Scientific name	Authority	First published in
Sapindus abstergens	Roxb. ex Wight & Arn.	Prodr. Fl. Ind. Orient. : 111 (1834)
Sapindus acutus	Roxb. ex Wight & Arn.	Prodr. Fl. Ind. Orient. : 111 (1834)
Sapindus mollis	Blume	Rumphia 3: 98 (1847 publ. 1849)
Sapindus maduriensis	Perr.	Mém. Soc. Linn. Paris 3: 144 (1825)
Sapindus emarginatus	Vahl	Symb. Bot. 3: 54 (1794)

Common names Top

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Filter by language:

Language	Common/alternative name
English	threeleaf soapberry
Arabic	صابونية ثلاثية الأوراق
Burmese	ကုလားကင်ပွန်း
Chinese	三叶无患子
Chinese	三葉無患子

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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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
  - Kenya
  - Tanzania
  - Uganda
- Western Indian Ocean
  - Rodrigues

Asia-tropical click to expand
- Indian Subcontinent
  - Bangladesh
  - India
  - Pakistan
  - Sri Lanka
- Indo-China
  - Andaman Islands
  - Myanmar

Southern America click to expand
- Caribbean
  - Trinidad-Tobago

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0001135030
UNII	AVK580175F
USDA Plants	SATR10
Tropicos	28600995
INPN	706772
KEW	urn:lsid:ipni.org:names:784697-1
The Plant List	tro-28600995
Open Tree Of Life	730999
NCBI Taxonomy	290988
IPNI	784697-1
iNaturalist	915030
GBIF	5421131
EPPO	SAKTF
EOL	483643
USDA GRIN	33092
Wikipedia	Sapindus_trifoliatus
CMAUP	NPO24019

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

A Pilot, Prospective, Randomized-Controlled Study to Evaluate the Efficacy and Safety of Arsha Hita™ in the Treatment of Anal Fissures

B. J. G, K. R. S, Shetty SK, Rao PN, Narvekar S, Nalawade M, Chawda MB, Chitnis KR, Seetharaman R, Tripathi RK

Cureus

13-Apr-2023

PMCID:	PMC10182782
doi:	10.7759/cureus.37531
PMID:	37193430

Do carbon stocks and floristic diversity of tropical homegardens vary along an elevational gradient and based on holding size in central Kerala, India?

Kumar BM

Agrofor Syst

07-Apr-2023

PMCID:	PMC10081327
doi:	10.1007/s10457-023-00821-7
PMID:	37193256

In Vitro Anti-Venom Potentials of Aqueous Extract and Oils of Toona ciliata M. Roem against Cobra Venom and Chemical Constituents of Oils

Okot DF, Namukobe J, Vudriko P, Anywar G, Heydenreich M, Omowumi OA, Byamukama R

Molecules

30-Mar-2023

PMCID:	PMC10096364
doi:	10.3390/molecules28073089
PMID:	37049851

Conserving traditional wisdom in a commodified landscape: Unpacking brand Ayurveda

Viale M, Vicol M

J Ayurveda Integr Med

18-Nov-2022

PMCID:	PMC10105222
doi:	10.1016/j.jaim.2022.100667
PMID:	36411197

Triterpenoid Saponins from Washnut (Sapindus mukorossi Gaertn.)—A Source of Natural Surfactants and Other Active Components

Sochacki M, Vogt O

Plants (Basel)

09-Sep-2022

PMCID:	PMC9502486
doi:	10.3390/plants11182355
PMID:	36145756

An Overview of Chili Leaf Curl Disease: Molecular Mechanisms, Impact, Challenges, and Disease Management Strategies in Indian Subcontinent

Shingote PR, Wasule DL, Parma VS, Holkar SK, Karkute SG, Parlawar ND, Senanayake DM

Front Microbiol

29-Jun-2022

PMCID:	PMC9277185
doi:	10.3389/fmicb.2022.899512
PMID:	35847087

A Contemporary Exploration of Traditional Indian Snake Envenomation Therapies

Deshpande AM, Sastry KV, Bhise SB

Trop Med Infect Dis

16-Jun-2022

PMCID:	PMC9227218
doi:	10.3390/tropicalmed7060108
PMID:	35736986

Genetic Diversity Analysis of Sapindus in China and Extraction of a Core Germplasm Collection Using EST-SSR Markers

Liu J, Gao S, Xu Y, Wang M, Ngiam JJ, Rui Wen NC, Yi JJ, Weng X, Jia L, Salojärvi J

Front Plant Sci

24-May-2022

PMCID:	PMC9171133
doi:	10.3389/fpls.2022.857993
PMID:	35685004

A Critical Review and Scientific Prospective on Contraceptive Therapeutics from Ayurveda and Allied Ancient Knowledge

Bhatt N, Deshpande M

Front Pharmacol

03-Jun-2021

PMCID:	PMC8210421
doi:	10.3389/fphar.2021.629591
PMID:	34149405

Advances and Perspectives in Tissue Culture and Genetic Engineering of Cannabis

Hesami M, Baiton A, Alizadeh M, Pepe M, Torkamaneh D, Jones AM

Int J Mol Sci

26-May-2021

PMCID:	PMC8197860
doi:	10.3390/ijms22115671
PMID:	34073522

Occupational immediate type allergy to soapnut and quillaja bark

Merget R, Raulf M, Sander I

Allergol Select

26-Jan-2021

PMCID:	PMC7841414
doi:	10.5414/ALX02131E
PMID:	33524084

Synthesis, Characterization, and Evaluation of Solution Properties of Sesame Fatty Methyl Ester Sulfonate Surfactant

R. C S, Kipkemboi PK, Rop K

ACS Omega

30-Oct-2020

PMCID:	PMC7658934
doi:	10.1021/acsomega.0c03698
PMID:	33195917

In vitro screening of peptidase inhibitory activity in some plants of North India

Samiksha, Sohal SK

Heliyon

13-Oct-2020

PMCID:	PMC7566102
doi:	10.1016/j.heliyon.2020.e05203
PMID:	33088962

Seed dormancy and germination in Dodonaea viscosa (Sapindaceae) from south-western Saudi Arabia

Al-Namazi AA, Al-Ammari BS, Davy AJ, Al-Turki TA

Saudi J Biol Sci

28-May-2020

PMCID:	PMC7451594
doi:	10.1016/j.sjbs.2020.05.036
PMID:	32874121

Exploration of anti-insect potential of trypsin inhibitor purified from seeds of Sapindus mukorossi against Bactrocera cucurbitae

Samiksha, Singh D, Kesavan AK, Sohal SK

Sci Rep

19-Nov-2019

PMCID:	PMC6863899
doi:	10.1038/s41598-019-53495-6
PMID:	31745144

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
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(2R,3R,4R,5R,6S)-2-[(2R,3R,4S,5R,6R)-5-hydroxy-2-[(2E,6E,10E)-12-[(2R,3R,4S,5R,6R)-5-hydroxy-6-(hydroxymethyl)-3-[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-3,7,11-trimethyldodeca-2,6,10-trienoxy]-6-(hydroxymethyl)-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	163011014	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OCC=C(C)CCC=C(C)CCC=C(C)COC3C(C(C(C(O3)CO)O)OC4C(C(C(CO4)O)O)O)OC5C(C(C(C(O5)C)O)O)O)CO)O)OC6C(C(C(CO6)O)O)O)O)O)O	1119.20	unknown	https://doi.org/10.1016/0031-9422(88)80128-6
(2R,3R,4R,5R,6S)-2-[(2R,3R,4S,5R,6R)-5-hydroxy-6-(hydroxymethyl)-2-[(2E,6E,10E)-12-hydroxy-3,7,11-trimethyldodeca-2,6,10-trienoxy]-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	163052223	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OCC=C(C)CCC=C(C)CCC=C(C)CO)CO)O)OC3C(C(C(CO3)O)O)O)O)O)O	678.80	unknown	https://doi.org/10.1016/0031-9422(88)80128-6
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5R,6R)-5-hydroxy-2-[(2E,6E,10E)-12-[(2R,3R,4S,5R,6R)-5-hydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-3,7,11-trimethyldodeca-2,6,10-trienoxy]-6-(hydroxymethyl)-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	101616724	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OCC=C(C)CCC=C(C)CCC=C(C)COC3C(C(C(C(O3)CO)O)OC4C(C(C(CO4)O)O)O)OC5C(C(C(C(O5)C)O)O)O)CO)O)OC6C(C(C(CO6)O)O)O)O)O)O	1119.20	unknown	https://doi.org/10.1016/0031-9422(88)80128-6
(2S,3S,4S,5S,6R)-2-[(2R,3R,4S,5R,6R)-5-hydroxy-6-(hydroxymethyl)-2-[(2E,6E,10E)-12-hydroxy-2,6,10-trimethyldodeca-2,6,10-trienoxy]-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	162944765	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OCC(=CCCC(=CCCC(=CCO)C)C)C)CO)O)OC3C(C(C(CO3)O)O)O)O)O)O	678.80	unknown	https://doi.org/10.1016/0031-9422(88)80128-6
2-[5-Hydroxy-2-[12-[5-hydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy-4-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-3,7,11-trimethyldodeca-2,6,10-trienoxy]-6-(hydroxymethyl)-4-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	163011013	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OCC=C(C)CCC=C(C)CCC=C(C)COC3C(C(C(C(O3)CO)O)OC4C(C(C(CO4)O)O)O)OC5C(C(C(C(O5)C)O)O)O)CO)O)OC6C(C(C(CO6)O)O)O)O)O)O	1119.20	unknown	https://doi.org/10.1016/0031-9422(88)80128-6
2-[5-Hydroxy-6-(hydroxymethyl)-2-(12-hydroxy-2,6,10-trimethyldodeca-2,6,10-trienoxy)-4-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	162944764	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OCC(=CCCC(=CCCC(=CCO)C)C)C)CO)O)OC3C(C(C(CO3)O)O)O)O)O)O	678.80	unknown	https://doi.org/10.1016/0031-9422(88)80128-6
2-[5-Hydroxy-6-(hydroxymethyl)-2-(12-hydroxy-3,7,11-trimethyldodeca-2,6,10-trienoxy)-4-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	163052222	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OCC=C(C)CCC=C(C)CCC=C(C)CO)CO)O)OC3C(C(C(CO3)O)O)O)O)O)O	678.80	unknown	https://doi.org/10.1016/0031-9422(88)80128-6
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,2S,5S,10S,14R,15R,18R,21R,22R)-1,2,8,8,15,21-hexamethyl-19-oxahexacyclo[12.10.0.02,11.05,10.015,22.018,21]tetracos-11-ene-5-carboxylic acid	162987188	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC6C5(CO6)C)C)C)C2C1)C)C(=O)O)C	454.70	unknown	https://doi.org/10.1007/BF02147773
(4aS,6aR,6aS,6bR,8aR,9R,10S,12aR,14bS)-10-[(2S,3R,4S,5S)-3-[(2S,3R,4R,5S,6S)-4-[(2S,3R,4R,5R)-5-acetyloxy-3,4-dihydroxyoxan-2-yl]oxy-3,5-dihydroxy-6-methyloxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	102316696	Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)O)O)OC8C(C(C(CO8)OC(=O)C)O)O)O	925.10	unknown	https://doi.org/10.1002/MRC.1675
(4aS,6bR,9S,10S,12aR)-10-[(2S,3R,4S,5S)-3-[(2S,3R,4R,5S,6S)-3,5-dihydroxy-6-methyl-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	6325965	Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)O)O)OC8C(C(C(CO8)O)O)O)O	883.10	unknown	https://doi.org/10.1016/0031-9422(88)80128-6
1,2,8,8,15,21-Hexamethyl-19-oxahexacyclo[12.10.0.02,11.05,10.015,22.018,21]tetracos-11-ene-5-carboxylic acid	156963326	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC6C5(CO6)C)C)C)C2C1)C)C(=O)O)C	454.70	unknown	https://doi.org/10.1007/BF02147773
10-[3-[4-(4-Acetyloxy-3,5-dihydroxyoxan-2-yl)oxy-3,5-dihydroxy-6-methyloxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	73818286	Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)O)O)OC8C(C(C(CO8)O)OC(=O)C)O)O	925.10	unknown	https://doi.org/10.1002/MRC.1675
10-[3-[4-(4,5-Diacetyloxy-3-hydroxyoxan-2-yl)oxy-3,5-dihydroxy-6-methyloxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	16196966	Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)O)O)OC8C(C(C(CO8)OC(=O)C)OC(=O)C)O)O	967.10	unknown	https://doi.org/10.1002/MRC.1675
10-[3-[4-(5-Acetyloxy-3,4-dihydroxyoxan-2-yl)oxy-3,5-dihydroxy-6-methyloxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	74029772	Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)O)O)OC8C(C(C(CO8)OC(=O)C)O)O)O	925.10	unknown	https://doi.org/10.1002/MRC.1675
3beta-[2-O-(3-O-alpha-L-Arabinopyranosyl-alpha-L-rhamnopyranosyl)-alpha-L-arabinopyranosyloxy]-23-hydroxyoleana-12-ene-28-oic acid	21637697	Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)O)O)OC8C(C(C(CO8)O)O)O)O	883.10	unknown	https://doi.org/10.1002/MRC.1675
3beta-[2-O-[3-O-(3-O-Acetyl-beta-D-xylopyranosyl)-alpha-L-rhamnopyranosyl]-alpha-L-arabinopyranosyloxy]-23-hydroxyoleana-12-ene-28-oic acid	21637699	Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)O)O)OC8C(C(C(CO8)O)OC(=O)C)O)O	925.10	unknown	https://doi.org/10.1002/MRC.1675
3beta-[2-O-[3-O-(3-O,4-O-Diacetyl-alpha-L-arabinopyranosyl)-alpha-L-rhamnopyranosyl]-alpha-L-arabinopyranosyloxy]-23-hydroxyoleana-12-ene-28-oic acid	102316698	Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)O)O)OC8C(C(C(CO8)OC(=O)C)OC(=O)C)O)O	967.10	unknown	https://doi.org/10.1002/MRC.1675
3beta-[2-O-[3-O-(3-O,4-O-Diacetyl-beta-D-xylopyranosyl)-alpha-L-rhamnopyranosyl]-alpha-L-arabinopyranosyloxy]-23-hydroxyoleana-12-ene-28-oic acid	21637700	Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)O)O)OC8C(C(C(CO8)OC(=O)C)OC(=O)C)O)O	967.10	unknown	https://doi.org/10.1002/MRC.1675
CID 15625347	15625347	Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)O)O)OC8C(C(C(CO8)O)O)O)O	883.10	unknown	https://doi.org/10.1002/MRC.1675
Sapindoside B	161686	Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)O)O)OC8C(C(C(CO8)O)O)O)O	883.10	unknown	https://doi.org/10.1002/MRC.1675 https://doi.org/10.1016/0031-9422(88)80128-6
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin	5280460	Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O	192.17	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
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
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
Gallocatechin	65084	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 / Flavonols
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
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 / Hydroxyflavonoids / 7-hydroxyflavonoids
(2S)-2-hydroxynaringenin	86311108	Click to see C1C(=O)C2=C(C=C(C=C2OC1(C3=CC=C(C=C3)O)O)O)O	288.25	unknown	via CMAUP database

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Sapindus trifoliatus

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