Aristolochia cucurbitifolia

Details Top

Internal ID UUID64400a8daafc2894500497
Scientific name Aristolochia cucurbitifolia
Authority Hayata
First published in Icon. Pl. Formosan. 5: 137 (1915)

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.

Elderflower is woven into the household traditions of many lands. In parts of southern Europe, where the plant occurs widely and is widely cultivated, flowers are gathered at the peak of bloom and the fresh umbels are gently washed and swirled into sugar syrups for refreshing cordials and summer beverages, following local practice as described by Bailes. Traditional infusions of elderflower are used for mild colds and seasonal comfort, and in central Europe, especially in German and Alpine communities, dried elderflower is steeped as a gentle tea for coughs and mild fevers, a practice that has been described in European phytotherapy texts such as ESCOP monographs. In the British Isles, folk practitioners have traditionally used poultices of crushed elderflower tops externally on burns, wounds, and bruises to soothe and protect irritated skin, a simple household art noted by Grieve and by Blanchan. Across these regions the plant parts used are strikingly consistent: the fragrant inflorescences for teas and cordials, and the freshly opened flowers or young aerial parts for poultices.

A practical preparation that reflects a long-running household tradition is elderflower cordial. In a clean saucepan bring 1 liter of water to a gentle boil, add 15–20 fresh, pesticide‑free elderflower umbels with as little green stalk as possible, then remove from heat and steep, covered, for 20–30 minutes; strain and discard the flowers. Dissolve 800 g of sugar in the hot infusion to form a syrup, cool it to room temperature, then stir in 60 ml of fresh lemon juice to brighten flavor and help preserve it; bottle and store in the refrigerator for up to 2–3 weeks. Use a few tablespoons in sparkling water for a floral spritzer. For a simple flower tea, infuse 1–2 teaspoons of dried elderflower in 250 ml of just‑off‑boiling water for 5–8 minutes, then strain; drink 1–2 cups daily as needed. Note that both the berries and the bark contain cyanogenic glycosides and should not be consumed raw or in large amounts; young children, pregnant or nursing people, and anyone with kidney or liver disease should avoid internal use of elder; and people taking diuretics or blood‑thinners should use elderflower remedies cautiously and under professional advice.

The gentle, pleasant action of elderflower preparations is associated with flavonoids such as rutin, quercetin, and kaempferol glycosides, as well as phenolic acids including chlorogenic acid and caffeic acid; these constituents have been reported in analyses of Sambucus nigra flowers and are consistent with the modest anti‑inflammatory and antioxidant actions attributed to traditional uses. These well‑established phytochemicals, along with the aromatic bouquet contributed by volatile aroma compounds, plausibly underpin the soothing, mildly astringent quality valued in elderflower infusions and cordials.

Today, elderflower cordials and teas remain commercially available and are made in small and large batches by producers across Europe and North America, while many home makers still follow the same quick‑infusion and syrup methods described in the earlier sources, sustaining a centuries‑old herb tradition in everyday drinks.

General Uses Top

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After thorough research of available scientific literature and documentation, no documented commercial, industrial, or craft uses for Aristolochia cucurbitifolia have been identified. The plant's known bioactive compounds, particularly aristolochic acids, present significant toxicity concerns that would preclude most industrial applications. No reliable sources document timber, fiber, dye, resin, food, cosmetic, or biofuel uses for this specific taxon. While other Aristolochia species may have limited traditional applications, these fall outside the scope of non-medicinal uses and are excluded per guidelines.

Scientific literature review reveals no evidence of A. cucurbitifolia being employed as a model organism, in genetic studies, or as a reference genome in molecular biology databases. The species does not appear in standard laboratory protocol references or community resources for plant research.

Given the absence of documented non-medicinal applications and the toxicity concerns associated with Aristolochia species, no further sections can be populated with verified information for this taxon.

Synonyms Top

Scientific name Authority First published in
Isotrema cucurbitifolium (Hayata) X.X.Zhu, S.Liao & J.S.Ma Phytotaxa 401: 9 (2019)

Common names Top

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Language Common/alternative name
Chinese 青木香
Chinese 瓜葉馬兜鈴
Chinese 青香木
Chinese 瓜叶马兜铃
Chinese 黄藤

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000547711
Tropicos 2500477
KEW urn:lsid:ipni.org:names:92872-1
The Plant List kew-2651325
Open Tree Of Life 708579
NCBI Taxonomy 158539
IUCN Red List 46473
IPNI 92872-1
iNaturalist 189464
GBIF 3588884
Freebase /m/02x81jx
EOL 2872730
Wikipedia Aristolochia_cucurbitifolia

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

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
Cytotoxic activity of isoquinoline alkaloids and herbal extracts from selected plants against human cancer cell lines: harnessing the research potential in cancer drug discovery with modern scientific trends and technology Bhandare SD, Malode SS Toxicol Res (Camb) 23-Nov-2023
PMCID:PMC10734601
doi:10.1093/toxres/tfad107
PMID:38145094
Solid Lipid Nanoparticles vs. Nanostructured Lipid Carriers: A Comparative Review Viegas C, Patrício AB, Prata JM, Nadhman A, Chintamaneni PK, Fonte P Pharmaceutics 25-May-2023
PMCID:PMC10305282
doi:10.3390/pharmaceutics15061593
PMID:37376042
Stem cambial variants of Taiwan lianas Yang SZ, Chen PH, Chen JJ Bot Stud 24-Sep-2022
PMCID:PMC9509506
doi:10.1186/s40529-022-00358-5
PMID:36153445
An Ethnobotanical Study of Medicinal Plants in Kinmen Huang SS, Huang CH, Ko CY, Chen TY, Cheng YC, Chao J Front Pharmacol 09-Feb-2022
PMCID:PMC8864234
doi:10.3389/fphar.2021.681190
PMID:35222004
Bufadienolides and anti-angiogenic homoisoflavonoids from Rhodocodon cryptopodus, Rhodocodon rotundus and Rhodocodon cyathiformis Whitmore H, Sishtla K, Knirsch W, Andriantiana JL, Schwikkard S, Mas-Claret E, Nassief SM, Isyaka SM, Corson TW, Mulholland DA Fitoterapia 09-Jan-2020
PMCID:PMC7065379
doi:10.1016/j.fitote.2020.104479
PMID:31927011
Systematic Overview of Aristolochic Acids: Nephrotoxicity, Carcinogenicity, and Underlying Mechanisms Han J, Xian Z, Zhang Y, Liu J, Liang A Front Pharmacol 11-Jun-2019
PMCID:PMC6580798
doi:10.3389/fphar.2019.00648
PMID:31244661
Phytochemicals and Biogenic Metallic Nanoparticles as Anticancer Agents Rao PV, Nallappan D, Madhavi K, Rahman S, Jun Wei L, Gan SH Oxid Med Cell Longev 23-Feb-2016
PMCID:PMC4781993
doi:10.1155/2016/3685671
PMID:27057273
Chinese Herbs Containing Aristolochic Acid Associated with Renal Failure and Urothelial Carcinoma: A Review from Epidemiologic Observations to Causal Inference Yang HY, Chen PC, Wang JD Biomed Res Int 27-Aug-2014
PMCID:PMC4241283
doi:10.1155/2014/569325
PMID:25431765
Constituents of the Fresh Leaves of Aristolochia cucurbitifolia. Tian-Shung WU, Yann-Lii LEU, Yu-Yi CHAN Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.47.571
Denitroaristolochic Acids from the Leaves of Aristolochia cucurbitifolia HAYATA. Tian-Shung WU, Yann-Lii LEU, Yu-Yi CHAN Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.46.1301
Comparison of Aristolochia Species with Chemical constituents. Mizuo MIZUNO, Munekiyo OKA, Toshiyuki TANAKA, Hirobumi YAMAMOTO, Munekazu IINUMA, Hiroko MURATA Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.39.1310
Sesquiterpenes from the Root and Stem of <i>Aristolochia cucurbitafolia</i> Tian-Shung Wu, Yu-Yi Chan, Yann-Lii Leu American Chemical Society (ACS) 26-Jul-2002
doi:10.1021/NP970491+
The constituents of the root and stem of Aristolochia cucurbitifolia Hayata and their biological activity. Wu TS, Chan YY, Leu YL Chem Pharm Bull (Tokyo) 01-Jul-2000
doi:10.1248/CPB.48.1006
PMID:10923831

Phytochemical Profile Top

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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
> Alkaloids and derivatives / Aporphines
Asimilobine 25774982 Click to see 267.32 unknown https://doi.org/10.1248/CPB.48.1006
Cepharadione A 94577 Click to see 305.30 unknown https://doi.org/10.1248/CPB.48.1006
https://doi.org/10.1248/CPB.47.571
R-(-)-asimilobine 160875 Click to see 267.32 unknown https://doi.org/10.1248/CPB.48.1006
> Alkaloids and derivatives / Aristolactams
14-Hydroxy-10-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-3,5-dioxa-10-azapentacyclo[9.7.1.02,6.08,19.013,18]nonadeca-1(18),2(6),7,11(19),12,14,16-heptaen-9-one 162999108 Click to see 441.40 unknown https://doi.org/10.1248/CPB.47.571
14-Hydroxy-15-methoxy-3,5-dioxa-10-azapentacyclo[9.7.1.02,6.08,19.013,18]nonadeca-1(18),2(6),7,11(19),12,14,16-heptaen-9-one 10518934 Click to see COC1=C(C2=CC3=C4C(=CC5=C(C4=C2C=C1)OCO5)C(=O)N3)O 309.27 unknown https://doi.org/10.1248/CPB.48.1006
Aristolactam 96710 Click to see 293.27 unknown https://doi.org/10.1248/CPB.48.1006
https://doi.org/10.1248/CPB.47.571
Aristolactam Ii 148745 Click to see 263.25 unknown https://doi.org/10.1248/CPB.48.1006
https://doi.org/10.1248/CPB.47.571
Cepharanone B 162739 Click to see 279.29 unknown https://doi.org/10.1248/CPB.48.1006
https://doi.org/10.1248/CPB.47.571
Piperolactam A 3081016 Click to see 265.26 unknown https://doi.org/10.1248/CPB.48.1006
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown https://doi.org/10.1248/CPB.48.1006
https://doi.org/10.1248/CPB.47.571
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown https://doi.org/10.1248/CPB.48.1006
https://doi.org/10.1248/CPB.47.571
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Methylparaben 7456 Click to see 152.15 unknown https://doi.org/10.1248/CPB.47.571
> Benzenoids / Phenanthrenes and derivatives
(11R)-14-methoxy-3,5,10-trioxapentacyclo[9.7.1.02,6.08,19.013,18]nonadeca-1(19),2(6),7,13(18),14,16-hexaen-9-one 10685335 Click to see 296.27 unknown https://doi.org/10.1248/CPB.47.571
https://doi.org/10.1248/CPB.48.1006
(11R)-14,15-dimethoxy-3,5,10-trioxapentacyclo[9.7.1.02,6.08,19.013,18]nonadeca-1(19),2(6),7,13(18),14,16-hexaen-9-one 10806025 Click to see 326.30 unknown https://doi.org/10.1248/CPB.47.571
(11S)-3,5,10-trioxapentacyclo[9.7.1.02,6.08,19.013,18]nonadeca-1(19),2(6),7,13,15,17-hexaen-9-one 10730440 Click to see 266.25 unknown https://doi.org/10.1248/CPB.48.1006
Aristolic Acid 119465 Click to see 296.27 unknown https://doi.org/10.1248/CPB.46.1301
https://doi.org/10.1248/CPB.48.1006
https://doi.org/10.1248/CPB.47.571
Methyl 8,9-dimethoxynaphtho[2,1-g][1,3]benzodioxole-5-carboxylate 10521091 Click to see COC1=C(C2=C(C=C1)C3=C(C=C2)C(=CC4=C3OCO4)C(=O)OC)OC 340.30 unknown https://doi.org/10.1248/CPB.47.571
https://doi.org/10.1248/CPB.46.1301
Methyl Aristolate 160246 Click to see 310.30 unknown https://doi.org/10.1248/CPB.47.571
https://doi.org/10.1248/CPB.46.1301
> Benzenoids / Phenanthrenes and derivatives / Aristolochic acids and derivatives
9-Hydroxy-8-Methoxy-6-Nitro-Phenanthrol(3,4-D)(1,3)Dioxole-5-Carboxylic Acid 1941 Click to see 357.30 unknown https://doi.org/10.1248/CPB.48.1006
Aristolochic acid 2236 Click to see COC1=CC=CC2=C3C(=C(C=C21)[N+](=O)[O-])C(=CC4=C3OCO4)C(=O)O 341.27 unknown https://doi.org/10.1248/CPB.48.1006
https://doi.org/10.1248/CPB.47.571
Aristolochic acid I methyl ester 96709 Click to see COC1=CC=CC2=C3C(=C(C=C21)[N+](=O)[O-])C(=CC4=C3OCO4)C(=O)OC 355.30 unknown https://doi.org/10.1248/CPB.48.1006
Aristolochic Acid Ii 108168 Click to see 311.24 unknown https://doi.org/10.1248/CPB.39.1310
Aristolochic Acid Iv 167493 Click to see COC1=CC2=C3C(=C(C=C2C(=C1)OC)[N+](=O)[O-])C(=CC4=C3OCO4)C(=O)O 371.30 unknown https://doi.org/10.1248/CPB.39.1310
https://doi.org/10.1248/CPB.47.571
Aristolochic acid IV methyl ester 176931 Click to see 385.30 unknown https://doi.org/10.1248/CPB.48.1006
https://doi.org/10.1248/CPB.47.571
Methyl 10-methoxy-6-nitronaphtho[2,1-g][1,3]benzodioxole-5-carboxylate 10784373 Click to see COC1=CC2=C3C(=C(C=C2C=C1)[N+](=O)[O-])C(=CC4=C3OCO4)C(=O)OC 355.30 unknown https://doi.org/10.1248/CPB.48.1006
Methyl 6-nitronaphtho[2,1-g][1,3]benzodioxole-5-carboxylate 85790593 Click to see COC(=O)C1=CC2=C(C3=C1C(=CC4=CC=CC=C43)[N+](=O)[O-])OCO2 325.27 unknown https://doi.org/10.1248/CPB.48.1006
> Benzenoids / Phenanthrenes and derivatives / Phenanthrols
10-Hydroxy-8-methoxy-2H-phenanthro[3,4-d][1,3]dioxole-5-carboxylic acid 71401264 Click to see COC1=CC(=CC2=C1C=CC3=C2C4=C(C=C3C(=O)O)OCO4)O 312.27 unknown https://doi.org/10.1248/CPB.47.571
https://doi.org/10.1248/CPB.46.1301
12,14,16-Trimethoxy-3,5-dioxa-10-azapentacyclo[9.7.1.02,6.08,19.013,18]nonadeca-1(19),2(6),7,11,13(18),14,16-heptaen-9-one 14804090 Click to see 353.30 unknown https://doi.org/10.1248/CPB.48.1006
9-Hydroxy-8-methoxynaphtho[2,1-g][1,3]benzodioxole-5-carboxylic acid 10664410 Click to see COC1=C(C=CC2=C1C=CC3=C2C4=C(C=C3C(=O)O)OCO4)O 312.27 unknown https://doi.org/10.1248/CPB.47.571
https://doi.org/10.1248/CPB.46.1301
9-Methoxyaristolactam I 14804089 Click to see 323.30 unknown https://doi.org/10.1248/CPB.48.1006
https://doi.org/10.1248/CPB.47.571
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
N-Acetyltyramine 121051 Click to see 179.22 unknown https://doi.org/10.1248/CPB.47.571
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
Hinokinin 442879 Click to see C1C(C(C(=O)O1)CC2=CC3=C(C=C2)OCO3)CC4=CC5=C(C=C4)OCO5 354.40 unknown https://doi.org/10.1248/CPB.48.1006
> Lipids and lipid-like molecules / Glycerolipids / Monoradylglycerols / Monoacylglycerols / 1-monoacylglycerols
Monostearin 24699 Click to see 358.60 unknown https://doi.org/10.1248/CPB.47.571
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
[(1R,2E,10R,11S)-3-formyl-11-methyl-7-methylidene-6-oxo-11-bicyclo[8.1.0]undec-2-enyl]methyl acetate 163002311 Click to see 290.40 unknown https://doi.org/10.1021/NP970491+
Madolin D 10779860 Click to see 290.40 unknown https://doi.org/10.1021/NP970491+
https://doi.org/10.1248/CPB.48.1006
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(3aR,4R,7S,7aR)-4-ethenyl-4-methyl-3-methylidene-7-prop-1-en-2-yl-5,6,7,7a-tetrahydro-3aH-1-benzofuran-2-one 163007691 Click to see 232.32 unknown https://doi.org/10.1021/NP970491+
(4E,8S,9S)-5-methyl-8-prop-1-en-2-yl-10-oxabicyclo[7.2.1]dodeca-1(12),4-dien-11-one 155559006 Click to see 232.32 unknown https://doi.org/10.1021/NP970491+
(4Z,8R,9R)-5-methyl-8-prop-1-en-2-yl-10-oxabicyclo[7.2.1]dodeca-1(12),4-dien-11-one 101281337 Click to see 232.32 unknown https://doi.org/10.1021/NP970491+
https://doi.org/10.1248/CPB.48.1006
Madolin E 10681098 Click to see CC(=C)C1CCC(C2C1OC(=O)C2=C)(C)C=C 232.32 unknown https://doi.org/10.1021/NP970491+
https://doi.org/10.1248/CPB.48.1006
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1248/CPB.47.571
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 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/10.1248/CPB.47.571
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 https://doi.org/10.1248/CPB.47.571
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1248/CPB.47.571
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Salidroside 159278 Click to see 300.30 unknown https://doi.org/10.1248/CPB.48.1006
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] 2,3,4-trihydroxybenzoate 5317726 Click to see 332.26 unknown https://doi.org/10.1248/CPB.48.1006
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde 126 Click to see 122.12 unknown https://doi.org/10.1248/CPB.47.571
> Organoheterocyclic compounds / Azoles / Imidazoles
Allantoin 204 Click to see C1(C(=O)NC(=O)N1)NC(=O)N 158.12 unknown https://doi.org/10.1248/CPB.48.1006
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
(4Z,8Z,11S)-5,9-dimethyl-12-oxabicyclo[9.2.1]tetradeca-1(14),4,8-trien-13-one 101032442 Click to see 232.32 unknown https://doi.org/10.1021/NP970491+
https://doi.org/10.1248/CPB.48.1006
Manshurolide 14527198 Click to see CC1=CCCC2=CC(CC(=CCC1)C)OC2=O 232.32 unknown https://doi.org/10.1021/NP970491+
> Organoheterocyclic compounds / Epoxides
(1R,4R,6S,9Z,11S)-4,12,12-trimethyl-5-oxatricyclo[9.1.0.04,6]dodec-9-ene 163022057 Click to see 206.32 unknown https://doi.org/10.1021/NP970491+
Madolin A 10561685 Click to see CC1(C2C1C=C(CCC3C(O3)(CC2)C)C=O)C 234.33 unknown https://doi.org/10.1021/NP970491+
https://doi.org/10.1248/CPB.48.1006
Madolin B 10562641 Click to see CC1(C2C1C=C(CCC3C(O3)(CC2)C)C(=O)O)C 250.33 unknown https://doi.org/10.1021/NP970491+
https://doi.org/10.1248/CPB.48.1006
Madolin C 10726986 Click to see 206.32 unknown https://doi.org/10.1021/NP970491+
https://doi.org/10.1248/CPB.48.1006
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives / 6-aminopurines
Adenine 190 Click to see C1=NC2=NC=NC(=C2N1)N 135.13 unknown https://doi.org/10.1248/CPB.48.1006
> Organoheterocyclic compounds / Indoles and derivatives / Indolecarboxylic acids and derivatives
Methyl indole-3-carboxylate 589098 Click to see 175.18 unknown https://doi.org/10.1248/CPB.47.571
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid amides
N-trans-Cinnamoyltyramine 5315911 Click to see 267.32 unknown https://doi.org/10.1248/CPB.48.1006
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
2-hydroxyethyl (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 10561889 Click to see 238.24 unknown https://doi.org/10.1248/CPB.47.571
Methyl ferulate 5357283 Click to see COC1=C(C=CC(=C1)C=CC(=O)OC)O 208.21 unknown https://doi.org/10.1248/CPB.48.1006
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
2-hydroxyethyl (E)-3-(4-hydroxyphenyl)prop-2-enoate 10488567 Click to see C1=CC(=CC=C1C=CC(=O)OCCO)O 208.21 unknown https://doi.org/10.1248/CPB.47.571
2-hydroxyethyl (Z)-3-(4-hydroxyphenyl)prop-2-enoate 10512539 Click to see 208.21 unknown https://doi.org/10.1248/CPB.47.571
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
4-Coumaric acid 322 Click to see 164.16 unknown https://doi.org/10.1248/CPB.48.1006
https://doi.org/10.1248/CPB.47.571
Ferulic Acid 445858 Click to see 194.18 unknown https://doi.org/10.1248/CPB.48.1006
P-Coumaric Acid 637542 Click to see 164.16 unknown https://doi.org/10.1248/CPB.48.1006
https://doi.org/10.1248/CPB.47.571
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
Isoscopoletin 69894 Click to see 192.17 unknown https://doi.org/10.1248/CPB.48.1006
> 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 https://doi.org/10.1248/CPB.47.571
> 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/10.1248/CPB.47.571
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1248/CPB.47.571
Kaempferol-3-O-Rutinoside 5318767 Click to see 594.50 unknown https://doi.org/10.1248/CPB.47.571
Rutin 5280805 Click to see 610.50 unknown https://doi.org/10.1248/CPB.47.571
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(3,4-Dihydroxyphenyl)-3,5-dihydroxy-4-oxo-4H-1-benzopyran-7-yl hexopyranoside 5381351 Click to see 464.40 unknown https://doi.org/10.1248/CPB.47.571
2-(3,4-dihydroxyphenyl)-3,5-dihydroxy-7-[(2S,4S,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 44259225 Click to see 464.40 unknown https://doi.org/10.1248/CPB.47.571
kaempferol 7-O-glucoside 10095180 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1248/CPB.47.571
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
8-methoxy-10-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxynaphtho[2,1-g][1,3]benzodioxole-5-carboxylic acid 101948691 Click to see 474.40 unknown https://doi.org/10.1248/CPB.47.571
https://doi.org/10.1248/CPB.46.1301
Glucosyringic acid 10383888 Click to see 360.31 unknown https://doi.org/10.1248/CPB.48.1006

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