Juglans mandshurica

Upload a new image!

Details

Description

Synonyms

Common Names

Subtypes (subspecies, varieties, subvarieties, forms)

Germination/Propagation

Distribution

Links to other databases

Genome

Scientific Literature

Phytochemical Profile

Biological Material

Contributors

Collections

Details Top

Internal ID	UUID644046ea4b40c158712798
Scientific name	Juglans mandshurica
Authority	Maxim.
First published in	Bull. Cl. Phys.-Math. Acad. Imp. Sci. Saint-Pétersbourg 15: 127 (1856)

Description Top

Suggest a correction or write a new one!

Juglans mandshurica, also known as Monkey nuts or Tigernut, is a deciduous tree native to the Eastern Asiatic Region. It was first described by a Russian botanist in 1856 and can grow up to 25 meters tall. The leaves are long and pinnate, with serrated edges and pointed tips. The tree produces male and female flowers, with the female flowers developing into nuts in the fall. Despite its hardiness and fast growth, it is mainly cultivated as an ornamental tree in colder regions. The nuts are edible but small and difficult to extract, and the timber is less valuable than other walnut species. The Manchurian walnut is known for its low levels of allelopathic compounds and is not known to cause significant effects in cultivation. There is a similar species, Juglans cathayensis, which is sometimes recognized as a separate species. The Japanese walnut is also closely related and is sometimes considered a variety of Juglans mandshurica.

Synonyms Top

Scientific name	Authority	First published in
Juglans stenocarpa	Maxim.	Mém. Acad. Imp. Sci. St.-Pétersbourg Divers Savans 9: 78 (1859)
Juglans cathayensis	Dode	Bull. Soc. Dendrol. France 11: 47 (1909)
Juglans draconis	Dode	Bull. Soc. Dendrol. France 11: 49 (1909)
Juglans cathayensis var. formosana	(Hayata) A.M.Lu & R.H.Chang	Fl. Reipubl. Popularis Sin. 21: 35 (1979)
Juglans formosana	Hayata	J. Coll. Sci. Imp. Univ. Tokyo 30(1): 283 (1911)
Juglans collapsa	Dode	Bull. Soc. Dendrol. France 11: 49 (1909)

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
English	manchurian walnut
Arabic	جوز منشوري
Azerbaijani	mancuriya qozu
Belarusian	Арэх маньчжурскі
Bulgarian	манджурски орех
Czech	ořešák mandžuský
German	mandschurische walnuss
Finnish	mantsurianjalopähkinä
Finnish	mantshurianjalopähkinä
Finnish	mantsurian jalopähkinä
Finnish	mantšurianjalopähkinä
Armenian	ընկուզենի մանջուրական
Japanese	マンシュウグルミ
Georgian	მანჯურიული კაკალი
Kazakh	Маньчжур жаңғағы
Korean	추자나무
Korean	가래나무
Lithuanian	mandžiūrinis riešutmedis
Norwegian Bokmål	mandsjurvalnøtt
Polish	orzech mandżurski
Russian	Маньчжурский орех
Russian	Орех маньчжурский
Russian	Орех манчжурский
Russian	Орешина маньчжурская
Russian	Орех думбейский
Russian	Манчжурский орех
Swedish	manchurisk valnöt
Turkish	mançurya cevizi
Ukrainian	Горіх маньчжурський
Chinese	野核桃油
Chinese	野核桃仁
Chinese	野核桃
Chinese	胡桃楸（核桃楸）
Chinese	胡桃楸
Chinese	核桃楸皮
Chinese	核桃楸果仁
Chinese	核桃楸果
Chinese	核桃楸
Chinese	楸子

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!

No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!

No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!

No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!

No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!

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
- Caucasus
  - North Caucasus
  - Transcaucasus
- China
  - China North-central
  - China South-central
  - China Southeast
  - Inner Mongolia
  - Manchuria
- Eastern Asia
  - Japan
  - Korea
  - Taiwan
- Middle Asia
  - Tadzhikistan
- Russian Far East
  - Amur
  - Khabarovsk
  - Kuril Islands
  - Primorye
  - Sakhalin

Europe click to expand
- Eastern Europe
  - Central European Russia

Northern America click to expand
- Northeastern U.S.A.
  - New York
- Southeastern U.S.A.
  - Maryland

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0001067447
UNII	U76Q86AD53
USDA Plants	JUMA8
Tropicos	16700044
INPN	1016949
KEW	urn:lsid:ipni.org:names:442388-1
The Plant List	tro-16700044
Plantarium	21010
PFAF	Juglans mandschurica
PaleoBotany	19911
Open Tree Of Life	70093
Observations.org	133329
NCBI Taxonomy	91218
IPNI	442388-1
iNaturalist	366815
IFPNI	F471ED18-38B6-4EE6-852E-FEABF61CDF24
GBIF	4205640
Freebase	/m/03cf0bl
EPPO	IUGMN
EOL	2872272
USDA GRIN	20758
Wikipedia	Juglans_mandshurica

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_022457165.1	NFU_Jman_1.0	Complete Genome	Northeast Forestry University	2022-03-10	25.2x	503.68 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

Pest categorisation of Eulecanium giganteum

Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Grégoire J, Malumphy C, Akrivou A, Kertesz V, Papachristos D, Sfyra O, MacLeod A

EFSA J

03-Apr-2024

PMCID:	PMC10988561
doi:	10.2903/j.efsa.2024.8666
PMID:	38576539

Genome-wide identification analysis of the 4-Coumarate: CoA ligase (4CL) gene family expression profiles in Juglans regia and its wild relatives J. Mandshurica resistance and salt stress

Ma J, Zuo D, Zhang X, Li H, Ye H, Zhang N, Li M, Dang M, Geng F, Zhou H, Zhao P

BMC Plant Biol

23-Mar-2024

PMCID:	PMC10960452
doi:	10.1186/s12870-024-04899-8
PMID:	38519917

Effects of Seed Size and Cache Density on the Seed Fate of Quercus wutaishanica Mediated by Rodents

Cheng J, Zhang M, Yan X

Life (Basel)

21-Feb-2024

PMCID:	PMC10971020
doi:	10.3390/life14030286
PMID:	38541612

Complete Chloroplast Genomes of Four Oaks from the Section Cyclobalanopsis Improve the Phylogenetic Analysis and Understanding of Evolutionary Processes in the Genus Quercus

Wang LL, Li Y, Zheng SS, Kozlowski G, Xu J, Song YG

Genes (Basel)

11-Feb-2024

PMCID:	PMC10888318
doi:	10.3390/genes15020230
PMID:	38397219

New Insights into Antioxidant Peptides: An Overview of Efficient Screening, Evaluation Models, Molecular Mechanisms, and Applications

Zhang Y, Li Y, Quan Z, Xiao P, Duan JA

Antioxidants (Basel)

05-Feb-2024

PMCID:	PMC10886007
doi:	10.3390/antiox13020203
PMID:	38397801

Effect of forest planting patterns on the formation of soil organic carbon during litter lignocellulose degradation from a microbial perspective

Wu D, Yin C, Fan Y, Chi H, Liu Z, Jin G

Front Microbiol

22-Dec-2023

PMCID:	PMC10771852
doi:	10.3389/fmicb.2023.1327481
PMID:	38188580

Genome-Wide Identification of the CBF Gene Family and ICE Transcription Factors in Walnuts and Expression Profiles under Cold Conditions

Zhou H, Ma J, Liu H, Zhao P

Int J Mol Sci

19-Dec-2023

PMCID:	PMC10778614
doi:	10.3390/ijms25010025
PMID:	38203199

Improved Therapeutic Efficacy of MT102, a New Anti-Inflammatory Agent, via a Self-Microemulsifying Drug Delivery System, in Ulcerative Colitis Mice

Baral KC, Lee SH, Song JG, Jeong SH, Han HK

Pharmaceutics

02-Dec-2023

PMCID:	PMC10747691
doi:	10.3390/pharmaceutics15122720
PMID:	38140061

Beneficial and biocontrol effects of Trichoderma atroviride, a dominant species in white birch rhizosphere soil

Liu K, Zhang YZ, Du HY, Wang ZY, Gu PW, Liu ZH, Yu ZY

Front Microbiol

30-Oct-2023

PMCID:	PMC10642753
doi:	10.3389/fmicb.2023.1265435
PMID:	37965558

Assessing mammal population densities in response to urbanization using camera trap distance sampling

Li Z, Shi X, Lu J, Fu X, Fu Y, Cui Y, Chen L, Duo L, Wang L, Wang T

Ecol Evol

18-Oct-2023

PMCID:	PMC10582676
doi:	10.1002/ece3.10634
PMID:	37859829

Promoter cloning and activities analysis of JmLFY, a key gene for flowering in Juglans mandshurica

Zhang L, Fu J, Dong T, Zhang M, Wu J, Liu C

Front Plant Sci

12-Oct-2023

PMCID:	PMC10602732
doi:	10.3389/fpls.2023.1243030
PMID:	37900747

Sleep Promotion by 3-Hydroxy-4-Iminobutyric Acid in Walnut Diaphragma juglandis Fructus

Ji J, Ye Y, Sheng L, Sun J, Hong Q, Liu C, Ding J, Geng S, Xu D, Zhang Y, Sun X

Research (Wash D C)

19-Sep-2023

PMCID:	PMC10508226
doi:	10.34133/research.0216
PMID:	37732131

Diversity and taxonomy of the genus Amanita (Amanitaceae, Agaricales) in the Yanshan Mountains, Northern China

Zhou H, Guo M, Zhuo L, Yan H, Sui X, Gao Y, Hou C

Front Plant Sci

14-Sep-2023

PMCID:	PMC10539691
doi:	10.3389/fpls.2023.1226794
PMID:	37780523

Conserving a threatened North American walnut: a chromosome-scale reference genome for butternut (Juglans cinerea)

Guzman-Torres CR, Trybulec E, LeVasseur H, Akella H, Amee M, Strickland E, Pauloski N, Williams M, Romero-Severson J, Hoban S, Woeste K, Pike CC, Fetter KC, Webster CN, Neitzey ML, O’Neill RJ, Wegrzyn JL

G3 (Bethesda)

13-Sep-2023

PMCID:	PMC10849370
doi:	10.1093/g3journal/jkad189
PMID:	37703053

Searching for Natural Plants with Antimelanogenesis and Antityrosinase Properties for Cosmeceutical or Nutricosmetics Applications: A Systematic Review

Tung XY, Yip JQ, Gew LT

ACS Omega

06-Sep-2023

PMCID:	PMC10515176
doi:	10.1021/acsomega.3c02994
PMID:	37744793

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 / Anthracenes / Anthracenecarboxylic acids and derivatives / Anthracenecarboxylic acids
1,5-Dihydroxy-9,10-anthraquinone-3-carboxylic acid	24946032	Click to see C1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C(=CC(=C3)C(=O)O)O	284.22	unknown	https://doi.org/10.1002/HLCA.201000462
4-Ethoxycarbonyl-8-hydroxy-9,10-dioxoanthracene-2-carboxylic acid	54597552	Click to see CCOC(=O)C1=CC(=CC2=C1C(=O)C3=C(C2=O)C(=CC=C3)O)C(=O)O	340.30	unknown	https://doi.org/10.1002/HLCA.201000462
Ethyl 4,8-dihydroxy-9,10-dioxoanthracene-2-carboxylate	54597553	Click to see CCOC(=O)C1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C(=CC=C3)O	312.27	unknown	https://doi.org/10.1002/HLCA.201000462
> Benzenoids / Benzene and substituted derivatives / Benzenesulfonamides
4-[2-(5-bromo-2-oxoindol-3-yl)hydrazinyl]benzenesulfonamide	5858639	Click to see C1=CC(=CC=C1NNC2=C3C=C(C=CC3=NC2=O)Br)S(=O)(=O)N	395.23	unknown	https://doi.org/10.1002/CHIN.200334202
> 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/BF02979196 https://doi.org/10.1007/S10600-011-9895-3
> Benzenoids / Benzene and substituted derivatives / Phenylmethylamines / Phenylbenzamines
Lavendustin c	3896	Click to see C1=CC(=C(C=C1NCC2=C(C=CC(=C2)O)O)C(=O)O)O	275.26	unknown	https://doi.org/10.1002/CHIN.200334202
> Benzenoids / Naphthalenes / Naphthoquinones
5-Hydroxy-2-methoxy-1,4-naphthoquinone	10104346	Click to see COC1=CC(=O)C2=C(C1=O)C=CC=C2O	204.18	unknown	https://doi.org/10.1021/NP970413M
Juglone	3806	Click to see C1=CC2=C(C(=O)C=CC2=O)C(=C1)O	174.15	unknown	https://doi.org/10.1016/S0031-9422(00)81321-7
> Benzenoids / Tetralins
(4R)-4-hydroxy-3,4-dihydro-2H-naphthalen-1-one	49836756	Click to see C1CC(=O)C2=CC=CC=C2C1O	162.18	unknown	https://doi.org/10.1248/CPB.53.934
(4R)-5-hydroxy-4-methoxy-3,4-dihydro-2H-naphthalen-1-one	11788768	Click to see COC1CCC(=O)C2=C1C(=CC=C2)O	192.21	unknown	https://doi.org/10.1248/CPB.53.934
(4R)-5,8-dihydroxy-4-methoxy-3,4-dihydro-2H-naphthalen-1-one	11171801	Click to see COC1CCC(=O)C2=C(C=CC(=C12)O)O	208.21	unknown	https://doi.org/10.1248/CPB.53.934
(S)-4,8-Dihydroxy-5-methoxytetralin-1-one	101695570	Click to see COC1=C2C(CCC(=O)C2=C(C=C1)O)O	208.21	unknown	https://doi.org/10.1248/CPB.53.934
(S)-Isosclerone	10442251	Click to see C1CC(=O)C2=C(C1O)C=CC=C2O	178.18	unknown	https://doi.org/10.1248/CPB.53.934
1(2H)-Naphthalenone, 3,4-dihydro-4-hydroxy-, (4S)-	11240662	Click to see C1CC(=O)C2=CC=CC=C2C1O	162.18	unknown	https://doi.org/10.1248/CPB.53.934
4-hydroxy-3,4-dihydronaphthalen-1(2H)-one	152325	Click to see C1CC(=O)C2=CC=CC=C2C1O	162.18	unknown	https://doi.org/10.1248/CPB.53.934
4,8-dihydroxy-5-methoxy-3,4-dihydro-2H-naphthalen-1-one	15297928	Click to see COC1=C2C(CCC(=O)C2=C(C=C1)O)O	208.21	unknown	https://doi.org/10.1248/CPB.53.934
5-hydroxy-4-methoxy-3,4-dihydro-2H-naphthalen-1-one	72814799	Click to see COC1CCC(=O)C2=C1C(=CC=C2)O	192.21	unknown	https://doi.org/10.1248/CPB.53.934
5,8-dihydroxy-4-methoxy-3,4-dihydro-2H-naphthalen-1-one	85420015	Click to see COC1CCC(=O)C2=C(C=CC(=C12)O)O	208.21	unknown	https://doi.org/10.1248/CPB.53.934
Isosclerone	13369486	Click to see C1CC(=O)C2=C(C1O)C=CC=C2O	178.18	unknown	https://doi.org/10.1248/CPB.53.934 https://doi.org/10.1002/CHIN.200334202
Regiolone	44576009	Click to see C1CC(=O)C2=C(C1O)C=CC=C2O	178.18	unknown	https://doi.org/10.1248/CPB.53.934
> Lignans, neolignans and related compounds / Lignan glycosides
(9S)-4-hydroxy-17-methoxy-9-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2-oxatricyclo[13.2.2.13,7]icosa-1(17),3,5,7(20),15,18-hexaen-10-one	163045431	Click to see COC1=C2C=CC(=C1)CCCCC(=O)C(CC3=CC(=C(C=C3)O)O2)OC4C(C(C(C(O4)CO)O)O)O	504.50	unknown	https://doi.org/10.1021/NP970413M
4-Hydroxy-17-methoxy-9-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2-oxatricyclo[13.2.2.13,7]icosa-1(17),3,5,7(20),15,18-hexaen-10-one	85244584	Click to see COC1=C2C=CC(=C1)CCCCC(=O)C(CC3=CC(=C(C=C3)O)O2)OC4C(C(C(C(O4)CO)O)O)O	504.50	unknown	https://doi.org/10.1021/NP970413M
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(4S)-4-(3-hydroxyphenyl)-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutanoic acid	101728055	Click to see C1=CC(=CC(=C1)O)C(CCC(=O)O)OC2C(C(C(C(O2)CO)O)O)O	358.34	unknown	https://doi.org/10.3987/COM-04-10054
4-(3-Hydroxyphenyl)-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutanoic acid	163021910	Click to see C1=CC(=CC(=C1)O)C(CCC(=O)O)OC2C(C(C(C(O2)CO)O)O)O	358.34	unknown	https://doi.org/10.3987/COM-04-10054
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
(2S)-2-methylhexadecan-1-ol	98062188	Click to see CCCCCCCCCCCCCCC(C)CO	256.50	unknown	https://doi.org/10.1007/S10600-011-9895-3
2-Methyl-1-hexadecanol	17218	Click to see CCCCCCCCCCCCCCC(C)CO	256.50	unknown	https://doi.org/10.1007/S10600-011-9895-3
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
Proximadiol	165258	Click to see CC12CCCC(C1CC(CC2)C(C)(C)O)(C)O	240.38	unknown	https://doi.org/10.1021/NP0201063
> Lipids and lipid-like molecules / Sphingolipids / Glycosphingolipids
(2R)-N-[(E,2S,3S,4R)-3,4-dihydroxy-1-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoctadec-8-en-2-yl]-2-hydroxydocosanamide	162925309	Click to see CCCCCCCCCCCCCCCCCCCCC(C(=O)NC(COC1C(C(C(C(O1)CO)O)O)O)C(C(CCCC=CCCCCCCCCC)O)O)O	816.20	unknown	https://doi.org/10.1007/S10600-011-9895-3
N-[3,4-dihydroxy-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoctadec-8-en-2-yl]-2-hydroxydocosanamide	72764896	Click to see CCCCCCCCCCCCCCCCCCCCC(C(=O)NC(COC1C(C(C(C(O1)CO)O)O)O)C(C(CCCC=CCCCCCCCCC)O)O)O	816.20	unknown	https://doi.org/10.1007/S10600-011-9895-3
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(4S)-4-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-naphthalen-1-one	162996749	Click to see C1CC(=O)C2=CC=CC=C2C1OC3C(C(C(C(O3)CO)O)O)O	324.32	unknown	https://doi.org/10.1248/CPB.52.566
(4S)-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxytetralin-1-one	21577027	Click to see C1CC(=O)C2=CC=CC=C2C1OC3C(C(C(C(O3)CO)O)O)O	324.32	unknown	https://doi.org/10.1248/CPB.52.566
(4S)-5-hydroxy-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-naphthalen-1-one	21577028	Click to see C1CC(=O)C2=C(C1OC3C(C(C(C(O3)CO)O)O)O)C(=CC=C2)O	340.32	unknown	https://doi.org/10.1248/CPB.52.566
(4S)-5,8-dihydroxy-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-naphthalen-1-one	21577030	Click to see C1CC(=O)C2=C(C=CC(=C2C1OC3C(C(C(C(O3)CO)O)O)O)O)O	356.32	unknown	https://doi.org/10.1248/CPB.52.566
(4S)-6-hydroxy-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-naphthalen-1-one	21577029	Click to see C1CC(=O)C2=C(C1OC3C(C(C(C(O3)CO)O)O)O)C=C(C=C2)O	340.32	unknown	https://doi.org/10.1248/CPB.52.566
4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-naphthalen-1-one	73802864	Click to see C1CC(=O)C2=CC=CC=C2C1OC3C(C(C(C(O3)CO)O)O)O	324.32	unknown	https://doi.org/10.1248/CPB.52.566
5-hydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-naphthalen-1-one	73802865	Click to see C1CC(=O)C2=C(C1OC3C(C(C(C(O3)CO)O)O)O)C(=CC=C2)O	340.32	unknown	https://doi.org/10.1248/CPB.52.566
5,8-dihydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-naphthalen-1-one	73802867	Click to see C1CC(=O)C2=C(C=CC(=C2C1OC3C(C(C(C(O3)CO)O)O)O)O)O	356.32	unknown	https://doi.org/10.1248/CPB.52.566
6-hydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-naphthalen-1-one	73802866	Click to see C1CC(=O)C2=C(C1OC3C(C(C(C(O3)CO)O)O)O)C=C(C=C2)O	340.32	unknown	https://doi.org/10.1248/CPB.52.566
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[4-hydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxynaphthalen-1-yl]oxyoxane-3,4,5-triol	101728054	Click to see C1=CC2=C(C=CC(=C2C(=C1)OC3C(C(C(C(O3)CO)O)O)O)O)OC4C(C(C(C(O4)CO)O)O)O	500.40	unknown	https://doi.org/10.3987/COM-04-10054
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[5-hydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxynaphthalen-1-yl]oxyoxane-3,4,5-triol	101728057	Click to see C1=CC2=C(C=CC(=C2C(=C1)O)OC3C(C(C(C(O3)CO)O)O)O)OC4C(C(C(C(O4)CO)O)O)O	500.40	unknown	https://doi.org/10.3987/COM-04-10054
(2S,3R,4R,5R,6R)-2-methyl-6-[[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(4-methoxynaphthalen-1-yl)oxyoxan-2-yl]methoxy]oxane-3,4,5-triol	101033302	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC=C(C4=CC=CC=C43)OC)O)O)O)O)O)O	482.50	unknown	https://doi.org/10.1055/S-0029-1243129
(2S,3R,4S,5S,6R)-2-(4,8-dihydroxynaphthalen-1-yl)oxy-6-[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxane-3,4,5-triol	101033300	Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C4C(=C(C=C3)O)C=CC=C4O)O)O)O)O)O)O	470.40	unknown	https://doi.org/10.1055/S-0029-1243129
(2S,3R,4S,5S,6R)-2-(4,8-dihydroxynaphthalen-1-yl)oxy-6-[[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxane-3,4,5-triol	101033301	Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C4C(=C(C=C3)O)C=CC=C4O)O)O)O)O)O)O	470.40	unknown	https://doi.org/10.1248/CPB.48.194 https://doi.org/10.1055/S-0029-1243129
(4S)-4,8-dihydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-naphthalen-1-one	21577031	Click to see C1CC(=O)C2=C(C=CC(=C2C1O)OC3C(C(C(C(O3)CO)O)O)O)O	356.32	unknown	https://doi.org/10.1248/CPB.52.566
[(2R,3S,4S,5R,6S)-6-(4,8-dihydroxynaphthalen-1-yl)oxy-3,4,5-trihydroxyoxan-2-yl]methyl 3,5-dihydroxy-4-methoxybenzoate	10815375	Click to see COC1=C(C=C(C=C1O)C(=O)OCC2C(C(C(C(O2)OC3=C4C(=C(C=C3)O)C=CC=C4O)O)O)O)O	504.40	unknown	https://doi.org/10.1248/CPB.48.194
[(2R,3S,4S,5R,6S)-6-[(4,8-dihydroxy-1-naphthyl)oxy]-3,4,5-trihydroxy-tetrahydropyran-2-yl]methyl 3,4,5-trihydroxybenzoate	477406	Click to see C1=CC2=C(C=CC(=C2C(=C1)O)OC3C(C(C(C(O3)COC(=O)C4=CC(=C(C(=C4)O)O)O)O)O)O)O	490.40	unknown	https://doi.org/10.1248/CPB.48.194
[(2R,3S,4S,5R,6S)-6-[[(8S)-4,8-dihydroxy-5-oxo-7,8-dihydro-6H-naphthalen-1-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate	10346156	Click to see C1CC(=O)C2=C(C=CC(=C2C1O)OC3C(C(C(C(O3)COC(=O)C4=CC(=C(C(=C4)O)O)O)O)O)O)O	508.40	unknown	https://doi.org/10.1248/CPB.48.194
[(2R,3S,4S,5R,6S)-6-[[(8S)-4,8-dihydroxy-5-oxo-7,8-dihydro-6H-naphthalen-1-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl 3,5-dihydroxy-4-methoxybenzoate	101012984	Click to see COC1=C(C=C(C=C1O)C(=O)OCC2C(C(C(C(O2)OC3=C4C(CCC(=O)C4=C(C=C3)O)O)O)O)O)O	522.50	unknown	https://doi.org/10.1248/CPB.48.194
[6-(4,8-Dihydroxynaphthalen-1-yl)oxy-3,4,5-trihydroxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate	78190003	Click to see C1=CC2=C(C=CC(=C2C(=C1)O)OC3C(C(C(C(O3)COC(=O)C4=CC(=C(C(=C4)O)O)O)O)O)O)O	490.40	unknown	https://doi.org/10.1248/CPB.48.194
[6-(4,8-Dihydroxynaphthalen-1-yl)oxy-3,4,5-trihydroxyoxan-2-yl]methyl 3,5-dihydroxy-4-methoxybenzoate	85277275	Click to see COC1=C(C=C(C=C1O)C(=O)OCC2C(C(C(C(O2)OC3=C4C(=C(C=C3)O)C=CC=C4O)O)O)O)O	504.40	unknown	https://doi.org/10.1248/CPB.48.194
[6-[(4,8-dihydroxy-5-oxo-7,8-dihydro-6H-naphthalen-1-yl)oxy]-3,4,5-trihydroxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate	85116707	Click to see C1CC(=O)C2=C(C=CC(=C2C1O)OC3C(C(C(C(O3)COC(=O)C4=CC(=C(C(=C4)O)O)O)O)O)O)O	508.40	unknown	https://doi.org/10.1248/CPB.48.194
[6-[(4,8-dihydroxy-5-oxo-7,8-dihydro-6H-naphthalen-1-yl)oxy]-3,4,5-trihydroxyoxan-2-yl]methyl 3,5-dihydroxy-4-methoxybenzoate	162873304	Click to see COC1=C(C=C(C=C1O)C(=O)OCC2C(C(C(C(O2)OC3=C4C(CCC(=O)C4=C(C=C3)O)O)O)O)O)O	522.50	unknown	https://doi.org/10.1248/CPB.48.194
2-(4,8-Dihydroxynaphthalen-1-yl)oxy-6-[(3,4,5-trihydroxyoxan-2-yl)oxymethyl]oxane-3,4,5-triol	162886438	Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C4C(=C(C=C3)O)C=CC=C4O)O)O)O)O)O)O	470.40	unknown	https://doi.org/10.1248/CPB.48.194 https://doi.org/10.1055/S-0029-1243129
2-(Hydroxymethyl)-6-[4-hydroxy-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxynaphthalen-1-yl]oxyoxane-3,4,5-triol	162931575	Click to see C1=CC2=C(C=CC(=C2C(=C1)OC3C(C(C(C(O3)CO)O)O)O)O)OC4C(C(C(C(O4)CO)O)O)O	500.40	unknown	https://doi.org/10.3987/COM-04-10054
2-(Hydroxymethyl)-6-[5-hydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxynaphthalen-1-yl]oxyoxane-3,4,5-triol	162937910	Click to see C1=CC2=C(C=CC(=C2C(=C1)O)OC3C(C(C(C(O3)CO)O)O)O)OC4C(C(C(C(O4)CO)O)O)O	500.40	unknown	https://doi.org/10.3987/COM-04-10054
2-Methyl-6-[[3,4,5-trihydroxy-6-(4-methoxynaphthalen-1-yl)oxyoxan-2-yl]methoxy]oxane-3,4,5-triol	162942848	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC=C(C4=CC=CC=C43)OC)O)O)O)O)O)O	482.50	unknown	https://doi.org/10.1055/S-0029-1243129
4,8-dihydroxy-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-naphthalen-1-one	73802868	Click to see C1CC(=O)C2=C(C=CC(=C2C1O)OC3C(C(C(C(O3)CO)O)O)O)O	356.32	unknown	https://doi.org/10.1248/CPB.52.566
alpha-Hydrojuglone 4-glucoside	477404	Click to see C1=CC2=C(C=CC(=C2C(=C1)O)OC3C(C(C(C(O3)CO)O)O)O)O	338.31	unknown	https://doi.org/10.1248/CPB.48.194
methyl 1,5-dihydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxynaphthalene-2-carboxylate	10046260	Click to see COC(=O)C1=CC(=C2C(=C1O)C=CC=C2O)OC3C(C(C(C(O3)CO)O)O)O	396.30	unknown	https://doi.org/10.1021/NP970413M
Methyl 1,5-dihydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxynaphthalene-2-carboxylate	75048925	Click to see COC(=O)C1=CC(=C2C(=C1O)C=CC=C2O)OC3C(C(C(C(O3)CO)O)O)O	396.30	unknown	https://doi.org/10.1021/NP970413M
> Organoheterocyclic compounds / Naphthopyrans / Naphthopyranones / Naphthopyranone glycosides
2,3,7,11-tetrahydroxy-12-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxynaphtho[2,3-c]isochromen-5-one	54597492	Click to see C1=CC2=C(C(=C1)O)C(=C3C4=CC(=C(C=C4C(=O)OC3=C2O)O)O)OC5C(C(C(C(O5)CO)O)O)O	488.40	unknown	https://doi.org/10.1002/HLCA.201000462
> Organoheterocyclic compounds / Quinolines and derivatives / Phenylquinolines
(E)-3-(1H-benzo[d]imidazol-2-yl)-1-(6-chloro-2-hydroxy-4-phenylquinolin-3-yl)prop-2-en-1-one	5343381	Click to see C1=CC=C(C=C1)C2=C(C(=O)NC3=C2C=C(C=C3)Cl)C(=O)C=CC4=NC5=CC=CC=C5N4	425.90	unknown	https://doi.org/10.1021/NP0201063 https://doi.org/10.1002/CHIN.200334202
> Phenylpropanoids and polyketides / Diarylheptanoids / Cyclic diarylheptanoids / Meta,para-diphenylether diarylheptanoids
(+)-Galeon	16116346	Click to see COC1=C2C=CC(=C1)CCCCC(=O)CCC3=CC(=C(C=C3)O)O2	326.40	unknown	https://doi.org/10.1002/CHIN.200334202 https://doi.org/10.1021/NP0201063
4,17-Dimethoxy-2-oxatricyclo[13.2.2.13,7]icosa-1(17),3,5,7(20),15,18-hexaene-10,16-diol	44567146	Click to see COC1=C2C=C(CCC(CCCCC3=C(C(=C(O2)C=C3)OC)O)O)C=C1	358.40	unknown	https://doi.org/10.1021/NP0201063
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
(2S,4S,6R)-2-[(1S)-1-hydroxy-2-(4-hydroxyphenyl)ethyl]-6-(4-hydroxy-3-methoxyphenyl)oxan-4-ol	46184734	Click to see COC1=C(C=CC(=C1)C2CC(CC(O2)C(CC3=CC=C(C=C3)O)O)O)O	360.40	unknown	https://doi.org/10.1002/CHIN.200334202
1-(4-Hydroxyphenyl)-7-(4-hydroxy-3-methoxyphenyl)-4-hepten-3-one	78200757	Click to see COC1=C(C=CC(=C1)CCC=CC(=O)CCC2=CC=C(C=C2)O)O	326.40	unknown	https://doi.org/10.1021/NP0201063
2-[1-Hydroxy-2-(4-hydroxyphenyl)ethyl]-6-(4-hydroxy-3-methoxyphenyl)oxan-4-ol	44567145	Click to see COC1=C(C=CC(=C1)C2CC(CC(O2)C(CC3=CC=C(C=C3)O)O)O)O	360.40	unknown	https://doi.org/10.1021/NP0201063
7-(4-Hydroxy-3-methoxy-phenyl)-1-(4-hydroxy-phenyl)-hept-4-en-3-one	637455	Click to see COC1=C(C=CC(=C1)CCC=CC(=O)CCC2=CC=C(C=C2)O)O	326.40	unknown	https://doi.org/10.1021/NP0201063
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids / Curcuminoids
(5S)-7-(4-hydroxy-3-methoxyphenyl)-1-(4-hydroxyphenyl)-5-methoxyheptan-3-one	163013521	Click to see COC1=C(C=CC(=C1)CCC(CC(=O)CCC2=CC=C(C=C2)O)OC)O	358.40	unknown	https://doi.org/10.1002/CHIN.200334202
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
(+/-)-Taxifolin	471	Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O	304.25	unknown	https://doi.org/10.1248/CPB.48.194 https://doi.org/10.1248/BPB.26.1042
Taxifolin	439533	Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O	304.25	unknown	https://doi.org/10.1248/CPB.48.194 https://doi.org/10.1007/BF02976598 https://doi.org/10.1248/BPB.26.1042
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Myricetin	5281672	Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O	318.23	unknown	https://doi.org/10.1007/BF02976598
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/BF02976598
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxy-phenyl)-5,7-dihydroxy-3-(3,4,5-trihydroxy-6-methyl-tetrahydro-pyran-2-yloxy)-chromen-4-one	5353915	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/BPB.26.1042 https://doi.org/10.1248/CPB.48.194
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	5378597	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	https://doi.org/10.1007/S10600-011-9895-3
5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one	12047524	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	432.40	unknown	https://doi.org/10.1248/CPB.48.194
5,7-dihydroxy-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2-(3,4,5-trihydroxyphenyl)chromen-4-one	129010103	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.48.194
Afzelin	5316673	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	432.40	unknown	https://doi.org/10.1248/CPB.48.194 https://doi.org/10.1007/BF02976598 https://doi.org/10.1248/BPB.26.1042
Hyperoside	5281643	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	https://doi.org/10.1007/S10600-011-9895-3
Kaempferol-3-O-rhamnoside	5835713	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	432.40	unknown	https://doi.org/10.1248/CPB.48.194 https://doi.org/10.1248/BPB.26.1042
Myricetin 3-beta-D-glucopyranoside	12311099	Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O	480.40	unknown	https://doi.org/10.1007/S10600-011-9895-3
Myricetin 3-galactoside	5491408	Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O	480.40	unknown	https://doi.org/10.1007/S10600-011-9895-3
Myricetin 3-rhamnoside	5352000	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.48.194 https://doi.org/10.1248/BPB.26.1042
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.48.194 https://doi.org/10.1007/BF02976598 https://doi.org/10.1248/BPB.26.1042
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/BPB.26.1042 https://doi.org/10.1248/CPB.48.194 https://doi.org/10.1007/BF02976598
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
irilin D	10495590	Click to see COC1=C(C2=C(C=C1O)OC=C(C2=O)C3=CC(=C(C=C3)O)O)O	316.26	unknown	https://doi.org/10.1248/CPB.48.194
> Phenylpropanoids and polyketides / Tannins
1,2,3,6-Tetragalloyl-beta-D-glucopyranose	5153644	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)O	788.60	unknown	https://doi.org/10.1248/BPB.26.1042 https://doi.org/10.1248/CPB.48.194
1,2,6-Trigalloyl-beta-D-glucopyranose	3357644	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)O)O	636.50	unknown	https://doi.org/10.1248/BPB.26.1042 https://doi.org/10.1248/CPB.48.194
1,2,6-Trigalloylglucose	440308	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)O)O	636.50	unknown	https://doi.org/10.1248/BPB.26.1042 https://doi.org/10.1248/CPB.48.194
NP-003686	73178	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)O	788.60	unknown	https://doi.org/10.1248/BPB.26.1042 https://doi.org/10.1248/CPB.48.194
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
[(2R,3S,4S,5R,6S)-6-[(4,8-dihydroxy-1-naphthyl)oxy]-3,4,5-trihydroxy-tetrahydropyran-2-yl]methyl 4-hydroxy-3,5-dimethoxy-benzoate	477405	Click to see COC1=CC(=CC(=C1O)OC)C(=O)OCC2C(C(C(C(O2)OC3=C4C(=C(C=C3)O)C=CC=C4O)O)O)O	518.50	unknown	https://doi.org/10.1248/CPB.48.194
[(2R,3S,4S,5R,6S)-6-[[(8S)-4,8-dihydroxy-5-oxo-7,8-dihydro-6H-naphthalen-1-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl 4-hydroxy-3,5-dimethoxybenzoate	101012983	Click to see COC1=CC(=CC(=C1O)OC)C(=O)OCC2C(C(C(C(O2)OC3=C4C(CCC(=O)C4=C(C=C3)O)O)O)O)O	536.50	unknown	https://doi.org/10.1021/NP970413M https://doi.org/10.1248/CPB.48.194
[6-(4,8-Dihydroxynaphthalen-1-yl)oxy-3,4,5-trihydroxyoxan-2-yl]methyl 4-hydroxy-3,5-dimethoxybenzoate	78190002	Click to see COC1=CC(=CC(=C1O)OC)C(=O)OCC2C(C(C(C(O2)OC3=C4C(=C(C=C3)O)C=CC=C4O)O)O)O	518.50	unknown	https://doi.org/10.1248/CPB.48.194
[6-[(4,8-dihydroxy-5-oxo-7,8-dihydro-6H-naphthalen-1-yl)oxy]-3,4,5-trihydroxyoxan-2-yl]methyl 4-hydroxy-3,5-dimethoxybenzoate	85244968	Click to see COC1=CC(=CC(=C1O)OC)C(=O)OCC2C(C(C(C(O2)OC3=C4C(CCC(=O)C4=C(C=C3)O)O)O)O)O	536.50	unknown	https://doi.org/10.1021/NP970413M https://doi.org/10.1248/CPB.48.194

Biological Material Top

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections	0
In public collections	0

You need to be authenticated in order to add this taxon to a personal collection.

Juglans mandshurica

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top