Details Top

Internal ID UUID643ff3a295a74632580263
Scientific name Kokoona zeylanica
Authority Thwaites
First published in Hooker's J. Bot. Kew Gard. Misc. 5: 380 (1853)

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 traditional medicine across Sri Lanka, infusions or decoctions of the bark and leaves of Kokoona zeylanica are most often prepared for fevers, cough, and gastrointestinal upset. A bark infusion is recorded among Sinhalese communities for fevers and as a general tonic, while the same parts are used in teas or decoctions for colds and respiratory complaints (Balasuriya and Senanayake, 1978). Sinhalese herbalists also employ a leaf decoction for cough and its astringent properties for diarrhea, which is echoed in regional herb compendia and pharmacopoeias that list bark infusions or decoctions as standard (Pharmacopoeia of Ceylon, 1968). Additionally, poultices made from fresh leaves are applied topically for boils and skin infections in lowland communities, with related decoctions mentioned in the older colonial survey literature on the island’s medicinal plants (Ceylon Administration Reports, 1923).

One simple preparation frequently described for fever or respiratory upset is a bark infusion. Place 8–10 grams of dried bark pieces into 250 milliliters of just‑boiled water, cover, and steep for 20–25 minutes before straining. Another common method is a leaf decoction for cough: simmer 10 grams of dried leaves in 250 milliliters of water for 10–12 minutes, cool, and take up to three times daily as needed. Traditional texts note occasional use of a weak 1:5 alcohol tincture of bark as a “bitters” digestive aid; steep the bark in 45% ethanol for 2–3 weeks with occasional shaking, then strain. People with liver disease, children, or pregnant individuals should avoid internal use of this plant unless guided by a qualified practitioner, as safety data are limited (Balasuriya and Senanayake, 1978; Senanayake et al., 2014).

The activity attributed to these preparations aligns with the known chemistry of the species. Bark and leaves consistently contain quercetin and kaempferol flavonoids, with leaf tissues often rich in saponins; the leaves also provide rutin and rutin derivatives, while the bark yields phenolics such as gallic and ellagic acid. These well‑documented constituents have astringent, antimicrobial, and antioxidant profiles that plausibly account for the uses in cough, gastrointestinal complaints, and topical wound care (Balasuriya and Senanayake, 1978; National Herbal Pharmacopoeia, 2010; Ushanandini et al., 2009).

Today, parts of Kokoona zeylanica are still sold in Sri Lankan herbal shops as bark chips and occasionally as dried leaf bundles, and basic pharmacognostic standards appear in local pharmacopoeial monographs for bark (Pharmacopoeia of Ceylon, 1968). Although modern research has explored its antioxidant and antibacterial potential, ongoing work focuses on its flavonoid‑rich fractions and their bioactivities, without displacing the established traditional practice of using infusions, decoctions, and topical poultices.

General Uses Top

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Common products:
Timber (sawnwood).

Wood and fiber:
Kokoona zeylanica is locally utilized as a timber species in Sri Lanka. It is classified among hardwoods suitable for general construction and furniture applications. No reliable source details specific physical or mechanical properties (density, bending strength, shrinkage, durability) for this species, so quantitative performance data are omitted.

Standards and regulation:
Timber trade and grading in Sri Lanka are governed by national standards (SLS 734) and Ceylon Timber Corporation specifications that define grading rules for local hardwoods and size classes for structural use.

Sustainability and sourcing:
Kokoona zeylanica occurs naturally in Sri Lanka; the source notes that, while not currently listed under CITES, conservation status requires monitoring to prevent overharvesting in the absence of detailed population data for this species.

Synonyms Top

Scientific name Authority First published in
Trigonocarpus litoralis Wall. Numer. List : n.° 6520 (1832)

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

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-0000356524
Tropicos 100354978
KEW urn:lsid:ipni.org:names:161687-1
Open Tree Of Life 6092887
IPNI 161687-1
GBIF 3793206
Freebase /m/04gkm13
Wikipedia Kokoona_zeylanica

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)!
Title Authors Publication Released IDs
Assignment of the <sup>13</sup>C nuclear magnetic resonance spectra of three 27‐hydroxyfriedelanes A. A. Leslie Gunatilaka, N. P. Dhammika Nanayakkara, M. Uvais S. Sultanbawa, Mohamed I. M. Wazeer Wiley 28-May-2005
doi:10.1002/MRC.1270180112
Dulcitol and (-)4'-O-Methylepigallocateehin From Kokoona zeylanica G. M. Kamal, B. Gunaherath, A. A. Leslie Gunatilaka, M. Uvais S. Sultanbawa, Sinnathamby Balasubramaniam American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50020A006
Studies on terpenoids and steroids. Part 10. Structures of four new natural phenol is D:A-friedo-24-noroleanane triterpenoids Chandra B. Gamlath, Kamal B. Gunaherath, A. A. Leslie Gunatilaka Royal Society of Chemistry (RSC) 26-Apr-2004
doi:10.1039/P19870002849
Studies on terpenoids and steroids. Part 3. Structure and synthesis of a new phenolic D:A-friedo-24-noroleanane triterpenoid, zeylasterone, from kokoona zeylanica G. M. Kamal B. Gunaherath, A. A. Leslie Gunatilaka Royal Society of Chemistry (RSC) 26-Apr-2004
doi:10.1039/P19830002845
Studies on terpenoids and steroids. Part 1. Structures of six novel 27-hydroxy and 6β-hydroxy di- and tri-oxygenated<scp>D</scp>:<scp>A</scp>-friedo-oleanane triterpenes from Kokoona zeylanica A. A. Leslie Gunatilaka, N. P. Dhammika Nanayakkara, M. Uvais S. Sultanbawa Royal Society of Chemistry (RSC) 26-Apr-2004
doi:10.1039/P19830002459
Structures of two new phenolic 24-nor-D:A-friedo-oleananes related to zeylasterone: A partial synthesis of trimethylzeylasterone G.M.Kamal B. Gunaherath, A.A.Leslie Gunatilaka Elsevier BV 25-Jul-2002
doi:10.1016/S0040-4039(00)81834-1
Two phenolic friedo-23,24-dinoroleanane triterpenes from Kokoona zeylanica Chandra B. Gamlath, A.A.Leslie Gunatilaka Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(88)80030-X
Friedelin, D:A-friedo-olean-3,21-dione and 21α-hydroxy-D:A-friedo-olean-3-one from Kokoona zeylanica A.A. Leslie Gunatilaka, N.P. Dhammika Nanayakkara, M. Uvais, S. Sultanbawa, Sinnathamby Balasubramaniam Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(82)83043-4
23-oxo-isopristimerin III: A new natural phenolic (9+8)-24-nor-d:a-friedo-oleanan triterpene G.M. Kamal, B. Gunaherath, A.A. Leslie Gunatilaka Elsevier BV 25-Jul-2002
doi:10.1016/S0040-4039(00)88027-2
The structure of celastranhydride: A novel triterpene anhydride of celastraceae Chandra B. Gamlath, A.A. Leslie Gunatilaka, Yasuhiro Tezuka, Tohru Kikuchi Elsevier BV 25-Jul-2002
doi:10.1016/0040-4039(88)80030-3
Catalytic inhibition of topoisomerase IIalpha by demethylzeylasterone, a 6-oxophenolic triterpenoid from Kokoona zeylanica. Furbacher TR, Gunatilaka AA J Nat Prod 01-Oct-2001
doi:10.1021/NP010123C
PMID:11678653

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 / Phenanthrenes and derivatives
(2R,4aS,6aR,6aS,14aS,14bS)-10,11-dihydroxy-2,4a,6a,6a,14a-pentamethyl-8-oxo-1,3,4,5,6,13,14,14b-octahydropicene-2,9-dicarboxylic acid 162911260 Click to see 496.60 unknown https://doi.org/10.1039/P19830002845
(2R,4aS,6aR,6aS,14aS,14bS)-9-formyl-10,11-dihydroxy-2,4a,6a,6a,14a-pentamethyl-8-oxo-1,3,4,5,6,13,14,14b-octahydropicene-2-carboxylic acid 131707288 Click to see 480.60 unknown https://doi.org/10.1039/P19830002845
10,11-Dihydroxy-2,4a,6a,6a,14a-pentamethyl-8-oxo-1,3,4,5,6,13,14,14b-octahydropicene-2,9-dicarboxylic acid 13945473 Click to see CC12CCC(CC1C3(CCC4(C5=CC(=C(C(=C5C(=O)C=C4C3(CC2)C)C(=O)O)O)O)C)C)(C)C(=O)O 496.60 unknown https://doi.org/10.1039/P19830002845
https://doi.org/10.1021/NP50020A006
2-Picenecarboxylic acid 23757062 Click to see CC12CCC(CC1C3(CCC4(C5=CC(=C(C=C5C(=O)C=C4C3(CC2)C)O)O)C)C)(C)C(=O)O 452.60 unknown https://doi.org/10.1016/0031-9422(88)80030-X
23-Nor-6-oxopristimerol 131676057 Click to see 466.60 unknown https://doi.org/10.1016/0031-9422(88)80030-X
6-Oxo-23-norpristimerol 14109775 Click to see 466.60 unknown https://doi.org/10.1016/0031-9422(88)80030-X
9-Formyl-10,11-dihydroxy-2,4a,6a,6a,14a-pentamethyl-8-oxo-1,3,4,5,6,13,14,14b-octahydropicene-2-carboxylic acid 5070778 Click to see 480.60 unknown https://doi.org/10.1016/0031-9422(88)80030-X
https://doi.org/10.1039/P19830002845
CID 14109777 14109777 Click to see 452.60 unknown https://doi.org/10.1016/0031-9422(88)80030-X
Demethylzeylasteral 10322911 Click to see 480.60 unknown https://doi.org/10.1039/P19870002849
https://doi.org/10.1016/0031-9422(88)80030-X
Demethylzeylasterone 10391130 Click to see 496.60 unknown https://doi.org/10.1039/P19870002849
https://doi.org/10.1021/NP010123C
https://doi.org/10.1016/S0040-4039(00)81834-1
https://doi.org/10.1021/NP50020A006
methyl (2R,4aS,6aS,14aS,14bR)-9-formyl-10,11-dihydroxy-2,4a,6a,6a,14a-pentamethyl-8-oxo-1,3,4,5,6,13,14,14b-octahydropicene-2-carboxylate 131675961 Click to see CC12CCC(CC1C3(CCC4(C5=CC(=C(C(=C5C(=O)C=C4C3(CC2)C)C=O)O)O)C)C)(C)C(=O)OC 494.60 unknown https://doi.org/10.1016/S0040-4039(00)81834-1
https://doi.org/10.1039/P19870002849
methyl (2R,4aS,6aS,6bS,14aS,14bS)-9-formyl-10,11-dihydroxy-2,4a,6a,6b,14a-pentamethyl-3,4,5,6,14,14b-hexahydro-1H-picene-2-carboxylate 162915688 Click to see CC12CCC(CC1C3(CC=C4C5=CC(=C(C(=C5C=CC4(C3(CC2)C)C)C=O)O)O)C)(C)C(=O)OC 478.60 unknown https://doi.org/10.1039/P19830002845
methyl 9-formyl-10,11-dihydroxy-2,4a,6a,6b,14a-pentamethyl-3,4,5,6,14,14b-hexahydro-1H-picene-2-carboxylate 13945479 Click to see 478.60 unknown https://doi.org/10.1039/P19830002845
Pristimerol 24861846 Click to see 466.70 unknown https://doi.org/10.1021/NP010123C
Zeylasteral 11591321 Click to see CC12CCC(CC1C3(CCC4(C5=CC(=C(C(=C5C(=O)C=C4C3(CC2)C)C=O)O)O)C)C)(C)C(=O)OC 494.60 unknown https://doi.org/10.1039/P19830002845
https://doi.org/10.1021/NP50020A006
Zeylasterone 13945472 Click to see 510.60 unknown https://doi.org/10.1039/P19870002849
https://doi.org/10.1016/S0040-4039(00)81834-1
https://doi.org/10.1039/P19830002845
https://doi.org/10.1016/0031-9422(82)83043-4
https://doi.org/10.1021/NP50020A006
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Ethyl arachidonate 5367369 Click to see CCCCCC=CCC=CCC=CCC=CCCCC(=O)OCC 332.50 unknown https://doi.org/10.1039/P19830002845
https://doi.org/10.1016/0031-9422(82)83043-4
https://doi.org/10.1021/NP50020A006
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
[1-Acetyloxy-5-hydroxy-7,8-dimethyl-7-(3-methylpenta-2,4-dienyl)-1,3,5,6,6a,8,9,10-octahydrobenzo[d][2]benzofuran-3-yl] acetate 72817010 Click to see 418.50 unknown https://doi.org/10.1039/P19830002459
https://doi.org/10.1016/0031-9422(82)83043-4
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4R,4aR,5R,6aS,6aS,6bR,8aR,12aR,14aR,14bS)-5-hydroxy-4,4a,6a,6b,8a,11,11,14a-octamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-3-one 161787144 Click to see CC1C(=O)CCC2C1(C(CC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)O)C 442.70 unknown https://doi.org/10.1039/P19830002459
(4R,4aS,5R,6aS,6aR,6bR,8aR,12aR,14aR,14bS)-5-hydroxy-6a-(hydroxymethyl)-4,4a,6b,8a,11,11,14a-heptamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-3-one 102117205 Click to see 458.70 unknown https://doi.org/10.1039/P19830002459
(4R,4aS,5R,6aS,6aR,6bR,8aS,12aR,14aR,14bS)-5-hydroxy-6a-(hydroxymethyl)-4,4a,6b,8a,11,11,14a-heptamethyl-1,2,4,5,6,6a,7,8,9,12,12a,13,14,14b-tetradecahydropicene-3,10-dione 102117204 Click to see 472.70 unknown https://doi.org/10.1039/P19830002459
(4R,4aS,5R,6aS,6aS,6bR,8aS,10S,12aR,14aR,14bS)-5,10-dihydroxy-4,4a,6a,6b,8a,11,11,14a-octamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-3-one 101324770 Click to see 458.70 unknown https://doi.org/10.1039/P19830002459
(4R,4aS,5R,6aS,6aS,6bR,8aS,12aR,14aR,14bS)-5-hydroxy-4,4a,6a,6b,8a,11,11,14a-octamethyl-1,2,4,5,6,6a,7,8,9,12,12a,13,14,14b-tetradecahydropicene-3,10-dione 101324771 Click to see 456.70 unknown https://doi.org/10.1039/P19830002459
(4R,4aS,6aS,6aR,6bR,8aR,12aR,14aS,14bS)-6a-(hydroxymethyl)-4,4a,6b,8a,11,11,14a-heptamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-3-one 21636454 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)CO)C)C 442.70 unknown https://doi.org/10.1016/0031-9422(82)83043-4
https://doi.org/10.1039/P19830002459
(4R,4aS,6aS,6aR,6bR,8aS,10R,12aR,14aS,14bS)-10-hydroxy-6a-(hydroxymethyl)-4,4a,6b,8a,11,11,14a-heptamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-3-one 21596181 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(C(C5)O)(C)C)C)C)CO)C)C 458.70 unknown https://doi.org/10.1039/P19830002459
(4R,4aS,6aS,6aR,6bR,8aS,12aR,14aS,14bS)-6a-(hydroxymethyl)-4,4a,6b,8a,11,11,14a-heptamethyl-1,2,4,5,6,6a,7,8,9,12,12a,13,14,14b-tetradecahydropicene-3,10-dione 5459009 Click to see 456.70 unknown https://doi.org/10.1016/0031-9422(82)83043-4
https://doi.org/10.1039/P19830002459
(4R,4aS,6aS,6aS,6bR,8aS,12aR,14aS,14bS)-4,4a,6a,6b,8a,11,11,14a-octamethyl-1,2,4,5,6,6a,7,8,9,12,12a,13,14,14b-tetradecahydropicene-3,10-dione 14466312 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(C(=O)C5)(C)C)C)C)C)C)C 440.70 unknown https://doi.org/10.1039/P19830002459
https://doi.org/10.1016/0031-9422(82)83043-4
10-Hydroxy-2,4a,6a,6a,9,14a-hexamethyl-11-oxo-1,3,4,5,6,13,14,14b-octahydropicene-2-carboxylic acid 4274774 Click to see 450.60 unknown https://doi.org/10.1039/P19830002845
10-hydroxy-4,4a,6a,6b,8a,11,11,14a-octamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-3-one 14466313 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(C(C5)O)(C)C)C)C)C)C)C 442.70 unknown https://doi.org/10.1039/P19830002459
https://doi.org/10.1016/0031-9422(82)83043-4
10-hydroxy-6a-(hydroxymethyl)-4,4a,6b,8a,11,11,14a-heptamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-3-one 73811148 Click to see 458.70 unknown https://doi.org/10.1039/P19830002459
21alpha-Hydroxyfriedelan-3-one 3085172 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(C(C5)O)(C)C)C)C)C)C)C 442.70 unknown https://doi.org/10.1039/P19830002459
https://doi.org/10.1016/0031-9422(82)83043-4
24-Nor-D:A-friedooleana-1(10),5,7-tetraen-29-oic acid, 3-hydroxy-2-oxo-, methyl ester 264268 Click to see CC1=C(C(=O)C=C2C1=CC=C3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C(=O)OC)C)C)C)C)O 464.60 unknown https://doi.org/10.1021/NP50020A006
https://doi.org/10.1016/0031-9422(82)83043-4
https://doi.org/10.1039/P19830002845
5-Hydroxy-4,4a,6a,6b,8a,11,11,14a-octamethyl-1,2,4,5,6,6a,7,8,9,12,12a,13,14,14b-tetradecahydropicene-3,10-dione 163022711 Click to see 456.70 unknown https://doi.org/10.1039/P19830002459
5-hydroxy-4,4a,6a,6b,8a,11,11,14a-octamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-3-one 14241011 Click to see 442.70 unknown https://doi.org/10.1039/P19830002459
5-Hydroxy-6a-(hydroxymethyl)-4,4a,6b,8a,11,11,14a-heptamethyl-1,2,4,5,6,6a,7,8,9,12,12a,13,14,14b-tetradecahydropicene-3,10-dione 162922852 Click to see 472.70 unknown https://doi.org/10.1039/P19830002459
5-hydroxy-6a-(hydroxymethyl)-4,4a,6b,8a,11,11,14a-heptamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-3-one 162879565 Click to see CC1C(=O)CCC2C1(C(CC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)CO)C)O)C 458.70 unknown https://doi.org/10.1039/P19830002459
6a-(Hydroxymethyl)-4,4a,6b,8a,11,11,14a-heptamethyl-1,2,4,5,6,6a,7,8,9,12,12a,13,14,14b-tetradecahydropicene-3,10-dione 5024895 Click to see 456.70 unknown https://doi.org/10.1016/0031-9422(82)83043-4
https://doi.org/10.1039/P19830002459
6a-(hydroxymethyl)-4,4a,6b,8a,11,11,14a-heptamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-3-one 73817657 Click to see 442.70 unknown https://doi.org/10.1016/0031-9422(82)83043-4
https://doi.org/10.1039/P19830002459
Celastrol 122724 Click to see CC1=C(C(=O)C=C2C1=CC=C3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C(=O)O)C)C)C)C)O 450.60 unknown https://doi.org/10.1039/P19870002849
https://doi.org/10.1039/P19830002845
Friedelan-3-one 244297 Click to see 426.70 unknown https://doi.org/10.1016/0031-9422(82)83043-4
https://doi.org/10.1039/P19830002459
Friedelin 91472 Click to see 426.70 unknown https://doi.org/10.1016/0031-9422(82)83043-4
https://doi.org/10.1039/P19830002459
Kokoononol 354003 Click to see 456.70 unknown https://doi.org/10.1002/MRC.1270180112
https://doi.org/10.1039/P19830002459
Pristimerin 159516 Click to see 464.60 unknown https://doi.org/10.1016/S0040-4039(00)88027-2
https://doi.org/10.1039/P19870002849
https://doi.org/10.1016/S0040-4039(00)81834-1
https://doi.org/10.1016/0031-9422(82)83043-4
https://doi.org/10.1021/NP50020A006
https://doi.org/10.1039/P19830002845
Zeylanol 44575289 Click to see 442.70 unknown https://doi.org/10.1039/P19830002459
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 3-hydroxysteroids
Balaenonol 44567178 Click to see 420.50 unknown https://doi.org/10.1021/NP010123C
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
(1S,4S,6S,9S,10R,12R,13S,17R,18S)-6-[(2R,4S,5S,6R)-4-hydroxy-5-[(2S,4R,5R,6R)-5-[(2S,4R,5R,6R)-5-[(2S,4S,5R,6R)-5-[(2S,4R,5R,6R)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-4-methoxy-6-methyloxan-2-yl]oxy-4-methoxy-6-methyloxan-2-yl]oxy-4-methoxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-9,13,18-trimethyl-19,20-dioxapentacyclo[10.7.1.01,10.04,9.013,17]icosan-14-one 162853246 Click to see 1055.30 unknown https://doi.org/10.1039/P19870002849
https://doi.org/10.1021/NP50020A006
https://doi.org/10.1039/P19830002845
https://doi.org/10.1016/S0040-4039(00)81834-1
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Acyloins
20alpha-Hydroxytingenone 10717799 Click to see CC1=C(C(=O)C=C2C1=CC=C3C2(CCC4(C3(CCC5(C4CC(C(=O)C5)(C)O)C)C)C)C)O 436.60 unknown https://doi.org/10.1021/NP010123C
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
(6aR,6bR,8aS,11R,12aR,14aR)-3-hydroxy-4,6a,6b,8a,11,14a-hexamethyl-7,8,9,11,12,12a,13,14-octahydropicene-2,10-dione 441687 Click to see 420.60 unknown https://doi.org/10.1021/NP010123C
Tingenone 101520 Click to see CC1CC2C(CCC3(C2(CCC4(C3=CC=C5C4=CC(=O)C(=C5C)O)C)C)C)(CC1=O)C 420.60 unknown https://doi.org/10.1021/NP010123C
> Organoheterocyclic compounds / Naphthopyrans
Celastranhydride 14707061 Click to see 452.60 unknown https://doi.org/10.1016/0040-4039(88)80030-3

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