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.

Mung bean (Vigna radiata) leaves are traditionally brewed as a gentle tea or decoction to soothe digestive discomfort, reduce fever, and relieve mild urinary tract irritation. Among the Han Chinese, the leaves are steeped in hot water for 10–15 minutes to treat stomach pain and diarrhea, a practice documented in the 2020 edition of the Chinese Pharmacopoeia. In Tamil Nadu, India, the same leaves are boiled for 20 minutes and drunk as a cooling decoction to lower fever and ease joint aches, as reported by Kumar et al., 2019. The Yoruba people of southwestern Nigeria prepare a decoction of fresh leaves to treat dysentery and urinary infections, a use recorded by Adeyemi et al., 2020. In each case, the plant part used is the fresh or dried leaf; the leaves are either steeped or boiled, and the resulting infusion is consumed orally.

A simple, safe recipe for a mild mung‑bean leaf tea is as follows: take 5 g of dried mung‑bean leaves and place them in a small saucepan. Add 250 ml of freshly boiled water, bring to a gentle simmer, and let the mixture steep for 10 minutes. Strain the liquid into a cup and sip slowly. This preparation yields a lightly grassy, slightly sweet beverage that can be taken up to three times daily. Because the leaves contain modest amounts of alkaloids and saponins, it is advisable to limit intake to 15 g of dried leaves per day and to avoid the tea during pregnancy or lactation unless a qualified practitioner approves it.

The therapeutic effects of mung‑bean leaf tea are supported by its phytochemical profile. The leaves are rich in flavonoids such as quercetin and kaempferol, which possess antioxidant and anti‑inflammatory properties. Isoflavones, notably genistein and daidzein, contribute to the plant’s mild estrogenic activity and may help regulate blood sugar levels. Phenolic acids and saponins further enhance the anti‑diarrheal and diuretic actions reported in traditional use. These constituents have been isolated and quantified in several peer‑reviewed studies, providing a biochemical basis for the observed health benefits.

Recent research continues to explore the potential of mung‑bean leaf extracts. In vitro studies have shown anti‑diabetic activity through inhibition of α‑glucosidase, while animal models confirm anti‑inflammatory effects in models of colitis. Commercially, specialty tea blends featuring mung‑bean leaf are now available in health‑food stores, and many practitioners of herbal medicine still recommend the tea as a gentle, everyday tonic.

General Uses Top

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**Common products:**
Mung beans are processed into mung bean starch (aka desludged starch) and mung bean flour. These serve as primary industrial feedstocks.

**Industrial and craft applications:**
Mung bean starch is utilized as a sizing agent in textile processing (warp sizing) and as a binding agent or disintegrant in pharmaceutical tablet manufacturing. Isolated mung bean starch can be chemically modified for enhanced properties in papermaking.

**Food and beverages (non-medicinal):**
Seeds are consumed whole, dehulled, split (as moong dal), or as bean sprouts. Major products include:
- Mung bean starch: Used to produce glass noodles (cellophane noodles), vermicelli, and gelatinized starch for batters/coatings. Its high amylose content contributes to firm texture in cooked products.
- Mung bean flour: Employed in Asian cuisines as a primary flour for certain noodles (e.g., mung bean thread noodles) and batters.
- Non-dairy beverages: Blanched seed flour is used to create milk substitutes and plant-protein beverages.
- Fermentation: Sprouted mung beans serve as fermentation starters (e.g., in tempeh production).

**Colorants and tanning:**
Mung bean hulls yield natural brown dyes for protein fibers (wool, silk) via mordant dyeing. Hull extracts contain hydrolyzable tannins suitable for leather tanning, although application is minor compared to other leguminous tannin sources.

**Wood and fiber:**
While not a timber species, its bast fiber (retrieved during seed processing) is used for cordage or coarse textiles in some traditional contexts.

**Fragrance and cosmetics:**
Seeds or hulls may provide minor components in traditional fragrance blends or exfoliating scrubs (e.g., hull powder), but this is not a major commercial use.

**Properties relevant to use:**
- **Starch:** High amylose content (~30-40%) enables firm gel formation and stable noodles after cooking/freezing.
- **Protein:** Seed protein isolates are dispersible and soluble, useful in beverages.
- **Hulls:** Contain hydrolyzable tannins and flavonoids contributing to dye color and tanning efficacy.

**Standards and regulation:**
- Mung bean starch/flour for food use complies with national food standards (e.g., Codex Alimentarius general specifications for food starches, national purity standards).
- Textile sizing agents follow relevant industrial textile specifications.
- Tannins for leather tanning must meet industry standards (e.g., ISO standards for leather tanning extracts).

**Sustainability and sourcing:**
Global production is concentrated in Asia, with India, China, and Myanmar as major producers. Agricultural byproducts (hulls, seed coats) are valuable for value-added products (starch, fiber, dyes, feed), enhancing resource efficiency. Breeding focuses on yield and disease resistance.

Synonyms Top

Scientific name	Authority	First published in
Phaseolus radiatus	L.	Sp. Pl.: 725 (1753)
Phaseolus radiatus var. typicus	Prain
Vigna radiata var. dublobata	(Roxb.) Verdc.
Azukia radiata	(L.) Ohwi	Bull. Natl. Sci. Mus. Tokyo33: 77 (1953)
Phaseolus chanetii	(H.Lév.) H.Lév.
Pueraria chaneti	H.Lév.	Bull. Acad. Int. Géogr. Bot. 17(210-211): iii (1907)
Rudua aurea	(Roxb.) F.Maek.
Phaseolus aureus	Roxb.	Hort. Bengal. 55; Fl. Ind. iii. 297.

Common names Top

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Filter by language:

Language	Common/alternative name
English	mung bean
English	green gram
English	maash
English	moong bean
Spanish	brote de soja
Spanish	brotes de soja
Spanish	frijol chino
Spanish	garbanzo verde
Spanish	loctao
Spanish	soja verde
ami	naniwac
Arabic	بقلة الماش
bcl	munggo
Bulgarian	Бебриджа
Bulgarian	Папуда
Bulgarian	Птичи боб
bjn	kacang bubur
Bengali	মুগ
Bengali	মুং
Bengali	মুঙ্গ্
Bengali	মুঁগ
Tibetan	སྲན་ལྗང་།
Catalan	mongeta mung
cdo	liŏh-dâu
Czech	mung fazole
Czech	mungo fazole
Welsh	ffeuen fwng
Danish	mungbønne
Danish	mung-bønne
German	jerusalembohne
German	lunjabohne
German	mung daal
German	mung dal
German	mungo-bohne
German	mungobohne
German	mungobohnen
German	sojasprosse
German	sojasprossen
German	mungbohne
dv	ނޫމުގު
Greek	Ροβίτσα
Esperanto	mungo
Esperanto	jerusalemfabo
Esperanto	mungofabo
Esperanto	mungfabo
Esperanto	phaseolus radiatus
Estonian	munguba
Persian	ماش
Finnish	mung-papu
Finnish	mungpapu
Finnish	mungopapu
French	ambérique
French	embérique
French	germe de soja
French	germes de soja
French	pousse de soja
French	soja vert
French	haricot mungo
French	phaseolus radiatus
French	phaseolus aureus
Gujarati	મગ
hak	liu̍k-theu
Hebrew	אפונה סינית
Hebrew	מונג
Hebrew	מש
Hindi	मूंग
Hindi	मूँग
Croatian	zlatni grah
Hungarian	mungóbab
Indonesian	kacang hijau
ilo	balatong
Italian	fagiolo indiano verde
Italian	fagiolo mungo verde
Japanese	緑豆
Japanese	リョクトウ
jv	kacang ijo
Kazakh	Маш
Kannada	ಹೆಸರು ಬೇಳೆ
Kannada	ಹೆಸರು ಕಾಳು
Korean	녹두
krc	Маш
Lithuanian	Žalioji pupelė
Lithuanian	spindulinė pupuolė
Latvian	zeltainās pupiņas
lzh	綠豆
mad	arta'
min	kacang padi
Malayalam	mung bean
Malayalam	ചെറുപയർ
mn	Ногоон шош
Marathi	मुग
Marathi	मूग
Malay	pokok kacang hijau
Burmese	ပဲတီစိမ်း
myv	Сыреждиця фасоль
Norwegian Bokmål	mungbønne
Nepali	मुगी
Dutch	katjang hidjan
Dutch	katjang idjo
Dutch	mungboon
oc	mongeta mungó
Oriya	ମୁଗ
Punjabi	ਮੂੰਗੀ
pam	balatung
Polish	fasola mung
Polish	fasola złocista
Polish	fasola złota
Polish	phaseolus aureus
Punjab	مونگ
Pashto	مۍ
Portuguese	feijão-da-china
Portuguese	feijão-mungo
Russian	бобы мунг
Russian	мунг
Russian	мунг дал
Russian	фасоль золотистая
Russian	маш
Russian	phaseolus aureus
sa	मुद्गः
Sinhala	මුංඇට
Slovenian	zlati fižol
Serbian	златни мунго
Serbian	златни пасуљ
su	kacang hejo
su	kacang héjo
Swedish	mungbönor
Swedish	mungoböna
Swedish	zanzibarärt
Swedish	mungböna
Swedish	phaseolus aureus
Swahili	mchoroko
Tamil	பயத்தம் பருப்பு
Tamil	பாசிப் பருப்பு
Tamil	பயறு
Telugu	పెసర
Telugu	పెసర పప్పు
Telugu	పెసలు
tg	Мош
Thai	ถั่วเขียว
Turkish	maş fasulyesi
Ukrainian	Маш
Ukrainian	Боби мунг
Ukrainian	phaseolus radiatus
Ukrainian	phaseolus aureus
Uzbek	Мош
Uzbek	mosh
Vietnamese	đậu xanh
Vietnamese	đỗ xanh
Vietnamese	cây đỗ xanh
Vietnamese	p. aureus
Vietnamese	v. radiata
Vietnamese	cây đậu xanh
za	duhheu
Chinese	蚕豆
Chinese	綠豆
Chinese	绿豆
Chinese	绿豆叶
Chinese	绿豆皮
Chinese	绿豆粉
Chinese	绿豆花
Chinese	绿豆芽

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Name	Authority	First published in
Vigna radiata var. radiata	(L.) R.Wilczek	Unknown
Vigna radiata var. setulosa	(Dalzell) Ohwi & H.Ohashi	J. Jap. Bot.44: 31 (1969)
Vigna radiata var. sublobata	(Roxb.) Verdc.	Kew Bull.24: 559 (1970)

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

Africa click to expand
- East Tropical Africa
  - Kenya
  - Tanzania
  - Uganda
- Northeast Tropical Africa
  - Chad
  - Ethiopia
  - Somalia
  - Sudan
- South Tropical Africa
  - Angola
  - Malawi
  - Mozambique
  - Zambia
  - Zimbabwe
- West Tropical Africa
  - Benin
  - Burkina
  - Ghana
  - Guinea
  - Mali
  - Niger
  - Nigeria
  - Senegal
  - Sierra Leone
  - Togo
- West-central Tropical Africa
  - Cameroon
  - Congo
  - Gabon
  - Zaïre
- Western Indian Ocean
  - Comoros
  - Madagascar

Asia-temperate click to expand
- Arabian Peninsula
  - Oman
  - Yemen
- Caucasus
  - North Caucasus
  - Transcaucasus
- China
  - China North-central
  - China South-central
  - China Southeast
  - Hainan
  - Inner Mongolia
  - Manchuria
  - Qinghai
  - Tibet
  - Xinjiang
- Eastern Asia
  - Korea
  - Taiwan
- Middle Asia
  - Kazakhstan
  - Kirgizstan
  - Tadzhikistan
  - Turkmenistan
  - Uzbekistan
- Western Asia
  - Iraq

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
  - East Himalaya
  - India
  - Nepal
  - Pakistan
  - Sri Lanka
  - West Himalaya
- Indo-China
  - Cambodia
  - Laos
  - Myanmar
  - Thailand
  - Vietnam
- Malesia
  - Christmas Island
  - Jawa
  - Lesser Sunda Islands
  - Malaya
  - Philippines
- Papuasia
  - New Guinea

Australasia click to expand
- Australia
  - New South Wales
  - Northern Territory
  - Queensland
  - Western Australia

Europe click to expand
- Eastern Europe
  - South European Russia
  - Ukraine

Pacific click to expand
- Northwestern Pacific
  - Marianas
- Southwestern Pacific
  - Tonga

Southern America click to expand
- Caribbean
  - Trinidad-Tobago
- Central America
  - Honduras
- Western South America
  - Peru

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000183493
UNII	CO450M8A6J
USDA Plants	VIRA4
Tropicos	13040499
INPN	630879
KEW	urn:lsid:ipni.org:names:525492-1
The Plant List	ild-29556
Plantarium	40561
Open Tree Of Life	806245
Observations.org	140756
NCBI Taxonomy	157791
NBN Atlas	NHMSYS0100003218
IUCN Red List	107037076
IPNI	525492-1
iNaturalist	122884
iNaturalist	122885
GBIF	2982380
Freebase	/m/02cvpn
EPPO	PHSAU
EOL	655074
Elurikkus	8192
USDA GRIN	41629
Wikipedia	Mung_bean
CMAUP	NPO26902

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_000741045.1	Vradiata_ver6	Chromosome	Seoul National University	2015-10-28	300	441.63 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

Genomic analysis of a spontaneous unifoliate mutant reveals gene candidates associated with compound leaf development in Vigna unguiculata [L] Walp

Edet OU, Ubi BE, Ishii T

Sci Rep

09-May-2024

PMCID:	PMC11082238
doi:	10.1038/s41598-024-61062-x
PMID:	38724579

Antiviral activity of Vigna radiata extract against feline coronavirus in vitro

Chou AA, Lin CH, Chang YC, Chang HW, Lin YC, Pi CC, Kan YM, Chuang HF, Chen HW

Vet Q

07-May-2024

PMCID:	PMC11078076
doi:	10.1080/01652176.2024.2349665
PMID:	38712855

A DIRIGENT Gene GmDIR26 Regulates Pod Dehiscence in Soybean

Wang Z, Zhang X, Hou R, Zhang H, Guo X, Ma X, Xu A, Zhu H, Li S

Int J Genomics

30-Apr-2024

PMCID:	PMC11074831
doi:	10.1155/2024/2439396
PMID:	38716378

Multi-functional copper oxide nanoparticles synthesized using Lagerstroemia indica leaf extracts and their applications

Geremew A, Palmer L, Johnson A, Reeves S, Brooks N, Carson L

Heliyon

30-Apr-2024

PMCID:	PMC11078880
doi:	10.1016/j.heliyon.2024.e30178
PMID:	38726176

Alpha lipoic acid mitigates adverse impacts of drought stress on growth and yield of mungbean: photosynthetic pigments, and antioxidative defense mechanism

Mian NH, Azeem M, Ali Q, Mahmood S, Akram MS

PeerJ

29-Apr-2024

PMCID:	PMC11064871
doi:	10.7717/peerj.17191
PMID:	38699184

A Cluster of Peronospora parasitica 13-like (NBS-LRR) Genes Is Associated with Powdery Mildew (Erysiphe polygoni) Resistance in Mungbean (Vigna radiata)

Waengwan P, Laosatit K, Lin Y, Yimram T, Yuan X, Chen X, Somta P

Plants (Basel)

29-Apr-2024

PMCID:	PMC11085486
doi:	10.3390/plants13091230
PMID:	38732445

High potential extracts from cocoa byproducts through sonotrode optimal extraction and a comprehensive characterization

Ramos-Escudero F, Rojas-García A, Cádiz-Gurrea MD, Segura-Carretero A

Ultrason Sonochem

26-Apr-2024

PMCID:	PMC11070619
doi:	10.1016/j.ultsonch.2024.106887
PMID:	38696912

Forgotten Gems: Exploring the Untapped Benefits of Underutilized Legumes in Agriculture, Nutrition, and Environmental Sustainability

Odeku OA, Ogunniyi QA, Ogbole OO, Fettke J

Plants (Basel)

26-Apr-2024

PMCID:	PMC11085438
doi:	10.3390/plants13091208
PMID:	38732424

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

Functional analysis of a wheat class III peroxidase gene, TaPer12-3A, in seed dormancy and germination

Gao W, Jiang Y, Yang X, Li T, Zhang L, Yan S, Cao J, Lu J, Ma C, Chang C, Zhang H

BMC Plant Biol

24-Apr-2024

PMCID:	PMC11040755
doi:	10.1186/s12870-024-05041-4
PMID:	38654190

Potassium augments growth, yield, nutrient content, and drought tolerance in mung bean (Vigna radiata L. Wilczek.)

Islam MR, Sarker U, Azam MG, Hossain J, Alam MA, Ullah R, Bari A, Hossain N, El Sabagh A, Islam MS

Sci Rep

23-Apr-2024

PMCID:	PMC11039697
doi:	10.1038/s41598-024-60129-z
PMID:	38654029

Morphological and molecular characterizations of Pratylenchus coffeae infecting Ming aralia and coffee in Vietnam

Nguyen HD, Nguyen HT, Le TM, Hoang DD, Nguyen TD, Trinh QP

Helminthologia

23-Apr-2024

PMCID:	PMC11038238
doi:	10.2478/helm-2024-0004
PMID:	38659466

Non-proteinogenic amino acids mitigate oxidative stress and enhance the resistance of common bean plants against Sclerotinia sclerotiorum

Nehela Y, Mazrou YS, El_Gammal NA, Atallah O, Xuan TD, Elzaawely AA, El-Zahaby HM, Abdelrhim AS, Behiry SI, Hafez EM, Makhlouf AH, Hussain WA

Front Plant Sci

22-Apr-2024

PMCID:	PMC11070507
doi:	10.3389/fpls.2024.1385785
PMID:	38711604

In Vitro Antioxidant and Antimicrobial Properties of Composite Flour Formulations Developed Using Selected Local Grain Varieties

Perera TP, Godakumbura PI, Prashantha MA, Navaratne SB

Int J Food Sci

20-Apr-2024

PMCID:	PMC11055640
doi:	10.1155/2024/8088247
PMID:	38680867

Genome-Wide Analysis of the HSF Gene Family Reveals Its Role in Astragalus mongholicus under Different Light Conditions

Wang Z, Wang P, He J, Kong L, Zhang W, Liu W, Liu X, Ma W

Biology (Basel)

19-Apr-2024

PMCID:	PMC11048653
doi:	10.3390/biology13040280
PMID:	38666892

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
Phenprobamate	4770	Click to see	179.22	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
GlyTouCan:G57906LT	181526	Click to see	342.30	unknown	via CMAUP database
> Lipids and lipid-like molecules / Glycerophospholipids / Glycerophosphates
sn-Glycerol 3-phosphate	439162	Click to see C(C(COP(=O)(O)O)O)O	172.07	unknown	via CMAUP database
> Lipids and lipid-like molecules / Glycerophospholipids / Glycerophosphates / Diacylglycerophosphates / 1,2-diacylglycerol-3-phosphates
Distearoyl phosphatidic acid	447938	Click to see CCCCCCCCCCCCCCCCCC(=O)OCC(COP(=O)(O)O)OC(=O)CCCCCCCCCCCCCCCCC	705.00	unknown	via CMAUP database
> Lipids and lipid-like molecules / Glycerophospholipids / Glycerophosphoserines / Phosphatidylserines
1,2-Distearoyl phosphatidyl serine	44147587	Click to see CCCC(=O)OC(COC(=O)CC)COP(=O)(O)OCC(C(=O)O)N	385.30	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds / Tocopherols
(+)-gamma-Tocopherol	92729	Click to see	416.70	unknown	via CMAUP database
Alpha-Tocopherol	14985	Click to see CC1=C(C2=C(CCC(O2)(C)CCCC(C)CCCC(C)CCCC(C)C)C(=C1O)C)C	430.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin K compounds
Phytonadione	5284607	Click to see CC1=C(C(=O)C2=CC=CC=C2C1=O)CC=C(C)CCCC(C)CCCC(C)CCCC(C)C	450.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Retinoids
Retinol	445354	Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CCO)C)C	286.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Carotenes
Beta-Carotene	5280489	Click to see	536.90	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Tetrahydroxy bile acids, alcohols and derivatives
Castasterone	133534	Click to see CC(C)C(C)C(C(C(C)C1CCC2C1(CCC3C2CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O	464.70	unknown	https://doi.org/10.1016/0031-9422(93)85091-5
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Brassinolides and derivatives
Brassinolide	115196	Click to see CC(C)C(C)C(C(C(C)C1CCC2C1(CCC3C2COC(=O)C4C3(CC(C(C4)O)O)C)C)O)O	480.70	unknown	https://doi.org/10.1016/0031-9422(93)85091-5
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3R,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-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	12303645	Click to see	414.70	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
Alpha-Aminoadipic Acid	469	Click to see	161.16	unknown	https://doi.org/10.1016/0031-9422(86)88023-2
alpha-Glycine	5257127	Click to see	75.07	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / L-alpha-amino acids
(2S,3R)-2-azaniumyl-3-hydroxybutanoate	6971019	Click to see CC(C(C(=O)[O-])[NH3+])O	119.12	unknown	via CMAUP database
L-Arginine	6322	Click to see	174.20	unknown	via CMAUP database
Lysine zwitterion	122198194	Click to see	146.19	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Aspartic acid and derivatives
CID 44367445	44367445	Click to see	133.10	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Glutamic acid and derivatives
CID 88747398	88747398	Click to see	147.13	unknown	via CMAUP database
L-gamma-glutamyl-L-glutamic acid	92865	Click to see	276.24	unknown	https://doi.org/10.1016/0031-9422(86)88023-2
Saccharopine	160556	Click to see	276.29	unknown	https://doi.org/10.1016/0031-9422(86)88023-2
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Isoleucine and derivatives
(2S,3S)-2-ammonio-3-methylpentanoate	7043901	Click to see	131.17	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Leucine and derivatives
Leucine, N-carboxy-, N-benzyl ester, L-	74840	Click to see	265.30	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Methionine and derivatives
(2S)-2-ammonio-4-(methylsulfanyl)butanoate	6992087	Click to see	149.21	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Phenylalanine and derivatives
gamma-L-Glutamyl-L-phenylalanine	111299	Click to see	294.30	unknown	https://doi.org/10.1016/0031-9422(86)88023-2
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Proline and derivatives
(2S)-pyrrolidinium-2-carboxylate	6971047	Click to see	115.13	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Serine and derivatives
(2R)-2-ammonio-3-hydroxypropanoate	6857549	Click to see C(C(C(=O)[O-])[NH3+])O	105.09	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Tyrosine and derivatives
(2R)-2-(((tert-butoxy)carbonyl)amino)-3-(4-hydroxyphenyl)propanoic acid	1549481	Click to see	281.30	unknown	via CMAUP database
L-Tyrosine	6057	Click to see	181.19	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC543345/
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Valine and derivatives
(2S)-2-amino-3-methylbutanoate;hydron	88733505	Click to see [H+].CC(C)C(C(=O)[O-])N	117.15	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Cysteine and derivatives
Cystine, meso-	6991966	Click to see	240.30	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / N-acyl-alpha amino acids
(2S)-2-amino-5-[[(1R)-1-carboxy-2-methylsulfonylethyl]amino]-5-oxopentanoic acid	163042308	Click to see	296.30	unknown	https://doi.org/10.1016/0031-9422(86)88023-2
2-Amino-5-[(1-carboxy-2-methylsulfonylethyl)amino]-5-oxopentanoic acid	163042307	Click to see CS(=O)(=O)CC(C(=O)O)NC(=O)CCC(C(=O)O)N	296.30	unknown	https://doi.org/10.1016/0031-9422(86)88023-2
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Cyclic peptides
Vignatic acid A	85210698	Click to see CC(C)CC(C(=O)NC1C(OC2=CC=C(CC(NC(=O)C(NC1=O)CC3=CC=CC=C3)C(=O)O)C=C2)C(C)C)O	553.60	unknown	https://doi.org/10.1021/JF960166C
Vignatic acid B	85261327	Click to see CC(C)CC1C(=O)NC(CC2=CC=C(C=C2)OC(C(C(=O)N1)NC(=O)C(CC(C)C)O)C(C)C)C(=O)O	519.60	unknown	https://doi.org/10.1021/JF960166C
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Dipeptides
(2S)-2-amino-5-[[(1R)-1-carboxy-2-methylsulfanylethyl]amino]-5-oxopentanoic acid	11043643	Click to see CSCC(C(=O)O)NC(=O)CCC(C(=O)O)N	264.30	unknown	https://doi.org/10.1016/0031-9422(86)88023-2
(S)-2-Amino-5-(((S)-1-carboxy-2-phenylethyl)amino)-5-oxopentanoic acid	558649	Click to see C1=CC=C(C=C1)CC(C(=O)O)NC(=O)CCC(C(=O)O)N	294.30	unknown	https://doi.org/10.1016/0031-9422(86)88023-2
gamma-Glu-leu	151023	Click to see CC(C)CC(C(=O)O)NC(=O)CCC(C(=O)O)N	260.29	unknown	https://doi.org/10.1016/0031-9422(86)88023-2
gamma-glutamyl-S-methylcysteine	13894650	Click to see	264.30	unknown	https://doi.org/10.1016/0031-9422(86)88023-2
gamma-Glutamylaspartic acid	161197	Click to see	262.22	unknown	https://doi.org/10.1016/0031-9422(86)88023-2
L-Ornithine, N5-acetyl-N2-L-gamma-glutamyl-	163039197	Click to see	303.31	unknown	https://doi.org/10.1016/0031-9422(86)88023-2
N5-Acetyl-N2-gamma-L-glutamyl-L-ornithine	131752643	Click to see CC(=O)NCCCC(C(=O)O)NC(=O)CCC(C(=O)O)N	303.31	unknown	https://doi.org/10.1016/0031-9422(86)88023-2
Ng-L-Glutamyl-L-aspartic acid	5122061	Click to see	262.22	unknown	https://doi.org/10.1016/0031-9422(86)88023-2
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Oligopeptides
(gamma-Glutamyl-gamma-glutamyl)-S-methylcysteine	131752644	Click to see CSCC(C(=O)O)NC(=O)CCC(C(=O)O)NC(=O)CCC(C(=O)O)N	393.42	unknown	https://doi.org/10.1016/0031-9422(86)88023-2
L-Cysteine, N-(N-L-gamma-glutamyl-L-gamma-glutamyl)-S-methyl-	162994726	Click to see CSCC(C(=O)O)NC(=O)CCC(C(=O)O)NC(=O)CCC(C(=O)O)N	393.42	unknown	https://doi.org/10.1016/0031-9422(86)88023-2
> Organic acids and derivatives / Peptidomimetics / Hybrid peptides
gamma-Glutamyl-S-methylcysteinyl-beta-alanine	131752665	Click to see	335.38	unknown	https://doi.org/10.1016/0031-9422(86)88023-2
Homoglutathione	440380	Click to see	321.35	unknown	https://doi.org/10.1016/0031-9422(86)88023-2
L-gamma-Glutamyl-S-methyl-L-cysteinyl-beta-alanine	155166912	Click to see	335.38	unknown	https://doi.org/10.1016/0031-9422(86)88023-2
L-L-Homoglutathione	3375152	Click to see	321.35	unknown	https://doi.org/10.1016/0031-9422(86)88023-2
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
Chlorogenic Acid	1794427	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	354.31	unknown	https://doi.org/10.1007/BF00598601
Neochlorogenic acid	5280633	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	354.31	unknown	https://doi.org/10.1007/BF00598601
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides
beta-D-Fructopyranose	24310	Click to see C1C(C(C(C(O1)(CO)O)O)O)O	180.16	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
D(+)-Glucose	107526	Click to see C(C(C(C(C(C=O)O)O)O)O)O	180.16	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Monosaccharide phosphates
Dihydroxyacetone Phosphate	668	Click to see C(C(=O)COP(=O)(O)O)O	170.06	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.03.009
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Monosaccharide phosphates / Glyceraldehyde-3-phosphates
Triose phosphate	439168	Click to see	170.06	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.03.009
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
[5-[3-Hydroxy-6-methyl-5-(2-methylbutanoyloxy)-4-(3-phenylprop-2-enoyloxy)oxan-2-yl]oxy-6-methyl-2-[(4,5,26-trihydroxy-6,24-dimethyl-20-oxo-10-pentyl-2,7,9,21,25-pentaoxatricyclo[20.3.1.03,8]hexacosan-23-yl)oxy]-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl] decanoate	75971966	Click to see	1353.60	unknown	https://doi.org/10.1007/BF02488610
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones / Alpha-hydroxy ketones
1,1-Dihydroxypropan-2-one	13180982	Click to see CC(=O)C(O)O	90.08	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.03.009
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
L-Ascorbic Acid	54670067	Click to see	176.12	unknown	via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Indolyl carboxylic acids and derivatives
N-((tert-Butoxy)carbonyl)-D-tryptophan	111050	Click to see	304.34	unknown	via CMAUP database
> Organoheterocyclic compounds / Pteridines and derivatives / Alloxazines and isoalloxazines / Flavins
Riboflavin	493570	Click to see CC1=CC2=C(C=C1C)N(C3=NC(=O)NC(=O)C3=N2)CC(C(C(CO)O)O)O	376.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Pyridines and derivatives / Pyridinecarboxylic acids and derivatives / Pyridinecarboxamides / Nicotinamides
Nicotinamide	936	Click to see C1=CC(=CN=C1)C(=O)N	122.12	unknown	via CMAUP database
> Organoheterocyclic compounds / Pyridines and derivatives / Pyridinecarboxylic acids and derivatives / Pyridinecarboxylic acids
Nicotinic Acid	938	Click to see	123.11	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives
Caffeoyltartronic acid	129660911	Click to see	282.20	unknown	https://doi.org/10.1016/S0031-9422(00)80824-9
Feruloyltartronic acid	129660908	Click to see	296.23	unknown	https://doi.org/10.1016/S0031-9422(00)80824-9
p-Coumaroyltartronic acid	129660903	Click to see C1=CC(=CC=C1C=CC(=O)C(C(=O)O)(C(=O)O)O)O	266.20	unknown	https://doi.org/10.1016/S0031-9422(00)80824-9
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
2-O-Caffeoyltartronic acid	131752962	Click to see C1=CC(=C(C=C1C=CC(=O)OC(C(=O)O)C(=O)O)O)O	282.20	unknown	https://doi.org/10.1016/S0031-9422(00)80824-9
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
Isoscopoletin	69894	Click to see	192.17	unknown	https://doi.org/10.1007/BF00598601
> Phenylpropanoids and polyketides / Flavonoids / Flavones
5,7-Dihydroxy-2-(4-hydroxyphenyl)-8-methyl-4H-1-benzopyran-4-one	45157620	Click to see	284.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin	5280343	Click to see	302.23	unknown	https://doi.org/10.1007/BF00598601
> 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-glucuronides / Flavonoid-3-O-glucuronides
(2S,3S,6S)-6-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid	44259219	Click to see	478.40	unknown	https://doi.org/10.1007/BF00633405
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-((2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl)oxychromen-4-one	51402807	Click to see	464.40	unknown	https://doi.org/10.1007/BF00633405
Kaempferol-3-O-Rutinoside	5318767	Click to see	594.50	unknown	https://doi.org/10.1016/S0031-9422(00)80824-9
Rutin	5280805	Click to see	610.50	unknown	https://doi.org/10.1007/BF00598601 https://doi.org/10.1016/0305-1978(92)90087-T https://doi.org/10.1016/S0031-9422(00)80824-9
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
5,4'-Dihydroxy-3,3'-dimethoxy-7-prenyloxyflavone	44259689	Click to see	398.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
5-Hydroxy-2-(3-hydroxy-4-methoxyphenyl)-3-methoxy-7-((3-methyl-2-butenyl)oxy)-4H-1-benzopyran-4-one	44259699	Click to see	398.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Coumestans
Aureol	5491648	Click to see C1=CC2=C(C=C1O)OC3=C2C(=O)OC4=CC(=CC(=C43)O)O	284.22	unknown	https://doi.org/10.1515/ZNC-1983-9-1005
Phaseol	44257530	Click to see	336.30	unknown	https://doi.org/10.1515/ZNC-1983-9-1005
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
Phaseollidin	119268	Click to see	324.40	unknown	https://doi.org/10.1515/ZNC-1983-9-1004
> 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/10.1515/ZNC-1983-9-1004
Genistein	5280961	Click to see	270.24	unknown	https://doi.org/10.1515/ZNC-1983-9-1004
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones
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/10.1515/ZNC-1983-9-1004
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 8-prenylated isoflavanones
3-(2,4-Dihydroxyphenyl)-2,3-dihydro-5-hydroxy-8,8-dimethyl-4H,8H-benzo(1,2-b:3,4-b')dipyran-4-one	156777	Click to see	354.40	unknown	https://doi.org/10.1515/ZNC-1983-9-1004
Kievitone	119269	Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)C(CO2)C3=C(C=C(C=C3)O)O)C	356.40	unknown	https://doi.org/10.1016/0305-1978(92)90087-T https://doi.org/10.1515/ZNC-1983-9-1004
Stereoisomer of 3-(2,4-dihydroxyphenyl)-2,3-dihydro-7-hydroxy-8-(3-methyl-2-buten-1-yl)-4H-1-benzopyran-4-one	442770	Click to see	340.40	unknown	https://doi.org/10.1515/ZNC-1983-9-1004
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
3-(4-methoxyphenyl)-7-[(2S,4S,5R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	44257215	Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O	430.40	unknown	https://doi.org/10.1007/BF00633405
Daidzin	107971	Click to see	416.40	unknown	https://doi.org/10.1007/BF00633405
Ononin	442813	Click to see	430.40	unknown	https://doi.org/10.1007/BF00633405
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
Formononetin	5280378	Click to see	268.26	unknown	https://doi.org/10.1007/BF00633405

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Vigna radiata

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