Details Top

Internal ID UUID64400dbe3b79a038246917
Scientific name Brassica carinata
Authority A.Braun
First published in Flora 24: 267 (1841)

Ethnobotanical Use Top

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Important notice
  • 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.

Ethiopian mustard is widely consumed as a leafy vegetable in the Horn of Africa, especially Ethiopia, where fresh or boiled leaves are cooked into wot (a spicy stew). Leaves are also eaten as a salad or boiled side dish in Eritrea (Bekele-Tesemma, 2007; Jansen, 1981). Among the Kewun in Kenya, young shoots and tender leaves are similarly boiled and eaten, and the plant is included among staple leafy vegetables (Maundu, 1999). In southern Ethiopia’s Shasha Forest area, schoolchildren harvest the tender tops and young leaves, typically boiling them as a leafy vegetable; boiling alone is documented as a common preparation method, though short infusions of leaves are not described in this group (Cotton, 1996).

Practical cooking example: Whole, blanched leaves or tender tops (about 2 cups loosely packed) are rinsed, added to a pot with a pinch of salt, covered, and gently boiled for 10–12 minutes until soft; the cooking water is usually consumed as broth. Avoid prolonged boiling if you prefer retain flavor and nutrients; serve with a squeeze of lemon or mixed with other cooked greens (Bekele-Tesemma, 2007; Cotton, 1996; Maundu, 1999). No formal dose or safety limits are reported for culinary quantities, but tolerate taste; proceed cautiously if you have thyroid conditions or are on blood‑thinning medication, as with other cruciferous vegetables. The species is a self‑compatible annual or short‑lived perennial; it is an “escaped” cultivar—descended from cultivated Ethiopian mustard and not considered invasive in its native African range.

Active constituents: Protein and carbohydrate content are well documented, including favorable amino acids, vitamin C, and folates; the leaves and seeds also contain glucosinolates such as sinalbin and glucobrassicin (Nuez et al., 2004). Glucosinolates are chemically stable in living tissues and become bioactive upon cell damage, which may underlie some of the described flavor and traditional use as a bitter, “pungent” green (Jansen, 1981).

Modern relevance: Ethnobotanical work continues to track its dietary role and occasional medicinal uses; the plant is a recognized staple green with stable cultivation in Ethiopia, Kenya, and Eritrea, and it appears in the PROTA database and contemporary ethnobotanical surveys (PROTA4U, 2014; Maundu, 1999; Bekele-Tesemma, 2007; Cotton, 1996; Jansen, 1981; Nuez et al., 2004).

General Uses Top

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Common products:
- Seed oil (high‑erucic acid oil), seed meal (protein‐rich animal feed after glucosinolate removal), and whole‑plant green manure for soil improvement.

Industrial and craft applications:
- Oil serves as a feedstock for biodiesel, renewable diesel, and aviation‑grade hydroprocessed esters and fatty acids (HEFA) used as jet‑fuel components. High‑erucic acid oil is a precursor for erucamide, a slip‑agent in plastics and a component of hydraulic fluids, lubricants, and metalworking fluids. Hydrogenated oil yields waxes and is incorporated into oil‑based paints, inks, and varnishes.

Food and beverages (non‑medicinal):
- Low‑erucic‑acid cultivars are marketed as culinary oil for salad dressings, frying, and deep‑frying. Carinata seed can be milled to produce a mustard‑type condiment analogous to other Brassica mustards. The oil’s neutral flavor and stability make it suitable for processed food applications where high‑erucic oils are permissible.

Properties relevant to use:
- Seed oil typically contains 40–55 % erucic acid, 5–10 % linoleic acid, 5–8 % oleic acid, and low saturated fatty‑acid levels (≈5 %). It exhibits a high iodine value (≈110–120) and good oxidative stability due to its monounsaturated profile. Seed meal averages 35–40 % crude protein but contains glucosinolates (≈10–20 µmol g⁻¹) that require detoxification for feed use.

Standards and regulation:
- For food‑grade oil, Codex Alimentarius and the EU (Regulation (EC) No 178/2002) limit erucic acid to ≤2 % of total fatty acids in refined vegetable oil. The U.S. FDA similarly permits ≤2 % erucic acid in “oil for food” (21 CFR § 184.1505). Industrial and biofuel oils are not subject to these erucic‑acid limits. ISO 5508 provides a method for determining erucic acid content.

Sustainability and sourcing:
- Carinata is cultivated in Ethiopia, Kenya, the United States, and Canada. It tolerates drought, low nitrogen inputs, and marginal soils, allowing production on land unsuitable for major food crops. As a rotation crop it improves soil structure and suppresses weeds. Its use as a low‑carbon biofuel feedstock contributes to greenhouse‑gas mitigation and can be paired with carbon‑offset programs.

Synonyms Top

Scientific name Authority First published in
Sinabraca carinata (A.Braun) G.H.Loos Florist. Rundbr., Beih. 7: 131 (2004)
Brassica integrifolia var. carinata (Broun) O.E.Schulz Pflanzenr. IV, 105(70): 58 1919
Brassica juncea var. agrestis Prain Agric. Ledger 1: 47 1898
Brassica juncea var. cuneifolia Prain Agric. Ledger 1: 47 1898
Brassica juncea var. edona Makino Somoku-Dzusetsu ed. 3, 3: 12, t. 37 1912
Brassica juncea subsp. urbaniana (O.E.Schulz) Thell. Verh. Bot. Vereins Prov. Brandenburg 50(2): 158 1908
Brassica nigra var. laevigata (DC.) Alef. Landw. Fl. 234 1866
Brassica timoriana F.Muell. Descr. Notes Papuan Pl. 2: 4 (1876)
Brassica urbaniana var. lyrifolia Stokes Bot. Mat. Med. 3: 481 1812
Sinapis abyssinica A.Braun ex Regel Index Seminum (LE, Petropolitanus) 1856: 34 (1856)

Common names Top

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Language Common/alternative name
English abyssinian mustard
English african kale
English ethiopian mustard
Amharic ጎመንዘር
Welsh rêp ethiopia
Persian خردل کاریناتا
Finnish etiopiansinappi
French moutarde d'Éthiopie
frr abessiinsk senep
Japanese アビシニアガラシ
Korean 고먼
Dutch ethiopische mosterd
Swedish etiopisk kål
Swahili sukuma ya kiasili
Chinese 埃塞俄比亚芥

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • East Tropical Africa
      • Kenya
      • Tanzania
      • Uganda
    • Northeast Tropical Africa
      • Eritrea
      • Ethiopia
    • West Tropical Africa
      • Ivory Coast
    • West-central Tropical Africa
      • Gabon

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000570995
USDA Plants BRCA30
Tropicos 4100066
KEW urn:lsid:ipni.org:names:279278-1
The Plant List kew-2682106
Open Tree Of Life 749459
NCBI Taxonomy 52824
NBN Atlas NHMSYS0000456596
Nature Serve 2.161199
IPNI 279278-1
iNaturalist 159414
GBIF 3042925
Freebase /m/047gc68
EPPO BRSCA
EOL 490690
USDA GRIN 7642
Wikipedia Brassica_carinata
CMAUP NPO6065

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
Name Level Submitter Released Coverage Size
GCA_051989265.1 ASM5198926v1 Chromosome Centre for Genetic Manipulation of Crop Plants, University of Delhi South Campus 2025-08-13 61 0.97 Gb

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
Deciphering variations, identification of marker–trait associations and candidate genes for seed oil content under terminal heat stress in Indian mustard (Brassica juncea L. Czern & Coss) germplasm stock Pal L, Sandhu SK, Kaur J, Bhatia D 3 Biotech 28-Apr-2024
PMCID:PMC11056352
doi:10.1007/s13205-024-03985-w
PMID:38689736
Traditional lore on the healing effects of therapeutic plants used by the local communities around Simien Mountains National Park, northwestern Ethiopia Seraw E, Melkamu Y, Masresha G J Ethnobiol Ethnomed 17-Apr-2024
PMCID:PMC11025143
doi:10.1186/s13002-024-00678-9
PMID:38632559
Genome-wide identification and stress response analysis of BcaCPK gene family in amphidiploid Brassica carinata Zuo D, Lei S, Qian F, Gu L, Wang H, Du X, Zeng T, Zhu B BMC Plant Biol 17-Apr-2024
PMCID:PMC11022436
doi:10.1186/s12870-024-05004-9
Lineage-specific gene duplication and expansion of DUF1216 gene family in Brassicaceae Zhang ZB, Xiong T, Wang XJ, Chen YR, Wang JL, Guo CL, Ye ZY PLoS One 16-Apr-2024
PMCID:PMC11020792
doi:10.1371/journal.pone.0302292
PMID:38626181
Microbe cultivation guidelines to optimize rhamnolipid applications Kłosowska-Chomiczewska IE, Macierzanka A, Parchem K, Miłosz P, Bladowska S, Płaczkowska I, Hewelt-Belka W, Jungnickel C Sci Rep 10-Apr-2024
PMCID:PMC11006924
doi:10.1038/s41598-024-59021-7
PMID:38600115
Do Brassica Vegetables Affect Thyroid Function?—A Comprehensive Systematic Review Galanty A, Grudzińska M, Paździora W, Służały P, Paśko P Int J Mol Sci 03-Apr-2024
PMCID:PMC11012840
doi:10.3390/ijms25073988
PMID:38612798
BcABF1 Plays a Role in the Feedback Regulation of Abscisic Acid Signaling via the Direct Activation of BcPYL4 Expression in Pakchoi Yang X, Wang M, Zhou Q, Xu X, Li Y, Hou X, Xiao D, Liu T Int J Mol Sci 30-Mar-2024
PMCID:PMC11011251
doi:10.3390/ijms25073877
PMID:38612692
A GASA Protein Family Gene, CmGEG, Inhibits Petal Growth in Chrysanthemum He Z, Jiang R, Wang X, Wang Y Int J Mol Sci 16-Mar-2024
PMCID:PMC10970651
doi:10.3390/ijms25063367
PMID:38542341
Pb uptake, accumulation, and translocation in plants: Plant physiological, biochemical, and molecular response: A review Ur Rahman S, Qin A, Zain M, Mushtaq Z, Mehmood F, Riaz L, Naveed S, Ansari MJ, Saeed M, Ahmad I, Shehzad M Heliyon 07-Mar-2024
PMCID:PMC10945279
doi:10.1016/j.heliyon.2024.e27724
PMID:38500979
Chromosome-scale reference genome of broccoli (Brassica oleracea var. italica Plenck) provides insights into glucosinolate biosynthesis Wu Q, Mao S, Huang H, Liu J, Chen X, Hou L, Tian Y, Zhang J, Wang J, Wang Y, Huang K Hortic Res 28-Feb-2024
PMCID:PMC11077082
doi:10.1093/hr/uhae063
PMID:38720933
Enzymatic properties of UDP-glycosyltransferase 89B1 from radish and modulation of enzyme catalytic activity via loop region mutation Ohashi H, Koma D, Yamanaka H, Ohmoto T PLoS One 28-Feb-2024
PMCID:PMC10901349
doi:10.1371/journal.pone.0299755
PMID:38416725
Ethnobotanical study of traditional medicinal plants used by the local Gamo people in Boreda Abaya District, Gamo Zone, southern Ethiopia Zemede J, Mekuria T, Ochieng CO, Onjalalaina GE, Hu GW J Ethnobiol Ethnomed 28-Feb-2024
PMCID:PMC10900619
doi:10.1186/s13002-024-00666-z
PMID:38419092
Productivity of two Brassica oilseed crops in a Mediterranean environment and assessment of the qualitative characteristics of raw materials for bioenergy purposes Licata M, Farruggia D, Di Miceli G, Salamone F, Iacuzzi N, Tuttolomondo T Heliyon 23-Feb-2024
PMCID:PMC10907774
doi:10.1016/j.heliyon.2024.e26818
PMID:38434387
Cytonuclear Interactions and Subgenome Dominance Shape the Evolution of Organelle-Targeted Genes in the Brassica Triangle of U Kan S, Liao X, Lan L, Kong J, Wang J, Nie L, Zou J, An H, Wu Z Mol Biol Evol 23-Feb-2024
PMCID:PMC10919925
doi:10.1093/molbev/msae043
PMID:38391484
The complete chloroplast genome of Brassica rapa var. purpuraria (L.H.Bailey) Kitam 1950 and its phylogenetic analysis Zhou X, Ren H, Zhang J, Xu D, Xiao W, Huang H, Li G, Zhang H, Zheng Y Mitochondrial DNA B Resour 24-Jan-2024
PMCID:PMC10810650
doi:10.1080/23802359.2024.2305403
PMID:38274856

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives
N-Formyl-4-hydroxybenzamide 71370414 Click to see C1=CC(=CC=C1C(=O)NC=O)O 165.15 unknown via CMAUP database
N-Formylbenzamide 151196 Click to see 149.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzamides
4-Hydroxybenzamide 65052 Click to see 137.14 unknown via CMAUP database
Benzamide, N-[(2S)-2-hydroxy-2-phenylethyl]- 6542363 Click to see 241.28 unknown via CMAUP database
> Lignans, neolignans and related compounds / Cyclobutane lignans
[(1R,2R,3S,4S)-2-(2,4-dihydroxybenzoyl)-3,4-diphenylcyclobutyl]-(2,4-dihydroxyphenyl)methanone 102228233 Click to see 480.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,2R,5S,6R,9R,10S,11S,14R,15R,19S,21R,22R)-10-(hydroxymethyl)-2,5,6,10,14,21-hexamethyl-23-oxahexacyclo[19.2.1.02,19.05,18.06,15.09,14]tetracos-17-ene-11,22-diol 44253988 Click to see CC12CCC(C(C1CCC3(C2CC=C4C3(CCC5(C4CC6(CC5OC6O)C)C)C)C)(C)CO)O 472.70 unknown via CMAUP database
(1R,2R,5S,6R,9R,10S,11S,14R,15R,19S,21R,22R)-10-(hydroxymethyl)-22-methoxy-2,5,6,10,14,21-hexamethyl-23-oxahexacyclo[19.2.1.02,19.05,18.06,15.09,14]tetracos-17-en-11-ol 44253989 Click to see 486.70 unknown via CMAUP database
(1R,2R,5S,6R,9R,10S,11S,14R,15R,19S,21R)-11-hydroxy-10-(hydroxymethyl)-2,5,6,10,14,21-hexamethyl-23-oxahexacyclo[19.2.1.02,19.05,18.06,15.09,14]tetracos-17-en-22-one 102482971 Click to see 470.70 unknown via CMAUP database
(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 via CMAUP database
(2R,4aS,6aR,6aS,6bR,8aR,9S,12aR,14bR)-9-(hydroxymethyl)-2,4a,6a,6b,9,12a-hexamethyl-10-oxo-3,4,5,6,6a,7,8,8a,11,12,13,14b-dodecahydro-1H-picene-2-carboxylic acid 44253990 Click to see CC12CCC(CC1C3=CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)CO)C)(C)C(=O)O 470.70 unknown via CMAUP database
(3S,4S,4aR,6aR,6bS,8aR,9R,11R,12aS,14aR,14bR)-4,11-bis(hydroxymethyl)-4,6a,6b,8a,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-3,9-diol 14335966 Click to see 474.70 unknown via CMAUP database
24-Hydroxy-beta-amyrin 14167253 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1)C)C)C 442.70 unknown via CMAUP database
Melilotigenin B 91895471 Click to see CC1(CC2C3=CCC4C5(CCC(=O)C(C5CCC4(C3(CCC2(C(=O)C1)C)C)C)(C)CO)C)C 454.70 unknown via CMAUP database
Melilotigenin C 10551785 Click to see CC1(CC2C3=CCC4C5(CCC(=O)C(C5CCC4(C3(CCC2(C(C1)O)C)C)C)(C)CO)C)C 456.70 unknown via CMAUP database
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 via CMAUP database
Soyasapogenol E 13632872 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(C(=O)C1)C)C)C)(C)CO)O)C)C 456.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glucosinolates / Alkylglucosinolates
Sinigrin 6911854 Click to see 359.40 unknown https://doi.org/10.1016/0031-9422(88)80190-0
https://doi.org/10.1021/JF00029A028
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
Hexanal 6184 Click to see 100.16 unknown https://doi.org/10.1016/0031-9422(88)83085-1
> Organoheterocyclic compounds / Benzopyrans
Oxytropisoflavan B 46918734 Click to see COC1=C(C(=C(C=C1)C2CC3(CCC(=O)C=C3OC2)O)O)OC 320.30 unknown via CMAUP database
> Organoheterocyclic compounds / Benzothiazoles
Benzothiazole 7222 Click to see C1=CC=C2C(=C1)N=CS2 135.19 unknown https://doi.org/10.1016/0031-9422(88)83085-1
> Organoheterocyclic compounds / Indoles and derivatives / Benzoylindoles
(3-Hydroxyindol-1-yl)-(3-hydroxyphenyl)methanone 46850207 Click to see 253.25 unknown via CMAUP database
(3-Hydroxyindol-1-yl)-(4-hydroxyphenyl)methanone 46850031 Click to see 253.25 unknown via CMAUP database
(3-Hydroxyindol-1-yl)-[4-hydroxy-3-(3-methylbut-2-enyl)phenyl]methanone 46850206 Click to see CC(=CCC1=C(C=CC(=C1)C(=O)N2C=C(C3=CC=CC=C32)O)O)C 321.40 unknown via CMAUP database
(3-Hydroxyindol-1-yl)-phenylmethanone 46850030 Click to see C1=CC=C(C=C1)C(=O)N2C=C(C3=CC=CC=C32)O 237.25 unknown via CMAUP database
(4-Hydroxy-3-methoxyindol-1-yl)-(4-hydroxyphenyl)methanone 46850205 Click to see 283.28 unknown via CMAUP database
(4-Hydroxyphenyl)-(3-methoxyindol-1-yl)methanone 46850032 Click to see COC1=CN(C2=CC=CC=C21)C(=O)C3=CC=C(C=C3)O 267.28 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Indoles / 3-alkylindoles
Brassinin 3035211 Click to see CSC(=S)NCC1=CNC2=CC=CC=C21 236.40 unknown https://doi.org/10.1016/S0960-894X(98)00564-2
Cyclobrassinin 184579 Click to see 234.30 unknown https://doi.org/10.1016/S0960-894X(98)00564-2
> Organosulfur compounds / Isothiocyanates
Butyl isothiocyanate 11613 Click to see CCCCN=C=S 115.20 unknown https://doi.org/10.1016/0031-9422(88)83085-1
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Antithiamine factor 5321318 Click to see 238.24 unknown https://doi.org/10.1016/S0031-9422(02)00488-0
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Sinapinic acid 637775 Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)O 224.21 unknown https://doi.org/10.1016/S0031-9422(02)00488-0
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
Dihydromyricetin 161557 Click to see C1=C(C=C(C(=C1O)O)O)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O 320.25 unknown https://doi.org/10.1016/S0031-9422(02)00488-0
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2S)-7-hydroxyflavanone 688857 Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC=CC=C3 240.25 unknown via CMAUP database
Liquiritigenin 114829 Click to see 256.25 unknown via CMAUP database
Pinocembrin 68071 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
(2S,3R)-3,5,7-trihydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one 11449086 Click to see 288.25 unknown https://doi.org/10.1016/S0031-9422(02)00488-0
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/10.1016/S0031-9422(02)00488-0
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown via CMAUP database
Chrysin 5281607 Click to see 254.24 unknown via CMAUP database
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Isorhamnetin 5281654 Click to see 316.26 unknown via CMAUP database
Kaempferol 5280863 Click to see 286.24 unknown https://doi.org/10.1016/S0031-9422(02)00488-0
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 via CMAUP database
Quercetin 5280343 Click to see 302.23 unknown https://doi.org/10.1016/S0031-9422(02)00488-0
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
3-[(2S,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-7-methoxychromen-4-one 60200223 Click to see 608.50 unknown via CMAUP database
3-[(2S,3R,4S,5R,6R)-6-[[(2R,3R,4R,5S,6S)-3,5-dihydroxy-6-methyl-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 21668680 Click to see 726.60 unknown via CMAUP database
3-[(2S,3R,4S,5R,6R)-6-[[(2R,3R,4R,5S,6S)-3,5-dihydroxy-6-methyl-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxymethyl]-4,5-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 10865825 Click to see 872.80 unknown via CMAUP database
Biorobin 15944778 Click to see 594.50 unknown via CMAUP database
Mauritianin 10919701 Click to see 740.70 unknown via CMAUP database
Oxytroflavoside A 60200065 Click to see 752.70 unknown via CMAUP database
Oxytroflavoside B 60200066 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)OC)C5=CC=C(C=C5)O)CO)O)OC(=O)CC(C)(CC(=O)O)O)O)O)O 752.70 unknown via CMAUP database
Oxytroflavoside C 60200220 Click to see 752.70 unknown via CMAUP database
Oxytroflavoside D 60200221 Click to see 606.50 unknown via CMAUP database
Oxytroflavoside E 60200222 Click to see 768.70 unknown via CMAUP database
Oxytroflavoside G 60200370 Click to see 754.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Kaempferol 3-O-(Alpha-L-Rhamnopyranosyl(1->2)-Beta-D-Galactopyranosyl)-7-O-Alpha-L-Rhamnopyranoside 57397583 Click to see 740.70 unknown via CMAUP database
Robinin 5281693 Click to see 740.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(-)-Pinostrobin 73201 Click to see 270.28 unknown via CMAUP database
(2S)-2-(4-hydroxyphenyl)-7-methoxy-2,3-dihydrochromen-4-one 14157884 Click to see COC1=CC2=C(C=C1)C(=O)CC(O2)C3=CC=C(C=C3)O 270.28 unknown via CMAUP database
(R,S)-7-Methoxy-2-phenyl-chroman-4-one 688883 Click to see COC1=CC2=C(C=C1)C(=O)CC(O2)C3=CC=CC=C3 254.28 unknown via CMAUP database
Sakuranetin 73571 Click to see 286.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Homoisoflavonoids / Homoisoflavans / Homoisoflavanones
(3S)-7-hydroxy-3-[(4-hydroxyphenyl)methyl]-2,3-dihydrochromen-4-one 26088035 Click to see 270.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
(-)-Maackiain 91510 Click to see 284.26 unknown via CMAUP database
(6Ar,11Ar)-3,8-Dihydroxy-9,10-Dimethoxypterocarpan 46918735 Click to see 316.30 unknown via CMAUP database
(l)-Edunol 182148 Click to see 352.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
Daidzein 5281708 Click to see 254.24 unknown via CMAUP database
Pseudobaptigenin 5281805 Click to see C1OC2=C(O1)C=C(C=C2)C3=COC4=C(C3=O)C=CC(=C4)O 282.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavanquinones
5-[(3R)-7-hydroxy-3,4-dihydro-2H-chromen-3-yl]-2,3-dimethoxycyclohexa-2,5-diene-1,4-dione 10403457 Click to see COC1=C(C(=O)C(=CC1=O)C2CC3=C(C=C(C=C3)O)OC2)OC 316.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
Daidzein-4'-glucoside 49862229 Click to see 416.40 unknown via CMAUP database
Sophoricoside 5321398 Click to see 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 3-O-methylated isoflavonoids / 3-O-methylisoflavones
3'-Methoxydaidzein 5319422 Click to see COC1=C(C=CC(=C1)C2=COC3=C(C2=O)C=CC(=C3)O)O 284.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids
Isomucronulatol, (-)- 10380176 Click to see 302.32 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 3-hydroxy,4-methoxyisoflavonoids
(3R)-2',3',7-trihydroxy-4'-methoxyisoflavan 15939757 Click to see COC1=C(C(=C(C=C1)C2CC3=C(C=C(C=C3)O)OC2)O)O 288.29 unknown via CMAUP database
(R)-Mucronulatol 13873811 Click to see 302.32 unknown via CMAUP database
Calycosin 5280448 Click to see 284.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
2'-Hydroxybiochanin A 5282075 Click to see 300.26 unknown via CMAUP database
Formononetin 5280378 Click to see 268.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 7-O-methylated isoflavonoids / 7-O-methylisoflavones
Isoformononetin 3764 Click to see 268.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
2',4'-Dihydroxydihydrochalcone 586491 Click to see 242.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
1-(2,4-Dihydroxyphenyl)-3-(4-Hydroxyphenyl)Prop-2-En-1-One 425 Click to see 256.25 unknown via CMAUP database
1-(2,4-Dihydroxyphenyl)-3-phenylprop-2-en-1-one 344530 Click to see C1=CC=C(C=C1)C=CC(=O)C2=C(C=C(C=C2)O)O 240.25 unknown via CMAUP database
2-Propen-1-one, 1-(2-hydroxy-4-methoxyphenyl)-3-(4-hydroxyphenyl)- 592216 Click to see COC1=CC(=C(C=C1)C(=O)C=CC2=CC=C(C=C2)O)O 270.28 unknown via CMAUP database
2',4'-Dihydroxychalcone 5376979 Click to see 240.25 unknown via CMAUP database
2a(2),4a(2)-Dihydroxy-4-methoxychalcone 166795 Click to see 270.28 unknown via CMAUP database
4'-Methoxy-2'-hydroxy chalcone 265720 Click to see 254.28 unknown via CMAUP database
Isoliquiritigenin 638278 Click to see 256.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 3-prenylated chalcones
2',4',4-Trihydroxy-3'-prenylchalcone 193568 Click to see 324.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Cinnamylphenols
1-(4-Hydroxy-2-methoxyphenyl)-3-phenylprop-2-en-1-one 71442332 Click to see 254.28 unknown via CMAUP database

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