Scientific name	Authority	First published in
Rhus osbeckii	Steud.	Nomencl. Bot. [Steudel], ed. 2. 2: 452. 1841
Rhus japonica	Buch.-Ham. ex D.Don	Prodr. Fl. Nepal. : 248 (1825)
Rhus simonii	Carrière	Rev. Hort. (Paris) 37: 339 (1866)
Rhus semialata	Murray	Commentat. Soc. Regiae Sci. Gott. 6: 27 (1784)
Rhus javanica var. chinensis	(Mill.) T.Yamaz.	J. Jap. Bot. 68: 240 (1993)
Toxicodendron semialatum	Kuntze	Revis. Gen. Pl. 1: 154 (1891)
Schinus indicus	Burm.f.	Fl. Indica : 215 (1768)
Rhus semialata var. osbeckii	DC.	Prodr. 2: 67 1825
Rhus semialata	Brandis	For. Fl. Brit. Ind. 119 1874

Common names Top

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Filter by language:

Language	Common/alternative name
English	chinese sumac
Arabic	سماق صيني
Assamese	নগা টেঙা
Persian	راس چینی
Upper Sorbian	chinski sumak
Japanese	カツノキ
Japanese	カチノキ
Japanese	エンブシ
Japanese	ゴバイシ
Japanese	フシノキ
Japanese	五倍子
Japanese	ヌルデ
Japanese	白膠木
Japanese	塩麩子
Japanese	付子の木
Korean	붉나무
Norwegian Bokmål	kinesisk sumak
Nepali	भक्मिलो
Nepali	भकिमिलो
Russian	Сумах китайский
szy	belus
Thai	ส้มผด
Chinese	酸酱头
Chinese	角倍
Chinese	肤杨树
Chinese	山鹽菁
Chinese	鹽膚木
Chinese	一种维管植物
Chinese	乌桃叶
Chinese	盐肤木
Chinese	盐酸树
Chinese	五倍子苗
Chinese	地耳草(田基黄）
Chinese	滨盐肤木(盐肤木）
Chinese	盐肤叶
Chinese	盐肤子
Chinese	盐肤木根
Chinese	盐肤木根皮
Chinese	盐肤木皮
Chinese	盐肤木花
Chinese	盐芙木
Chinese	盐霜柏
Chinese	盐麸木
Chinese	五倍子
Chinese	乌烟桃
Chinese	乌盐泡
Chinese	乌酸桃
Chinese	五倍子树
Chinese	五倍柴
Chinese	倍子柴
Chinese	土椿树
Chinese	山梧桐
Chinese	木五倍子
Chinese	盐树根
Chinese	盐酸白
Chinese	红叶桃
Chinese	红盐果

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Name	Authority	First published in
Rhus chinensis var. roxburghii	(DC.) Rehder	J. Arnold Arbor. 20: 416. 1939 (1939)

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

Asia-temperate click to expand
- China
  - China North-central
  - China South-central
  - China Southeast
  - Hainan
  - Tibet
- Eastern Asia
  - Japan
  - Korea
  - Nansei-shoto
  - Taiwan
- Western Asia
  - Turkey

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
  - East Himalaya
  - India
  - Nepal
  - Pakistan
  - West Himalaya
- Indo-China
  - Cambodia
  - Laos
  - Myanmar
  - Thailand
  - Vietnam
- Malesia
  - Sumatera

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000402760
UNII	J6BED8187F
USDA Plants	RHCH9
Tropicos	1300863
Flora of Italy	8592
KEW	urn:lsid:ipni.org:names:70452-1
The Plant List	kew-2422836
Missouri Botanical Garden	275959
PaleoBotany	82452
Open Tree Of Life	931763
NCBI Taxonomy	289753
IUCN Red List	135819132
IPNI	70452-1
iNaturalist	472886
GBIF	3190553
Freebase	/m/0dll529
EPPO	RHUCH
EOL	483507
USDA GRIN	31679
Wikipedia	Rhus_chinensis
CMAUP	NPO14827

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

Identification and functional analysis of the LEAFY gene in longan flower induction

Jue D, Li Z, Zhang W, Tang J, Xie T, Sang X, Guo Q

BMC Genomics

25-Mar-2024

PMCID:	PMC10962150
doi:	10.1186/s12864-024-10229-x
PMID:	38528464

Plant-Derived Substances for Prevention of Necrotising Enterocolitis: A Systematic Review of Animal Studies

Mackay CA, Rath C, Rao S, Patole S

Nutrients

14-Mar-2024

PMCID:	PMC10975714
doi:	10.3390/nu16060832
PMID:	38542743

Soil carbon emissions and influential factors across various stages of vegetation succession in vegetated concrete

Xu Y, Luo T, Wu B, Xia Z, Xu W, Gao J

Sci Rep

12-Mar-2024

PMCID:	PMC10933349
doi:	10.1038/s41598-024-56473-9
PMID:	38472340

Conductivity-Based Gas Sensors Using Tamarindus indica Polysaccharide-Capped Gold Nanoparticles for the Detection of Volatile Gases

Selvanayakam S, Esakkidurai SP, Kalaiyar S

ACS Omega

24-Feb-2024

PMCID:	PMC10918775
doi:	10.1021/acsomega.3c09137
PMID:	38463309

Ethnobotanical study of medicinal plants used by the Yi people in Mile, Yunnan, China

Li H, Huang C, Li Y, Wang P, Sun J, Bi Z, Xia S, Xiong Y, Bai X, Huang X

J Ethnobiol Ethnomed

23-Feb-2024

PMCID:	PMC10893717
doi:	10.1186/s13002-024-00656-1
PMID:	38395900

From Plant to Chemistry: Sources of Antinociceptive Non-Opioid Active Principles for Medicinal Chemistry and Drug Design

Turnaturi R, Piana S, Spoto S, Costanzo G, Reina L, Pasquinucci L, Parenti C

Molecules

09-Feb-2024

PMCID:	PMC10892999
doi:	10.3390/molecules29040815
PMID:	38398566

Uncovering floral composition of paper wasp nests (Hymenoptera: Vespidae: Polistes) through DNA metabarcoding

Mohamadzade Namin S, Son M, Jung C

Sci Rep

03-Feb-2024

PMCID:	PMC10838270
doi:	10.1038/s41598-024-52834-6
PMID:	38310136

Ultra-High-Performance Liquid Chromatography–Electrospray Ionization–High-Resolution Mass Spectrometry for Distinguishing the Origin of Ellagic Acid Extracts: Pomegranate Peels or Gallnuts

Wei J, Xu R, Zhang Y, Zhao L, Li S, Zhao Z

Molecules

31-Jan-2024

PMCID:	PMC10856690
doi:	10.3390/molecules29030666
PMID:	38338410

Partial Correspondence between Host Plant-Related Differentiation and Symbiotic Bacterial Community in a Polyphagous Insect

Cheng Z, Liu Q, Huang X

Animals (Basel)

16-Jan-2024

PMCID:	PMC10812459
doi:	10.3390/ani14020283
PMID:	38254452

Update of Natural Products and Their Derivatives Targeting Epstein–Barr Infection

Pennisi R, Trischitta P, Costa M, Venuti A, Tamburello MP, Sciortino MT

Viruses

15-Jan-2024

PMCID:	PMC10818872
doi:	10.3390/v16010124
PMID:	38257824

Chinese Sumac (Rhus chinensis Mill.) Fruits Prevent Hyperuricemia and Uric Acid Nephropathy in Mice Fed a High-Purine Yeast Diet

Ma N, Cai S, Sun Y, Chu C

Nutrients

05-Jan-2024

PMCID:	PMC10819650
doi:	10.3390/nu16020184
PMID:	38257077

A chromosome-level genome assembly of the Rhus gall aphid Schlechtendalia chinensis provides insight into the endogenization of Parvovirus-like DNA sequences

Ahmad A, von Dohlen C, Ren Z

BMC Genomics

02-Jan-2024

PMCID:	PMC10759679
doi:	10.1186/s12864-023-09916-y
PMID:	38166596

Chemical Fingerprint Analysis and Content Determination of Horned Gallnut and Bellied Gallnut in Galla Chinensis

Long X, Guo S, Gu J, Zhang L, Liu H, Fan Y, Wen W

Int J Anal Chem

31-Dec-2023

PMCID:	PMC10771921
doi:	10.1155/2023/8849341
PMID:	38188368

The genus Rachicladosporium: introducing new species from sooty mould communities and excluding cold adapted species

Piątek M, Stryjak-Bogacka M, Czachura P, Owczarek-Kościelniak M

Sci Rep

21-Dec-2023

PMCID:	PMC10739867
doi:	10.1038/s41598-023-49696-9
PMID:	38129458

Effects of natural products on polycystic ovary syndrome: From traditional medicine to modern drug discovery

Jung W, Choi H, Kim J, Kim J, Kim W, Nurkolis F, Kim B

Heliyon

11-Oct-2023

PMCID:	PMC10589870
doi:	10.1016/j.heliyon.2023.e20889
PMID:	37867816

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
Methyl 2,4,6-trihydroxybenzoate	76600	Click to see COC(=O)C1=C(C=C(C=C1O)O)O	184.15	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
3,4,5-Trihydroxybenzoate	54675821	Click to see C1=C(C=C(C(=C1O)[O-])O)C(=O)O	169.11	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid	370	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)O	170.12	unknown	https://doi.org/10.1007/S10600-015-1336-2 https://doi.org/10.1248/CPB.55.804
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
Ethyl gallate	13250	Click to see CCOC(=O)C1=CC(=C(C(=C1)O)O)O	198.17	unknown	https://doi.org/10.1007/S10600-015-1336-2
Methyl gallate	7428	Click to see COC(=O)C1=CC(=C(C(=C1)O)O)O	184.15	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Salicylic acid and derivatives / Salicylic acids
Anacardic acid	167551	Click to see CCCCCCCCCCCCCCCC1=C(C(=CC=C1)O)C(=O)O	348.50	unknown	https://doi.org/10.1002/PTR.2650010307 https://doi.org/10.1055/S-2006-960083
> Benzenoids / Phenols / Methoxyphenols
Vanillin	1183	Click to see COC1=C(C=CC(=C1)C=O)O	152.15	unknown	https://doi.org/10.1248/CPB.55.804
> Lignans, neolignans and related compounds / Aryltetralin lignans
Rhusemialin A	16724385	Click to see COC1=CC(=CC(=C1O)OC)C2C(C(CC3=CC(=C(C(=C23)OC)O)OC)CO)COC(=O)C=CC4=CC(=C(C=C4)O)O	582.60	unknown	https://doi.org/10.1248/CPB.55.804
> Lignans, neolignans and related compounds / Lignan glycosides
[(2R,3S,4S,5R,6S)-4,5-dihydroxy-6-[[(6R,7R,8S)-8-(4-hydroxy-3,5-dimethoxyphenyl)-6,7-bis(hydroxymethyl)-1,3-dimethoxy-5,6,7,8-tetrahydronaphthalen-2-yl]oxy]-3-[(E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxyoxan-2-yl]methyl (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate	163042029	Click to see COC1=CC(=CC(=C1O)OC)C2C(C(CC3=CC(=C(C(=C23)OC)OC4C(C(C(C(O4)COC(=O)C=CC5=CC(=C(C=C5)O)OC)OC(=O)C=CC6=CC(=C(C=C6)O)OC)O)O)OC)CO)CO	934.90	unknown	https://doi.org/10.1248/CPB.55.804
Rhusemialin B	16724500	Click to see COC1=CC(=CC(=C1O)OC)C2C(C(CC3=CC(=C(C(=C23)OC)OC4C(C(C(C(O4)COC(=O)C=CC5=CC(=C(C=C5)O)OC)O)O)O)OC)CO)CO	758.80	unknown	https://doi.org/10.1248/CPB.55.804
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
5-Hydroxy-3-propan-2-ylidene-7-(3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraenyl)-1-benzofuran-2-one	73298903	Click to see CC(=CCCC(=CCCC(=CCCC(=CCC1=C2C(=CC(=C1)O)C(=C(C)C)C(=O)O2)C)C)C)C	462.70	unknown	https://doi.org/10.1055/S-2007-967113
5-Hydroxy-7-(3,7,11,15-tetramethyl-2,6,10,14-hexadecatetraenyl)-2(3h)-benzofuranone	16728597	Click to see CC(=CCCC(=CCCC(=CCCC(=CCC1=CC(=CC2=C1OC(=O)C2)O)C)C)C)C	422.60	unknown	https://doi.org/10.1055/S-2007-967113
5-hydroxy-7-(3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraenyl)-3H-1-benzofuran-2-one	73313070	Click to see CC(=CCCC(=CCCC(=CCCC(=CCC1=CC(=CC2=C1OC(=O)C2)O)C)C)C)C	422.60	unknown	https://doi.org/10.1055/S-2007-967113
Rhuscholide A	16655065	Click to see CC(=CCCC(=CCCC(=CCCC(=CCC1=C2C(=CC(=C1)O)C(=C(C)C)C(=O)O2)C)C)C)C	462.70	unknown	https://doi.org/10.1055/S-2007-967113
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(2E)-6-[(1S,2S,5R,6S,9R,10R,13R,15S)-15-hydroxy-9,10,14,14-tetramethyl-16-oxapentacyclo[13.2.2.01,13.02,10.05,9]nonadecan-6-yl]-2-methylhepta-2,6-dienoic acid	163000018	Click to see CC(=CCCC(=C)C1CCC2(C1CCC3C2(CCC4C35CCC(C4(C)C)(OC5)O)C)C)C(=O)O	470.70	unknown	https://doi.org/10.1016/0031-9422(91)83667-A
(4aS,6aR,6aR,6bR,8R,8aR,12aR,14aS)-8-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-10-oxo-4,5,6,6a,7,8,8a,11,12,13,14,14a-dodecahydro-3H-picene-4a-carboxylic acid	162961980	Click to see CC1(CCC2(CCC3(C(C2=C1)CCC4C3(CC(C5C4(CCC(=O)C5(C)C)C)O)C)C)C(=O)O)C	470.70	unknown	https://doi.org/10.1055/S-2007-967113
2,2,6a,6b,9,9,12a-heptamethyl-10-oxo-4,5,6,6a,7,8,8a,11,12,13,14,14a-dodecahydro-3H-picene-4a-carboxylic acid	14345396	Click to see CC1(CCC2(CCC3(C(C2=C1)CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C)C(=O)O)C	454.70	unknown	https://doi.org/10.1055/S-2007-967113
3-Oxolup-20(29)-en-28-oic acid	289985	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C(=O)O	454.70	unknown	https://doi.org/10.1055/S-2007-967113
6-(15-Hydroxy-9,10,14,14-tetramethyl-16-oxapentacyclo[13.2.2.01,13.02,10.05,9]nonadecan-6-yl)-2-methylhepta-2,6-dienoic acid	163000014	Click to see CC(=CCCC(=C)C1CCC2(C1CCC3C2(CCC4C35CCC(C4(C)C)(OC5)O)C)C)C(=O)O	470.70	unknown	https://doi.org/10.1016/0031-9422(91)83667-A
6beta-Hydroxy-3-oxo-12-oleanen-28-oic acid	73313071	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CC(C5C4(CCC(=O)C5(C)C)C)O)C)C2C1)C)C(=O)O)C	470.70	unknown	https://doi.org/10.1055/S-2007-967113
6beta-Hydroxy-3-oxooleana-12-ene-28-oic acid	44593478	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CC(C5C4(CCC(=O)C5(C)C)C)O)C)C2C1)C)C(=O)O)C	470.70	unknown	https://doi.org/10.1055/S-2007-967113
8-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-10-oxo-4,5,6,6a,7,8,8a,11,12,13,14,14a-dodecahydro-3H-picene-4a-carboxylic acid	73313072	Click to see CC1(CCC2(CCC3(C(C2=C1)CCC4C3(CC(C5C4(CCC(=O)C5(C)C)C)O)C)C)C(=O)O)C	470.70	unknown	https://doi.org/10.1055/S-2007-967113
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/10.1055/S-2007-967113
Betulonic acid	122844	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C(=O)O	454.70	unknown	https://doi.org/10.1055/S-2007-967113
Lup-20(29)-ene-3beta,28-diol	221023	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/10.1055/S-2007-967113
Moronic acid	489941	Click to see CC1(CCC2(CCC3(C(C2=C1)CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C)C(=O)O)C	454.70	unknown	https://doi.org/10.1055/S-2007-967113
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(2S,3R,4S,5S,6R)-2-[[(1R,2S,4S,5S,6R)-2-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-(5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl)oxyoxan-3-yl]oxy-4-methyl-3,7,8-trioxabicyclo[4.2.0]octan-5-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	11968844	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)OC8C9C(C(C(O8)C)OC2C(C(C(C(O2)CO)O)O)O)OO9)C)C)C)OC1	885.00	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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/10.1007/S10600-015-1336-2 https://doi.org/10.1016/0031-9422(91)83667-A
24-Ethylcholest-5-en-3beta-ol	22012	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1016/0031-9422(91)83667-A https://doi.org/10.1007/S10600-015-1336-2
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Shikimic acids and derivatves
3,4,5-Trihydroxy-1-cyclohexene-1-carboxylic acid	1094	Click to see C1C(C(C(C=C1C(=O)O)O)O)O	174.15	unknown	https://doi.org/10.1248/CPB.14.877
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Sucrose	5988	Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O	342.30	unknown	https://doi.org/10.1248/CPB.14.877
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
(2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanal	107526	Click to see C(C(C(C(C(C=O)O)O)O)O)O	180.16	unknown	https://doi.org/10.1248/CPB.14.877
D-Glucose	5793	Click to see C(C1C(C(C(C(O1)O)O)O)O)O	180.16	unknown	https://doi.org/10.1248/CPB.14.877
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
3-Galloyl-gallic acid	87339261	Click to see C1C(=CC(=C(C1(C(=O)C2=CC(=C(C(=C2)O)O)O)O)O)O)C(=O)O	324.24	unknown	https://doi.org/10.1055/S-2008-1081300
p-Digallussaure	129628530	Click to see C1=C(C=C(C(C1O)(C(=O)C2=CC(=C(C(=C2)O)O)O)O)O)C(=O)O	324.24	unknown	https://doi.org/10.1055/S-2008-1081300
> Organoheterocyclic compounds / Azolidines / Imidazolidines / Hydantoins
parazoanthine A	44482058	Click to see C1=CC(=CC=C1C=CN2C(=O)C(NC2=O)CCCN=C(N)N)O	317.34	unknown	https://doi.org/10.1016/S0031-9422(99)00399-4
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans
Riccionidin A	441775	Click to see C1=C2C=C3C(=C4C(=CC(=CC4=[OH+])O)O3)OC2=CC(=C1O)O	285.23	unknown	https://doi.org/10.1016/S0031-9422(99)00399-4
> Organoheterocyclic compounds / Naphthopyrans
(1S,2S,5S,11S,14R,15R,18R,20S)-20-hydroxy-8,8,14,15,19,19-hexamethyl-21-oxahexacyclo[18.2.2.01,18.02,15.05,14.06,11]tetracos-6-ene-11-carboxylic acid	21669113	Click to see CC1(CCC2(CCC3(C(C2=C1)CCC4C3(CCC5C46CCC(C5(C)C)(OC6)O)C)C)C(=O)O)C	470.70	unknown	https://doi.org/10.1016/0031-9422(91)83667-A
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Methyl ferulate	5357283	Click to see COC1=C(C=CC(=C1)C=CC(=O)OC)O	208.21	unknown	https://doi.org/10.1248/CPB.55.804
> 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	https://doi.org/10.1007/S10600-015-1336-2
> Phenylpropanoids and polyketides / Depsides and depsidones
Digallic acid	341	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2=CC(=CC(=C2O)O)C(=O)O	322.22	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
(3S,4S,5R,6R)-3,4,5,6-tetrahydroxy-6-(hydroxymethyl)-3,4,5-tris(3,4,5-trihydroxybenzoyl)-1,7-bis(3,4,5-trihydroxyphenyl)heptane-1,2,7-trione	129641892	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)C(=O)C(C(=O)C2=CC(=C(C(=C2)O)O)O)(C(C(=O)C3=CC(=C(C(=C3)O)O)O)(C(C(=O)C4=CC(=C(C(=C4)O)O)O)(C(CO)(C(=O)C5=CC(=C(C(=C5)O)O)O)O)O)O)O	940.70	unknown	https://doi.org/10.1021/NP50040A016 https://doi.org/10.1016/S0031-9422(99)00399-4
Decagalloylglucose	87729803	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)C(C(C(=O)C2=CC(=C(C(=C2)O)O)O)(C(C(=O)C3=CC(=C(C(=C3)O)O)O)(C(C(=O)C4=CC(=C(C(=C4)O)O)O)(C(C(=O)C5=CC(=C(C(=C5)O)O)O)(C(=O)C(=O)C6=CC(=C(C(=C6)O)O)O)OC(=O)C7=CC(=C(C(=C7)O)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O)OC(=O)C9=CC(=C(C(=C9)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)O	1701.20	unknown	https://doi.org/10.1016/S0031-9422(99)00399-4
Heptagalloylglucose	129636907	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)C(=O)C(C(=O)C2=CC(=C(C(=C2)O)O)O)(C(C(=O)C3=CC(=C(C(=C3)O)O)O)(C(C(=O)C4=CC(=C(C(=C4)O)O)O)(C(C(=O)C5=CC(=C(C(=C5)O)O)O)(C(C(=O)C6=CC(=C(C(=C6)O)O)O)(C(=O)C7=CC(=C(C(=C7)O)O)O)O)O)O)O)O	1244.90	unknown	https://doi.org/10.1021/NP50040A016 https://doi.org/10.1016/S0031-9422(99)00399-4
Hexagalloylglucose	129630523	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)C(C=O)(C(C(=O)C2=CC(=C(C(=C2)O)O)O)(C(C(=O)C3=CC(=C(C(=C3)O)O)O)(C(C(=O)C4=CC(=C(C(=C4)O)O)O)(C(C(=O)C5=CC(=C(C(=C5)O)O)O)(C(=O)C6=CC(=C(C(=C6)O)O)O)O)O)O)O)O	1092.80	unknown	https://doi.org/10.1016/S0031-9422(99)00399-4 https://doi.org/10.1021/NP50040A016
Nonagalloylglucose	53831489	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)C(=O)C(C(=O)C2=CC(=C(C(=C2)O)O)O)(C(C(=O)C3=CC(=C(C(=C3)O)O)O)(C(C(=O)C4=CC(=C(C(=C4)O)O)O)(C(CO)(C(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O)OC(=O)C7=CC(=C(C(=C7)O)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O)OC(=O)C9=CC(=C(C(=C9)O)O)O	1549.10	unknown	https://doi.org/10.1016/S0031-9422(99)00399-4
Octagalloylglucose	54085664	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)C(=O)C(C(=O)C2=CC(=C(C(=C2)O)O)O)(C(C(=O)C3=CC(=C(C(=C3)O)O)O)(C(C(=O)C4=CC(=C(C(=C4)O)O)O)(C(CO)(C(=O)C5=CC(=C(C(=C5)O)O)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O)OC(=O)C7=CC(=C(C(=C7)O)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O	1397.00	unknown	https://doi.org/10.1021/NP50040A016 https://doi.org/10.1016/S0031-9422(99)00399-4
Undecagalloylglucos	53869671	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)C(=O)C(C(=O)C2=CC(=C(C(=C2)O)O)O)(C(C(=O)C3=CC(=C(C(=C3)O)O)O)(C(C(=O)C4=CC(=C(C(=C4)O)O)O)(C(C(=O)C5=CC(=C(C(=C5)O)O)O)(C(C(=O)C6=CC(=C(C(=C6)O)O)O)(C(=O)C7=CC(=C(C(=C7)O)O)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O)OC(=O)C9=CC(=C(C(=C9)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O	1853.30	unknown	https://doi.org/10.1016/S0031-9422(99)00399-4
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Fisetin	5281614	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(O2)C=C(C=C3)O)O)O)O	286.24	unknown	https://doi.org/10.1007/S10600-015-1336-2
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/10.1007/S10600-015-1336-2
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
Quercetin 3'-alpha-D-glucopyranoside	67128564	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)OC4C(C(C(C(O4)CO)O)O)O)O	464.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxyphenyl)-5,7-Dihydroxy-3-[(2S,3R,4S,5R,6R)-3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-yl]Oxy-Chromen-4-one	12304323	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
Myricitrin	5281673	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)O	464.40	unknown	https://doi.org/10.1248/CPB.14.877
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/10.1248/CPB.14.877
> Phenylpropanoids and polyketides / Tannins
Pentagalloylglucose	65238	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O	940.70	unknown	https://doi.org/10.1016/S0031-9422(99)00399-4 https://doi.org/10.1021/NP50040A016

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Rhus chinensis

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