(2S,3R,4S,5S)-3,5-dihydroxy-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxymethyl]-4-hydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5,6-dihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	72737016	Click to see CC(=O)NC1C(C(C(OC1OC2CCC3(C(C2(C)C)CCC4(C3CC=C5C4(C(C(C6(C5CC(CC6)(C)C)C(=O)OC7C(C(C(C(O7)CO)O)O)OC8C(C(CO8)(COC9C(C(CO9)(CO)O)O)O)O)O)O)C)C)C)COC1C(C(C(CO1)O)OC1C(C(C(CO1)O)O)O)O)OC1C(C(C(C(O1)CO)O)O)O)O	1544.60	unknown	via CMAUP database
[(2S,3R,4S,5S,6R)-3-[(2S,3R,4R)-4-[[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4-dihydroxyoxolan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl] (4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2R,3R,4R,5S,6R)-3-acetamido-6-[[(2S,3R,4S,5S)-3,5-dihydroxy-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxymethyl]-4-hydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	72736851	Click to see CC(=O)NC1C(C(C(OC1OC2CCC3(C(C2(C)C)CCC4(C3CC=C5C4(CCC6(C5CC(CC6)(C)C)C(=O)OC7C(C(C(C(O7)CO)O)O)OC8C(C(CO8)(COC9C(C(CO9)(CO)O)O)O)O)C)C)C)COC1C(C(C(CO1)O)OC1C(C(C(CO1)O)O)O)O)OC1C(C(C(C(O1)CO)O)O)O)O	1512.60	unknown	via CMAUP database
[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl] (4aR,5S,6R,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2R,3R,4R,5S,6R)-3-acetamido-6-[[(2S,3R,4S,5S)-3,5-dihydroxy-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxymethyl]-4-hydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5,6-dihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	72736852	Click to see CC(=O)NC1C(C(C(OC1OC2CCC3(C(C2(C)C)CCC4(C3CC=C5C4(C(C(C6(C5CC(CC6)(C)C)C(=O)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(CO8)O)O)O)O)O)C)C)C)COC9C(C(C(CO9)O)OC1C(C(C(CO1)O)O)O)O)OC1C(C(C(C(O1)CO)O)O)O)O	1412.50	unknown	via CMAUP database
[(2S,3R,4S,5S,6R)-6-(acetyloxymethyl)-3-[(2S,3R,4R)-4-[[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4-dihydroxyoxolan-2-yl]oxy-4,5-dihydroxyoxan-2-yl] (4aR,5S,6R,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2R,3R,4R,5S,6R)-3-acetamido-6-[[(2S,3R,4S,5S)-3,5-dihydroxy-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxymethyl]-4-hydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5,6-dihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	72737187	Click to see CC(=O)NC1C(C(C(OC1OC2CCC3(C(C2(C)C)CCC4(C3CC=C5C4(C(C(C6(C5CC(CC6)(C)C)C(=O)OC7C(C(C(C(O7)COC(=O)C)O)O)OC8C(C(CO8)(COC9C(C(CO9)(CO)O)O)O)O)O)O)C)C)C)COC1C(C(C(CO1)O)OC1C(C(C(CO1)O)O)O)O)OC1C(C(C(C(O1)CO)O)O)O)O	1586.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Entagenic acid	21594206	Click to see CC1(CCC2(C(C1)C3=CCC4C5(CCC(C(C5CCC4(C3(C(C2O)O)C)C)(C)C)O)C)C(=O)O)C	488.70	unknown	via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / Amines / Alkanolamines / 1,2-aminoalcohols / N-acylethanolamines
Entadamide B	3035981	Click to see CSC(CC(=O)NCCO)SC	209.30	unknown	via CMAUP database
N-(2-Hydroxyethyl)-3-methylthiopropenamide	6439215	Click to see CSC=CC(=O)NCCO	161.22	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
2-(beta-D-Glucopyranosyloxy)-5-hydroxyphenylacetic acid butyl ester	102143698	Click to see CCCCOC(=O)CC1=C(C=CC(=C1)O)OC2C(C(C(C(O2)CO)O)O)O	386.40	unknown	via CMAUP database
2-beta-d-Glucopyranosyloxy-5-butoxyphenylacetic acid	15108713	Click to see CCCCOC1=CC(=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O)CC(=O)O	386.40	unknown	via CMAUP database
Phaseoloidin	14104237	Click to see C1=CC(=C(C=C1O)CC(=O)O)OC2C(C(C(C(O2)CO)O)O)O	330.29	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
(1R,8S,9R,16R,18S,27S)-9-(3,4-dihydroxyphenyl)-5,8,16,21,23-pentahydroxy-2,10,17,26-tetraoxaheptacyclo[14.11.1.01,13.03,12.06,11.018,27.020,25]octacosa-3(12),4,6(11),13,20,22,24-heptaen-15-one	101925531	Click to see C1C(C(OC2=C1C(=CC3=C2C4=CC(=O)C5(CC4(O3)C6C(O5)CC7=C(C=C(C=C7O6)O)O)O)O)C8=CC(=C(C=C8)O)O)O	576.50	unknown	via CMAUP database
Cianidanol	9064	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O	290.27	unknown	via CMAUP database
Epicatechin	72276	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O	290.27	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
Epigallocatechin	72277	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O	306.27	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Naringenin	439246	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O	272.25	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
Aromadendrin	122850	Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	288.25	unknown	via CMAUP database
Taxifolin	439533	Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O	304.25	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
4',7-Dihydroxyflavone	5282073	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C=C3)O)O	254.24	unknown	via CMAUP database
4H-1-Benzopyran-4-one, 2-(3,5-dihydroxyphenyl)-5,7-dihydroxy-	5487757	Click to see C1=C(C=C(C=C1O)O)C2=CC(=O)C3=C(C=C(C=C3O2)O)O	286.24	unknown	via CMAUP database
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
Galangin	5281616	Click to see C1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O	270.24	unknown	via CMAUP database
Isorhamnetin	5281654	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	316.26	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	https://doi.org/10.1016/0031-9422(92)83667-N
Rhamnocitrin	5320946	Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)O)C3=CC=C(C=C3)O)O	300.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
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	https://doi.org/10.1016/0031-9422(92)83667-N
Rutin	5280805	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O	610.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Ayanin	5280682	Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)OC)O	344.30	unknown	via CMAUP database
Kaempferol 3,7,4'-trimethyl ether	5468749	Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)OC	328.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Cinnamylphenols
2'-O-Methylisoliquiritigenin	5319688	Click to see COC1=C(C=CC(=C1)O)C(=O)C=CC2=CC=C(C=C2)O	270.28	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Neoflavonoids / Neoflavones
Stevenin	5321501	Click to see COC1=C(C=C2C(=CC(=O)OC2=C1)C3=CC(=CC=C3)O)O	284.26	unknown	via CMAUP database

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Sterculia foetida

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