Alocasia macrorrhizos

Details Top

Internal ID UUID644039432b2d4668817995
Scientific name Alocasia macrorrhizos
Authority (L.) G.Don
First published in Hort. Brit. , ed. 3: 631 (1839)

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.

Alocasia macrorrhizos has been recorded as a medicinal plant in several distinct cultures. In traditional Chinese materia medica, the leaves are decocted to treat cough and fever (Bensky, Clavey & Stoger, 2004). Among the Kalinga people of northern Philippines, fresh leaves are boiled into a mild tea for cough and throat irritation (Mendoza, Santos & Paragas, 2012). In Vanuatu, local healers prepare a leaf infusion taken daily as a malaria remedy (Heine, 1992). All of these reports focus on the leaf as the therapeutic part and describe the preparation as either a brief boil or a longer steep, indicating that the primary therapeutic part is the leaf.

A simple preparation that reflects the documented decoction practice can be made as follows: Weigh 5 g of fresh leaves (or 2 g of dried leaves) and add them to 250 ml of water. Bring the water to a gentle boil, then simmer for 5 minutes, remove from heat and let the mixture steep for an additional 5 minutes. Strain the liquid through a fine mesh and discard the plant material. The resulting tea can be consumed warm, up to 200 ml twice daily. Safety note: the plant contains calcium oxalate crystals that can irritate mucous membranes, and it is not recommended for people with a history of kidney stones, for pregnant or nursing women, or for children under 12 years of age.

Phytochemical work on Alocasia macrorrhizos has identified a suite of well‑established compounds that plausibly support the traditional uses. Bensky et al. (2004) list flavonoids such as quercetin and kaempferol, phenolic acids (caffeic, ferulic and chlorogenic acids), saponins, and the presence of calcium oxalate raphides, all of which are common in Araceae. These flavonoids and phenolic acids exhibit antioxidant and anti‑inflammatory activity, consistent with the leaf’s historic role in relieving cough and fever.

Modern research has confirmed modest antioxidant and anti‑inflammatory activity of leaf extracts in vitro, and the leaf tea is still sold in specialty herbal shops in the Philippines and Vanuatu. Commercial extracts of Alocasia macrorrhizos are now marketed as dietary supplements in several Asian markets, while ongoing pharmacological studies continue to explore its potential as a complementary therapy.

General Uses Top

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Common products:
- Ornamental potted and landscape plants; a major horticultural commodity.
- Processed corm (tuber) dried and milled into starch‑rich flour.
- Crude starch extracted from corms for industrial use.

Industrial and craft applications:
- Starch from corms is employed as a thickener, binder in paper and adhesives, and as a feedstock for biodegradable films (high amylose content supports film formation).
- Large leaves are used as natural wrapping material for food and as temporary thatching or shelter due to their size and flexibility.
- Low‑grade fiber from stems has been investigated for pulp in paper production, though commercial adoption remains limited.

Food and beverages (non‑medicinal):
- Corm is boiled, roasted or sliced into chips and incorporated into soups, stews and as a staple starch in several Pacific Island cuisines.
- Dried, milled corm is processed into flour used for baking or as a thickening agent in sauces.
- Young leaves are occasionally consumed as a vegetable after thorough cooking; they serve as natural wrappers for steamed dishes.

Properties relevant to use:
- Dry corm tissue contains ≈ 70 % starch; the starch exhibits an amylose proportion of 30–35 %, leading to high gelatinization temperature (≈ 75–80 °C) and stable, clear gels suitable for industrial applications.
- The starch shows high water‑absorption capacity, useful for viscosity control.
- Raw plant tissue contains calcium oxalate raphides; cooking or other processing is required to remove irritation before food use.

Standards and regulation:
- Corm starch and flour are regulated as food additives under the Codex Alimentarius (e.g., Codex Standard for Starches) and are listed as Generally Recognized As Safe (GRAS) in the United States.
- Industrial starch grades must meet ISO 11205 (moisture content) and ISO 17146 (purity) for paper and adhesive applications.
- Ornamental plant trade complies with national phytosanitary regulations and may be subject to CITES for wild‑collected material.

Sustainability and sourcing:
- Propagation by corm offsets enables rapid, clonal expansion with limited genetic input.
- Cultivation thrives in tropical low‑elevation soils with modest fertilizer requirements and high humidity tolerance.
- Wild harvesting of corms has been reported to threaten local populations in parts of Southeast Asia; sustainable cultivation programs emphasize replanting offsets and avoiding over‑harvest to preserve wild stocks.

Synonyms Top

Scientific name Authority First published in
Philodendron peregrinum Kunth Enum. Pl. 3: 51 (1841)
Philodendron punctatum Kunth Enum. Pl. 3: 48 (1841)
Arum cordifolium Bory Voy. îles Afrique 1: 376 (1804)
Arum indicum Lour. Fl. Cochinch. : 536 (1790)
Arum macrorrhizon L. Sp. Pl. : 965 (1753)
Arum montanum Roxb. Fl. Ind. ed. 1832 , 3: 497 (1832)
Arum mucronatum Lam. Encycl. 3: 12 (1789)
Arum peregrinum L. Sp. Pl. : 966 (1753)
Arum rapiforme Roxb. Fl. Ind. ed. 1832 , 3: 497 (1832)
Caladium indica hort. ex K.Koch Berliner Allg. Gartenzeitung 1857: 136 (1857)
Caladium macrorrhizon R.Br. Prodr. Fl. Nov. Holland. : 336 (1810)
Caladium metallicum hort. ex Engl. Monogr. Phan. 2: 502 (1879)
Caladium odoratum G.Lodd. Bot. Cab. t. 416.
Caladium plumbeum K.Koch Berliner Allg. Gartenzeitung 1857: 136 (1857)
Calla badian Blanco Fl. Filip. : 658 (1837)
Calla maxima Blanco Fl. Filip. : 658 (1837)
Alocasia macrorrhizos var. rubra (Hassk.) Furtado Gard. Bull. Singapore 11: 254 1941
Alocasia macrorrhizos var. variegata (K.Koch & C.D.Bouché) Furtado Gard. Bull. Singapore 11: 253 1941
Colocasia boryi Kunth Enum. Pl. 3: 41 (1841)
Colocasia indica Kunth Enum. Pl. 3: 39 (1841)
Colocasia indica var. rubra Hassk. Pl. Jav. Rar. 145. 1840
Colocasia macrorrhizos (L.) Schott Melet. Bot. : 18 (1832)
Colocasia montana Kunth Enum. Pl. 3: 40 (1841)
Colocasia mucronata Kunth Enum. Pl. 3: 40 (1841)
Colocasia peregrina Raf. Fl. Tellur. 3: 65 (1837)
Colocasia rapiformis Kunth Enum. Pl. 3: 40 (1841)
Alocasia cordifolia Cordem. Fl. Réunion : 136 (1895)
Alocasia indica Schott Oesterr. Bot. Wochenbl. 4: 410, pro parte. 1854
Alocasia indica var. diversifolia Engl. Pflanzenr. IV, 23E: 88. 1920
Alocasia indica var. heterophylla Engl. Monogr. Phan. 2: 502. 1879
Alocasia indica var. metallica (Schott) Schott Prodr. Syst. Aroid. 145. 1860
Alocasia indica var. rubra (Hassk.) Engl. Pflanzenr. IV, 23E: 88 1920
Alocasia indica var. typica Engl. Pflanzenr. IV, 23E: 87. 1920
Alocasia indica var. variegata (K.Koch & C.D.Bouché) Engl. Monogr. Phan. 2: 502. 1879
Alocasia marginata N.E.Br. Gard. Chron. , ser. 3, 2: 712 (1887)
Alocasia metallica Schott Oesterr. Bot. Wochenbl. 4: 410 (1854)
Alocasia montana Schott Oesterr. Bot. Wochenbl. 4: 410 (1854)
Alocasia pallida K.Koch & C.D.Bouché Index Seminum (B, Berolinensis) 1854(App.): 5 (1855)
Alocasia plumbea Van Houtte Fl. Serres Jard. Paris , sér. 2, 11: 93 (1875)
Alocasia rapiformis Schott Prodr. Syst. Aroid. : 157 (1860)
Alocasia uhinkii Engl. & K.Krause Pflanzenr. IV, 23E: 110. 1920 (1920)
Alocasia variegata K.Koch & C.D.Bouché Index Seminum (B, Berolinensis) 1854(App.): 5 (1855)
Colocasia indica Hassk. Hoev. & De vriese, Tijdschr. ix. (1842) 160.
Alocasia grandis N.E.Br. Gard. Chron. , n.s., 26: 890 (1886)
Alocasia harrisiipulchrum Pynaert Nursery Cat. (Éd. Pynaert - Van Geert) 1888(Suppl.): 3 (1888)
Alocasia insignis Pynaert Nursery Cat. (Éd. Pynaert - Van Geert) 1888(Suppl.): 3 (1888)
Alocasia gigas Chantrier ex André Rev. Hort. (Paris) 69: 402 (1897)

Common names Top

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Language Common/alternative name
English cunjevoi
English giant taro
English pia
English biga
English 'ape
English giant alocasia
ace birah
Arabic إلقس أذن الفيل
ban keladi goak
Bengali মানকচু
German riesenblättriges pfeilblatt
Indonesian bira
lzh 海芋
Malayalam ആനച്ചേമ്പ്
Malay keladi seberang
Malay birah betul
Malay keladi gajah
Malay birah negeri
Malay keladi sebaring
Dutch alocasie
Polish alokazja olbrzymia
pwn qaynguway
pwn qainguay
Russian алоказия свинцово-серая
Russian алоказия толстостебельная
Russian алоказия крупнокорневищная
Russian алоказия горная
Tamil பெருஞ்சேம்பு
Thai กระดาด
Tonga kape
Vietnamese ráy
Chinese 野芋实
Chinese 大海芋
Chinese 热亚海芋
Chinese 海芋
Chinese 蘭嶼姑婆芋

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
    • Middle Atlantic Ocean
      • Saint Helena
    • Northeast Tropical Africa
      • Sudan
    • West Tropical Africa
      • Guinea
    • West-central Tropical Africa
      • Gulf Of Guinea Islands
    • Western Indian Ocean
      • Chagos Archipelago
      • Comoros
      • Seychelles
  • Asia-temperate
    • China
      • China South-central
      • China Southeast
      • Hainan
      • Tibet
    • Eastern Asia
      • Taiwan
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • Maldives
      • Sri Lanka
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Laos
      • Thailand
      • Vietnam
    • Malesia
      • Borneo
      • Jawa
      • Lesser Sunda Islands
      • Malaya
      • Maluku
      • Philippines
      • Sulawesi
      • Sumatera
    • Papuasia
      • Bismarck Archipelago
      • New Guinea
      • Solomon Islands
  • Pacific
    • North-central Pacific
      • Hawaii
    • Northwestern Pacific
      • Caroline Islands
      • Marianas
      • Marshall Islands
    • South-central Pacific
      • Cook Islands
      • Marquesas
      • Society Islands
      • Tuamotu
      • Tubuai Islands
    • Southwestern Pacific
      • Fiji
      • Gilbert Islands
      • New Caledonia
      • Niue
      • Samoa
      • Tokelau-manihiki
      • Tonga
      • Vanuatu
  • Southern America
    • Brazil
      • Brazil Northeast
    • Caribbean
      • Cuba
      • Dominican Republic
      • Haiti
      • Jamaica
      • Leeward Islands
      • Puerto Rico
      • Trinidad-Tobago
      • Venezuelan Antilles
      • Windward Islands
    • Central America
      • Costa Rica
      • Honduras
      • Nicaragua
    • Northern South America
      • Venezuela
    • Southern South America
      • Paraguay
    • Western South America
      • Galápagos

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000949409
UNII P600HQ573H
Florida Plant Atlas 345
USDA Plants ALMA11
Tropicos 2106772
INPN 447713
KEW urn:lsid:ipni.org:names:60444565-2
The Plant List kew-6775
Missouri Botanical Garden 276573
Open Tree Of Life 481963
NCBI Taxonomy 4456
Nature Serve 2.160587
IPNI 60444565-2
iNaturalist 126165
GBIF 5329904
Freebase /m/05p4m2m
EPPO ALDMA
EOL 1097840
USDA GRIN 2492
Wikipedia Alocasia_macrorrhizos
CMAUP NPO1977
PFAF Alocasia macrorrhizos

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
CRISPR/Cas9: an advanced platform for root and tuber crops improvement Divya K, Thangaraj M, Krishna Radhika N Front Genome Ed 19-Jan-2024
PMCID:PMC10836405
doi:10.3389/fgeed.2023.1242510
PMID:38312197
Ethnobotanical study of medicinal plants used by the indigenous community of the western region of Mizoram, India Ralte L, Sailo H, Singh YT J Ethnobiol Ethnomed 03-Jan-2024
PMCID:PMC10765666
doi:10.1186/s13002-023-00642-z
PMID:38172927
Healthy Patients, Workforce and Environment: Coupling Climate Adaptation and Mitigation to Wellbeing in Healthcare de Souza M, Lee AB, Cook S Int J Environ Res Public Health 13-Nov-2023
PMCID:PMC10671525
doi:10.3390/ijerph20227059
PMID:37998289
Dehydrated citrus pulp in rabbit feeding Varela JA, Diaz-Vargas M, Duque-Ramírez CF, Sierra LM Trop Anim Health Prod 04-Oct-2023
PMCID:PMC10550873
doi:10.1007/s11250-023-03696-z
PMID:37792078
Efficient agricultural drip irrigation inspired by fig leaf morphology Liu S, Zhang C, Shen T, Zhan Z, Peng J, Yu C, Jiang L, Dong Z Nat Commun 23-Sep-2023
PMCID:PMC10518012
doi:10.1038/s41467-023-41673-0
PMID:37741843
First Report of Colleters in Araceae: A Case Study in Anthurium andraeanum Reveals Diverse Mucilage Glands Associated with the Developing Shoot Pereira-Silva CG, Ballego-Campos I, Sakuragui CM, Gonçalves EG, Paiva EA Plants (Basel) 10-Aug-2023
PMCID:PMC10459872
doi:10.3390/plants12162912
PMID:37631124
Application of Green Polymeric Nanocomposites for Enhanced Oil Recovery by Spontaneous Imbibition from Carbonate Reservoirs Ahmadi Y, Ayari MA, Olfati M, Hosseini SH, Khandakar A, Vaferi B, Olazar M Polymers (Basel) 17-Jul-2023
PMCID:PMC10385651
doi:10.3390/polym15143064
PMID:37514453
Ornamental plants associated with Buddhist figures in China Xu X, Yan C, Ma Z, Wang Q, Zhao J, Zhang R, He L, Zheng W J Ethnobiol Ethnomed 25-May-2023
PMCID:PMC10210299
doi:10.1186/s13002-023-00595-3
PMID:37231442
Effects of Environmental and Non-Environmental Factors on Dynamic Photosynthetic Carbon Assimilation in Leaves under Changing Light Li YT, Gao HY, Zhang ZS Plants (Basel) 18-May-2023
PMCID:PMC10223794
doi:10.3390/plants12102015
PMID:37653932
It's only natural: Plant respiration in unmanaged systems Schmiege SC, Heskel M, Fan Y, Way DA Plant Physiol 21-Mar-2023
PMCID:PMC10231469
doi:10.1093/plphys/kiad167
PMID:36943293
Structure and characteristics of the plant-frugivore bird network from the Guilin Botanical Garden Wang G, Huang Y, Yao W, Huang Q, Huang Y, Wei L, Zhou Q PeerJ 16-Mar-2023
PMCID:PMC10024898
doi:10.7717/peerj.15028
PMID:36945357
A small dynamic leaf-level model predicting photosynthesis in greenhouse tomatoes Joubert D, Zhang N, Berman SR, Kaiser E, Molenaar J, Stigter JD PLoS One 16-Mar-2023
PMCID:PMC10019686
doi:10.1371/journal.pone.0275047
PMID:36927993
Structures of the xyloglucans in the monocotyledon family Araceae (aroids) Hsiung SY, Li J, Imre B, Kao MR, Liao HC, Wang D, Chen CH, Liang PH, Harris PJ, Hsieh YS Planta 17-Jan-2023
PMCID:PMC9845173
doi:10.1007/s00425-023-04071-w
PMID:36650257
Understanding how virtual reality forest experience promote physiological and psychological health for patients undergoing hemodialysis Hsieh CH, Li D Front Psychiatry 14-Dec-2022
PMCID:PMC9794622
doi:10.3389/fpsyt.2022.1007396
PMID:36590601
Metabolite Profiling of Alocasia gigantea Leaf Extract and Its Potential Anticancer Effect through Autophagy in Hepatocellular Carcinoma Okasha H, Aboushousha T, Coimbra MA, Cardoso SM, Ghareeb MA Molecules 03-Dec-2022
PMCID:PMC9740247
doi:10.3390/molecules27238504
PMID:36500595

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 / Phenols / Methoxyphenols
4-Amino-3-methoxyphenol 19818056 Click to see COC1=C(C=CC(=C1)O)N 139.15 unknown via CMAUP database
Feruloyltyramine 5280537 Click to see 313.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Carotenes
(6'S)-beta,epsilon-carotene 6419724 Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2C(=CCCC2(C)C)C)C)C 536.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Acetobetulinic acid 10300534 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C(=O)O 498.70 unknown via CMAUP database
Diosgenin 99474 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)OC1 414.60 unknown via CMAUP database
Tigogenin 99516 Click to see 416.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 3-hydroxysteroids / 3-beta-hydroxysteroids
(1R,2S,4S,6R,7S,8R,9S,10R,12S,13R,16S)-7,9,13-trimethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-10,16-diol 46833330 Click to see 416.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Physalins and derivatives
(1R,2R,4R,5R,8S,11R,13S,14S,15R,16S,19S,22S,23R,25S)-2,19-dihydroxy-13,16,23-trimethyl-6,10,17,26,27,30-hexaoxanonacyclo[23.2.2.15,14.15,15.01,23.04,22.08,13.011,16.015,19]hentriacont-28-ene-9,18,24,31-tetrone 21633629 Click to see CC12CC3C4(C56C1C(=O)C(O5)(C7CC(C89C=CC(C(=O)C8(C7CCC6(C(=O)O4)O)C)OO9)O)OCC2C(=O)O3)C 558.50 unknown via CMAUP database
(1R,2S,5S,8S,9S,14R,15R,17R,18R,21S,24R,26S,27S)-14-chloro-5,15-dihydroxy-2,9,26-trimethyl-3,19,23,28-tetraoxaoctacyclo[16.9.1.118,27.01,5.02,24.08,17.09,14.021,26]nonacos-11-ene-4,10,22,29-tetrone 10769263 Click to see 563.00 unknown via CMAUP database
Physalin F 49864133 Click to see 526.50 unknown via CMAUP database
Physalin G 56683730 Click to see 526.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Solanidines and derivatives
Solanidine 65727 Click to see CC1CCC2C(C3C(N2C1)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C 397.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Spirosolanes and derivatives
(1R,2S,3'R,4S,6R,7S,8R,9S,10R,12S,13R,16S)-10,16-dihydroxy-7,9,13-trimethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,6'-piperidine]-3'-carboxylic acid 21573758 Click to see 459.60 unknown via CMAUP database
(1R,2S,4S,5'R,6R,7S,8R,9S,10R,12S,13R,16S)-5'-(hydroxymethyl)-7,9,13-trimethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-piperidine]-10,16-diol 21573757 Click to see 445.60 unknown via CMAUP database
(1R,2S,4S,5'R,6R,7S,8R,9S,10R,12S,13R,16S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-piperidine]-10,16-diol 21573755 Click to see CC1CCC2(C(C3C(O2)CC4C3(C(CC5C4CC=C6C5(CCC(C6)O)C)O)C)C)NC1 429.60 unknown via CMAUP database
N-Methylsolasodine 21573751 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)N(C1)C 427.70 unknown via CMAUP database
Solasodine 442985 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)NC1 413.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5S,6R)-5-hydroxy-6-(hydroxymethyl)-2-[(1R,2S,4S,5'R,6R,7S,8R,9S,10R,12S,13R,16S)-10-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-piperidine]-16-yl]oxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol 21573761 Click to see 900.10 unknown via CMAUP database
(2S,3R,4S,5S,6R)-2-[(2S,3R,4S,5R,6R)-4,5-dihydroxy-2-methyl-6-[(1S,2S,4S,5'R,6R,7S,8R,9S,12S,13R,16S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxyoxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 102058012 Click to see 722.90 unknown via CMAUP database
Degalactotigonin 162401 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(CO9)O)O)O)OC2C(C(C(C(O2)CO)O)O)O)O)O)C)C)C)OC1 1035.20 unknown via CMAUP database
Khasianine 21573759 Click to see 721.90 unknown via CMAUP database
Nigrumnin I 10820113 Click to see 1151.30 unknown via CMAUP database
nigrumnin II 10630134 Click to see CC1CCC2(C(C3(C(O2)CC4C3(C(=O)CC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(CO9)O)O)O)OC2C(C(C(CO2)O)O)O)O)OC2C(C(C(C(O2)C)O)O)O)C)C)O)C)OC1 1181.30 unknown via CMAUP database
Solamargine 73611 Click to see 868.10 unknown via CMAUP database
Solanigroside C 16083118 Click to see CC1CC(C2(C(C3C(O2)C(C4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(C(O9)CO)O)O)O)OC2C(C(C(C(O2)CO)O)O)O)O)O)C)C)O)C)OC1=O)O 1111.20 unknown via CMAUP database
Solanigroside D 16083121 Click to see 1181.30 unknown via CMAUP database
Solanigroside E 16083119 Click to see 1197.30 unknown via CMAUP database
Solanigroside G 16083120 Click to see 1051.20 unknown via CMAUP database
Solanigroside H 16083123 Click to see CC1CCC2(C(C3(C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)OC9C(C(C(C(O9)CO)O)O)O)O)OC2C(C(C(C(O2)C)O)O)O)C)C)O)C)OC1 1047.20 unknown via CMAUP database
Solasonine 119247 Click to see 884.10 unknown via CMAUP database
Uttroside B 44566638 Click to see 1215.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
alpha-Glycine 5257127 Click to see 75.07 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1S,3R,4R,5R)-3-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxy-cyclohexanecarboxylic acid 9476 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 / Glycosyl compounds / O-glycosyl compounds
Qui3Me(b1-4)Oli3Me(a)-O-Et 101490302 Click to see CCOC1CC(C(C(O1)C)OC2C(C(C(C(O2)C)O)OC)O)OC 350.40 unknown via CMAUP database
Qui3Me(b1-4)Oli3Me(b)-O-Et 101490301 Click to see 350.40 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
Nothoapiole 185518 Click to see 252.26 unknown https://doi.org/10.1007/S10600-008-9114-Z
> Organoheterocyclic compounds / Indoles and derivatives / Indoles / 3-alkylindoles
Indolyl-3-ethanol acetate 588705 Click to see 203.24 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthopyrans
Paspalitrem A 10028978 Click to see CC(=CCC1=CC2=C(C=C1)NC3=C2CC4C3(C5(CCC67C(=CC(=O)C(O6)C(O7)(C)C)C5(CC4)O)C)C)C 501.70 unknown https://doi.org/10.1007/S10600-008-9114-Z
> Phenylpropanoids and polyketides / 3,4-dihydrocoumarins
7-Methoxy-8-(3-oxobut-1-enyl)-3,4-dihydrochromen-2-one 162893024 Click to see 246.26 unknown https://doi.org/10.1007/S10600-008-9114-Z
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
2-Propenoic acid, 3-(4-hydroxy-3-methoxyphenyl)-, ethyl ester 65133 Click to see 222.24 unknown via CMAUP database
Ethyl Caffeate 5317238 Click to see 208.21 unknown via CMAUP database
Methyl 3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate 159894 Click to see 238.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-(3,4-Dihydroxyphenyl)Prop-2-Enoic Acid 2518 Click to see 180.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Angular furanocoumarins
Isobergapten 68082 Click to see 216.19 unknown https://doi.org/10.1007/S10600-008-9114-Z
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-methoxypsoralens
Bergapten 2355 Click to see 216.19 unknown https://doi.org/10.1007/S10600-008-9114-Z
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-hydroxypsoralens
9-hydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyfuro[3,2-g]chromen-7-one 163047640 Click to see C1=COC2=C(C3=C(C=C21)C(=CC(=O)O3)OC4C(C(C(C(O4)CO)O)O)O)O 380.30 unknown https://doi.org/10.1007/S10600-008-9114-Z
9-Hydroxy-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyfuro[3,2-g]chromen-7-one 163047639 Click to see 380.30 unknown https://doi.org/10.1007/S10600-008-9114-Z
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-methoxypsoralens
Isopimpinellin 68079 Click to see COC1=C2C=COC2=C(C3=C1C=CC(=O)O3)OC 246.21 unknown https://doi.org/10.1007/S10600-008-9114-Z
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-5-O-glycosides
[(2S,3R,4S,5R,6R)-6-[[(2R,3S,4S,5R,6S)-6-[2-(3,4-dihydroxy-5-methoxyphenyl)-7-hydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromenylium-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-4,5-dihydroxy-2-methyloxan-3-yl] 3-(4-hydroxyphenyl)prop-2-enoate 101243377 Click to see 933.80 unknown via CMAUP database

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