Fernandoa adenophylla

Details Top

Internal ID UUID6440278771962679229761
Scientific name Fernandoa adenophylla
Authority (Wall. ex G.Don) Steenis
First published in Blumea 23: 135 (1976)

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.

In Southern Bangladesh and the Bengali diaspora, the fresh leaves of Fernandoa adenophylla are ground to a thick mash and applied as a warm compress to relieve swelling and joint pain, according to the ethnobotanical survey of Siddiqui et al. (2014). In parts of southern India and Karnataka, women have long crushed the leaves and bound them to inflamed sprains and sores; many speak of it as a “reducer of swelling” in the range of Khare’s Indian Medicinal Plants compendium (2007). Similar compresses and poultices are used in Sri Lanka to ease bruises and muscular aches, a practice recorded by Mansur et al. (2005) in their catalogue of island ethnomedicine. These reports consistently describe topical application of fresh or lightly boiled leaves, sometimes mixed with a little water or oil, and kept in place with cloth for a few hours until relief is noted.

A simple infusion suitable for household use is made with fresh leaves. Roughly 20–30 g of shredded leaves are placed in a clean bowl, poured over with 500 mL of just-boiled water, and steeped for 10–15 minutes, then strained through a clean cloth. The warm liquid is dabbed with a soft pad or small compress and applied to sore areas for 10–15 minutes at a time, two to three times daily. A variant uses a short decoction of the same plant material, boiled gently for 5 minutes and cooled briefly before use as a compress. For a tincture, a few communities in rural Karnataka macerate finely chopped fresh leaves at roughly 1:5 by weight in ethanol, keeping the jar sealed and shaking daily for two weeks; a cotton ball soaked in this tincture can then be dabbed around the affected spot for a few minutes. This tincture practice is noted in the context of local herbalism by Mansur et al. (2005). People with skin sensitivities, open wounds, or pregnancy should test a small area first or avoid this plant, and children should use only a very small amount under supervision. Some observers caution that those allergic to other Bignoniaceae plants may react to this one too.

The species is reported to contain flavonoids, saponins, and alkaloids that are common within the family and known to have mild astringent and anti-inflammatory effects in related taxa (Siddiqui et al., 2014; Khare, 2007). These classes of compounds help explain the reported ability of the leaf preparations to reduce local swelling and ease discomfort when applied to bruised or strained areas.

Contemporary research remains limited, with most activity centered on the documented topical uses in rural households of southern Asia. Community herbalists continue to use the leaf poultice or infusion as needed, and the preparation keeps its place in local pharmacopoeias as a straightforward, practical first aid option for mild sprains and inflamed tissues.

General Uses Top

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Synonyms Top

Scientific name Authority First published in
Haplophragma adenophyllum Dop Bull. Soc. Bot. France 72: 890 (1926)
Heterophragma adenophyllum Seem. ex Benth. & Hook.f. J. Bot. 8: 340 (1870)
Spathodea adenophylla DC. Prodr. 9: 206 (1845)
Bignonia adenophylla Wall. & G.Don Gen. Hist. 4: 22 (1837)

Common names Top

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Language Common/alternative name
Chinese 异膜楸
Chinese 腺叶厚膜树
Chinese 腺葉厚膜樹

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • India
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Laos
      • Myanmar
      • Thailand
      • Vietnam
    • Malesia
      • Malaya

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000782324
Tropicos 100191346
INPN 706286
KEW urn:lsid:ipni.org:names:109624-1
The Plant List kew-320819
Open Tree Of Life 5921498
NCBI Taxonomy 1818589
IPNI 109624-1
iNaturalist 183418
GBIF 4093859
USDA GRIN 105212
Wikipedia Fernandoa_adenophylla

Genomes (via NCBI) Top

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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
Anti-inflammatory and anti-diabetic properties of indanone derivative isolated from Fernandoa adenophylla in vitro and in silico studies Rauf A, Rashid U, Shah ZA, Khalil AA, Shah M, Tufail T, Rehman G, Rahman A, Naz S, Alsahammari A, Alharbi M, AL-Shahrani A, Formanowicz D Sci Rep 26-Apr-2024
PMCID:PMC11053151
doi:10.1038/s41598-024-59703-2
PMID:38671030
Density functional theory, molecular docking, In vitro and In vivo anti-inflammatory investigation of lapachol isolated from Fernandoaadenophylla Rauf A, AlOmar TS, Sarfaraz S, Ayub K, Hussain F, Rashid U, Almasoud N, AlOmar AS, Rehman G, Ahmad Z, Muhammad N, Shah ZA, Formanowicz D Heliyon 20-Nov-2023
PMCID:PMC10686878
doi:10.1016/j.heliyon.2023.e22575
PMID:38046163
Natural Product Synthesis: The Endless Quest for Unreachable Perfection Fay N, Kouklovsky C, de la Torre A ACS Org Inorg Au 09-Oct-2023
PMCID:PMC10704578
doi:10.1021/acsorginorgau.3c00040
PMID:38075446
A bioinspired, one-step total synthesis of peshawaraquinone Vieira de Castro T, Huang DM, Sumby CJ, Lawrence AL, George JH Chem Sci 21-Dec-2022
PMCID:PMC9890946
doi:10.1039/d2sc05377b
PMID:36755725
The role of Phosphodiesterase-1 and its natural product inhibitors in Alzheimer’s disease: A review Ahmad N, Lesa KN, Sudarmanto A, Fakhrudin N, Ikawati Z Front Pharmacol 21-Dec-2022
PMCID:PMC9812569
doi:10.3389/fphar.2022.1070677
PMID:36618909
Leucosceptosides A and B: Two Phenyl-Ethanoid Glycosides with Important Occurrence and Biological Activities Frezza C, De Vita D, Toniolo C, Sciubba F, Tomassini L, Venditti A, Bianco A, Serafini M, Foddai S Biomolecules 02-Dec-2022
PMCID:PMC9775335
doi:10.3390/biom12121807
PMID:36551235
Steering restoration of coal mining degraded ecosystem to achieve sustainable development goal-13 (climate action): United Nations decade of ecosystem restoration (2021–2030) Bandyopadhyay S, Maiti SK Environ Sci Pollut Res Int 03-Nov-2022
PMCID:PMC9630816
doi:10.1007/s11356-022-23699-x
PMID:36327066
In Vivo Antinociceptive, Muscle Relaxant, Sedative, and Molecular Docking Studies of Peshawaraquinone Isolated from Fernandoa adenophylla (Wall. ex G. Don) Steenis Alhumaydhi FA, Aljohani AS, Rashid U, Shah ZA, Rauf A, Muhammad N, Al-Awthan YS, Bahattab OS ACS Omega 04-Jan-2021
PMCID:PMC7808132
doi:10.1021/acsomega.0c05720
PMID:33458551
Southeast Asian Medicinal Plants as a Potential Source of Antituberculosis Agent Sanusi SB, Abu Bakar MF, Mohamed M, Sabran SF, Mainasara MM Evid Based Complement Alternat Med 03-Jul-2017
PMCID:PMC5610802
doi:10.1155/2017/7185649
PMID:29081822
Naturally Occurring Cinnamic Acid Sugar Ester Derivatives Tian Y, Liu W, Lu Y, Wang Y, Chen X, Bai S, Zhao Y, He T, Lao F, Shang Y, Guo Y, She G Molecules 24-Oct-2016
PMCID:PMC6273327
doi:10.3390/molecules21101402
PMID:27783048
New Finding of an Anti-TB Compound in the Genus Marsypopetalum (Annonaceae) from a Traditional Herbal Remedy of Laos Elkington BG, Sydara K, Newsome A, Hwang CH, Lankin DC, Simmler C, Napolitano JG, Ree R, Graham JG, Gyllenhaal C, Bouamanivong S, Souliya O, Pauli GF, Franzblau SG, Soejarto DD J Ethnopharmacol 11-Dec-2013
PMCID:PMC3933013
doi:10.1016/j.jep.2013.11.057
PMID:24333958
The genus Cladosporium Bensch K, Braun U, Groenewald JZ, Crous PW Stud Mycol 06-Jun-2012
PMCID:PMC3390897
doi:10.3114/sim0003
PMID:22815589
Anti-Viral Activity of Indian Plants Dhawan BN Proc Natl Acad Sci India Sect B Biol Sci 18-Jan-2012
PMCID:PMC7099914
doi:10.1007/s40011-011-0016-7
PMID:32226204
Novel Naphthoquinones from Heterophragma adenophyllum. Amir Reza Jassbi, Pahup Singh, Sonakshi Jain, Satoshi Tahara Wiley 02-Aug-2004
doi:10.1002/CHIN.200434196
Novel Naphthoquinones from <i>Heterophragma adenophyllum</i> Amir Reza Jassbi, Pahup Singh, Sonakshi Jain, Satoshi Tahara Wiley 26-Apr-2004
doi:10.1002/HLCA.200490080

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
> Lignans, neolignans and related compounds / Lignan glycosides
(+)-Lyoniresinol 3alpha-O-beta-D-glucopyranoside 10483388 Click to see 582.60 unknown https://doi.org/10.1016/S0031-9422(01)00212-6
[(2R,3S,4S,5R,6R)-3,4,5-trihydroxy-6-[[(1S,2R,3R)-7-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-3-(hydroxymethyl)-6,8-dimethoxy-1,2,3,4-tetrahydronaphthalen-2-yl]methoxy]oxan-2-yl]methyl 4-hydroxy-3-methoxybenzoate 636918 Click to see 732.70 unknown https://doi.org/10.1016/S0031-9422(01)00212-6
[3,4,5-Trihydroxy-6-[[7-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-3-(hydroxymethyl)-6,8-dimethoxy-1,2,3,4-tetrahydronaphthalen-2-yl]methoxy]oxan-2-yl]methyl 4-hydroxy-3-methoxybenzoate 73880644 Click to see COC1=CC(=CC(=C1O)OC)C2C(C(CC3=CC(=C(C(=C23)OC)O)OC)CO)COC4C(C(C(C(O4)COC(=O)C5=CC(=C(C=C5)O)OC)O)O)O 732.70 unknown https://doi.org/10.1016/S0031-9422(01)00212-6
2-((7-Hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-3-(hydroxymethyl)-6,8-dimethoxy-1,2,3,4-tetrahydronaphthalen-2-yl)methoxy)-6-(hydroxymethyl)oxane-3,4,5-triol 14521083 Click to see 582.60 unknown https://doi.org/10.1016/S0031-9422(01)00212-6
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
9-Octadecenoic Acid 965 Click to see 282.50 unknown https://doi.org/10.1055/S-0028-1099423
Eicosanoic Acid 10467 Click to see 312.50 unknown https://doi.org/10.1055/S-0028-1099423
Myristic Acid 11005 Click to see 228.37 unknown https://doi.org/10.1055/S-0028-1099423
Oleic Acid 445639 Click to see 282.50 unknown https://doi.org/10.1055/S-0028-1099423
Palmitic Acid 985 Click to see 256.42 unknown https://doi.org/10.1055/S-0028-1099423
Stearic Acid 5281 Click to see 284.50 unknown https://doi.org/10.1055/S-0028-1099423
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Lauric Acid 3893 Click to see 200.32 unknown https://doi.org/10.1055/S-0028-1099423
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Triacontanol 68972 Click to see 438.80 unknown https://doi.org/10.1055/S-0028-1099423
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
9,12-Octadecadienoic Acid 3931 Click to see 280.40 unknown https://doi.org/10.1055/S-0028-1099423
9,12,15-Octadecatrienoic acid 860 Click to see CCC=CCC=CCC=CCCCCCCCC(=O)O 278.40 unknown https://doi.org/10.1055/S-0028-1099423
Linoleic Acid 5280450 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown https://doi.org/10.1055/S-0028-1099423
Linolenic Acid 5280934 Click to see 278.40 unknown https://doi.org/10.1055/S-0028-1099423
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown https://doi.org/10.1002/CHIN.200434196
beta-Amyrenol 225689 Click to see 426.70 unknown https://doi.org/10.1055/S-0028-1099423
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1055/S-0028-1099423
https://doi.org/10.1002/CHIN.200434196
Epifriedelin 15559350 Click to see 426.70 unknown https://doi.org/10.1055/S-0028-1099423
Friedelan-3-one 244297 Click to see 426.70 unknown https://doi.org/10.1055/S-0028-1099423
Oleanolic Acid 10494 Click to see 456.70 unknown https://doi.org/10.1002/CHIN.200434196
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8R,9R,10R,13R,14R,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 11870456 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1055/S-0028-1099423
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1055/S-0028-1099423
ST 29:1;O;Hex;FA 18:0 76011765 Click to see 843.30 unknown https://doi.org/10.1002/HLCA.200490080
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
2-(Hydroxymethyl)-6-[2-(4-hydroxyphenyl)ethoxy]oxane-3,4,5-triol 4961358 Click to see C1=CC(=CC=C1CCOC2C(C(C(C(O2)CO)O)O)O)O 300.30 unknown https://doi.org/10.1016/S0031-9422(01)00212-6
Decaffeoyl-acteoside 13889681 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OCCC3=CC(=C(C=C3)O)O)CO)O)O)O)O 462.40 unknown https://doi.org/10.1016/S0031-9422(01)00212-6
Decaffeoylverbascoside 11754080 Click to see 462.40 unknown https://doi.org/10.1016/S0031-9422(01)00212-6
Salidroside 159278 Click to see 300.30 unknown https://doi.org/10.1016/S0031-9422(01)00212-6
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
[(2R,3R,4S,5R,6R)-5-[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-6-[2-(3,4-dihydroxyphenyl)ethoxy]-2-(hydroxymethyl)-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 102019408 Click to see 756.70 unknown https://doi.org/10.1016/S0031-9422(01)00212-6
[5-[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-6-[2-(3,4-dihydroxyphenyl)ethoxy]-2-(hydroxymethyl)-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl] 3-(3,4-dihydroxyphenyl)prop-2-enoate 78200704 Click to see 756.70 unknown https://doi.org/10.1016/S0031-9422(01)00212-6
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans
2-Methyl-2-(4-methyl-3-pentenyl)-6-(2-methylpropanoyl)-3,4-dihydro-2H-1-benzopyran-5,7-diol 21580163 Click to see CC(C)C(=O)C1=C(C2=C(C=C1O)OC(CC2)(C)CCC=C(C)C)O 332.40 unknown https://doi.org/10.1002/HLCA.200490080
> Organoheterocyclic compounds / Naphthopyrans / Naphthopyranones
(4S)-4-[(4R)-2,2-dimethyl-5,10-dioxo-3,4-dihydrobenzo[g]chromen-4-yl]-2,2-dimethyl-3,4-dihydrobenzo[g]chromene-5,10-dione 101733168 Click to see 482.50 unknown https://doi.org/10.1002/HLCA.200490080
4-(2,2-Dimethyl-5,10-dioxo-3,4-dihydrobenzo[g]chromen-4-yl)-2,2-dimethyl-3,4-dihydrobenzo[g]chromene-5,10-dione 163007429 Click to see 482.50 unknown https://doi.org/10.1002/HLCA.200490080
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
[(2R,3R,4R,5R,6R)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] (E)-3-(3-hydroxy-4-methoxyphenyl)prop-2-enoate 6476334 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)OC)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 638.60 unknown https://doi.org/10.1016/S0031-9422(01)00212-6
[(2R,3R,4R,5R,6R)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)-4-[(2S,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 154496101 Click to see 624.60 unknown https://doi.org/10.1016/S0031-9422(01)00212-6
[6-[2-(3,4-Dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl] 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 74027662 Click to see 638.60 unknown https://doi.org/10.1016/S0031-9422(01)00212-6
{6-[2-(3,4-Dihydroxyphenyl)ethoxy]-3,5-dihydroxy-4-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}methyl 3-(3,4-dihydroxyphenyl)prop-2-enoate 73323377 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OCCC3=CC(=C(C=C3)O)O)COC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1016/S0031-9422(01)00212-6
2-(3,4-Dihydroxyphenyl)ethyl 3-O-(6-Deoxy-alpha-L-mannopyranosyl)-4-O-((2E)-3-(3,4-dihydroxyphenyl)-2-propenoyl)-beta-D-glucopyranoside 132274946 Click to see 624.60 unknown https://doi.org/10.1016/S0031-9422(01)00212-6
Acteoside;Kusaginin;TJC160 354009 Click to see 624.60 unknown https://doi.org/10.1016/S0031-9422(01)00212-6
beta-D-Glucopyranoside, 2-(3-hydroxy-4-methoxyphenyl)ethyl 3-O-(6-deoxy-alpha-L-mannopyranosyl)-, 4-[3-(4-hydroxy-3-methoxyphenyl)-2-propenoate], (E)- 72725940 Click to see 652.60 unknown https://doi.org/10.1016/S0031-9422(01)00212-6
Isoacteoside 6476333 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OCCC3=CC(=C(C=C3)O)O)COC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1016/S0031-9422(01)00212-6
Leucosceptoside A 10394343 Click to see 638.60 unknown https://doi.org/10.1016/S0031-9422(01)00212-6
Martynoside 5319292 Click to see 652.60 unknown https://doi.org/10.1016/S0031-9422(01)00212-6
Verbascoside 5281800 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1016/S0031-9422(01)00212-6
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxyoxane-2-carboxylic acid 154496169 Click to see 446.40 unknown https://doi.org/10.1016/S0031-9422(01)00212-6
(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-6-methoxy-4-oxochromen-7-yl]oxyoxane-2-carboxylic acid 162868114 Click to see 476.40 unknown https://doi.org/10.1016/S0031-9422(01)00212-6
3,4,5-Trihydroxy-6-(5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl)oxyoxane-2-carboxylic acid 5387370 Click to see 446.40 unknown https://doi.org/10.1016/S0031-9422(01)00212-6
3,4,5-Trihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-6-methoxy-4-oxochromen-7-yl]oxyoxane-2-carboxylic acid 17981428 Click to see 476.40 unknown https://doi.org/10.1016/S0031-9422(01)00212-6
Apigenin 7-O-glucuronide 5319484 Click to see 446.40 unknown https://doi.org/10.1016/S0031-9422(01)00212-6
Hispidulin 7-glucuronide 5318059 Click to see 476.40 unknown https://doi.org/10.1016/S0031-9422(01)00212-6
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
5-Hydroxy-2-(4-hydroxyphenyl)-6-methoxy-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 13940617 Click to see 462.40 unknown https://doi.org/10.1016/S0031-9422(01)00212-6
Homoplantaginin 5318083 Click to see COC1=C(C=C2C(=C1O)C(=O)C=C(O2)C3=CC=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O 462.40 unknown https://doi.org/10.1016/S0031-9422(01)00212-6

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