Content in this section summarizes historical and cultural records. It is not medical advice.
Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Citrus japonica, commonly known as the Japanese mandarin or satsuma, has a long history of use as a soothing infusion in East Asian folk medicine. Among the Japanese, the dried peel is steeped in hot water to produce a fragrant tea that is traditionally drunk after meals to aid digestion and relieve mild stomach discomfort (Kondo et al., 2015). In Korea, a similar practice is documented: the peel is boiled to make a decoction that is taken during colds to help clear congestion and reduce cough (Kim et al., 2018). Chinese herbalists have also recorded the use of the fruit’s peel in a decoction for treating stomach upset and abdominal pain, noting that the tea can be taken twice daily for several days (Li et al., 2019). In all three cultures, the primary plant part used is the peel; occasionally, the fresh fruit or the leaves are macerated in alcohol to produce a tincture that is applied topically as a poultice for minor skin irritations.

A simple, safe recipe for a citrus‑peel tea is as follows: take 5 g of dried Citrus japonica peel, place it in a teapot, pour 200 ml of freshly boiled water, cover, and steep for 5 minutes. Strain the liquid and enjoy warm. This preparation delivers a gentle dose of the fruit’s natural flavonoids and essential oils. For safety, people with known citrus allergies should avoid this tea, and pregnant women are advised to limit intake of high‑concentration essential oils such as limonene, which can be present in large amounts in citrus peels.

The therapeutic effects of Citrus japonica tea are largely attributed to its well‑established phytochemicals. Hesperidin and naringin, two flavanones abundant in the peel, have been shown to possess antioxidant and anti‑inflammatory properties. Limonene, a monoterpene in the peel’s essential oil, contributes to the aroma and may help relieve digestive discomfort. These constituents provide a scientific basis for the traditional use of the tea as a mild digestive aid and cough suppressant.

Modern research continues to explore the health benefits of Citrus japonica. Recent studies have confirmed its antioxidant capacity and its potential to modulate gut microbiota, supporting its role in digestive health. Commercially, the fruit’s peel is now available in specialty tea blends marketed for relaxation and digestive support, keeping the centuries‑old tradition of satsuma tea alive in contemporary wellness culture.

General Uses Top

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Food and beverages (non-medicinal):
The fruit is consumed fresh, dried, or candied, and as jam and preserves; it is also used as a flavoring in confectionery and beverages (CITRUS: The Worldwide Compendium). Fruit processing yields essential oil and, in some regions, juice; the latter is standardized by commercial practices such as those of the International Citrus Juice Federation for traceability and composition. For example, the Japanese cultivar “Kiyomi” shows Brix values of 9–11 with acidity around 1.2–1.8 g/100 mL and high linalool/linalool acetate contents.

Fragrance and cosmetics:
Peel essential oil is produced by cold expression or hydrodistillation and used as a fragrance ingredient in perfumes and aromatic compositions. Flavedo and zest are utilized as flavoring and aroma notes in food and beverages; aroma compounds are dominated by monoterpenes (limonene) and oxygenated constituents (linalool and its acetate) that impart characteristic citrusy, floral tones. No medicinal claims or topical applications are proposed.

Properties relevant to use:
Citrus peel and essential oil are rich in limonene, a solvent with good stability that facilitates fragrance formulation; some compositions also contain linalool and linalyl acetate, both used in perfumery for their floral attributes. Essential oils and extracts are handled under established fragrance-industry safety and labeling frameworks.

Standards and regulation:
Fragrance materials are typically managed in accordance with IFRA Standards on safe use and restricted substances; essential oils are handled under relevant transportation regulations (e.g., UN 1169, Class 3). Food uses follow standard processing and sanitation practices; while genus-level citrus standards exist (e.g., Codex Alimentarius for citrus juices and fresh produce), cultivar-specific requirements are implemented regionally.

Synonyms Top

Scientific name	Authority	First published in
Sclerostylis hindsii	Champ. ex Benth.	Hooker's J. Bot. Kew Gard. Misc. 3: 327 (1851)
Atalantia hindsii	(Champ. ex Benth.) Oliv.	Fl. Hongk. 51. 1861 [Feb 1861]
Citrofortunella madurensis	(Lour.) D.Rivera, Obón, S.Ríos, Selma, F.Méndez, Verde & F.Cano	Varied. Tradic. Frutales Río Segura Cat. Etnobot. Cítricos 191. 1998
Citrus aurantium var. globifera	Engl.	Nat. Pflanzenfam. 3(4): 199 1896
Citrus aurantium var. japonica	(Thunb.) Hook.f.	Bot. Mag. 100: t. 6128 1874
Citrus aurantium subsp. japonica	(Thunb.) Engl.	Nat. Pflanzenfam. 3(4): 199 1896
Citrus aurantium var. olivicormis	Risso ex Loisel.	Traité Arbr. Arbust. 7: 95 1816
Citrus hindsii	(Champ. ex Benth.) Govaerts	World Checkl. Seed Pl. 3(1): 15 (1999)
Citrus inermis	Roxb.	Fl. Ind. ed. 1832 , 3: 393 (1832)
Citrus japonica var. madurensis	(Lour.) Guillaumin	Agric. Prat. Pays Chauds n.s., 14: 121 1932
Citrus madurensis	Lour.	Fl. Cochinch. : 467 (1790)
Citrus margarita	Lour.	Fl. Cochinch. : 467 (1790)
Fortunella crassifolia	Swingle	J. Washington Acad. Sci. 4: 172 (1915)
Fortunella hindsii	Swingle	J. Washington Acad. Sci. 5: 175 (1915)
Fortunella japonica	Swingle	J. Washington Acad. Sci. 5: 171 (1915)
Fortunella margarita	Swingle	J. Washington Acad. Sci. 5: 170 (1915)
Fortunella venosa	(Champ. ex Hook.) C.C.Huang	Guihaia 11: 8 (1991)
Citrus japonica var. fructu-elliptica	Siebold & Zucc.	Fl. Jap. 1: 35 1835
Fortunella hindsii var. chintou	Swingle	J. Arnold Arbor. 21: 130 1940
Fortunella bawangica	C.C.Huang	Rhodora 111(948): 537. 2010 [dt. 2009; issued 11 Feb 2010]
Fortunella obovata	hort. ex Tanaka	Mem. Tanaka Citrus Exper. Stat. i. No. 1, 45 (1927), in obs., nomen.
Sclerostylis venosa	Champ. ex Benth.	Hooker's J. Bot. Kew Gard. Misc. 3: 327 (1851)
Fortunella chintou	(Swingle) C.C.Huang
Citrus japonica var. margarita	(Lour.) Guillaumin
Citrus microcarpa	Bunge	Mém. Acad. Imp. Sci. St.-Pétersbourg Divers Savans 2: 84 1833
Citrus nobilis var. microcarpa	Hassk.	Flora 25(2, Beibl. 3): 43 (1842)
Citrus japonica subf. crassifolia	(Swingle) M.Hiroe	Forest Pl. Hist. Jap. Islands 1: 217. 1974
Citrus japonica subf. hindsii	(Swingle) M.Hiroe	Forest Pl. Hist. Jap. Islands 1: 217. 1974
Fortunella japonica var. margarita	(Lour.) Makino	Ill. Fl. Nippon 385. 1940 [2 Oct 1940]

Common names Top

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Filter by language:

Language	Common/alternative name
English	cumquat
English	kumquat
Spanish	naranjo chino
Spanish	naranjo enano
Spanish	quinoto
Afrikaans	koemkwart
Afrikaans	koemkwate
Afrikaans	kumkwart
Afrikaans	kumkwate
Afrikaans	koemkwat
Arabic	كمكوات
Arabic	برتقال ياباني
Azerbaijani	kinkan
Azerbaijani	yapon kinkanı
azb	کینکان
Bulgarian	кумкуат
Catalan	cumquat
ceb	kumkuwat
Czech	kumkvat
Czech	kumquat
cv	Кумкват
Danish	kumquat
German	zwergorange
German	zwergpomeranze
German	kumquat
Greek	Κουμκουάτ
Esperanto	nanaj oranĝoj
Esperanto	kumkvato
Esperanto	japana citruso
Estonian	kinkan
Basque	kumquata
Basque	kumkuat
Persian	پورنج
Persian	پورنج مارومی
Finnish	kumkvatit
French	kumquat
frr	kumquat
Galician	laranxa anana
Galician	laranxa chinesa
Galician	kumquat
Hebrew	תפוז סיני
Hebrew	קומקוואט
Croatian	kumkvat
Upper Sorbian	kumkwat
Upper Sorbian	japanski kumkwat
Hungarian	törpemandarin
Hungarian	kamkvat
Hungarian	savanyú narancs
Hungarian	kumkvat
Armenian	Կումկվատ
Indonesian	kumkuat
Icelandic	egglaga gullappelsína
Icelandic	kúmkvat
Italian	cumquat
Italian	kingen
Italian	mandarino cinese
Italian	kumquat
Japanese	マルミキンカン
Japanese	キンキツ
Japanese	金柑
Japanese	金橘
Japanese	キンカン
Japanese	フォルトゥネッラ・ジャポニカ
Japanese	チートルス・ジャポニカ
jv	kumquat
Georgian	კუმკვატი
Georgian	კინკანი
Korean	금귤
Korean	금귤나무
Korean	금감
Korean	낑깡
Korean	동귤
Korean	알귤
koi	Кумкват
kv	Кумкват
lbe	Кумкват
Lithuanian	kinkanas
Lithuanian	japoninis kinkanas
lzh	金橘
Malayalam	കുംകാറ്റ് ഓറഞ്ച്
mrj	Кумкват
Malay	kumkuat
Norwegian Bokmål	kumquat
Norwegian Bokmål	kumkvat
nds	kumquat
Nepali	मुन्तला
Dutch	kumquat
Norwegian Nynorsk	kumkvat
Polish	kumkwat
Portuguese	cunquate
Romanian	kumquat
Russian	Фортунелла
Russian	Кумкват
Slovak	kumkvát
Slovak	kumkvat
Slovenian	kumkvati
Slovenian	kumkvat
Serbian	Кумкват
Swedish	kumquat
Thai	ส้มกิมจ๊อ
Thai	ส้มจี๊ด
Tonga	kamikuati
Turkish	kamkat
udm	Кумкват
Ukrainian	Кумкват
Uzbek	kumquat
Vietnamese	kim quất
Vietnamese	quất
Chinese	金橘
Chinese	金柑
Chinese	园金柑
Chinese	山橘
Chinese	山橘（山桔）
Chinese	山橘叶
Chinese	山橘根
Chinese	金橘叶
Chinese	金橘核
Chinese	金橘根
Chinese	金橘露
Chinese	罗浮
Chinese	金桔
Chinese	山桔芸香科柑橘属植物或其果实

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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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
- West Tropical Africa
  - Gambia

Asia-temperate click to expand
- China
  - China Southeast
  - Hainan
- Eastern Asia
  - Japan
  - Korea

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
- Indo-China
  - Vietnam

Northern America click to expand
- Southwestern U.S.A.
  - California

Southern America click to expand
- Caribbean
  - Cuba
  - Dominican Republic
  - Haiti
  - Puerto Rico
  - Trinidad-Tobago

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000608080
UNII	YQ1UE03Q6W
Tropicos	28100019
INPN	91806
KEW	urn:lsid:ipni.org:names:771939-1
The Plant List	kew-2724150
Open Tree Of Life	370009
Observations.org	367651
NCBI Taxonomy	76966
IPNI	771939-1
iNaturalist	343817
iNaturalist	343818
GBIF	3831801
Freebase	/m/0bbrzk6
USDA GRIN	10724
Wikipedia	Kumquat
CMAUP	NPO27623
USDA Plants	FOJA
PFAF	Citrus japonica
Freebase	/m/043mmn5
EPPO	FOLJA
EOL	47126196
Calflora (Californian flora)	9124

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

Green synthesized AgNPs as a probe for colorimetric detection of Hg (II) ions in aqueous medium and fluorescent imaging in liver cell lines and its antibacterial activity

Tewari S, Sahani S, Yaduvanshi N, Painuli R, Sankararamakrishnan N, Dwivedi J, Sharma S, Han SS

Discov Nano

02-May-2024

PMCID:	PMC11065856
doi:	10.1186/s11671-024-04014-8
PMID:	38696067

Mango headspace volatiles trigger differential responses of the mango fruit fly Ceratitis cosyra and its parasitoids

Miano RN, Dekker T, Rohwer E, Biasazin TD, Ndlela S, Yusuf AA, Cheseto X, Mohamed SA

Heliyon

23-Apr-2024

PMCID:	PMC11066407
doi:	10.1016/j.heliyon.2024.e30068
PMID:	38707327

Glucosidase inhibition and compound identification of stingless bee honey and preserved fruits of Citrus japonica

Thummajitsakul S, Suppasat T, Silprasit K

Heliyon

16-Apr-2024

PMCID:	PMC11053177
doi:	10.1016/j.heliyon.2024.e29740
PMID:	38681540

Transient Expression Assay and Microscopic Observation in Kumquat Fruit

Gong J, Sun X

Bio Protoc

05-Apr-2024

PMCID:	PMC11006802
doi:	10.21769/BioProtoc.4968
PMID:	38618180

Integrated proteomic, transcriptomic, and metabolomic profiling reveals that the gibberellin–abscisic acid hub runs flower development in the Chinese orchid Cymbidium sinense

Ahmad S, Lu C, Gao J, Wei Y, Xie Q, Jin J, Zhu G, Yang F

Hortic Res

12-Mar-2024

PMCID:	PMC11088716
doi:	10.1093/hr/uhae073
PMID:	38738212

Genome-Wide Identification and Characterization of the Sweet Orange (Citrus sinensis) GATA Family Reveals a Role for CsGATA12 as a Regulator of Citrus Bacterial Canker Resistance

Fan J, Xian B, Huang X, Yu Q, Zhang M, Zhang C, Jia R, Chen S, He Y, Li Q

Int J Mol Sci

02-Mar-2024

PMCID:	PMC10931568
doi:	10.3390/ijms25052924
PMID:	38474170

A tetraploid-dominated cytochimera developed from a natural bud mutant of the nonapomictic mandarin variety ‘Orah’

Dang J, Li C, Sun D, Guo Q, Liang G

Mol Breed

23-Feb-2024

PMCID:	PMC10891019
doi:	10.1007/s11032-024-01456-x
PMID:	38404720

PbrWRKY62-PbrADC1 module involves in superficial scald development of Pyrus bretschneideri Rehd.fruit via regulating putrescine biosynthesis

Zhang X, Zhu L, Qian M, Jiang L, Gu P, Jia L, Qian C, Luo W, Ma M, Wu Z, Qiao X, Wang L, Zhang S

Mol Hortic

20-Feb-2024

PMCID:	PMC10877817
doi:	10.1186/s43897-024-00081-8
PMID:	38373989

Meta-analysis of citrus-derived additives on chicken meat quality and safety: a comprehensive evaluation of acceptability, physicochemical properties, and microbial contamination

Budiarto R, Ujilestari T, Rumhayati B, Adli DN, Hudaya MF, Sitaresmi PI, Widodo S, Wulandari W, Wahyono T, Sholikin MM

Poult Sci

15-Feb-2024

PMCID:	PMC10912930
doi:	10.1016/j.psj.2024.103556
PMID:	38430777

Dihydromyrcenol Modulates Involucrin Expression through the Akt Signaling Pathway

Yang S, Kang W, Choi D, Roh J, Park T

Int J Mol Sci

13-Feb-2024

PMCID:	PMC10889318
doi:	10.3390/ijms25042246
PMID:	38396923

Untargeted Metabolomic Analyses and Antilipidemic Effects of Citrus Physiological Premature Fruit Drop

Wang C, Peng M, Gao Z, Han Q, Fu F, Li G, Su D, Huang L, Guo J, Shan Y

Int J Mol Sci

04-Feb-2024

PMCID:	PMC10855584
doi:	10.3390/ijms25031876
PMID:	38339154

Correction: He et al. Biology, Ecology and Management of Tephritid Fruit Flies in China: A Review. Insects 2023, 14, 196

He Y, Xu Y, Chen X

Insects

31-Jan-2024

PMCID:	PMC10889426
doi:	10.3390/insects15020093
PMID:	38392559

Highly Promiscuous Flavonoid Di-O-glycosyltransferases from Carthamus tinctorius L.

Xu X, Xia M, Han Y, Tan H, Chen Y, Song X, Yuan S, Zhang Y, Su P, Huang L

Molecules

26-Jan-2024

PMCID:	PMC10856022
doi:	10.3390/molecules29030604
PMID:	38338349

Advancing tree genomics to future proof next generation orchard production

Kerr SC, Shehnaz S, Paudel L, Manivannan MS, Shaw LM, Johnson A, Velasquez JT, Tanurdžić M, Cazzonelli CI, Varkonyi-Gasic E, Prentis PJ

Front Plant Sci

19-Jan-2024

PMCID:	PMC10834703
doi:	10.3389/fpls.2023.1321555
PMID:	38312357

Low-Cost Plant-Based Metal and Metal Oxide Nanoparticle Synthesis and Their Use in Optical and Electrochemical (Bio)Sensors

Ciobotaru IC, Oprea D, Ciobotaru CC, Enache TA

Biosensors (Basel)

15-Dec-2023

PMCID:	PMC10741781
doi:	10.3390/bios13121031
PMID:	38131791

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
> Alkaloids and derivatives / Eburnan-type alkaloids
Eburnamenine	6857502	Click to see	278.40	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzamides
Octadecanoic acid, 4-[4-[2-(benzoylamino)ethyl]phenoxy]-1-[(3,3-dimethyloxiranyl)methyl]-2-methyl-2-butenyl ester	162987554	Click to see	676.00	unknown	https://doi.org/10.1016/0040-4020(76)87016-0
> Benzenoids / Phenol ethers
[(Z,2S)-5-[4-(2-benzamidoethyl)phenoxy]-1-[(2R)-3,3-dimethyloxiran-2-yl]-3-methylpent-3-en-2-yl] octadecanoate	163193114	Click to see	676.00	unknown	https://doi.org/10.1016/0040-4020(76)87016-0
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(1R,4R,7R,9R,10S,13S)-5,5-bis(hydroxymethyl)-9-methyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-7-ol	162920705	Click to see	320.50	unknown	https://doi.org/10.1002/CHIN.200324150
(1R,4R,7S,9R,10S,13S)-5,5-bis(hydroxymethyl)-9-methyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-7-ol	11897962	Click to see	320.50	unknown	https://doi.org/10.1002/CHIN.200324150
(1R,4R,9R,10S,13S)-5,5-bis(hydroxymethyl)-9-methyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-7-one	163034477	Click to see	318.40	unknown	https://doi.org/10.1002/CHIN.200324150
5,5-Bis(hydroxymethyl)-9-methyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-7-ol	53396113	Click to see	320.50	unknown	https://doi.org/10.1002/CHIN.200324150
> Lipids and lipid-like molecules / Prenol lipids / Isoprenoid phosphates
Geranyl Diphosphate	445995	Click to see	314.21	unknown	https://doi.org/10.1007/BF00393177
Isopentenyl pyrophosphate	1195	Click to see CC(=C)CCOP(=O)(O)OP(=O)(O)O	246.09	unknown	https://doi.org/10.1007/BF00393177
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-alpha-Pinene	440968	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	https://doi.org/10.1007/BF00393177
(+-)-alpha-Pinene	6654	Click to see	136.23	unknown	https://doi.org/10.1007/BF00393177
Sabinene	18818	Click to see	136.23	unknown	https://doi.org/10.1021/ACS.JNATPROD.9B00361
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Limonene, (-)-	439250	Click to see	136.23	unknown	https://doi.org/10.1007/BF00393177
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
2H-1-Benzopyran-2-one, 7-[[(2E)-3,7-dimethyl-2,6-octadienyl]oxy]-	400073	Click to see CC(=CCCC(=CCOC1=CC2=C(C=C1)C=CC(=O)O2)C)C	298.40	unknown	https://doi.org/10.3109/13880209.2012.747546 https://doi.org/10.1016/J.BBRC.2007.11.119 https://doi.org/10.1021/JF303060B https://doi.org/10.1159/000078001 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4550746/ https://doi.org/10.1089/JMF.2013.0029 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3382769/ https://doi.org/10.1002/BIOF.5520330103 https://doi.org/10.1093/JN/135.12.2987S https://doi.org/10.1080/01635580701308216 https://doi.org/10.1016/J.PHYTOCHEM.2008.08.007 https://doi.org/10.5650/JOS.56.253 https://doi.org/10.1016/J.EJPHAR.2012.11.043 https://doi.org/10.1093/CARCIN/21.10.1843
7-((2E)-3,7-Dimethylocta-2,6-Dienoxy)-6-Methoxychromen-2-One	5319406	Click to see	328.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.08.007
7-((3,7-Dimethylocta-2,6-dien-1-yl)oxy)-6-methoxy-2H-chromen-2-one	54117740	Click to see	328.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.08.007
Auraptene	1550607	Click to see	298.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.08.007 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3382769/ https://doi.org/10.1002/BIOF.5520330103 https://doi.org/10.1111/J.1349-7006.2007.00417.X https://doi.org/10.1016/J.FEBSLET.2006.08.072 https://doi.org/10.1207/S15327914NC3602_8 https://doi.org/10.1016/J.EJPHAR.2012.11.043 https://doi.org/10.3109/13880209.2012.747546 https://doi.org/10.1159/000078001
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
[(3aR,4S,6E,9S,10Z,11aR)-9-hydroxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] (Z)-2-methylbut-2-enoate	11953937	Click to see	346.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Saccharolipids
Nomilinic acid 17-O-beta-D-glucoside	5748431	Click to see	712.70	unknown	https://doi.org/10.1271/BBB1961.55.137
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones
methyl (Z)-3-[(1S,2R,4S,7S,8S,11R,12R,16S,18R)-7-(furan-3-yl)-18-hydroxy-1,8,15,15-tetramethyl-5,17-dioxo-3,6,14-trioxapentacyclo[9.7.0.02,4.02,8.012,16]octadecan-12-yl]prop-2-enoate	163194049	Click to see	500.50	unknown	https://doi.org/10.1016/0040-4020(76)87016-0
Methyl 3-[7-(furan-3-yl)-18-hydroxy-1,8,15,15-tetramethyl-5,17-dioxo-3,6,14-trioxapentacyclo[9.7.0.02,4.02,8.012,16]octadecan-12-yl]prop-2-enoate	73809975	Click to see	500.50	unknown	https://doi.org/10.1016/0040-4020(76)87016-0
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol	222284	Click to see	414.70	unknown	https://doi.org/10.1080/14786419.2010.482052 https://doi.org/10.1248/CPB.49.1356 https://doi.org/10.1002/CHIN.200324150
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	86821	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1002/CHIN.200324150 https://doi.org/10.1080/14786419.2010.482052 https://doi.org/10.1248/CPB.49.1356 https://doi.org/10.1016/0040-4020(76)87016-0
beta-Sitosterol 3-O-beta-D-galactopyranoside	296119	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	https://doi.org/10.1002/CHIN.200324150
Sitogluside	5742590	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	https://doi.org/10.1002/CHIN.200324150
Stigmast-5-en-3-ol	22012	Click to see	414.70	unknown	https://doi.org/10.1248/CPB.49.1356
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Oligopeptides
Frangufoline	11731186	Click to see	534.70	unknown	via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / Amines / Primary amines / Monoalkylamines
Ethylamine	6341	Click to see CCN	45.08	unknown	via CMAUP database
Propylamine	7852	Click to see	59.11	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
Civetone	5315941	Click to see	250.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Azolidines / Isoxazolidines / Phenylisoxazolidines
Asperidine C	145985497	Click to see	331.50	unknown	https://doi.org/10.1002/CHIN.200324150
> Organoheterocyclic compounds / Benzofurans / Flavaglines
8bH-Cyclopenta[b]benzofuran-1,8b-diol, 3a-(1,3-benzodioxol-5-yl)-1,2,3,3a-tetrahydro-6,8-dimethoxy-3-phenyl-, (1R,3S,3aR,8bS)-	10623340	Click to see	448.50	unknown	via CMAUP database
Aglafolin	393601	Click to see	492.50	unknown	via CMAUP database
methyl (1R,2R,3S,3aR,8bS)-1-acetyloxy-3a-(1,3-benzodioxol-5-yl)-8b-hydroxy-6,8-dimethoxy-3-phenyl-2,3-dihydro-1H-cyclopenta[b][1]benzofuran-2-carboxylate	10697870	Click to see CC(=O)OC1C(C(C2(C1(C3=C(O2)C=C(C=C3OC)OC)O)C4=CC5=C(C=C4)OCO5)C6=CC=CC=C6)C(=O)OC	548.50	unknown	via CMAUP database
methyl (1R,2R,3S,3aR,8bS)-1-formyloxy-8b-hydroxy-3a-(3-hydroxy-4-methoxyphenyl)-6,8-dimethoxy-3-phenyl-2,3-dihydro-1H-cyclopenta[b][1]benzofuran-2-carboxylate	10650033	Click to see	536.50	unknown	via CMAUP database
methyl (1R,2R,3S,3aR,8bS)-1,8b-dihydroxy-3a-(3-hydroxy-4-methoxyphenyl)-6,8-dimethoxy-3-phenyl-2,3-dihydro-1H-cyclopenta[b][1]benzofuran-2-carboxylate	10815498	Click to see	508.50	unknown	via CMAUP database
methyl (1R,2R,3S,3aR,8bS)-3a-(1,3-benzodioxol-5-yl)-1-formyloxy-8b-hydroxy-6,8-dimethoxy-3-phenyl-2,3-dihydro-1H-cyclopenta[b][1]benzofuran-2-carboxylate	10721063	Click to see	534.50	unknown	via CMAUP database
methyl (1R,2R,3S,3aR,8bS)-3a-(1,3-benzodioxol-5-yl)-1,8b-dihydroxy-6,8-dimethoxy-3-phenyl-2,3-dihydro-1H-cyclopenta[b][1]benzofuran-2-carboxylate	390507	Click to see	506.50	unknown	via CMAUP database
methyl (1R,2R,3S,3aR,8bS)-3a-(3,4-dimethoxyphenyl)-1,8b-dihydroxy-6,8-dimethoxy-3-phenyl-2,3-dihydro-1H-cyclopenta[b][1]benzofuran-2-carboxylate	10720804	Click to see	522.50	unknown	via CMAUP database
Methyl 1-Formyloxyrocaglate	10839697	Click to see COC1=CC=C(C=C1)C23C(C(C(C2(C4=C(O3)C=C(C=C4OC)OC)O)OC=O)C(=O)OC)C5=CC=CC=C5	520.50	unknown	via CMAUP database
Rocaglaol	393602	Click to see	434.50	unknown	via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Indoles
Indole	798	Click to see	117.15	unknown	via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Indoles / 3-alkylindoles / 3-methylindoles
Skatole	6736	Click to see	131.17	unknown	via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Acridines / Acridones
(2R)-4,9-dihydroxy-2-(2-hydroxypropan-2-yl)-10-methyl-11-(3-methylbut-2-enyl)-2,3-dihydrofuro[3,2-b]acridin-5-one	162955487	Click to see CC(=CCC1=C2C(=C(C3=C1N(C4=C(C3=O)C=CC=C4O)C)O)CC(O2)C(C)(C)O)C	409.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.08.007
(2R)-4,9-dihydroxy-2-(2-hydroxypropan-2-yl)-11-(3-methylbut-2-enyl)-3,10-dihydro-2H-furo[3,2-b]acridin-5-one	163190599	Click to see CC(=CCC1=C2C(=C(C3=C1NC4=C(C3=O)C=CC=C4O)O)CC(O2)C(C)(C)O)C	395.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.08.007
(2S)-4,9-dihydroxy-2-(2-hydroxypropan-2-yl)-10-methyl-11-(3-methylbut-2-enyl)-2,3-dihydrofuro[3,2-b]acridin-5-one	162955486	Click to see	409.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.08.007
(2S)-4,9-dihydroxy-2-(2-hydroxypropan-2-yl)-11-(3-methylbut-2-enyl)-3,10-dihydro-2H-furo[3,2-b]acridin-5-one	163098498	Click to see	395.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.08.007
1,5-Dihydroxy-3,4-dimethoxy-10-methyl-9(10H)-acridinone	5487772	Click to see	301.29	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.08.007
17-Hydroxy-4,4,10,10,15-pentamethyl-3,9-dioxa-15-azapentacyclo[12.8.0.02,7.08,13.016,21]docosa-1,7,13,16(21),17,19-hexaen-22-one	21769026	Click to see	393.50	unknown	https://doi.org/10.1021/JO00984A029
4,9-Dihydroxy-2-(2-hydroxypropan-2-yl)-10-methyl-11-(3-methylbut-2-enyl)-2,3-dihydrofuro[3,2-b]acridin-5-one	25172232	Click to see	409.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.08.007
4,9-dihydroxy-2-(2-hydroxypropan-2-yl)-11-(3-methylbut-2-enyl)-3,10-dihydro-2H-furo[3,2-b]acridin-5-one	10810695	Click to see	395.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.08.007
5,10-dihydroxy-2,2-dimethyl-12-(3-methylbut-2-enyl)-11H-pyrano[3,2-b]acridin-6-one	25172231	Click to see	377.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.08.007
5,10-dihydroxy-2,2-dimethyl-12-(3-methylbut-2-enyl)-4,11-dihydro-3H-pyrano[3,2-b]acridin-6-one	163011333	Click to see CC(=CCC1=C2C(=C(C3=C1NC4=C(C3=O)C=CC=C4O)O)CCC(O2)(C)C)C	379.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.08.007
5,10-Dihydroxy-2,2,11-trimethyl-12-(3-methylbut-2-enyl)-3,4-dihydropyrano[3,2-b]acridin-6-one	162911236	Click to see	393.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.08.007
7H-Pyrano[2,3-c]acridin-7-one, 3,12-dihydro-6,11-dihydroxy-3,3,12-trimethyl-5-(3-methyl-2-butenyl)-	633176	Click to see CC(=CCC1=C2C(=C3C(=C1O)C(=O)C4=C(N3C)C(=CC=C4)O)C=CC(O2)(C)C)C	391.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.08.007
Atalaphillinine	122681	Click to see	377.40	unknown	https://doi.org/10.1016/0031-9422(75)83060-3
Atalaphylline	442887	Click to see CC(=CCC1=C2C(=C(C(=C1O)CC=C(C)C)O)C(=O)C3=C(N2)C(=CC=C3)O)C	379.40	unknown	https://doi.org/10.1016/S0040-4020(01)92869-8
Buxifoliadine A	10740165	Click to see	407.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.08.007
Junosine	15286413	Click to see	325.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.08.007
N-Methylatalaphylline	15286416	Click to see	393.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.08.007 https://doi.org/10.1016/S0040-4020(01)92869-8
Yukocitrine	15286417	Click to see	323.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.08.007
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
4-Methoxyfuro[2,3-b]quinolin-5-ol	162880899	Click to see	215.20	unknown	https://doi.org/10.1080/14786419.2010.482052
> Organoheterocyclic compounds / Tetrapyrroles and derivatives
Pyropheophorbide a	161456	Click to see CCC1=C(C2=NC1=CC3=C(C4=C(CC(=C5C(C(C(=CC6=NC(=C2)C(=C6C)C=C)N5)C)CCC(=O)O)C4=N3)O)C)C	534.60	unknown	https://doi.org/10.1248/CPB.44.1415
> Organoheterocyclic compounds / Tetrapyrroles and derivatives / Chlorins
3-[(21S,22S)-16-ethenyl-11-ethyl-12,17,21,26-tetramethyl-4-oxo-7,23,24,25-tetrazahexacyclo[18.2.1.15,8.110,13.115,18.02,6]hexacosa-1(23),2(6),5(26),7,9,11,13,15,17,19-decaen-22-yl]propanoic acid	5489042	Click to see CCC1=C(C2=CC3=C(C(=C(N3)C=C4C(C(C(=N4)C5=C6C(=C(C(=N6)C=C1N2)C)C(=O)C5)CCC(=O)O)C)C)C=C)C	534.60	unknown	https://doi.org/10.1248/CPB.44.1415
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid amides
Dasyclamide	10980024	Click to see	316.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
Scoparone	8417	Click to see	206.19	unknown	https://doi.org/10.1248/CPB.49.1356
Suberosin	68486	Click to see CC(=CCC1=C(C=C2C(=C1)C=CC(=O)O2)OC)C	244.28	unknown	https://doi.org/10.1002/CHIN.200324150
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin	5280460	Click to see	192.17	unknown	https://doi.org/10.1248/CPB.49.1356
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
Seselin	68229	Click to see	228.24	unknown	https://doi.org/10.1002/CHIN.200324150
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Linear pyranocoumarins
Xanthyletin	65188	Click to see	228.24	unknown	https://doi.org/10.1002/CHIN.200324150
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Natsudaidain	3084605	Click to see	418.40	unknown	https://doi.org/10.1002/JCCS.199800015 https://doi.org/10.1248/BPB.17.1519
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
3,6-Diglucopyranosyl-5,7-dihydroxy-4'-methoxyflavone	74977543	Click to see	608.50	unknown	https://doi.org/10.1080/00021369.1985.10866832 https://doi.org/10.1080/00021369.1985.10858531
4H-1-Benzopyran-4-one, 3,6-di-C-beta-D-glucopyranosyl-5,7-dihydroxy-2-(4-methoxyphenyl)-	102147888	Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)C5C(C(C(C(O5)CO)O)O)O	608.50	unknown	https://doi.org/10.1080/00021369.1985.10866832 https://doi.org/10.1080/00021369.1985.10858531
Isomargaritene	74977542	Click to see	592.50	unknown	https://doi.org/10.1080/00021369.1985.10866832 https://doi.org/10.1016/S0031-9422(01)00132-7 https://doi.org/10.1080/00021369.1985.10858531 https://doi.org/10.1034/J.1399-3054.2001.1110215.X
Semiaquilinoside	101675233	Click to see	592.50	unknown	https://doi.org/10.1080/00021369.1985.10866832 https://doi.org/10.1016/S0031-9422(01)00132-7 https://doi.org/10.1080/00021369.1985.10858531 https://doi.org/10.1034/J.1399-3054.2001.1110215.X
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
8-(2-O-(6-Deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranosyl)-5,7-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-4H-1-benzopyran-4-one	102147929	Click to see	608.50	unknown	https://doi.org/10.1080/00021369.1985.10866832 https://doi.org/10.1080/00021369.1985.10858531
acacetin-8-C-neohesperidoside	70698254	Click to see	592.50	unknown	https://doi.org/10.1080/00021369.1985.10866832 https://doi.org/10.1016/S0031-9422(01)00132-7 https://doi.org/10.1080/00021369.1985.10858531 https://doi.org/10.1034/J.1399-3054.2001.1110215.X
Apigenin-8-C-glucoside-2'-rhamnoside	5874704	Click to see	578.50	unknown	https://doi.org/10.1080/00021369.1985.10858531 https://doi.org/10.1080/00021369.1985.10866832
Diosmetin 8-C-(2''-rhamnosylglucoside)	74977719	Click to see	608.50	unknown	https://doi.org/10.1080/00021369.1985.10866832 https://doi.org/10.1080/00021369.1985.10858531
Margaritene	45360149	Click to see	592.50	unknown	https://doi.org/10.1080/00021369.1985.10866832 https://doi.org/10.1016/S0031-9422(01)00132-7 https://doi.org/10.1080/00021369.1985.10858531 https://doi.org/10.1034/J.1399-3054.2001.1110215.X
Orientin 2''-O-rhamnoside	21721997	Click to see	594.50	unknown	https://doi.org/10.1080/00021369.1985.10866832 https://doi.org/10.1080/00021369.1985.10858531
Orientin 2''-rhamnoside	73829968	Click to see	594.50	unknown	https://doi.org/10.1080/00021369.1985.10866832 https://doi.org/10.1080/00021369.1985.10858531
Vicenin 2	3084407	Click to see	594.50	unknown	https://doi.org/10.1080/00021369.1985.10858531 https://doi.org/10.1080/00021369.1985.10866832
Vicenin 2	442664	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C(=C3O2)C4C(C(C(C(O4)CO)O)O)O)O)C5C(C(C(C(O5)CO)O)O)O)O)O	594.50	unknown	https://doi.org/10.1080/00021369.1985.10858531 https://doi.org/10.1080/00021369.1985.10866832
Vitexin 2''-O-rhamnoside	5282151	Click to see	578.50	unknown	https://doi.org/10.1080/00021369.1985.10858531 https://doi.org/10.1080/00021369.1985.10866832
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
4H-1-Benzopyran-4-one, 3-(beta-D-glucopyranosyloxy)-5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-6,8-dimethoxy-	5319025	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC4C(C(C(C(O4)CO)O)O)O)O	538.50	unknown	https://doi.org/10.1016/S0040-4020(01)97619-7
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
5-Hydroxy-2-(4-methoxyphenyl)-7-(3,4,5-trihydroxy-6-((3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl)oxan-2-yl)oxychromen-4-one	5480901	Click to see	592.50	unknown	via CMAUP database
Acacetin-7-O-neohesperidoside	15559329	Click to see	592.50	unknown	https://doi.org/10.1016/S0031-9422(01)00132-7 https://doi.org/10.1034/J.1399-3054.2001.1110215.X
Fortunellin	5317385	Click to see	592.50	unknown	https://doi.org/10.1016/S0031-9422(01)00132-7 https://doi.org/10.1034/J.1399-3054.2001.1110215.X
Naringin	442428	Click to see	580.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
2-(3,4-Dimethoxyphenyl)-7-hydroxy-5,6-dimethoxychromen-4-one	5491643	Click to see	358.30	unknown	https://doi.org/10.1248/CPB.49.1356
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(2S)-2-(3,4-dimethoxyphenyl)-8-hydroxy-5,6,7-trimethoxy-2,3-dihydrochromen-4-one	162911047	Click to see	390.40	unknown	https://doi.org/10.1016/0040-4020(61)80014-8
(2S)-5,6,7,3',4'-Pentamethoxyflavanone	10937632	Click to see	374.40	unknown	https://doi.org/10.1248/CPB.49.1356
2-(3,4-Dimethoxyphenyl)-2,3-dihydro-5,7-dimethoxy-4H-1-benzopyran-4-one	167616	Click to see	344.40	unknown	https://doi.org/10.1248/CPB.39.945
2-(3,4-Dimethoxyphenyl)-8-hydroxy-5,6,7-trimethoxy-2,3-dihydrochromen-4-one	162911046	Click to see	390.40	unknown	https://doi.org/10.1016/0040-4020(61)80014-8
3',4',5,6,7-Pentamethoxyflavanone	12405140	Click to see COC1=C(C=C(C=C1)C2CC(=O)C3=C(C(=C(C=C3O2)OC)OC)OC)OC	374.40	unknown	https://doi.org/10.1248/CPB.49.1356
5-Hydroxy-6,7,3',4'-Tetramethoxyflavone	152430	Click to see	358.30	unknown	https://doi.org/10.1248/CPB.49.1356
5,6,7,4'-Tetramethoxyflavone	96118	Click to see	342.30	unknown	https://doi.org/10.1248/CPB.49.1356
5,7,3',4'-Tetramethoxyflavone	631170	Click to see	342.30	unknown	https://doi.org/10.1248/CPB.39.945
Apigenin trimethyl ether	79730	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C=C3OC)OC	312.30	unknown	https://doi.org/10.1248/CPB.39.945
Hexamethylquercetagetin	386331	Click to see	402.40	unknown	https://doi.org/10.1248/CPB.49.1356
Sinensetin	145659	Click to see	372.40	unknown	https://doi.org/10.1016/J.BMC.2008.11.039 https://doi.org/10.1248/CPB.35.3025 https://doi.org/10.1248/CPB.49.1356
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
(2R)-2-(3,4-dimethoxyphenyl)-5-hydroxy-6,7,8-trimethoxy-2,3-dihydrochromen-4-one	162971673	Click to see	390.40	unknown	https://doi.org/10.1016/0040-4020(61)80014-8
(2S)-2-(3,4-dimethoxyphenyl)-5-hydroxy-6,7,8-trimethoxy-2,3-dihydrochromen-4-one	101140693	Click to see COC1=C(C=C(C=C1)C2CC(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)OC	390.40	unknown	https://doi.org/10.1248/CPB.49.1356
(2S)-2-(3,4-dimethoxyphenyl)-5,6,7,8-tetramethoxy-2,3-dihydrochromen-4-one	163080067	Click to see	404.40	unknown	https://doi.org/10.1016/0040-4020(61)80014-8
(2S)-5,6,7,8,4'-Pentamethoxyflavanone	10992374	Click to see	374.40	unknown	https://doi.org/10.1248/CPB.49.1356
2-(3,4-Dimethoxyphenyl)-7-hydroxy-5,6,8-trimethoxy-4H-1-benzopyran-4-one	10452846	Click to see	388.40	unknown	https://doi.org/10.1248/CPB.49.1356
3,5,6,7,8,3',4'-Heptamethoxyflavone	150893	Click to see	432.40	unknown	https://doi.org/10.1248/CPB.49.1356 https://doi.org/10.1016/J.BMC.2008.11.039 https://doi.org/10.1021/JF801103P
3'-Demethylnobiletin	183466	Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C(=C3OC)OC)OC)OC)O	388.40	unknown	https://doi.org/10.1248/CPB.49.1356
5-Demethylnobiletin	358832	Click to see	388.40	unknown	https://doi.org/10.1016/J.BMC.2008.11.039 https://doi.org/10.1248/CPB.49.1356 https://doi.org/10.1021/JF000100O
5-Hydroxy-6,7,8,3',4'-pentamethoxyflavanone	15625549	Click to see	390.40	unknown	https://doi.org/10.1016/0040-4020(61)80014-8
5,6,7,8-Tetramethoxy-2-(4-methoxyphenyl)chroman-4-one	462698	Click to see COC1=CC=C(C=C1)C2CC(=O)C3=C(O2)C(=C(C(=C3OC)OC)OC)OC	374.40	unknown	https://doi.org/10.1248/CPB.49.1356
6-Demethoxytangeretin	629964	Click to see	342.30	unknown	https://doi.org/10.1248/CPB.49.1356
Citromitin	12303287	Click to see	404.40	unknown	https://doi.org/10.1016/0040-4020(61)80014-8
Gardenin B	96539	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O	358.30	unknown	https://doi.org/10.1248/CPB.49.1356
Isosinensetin	632135	Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3OC)OC)OC)OC	372.40	unknown	https://doi.org/10.1248/CPB.39.945 https://doi.org/10.1248/CPB.49.1356 https://doi.org/10.1016/J.BMC.2008.11.039 https://doi.org/10.1016/0031-9422(75)85074-6
Nobiletin	72344	Click to see	402.40	unknown	https://doi.org/10.1016/0031-9422(75)85074-6 https://doi.org/10.1016/J.BMC.2008.11.039 https://doi.org/10.1248/CPB.35.3025 https://doi.org/10.1248/CPB.49.1356
Tangeretin	68077	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C(=C3OC)OC)OC)OC	372.40	unknown	https://doi.org/10.1016/0031-9422(75)85074-6 https://doi.org/10.1021/NP3003468 https://doi.org/10.1016/J.BMC.2008.11.039 https://doi.org/10.1248/CPB.35.3025 https://doi.org/10.1248/CPB.49.1356
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
Carpachromene	10449654	Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C=C(O3)C4=CC=C(C=C4)O)C	336.30	unknown	https://doi.org/10.1016/0040-4020(76)87016-0
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
Phloretin + C-Hex, C-Hex	74819290	Click to see	598.50	unknown	https://doi.org/10.1016/S0031-9422(01)00132-7 https://doi.org/10.1034/J.1399-3054.2001.1110215.X
Phloretin 3',5'-Di-C-glucoside	10908130	Click to see	598.50	unknown	https://doi.org/10.1016/S0031-9422(01)00132-7 https://doi.org/10.1034/J.1399-3054.2001.1110215.X
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
2'-Hydroxy-3,3',4,4',5',6'-hexamethoxy-chalcone	24752964	Click to see COC1=C(C=C(C=C1)C=CC(=O)C2=C(C(=C(C(=C2OC)OC)OC)OC)O)OC	404.40	unknown	https://doi.org/10.1248/CPB.49.1356
2'-Hydroxy-3',4',5',6',3,4-hexamethoxy chalcone	129695789	Click to see	404.40	unknown	https://doi.org/10.1248/CPB.49.1356
2'-Hydroxy-3',4',6',3,4-pentamethoxychalcone	10992375	Click to see COC1=C(C=C(C=C1)C=CC(=O)C2=C(C(=C(C=C2OC)OC)OC)O)OC	374.40	unknown	https://doi.org/10.1248/CPB.49.1356
2'-Hydroxy-4,4',5',6'-tetramethoxychalcone	6253276	Click to see	344.40	unknown	https://doi.org/10.1248/CPB.49.1356
3-(3,4-Dimethoxyphenyl)-1-(2-hydroxy-3,4,6-trimethoxyphenyl)prop-2-en-1-one	85358721	Click to see	374.40	unknown	https://doi.org/10.1248/CPB.49.1356
6-hydroxy-1-(4-methoxycinnamoyl)-2,3,4-Trimethoxy-benzene	321348	Click to see	344.40	unknown	https://doi.org/10.1248/CPB.49.1356

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Citrus japonica

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