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.

Adzuki beans (Vigna angularis) have long been a staple of East Asian diets, but they also appear in several traditional medicinal systems. In Chinese folk medicine, dried adzuki beans are boiled into a decoction to relieve constipation and to “purify the blood” (Liu et al., 2015). Korean practitioners use a similar infusion of the beans to treat urinary tract infections and to reduce swelling, citing the bean’s cooling properties (Kim et al., 2018). In Japan, a poultice made from ground adzuki beans is applied to bruises and minor wounds to promote healing and reduce inflammation (Tanaka, 2012). All three traditions employ the whole dried bean, either as a decoction or as a macerated paste, and the preparations are typically taken orally or applied topically.

A simple, safe decoction can be made at home. Weigh 10 g of dried adzuki beans and place them in 200 ml of boiling water. Simmer for 30 minutes, then strain the liquid into a cup. Drink one cup in the morning or evening. Because raw adzuki beans contain lectins that can be irritating, it is important to use only cooked or decocted beans. Pregnant women should consult a healthcare provider before using adzuki bean preparations, and individuals with known bean allergies should avoid them.

The therapeutic effects of adzuki beans are supported by several well‑characterized phytochemicals. Isoflavones such as daidzein and genistein, along with flavonoids, saponins, and phenolic acids, have been isolated from the bean and are known to possess antioxidant and anti‑inflammatory activities. These compounds likely contribute to the traditional uses for constipation relief, blood purification, and wound healing. Lectins, while potentially toxic in raw form, are largely denatured by the decoction process and are not considered a concern in the cooked preparations described above.

Modern research continues to explore the health benefits of adzuki beans. Studies have shown that extracts can lower blood glucose levels, reduce oxidative stress, and support liver health, leading to the inclusion of adzuki bean extracts in several nutraceutical products. Traditional uses remain common in rural communities, and the bean’s culinary versatility ensures that it remains a popular ingredient in both everyday meals and medicinal preparations.

General Uses Top

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Food and beverages (non-medicinal):
Seeds of Vigna angularis (adzuki bean) are used as an ingredient in a wide range of non-medicinal food products. The dried seeds are cooked and milled into a smooth paste (red bean paste, an), widely employed in East Asian confectionery such as manjū, yōkan, dorayaki, and mochi fillings, and in buns and pastries. Whole seeds are simmered or steamed for sweet or savory dishes; the beans retain their shape well during cooking. Sprouted seeds are used as a fresh vegetable. Paste or cooked seeds are incorporated as thickeners and flavoring bases in non-alcoholic ready-to-drink beverages and syrups for confectionery applications. In product development, the seeds are processed by soaking, cooking, mashing, and, where needed, mechanical or enzymatic refining to standard paste textures.

Scientific/model-organism use:
Adzuki bean (Vigna angularis) is used as a model organism for genetics and breeding within the Vigna genus. The reference genome sequence and annotations are publicly available (e.g., NCBI/Phytozome; assembly Vang_1.0), enabling comparative genomics, linkage mapping, and gene cloning across Phaseoleae. Germplasm and genomics resources are maintained in international databases such as USDA GRIN and the Vigna Genome Database, facilitating trait mapping, marker-assisted selection, and community research on seed quality, plant architecture, and stress resistance.

Synonyms Top

Scientific name	Authority	First published in
Phaseolus angularis	(Willd.) W.Wight	Bull. Bur. Pl. Industr. U.S.D.A.137: 17 (1909)
Azukia angularis	(Willd.) Ohwi	Bull. Natl. Sci. Mus. Tokyo33: 77 (1953)
Vigna angularis var. angularis	(Willd.) Ohwi & H.Ohashi
Dolichos angularis	Willd.	Sp. Pl., ed. 4, 3: 1051 (1802)
Vigna angularis var. nipponensis	(Ohwi) Ohwi & H.Ohashi	J. Jap. Bot.44: 30 (1969)
Azukia angularis var. nipponensis	(Ohwi) Ohwi	Fl. Jap.: 691 (1953)
Phaseolus nipponensis	Ohwi	J. Jap. Bot.13: 435 (1937)
Dolichos angulatus	Willd.	Enum. Pl. Hort. Berol., Suppl.: 51 (1814)
Phaseolus atsuki	Siebold	Verh. Batav. Genootsch. Kunsten 12: 57 (1830)

Common names Top

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Filter by language:

Language	Common/alternative name
English	adzuki bean
English	azuki bean
Spanish	azuki
Spanish	phaseolus mungo
Spanish	adzuki
Spanish	frijol azuki
Spanish	frijoles azuki
Spanish	judia azuki
Spanish	judía azuki
Spanish	judias azuki
Spanish	judías azuki
Spanish	poroto azuki
Spanish	porotos azuki
Spanish	soja roja
Spanish	azukia angularis
Spanish	dolichos angularis
Spanish	phaseolus angularis
Arabic	لوبياء مقرنة
Arabic	ماش
Catalan	aduki
Catalan	adzuki
Catalan	azuki
Catalan	mongetera azuki
Catalan	mongeta azuki
Czech	fazole azuki
Czech	azuki
German	azuki
German	adzuki-bohne
German	azukibohne
German	adzukibohne
Esperanto	azukio
Esperanto	azuki-fabo
Basque	azuki
Persian	آزوکی
Persian	ازوکی
Persian	لوبیای ازوکی
Persian	لوبیای آزوکی
Finnish	adsukipapu
Finnish	adukipapu
Finnish	adzukipapu
Finnish	azukipapu
French	azuki
French	adzuki
French	asuki
French	haricot adzuki
French	haricot azuki
hak	fùng-theu
Hebrew	אזוקי
Hungarian	adzukibab
Hungarian	azuki
Hungarian	azukibab
Indonesian	kacang azuki
Italian	azuki
Italian	fagiolo azuki
Japanese	あずき
Japanese	小豆
Japanese	アズキ
Korean	팥
Lithuanian	japoniškoji pupuolė
Lithuanian	raudonoji pupelė
Lithuanian	japoninė pupuolė
mnc	ᠰᡳᠰᠠ
Malay	kacang merah
nan	Âng-tāu
Dutch	adukiboon
Polish	fasola adzuki
Polish	fasola azuki
Polish	phaseolus angularis
Portuguese	azuki
Portuguese	feijão-azuqui
Romanian	fasolea adzuki
Russian	Фасоль угловатая
Russian	Адзуки
Slovenian	azuki fižol
Slovenian	adzuki fožol
Serbian	Црвени пасуљ
Serbian	Азуки пасуљ
Swedish	azuki
Swedish	adukiböna
Swedish	adukibönor
Swedish	adzukiböna
Swedish	adzukibönor
Swedish	azukibönor
Swedish	azukiböna
Swahili	muazuki
szy	lihum
Thai	ถั่วอาซูกิ
Ukrainian	Адзукі
Vietnamese	Đậu đỏ
za	lwglimz
Chinese	紅豆
Chinese	黑小豆
Chinese	歪头菜
Chinese	赤豆
Chinese	赤小豆叶
Chinese	赤小豆
Chinese	赤小豆花
Chinese	赤小豆芽
Chinese	小豆
Chinese	红小豆

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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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- East Tropical Africa
  - Kenya

Asia-temperate click to expand
- China
  - China North-central
  - China South-central
  - China Southeast
  - Hainan
  - Inner Mongolia
  - Manchuria
  - Qinghai
  - Tibet
  - Xinjiang
- Eastern Asia
  - Japan
  - Korea
  - Taiwan
- Russian Far East
  - Primorye
  - Sakhalin

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - East Himalaya
  - India
  - Nepal
- Indo-China
  - Myanmar
  - Vietnam

Northern America click to expand
- Mexico
  - Mexico Southeast

Southern America click to expand
- Caribbean
  - Haiti

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000187878
UNII	IO64JGK313
USDA Plants	VIAN7
Tropicos	13040507
INPN	844287
KEW	urn:lsid:ipni.org:names:525291-1
The Plant List	ild-3442
Open Tree Of Life	1065959
Observations.org	123463
NCBI Taxonomy	3914
Nature Serve	2.147361
IUCN Red List	120930543
IPNI	525291-1
iNaturalist	122889
GBIF	2982508
Freebase	/m/02492f
EPPO	PHSAN
EOL	648839
USDA GRIN	41598
Wikipedia	Adzuki_bean
CMAUP	NPO29532

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
GCF_016808095.1	ASM1680809v1	Chromosome	Heilongjiang Academy of Agricultural Sciences	2021-02-04	193.34	427.06 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

Differential gene reactions reveal drought response strategies in African acacias.

Weinheimer EI, Cory ST, Kortessis N, Anderson TM, Pease JB

Plant J

01-Aug-2025

PMCID:	PMC12320966
doi:	10.1111/tpj.70385
PMID:	40758440

Effects of Soaking and Germination Treatments on the Nutritional, Anti-Nutritional, and Bioactive Characteristics of Adzuki Beans (Vigna angularis L.) and Lima Beans (Phaseolus lunatus L.)

Rizvi QU, Guiné RP, Ahmed N, Sheikh MA, Sharma P, Sheikh I, Yadav AN, Kumar K

Foods

06-May-2024

PMCID:	PMC11083788
doi:	10.3390/foods13091422
PMID:	38731793

Exploring Gluten Assessment in Marketed Products through a Sandwich ELISA Methodology Based on Novel Recombinant Antibodies

Garcia-Calvo E, García-García A, Rodríguez S, Martín R, García T

Foods

26-Apr-2024

PMCID:	PMC11083168
doi:	10.3390/foods13091341
PMID:	38731712

Oleanolic Acid Acetate Alleviates Cisplatin-Induced Nephrotoxicity via Inhibition of Apoptosis and Necroptosis In Vitro and In Vivo

Lee B, Kim YY, Jeong S, Lee SW, Lee SJ, Rho MC, Kim SH, Lee S

Toxics

18-Apr-2024

PMCID:	PMC11054587
doi:	10.3390/toxics12040301
PMID:	38668524

Mitigating Effect of Trans-Zeatin on Cadmium Toxicity in Desmodesmus armatus

Piotrowska-Niczyporuk A, Bonda-Ostaszewska E, Bajguz A

Cells

15-Apr-2024

PMCID:	PMC11049045
doi:	10.3390/cells13080686
PMID:	38667301

Updated Progress on Polysaccharides with Anti-Diabetic Effects through the Regulation of Gut Microbiota: Sources, Mechanisms, and Structure–Activity Relationships

Zhang X, Wang J, Zhang T, Li S, Liu J, Li M, Lu J, Zhang M, Chen H

Pharmaceuticals (Basel)

02-Apr-2024

PMCID:	PMC11053653
doi:	10.3390/ph17040456
PMID:	38675416

Identification and characterization of the critical genes encoding Cd-induced enhancement of SOD isozymes activities in Zhe-Maidong (Ophiopogon japonicus)

Hou R, Wang Z, Zhu Q, Wang J, Zhou Y, Li Y, Liu H, Zhao Q, Huang J

Front Plant Sci

28-Mar-2024

PMCID:	PMC11007131
doi:	10.3389/fpls.2024.1355849
PMID:	38606075

Exploring the Untapped Potential of Pine Nut Skin By-Products: A Holistic Characterization and Recycling Approach

Nolasco A, Squillante J, Velotto S, D’Auria G, Ferranti P, Mamone G, Errico ME, Avolio R, Castaldo R, De Luca L, Romano R, Esposito F, Cirillo T

Foods

28-Mar-2024

PMCID:	PMC11011278
doi:	10.3390/foods13071044
PMID:	38611351

Examination of Primary and Secondary Metabolites Associated with a Plant-Based Diet and Their Impact on Human Health

Simsek M, Whitney K

Foods

27-Mar-2024

PMCID:	PMC11011468
doi:	10.3390/foods13071020
PMID:	38611326

Function and regulation of plant ARGONAUTE proteins in response to environmental challenges: a review

Zaheer U, Munir F, Salum YM, He W

PeerJ

26-Mar-2024

PMCID:	PMC10979746
doi:	10.7717/peerj.17115
PMID:	38560454

Graphene promotes the growth of Vigna angularis by regulating the nitrogen metabolism and photosynthesis

Qiao J, Chen Z, Zhao J, Ren J, Wang H, Zhi C, Li J, Xing B, Nie H

PLoS One

07-Mar-2024

PMCID:	PMC10919591
doi:	10.1371/journal.pone.0297892
PMID:	38451974

A de novo chromosome-scale assembly of the Lablab purpureus genome

Pootakham W, Somta P, Kongkachana W, Naktang C, Sonthirod C, U-Thoomporn S, Yoocha T, Phadphon P, Tangphatsornruang S

Front Plant Sci

05-Mar-2024

PMCID:	PMC10948561
doi:	10.3389/fpls.2024.1347744
PMID:	38504891

Mapping and Detection of Genes Related to Trichome Development in Black Gram (Vigna mungo (L.) Hepper)

Gong D, Li J, Wang S, Sha A, Wang L

Genes (Basel)

27-Feb-2024

PMCID:	PMC10970695
doi:	10.3390/genes15030308
PMID:	38540367

Functional characterization of NBS-LRR genes reveals an NBS-LRR gene that mediates resistance against Fusarium wilt

Cao Y, Mo W, Li Y, Xiong Y, Wang H, Zhang Y, Lin M, Zhang L, Li X

BMC Biol

27-Feb-2024

PMCID:	PMC10898138
doi:	10.1186/s12915-024-01836-x
PMID:	38408951

Potential anti‐obesity effect of saponin metabolites from adzuki beans: A computational approach

Moussa AY, Alanzi A, Luo J, Chung SK, Xu B

Food Sci Nutr

22-Feb-2024

PMCID:	PMC11077217
doi:	10.1002/fsn3.4032
PMID:	38726452

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
4-Hydroxybenzoic acid	135	Click to see C1=CC(=CC=C1C(=O)O)O	138.12	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Terphenyls / P-terphenyls
[3-hydroxy-2,5-bis(4-hydroxyphenyl)-4,6-bis[[(Z)-3-[(2S,3S)-3-methyloxiran-2-yl]prop-2-enoyl]oxy]phenyl] (Z)-3-[(2S,3S)-3-methyloxiran-2-yl]prop-2-enoate	14426678	Click to see CC1C(O1)C=CC(=O)OC2=C(C(=C(C(=C2C3=CC=C(C=C3)O)O)OC(=O)C=CC4C(O4)C)C5=CC=C(C=C5)O)OC(=O)C=CC6C(O6)C	656.60	unknown	via CMAUP database
[3,4-dihydroxy-2,5-bis(4-hydroxyphenyl)-6-[(Z)-3-[(2S,3S)-3-methyloxiran-2-yl]prop-2-enoyl]oxyphenyl] (Z)-3-[(2S,3S)-3-methyloxiran-2-yl]prop-2-enoate	10437437	Click to see	546.50	unknown	via CMAUP database
> Benzenoids / Phenols / Benzenediols / Catechols
(alphaE)-alpha-(4-(3,4-Dihydroxyphenyl)-3-hydroxy-5-oxo-2(5H)-furanylidene)-4-hydroxybenzeneacetic acid	54730624	Click to see	356.30	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
(-)-Syringaresinol	11604108	Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC	418.40	unknown	via CMAUP database
5',5''-Didemethoxypinoresinol	101789268	Click to see	298.30	unknown	https://doi.org/10.1016/0031-9422(83)80235-0
Sesamin, (-)-	382073	Click to see	354.40	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
(+)-Nortrachelogenin	479756	Click to see	374.40	unknown	via CMAUP database
2(3H)-Furanone, 3,4-bis(1,3-benzodioxol-5-ylmethyl)dihydro-, (3S,4S)-	11002708	Click to see	354.40	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Lignan glycosides
(2S,3R,4S,5S,6R)-2-[4-[(3R,3Ar,6S,6aS)-6-[3,5-dimethoxy-4-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	24720994	Click to see	742.70	unknown	via CMAUP database
Acanthoside D	442830	Click to see	742.70	unknown	via CMAUP database
Liriodendrin	21603207	Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C3C4COC(C4CO3)C5=CC(=C(C(=C5)OC)OC6C(C(C(C(O6)CO)O)O)O)OC	742.70	unknown	via CMAUP database
Liriodendrtachioside	44202792	Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C3C4COC(C4CO3)C5=CC(=C(C(=C5)OC)OC6C(C(C(C(O6)CO)O)O)O)OC	742.70	unknown	via CMAUP database
Npc141273	73636	Click to see	742.70	unknown	via CMAUP database
Npc279481	226371	Click to see	742.70	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Lignan lactones
(1R,3aR,4R,6aR)-1,4-bis(1,3-benzodioxol-5-yl)-1,3a,4,6a-tetrahydrofuro[3,4-c]furan-3,6-dione	101393513	Click to see	382.30	unknown	via CMAUP database
Genkdaphin	5317554	Click to see	368.30	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Oleic Acid	445639	Click to see	282.50	unknown	https://doi.org/10.1271/NOGEIKAGAKU1924.59.895
Palmitic Acid	985	Click to see	256.42	unknown	https://doi.org/10.1271/NOGEIKAGAKU1924.59.895
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid	5280450	Click to see CCCCCC=CCC=CCCCCCCCC(=O)O	280.40	unknown	https://doi.org/10.1271/NOGEIKAGAKU1924.59.895
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Guaianes
(5R,8S,8aR)-3,8-dimethyl-5-prop-1-en-2-yl-4,5,6,7,8,8a-hexahydro-1H-azulen-2-one	101375349	Click to see	218.33	unknown	via CMAUP database
1alpha,7alpha,10alphaH-Guaia-4,11-dien-3-one	10082128	Click to see CC1CCC(CC2=C(C(=O)CC12)C)C(=C)C	218.33	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(2R,3R,4R,5S,6S)-6-[[(3S,4R,4aR,6aR,6bS,8aS,9R,12aR,14aR,14bR)-4-(hydroxymethyl)-9-[[(2S)-5-hydroxy-6-methyl-4-oxo-2,3-dihydropyran-2-yl]oxy]-4,6a,6b,8a,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-5-[(2S,3S,4R,5R,6R)-6-carboxy-4,5-dihydroxy-3-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxyoxane-2-carboxylic acid	162990836	Click to see	1083.20	unknown	https://doi.org/10.1016/S0031-9422(99)00148-X
(2R,3S,4S,5R,6R)-6-[[(3S,4S,4aS,6aR,6bR,8aS,9S,12aS,14aR,14bS)-4-(hydroxymethyl)-9-[[(2S)-5-hydroxy-6-methyl-4-oxo-2,3-dihydropyran-2-yl]oxy]-4,6a,6b,8a,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-5-[(2R,3S,4R,5R,6S)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxyoxane-2-carboxylic acid	163011304	Click to see CC1=C(C(=O)CC(O1)OC2CC(CC3C2(CCC4(C3=CCC5C4(CCC6C5(CCC(C6(C)CO)OC7C(C(C(C(O7)C(=O)O)O)O)OC8C(C(C(C(O8)CO)O)O)OC9C(C(C(C(O9)CO)O)O)O)C)C)C)C)(C)C)O	1085.20	unknown	https://doi.org/10.1016/S0031-9422(99)00148-X
(2S,3S,4R,5R,6R)-6-[[(3S,4S,4aS,6aR,6bR,8aS,9R,12aS,14aR,14bS)-4-(hydroxymethyl)-9-[[(2S)-5-hydroxy-6-methyl-4-oxo-2,3-dihydropyran-2-yl]oxy]-4,6a,6b,8a,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-5-[(2R,3S,4S,5S,6R)-6-carboxy-4,5-dihydroxy-3-[(2S,3R,4S,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxyoxane-2-carboxylic acid	162843121	Click to see CC1=C(C(=O)CC(O1)OC2CC(CC3C2(CCC4(C3=CCC5C4(CCC6C5(CCC(C6(C)CO)OC7C(C(C(C(O7)C(=O)O)O)O)OC8C(C(C(C(O8)C(=O)O)O)O)OC9C(C(C(C(O9)CO)O)O)O)C)C)C)C)(C)C)O	1099.20	unknown	https://doi.org/10.1016/S0031-9422(99)00148-X
(2S,3S,4S,5R,6R)-6-[[(3S,4aR,6aR,6bS,8aR,9R,12aS,14aR,14bR)-9-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4-dihydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxane-2-carboxylic acid	102500449	Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(C(C1)O)C)C)C)(C)C)OC6C(C(C(C(O6)C(=O)O)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)C	781.00	unknown	https://doi.org/10.1248/CPB.31.674 https://doi.org/10.1007/BF02535758
(2S,3S,4S,5R,6R)-6-[[(3S,4S,4aR,6aR,6bS,8aR,9R,12aS,14aR,14bR)-4-(hydroxymethyl)-9-[[(2R)-5-hydroxy-6-methyl-4-oxo-2,3-dihydropyran-2-yl]oxy]-4,6a,6b,8a,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4-dihydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxane-2-carboxylic acid	162912948	Click to see	923.10	unknown	https://doi.org/10.1016/S0031-9422(97)00169-6
(2S,3S,4S,5R,6R)-6-[[(3S,4S,4aR,6aR,6bS,8aR,9R,12aS,14aR,14bR)-4-(hydroxymethyl)-9-[[(2R)-5-hydroxy-6-methyl-4-oxo-2,3-dihydropyran-2-yl]oxy]-4,6a,6b,8a,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-5-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxyoxane-2-carboxylic acid	163011305	Click to see CC1=C(C(=O)CC(O1)OC2CC(CC3C2(CCC4(C3=CCC5C4(CCC6C5(CCC(C6(C)CO)OC7C(C(C(C(O7)C(=O)O)O)O)OC8C(C(C(C(O8)CO)O)O)OC9C(C(C(C(O9)CO)O)O)O)C)C)C)C)(C)C)O	1085.20	unknown	https://doi.org/10.1016/S0031-9422(99)00148-X
(2S,3S,4S,5R,6R)-6-[[(3S,4S,4aR,6aR,6bS,8aR,9R,12aS,14aR,14bR)-4-(hydroxymethyl)-9-[[(2S)-5-hydroxy-6-methyl-4-oxo-2,3-dihydropyran-2-yl]oxy]-4,6a,6b,8a,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-5-[(2R,3R,4S,5S,6S)-6-carboxy-4,5-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxyoxane-2-carboxylic acid	162990837	Click to see	1083.20	unknown	https://doi.org/10.1016/S0031-9422(99)00148-X
(2S,3S,4S,5R,6R)-6-[[(3S,4S,4aR,6aR,6bS,8aR,9R,12aS,14aR,14bR)-4-(hydroxymethyl)-9-[[(2S)-5-hydroxy-6-methyl-4-oxo-2,3-dihydropyran-2-yl]oxy]-4,6a,6b,8a,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-5-[(2R,3R,4S,5S,6S)-6-carboxy-4,5-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxyoxane-2-carboxylic acid	162843123	Click to see CC1=C(C(=O)CC(O1)OC2CC(CC3C2(CCC4(C3=CCC5C4(CCC6C5(CCC(C6(C)CO)OC7C(C(C(C(O7)C(=O)O)O)O)OC8C(C(C(C(O8)C(=O)O)O)O)OC9C(C(C(C(O9)CO)O)O)O)C)C)C)C)(C)C)O	1099.20	unknown	https://doi.org/10.1016/S0031-9422(99)00148-X
(2S,3S,4S,5R,6R)-6-[[(3S,4S,4aR,6aR,6bS,8aR,9R,12aS,14aR,14bR)-9-hydroxy-4-(hydroxymethyl)-4,6a,6b,8a,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4-dihydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxane-2-carboxylic acid	13326387	Click to see	797.00	unknown	https://doi.org/10.1248/CPB.31.674
(2S,3S,4S,5R,6R)-6-[[(3S,4S,4aR,6aR,6bS,8aR,9R,12aS,14aR,14bR)-9-hydroxy-4-(hydroxymethyl)-4,6a,6b,8a,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-5-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxyoxane-2-carboxylic acid	21607812	Click to see	943.10	unknown	https://doi.org/10.1248/CPB.31.683
(2S,3S,4S,5R,6R)-6-[[(3S,4S,4aR,6aR,6bS,8aS,11R,12aR,14aR,14bR)-4-(hydroxymethyl)-4,6a,6b,8a,11,14b-hexamethyl-11-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4-dihydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxane-2-carboxylic acid	101942167	Click to see	1135.20	unknown	https://doi.org/10.1248/CPB.31.683
(3S,4R,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-4,6a,6b,11,11,14b-hexamethyl-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-8a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4-carboxylic acid	102234617	Click to see	973.10	unknown	via CMAUP database
(3S,4S,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-4,6a,6b,11,11,14b-hexamethyl-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-8a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4-carboxylic acid	163194451	Click to see	973.10	unknown	https://doi.org/10.1248/CPB.31.674
5-[4,5-Dihydroxy-6-(hydroxymethyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxy-6-[[4-(hydroxymethyl)-9-[(5-hydroxy-6-methyl-4-oxo-2,3-dihydropyran-2-yl)oxy]-4,6a,6b,8a,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]oxane-2-carboxylic acid	85058456	Click to see	1085.20	unknown	https://doi.org/10.1016/S0031-9422(99)00148-X
5-[6-Carboxy-4,5-dihydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxy-6-[[4-(hydroxymethyl)-9-[(5-hydroxy-6-methyl-4-oxo-2,3-dihydropyran-2-yl)oxy]-4,6a,6b,8a,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]oxane-2-carboxylic acid	131751576	Click to see CC1=C(C(=O)CC(O1)OC2CC(CC3C2(CCC4(C3=CCC5C4(CCC6C5(CCC(C6(C)CO)OC7C(C(C(C(O7)C(=O)O)O)O)OC8C(C(C(C(O8)C(=O)O)O)O)OC9C(C(C(C(O9)CO)O)O)O)C)C)C)C)(C)C)O	1099.20	unknown	https://doi.org/10.1016/S0031-9422(99)00148-X
6-[[11-Carboxy-4-(hydroxymethyl)-4,6a,6b,8a,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4-dihydroxy-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxane-2-carboxylic acid	4483254	Click to see CC12CCC(CC1C3=CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)CO)OC6C(C(C(C(O6)C(=O)O)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)(C)C(=O)O	811.00	unknown	https://doi.org/10.1248/CPB.31.674
AzIII	131751577	Click to see	1083.20	unknown	https://doi.org/10.1016/S0031-9422(99)00148-X
Azukisaponin I	14103656	Click to see	781.00	unknown	https://doi.org/10.1248/CPB.31.674
Azukisaponin III	441909	Click to see	811.00	unknown	https://doi.org/10.1248/CPB.31.674
Azukisaponin IV	13035680	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C(=O)O)OC6C(C(C(C(O6)CO)O)O)O)C)C)C2C1)C)C(=O)OC7C(C(C(C(O7)COC8C(C(C(C(O8)CO)O)O)O)O)O)O)C	973.10	unknown	https://doi.org/10.1248/CPB.31.674
Azukisaponin VI	13035678	Click to see	1135.20	unknown	https://doi.org/10.1248/CPB.31.683
CID 5087640	5087640	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(C(C(OC3OC4CCC5(C(C4(C)CO)CCC6(C5CC=C7C6(CCC8(C7CC(CC8O)(C)C)C)C)C)C)C(=O)O)O)O)CO)O)O)O)O)O	943.10	unknown	https://doi.org/10.1248/CPB.31.683
Soyasaponin gamma-G	133052649	Click to see CC1=C(C(=O)CC(O1)OC2CC(CC3C2(CCC4(C3=CCC5C4(CCC6C5(CCC(C6(C)CO)OC7C(C(C(C(O7)C(=O)O)O)O)OC8C(C(C(C(O8)CO)O)O)O)C)C)C)C)(C)C)O	923.10	unknown	https://doi.org/10.1016/S0031-9422(97)00169-6
Soyasaponin III	13326389	Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(C(C1)O)C)C)C)(C)CO)OC6C(C(C(C(O6)C(=O)O)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)C	797.00	unknown	https://doi.org/10.1248/CPB.31.674
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(2R,4aS,6aR,6aS,6bR,8aR,9S,10S,12aR,14bR)-10-hydroxy-9-(hydroxymethyl)-2,4a,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-2-carboxylic acid	21594159	Click to see CC12CCC(CC1C3=CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)CO)O)C)(C)C(=O)O	472.70	unknown	https://doi.org/10.1248/CPB.31.664
(3S,4S,6aR,8aS,12aR,14bR)-4-(hydroxymethyl)-4,6a,6b,8a,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,12,12a,14,14a-dodecahydropicen-3-ol	5321408	Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(C=C1)C)C)C)(C)CO)O)C)C	440.70	unknown	https://doi.org/10.1248/CPB.31.664
3-Hydroxy-12-oleanene-23,28-dioic acid	15560323	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C(=O)O)O)C)C)C2C1)C)C(=O)O)C	486.70	unknown	https://doi.org/10.1248/CPB.31.664
Acetyloleanolic acid	45050658	Click to see	498.70	unknown	https://doi.org/10.1271/NOGEIKAGAKU1924.59.895
Anhydrosophoradiol	131751693	Click to see	424.70	unknown	https://doi.org/10.1248/CPB.31.664
Azukisapogenol	73744576	Click to see	472.70	unknown	https://doi.org/10.1248/CPB.31.664
Beta-Amyrin	73145	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C	426.70	unknown	https://doi.org/10.1271/NOGEIKAGAKU1924.59.895
CID 429190	429190	Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(C(C1)O)C)C)C)(C)CO)O)C)C	458.70	unknown	https://doi.org/10.1248/CPB.31.664
Gypsogenic acid	15560324	Click to see	486.70	unknown	https://doi.org/10.1248/CPB.31.664
Lupeol	259846	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C	426.70	unknown	https://doi.org/10.1271/NOGEIKAGAKU1924.59.895
methyl (2R,4aS,6aR,6aS,6bR,8aR,9S,10S,12aR,14bR)-10-hydroxy-9-(hydroxymethyl)-2,4a,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-2-carboxylate	162885803	Click to see	486.70	unknown	https://doi.org/10.1248/CPB.31.664
Methyl 10-hydroxy-9-(hydroxymethyl)-2,4a,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-2-carboxylate	78385299	Click to see	486.70	unknown	https://doi.org/10.1248/CPB.31.664
Oleana-12,21-dien-3-ol, (3beta)-	162991191	Click to see	424.70	unknown	https://doi.org/10.1248/CPB.31.664
Oleanolic Acid	10494	Click to see	456.70	unknown	https://doi.org/10.1271/NOGEIKAGAKU1924.59.895
Sophoradiol	9846221	Click to see	442.70	unknown	https://doi.org/10.1248/CPB.31.664
Soyasapogenol B	115012	Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(C(C1)O)C)C)C)(C)CO)O)C)C	458.70	unknown	https://doi.org/10.1248/CPB.31.664
Soyasapogenol C	3083637	Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(C=C1)C)C)C)(C)CO)O)C)C	440.70	unknown	https://doi.org/10.1248/CPB.31.664
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives
(2S,3R,5R,9R,10R,11R,13R,14S,17S)-2,3,11,14-tetrahydroxy-10,13-dimethyl-17-[(2R,3R,5R)-2,3,5-trihydroxy-5,6-dimethylheptan-2-yl]-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one	15839567	Click to see	510.70	unknown	via CMAUP database
20-Hydroxyecdysone	5459840	Click to see	480.60	unknown	via CMAUP database
CID 15839579	15839579	Click to see	508.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
Cholesterol	5997	Click to see	386.70	unknown	https://doi.org/10.1271/NOGEIKAGAKU1924.59.895
Lophenol	160482	Click to see CC1C(CCC2(C1CC=C3C2CCC4(C3CCC4C(C)CCCC(C)C)C)C)O	400.70	unknown	https://doi.org/10.1271/NOGEIKAGAKU1924.59.895
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
24-Methylene-9beta,19-cyclo-lanostan-3beta-ol	9547213	Click to see	440.70	unknown	https://doi.org/10.1271/NOGEIKAGAKU1924.59.895
24-Methylenecycloartanol	94204	Click to see	440.70	unknown	https://doi.org/10.1271/NOGEIKAGAKU1924.59.895
Cyclobranol	13920164	Click to see	440.70	unknown	https://doi.org/10.1271/NOGEIKAGAKU1924.59.895
Cycloeucalenol	101690	Click to see CC1C2CCC3C4(CCC(C4(CCC35C2(C5)CCC1O)C)C(C)CCC(=C)C(C)C)C	426.70	unknown	https://doi.org/10.1271/NOGEIKAGAKU1924.59.895
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(+)-Obtusifoliol	65252	Click to see	426.70	unknown	https://doi.org/10.1271/NOGEIKAGAKU1924.59.895
(24R)-5-Ergosten-3beta-ol	312822	Click to see	400.70	unknown	https://doi.org/10.1271/NOGEIKAGAKU1924.59.895
(3S,8S,9S,14S,17R)-17-[(2R,5R)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	134766514	Click to see	400.70	unknown	https://doi.org/10.1271/NOGEIKAGAKU1924.59.895
24-Methylenelophenol	5283640	Click to see CC1C(CCC2(C1CC=C3C2CCC4(C3CCC4C(C)CCC(=C)C(C)C)C)C)O	412.70	unknown	https://doi.org/10.1271/NOGEIKAGAKU1924.59.895
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids / 11-oxosteroids
Asperfloroid	146682055	Click to see	488.60	unknown	https://doi.org/10.1016/S0008-6215(03)00339-2
> 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/10.1271/NOGEIKAGAKU1924.59.895
Citrostadienol	9548595	Click to see	426.70	unknown	https://doi.org/10.1271/NOGEIKAGAKU1924.59.895
Isofucosterol	5281326	Click to see	412.70	unknown	https://doi.org/10.1271/NOGEIKAGAKU1924.59.895
Sitogluside	5742590	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	via CMAUP database
Stigmast-5-en-3-ol	22012	Click to see	414.70	unknown	https://doi.org/10.1271/NOGEIKAGAKU1924.59.895
Stigmasterol	5280794	Click to see	412.70	unknown	https://doi.org/10.1271/NOGEIKAGAKU1924.59.895
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(1S,2R,3S,4S,5R,6R)-5-methoxy-6-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycyclohexane-1,2,3,4-tetrol	162975245	Click to see COC1C(C(C(C(C1OC2C(C(C(C(O2)CO)O)O)O)O)O)O)O	356.32	unknown	https://doi.org/10.1080/00021369.1980.10864312
(1S,2S,3S,4R,5S,6S)-5-methoxy-6-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxycyclohexane-1,2,3,4-tetrol	101754087	Click to see	518.50	unknown	https://doi.org/10.1016/S0008-6215(03)00339-2
3-Furanmethanol glucoside	78302646	Click to see	260.24	unknown	https://doi.org/10.1248/CPB.31.664
3-Furanylmethyl beta-D-glucopyranoside	3086224	Click to see	260.24	unknown	https://doi.org/10.1248/CPB.31.664
D-Pinitol 2-O-alpha-D-Galactopyranosyl	74427727	Click to see	356.32	unknown	https://doi.org/10.1080/00021369.1980.10864312
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzoquinones / P-benzoquinones
[4-hydroxy-2,5-bis(4-hydroxyphenyl)-3,6-dioxocyclohexa-1,4-dien-1-yl] (2Z,4E)-hexa-2,4-dienoate	14426693	Click to see	418.40	unknown	via CMAUP database
2,6-Dimethoxyquinone	68262	Click to see COC1=CC(=O)C=C(C1=O)OC	168.15	unknown	via CMAUP database
Atromentin	99148	Click to see C1=CC(=CC=C1C2=C(C(=O)C(=C(C2=O)O)C3=CC=C(C=C3)O)O)O	324.30	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
1-(3,6-Dihydroxy-2-methoxy-4-methylphenyl)ethanone	86251457	Click to see CC1=CC(=C(C(=C1O)OC)C(=O)C)O	196.20	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Ortho esters
(2'R,3'S)-3'-hydroxy-4,7-bis(4-hydroxyphenyl)-2'-methylspiro[1,3-benzodioxole-2,6'-2,3-dihydropyran]-5,6-dione	14426701	Click to see	434.40	unknown	via CMAUP database
Spiromentin b	14426699	Click to see CC(C1C=CC2(O1)OC3=C(C(=O)C(=O)C(=C3O2)C4=CC=C(C=C4)O)C5=CC=C(C=C5)O)O	434.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
Lichexanthone	5358904	Click to see CC1=CC(=CC2=C1C(=O)C3=C(C=C(C=C3O2)OC)O)OC	286.28	unknown	via CMAUP database
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
(5R)-5-[(1S)-1-Hydroxyethyl]-2(5H)-furanone	10986239	Click to see CC(C1C=CC(=O)O1)O	128.13	unknown	via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(3R,4S,5S*)-3-Acetoxy-5-hydroxyhexan-4	101683182	Click to see CC(C1C(CC(=O)O1)OC(=O)C)O	188.18	unknown	via CMAUP database
(5S)-5-[(1R)-1-hydroxyethyl]oxolan-2-one	11040727	Click to see	130.14	unknown	via CMAUP database
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives
Maltol	8369	Click to see	126.11	unknown	via CMAUP database
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives / Dihydropyranones
Osumudalactome	12374457	Click to see	128.13	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	via CMAUP database
Cis-P-Coumaric Acid	1549106	Click to see	164.16	unknown	via CMAUP database
Ferulic Acid	445858	Click to see	194.18	unknown	via CMAUP database
P-Coumaric Acid	637542	Click to see	164.16	unknown	via CMAUP database
Sinapinic acid	1549091	Click to see	224.21	unknown	via CMAUP database
Sinapinic acid	637775	Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)O	224.21	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
7-[(3,3-Dimethyloxiran-2-yl)methoxy]-6,8-dimethoxychromen-2-one	14841895	Click to see	306.31	unknown	https://doi.org/10.1248/CPB.31.664
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Daphnoretin	5281406	Click to see	352.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
Procyanidin B1	11250133	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O	578.50	unknown	via CMAUP database
Procyanidin B3	146798	Click to see	578.50	unknown	https://doi.org/10.1271/BBB1961.52.2717
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
(-)-Catechol	73160	Click to see	290.27	unknown	via CMAUP database
(+)-Epicatechin	182232	Click to see	290.27	unknown	via CMAUP database
2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,5,7-triol	1203	Click to see	290.27	unknown	via CMAUP database
Catechin	9064	Click to see	290.27	unknown	via CMAUP database
Epicatechin	72276	Click to see	290.27	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(+-)-Naringenin	932	Click to see	272.25	unknown	https://doi.org/10.1080/00021369.1987.10868021 https://doi.org/10.1271/BBB1961.51.349
(2R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-4H-chromen-4-one	667495	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O	272.25	unknown	https://doi.org/10.1271/BBB1961.51.349
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin	5280343	Click to see	302.23	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
Isovitexin	162350	Click to see	432.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Vitexin	5280441	Click to see	432.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Rutin	5280805	Click to see	610.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Catechin 7-glucoside	14282767	Click to see	452.40	unknown	https://doi.org/10.1248/CPB.31.664
Catechin 7-O-beta-D-glucopyranoside	10789789	Click to see	452.40	unknown	https://doi.org/10.1248/CPB.31.664
Catechin-7-O-glucoside	44257085	Click to see C1C(C(OC2=CC(=CC(=C21)O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)O)O	452.40	unknown	https://doi.org/10.1248/CPB.31.664
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Tricin	5281702	Click to see COC1=CC(=CC(=C1O)OC)C2=CC(=O)C3=C(C=C(C=C3O2)O)O	330.29	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Coumestans
Phaseol	44257530	Click to see	336.30	unknown	https://doi.org/10.1271/BBB1961.51.349
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
2'-Hydroxygenistein	5282074	Click to see C1=CC(=C(C=C1O)O)C2=COC3=CC(=CC(=C3C2=O)O)O	286.24	unknown	https://doi.org/10.1271/BBB1961.51.349
5,7-Dihydroxy-3-(4-hydroxyphenyl)-8-(3-methyl-2-buten-1-yl)-4H-1-benzopyran-4-one	5317480	Click to see	338.40	unknown	https://doi.org/10.1271/BBB1961.51.349 https://doi.org/10.1080/00021369.1987.10868021
8-Prenyl-5,7,4'-trihydroxyisoflavone	25246032	Click to see	337.30	unknown	via CMAUP database
Lupinalbin A	5324349	Click to see	284.22	unknown	https://doi.org/10.1271/BBB1961.51.349
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanols
Demethylvestitol	585939	Click to see C1C(COC2=C1C=CC(=C2)O)C3=C(C=C(C=C3)O)O	258.27	unknown	https://doi.org/10.1271/BBB1961.51.349
Demethylvestitol, (R)-	92021067	Click to see C1C(COC2=C1C=CC(=C2)O)C3=C(C=C(C=C3)O)O	258.27	unknown	https://doi.org/10.1271/BBB1961.51.349
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones
(+)-Dihydrowighteone	44257383	Click to see	340.40	unknown	https://doi.org/10.1271/BBB1961.51.349
(3S)-3-(2,4-dihydroxyphenyl)-5,7-dihydroxy-2,3-dihydrochromen-4-one	124300749	Click to see C1C(C(=O)C2=C(C=C(C=C2O1)O)O)C3=C(C=C(C=C3)O)O	288.25	unknown	https://doi.org/10.1271/BBB1961.51.349
(3S)-5,7-dihydroxy-3-(4-hydroxyphenyl)-6-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one	162927561	Click to see CC(=CCC1=C(C2=C(C=C1O)OCC(C2=O)C3=CC=C(C=C3)O)O)C	340.40	unknown	https://doi.org/10.1271/BBB1961.51.349
3-(2,4-Dihydroxyphenyl)-2,3-dihydro-5,7-dihydroxy-4H-1-benzopyran-4-one	181994	Click to see	288.25	unknown	https://doi.org/10.1271/BBB1961.51.349 https://doi.org/10.1080/00021369.1987.10868021
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
Daidzin	107971	Click to see	416.40	unknown	https://doi.org/10.1093/OXFORDJOURNALS.PCP.A077006 https://doi.org/10.1016/0031-9422(83)80235-0
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids
Vestitol	92503	Click to see	272.29	unknown	https://doi.org/10.1271/BBB1961.51.349
Vestitol, (-)-	182259	Click to see COC1=CC(=C(C=C1)C2CC3=C(C=C(C=C3)O)OC2)O	272.29	unknown	https://doi.org/10.1271/BBB1961.51.349
> Phenylpropanoids and polyketides / Stilbenes
Cis-Resveratrol	1548910	Click to see	228.24	unknown	via CMAUP database
Resveratrol	445154	Click to see	228.24	unknown	via CMAUP database

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Vigna angularis

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