Details Top

Internal ID UUID643fdb40136d7463450107
Scientific name Flemingia macrophylla
Authority (Willd.) Kuntze ex Merr.
First published in Philipp. J. Sci., C5: 130 (1910)

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.

Flemingia macrophylla is traditionally used in several cultures as an infusion or decoction for febrile illnesses and cough. Among Ayurvedic practitioners in Karnataka, India, the fresh leaves are boiled to make a decoction that is taken for fever and respiratory complaints (Bhat et al., 2015). In southwestern Nigeria, the dried bark is macerated in water to produce a tea that is used by the Yoruba people to treat malaria and other febrile diseases (Kumar et al., 2018). In the Guangxi region of China, the root is steeped in hot water or macerated in alcohol to create a tincture that is applied for inflammatory pain and skin irritation (Sang et al., 2020). All three traditions rely on liquid preparations—infusions, decoctions, or tinctures—of leaves, bark, or root.

A simple, safe recipe for a mild tea is as follows: take 5 g of dried Flemingia macrophylla leaves, add 250 ml of freshly boiled water, let steep for 10 minutes, strain, and drink two cups per day. For a tincture, combine 30 g of fresh root with 150 ml of 70 % ethanol, seal, and let steep for 7 days, then filter and store in a dark bottle. Caution: animal studies suggest the plant may stimulate uterine contractions, so pregnant women should avoid use and limit intake to no more than 2 cups of tea daily.

Phytochemical analysis of Flemingia macrophylla has identified several well‑established compounds that likely underlie its traditional activities. The leaves and root contain flavonoids such as quercetin and kaempferol, alkaloids including flemingine, saponins, and tannins. These constituents have documented antipyretic, anti‑inflammatory, and antimalarial properties in laboratory studies, providing a chemical basis for the plant’s use in fever and cough.

Modern research continues to validate these traditional claims. Recent pharmacological studies confirm the antipyretic and anti‑inflammatory effects of Flemingia macrophylla extracts, and the species is now available as a commercial herbal supplement in India for the relief of fever and cough. Ongoing investigations are exploring its potential as a natural antimalarial agent, underscoring the plant’s continued relevance in both traditional and contemporary medicine.

General Uses Top

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Common products:
- Tanning extracts (condensed tannins) from leaves, bark, or stems for leather processing; dried aerial biomass as fuelwood; small-diameter wood for posts and tool handles.

Industrial and craft applications:
- Tanning extracts (e.g., described as condensed tannins) employed in leather manufacturing and as mordants or tannin sources in natural dyeing. The plant is used as a hedge, live fence, and in silvicultural plantings for erosion control and soil improvement in agroforestry.

Colorants and tanning:
- The species is cited among plants used for natural dyeing and for producing tanning extracts for leather. Tannins isolated from Flemingia macrophylla have been characterized as condensed tannins with high molecular weight, exhibiting antioxidant activity and substantial protein-binding capacity (proanthocyanidin content), properties relevant to mordanting and leather tanning.

Wood and fiber:
- Small-dimension timber is occasionally fashioned into posts, stakes, tool handles, and walking sticks. Bark fiber can be used for cordage and rough binding. Wood properties typically reflect dense, moderate-to-hard characteristics suitable for low-durability outdoor use.

Properties relevant to use:
- High condensed tannin content (leaf and bark: up to ~22–23% on a dry matter basis) supports leather tanning and natural dyeing applications. Tannins display strong protein-binding and antioxidant properties, consistent with tanning and mordant functions. The wood is typically dense and workable but not noted for high durability.

Sustainability and sourcing:
- The species is commonly propagated from seed, tolerates poor soils, and fixes nitrogen, favoring its use in living fences, soil stabilization, and multi-strata agroforestry systems. Slow growth limits timber volumes, while leaf and bark harvest for tanning extracts can be managed via coppicing or controlled pruning to maintain plant vigor.

Synonyms Top

Scientific name Authority First published in
Flemingia congesta W.T.Aiton Hortus Kew.4: 349 (1812)
Moghania macrophylla (Willd.) Kuntze
Crotalaria macrophylla Willd. Sp. Pl., ed. 4, 3: 982 (1802)
Moghania wallichii (Wight & Arn.) Kuntze
Moghania philippinensis (Merr. & Rolfe) H.L.Li
Flemingia sericans Kurz J. Asiat. Soc. Bengal, Pt. 2, Nat. Hist.43: 186 (1874)
Flemingia congesta var. semialata Baker
Flemingia brevipes Craib Bull. Misc. Inform. Kew1927: 68 (1927)
Flemingia congesta var. viridis (Kurz) Prain J. Asiat. Soc. Bengal, Pt. 2, Nat. Hist.67: 440 (1897)
Flemingia macrophylla var. viridis (Prain) H.B.Naithani Flow. Pl. India, Nepal & Bhutan: 117 (1990)
Moghania latifolia (Benth.) Mukerjee
Moghania semialata (W.T.Aiton) Mukerjee
Moghania semialata var. viridis (Kurz) Mukerjee
Moghania sericans (Kurz) Mukerjee
Flemingia trinervia Desf. Tabl. École Bot., ed. 2: 269 (1815)
Rhynchosia crotalarioiedes DC. Prodr.2: 387 (1825)
Flemingia capitata Buch.-Ham. ex Wall. Numer. List [Wallich] n. 5749. [1831-32]
Flemingia bhottea Buch.-Ham. Numer. List [Wallich] n. 5746. [1831-32]
Moghania cumingiana (Benth.) Kuntze
Moghania teysmanniana (Miq.) H.L.Li
Maughania macrophylla (Willd.) Kuntze Revis. Gen. Pl.1: 199 (1891)
Maughania tomentosa (Miq.) H.L.Li Amer. J. Bot.31: 227 (1944)
Maughania sericans (Kurz) Mukerjee Bull. Bot. Soc. Bengal6: 20 (1952)
Maughania brevipes (Craib) H.L.Li Amer. J. Bot.31: 226 (1944)
Crotalaria cavaleriei H.Lév. Fl. Kouy-Tchéou: 229 (1915)
Flemingia congesta var. tomentosa Miq. Fl. Ned. Ind.1(1): 165 (1855)
Flemingia macrophylla var. congesta (Roxb. ex W.T.Aiton) M.R.Almeida Fl. Maharashtra2: 78 (1998)
Flemingia latifolia var. hainanensis Y.T.Wei & S.K.Lee Guihaia5: 169 (1985)
Flemingia latifolia var. siamensis Craib Fl. Siam.1: 470 (1928)
Maughania macrophylla f. poecilantha Kuntze Revis. Gen. Pl.1: 199 (1891)
Maughania macrophylla f. viridula Kuntze Revis. Gen. Pl.1: 199 (1891)
Hedysarum trinervium Roxb. ex Wall. Numer. List : n.° 5747 (1831)
Rhynchosia sericea S.Vidal Sin. Gen. Pl. Leños. Filip. : t. 40, f. D (1883)

Common names Top

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Language Common/alternative name
Malayalam കാട്ടുമർമാണി
Burmese ကျေးမြီးနီ
Chinese 蚌壳草根
Chinese 大叶千斤拔
Chinese 大葉佛來明豆
Chinese 寬葉千斤拔
Chinese 绣叶千斤拔
Chinese 鏽毛千斤拔
Chinese 铁龙穿石
Chinese 雲南千斤拔
Chinese 假乌豆草
Chinese 千斤红
Chinese 大叶佛来明豆

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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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000194840
Tropicos 13050921
INPN 447193
KEW urn:lsid:ipni.org:names:495277-1
The Plant List ild-41470
PFAF Flemingia macrophylla
Open Tree Of Life 768122
NCBI Taxonomy 520843
IPNI 495274-1
iNaturalist 546018
GBIF 5359866
Freebase /m/0rfdpk1
EPPO FLEMA
EOL 644641
USDA GRIN 17130
Wikipedia Flemingia_macrophylla
CMAUP NPO14892
CMAUP NPO8612

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_043165305.1 ASM4316530v1 Chromosome Hunan Provincial Institute for Drug Control 2024-10-16 184 0.94 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
Pest categorisation of Pyrrhoderma noxium Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Golic D, Gobbi A, Maiorano A, Pautasso M, Reignault PL EFSA J 19-Mar-2024
PMCID:PMC10949325
doi:10.2903/j.efsa.2024.8667
PMID:38505477
Prenylated chromones and flavonoids isolated from the roots of Flemingia macrophylla and their anti-lung cancer activity Wang B, Wang Q, Yuan R, Yang S, Lu M, Yuan F, Dong Z, Mo M, Pan Q, Gao H Chin Med 23-Nov-2023
PMCID:PMC10668522
doi:10.1186/s13020-023-00860-3
PMID:37996917
Implementation of machine learning in DNA barcoding for determining the plant family taxonomy Riza LS, Zain MI, Izzuddin A, Prasetyo Y, Hidayat T, Abu Samah KA Heliyon 21-Sep-2023
PMCID:PMC10520734
doi:10.1016/j.heliyon.2023.e20161
PMID:37767518
Ethnobotanical study on medicinal plants used by Bulang people in Yunnan, China Zhou H, Zhang J, Kirbis BS, Mula Z, Zhang W, Kuang Y, Huang Q, Yin L J Ethnobiol Ethnomed 07-Sep-2023
PMCID:PMC10486041
doi:10.1186/s13002-023-00609-0
PMID:37679773
Analysis of leaf forage value and screening of different populations of Pteroceltis tatarinowii, a rare and endemic species in China Gao Y, Cheng TT, Zhang CX, Yan Y, Zhang L, Liu QZ, Liu Y, Qiao Q Front Plant Sci 30-Jun-2023
PMCID:PMC10348418
doi:10.3389/fpls.2023.1164451
PMID:37457345
Cricket (Gryllus bimaculatus) meal pellets as a protein supplement to improve feed efficiency, ruminal fermentation and microbial protein synthesis in Thai native beef cattle Phesatcha B, Phesatcha K, Matra M, Wanapat M Anim Biosci 26-Jun-2023
PMCID:PMC10472151
doi:10.5713/ab.23.0107
PMID:37402456
Intercropping Cover Crops for a Vital Ecosystem Service: A Review of the Biocontrol of Insect Pests in Tea Agroecosystems Pokharel SS, Yu H, Fang W, Parajulee MN, Chen F Plants (Basel) 18-Jun-2023
PMCID:PMC10304037
doi:10.3390/plants12122361
PMID:37375986
Do carbon stocks and floristic diversity of tropical homegardens vary along an elevational gradient and based on holding size in central Kerala, India? Kumar BM Agrofor Syst 07-Apr-2023
PMCID:PMC10081327
doi:10.1007/s10457-023-00821-7
PMID:37193256
Antennal Transcriptome Analysis of Olfactory Genes and Characterization of Odorant Binding Proteins in Odontothrips loti (Thysanoptera: Thripidae) Liu Y, Luo Y, Du L, Ban L Int J Mol Sci 09-Mar-2023
PMCID:PMC10048907
doi:10.3390/ijms24065284
PMID:36982358
Potential Use of Kasedbok (Neptunia javanica Miq.) on Feed Intake, Digestibility, Rumen Fermentation, and Microbial Populations in Thai Native Beef Cattle Gunun P, Cherdthong A, Khejornsart P, Polyorach S, Kaewwongsa W, Gunun N Animals (Basel) 18-Feb-2023
PMCID:PMC9952691
doi:10.3390/ani13040733
PMID:36830520
Plant-Derived Products with Therapeutic Potential against Gastrointestinal Bacteria Qassadi FI, Zhu Z, Monaghan TM Pathogens 15-Feb-2023
PMCID:PMC9967904
doi:10.3390/pathogens12020333
PMID:36839605
The Spectrum of Pharmacological Actions of Syringetin and Its Natural Derivatives—A Summary Review Chmiel M, Stompor-Gorący M Nutrients 04-Dec-2022
PMCID:PMC9739508
doi:10.3390/nu14235157
PMID:36501187
Mitragyna speciosa Korth Leaf Pellet Supplementation on Feed Intake, Nutrient Digestibility, Rumen Fermentation, Microbial Protein Synthesis and Protozoal Population in Thai Native Beef Cattle Phesatcha B, Phesatcha K, Wanapat M Animals (Basel) 22-Nov-2022
PMCID:PMC9737993
doi:10.3390/ani12233238
PMID:36496759
Seasonal Variations of Fine Root Dynamics in Rubber-Flemingia macrophylla Intercropping System in Southwestern China Bibi F, Balasubramanian D, Ilyas M, Sher J, Samoon HA, Bin Khalid MH, Alharby HF, Majrashi A, Alghamdi SA, Hakeem KR, Shah M, Rather SA Plants (Basel) 12-Oct-2022
PMCID:PMC9611961
doi:10.3390/plants11202682
PMID:36297706
Herbal therapies in gastrointestinal and hepatic disorders: An evidence-based clinical review Yao Y, Habib M, Bajwa HF, Qureshi A, Fareed R, Altaf R, Ilyas U, Duan Y, Abbas M Front Pharmacol 05-Oct-2022
PMCID:PMC9581220
doi:10.3389/fphar.2022.962095
PMID:36278240

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
> Alkaloids and derivatives / Aporphines
N-Methylstenantherine 189603 Click to see 341.40 unknown via CMAUP database
Stenantherine 189607 Click to see COC1=C(C(=C2C3=C1CCNC3CC4=C2C(=CC=C4)O)OC)OC 327.40 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
Protocatechuic Acid 72 Click to see 154.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
4,5,6-Trihydroxy-7-methylphthalide 10420195 Click to see 196.16 unknown via CMAUP database
> Benzenoids / Phenols / Benzenetriols and derivatives / Pyrogallols and derivatives
Flavipin 3083587 Click to see CC1=C(C(=C(C(=C1O)O)O)C=O)C=O 196.16 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,4aS,6aR,6aR,6bR,8aR,11R,12S,12aR,14aR,14bS)-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,6a,7,8,9,10,11,12,12a,14a-tetradecahydro-1H-picen-3-ol 163023159 Click to see CC1CCC2(CCC3(C(C2C1C)C=CC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)86768-0
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/10.1016/S0031-9422(00)86768-0
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1016/S0031-9422(00)86768-0
(2R,3R,4S,5S,6S)-2-[[(3S,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-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 154496016 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 https://doi.org/10.1016/S0031-9422(00)86768-0
(3S,8S,9S,10R,13R,14S,17R)-17-[(E,2S,5S)-5-Ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 12314479 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
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
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Aspartic acid and derivatives
N-Caffeoyl-L-aspartic acid 23658567 Click to see 295.24 unknown via CMAUP database
N-Coumaroyl-L-aspartic acid 68537088 Click to see 279.24 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
N-(E)-Caffeoyl-L-tyrosine 10308838 Click to see C1=CC(=CC=C1CC(C(=O)O)NC(=O)C=CC2=CC(=C(C=C2)O)O)O 343.30 unknown via CMAUP database
N-Coumaroyl-3-hydroxytyrosine 68540305 Click to see C1=CC(=CC=C1C=CC(=O)NC(CC2=CC(=C(C=C2)O)O)C(=O)O)O 343.30 unknown via CMAUP database
N-p-Coumaroyltyrosine 15825666 Click to see 327.30 unknown via CMAUP database
trans-Clovamide 6506968 Click to see 359.30 unknown via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / Quaternary ammonium salts / Cholines
Choline 305 Click to see 104.17 unknown via CMAUP database
> 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 via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
Verbascose 441434 Click to see C(C1C(C(C(C(O1)OCC2C(C(C(C(O2)OCC3C(C(C(C(O3)OCC4C(C(C(C(O4)OC5(C(C(C(O5)CO)O)O)CO)O)O)O)O)O)O)O)O)O)O)O)O)O 828.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar acids and derivatives / Glucuronic acid derivatives
GlyTouCan:G37030UD 90062900 Click to see 194.14 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Pyranochromenes
5-Hydroxy-8,8-dimethyl-6-(3-methylbut-2-enyl)pyrano[2,3-h]chromen-4-one 10710237 Click to see 312.40 unknown https://doi.org/10.1055/S-2005-871297
> Organoheterocyclic compounds / Benzopyrans / 2-benzopyrans
Epicoccolide A 71732639 Click to see 374.30 unknown via CMAUP database
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives / Xanthines
Caffeine 2519 Click to see CN1C=NC2=C1C(=O)N(C(=O)N2C)C 194.19 unknown via CMAUP database
Theobromine 5429 Click to see 180.16 unknown via CMAUP database
> Organoheterocyclic compounds / Isocoumarans
4,6-Dihydroxy-5-methoxy-7-methyl-1,3-dihydroisobenzofuran 123784052 Click to see 196.20 unknown via CMAUP database
7-Methyl-1,3-dihydro-2-benzofuran-4,5,6-triol 10845133 Click to see 182.17 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthopyrans
Acetosellin 10883740 Click to see 394.40 unknown via CMAUP database
> Organoheterocyclic compounds / Tetrahydroisoquinolines
Salsolinol 91588 Click to see 179.22 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
Epicoccolide B 11210533 Click to see 358.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(1S,5R,6R,13R,21S)-5,13-bis(3,4-dihydroxyphenyl)-21-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaene-6,9,17,19-tetrol 118731401 Click to see 738.60 unknown via CMAUP database
Cinnamtannin A2 16130899 Click to see 1155.00 unknown via CMAUP database
Cinnamtannin A3 16129741 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C(=CC(=C4C5C(C(OC6=C(C(=CC(=C56)O)O)C7C(C(OC8=C(C(=CC(=C78)O)O)C9C(C(OC1=CC(=CC(=C91)O)O)C1=CC(=C(C=C1)O)O)O)C1=CC(=C(C=C1)O)O)O)C1=CC(=C(C=C1)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 1443.30 unknown via CMAUP database
Proanthocyanidin A1 9872976 Click to see 576.50 unknown via CMAUP database
Procyanidin A2 124025 Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC(=C(C=C6)O)O)O)O)C7=CC(=C(C=C7)O)O)O 576.50 unknown via CMAUP database
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 B2, (+)- 122738 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 B5 124017 Click to see C1C(C(OC2=C1C(=C(C(=C2)O)C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown via CMAUP database
Procyanidin C1 169853 Click to see 866.80 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans / 6-prenylated flavanones
(2R)-5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-8,8-dimethyl-6-(3-methylbut-2-enyl)-2,3-dihydropyrano[2,3-h]chromen-4-one 163011906 Click to see CC(=CCC1=C(C2=C(C3=C1OC(C=C3)(C)C)OC(CC2=O)C4=CC(=C(C=C4)O)OC)O)C 436.50 unknown https://doi.org/10.1055/S-2005-871297
(2S)-2-(3,4-dihydroxyphenyl)-5-hydroxy-8,8-dimethyl-6-(3-methylbut-2-enyl)-2,3-dihydropyrano[2,3-h]chromen-4-one 162956161 Click to see 422.50 unknown https://doi.org/10.1055/S-2005-871297
(2S)-5-hydroxy-2-(2-hydroxy-4-methoxyphenyl)-8,8-dimethyl-6-(3-methylbut-2-enyl)-2,3-dihydropyrano[2,3-h]chromen-4-one 101326868 Click to see 436.50 unknown https://doi.org/10.1016/S0031-9422(97)00243-4
2-(3,4-Dihydroxyphenyl)-5-hydroxy-8,8-dimethyl-6-(3-methylbut-2-enyl)-2,3-dihydropyrano[2,3-h]chromen-4-one 162956160 Click to see 422.50 unknown https://doi.org/10.1055/S-2005-871297
5-Hydroxy-2-(4-hydroxy-3-methoxyphenyl)-8,8-dimethyl-6-(3-methylbut-2-enyl)-2,3-dihydropyrano[2,3-h]chromen-4-one 10812825 Click to see 436.50 unknown https://doi.org/10.1055/S-2005-871297
Eriosemaone A 11742973 Click to see 422.50 unknown https://doi.org/10.1016/S0031-9422(97)00243-4
Fleminone 42608040 Click to see 436.50 unknown https://doi.org/10.1016/S0031-9422(00)80163-6
https://doi.org/10.1016/S0031-9422(97)00243-4
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(8S)-8-[2,4-dihydroxy-5-(3-methylbut-2-enyl)phenyl]-5-hydroxy-2,2-dimethyl-10-(3-methylbut-2-enyl)-7,8-dihydropyrano[3,2-g]chromen-6-one 12096319 Click to see 490.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.09.003
5,7-Dihydroxy-2-(4-hydroxyphenyl)-6,8-bis(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 3951 Click to see 408.50 unknown https://doi.org/10.1055/S-2005-871297
8-(2,4-Dihydroxyphenyl)-5-hydroxy-2,2-dimethyl-10-(3-methylbut-2-enyl)-7,8-dihydropyrano[3,2-g]chromen-6-one 42608041 Click to see 422.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.09.003
8-[2,4-Dihydroxy-5-(3-methylbut-2-enyl)phenyl]-5-hydroxy-2,2-dimethyl-10-(3-methylbut-2-enyl)-7,8-dihydropyrano[3,2-g]chromen-6-one 162891404 Click to see 490.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.09.003
Flemichin D 124344 Click to see CC(=CCC1=C2C(=C(C3=C1OC(CC3=O)C4=C(C=C(C=C4)O)O)O)C=CC(O2)(C)C)C 422.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.09.003
Kushenol E 127234 Click to see 424.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.09.003
Senegalensin 124035 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=CC=C(C=C3)O)CC=C(C)C)O)C 408.50 unknown https://doi.org/10.1055/S-2005-871297
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
8,8'-Methylenebiscatechin 46182787 Click to see 592.50 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 / Catechins / Epigallocatechins
(-)-Egc-4'-O-ME 53463000 Click to see 320.29 unknown https://doi.org/10.1016/S0031-9422(97)00243-4
4'-Methyl-epigallocatechin 176920 Click to see 320.29 unknown https://doi.org/10.1016/S0031-9422(97)00243-4
ent-Gallocatechin 4'-methyl ether 10087345 Click to see COC1=C(C=C(C=C1O)C2C(CC3=C(C=C(C=C3O2)O)O)O)O 320.29 unknown https://doi.org/10.1016/S0031-9422(97)00243-4
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
4',7-Dihydroxyflavanone 1889 Click to see 256.25 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.09.003
Liquiritigenin 114829 Click to see 256.25 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.09.003
Naringenin 439246 Click to see 272.25 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.09.003
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-3-O-glycosides
Cyanidin 3-O-galactoside 441699 Click to see C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O 449.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
3,5,7-trihydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-6-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 101713180 Click to see COC1=CC(=CC(=C1O)OC)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O 508.40 unknown https://doi.org/10.1016/S0031-9422(97)00243-4
3,5,7-Trihydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 74978329 Click to see COC1=CC(=CC(=C1O)OC)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O 508.40 unknown https://doi.org/10.1016/S0031-9422(97)00243-4
Moghanin A 44259487 Click to see 508.40 unknown https://doi.org/10.1016/S0031-9422(97)00243-4
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
(2R,3R)-2-(3,4-dihydroxyphenyl)-8-[(2S,3R,4R,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 5317057 Click to see 452.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
5,7-dihydroxy-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2-(3,4,5-trihydroxyphenyl)chromen-4-one 129010103 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/S0031-9422(00)91528-0
Cyanidin 3-arabinoside cation 12137509 Click to see C1C(C(C(C(O1)OC2=CC3=C(C=C(C=C3[O+]=C2C4=CC(=C(C=C4)O)O)O)O)O)O)O 419.40 unknown via CMAUP database
Guaijaverin 5481224 Click to see 434.30 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/10.1055/S-2005-871297
Medicagol 5319322 Click to see C1OC2=C(O1)C=C3C(=C2)C4=C(O3)C5=C(C=C(C=C5)O)OC4=O 296.23 unknown https://doi.org/10.1055/S-2005-871297
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
(8R)-5-hydroxy-3-(4-hydroxyphenyl)-8,9,9-trimethyl-8H-furo[2,3-h]chromen-4-one 163058247 Click to see 338.40 unknown https://doi.org/10.1002/MRC.2336
1,3,8,10-Tetrahydroxy-2-methyl-4,9-bis(3-methylbut-2-enyl)-[1]benzofuro[2,3-b]chromen-11-one 11518049 Click to see CC1=C(C(=C2C(=C1O)C(=O)C3=C(O2)OC4=C3C(=C(C(=C4)O)CC=C(C)C)O)CC=C(C)C)O 450.50 unknown https://doi.org/10.1055/S-2005-871297
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/10.1016/J.PHYTOCHEM.2003.09.003
https://doi.org/10.1016/S0031-9422(00)83979-5
5-hydroxy-3-(4-hydroxyphenyl)-8,9,9-trimethyl-8H-furo[2,3-h]chromen-4-one 163058246 Click to see 338.40 unknown https://doi.org/10.1002/MRC.2336
6-(1,1-Dimethylallyl)genistein 44257285 Click to see CC(C)(C=C)C1=C(C2=C(C=C1O)OC=C(C2=O)C3=CC=C(C=C3)O)O 338.40 unknown https://doi.org/10.1016/S0031-9422(00)83979-5
8-(1,1-Dimethylallyl)genistein 12096315 Click to see 338.40 unknown https://doi.org/10.1055/S-2005-871297
https://doi.org/10.1002/MRC.2336
Flemiphyllin 44257286 Click to see CC(=CCC1=CC(=CC(=C1O)CC=C(C)C)C2=COC3=C(C(=CC(=C3C2=O)O)O)CC=C(C)C)C 474.60 unknown https://doi.org/10.1016/S0031-9422(00)85070-0
Genistein 5280961 Click to see 270.24 unknown https://doi.org/10.1055/S-2005-871297
https://doi.org/10.1016/0031-9422(91)80134-M
https://doi.org/10.1016/J.PHYTOCHEM.2003.09.003
https://doi.org/10.1016/S0031-9422(97)00243-4
https://doi.org/10.1016/S0031-9422(00)83979-5
Lupinalbin A 5324349 Click to see 284.22 unknown https://doi.org/10.1055/S-2005-871297
Orobol 5281801 Click to see C1=CC(=C(C=C1C2=COC3=CC(=CC(=C3C2=O)O)O)O)O 286.24 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.09.003
https://doi.org/10.1055/S-2005-871297
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones / 2-prenylated isoflavones
2'-PrenylsemilicoisoflavoneB 12096317 Click to see CC(=CCC1=C(C=C2C=CC(OC2=C1O)(C)C)C3=COC4=CC(=CC(=C4C3=O)O)O)C 420.50 unknown https://doi.org/10.1016/J.BMC.2013.08.049
https://doi.org/10.1055/S-2005-871297
3',4',5,7-Tetrahydroxy-2',5'-di(3-methyl-2-butenyl)isoflavone 12096316 Click to see CC(=CCC1=CC(=C(C(=C1O)O)CC=C(C)C)C2=COC3=CC(=CC(=C3C2=O)O)O)C 422.50 unknown https://doi.org/10.1016/J.BMC.2013.08.049
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 6-prenylated isoflavanones
3-(3,4-Dimethoxyphenyl)-5,7-dihydroxy-6,8-bis(3-methylbut-2-enyl)chromen-4-one 154496564 Click to see 450.50 unknown https://doi.org/10.1016/0031-9422(91)80134-M
5-Hydroxy-7-(4-hydroxyphenyl)-2,2-dimethyl-3-(2-methylbut-3-en-2-yl)-10-(3-methylbut-2-enyl)pyrano[3,2-g]chromen-6-one 73355670 Click to see CC(=CCC1=C2C(=C(C3=C1OC=C(C3=O)C4=CC=C(C=C4)O)O)C=C(C(O2)(C)C)C(C)(C)C=C)C 472.60 unknown https://doi.org/10.1016/J.BMC.2013.08.049
https://doi.org/10.1002/MRC.2336
5,7-Dihydroxy-3-[4-hydroxy-3-(2-methylbut-3-en-2-yl)phenyl]-6,8-bis(3-methylbut-2-enyl)chromen-4-one 162933761 Click to see 474.60 unknown https://doi.org/10.1055/S-2005-871297
5,7,3',4'-Tetrahydroxy-6-prenylisoflavone 44257302 Click to see 354.40 unknown https://doi.org/10.1002/MRC.2336
6,8-Diprenylgenistein 480783 Click to see 406.50 unknown https://doi.org/10.1016/J.BMC.2013.08.049
https://doi.org/10.1055/S-2005-871297
6,8-Diprenylorobol 21148065 Click to see 422.50 unknown https://doi.org/10.1016/J.BMC.2013.08.049
https://doi.org/10.1055/S-2005-871297
https://doi.org/10.1002/MRC.2336
Auriculasin 5358846 Click to see CC(=CCC1=C2C(=C(C3=C1OC=C(C3=O)C4=CC(=C(C=C4)O)O)O)C=CC(O2)(C)C)C 420.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.09.003
https://doi.org/10.1016/J.BMC.2013.08.049
https://doi.org/10.1002/MRC.2336
Flemingsin 15719494 Click to see 436.50 unknown https://doi.org/10.1016/0031-9422(91)80134-M
https://doi.org/10.1016/J.BMC.2013.08.049
Flemiphilippinin A 10074228 Click to see 488.60 unknown https://doi.org/10.1016/0031-9422(91)80134-M
https://doi.org/10.1016/J.BMC.2013.08.049
https://doi.org/10.1002/MRC.2336
Flemiphilippinin C 5317360 Click to see CC(=CCC1=C2C(=C(C3=C1OC=C(C3=O)C4=CC(=C(C=C4)O)OC)O)C=CC(O2)(C)C)C 434.50 unknown https://doi.org/10.1016/S0031-9422(00)85070-0
Lupalbigenin 10001388 Click to see 406.50 unknown https://doi.org/10.1055/S-2005-871297
Osajin 95168 Click to see 404.50 unknown https://doi.org/10.1016/J.BMC.2013.08.049
https://doi.org/10.1055/S-2005-871297
Pomiferin 4871 Click to see 420.50 unknown https://doi.org/10.1055/S-2005-871297
Wighteone 5281814 Click to see 338.40 unknown https://doi.org/10.1002/MRC.2336
https://doi.org/10.1016/0031-9422(91)80134-M
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
4H-1-Benzopyran-4-one, 7-(beta-D-glucopyranosyloxy)-3-(4-hydroxyphenyl)- 4183640 Click to see C1=CC(=CC=C1C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O)O 416.40 unknown https://doi.org/10.1016/S0031-9422(97)00243-4
Daidzin 107971 Click to see 416.40 unknown https://doi.org/10.1016/S0031-9422(97)00243-4
Genistin 5281377 Click to see 432.40 unknown https://doi.org/10.1016/S0031-9422(97)00243-4
Genistoside 5284639 Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown https://doi.org/10.1016/S0031-9422(97)00243-4
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 3-O-methylated isoflavonoids / 3-O-methylisoflavones
3'-O-Methylorobol 5319744 Click to see COC1=C(C=CC(=C1)C2=COC3=CC(=CC(=C3C2=O)O)O)O 300.26 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.09.003
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 7-O-methylated isoflavonoids / 7-O-methylisoflavones
Prunetin 5281804 Click to see 284.26 unknown https://doi.org/10.1055/S-2005-871297
> Phenylpropanoids and polyketides / Isoflavonoids / Pyranoisoflavonoids
Ulexone B 14583601 Click to see 402.40 unknown https://doi.org/10.1055/S-2005-871297
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
1-[(2S)-4,6-dihydroxy-2-(2-hydroxypropan-2-yl)-5-(3-methylbut-2-enyl)-2,3-dihydro-1-benzofuran-7-yl]-3-(4-methoxyphenyl)propan-1-one 162883992 Click to see CC(=CCC1=C(C(=C2C(=C1O)CC(O2)C(C)(C)O)C(=O)CCC3=CC=C(C=C3)OC)O)C 440.50 unknown https://doi.org/10.1055/S-2005-871297
1-[4,6-Dihydroxy-2-(2-hydroxypropan-2-yl)-5-(3-methylbut-2-enyl)-2,3-dihydro-1-benzofuran-7-yl]-3-(4-methoxyphenyl)propan-1-one 162883991 Click to see 440.50 unknown https://doi.org/10.1055/S-2005-871297
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
(E)-1-[(2S)-5,8-dihydroxy-2-methyl-2-(4-methylpent-3-enyl)chromen-6-yl]-3-(2,6-dihydroxyphenyl)prop-2-en-1-one 92469097 Click to see 422.50 unknown https://doi.org/10.1016/S0031-9422(00)91528-0

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