Colchicum speciosum

Details Top

Internal ID UUID644025a955102230158836
Scientific name Colchicum speciosum
Authority Steven
First published in Observ. Pl. Ross. 2: 69 (1824)

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.

Among communities across South and Southeast Asia, Alstonia scholaris (L.) R.Br. is prepared as a mild tea from leaves or young bark to relieve fevers and colds (according to Rüedi, 2003), and as a stronger bark decoction to treat coughs, bronchitis, and throat pain (according to Kirtikar and Basu, 1935; Bhattacharjee, 2004). In tropical coastal India and Sri Lanka, leaf infusions are used for gut pain and dysentery (according to Bhattacharjee, 2004), while in Thailand the leaves are made into a poultice or mild tea for wound care and inflammation (according to Cheeptham et al., 2003). Throughout Southeast Asia and parts of India, the bark and leaf are also macerated in oil for massage or applied as a poultice for muscle and joint pain (according to Cheeptham et al., 2003; Rüedi, 2003). Importantly, these uses are associated with aqueous or macerated preparations rather than the stronger, latex‑rich milky latex preparations used topically for ulcers and severe wounds.

Practical preparation—throat‑soothing bark infusion: simmer 1 gram of dried bark in 250 ml water for 15 minutes, cool to warm, strain, and drink 2 to 3 cups daily. Do not use the milky latex preparation; it can cause severe skin irritation (according to Rüedi, 2003). Because official data on dose limits and contraindications for specific extracts of A. scholaris are not standardized, the safest advice is to use only under the guidance of a qualified practitioner, especially in pregnancy and while breastfeeding (according to Bhattacharjee, 2004).

Well‑documented constituents for Alstonia scholaris include indole alkaloids such as echitamine, alstonine, and reserpinine, as well as triterpenoids and iridoid glycosides, compounds that are consistent with the plant’s traditional use in fevers, coughs, and inflammation (according to Rüedi, 2003; Cheeptham et al., 2003; Bhattacharjee, 2004). Modern relevance: commercial leaf and bark extracts are still produced for cough and cold blends in parts of South Asia, and ongoing phytochemical work continues to map alkaloid profiles across regions, while traditional uses remain part of household practice where access to modern medicine is limited.

General Uses Top

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Common products:
The corms (bulbous underground stems) of Colchicum speciosum contain colchicine, a tropolone alkaloid that is extracted and supplied as a laboratory reagent. Commercial forms include purified colchicine (typically ≥95 % purity) packaged as a dry powder or in ethanol solution, and crude extracts standardized for colchicine content (often expressed as mg of colchicine per gram of extract). These products are marketed to research laboratories for polyploidy induction and other cytogenetic applications.

Scientific/model‑organism use:
Colchicine extracted from C. speciosum is widely employed as a mitotic inhibitor in plant cytogenetics, cell‑biology protocols, and polyploid breeding programs. Standard procedures for inducing polyploidy in wheat, barley, and other crops specify colchicine concentrations and treatment durations derived from corm extracts. The species is referenced in major botanical and chemical databases (e.g., GBIF, PLANTS, PubChem) as a source of colchicine for assay development and reference material, supporting genetics and molecular‑biology research.

Properties relevant to use:
Colchicine is a lipophilic alkaloid (C₂₂H₂₅NO₆) that binds tubulin, preventing microtubule polymerization. It is highly soluble in ethanol and sparingly soluble in water, which facilitates efficient extraction from corm tissue using ethanol‑based protocols. The compound remains stable under cool, dry storage conditions, allowing long‑term reagent stability suitable for laboratory use.

Standards and regulation:
Colchicine derived from Colchicum species is classified as a hazardous chemical under UN GHS (Category 2). Laboratories handling the reagent must comply with occupational‑safety regulations such as OSHA’s Hazard Communication Standard and EU REACH for chemical registration and risk assessment. Quality‑management systems for chemical reagents (e.g., ISO/IEC 17025) are commonly applied to ensure reliable analytical performance.

Sustainability and sourcing:
Wild populations of C. speciosum, native to the Caucasus and parts of Iran, have historically been harvested for colchicine extraction, raising conservation concerns. To mitigate pressure on natural stands, many research institutions and commercial suppliers now cultivate the species under controlled greenhouse or field conditions. Cultivation programs enable traceability, promote sustainable sourcing, and support consistent supply of colchicine‑rich corms for laboratory reagents.

Synonyms Top

Scientific name Authority First published in
Colchicum bornmuelleri Freyn Ber. Deutsch. Bot. Ges. 7: 319 (1889)
Colchicum giganteum hort. ex Stef. ex Stefanoff, Monogr. Colch. (Sborn. B'lghar. Akad. Nauk. xxii.) 82 (1926), inobs.
Colchicum hyrcanicum Woronow ex Stef. Monogr. Colchicum (Sbornuk B'lghar Akad. Nauk. xxii.), 80 (1926), in syn.
Colchicum lenkoranicum (Miscz.) Grossh. Fl. Kavkaza 1: 191 (1928)
Colchicum speciosum var. lenkoranicum Miscz. Fl. Caucas. Crit. 2: 108. 1901
Colchicum latifolium Griseb. Spic. Fl. Rumel. 2: 378 (1846)
Colchicum giganteum S.Arn. Gard. Chron. ser. 3, 32: 435 (1902)
Colchicum hyrcanicum Woronow Herb. Fl. Cauc. 62 (1914)

Common names Top

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Language Common/alternative name
English showy colchicum
Arabic سورنجان خلاب
Arabic لحلاح خلاب
Azerbaijani Əzəmətli vaxsızçiçək
Azerbaijani gözəl vaxtsızçiçək
azb گؤزل واختسیزچیچک
Czech ocún ozdobný
Persian گل حسرت زیبا
Persian گلحسرت زیبا
os Куыдзынуры
Polish zimowit powabny
Russian Безвременник великолепный
Swedish prakttidlösa
Turkish vargit çiçeği
Chinese 美麗秋水仙
Chinese 美丽秋水仙
Chinese 白花美丽秋水仙

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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Expose seeds to natural outdoor winter conditions for 3 months, then gradually increase light and temperature in the spring.
Sow seeds immediately as their viability decreases rapidly, or they best germinate when fresh. If stored, seeds might need temperature cycling and patience to germinate.
must have summer heat to germinate; may take 6 years to germinate; grow seedlings @ 4°C x 1 month

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • Caucasus
      • North Caucasus
      • Transcaucasus
    • Western Asia
      • Iran
      • Turkey

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000764019
USDA Plants COSP12
Tropicos 18404246
KEW urn:lsid:ipni.org:names:533389-1
The Plant List kew-302950
Open Tree Of Life 1001035
Observations.org 145334
NCBI Taxonomy 13445
IPNI 533389-1
iNaturalist 513871
GBIF 2739794
Freebase /m/0cm8kv7
EPPO CXHSP
EOL 1087047
Elurikkus 293993
USDA GRIN 11146
Wikipedia Colchicum_speciosum
CMAUP NPO4855

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
Targeting Epigenetic ‘Readers’ with Natural Compounds for Cancer Interception Damiani E, Duran MN, Mohan N, Rajendran P, Dashwood RH J Cancer Prev 30-Dec-2020
PMCID:PMC7783241
doi:10.15430/JCP.2020.25.4.189
PMID:33409252
Molecular docking analysis of alkaloid compounds with beta-catenin towards the treatment of colon cancer Ponnulakshmi R, Vishnupriya V, Mohan SK, Abilasha S, Ramajayam G, Vijayalakshmi P, Rajalakshmi M, Selvaraj J Bioinformation 31-Mar-2020
PMCID:PMC7147492
doi:10.6026/97320630016283
PMID:32308271
Antileukemic Activity of Twig Components of Caucasian Beech in Turkey Shida W, Tateishi H, Tahara Y, Fujita M, Husham Majeed Alsaadi D, Watanabe M, Koga R, Radwan MO, Ciftci HI, Gezici S, Kurauchi Y, Katsuki H, Otsuka M, Sugimura K, Wada M, Sekeroglu N, Watanabe T Molecules 25-Oct-2019
PMCID:PMC6864984
doi:10.3390/molecules24213850
PMID:31731511
Substances of Colchicum autumnale and their derivatives. XXXVII. Compounds from the flowers and corms of Colchicum speciosum STEV. V. Mašínová, F. Šantavý Institute of Organic Chemistry & Biochemistry 24-Mar-2014
doi:10.1135/CCCC19541283
Natural Products as a Source of Alzheimer’s Drug Leads Williams P, Sorribas A, Howes MJ Nat Prod Rep 12-Nov-2010
PMCID:PMC4917364
doi:10.1039/c0np00027b
PMID:21072430
X-Ray structural investigation of the alkaloid speciosine L. Yu. Izotova, K. M. Beketov, R. M. Yusupov, M. K. Yusupov, B. T. Ibragimov Springer Science and Business Media LLC 25-Jan-2006
doi:10.1007/BF02282367
A fully automatable enzymatic method for DNA extraction from plant tissues Manen JF, Sinitsyna O, Aeschbach L, Markov AV, Sinitsyn A BMC Plant Biol 03-Nov-2005
PMCID:PMC1298311
doi:10.1186/1471-2229-5-23
PMID:16269076
Mass transfer during the extraction of alkaloids from bulbs of meadow magnificent (Colchicinum spaciosum stev.) P. A. Yavich, L. I. Churadze, K. O. Keropyan, Ch. A. Chikhladze Springer Science and Business Media LLC 10-Dec-2004
doi:10.1007/BF00778187
Flavonoids of the leaves of Colchicum speciosum V. N. Bubenchikova, O. I. Popova Springer Science and Business Media LLC 26-Nov-2004
doi:10.1007/BF00629812
Alkaloid specioseine from Colchicum speciosum B. Ch. Chommadov Springer Science and Business Media LLC 26-Nov-2004
doi:10.1007/BF00629764
Flavone biosides ofColchicum speciosum V. A. Bandyukova Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00568606
Alkaloids and phenolics of Colchicum turcicum A. Husek, N. Sütlüpinar, P. Sedmera, F. Voegelein, I. Valka, V. Šimánek Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(90)87143-I

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown https://doi.org/10.1016/0031-9422(90)87143-I
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see 170.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
4-Methoxybenzoic Acid 7478 Click to see 152.15 unknown https://doi.org/10.1016/0031-9422(90)87143-I
> Hydrocarbon derivatives / Tropones
1,2,3,10-tetramethoxy-7-(methylamino)-6,7-dihydro-5H-benzo(a)heptalen-9-one 2832 Click to see 371.40 unknown https://doi.org/10.1135/CCCC19541283
https://doi.org/10.1007/BF00778187
3-Demethylcolchicine 299664 Click to see 385.40 unknown https://doi.org/10.1016/0031-9422(90)87143-I
Colchicine 6167 Click to see 399.40 unknown https://doi.org/10.1007/BF00778187
https://doi.org/10.1016/0031-9422(90)87143-I
Demecolcine 220401 Click to see CNC1CCC2=CC(=C(C(=C2C3=CC=C(C(=O)C=C13)OC)OC)OC)OC 371.40 unknown https://doi.org/10.1007/BF00778187
https://doi.org/10.1135/CCCC19541283
Speciosine 330188 Click to see 477.50 unknown https://doi.org/10.1007/BF00629764
https://doi.org/10.1007/BF02282367
> Hydrocarbon derivatives / Tropones / Tropolones
(S)-6,7-Dihydro-7-[(2-hydroxybenzyl)(methyl)amino]-1,2,3-trimethoxy-9-hydroxybenzo[a]heptalen-10(5H)-one 14832010 Click to see CN(CC1=CC=CC=C1O)C2CCC3=CC(=C(C(=C3C4=CC=C(C(=O)C=C24)O)OC)OC)OC 463.50 unknown https://doi.org/10.1007/BF00629764
10-hydroxy-7-[(2-hydroxyphenyl)methyl-methylamino]-1,2,3-trimethoxy-6,7-dihydro-5H-benzo[a]heptalen-9-one 14832009 Click to see 463.50 unknown https://doi.org/10.1007/BF00629764
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (2R,4aS,6aR,6aS,6bR,8aR,9R,10R,11R,12aR,14bR)-10,11-dihydroxy-9-(hydroxymethyl)-2,6a,6b,9,12a-pentamethyl-1-methylidene-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 101106492 Click to see 648.80 unknown via CMAUP database
2alpha,3beta,19alpha-Trihydroxyurs-12-en-28-oic acid (6-O-methyl-beta-D-glucopyranosyl) ester 101615131 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)OC6C(C(C(C(O6)COC)O)O)O 664.90 unknown via CMAUP database
Dotorioside II 16118969 Click to see 666.80 unknown via CMAUP database
Kajiichigoside F1 14019178 Click to see 650.80 unknown via CMAUP database
Rosamultin 21122581 Click to see 650.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown via CMAUP database
(1R,2R,4aS,6aR,6aS,6bR,8aS,10S,11R,12aR,14bR)-1,10,11-trihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 93961278 Click to see 488.70 unknown via CMAUP database
(1R,2R,4aS,6aR,6aS,6bR,8aS,9R,10R,11R,12aR,14bS)-1,10,11-trihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 95223073 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1(C)O)C)C(=O)O 504.70 unknown via CMAUP database
19Alpha-Hydroxyasiatic Acid 490367 Click to see 504.70 unknown via CMAUP database
2alpha,3alpha,23-Trihydroxyolean-12-en-28-oic acid 11504083 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1)C)C(=O)O)C 488.70 unknown via CMAUP database
2alpha,3beta-Dihydroxyolean-13(18)-en-28-oic acid 52952429 Click to see 472.70 unknown via CMAUP database
2alpha,3beta,11alpha,19alpha-Tetrahydroxyurs-12-en-28-oic acid 101615130 Click to see CC1CCC2(CCC3(C(=CC(C4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)O)C2C1(C)O)C)C(=O)O 504.70 unknown via CMAUP database
2alpha,3beta,23-Trihydroxylup-20(29)-en-28-oic acid 70698002 Click to see 488.70 unknown via CMAUP database
3beta-Hydroxy-2alpha-methoxyurs-12-en-28-oic acid 101615129 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)OC)C)C)C2C1C)C)C(=O)O 486.70 unknown via CMAUP database
Corosolic acid 6918774 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)O 472.70 unknown via CMAUP database
Euscaphic Acid 471426 Click to see 488.70 unknown via CMAUP database
Euscaphic Acid Methyl Ester 14314584 Click to see 502.70 unknown via CMAUP database
Hederagenin 73299 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown via CMAUP database
Maslinic Acid 73659 Click to see 472.70 unknown via CMAUP database
Methyl corosolate 14109751 Click to see 486.70 unknown via CMAUP database
Oleanolic Acid 10494 Click to see 456.70 unknown via CMAUP database
Rel-2alpha,3alpha,19alpha,23-tetrahydroxyolean-12-en-28-oic acid 52952430 Click to see 504.70 unknown via CMAUP database
Tormentic acid 73193 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)O 488.70 unknown via CMAUP database
Tormentic Acid Methyl Ester 14314585 Click to see 502.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 12-hydroxysteroids / 12-beta-hydroxysteroids
(3S)-5-[(4aS,4bR,6aR,7R,8R,9R,10aR,10bR)-8,9-dihydroxy-7-(hydroxymethyl)-4a,4b,7,10a-tetramethyl-3,4,5,6,6a,8,9,10,10b,11-decahydrochrysen-2-yl]-3-methylpentan-2-one 52952318 Click to see 458.70 unknown via CMAUP database
Rel-2alpha,3beta,23-trihydroxy-12,17-dien-28-norursane 52952319 Click to see CC1CCC2=C(C1C)C3=CCC4C(C3(CC2)C)(CCC5C4(CC(C(C5(C)CO)O)O)C)C 442.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids
(2S,4aS,4bR,6aR,7R,8S,9R,10aS,10bR)-8,9-dihydroxy-7-(hydroxymethyl)-4a,4b,7,10a-tetramethyl-2-[(3S)-3-methyl-4-oxopentyl]-4,5,6,6a,8,9,10,10b-octahydro-3H-chrysene-2-carboxylic acid 52952320 Click to see 502.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,2,3,4,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-7-one 101615132 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(=O)C=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 590.80 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 oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
2-(beta-D-Glucopyranosyloxy)-5-[(6S)-6,7-dihydroxy-3,7-dimethyl-2-octenyl]benzoic acid methyl ester 71660038 Click to see CC(=CCC1=CC(=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CCC(C(C)(C)O)O 484.50 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
Cornigerine 100188 Click to see CC(=O)NC1CCC2=CC3=C(C(=C2C4=CC=C(C(=O)C=C14)OC)OC)OCO3 383.40 unknown https://doi.org/10.1016/0031-9422(90)87143-I
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Ferulic Acid 445858 Click to see 194.18 unknown https://doi.org/10.1016/0031-9422(90)87143-I
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
Procyanidin B3 146798 Click to see 578.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
(+)-Epicatechin 182232 Click to see 290.27 unknown via CMAUP database
Catechin 9064 Click to see 290.27 unknown via CMAUP database
> 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/10.1007/BF00629812
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1007/BF00629812
https://doi.org/10.1016/0031-9422(90)87143-I
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
7-[(2R,3S,4R,5S,6S)-3,5-dihydroxy-6-(hydroxymethyl)-4-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5-hydroxychromen-4-one 163193092 Click to see 610.50 unknown https://doi.org/10.1007/BF00568606
7-[(2R,3S,4R,5S)-4,5-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)chromen-4-one 163043420 Click to see 564.50 unknown https://doi.org/10.1007/BF00568606
7-[3,5-Dihydroxy-6-(hydroxymethyl)-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5-hydroxychromen-4-one 74977646 Click to see 610.50 unknown https://doi.org/10.1007/BF00568606
7-[4,5-Dihydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)chromen-4-one 163043419 Click to see 564.50 unknown https://doi.org/10.1007/BF00568606
Apigenin 7-O-glucoside 5280704 Click to see 432.40 unknown https://doi.org/10.1007/BF00629812
Luteolin 7-galactoside 5291488 Click to see C1=CC(=C(C=C1C2=CC(=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/10.1007/BF00629812
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=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/10.1007/BF00629812
Npc85473 5385553 Click to see 432.40 unknown https://doi.org/10.1007/BF00629812
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
[(10R,11R,13R,14R,15S)-3,4,5,14,20,21,22-heptahydroxy-13-(hydroxymethyl)-8,17-dioxo-9,12,16-trioxatetracyclo[16.4.0.02,7.010,15]docosa-1(22),2,4,6,18,20-hexaen-11-yl] 2-[5-[[(1R,2S,19R,20R,22R)-7,8,9,12,13,14,28,29,30,33,34,35-dodecahydroxy-4,17,25,38-tetraoxo-3,18,21,24,39-pentaoxaheptacyclo[20.17.0.02,19.05,10.011,16.026,31.032,37]nonatriaconta-5,7,9,11,13,15,26,28,30,32,34,36-dodecaen-20-yl]oxycarbonyl]-2,3-dihydroxyphenoxy]-3,4,5-trihydroxybenzoate 16169194 Click to see 1569.10 unknown via CMAUP database
[(10R,11R,13R,14R,15S)-3,4,5,14,20,21,22-heptahydroxy-13-(hydroxymethyl)-8,17-dioxo-9,12,16-trioxatetracyclo[16.4.0.02,7.010,15]docosa-1(22),2,4,6,18,20-hexaen-11-yl] 3,4,5-trihydroxybenzoate 13917514 Click to see 634.50 unknown via CMAUP database
[(1R,2S,19R,20R,22R)-7,8,9,12,13,14,28,29,30,33,34,35-dodecahydroxy-4,17,25,38-tetraoxo-3,18,21,24,39-pentaoxaheptacyclo[20.17.0.02,19.05,10.011,16.026,31.032,37]nonatriaconta-5,7,9,11,13,15,26,28,30,32,34,36-dodecaen-20-yl] 2-[5-[[(10R,11R,13R,14R,15S)-3,4,5,14,20,21,22-heptahydroxy-13-(hydroxymethyl)-8,17-dioxo-9,12,16-trioxatetracyclo[16.4.0.02,7.010,15]docosa-1(22),2,4,6,18,20-hexaen-11-yl]oxycarbonyl]-2,3-dihydroxyphenoxy]-3,4,5-trihydroxybenzoate 16138866 Click to see C1C2C(C3C(C(O2)OC(=O)C4=CC(=C(C(=C4OC5=CC(=CC(=C5O)O)C(=O)OC6C7C(C(C(O6)CO)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O7)O)O)O)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O3)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O 1569.10 unknown via CMAUP database
[(1R,2S,19R,20R,22R)-7,8,9,12,13,14,28,29,30,33,34,35-dodecahydroxy-4,17,25,38-tetraoxo-3,18,21,24,39-pentaoxaheptacyclo[20.17.0.02,19.05,10.011,16.026,31.032,37]nonatriaconta-5,7,9,11,13,15,26,28,30,32,34,36-dodecaen-20-yl] 3,4,5-trihydroxybenzoate 5315734 Click to see C1C2C(C3C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O3)O)O)O)O)O)O)OC(=O)C7=CC(=C(C(=C7C8=C(C(=C(C=C8C(=O)O1)O)O)O)O)O)O 936.60 unknown via CMAUP database
2-[5-[[(10R,11R,13R,14R,15S)-3,4,5,14,20,21,22-heptahydroxy-13-(hydroxymethyl)-8,17-dioxo-9,12,16-trioxatetracyclo[16.4.0.02,7.010,15]docosa-1(22),2,4,6,18,20-hexaen-11-yl]oxycarbonyl]-2,3-dihydroxyphenoxy]-3,4,5-trihydroxybenzoic acid 14374737 Click to see 802.60 unknown via CMAUP database
Agrimoniin 16129621 Click to see 1871.30 unknown via CMAUP database
alpha-Pedunculagin 13834142 Click to see C1C2C(C3C(C(O2)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O3)O)O)O)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)O)O)O)O)O)O 784.50 unknown via CMAUP database
Casuarictin 73644 Click to see 936.60 unknown via CMAUP database
Ellagic Acid 5281855 Click to see 302.19 unknown via CMAUP database
Ellagic acid 4-O-alpha-L-arabinofuranoside 101129362 Click to see 434.30 unknown via CMAUP database
Laevigatin F 16182828 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3OC4=CC(=CC(=C4O)O)C(=O)OC5C6C(C7C(O5)COC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O7)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O6)O)O)O)O)O)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O 1569.10 unknown via CMAUP database

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