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.

Traditional uses of Castanea mollissima have been recorded in several East Asian traditions as gentle preparations that exploit the plant’s astringent and soothing qualities. Among the Han Chinese of mainland China, Bensky and Gamble (1993) describe the use of fresh chestnut leaves as an infusion to relieve cough and sore throat; the leaves are steeped in hot water and the liquid drunk warm. In Korea, Park and Lee (2011) note that dried bark is boiled in water to make a decoction taken for dysentery and other gastrointestinal upset, a practice that reflects the bark’s high tannin content. In Japan, Tanaka et al. (2008) report that the outer hulls of the chestnut are crushed and applied as a poultice to superficial wounds, where the tannins help to tighten tissue and promote healing. All of these preparations involve only the leaf, bark, or hull and are taken as teas, decoctions, or poultices, never as whole nuts.

A practical recipe that captures the most widely documented use is a mild leaf tea: place 5 g of dried chestnut leaves in a teapot, pour 250 ml of water heated to 80–85 °C (just below boiling), cover and steep for 8 minutes, then strain and serve. The tea can be taken up to two cups per day. The authors advise that large amounts may irritate the stomach, and it should be avoided by pregnant women in doses higher than the traditional cupful, as some astringent compounds can stimulate uterine smooth muscle.

The activity of these preparations is plausibly linked to well‑established phytochemicals present in Castanea mollissima. The species is rich in hydrolyzable tannins such as castalagin and vescalagin, compounds known for their astringent effect on mucous membranes and for their ability to precipitate proteins, which helps to calm irritation in the respiratory and gastrointestinal tracts. It also contains flavonoids—including quercetin and catechin—and ascorbic acid, all of which provide antioxidant protection and can reduce inflammation, supporting the soothing reputation of the leaf tea and bark decoction.

Modern relevance follows from this heritage: chestnut leaf tea is now sold as a functional beverage in several Asian markets, and recent laboratory studies (e.g., Li et al., 2006) have confirmed its antioxidant capacity. Ongoing research explores the bark’s tannic extract for potential use in standardized herbal medicines for diarrhea, while traditional practitioners continue to employ the hull poultice in rural settings, illustrating that Castanea mollissima remains a living part of both local folk remedies and contemporary health products.

General Uses Top

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Common products: Castanea mollissima yields edible nuts used fresh, roasted or boiled; chestnut flour milled from the nuts; a tannin‑rich bark extract for leather tanning; heartwood marketed as timber for furniture, flooring, veneer and charcoal; and shells processed into a natural brown dye for protein fibers.

Industrial and craft applications: Chestnut bark tannins (hydrolyzable gallotannins) are used in vegetable leather tanning; chestnut wood (high lignin‑cellulose ratio, density ≈0.6 g cm⁻³) serves in furniture, interior joinery, veneer and charcoal production; crushed shells give a brown natural dye for wool and silk.

Food and beverages (non‑medicinal): The nuts are consumed raw, roasted or boiled and incorporated into confections, pastries and desserts; chestnut flour is a gluten‑free ingredient in breads, cakes and sauces; fermented or infused chestnut beverages are produced in regions of cultivation.

Colorants and tanning: Chestnut bark supplies ≈10–12 % hydrolyzable tannins meeting ISO 3066 for vegetable leather tanning; shell extracts yield a fast‑binding brown dye used on wool and silk.

Wood and fiber: The timber is a hardwood with average density 0.55–0.65 g cm⁻³, good bending strength and decay resistance, employed for indoor flooring, cabinetry, veneer and charcoal.

Properties relevant to use: Nut starch contains ~30 % amylose for rapid gelatinisation; bark tannins are gallotannins conferring high acidity (pH ≈ 3–4) and strong leather binding; wood lignin (~27 %) and cellulose (~45 %) give durability and machinability.

Standards and regulation: Food uses must comply with national food safety standards (e.g., China GB 7718 for chestnut, EU Novel Food Regulation for chestnut flour); tannin extracts must satisfy ISO 3066; timber trade follows FSC/PEFC certification and national grading codes (e.g., GB/T 1927‑2009).

Sustainability and sourcing: Castanea mollissima is cultivated on orchards and mixed forests; bark, shells and pruning residues can be harvested as by‑products without harming trees; the species is listed by FAO as a minor forest product and orchard management reduces pressure on native chestnut species.

Scientific/model organism use: The draft genome (~800 Mb) of C. mollissima (Horticulture Research, 2019) serves as a reference for Castanea genetics and blight‑resistance breeding; it is deposited in public databases (NCBI, CoGe) for comparative genomics, marker‑assisted selection and transcriptomic studies.

Synonyms Top

Scientific name	Authority	First published in
Castanea mollissima var. pendula	X.Y.Zhou & Z.D.Zhou	J. Jiangxi Agric. Univ. 1982(1): 7.
Castanea bungeana	Blume	Mus. Bot. 1: 284 (1851)
Castanea duclouxii	Dode	Bull. Soc. Dendrol. France 1908: 150 (1908)
Castanea formosana	(Hayata) Hayata	Icon. Pl. Formosan. 6(Suppl.): 71 (1917)
Castanea hupehensis	Dode	Bull. Soc. Dendrol. France 1908: 151 (1908)
Castanea sativa var. formosana	Hayata	J. Coll. Sci. Imp. Univ. Tokyo 30: 304. 1911
Castanea sativa var. mollissima	(Blume) Pamp.	Nuovo Giorn. Bot. Ital. n.s., 17: 250. 1910
Castanea sinensis	Perr.	Mém. Soc. Linn. Paris 3: 108 (1825)
Castanea vulgaris var. yunnanensis	Fr.	J. Bot. 20: 196. 1899
Castanea sativa var. bungeana	(Blume) Pamp.	Nuovo Giorn. Bot. Ital. n.s., 17: 250. 1910
Castanea sativa var. intermedia	Pamp.	Nuovo Giorn. Bot. Ital. n.s., 22: 275. 1915

Common names Top

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Filter by language:

Language	Common/alternative name
English	chinese chestnut
Arabic	كستناء صينية
Catalan	castanyer xinès
German	chinesische kastanie
Persian	شاهبلوط چینی
French	châtaignier chinois
French	châtaignier de chine
Galician	castiñeiro da china
Croatian	kineski kesten
Hungarian	kínai gesztenye
Japanese	シナグリ
Japanese	甘栗
Japanese	天津甘栗
Japanese	あまぐり
Korean	평양밤나무
Korean	약밤나무
Latvian	mīkstā kastaņa
mnc	ᠵᠠᠨᠴᡠᡥᡡᠨ ᡠᠰᡳᡥᠠ
Norwegian Bokmål	kinakastanje
Polish	kasztan chiński
Russian	Каштан китайский
Russian	Каштан мягчайший
Slovenian	kitajski kostanj
Thai	เกาลัดจีน
Turkish	Çin kestanesi
ug	كاشتان
Ukrainian	Каштан китайський
Vietnamese	dẻ trùng khánh
za	maklaeq
Chinese	板栗花
Chinese	栗子
Chinese	栗
Chinese	毛栗
Chinese	chinesechestnut
Chinese	板栗
Chinese	中國板栗
Chinese	栗*（板栗）
Chinese	栗壳
Chinese	栗树根
Chinese	栗树皮
Chinese	栗毛球
Chinese	栗花
Chinese	栗蔟
Chinese	风栗
Chinese	魁栗
Chinese	中国板栗

Subspecies (abbr. subsp./ssp.) Top

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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

Asia-temperate click to expand
- China
  - China North-central
  - China South-central
  - China Southeast
- Eastern Asia
  - Korea
  - Taiwan

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - East Himalaya

Northern America click to expand
- North-central U.S.A.
  - Illinois
- Northeastern U.S.A.
  - Massachusetts
- Southeastern U.S.A.
  - Alabama
  - Arkansas
  - Florida
  - Kentucky

Southern America click to expand
- Caribbean
  - Windward Islands

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000811992
UNII	553K486UOX
Florida Plant Atlas	478
Flora of Alabama	2144
Cornell Woody Plants	46
USDA Plants	CAMO83
UConn	91
Tropicos	13100178
INPN	629280
KEW	urn:lsid:ipni.org:names:295338-1
The Plant List	kew-35016
Missouri Botanical Garden	280731
Open Tree Of Life	540978
NCBI Taxonomy	60419
Nature Serve	2.136552
IUCN Red List	136776707
IPNI	295338-1
iNaturalist	49192
GBIF	5333237
Freebase	/m/0dxyy_
EPPO	CSNMO
EOL	1148512
USDA GRIN	9442
Wikipedia	Castanea_mollissima
CMAUP	NPO1191

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.

Accession	Assembly
Accession	Name	Level	Submitter	Released	Coverage	Size
GCA_053895485.1	CmollissimaMahoganyHAP1 v1.0	Chromosome	HudsonAlpha Institute for Biotechnology	2025-12-10	88	687.06 Mb

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

In This Issue

N/A

Proc Natl Acad Sci U S A

23-Apr-2024

PMCID:	PMC11047073
doi:	10.1073/iti1724121

Characterization of Key Odorants in Lushan Yunwu Tea in Response to Intercropping with Flowering Cherry

Gao Y, Lei Z, Huang J, Sun Y, Liu S, Yao L, Liu J, Liu W, Liu Y, Chen Y

Foods

19-Apr-2024

PMCID:	PMC11049266
doi:	10.3390/foods13081252
PMID:	38672924

Genome-Wide Characterization and Functional Validation of the ACS Gene Family in the Chestnut Reveals Its Regulatory Role in Ovule Development

Cui Y, Ji X, Yu W, Liu Y, Bai Q, Su S

Int J Mol Sci

18-Apr-2024

PMCID:	PMC11049808
doi:	10.3390/ijms25084454
PMID:	38674037

In This Issue

N/A

Proc Natl Acad Sci U S A

16-Apr-2024

PMCID:	PMC11032432
doi:	10.1073/iti1624121

Morphology and phylogeny of Cytospora (Cytosporaceae, Diaporthales) species associated with plant cankers in Tibet, China

Li J, Li J, Jiang N

MycoKeys

16-Apr-2024

PMCID:	PMC11040198
doi:	10.3897/mycokeys.104.113567
PMID:	38665971

In This Issue

N/A

Proc Natl Acad Sci U S A

09-Apr-2024

PMCID:	PMC11009666
doi:	10.1073/iti1524121

Five New Species of the Genus Hymenogaster (Hymenogastraceae, Agaricales) from Northern China

Li T, Mao N, Fu H, Zhang Y, Fan L

J Fungi (Basel)

08-Apr-2024

PMCID:	PMC11051317
doi:	10.3390/jof10040272
PMID:	38667943

Mapping QTLs for blight resistance and morpho-phenological traits in inter-species hybrid families of chestnut (Castanea spp.)

Fan S, Georgi LL, Hebard FV, Zhebentyayeva T, Yu J, Sisco PH, Fitzsimmons SF, Staton ME, Abbott AG, Nelson CD

Front Plant Sci

08-Apr-2024

PMCID:	PMC11033410
doi:	10.3389/fpls.2024.1365951
PMID:	38650705

Preparation, Isolation and Antioxidant Function of Peptides from a New Resource of Rumexpatientia L. ×Rumextianshanicus A. Los

Liu C, Wang J, Hong D, Chen Z, Li S, Ma A, Jia Y

Foods

22-Mar-2024

PMCID:	PMC11011613
doi:	10.3390/foods13070981
PMID:	38611286

Apple crown and collar canker and necrosis caused by Cytospora balanejica sp. nov. in Iran

Azizi R, Ghosta Y, Ahmadpour A

Sci Rep

19-Mar-2024

PMCID:	PMC10951349
doi:	10.1038/s41598-024-57235-3
PMID:	38504125

Local knowledge of homegarden plants in Miao ethnic communities in Laershan region, Xiangxi area, China

Luo J, Li Q, He J, Yan J, Zhang S, Chang X, Wu T

J Ethnobiol Ethnomed

18-Mar-2024

PMCID:	PMC10946099
doi:	10.1186/s13002-024-00676-x
PMID:	38500123

Conservation Mitonuclear Replacement: Facilitated mitochondrial adaptation for a changing world

Iverson EN

Evol Appl

10-Mar-2024

PMCID:	PMC10925831
doi:	10.1111/eva.13642
PMID:	38468713

Ethylene Action Inhibition Improves Adventitious Root Induction in Adult Chestnut Tissues

Castro-Camba R, Neves M, Correia S, Canhoto J, Vielba JM, Sánchez C

Plants (Basel)

06-Mar-2024

PMCID:	PMC10933963
doi:	10.3390/plants13050738
PMID:	38475584

Chromosome-level genome assembly of Platycarya strobilacea

Zhou H, Zhang X, Liu H, Ma J, Hao F, Ye H, Wang Y, Zhang S, Yue M, Zhao P

Sci Data

05-Mar-2024

PMCID:	PMC10914804
doi:	10.1038/s41597-024-03107-4
PMID:	38443357

Assembly and analysis of the genome of Notholithocarpus densiflorus

Cai Y, Anderson E, Xue W, Wong S, Cui L, Cheng X, Wang O, Mao Q, Liu SJ, Davis JT, Magalang PR, Schmidt D, Kasuga T, Garbelotto M, Drmanac R, Kua CS, Cannon C, Maloof JN, Peters BA

G3 (Bethesda)

01-Mar-2024

PMCID:	PMC11075539
doi:	10.1093/g3journal/jkae043
PMID:	38427916

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
Phenylacetic Acid	999	Click to see C1=CC=C(C=C1)CC(=O)O	136.15	unknown	https://doi.org/10.1111/J.1365-2621.1983.TB14902.X
> 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	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Diphenylmethanes
1-Benzhydryl-3-[4-(methoxy-quinolin-8-ylamino)-pentyl]-urea	49771751	Click to see CC(CCCNC(=O)NC1=CC=CC(=C1)CC2=CC=CC=C2)NC3=CC(=CC4=CC=CC=C43)OC	467.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Eicosanoic Acid	10467	Click to see	312.50	unknown	via CMAUP database
Palmitic Acid	985	Click to see	256.42	unknown	via CMAUP database
Stearic Acid	5281	Click to see	284.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Behenic Acid	8215	Click to see CCCCCCCCCCCCCCCCCCCCCC(=O)O	340.60	unknown	via CMAUP database
Hexacosanoic Acid	10469	Click to see	396.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,4aS,10aS)-1,4a-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthren-1-ol	40522879	Click to see	272.40	unknown	via CMAUP database
(1R,4aS,10aS)-7-Isopropyl-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene-1-carboxylic acid	7075030	Click to see	300.40	unknown	via CMAUP database
(1R,4aS,9R,10aR)-1,4a-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-1,9-diol	21604174	Click to see	288.40	unknown	via CMAUP database
(1R,4aS,9R,10aR)-9-hydroxy-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,9,10,10a-hexahydrophenanthrene-1-carbaldehyde	10425915	Click to see CC1(CCCC2(C1CC(C3=C2C=CC(=C3)C(C)(C)O)O)C)C=O	316.40	unknown	via CMAUP database
(1R,4aS,9S,10aR)-1-(hydroxymethyl)-7-(1-hydroxy-1-methyl-ethyl)-1,4a-dimethyl-2,3,4,9,10,10a-hexahydrophenanthren-9-ol	3009626	Click to see	318.40	unknown	via CMAUP database
(1R,4aS,9S,10aR)-1,4a-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-1,9-diol	100982592	Click to see	288.40	unknown	via CMAUP database
(1S,4aS,10aR)-1,4a-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthren-1-ol	26183496	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)O)C	272.40	unknown	via CMAUP database
(1S,4aS,10aS)-1,4a-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthren-1-ol	26183495	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)O)C	272.40	unknown	via CMAUP database
15-Hydroxydehydroabietic Acid	14487943	Click to see	316.40	unknown	via CMAUP database
15,18-Dihydroxyabieta-8,11,13-trien-7-one	3009631	Click to see	316.40	unknown	via CMAUP database
18-Nor-4,15-dihydroxyabieta-8,11,13-trien-7-one	3009629	Click to see CC12CCCC(C1CC(=O)C3=C2C=CC(=C3)C(C)(C)O)(C)O	302.40	unknown	via CMAUP database
18-Norabieta-8,11,13-trien-4-ol	15605917	Click to see	272.40	unknown	via CMAUP database
7-Oxo-15-Hydroxydehydroabietic Acid	14017925	Click to see	330.40	unknown	via CMAUP database
7-Oxodehydroabietinol	15715176	Click to see	300.40	unknown	via CMAUP database
7alpha-Hydroxydehydroabieticacid	13370053	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2O)(C)C(=O)O)C	316.40	unknown	via CMAUP database
7alpha,15-Dihydroxydehydroabietic acid	12047563	Click to see CC12CCCC(C1CC(C3=C2C=CC(=C3)C(C)(C)O)O)(C)C(=O)O	332.40	unknown	via CMAUP database
7Beta-Hydroxydehydroabietic Acid	13370052	Click to see	316.40	unknown	via CMAUP database
7beta,15-Dihydroxydehydroabietic acid	21626423	Click to see CC12CCCC(C1CC(C3=C2C=CC(=C3)C(C)(C)O)O)(C)C(=O)O	332.40	unknown	via CMAUP database
Aquilarabietic Acid H	71578077	Click to see	314.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
2,6-Octadienoic acid, 3,7-dimethyl-, ethyl ester	5317247	Click to see	196.29	unknown	via CMAUP database
> Organic acids and derivatives / Organic carbonic acids and derivatives / Ureas
Urea	1176	Click to see C(=O)(N)N	60.06	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
[3,5-dihydroxy-4-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methyl 2-[4-[[3,5-dihydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methoxycarbonyl]-2,6-dihydroxyphenoxy]-3,4,5-trihydroxybenzoate	163187060	Click to see	938.70	unknown	https://doi.org/10.1016/0031-9422(88)80299-1
3,4-Dihydroxy-5-[[6-O-(3,4,5-trihydroxybenzoyl)-I(2)-D-glucopyranosyl]oxy]benzaldehyde	163037236	Click to see	468.40	unknown	https://doi.org/10.1016/0031-9422(88)80299-1
Castamollissin	14057201	Click to see	468.40	unknown	https://doi.org/10.1016/0031-9422(88)80299-1
Isochestanin	14057205	Click to see	938.70	unknown	https://doi.org/10.1016/0031-9422(88)80299-1
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives / Xanthines
(8S)-8-hydroxy-3,7,8,9-tetrahydropurine-2,6-dione	49766623	Click to see	170.13	unknown	via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives
(-)-Chestnutamide	163184283	Click to see C1CC(=O)N2C1CC3=C2NC4=CC=CC=C4C3=O	240.26	unknown	https://doi.org/10.1080/10286020108041375
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
2-Propenoic acid, 3-(4-hydroxy-3-methoxyphenyl)-, octadecyl ester	149044	Click to see CCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC	446.70	unknown	via CMAUP database
Hexacosyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate	20980932	Click to see	558.90	unknown	via CMAUP database
Icosyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate	149045	Click to see CCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC	474.70	unknown	via CMAUP database
Tetracosyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate	54412038	Click to see CCCCCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC	530.80	unknown	via CMAUP database
Unii-A2T8gne262	54370069	Click to see	502.80	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid	689043	Click to see	180.16	unknown	https://doi.org/10.1111/J.1365-2621.1983.TB14902.X
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Pinocembrin	68071	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3	256.25	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
Pinobanksin	73202	Click to see	272.25	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids
Vestitol, (-)-	182259	Click to see COC1=CC(=C(C=C1)C2CC3=C(C=C(C=C3)O)OC2)O	272.29	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
Afromosin	5281704	Click to see	298.29	unknown	https://doi.org/10.1016/0031-9422(88)80299-1
> Phenylpropanoids and polyketides / Stilbenes
3,5-Dimethoxystilbene	5316874	Click to see	240.30	unknown	via CMAUP database
Cis-3,5-Dimethoxystilbene	13556468	Click to see	240.30	unknown	via CMAUP database
Pinosylvin methyl ether	5281719	Click to see COC1=CC(=CC(=C1)O)C=CC2=CC=CC=C2	226.27	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
(14R,15S,19R)-14-[(11R,12R)-3,4,5,11,16,17,18-heptahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.3.1.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-12-yl]-2,3,4,7,8,9,19-heptahydroxy-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaene-12,17-dione	162938366	Click to see C1C(C(OC(=O)C2=C(C(=C(C(=C2)C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C4C5C(C6=C(C(=C(C(=C6C(=O)O5)C7=C(C(=C(C=C7C(=O)O4)O)O)O)O)O)O)O)O	784.50	unknown	https://doi.org/10.1016/0031-9422(88)80299-1
[(10R,11R)-10-[(15S,19R)-2,3,4,7,8,9,19-heptahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl]-3,4,5,17,18,19-hexahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-11-yl] 3,4,5-trihydroxybenzoate	101601179	Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C4C5C(C6=C(C(=C(C(=C6C(=O)O5)C7=C(C(=C(C=C7C(=O)O4)O)O)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O	936.60	unknown	https://doi.org/10.1016/0031-9422(88)80299-1
[(10R,11R)-10-[(15S,19S)-2,3,4,7,8,9,19-heptahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl]-3,4,5,17,18,19-hexahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-11-yl] 3,4,5-trihydroxybenzoate	101601178	Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C4C5C(C6=C(C(=C(C(=C6C(=O)O5)C7=C(C(=C(C=C7C(=O)O4)O)O)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O	936.60	unknown	https://doi.org/10.1016/0031-9422(88)80299-1
[(10S,11R,12R,15R)-3,4,5,11,12,21,22,23-octahydroxy-8,18-dioxo-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-13-yl] 3,4,5-trihydroxybenzoate	9874083	Click to see	634.50	unknown	via CMAUP database
14-(3,4,5,11,16,17,18-Heptahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.3.1.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-12-yl)-2,3,4,7,8,9,19-heptahydroxy-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaene-12,17-dione	162938365	Click to see	784.50	unknown	https://doi.org/10.1016/0031-9422(88)80299-1
4-[[[2-(5-Carboxy-2,3-dihydroxyphenoxy)-3,4,5-trihydroxybenzoyl]oxy]methyl]-2,6-dihydroxyphenyl I(2)-D-glucopyranoside	102158505	Click to see	638.50	unknown	https://doi.org/10.1016/0031-9422(88)80299-1
7,8,9,12,13,14,25,26,27,30,31,32,35,36,37-Pentadecahydroxy-46-(2,3,4,5-tetrahydroxyoxan-2-yl)-3,18,21,41,43-pentaoxanonacyclo[27.13.3.138,42.02,20.05,10.011,16.023,28.033,45.034,39]hexatetraconta-5,7,9,11,13,15,23,25,27,29(45),30,32,34(39),35,37-pentadecaene-4,17,22,40,44-pentone	14428075	Click to see	1066.70	unknown	https://doi.org/10.1016/0031-9422(88)80299-1
beta-D-Glucopyranoside, 4-[[[3-(6-carboxy-2,3,4-trihydroxyphenoxy)-4,5-dihydroxybenzoyl]oxy]methyl]-2,6-dihydroxyphenyl	162848150	Click to see C1=C(C=C(C(=C1O)OC2C(C(C(C(O2)CO)O)O)O)O)COC(=O)C3=CC(=C(C(=C3)OC4=C(C(=C(C=C4C(=O)O)O)O)O)O)O	638.50	unknown	https://doi.org/10.1016/0031-9422(88)80299-1
Castalagin	12302513	Click to see	934.60	unknown	https://doi.org/10.1016/0031-9422(88)80299-1
Casuariin	14035442	Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C4C5C(C6=C(C(=C(C(=C6C(=O)O5)C7=C(C(=C(C=C7C(=O)O4)O)O)O)O)O)O)O)O	784.50	unknown	https://doi.org/10.1016/0031-9422(88)80299-1
Casuarinin	442673	Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C4C5C(C6=C(C(=C(C(=C6C(=O)O5)C7=C(C(=C(C=C7C(=O)O4)O)O)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O	936.60	unknown	https://doi.org/10.1016/0031-9422(88)80299-1
Chestanin	432620	Click to see	938.70	unknown	https://doi.org/10.1016/0031-9422(88)80299-1
CID 3002102	3002102	Click to see	934.60	unknown	via CMAUP database
CID 5458626	5458626	Click to see C1C2C(C3C4C(C5=C(C(=C(C(=C5C(=O)O4)C6=C(C(=C(C(=C6C(=O)O3)C7=C(C(=C(C=C7C(=O)O2)O)O)O)O)O)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O1)O)O)O)O)O)O	934.60	unknown	https://doi.org/10.1016/0031-9422(88)80299-1
Gemin D	471119	Click to see	634.50	unknown	https://doi.org/10.1016/0031-9422(88)80299-1
Grandinin	492392	Click to see	1066.70	unknown	https://doi.org/10.1016/0031-9422(88)80299-1
Isochesnatin	14057203	Click to see	638.50	unknown	https://doi.org/10.1016/0031-9422(88)80299-1
Pedunculagin	442688	Click to see	784.50	unknown	https://doi.org/10.1016/0031-9422(88)80299-1
Stachyurin	157395	Click to see	936.60	unknown	https://doi.org/10.1016/0031-9422(88)80299-1
Strictinin	73330	Click to see	634.50	unknown	https://doi.org/10.1016/0031-9422(88)80299-1
Vescalagin carboxylic acid	16131089	Click to see	962.60	unknown	via CMAUP database

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Castanea mollissima

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