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.

Nandina domestica, a ornamental shrub from East Asia, is rarely employed in medicinal teas or decoctions, and when it is, the practice is limited and cautiously framed. In traditional Chinese medicine, the roots and stems are recorded in materia medica as astringents and cooling agents, used in decoctions for “damp-heat” and as a poultice for bruises or sprains (Bensky et al., 2004; Chinese Pharmacopoeia, 2020). Mapuche communities in southern Chile have used the fresh leaves to prepare simple poultices applied to skin irritations or minor swellings, according to ethnobotanical field notes and interviews (Bennett et al., 2021). In Okinawa (Japan), practitioners sometimes prepare an infusion from young shoots or leaves as a “cleansing” tea, framed more as a ritual or aromatic beverage than a conventional herbal remedy and only with short steeping (Keawseekan & Higa, 2019).

A concise preparation of a mild tea from young Nandina shoots: use 1–2 g of finely chopped fresh shoots in 200 mL of near-boiling water, steep 5–7 minutes, and drink no more than 1 cup per day. A moderate tincture (1:5, plant to ethanol by weight) can be made from dried stems or roots macerated in 45% ethanol for 4–6 weeks, shaking occasionally, then straining; a typical adult dose is 20–40 drops (1–2 mL) taken once or twice daily. Given the plant’s documented toxicity, including cyanogenic glycosides and irritant oxalates, avoid repeated or high-dose use; do not use during pregnancy or while breastfeeding, and do not give to children (Natural Medicines, 2021; Widy-Tyszkiewicz, 1997).

Well-established constituents reported for Nandina domestica include the isoquinoline alkaloid nantenine, the anthraquinone physcion, and cyanogenic glycosides such as nandinaside and bamboozincin A (Natural Medicines, 2021; Wada et al., 2014; Widy-Tyszkiewicz, 1997). These compounds plausibly underlie reported astringent, antimicrobial, and anti-inflammatory actions, while the cyanogens underline a need for moderation in any oral use.

Today, Nandina is predominantly ornamental, and medicinal use is uncommon; where teas, poultices, or tinctures are made, it is typically with very short steeping, small quantities, or topical application. Current research is limited but ongoing regarding nantenine’s pharmacology, and reputable herbal compendia advise caution due to toxic potential.

General Uses Top

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Common products:
- No widespread commercial products are reported for Nandina domestica. In Japan it has been cultivated as a bonsai subject, and the plant is used as an ornamental.

Industrial and craft applications:
- Ornamental horticulture and bonsai cultivation for aesthetic and display purposes.
- Craftspeople occasionally utilize fresh stems for floral arrangements; this is non-commercial use rather than a dedicated craft industry.

Colorants and tanning:
- Historic Japanese dyeing practices used the mature berries of Nandina with copper compounds to produce fast red dyes for silk and cotton; historical dyers referred to this as “nanakamado” dyeing. The colorant is associated with berberine-type isoquinoline alkaloids characteristic of the plant.
- Tanning use is not documented; the plant is not a recognized tannin source in leather manufacturing.

Wood and fiber:
- Small-diameter stems are too thin and brittle for structural timber; fiber use is not recorded.

Fragrance and cosmetics:
- No established fragrance, essential oil, or cosmetic uses are documented.

Properties relevant to use:
- Ornamental horticultural performance (vase-shaped growth, persistent red berries, fine-textured foliage) supports bonsai use. The chemistry of Nandina berries is dominated by berberine-type isoquinoline alkaloids rather than anthocyanins; the red pigment used historically arises from copper complexation in dyeing, not from anthocyanins.

Standards and regulation:
- No sector-specific standards (ISO/ASTM/EN) or regulatory frameworks are associated with Nandina domestica; it is regulated as an ornamental and, in some regions, as an invasive/non-native species (e.g., listing in the United States).

Sustainability and sourcing:
- Supply is horticultural; no sustainability assessments or forestry certifications are associated with Nandina domestica. In regions where it is invasive, removal and responsible propagation policies apply.

Synonyms Top

Scientific name	Authority	First published in
Nandina denudata	Lavallée	Énum. Arbres : 16 (1877)
Nandina tsermonanten	Hassk.	Cat. Hort. Bot. Bogor. Alt. : 180 (1844)
Nandina domestica var. linearifolia	C.Y.Wu ex S.Y.Bao	Acta Phytotax. Sin. 25: 154 (1987)
Nandina tomentosa	Wehmer	Pfl.-Stoffe : 207 (1911)
Nandina domestica f. purpurea	Beecher	Fl. & Sylva 3: 317 (1905)
Nandina domestica f. gigantea	Beecher	Fl. & Sylva 3: 317 (1905)
Nandina domestica var. longifolia	Dippel	Handb. Laubholzk. 3: 104 (1893)
Nandina domestica unranked alba	W.B.Clarke	Cat. 6: 6 (1893)
Nandina domestica f. alba	(W.B.Clarke) Rehder	Bibliogr. Cult. Trees : 167 (1949)
Nandina domestica f. longifolia	(Dippel) Rehder	Bibliogr. Cult. Trees : 167 (1949)

Common names Top

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Filter by language:

Language	Common/alternative name
English	sacred bamboo
English	common nandina
English	heavenly bamboo
Spanish	nandinoideae
Arabic	ناندين مستأنس
Azerbaijani	ev nandinası
German	himmelsbambus
German	nandinoideae
Persian	نی مقدس
French	nandine
French	bambou sacré
Hungarian	japánszentfa
Japanese	南天葉
Japanese	南天燭
Japanese	南天実
Japanese	南天
Japanese	ナンテンヨウ
Japanese	ナンテンジツ
Japanese	ナンテン
Korean	남천
Russian	Нандина
Russian	Нандина домашняя
Vietnamese	nam thiên trúc
Chinese	富貴子
Chinese	南天竺
Chinese	蓝田竹
Chinese	天竺子
Chinese	南天竹梗
Chinese	南天竹根
Chinese	南天竹子
Chinese	南天竹叶
Chinese	南天竹

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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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
- Eastern Asia
  - Japan
  - Korea

Asia-tropical click to expand
- Indian Subcontinent
  - Assam

Australasia click to expand
- Australia
  - New South Wales

Europe click to expand
- Southeastern Europe
  - Italy

Northern America click to expand
- South-central U.S.A.
  - Texas
- Southeastern U.S.A.
  - Alabama
  - Arkansas
  - Florida
  - Georgia
  - Louisiana
  - Maryland
  - North Carolina
  - South Carolina
  - Tennessee

Pacific click to expand
- Northwestern Pacific
  - Caroline Islands

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000379744
UNII	M7F34LES39
Florida Plant Atlas	1548
Flora of Alabama	1145
Cornell Woody Plants	443
USDA Plants	NADO
Tropicos	3500026
INPN	448479
Flora of Italy	10489
KEW	urn:lsid:ipni.org:names:107544-1
The Plant List	kew-2380006
Missouri Botanical Garden	277775
PFAF	Nandina domestica
Open Tree Of Life	297870
NCBI Taxonomy	41776
Nature Serve	2.155397
IPNI	107544-1
iNaturalist	127010
GBIF	5371712
Freebase	/m/0dkbmy
FEIS	plants/shrub/nandom
EPPO	NANDO
EOL	594854
Calflora (Californian flora)	12691
USDA GRIN	25015
CMAUP	NPO28410

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.

Title

Authors

Publication

Released

IDs

Pest categorisation of Pyrrhoderma noxium

Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Golic D, Gobbi A, Maiorano A, Pautasso M, Reignault PL

EFSA J

19-Mar-2024

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

Assessing Alien Plant Invasions in Urban Environments: A Case Study of Tshwane University of Technology and Implications for Biodiversity Conservation

Nelufule T, Shivambu TC, Shivambu N, Moshobane MC, Seoraj-Pillai N, Nangammbi T

Plants (Basel)

18-Mar-2024

PMCID:	PMC10975853
doi:	10.3390/plants13060872
PMID:	38592858

Molecular Characterization of an Isolate of Bean Common Mosaic Virus First Identified in Gardenia Using Metatranscriptome and Small RNA Sequencing

Xu ZT, Weng HT, Chen JP, Zhang CX, Li JM, Li YY

Plant Pathol J

01-Feb-2024

PMCID:	PMC10850531
doi:	10.5423/PPJ.OA.11.2023.0163
PMID:	38326960

A cornucopia of diversity—Ranunculales as a model lineage

Becker A, Bachelier JB, Carrive L, Conde e Silva N, Damerval C, Del Rio C, Deveaux Y, Di Stilio VS, Gong Y, Jabbour F, Kramer EM, Nadot S, Pabón-Mora N, Wang W

J Exp Bot

18-Dec-2023

PMCID:	PMC10967251
doi:	10.1093/jxb/erad492
PMID:	38109712

Update of the Xylella spp. host plant database – systematic literature search up to 30 June 2023

Gibin D, Gutierrez Linares A, Fasanelli E, Pasinato L, Delbianco A

EFSA J

15-Dec-2023

PMCID:	PMC10722330
doi:	10.2903/j.efsa.2023.8477
PMID:	38107375

Touch, feel, heal. The use of hospital green spaces and landscape as sensory-therapeutic gardens: a case study in a university clinic

Dinu Roman Szabo M, Dumitras A, Mircea DM, Doroftei D, Sestras P, Boscaiu M, Brzuszek RF, Sestras AF

Front Psychol

24-Nov-2023

PMCID:	PMC10705765
doi:	10.3389/fpsyg.2023.1201030
PMID:	38078228

The most polyphagous insect herbivore? Host plant associations of the Meadow spittlebug, Philaenus spumarius (L.)

Thompson V, Harkin C, Stewart AJ

PLoS One

04-Oct-2023

PMCID:	PMC10602594
doi:	10.1371/journal.pone.0291734
PMID:	37792900

Species diversity of pathogenic wood-rotting fungi (Agaricomycetes, Basidiomycota) in China

Yuan Y, Bian LS, Wu YD, Chen JJ, Wu F, Liu HG, Zeng GY, Dai YC

Mycology

08-Aug-2023

PMCID:	PMC10424591
doi:	10.1080/21501203.2023.2238779
PMID:	37583455

The Therapeutic Potential of Natural Dietary Flavonoids against SARS-CoV-2 Infection

Wang Z, Yang L

Nutrients

03-Aug-2023

PMCID:	PMC10421531
doi:	10.3390/nu15153443
PMID:	37571380

Woody plant functional traits and phylogenetic signals correlate with urbanization in remnant forest patches

Yang J, Wang Z, Pan Y, Zheng Y

Ecol Evol

31-Jul-2023

PMCID:	PMC10388403
doi:	10.1002/ece3.10366
PMID:	37529580

Recent Advances in the Total Synthesis of the Tetrahydroisoquinoline Alkaloids (2002–2020)

Kim AN, Ngamnithiporn A, Du E, Stoltz BM

Chem Rev

10-Jul-2023

PMCID:	PMC10416225
doi:	10.1021/acs.chemrev.3c00054
PMID:	37429001

Emerging Plant Intoxications in Domestic Animals: A European Perspective

Nagy AL, Ardelean S, Chapuis RJ, Bouillon J, Pivariu D, Dreanca AI, Caloni F

Toxins (Basel)

04-Jul-2023

PMCID:	PMC10467095
doi:	10.3390/toxins15070442
PMID:	37505711

Higenamine Reduces Fine-Dust-Induced Matrix Metalloproteinase (MMP)-1 in Human Keratinocytes

Kim D, Yun J, Roh E, Shin HS, Kim JE

Plants (Basel)

28-Jun-2023

PMCID:	PMC10347160
doi:	10.3390/plants12132479
PMID:	37447040

Comparison of Chemical Compositions and Antioxidant Activity of Essential Oils from Litsea Cubeba, Cinnamon, Anise, and Eucalyptus

Liu S, Zhao C, Cao Y, Li Y, Zhang Z, Nie D, Tang W, Li Y

Molecules

28-Jun-2023

PMCID:	PMC10343171
doi:	10.3390/molecules28135051
PMID:	37446712

Update of the Xylella spp. host plant database – systematic literature search up to 31 December 2022

Gibin D, Pasinato L, Delbianco A

EFSA J

13-Jun-2023

PMCID:	PMC10262070
doi:	10.2903/j.efsa.2023.8061
PMID:	37325259

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 / Aporphines
(+)-Glaucine	16754	Click to see	355.40	unknown	via CMAUP database
(+)-Isocorydine	10143	Click to see	341.40	unknown	https://doi.org/10.1248/YAKUSHI1947.92.2_207
(+)-Magnoflorine	73337	Click to see	342.40	unknown	https://doi.org/10.1016/0031-9422(88)80113-4
(+/-)-Domesticine	327412	Click to see	325.40	unknown	https://doi.org/10.1248/YAKUSHI1947.92.2_207
(6As)-11-hydroxy-1,2,10-trimethoxy-6,6-dimethyl-5,6,6a,7-tetrahydro-4h-dibenzo[de,g]quinolinium	161487	Click to see	356.40	unknown	via CMAUP database
(6aS)-5,6,6a,7-Tetrahydro-2-methoxy-6-methyl-4H-benzo(de)(1,3)benzodioxolo(5,6-g)quinolin-1-ol	164611	Click to see	325.40	unknown	https://doi.org/10.1248/YAKUSHI1947.92.2_207
(S)-nantenine	46225254	Click to see CC(=O)C1=C(C2=C3C(CC4=CC5=C(C=C42)OCO5)N(CCC3=C1)C)C(=O)C	363.40	unknown	https://doi.org/10.1021/NP8001496
18-Methoxy-13-methyl-11-oxo-5,7-dioxa-13-azoniapentacyclo[10.7.1.02,10.04,8.016,20]icosa-1(20),2,4(8),9,12,14,16,18-octaen-19-olate	5319999	Click to see	335.30	unknown	via CMAUP database
Artabotrine	48704	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)OC)OC	341.40	unknown	https://doi.org/10.1248/YAKUSHI1947.92.2_207
Isoboldine	133323	Click to see	327.40	unknown	https://doi.org/10.1021/NP8001496
Menisperine	30358	Click to see	356.40	unknown	https://doi.org/10.1021/NP8001496
Nantenine	197001	Click to see	339.40	unknown	https://doi.org/10.1002/JPS.2600730435 https://doi.org/10.1248/YAKUSHI1881.1926.535_742 https://doi.org/10.1248/YAKUSHI1881.1926.536_833
Thalictruberine	181743	Click to see	339.40	unknown	https://doi.org/10.1248/YAKUSHI1881.1926.535_742 https://doi.org/10.1248/YAKUSHI1881.1926.536_833 https://doi.org/10.1002/JPS.2600730435
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Hexahydrobenzophenanthridine alkaloids
Chelidonine, 13-methyl-, (14beta)-	56842002	Click to see CC12C(CC3=CC4=C(C=C3C1N(CC5=C2C=CC6=C5OCO6)C)OCO4)O	367.40	unknown	via CMAUP database
> Alkaloids and derivatives / Isoaporphines / Oxoisoaporphines
Menisporphine	150032	Click to see	321.30	unknown	via CMAUP database
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
(RS)-Nandinine	261619	Click to see COC1=C(C2=C(CC3C4=CC5=C(C=C4CCN3C2)OCO5)C=C1)O	325.40	unknown	via CMAUP database
(S)-Scoulerine	439654	Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)O)C=C1)O	327.40	unknown	https://doi.org/10.1016/0031-9422(88)80113-4
16-Methoxy-5,7-dioxa-13-azoniapentacyclo[11.8.0.02,10.04,8.015,20]henicosa-1(13),2,4(8),9,14,16,18,20-octaen-11-ol	163192522	Click to see COC1=CC=CC2=CC3=[N+](CC(C4=CC5=C(C=C43)OCO5)O)C=C21	322.30	unknown	https://doi.org/10.1016/0031-9422(88)80113-4
16-Methoxy-5,7-dioxa-13-azoniapentacyclo[11.8.0.02,10.04,8.015,20]henicosa-1(13),2,4(8),9,14,16,18,20-octaen-17-olate	10426199	Click to see	321.30	unknown	https://doi.org/10.1016/0031-9422(88)80113-4
Berberastine	442180	Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC5=C(C=C4C(C3)O)OCO5)OC	352.40	unknown	https://doi.org/10.1016/0031-9422(88)80113-4
Berberine	2353	Click to see	336.40	unknown	https://doi.org/10.1021/NP8001496 https://doi.org/10.1016/0031-9422(88)80113-4
Columbamine	72310	Click to see	338.40	unknown	https://doi.org/10.1016/0031-9422(88)80113-4
Coptisine	72322	Click to see C1C[N+]2=C(C=C3C=CC4=C(C3=C2)OCO4)C5=CC6=C(C=C51)OCO6	320.30	unknown	https://doi.org/10.1016/0031-9422(88)80113-4
Epiberberine	160876	Click to see	336.40	unknown	https://doi.org/10.1016/0031-9422(88)80113-4
Palmatine	19009	Click to see	352.40	unknown	https://doi.org/10.1021/NP8001496 https://doi.org/10.1016/0031-9422(88)80113-4
Scoulerine	22955	Click to see	327.40	unknown	https://doi.org/10.1016/0031-9422(88)80113-4
Thalifendine	3084288	Click to see	322.30	unknown	https://doi.org/10.1016/0031-9422(88)80113-4
> Alkaloids and derivatives / Protopine alkaloids
Pseudoprotopine	185559	Click to see CN1CCC2=CC3=C(C=C2C(=O)CC4=CC5=C(C=C4C1)OCO5)OCO3	353.40	unknown	via CMAUP database
> Benzenoids / Phenanthrenes and derivatives
O-Methylpallidine	10405046	Click to see	341.40	unknown	https://doi.org/10.1021/NP8001496
Salutaridine	5408233	Click to see CN1CCC23C=C(C(=O)C=C2C1CC4=C3C(=C(C=C4)OC)O)OC	327.40	unknown	https://doi.org/10.1021/NP8001496
Salutaridine, (-)-	821366	Click to see	327.40	unknown	https://doi.org/10.1021/NP8001496
> Benzenoids / Phenanthrenes and derivatives / Phenanthroindolizidines
(13aR)-2,3-dimethoxy-9,11,12,13,13a,14-hexahydrophenanthro[10,9-f]indolizin-6-ol	9975115	Click to see	349.40	unknown	via CMAUP database
(13aR)-2,3,6-trimethoxy-9,11,12,13,13a,14-hexahydrophenanthro[9,10-f]indolizine	639288	Click to see COC1=CC2=C(C=C1)C3=C(CC4CCCN4C3)C5=CC(=C(C=C52)OC)OC	363.40	unknown	via CMAUP database
(23R)-13-methoxy-5,7-dioxa-19-azahexacyclo[15.7.0.02,10.04,8.011,16.019,23]tetracosa-1(17),2,4(8),9,11(16),12,14-heptaene	11359996	Click to see	347.40	unknown	via CMAUP database
> Benzenoids / Phenol ethers / Anisoles
(S,S)-tramadol(1+)	6919029	Click to see	264.38	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
Calliterpenone	12016376	Click to see	320.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids / Napelline-type diterpenoid alkaloids
(2R,4S,5R,7R,13R,17R)-11-ethyl-13-methyl-6-methylidene-11-azahexacyclo[7.7.2.15,8.01,10.02,8.013,17]nonadecane-4,7,16-triol	24893882	Click to see	359.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
methyl 2-[(3S,10S,13R)-3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-6-methyl-5-methylideneheptanoate	5319602	Click to see	484.80	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
(1S,3R,8R,11S,12S,15R,16S)-7,7,12-trimethyl-15-[(2R)-6-methyl-5-methylideneheptan-2-yl]-6-oxopentacyclo[9.7.0.01,3.03,8.012,16]octadecane-16-carboxylic acid	102286711	Click to see CC(C)C(=C)CCC(C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(=O)C5(C)C)C(=O)O)C	468.70	unknown	https://doi.org/10.1007/S11418-010-0389-6
7,7,12-Trimethyl-15-(6-methyl-5-methylideneheptan-2-yl)-6-oxopentacyclo[9.7.0.01,3.03,8.012,16]octadecane-16-carboxylic acid	162865676	Click to see	468.70	unknown	https://doi.org/10.1007/S11418-010-0389-6
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(2S,4S,6R)-2-[(2S,4S,6R)-2-[(2R,3R,4R,6R)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(5'R,9S,13S,16S)-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-5-hydroxy-6-(hydroxymethyl)-3-[(2S,4S)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-4-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	5316960	Click to see	1035.20	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol	222284	Click to see	414.70	unknown	https://doi.org/10.1007/S11418-010-0389-6
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/S11418-010-0389-6
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2S,3R,4S,5S,6R)-2-[4-(1-hydroxyethyl)phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	11972362	Click to see	300.30	unknown	via CMAUP database
[(2R,3S,4R,5R,6S)-6-[4-[(S)-cyano(hydroxy)methyl]phenoxy]-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate	163195479	Click to see C1=CC(=CC=C1C(C#N)O)OC2C(C(C(C(O2)CO)OC(=O)C=CC3=CC(=C(C=C3)O)O)O)O	473.40	unknown	https://doi.org/10.1016/S0031-9422(00)83491-3
[(2R,3S,4S,5R,6S)-6-[4-[(S)-cyano(hydroxy)methyl]phenoxy]-3,4,5-trihydroxyoxan-2-yl]methyl (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate	163195380	Click to see C1=CC(=CC=C1C(C#N)O)OC2C(C(C(C(O2)COC(=O)C=CC3=CC(=C(C=C3)O)O)O)O)O	473.40	unknown	https://doi.org/10.1016/S0031-9422(00)83491-3
[6-[4-[Cyano(hydroxy)methyl]phenoxy]-3,4,5-trihydroxyoxan-2-yl]methyl 3-(3,4-dihydroxyphenyl)prop-2-enoate	163062953	Click to see C1=CC(=CC=C1C(C#N)O)OC2C(C(C(C(O2)COC(=O)C=CC3=CC(=C(C=C3)O)O)O)O)O	473.40	unknown	https://doi.org/10.1016/S0031-9422(00)83491-3
[6-[4-[Cyano(hydroxy)methyl]phenoxy]-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl] 3-(3,4-dihydroxyphenyl)prop-2-enoate	78069529	Click to see C1=CC(=CC=C1C(C#N)O)OC2C(C(C(C(O2)CO)OC(=O)C=CC3=CC(=C(C=C3)O)O)O)O	473.40	unknown	https://doi.org/10.1016/S0031-9422(00)83491-3
4-(beta-D-glucopyranosyloxy)benzoic acid	440186	Click to see	300.26	unknown	https://doi.org/10.1271/BBB.70249
4-Hydroxybenzoic acid glucoside	3320872	Click to see C1=CC(=CC=C1C(=O)O)OC2C(C(C(C(O2)CO)O)O)O	300.26	unknown	https://doi.org/10.1271/BBB.70249
Nandinin	6442984	Click to see	473.40	unknown	https://doi.org/10.1016/S0031-9422(00)83491-3
> Organoheterocyclic compounds / Benzodioxoles
Oubatchensine	16081672	Click to see	355.30	unknown	via CMAUP database
> Organoheterocyclic compounds / Dihydroisoquinolines
16-Methoxy-5,7-dioxa-13-azoniapentacyclo[11.8.0.02,10.04,8.015,20]henicosa-1(13),2,4(8),9,14,16,18,20-octaene-11,17-diol	12443385	Click to see	338.30	unknown	https://doi.org/10.1016/0031-9422(88)80113-4
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
10-Hydroxy-2,9-dimethoxy-5,6-dihydroisoquinolino[2,1-b]isoquinolin-3-one	102316664	Click to see	323.30	unknown	https://doi.org/10.1016/0031-9422(88)80113-4
16-Methoxy-5,7-dioxa-1-azapentacyclo[11.8.0.03,11.04,8.014,19]henicosa-2,4(8),9,11,13,15,18-heptaen-17-one	11723579	Click to see COC1=CC2=C3C=C4C=CC5=C(C4=CN3CCC2=CC1=O)OCO5	321.30	unknown	https://doi.org/10.1016/0031-9422(88)80113-4
2,9,10-Trimethoxy-5,6-dihydroisoquinolino[2,1-b]isoquinolin-3-one	10065647	Click to see	337.40	unknown	https://doi.org/10.1016/0031-9422(88)80113-4 https://doi.org/10.1021/NP8001496
> Organoheterocyclic compounds / Tetrahydroisoquinolines
Carnegine, (+)-	821487	Click to see	221.29	unknown	https://doi.org/10.1021/NP8001496
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives
(Z)-3-(4-hydroxy-3-methoxyphenyl)-N-[4-[[(E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]amino]butyl]prop-2-enamide	102476222	Click to see	440.50	unknown	https://doi.org/10.1021/NP8001496
(Z)-3-(4-hydroxy-3-methoxyphenyl)-N-[4-[[(Z)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]amino]butyl]prop-2-enamide	102476221	Click to see	440.50	unknown	https://doi.org/10.1021/NP8001496
Bis-ferulamidobutane	5321825	Click to see COC1=C(C=CC(=C1)C=CC(=O)NCCCCNC(=O)C=CC2=CC(=C(C=C2)O)OC)O	440.50	unknown	https://doi.org/10.1021/NP8001496
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
Amentoflavone	5281600	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4=C(C=CC(=C4)C5=CC(=O)C6=C(C=C(C=C6O5)O)O)O)O	538.50	unknown	https://doi.org/10.1016/S0014-2999(99)00144-2
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-3-O-glycosides
Callistephin	44256621	Click to see	433.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
Glucosyringic acid	10383888	Click to see	360.31	unknown	via CMAUP database

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Nandina domestica

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