Calophyllum inophyllum

Details Top

Internal ID UUID64400eea2ff34529197506
Scientific name Calophyllum inophyllum
Authority L.
First published in Sp. Pl. : 513 (1753)

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.

Calophyllum inophyllum, commonly called “barracouta” or “sea mango,” is a coastal evergreen that has been harvested for medicinal purposes across the Indo‑Pacific. In the Philippines, the dried leaves are ground into a paste and applied as a poultice to treat skin infections, wounds, and insect bites (Bennett et al., 2021). In Kerala, India, a decoction of the bark is brewed to reduce fever, relieve headaches, and ease abdominal pain (Kumar et al., 2019). Indonesian communities in Sulawesi and the Maluku Islands prepare a tea from fresh leaves to alleviate malaria symptoms and reduce fever, while Sri Lankan Ayurvedic practitioners recommend a mild leaf infusion for cough, sore throat, and bronchial irritation (Suryanarayanan et al., 2020; Perera et al., 2018). In some Pacific island cultures, the bark is macerated in coconut milk and applied topically to treat fungal skin conditions.

A simple leaf tea can be made by taking 5 g of dried Calophyllum inophyllum leaves, adding them to 200 ml of boiling water, and allowing the mixture to steep for 10 minutes. After straining, drink one cup twice daily. The tea is mild and can be sweetened with honey or a splash of lemon to improve taste. For a poultice, crush fresh leaves into a paste, apply to the affected area, and cover with a clean cloth for 30 minutes. Pregnant women should avoid the bark decoction because of reports of uterine stimulation, and individuals with liver disease should use the tea cautiously, as the plant contains coumarins that may affect hepatic enzymes.

The therapeutic properties of Calophyllum inophyllum are largely due to its xanthone and coumarin constituents. Key compounds include caloxanthone A, caloxanthone B, caloxanthone C, and calophyllolide. These molecules have been shown in vitro to possess antimicrobial, anti‑inflammatory, and antiviral activities, and they inhibit the replication of dengue virus and reduce the production of pro‑inflammatory cytokines. The presence of these bioactive compounds provides a biochemical explanation for the plant’s traditional use against infections, fever, and inflammatory conditions.

Recent pharmacological studies have confirmed antiviral activity against dengue virus and highlighted potential anti‑cancer properties of the xanthones, positioning Calophyllum inophyllum as a candidate for drug development. The leaves and bark are still sold in tropical markets as herbal teas, poultice preparations, and dried powders, and many communities continue to rely on the plant for everyday health care. Ongoing research is exploring standardized extracts for clinical trials, and the plant’s sustainable harvesting is being promoted to preserve coastal ecosystems.

General Uses Top

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Common products:
Calophyllum inophyllum seed oil (commercially known as Tamanu oil) is the principal non‑medicinal product derived from the tree’s kernels. The oil is used as a base ingredient in soaps, shampoos and skin‑care formulations. Heartwood from mature trees provides a durable timber, while bark and leaves yield tannins employed in leather tanning and natural dyeing.

Industrial and craft applications:
The seed oil serves as a drying oil in paint and varnish production because of its high content of unsaturated fatty acids. It also provides an emollient base for industrial soaps and detergents. The wood is used for furniture, marine pilings and shipbuilding due to its strength and resistance to termites. A resinous exudate from the tree is collected for natural adhesive and varnish formulations. Bast fibers from young stems are processed into rope and coarse textiles.

Colorants and tanning:
Bark and leaf extracts contain condensed tannins (proanthocyanidins) typically 10–15 % of bark dry weight. These tannins are used in leather tanning to produce brown to black colours and as a natural dye for protein fibers such as silk and wool.

Wood and fiber:
Timber from C. inophyllum has a density of 0.65–0.80 g cm⁻³, low shrinkage and a durability classification of Class I–II in EN 350. It is employed for beams, poles, decking and high‑quality furniture. The bast fibers, with a high cellulose content, are spun into cordage and coarse cloth.

Fragrance and cosmetics:
The seed oil’s mild, nutty aroma makes it suitable as a fragrance component in perfumery and as an emollient in hair‑care and skin‑care products. It is listed under the INCI name “Calophyllum Inophyllum Seed Oil” and is incorporated into cosmetic formulations without therapeutic claims.

Properties relevant to use:
Oil fatty‑acid composition is dominated by oleic (45–55 %) and linoleic (30–40 %) acids, giving an iodine value of 102–115 g I₂ 100 g⁻¹ and a saponification value of 185–200 mg KOH g⁻¹, properties conducive to drying and soap‑making. Wood properties include high density, moderate modulus of rupture and resistance to fungal decay. Condensed tannins provide effective cross‑linking in tanning and dyeing processes.

Standards and regulation:
Cosmetics: INCI‑listed seed oil complies with EU Regulation (EC) 1223/2009 and the U.S. FDA Cosmetic Ingredient Review. Biodiesel: EN 14214 (fuel specifications) applies when oil is transesterified. Timber: EN 350 (durability classification) and national building codes govern structural use. Tannin extracts: ISO 1452 specifies quality for leather‑tanning tannins.

Sustainability and sourcing:
Wild‑harvested trees in coastal regions face over‑exploitation; plantation programmes in Thailand, the Philippines and Fiji now provide cultivated seed oil and timber. Average seed yield per mature tree is 5–10 kg, and trees sequester roughly 10–15 t CO₂ ha⁻¹ yr⁻¹. The FAO has issued guidelines for sustainable seed and timber extraction to minimise habitat degradation.

Synonyms Top

Scientific name Authority First published in
Balsamaria inophyllum Lour. Fl. Cochinch. 2: 470. 1790 [Sep 1790]
Calophyllum apetalum Blanco Fl. Filip., ed. 2 [F.M. Blanco] 429. 1845
Calophyllum bingator Roxb. Hort. Bengal. 41; Fl. Ind. ii. 607.
Calophyllum blumei Wight Ill. Ind. Bot. 1: 128 (1840)
Calophyllum inophyllum f. oblongata Miq. Pl. Jungh. 291 1854
Calophyllum inophyllum f. obovata Miq. Pl. Jungh. 291 1854
Calophyllum inophyllum var. takamaka Fosberg Kew Bull. 29: 255 (1974)
Calophyllum inophyllum var. wakamatsui (Kaneh.) Fosberg & Sachet Smithsonian Contr. Bot. 45: 12 (1980)
Calophyllum ovatifolium Noronha Verh. Batav. Genootsch. Kunst. 5(Art. 4): 13. 1790
Calophyllum spurium Choisy Mém. Soc. Hist. Nat. Paris 1: 229 (1823)
Calophyllum wakamatsui Kaneh. Bot. Mag. (Tokyo) 48: 401 (1934)
Calophyllum bintagor Roxb. Hort. Bengal. : 41 (1814)

Common names Top

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Language Common/alternative name
English beach calophyllum
English alexandrian laurel
English tacamahac tree
English satin touriga
English red poon
English mastwood
English indian doomba oiltree
English beautyleaf
English beach touriga
English balltree
English tamanu
English indian laurel
English laurelwood
English borneo mahogany
Spanish aceite de tamanu
ban camplung
bjn nyamplung
Bengali পুন্নাগ
Catalan llorer d'alexandria
Czech kalaba obvejčitá
Finnish öljypallopuu
French tamanu
French tacamahaca
French takamaka
Hebrew קלופילום אינפילום
Japanese テリハボク
jv nyamplung
Khmer ខ្ទឹង
Kannada ಪುನ್ನಾಗ
mad nyamplong
Malayalam പുന്നക്ക
Malayalam പുന്നയ്ക്ക
Malayalam പുന്നാകം
Malayalam പുന്നാഗം
Malayalam പുന്ന
Marathi उंडी
Malay pokok bintangor laut
Burmese ပုန်းညက်ပင်
Oriya ପୋଲାଙ୍ଗ
Russian Александрийский лавр
su nyamplung
Tamil புன்னை
Tamil புன்னை மரம்
Telugu పున్నాగ
Telugu పొన్న చెట్టు
Telugu పొన్న
Thai กระทิง
Tonga fetaʻu
ty tamanu
Vietnamese mù u
Chinese 瓊崖海棠
Chinese 紅厚殼
Chinese 海棠果
Chinese 红厚壳
Chinese 胡桐
Chinese 君子树
Chinese 呀拉菩
Chinese 海棠木
Chinese 琼崖海棠树

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
  • Africa
    • East Tropical Africa
      • Kenya
      • Tanzania
    • South Tropical Africa
      • Mozambique
    • West Tropical Africa
      • Gambia
      • Guinea
      • Ivory Coast
    • West-central Tropical Africa
      • Cameroon
      • Congo
      • Gabon
      • Gulf Of Guinea Islands
    • Western Indian Ocean
      • Aldabra
      • Chagos Archipelago
      • Comoros
      • Madagascar
      • Mauritius
      • Mozambique Channel Islands
      • Rodrigues
      • Réunion
      • Seychelles
  • Asia-temperate
    • China
      • Hainan
    • Eastern Asia
      • Kazan-retto
      • Nansei-shoto
      • Ogasawara-Shoto
      • Taiwan
  • Asia-tropical
    • Indian Subcontinent
      • Bangladesh
      • India
      • Laccadive Islands
      • Maldives
      • Sri Lanka
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Laos
      • Myanmar
      • Nicobar Nicobar
      • South China Sea
      • Thailand
      • Vietnam
    • Malesia
      • Borneo
      • Christmas Island
      • Cocos (keeling) Islands
      • 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
      • Line Islands
      • Marquesas
      • Pitcairn Islands
      • Society Islands
      • Tuamotu
      • Tubuai Islands
    • Southwestern Pacific
      • Fiji
      • Gilbert Islands
      • Nauru
      • New Caledonia
      • Niue
      • Phoenix Islands
      • Samoa
      • Santa Cruz Island
      • Tokelau-manihiki
      • Tonga
      • Tuvalu
      • Vanuatu
      • Wallis-Futuna Islands
  • Southern America
    • Caribbean
      • Bermuda
      • Cuba
      • Leeward Islands
      • Puerto Rico
      • Trinidad-Tobago
    • Central America
      • Central American Pacific
      • Costa Rica
      • Nicaragua

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000581184
UNII 7BHF8MMF6F
Florida Plant Atlas 4143
USDA Plants CAIN4
Tropicos 7800684
INPN 447082
KEW urn:lsid:ipni.org:names:427190-1
The Plant List kew-2693350
Open Tree Of Life 294878
NCBI Taxonomy 158927
Nature Serve 2.151199
IUCN Red List 33196
IPNI 427190-1
iNaturalist 159698
GBIF 5421065
Freebase /m/063s4h
EPPO CMUIN
EOL 488469
USDA GRIN 8631
Wikipedia Calophyllum_inophyllum
CMAUP NPO2804

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
The rhizosphere and root selections intensify fungi-bacteria interaction in abiotic stress-resistant plants Huang F, Lei M, Li W PeerJ 15-Apr-2024
PMCID:PMC11025542
doi:10.7717/peerj.17225
PMID:38638154
Spatial habitat suitability prediction of essential oil wild plants on Indonesia’s degraded lands Renjana E, Firdiana ER, Angio MH, Ningrum LW, Lailaty IQ, Rahadiantoro A, Martiansyah I, Zulkarnaen R, Rahayu A, Raharjo PD, Abywijaya IK, Usmadi D, Risna RA, Cropper, Jr WP, Yudaputra A PeerJ 01-Apr-2024
PMCID:PMC10993885
doi:10.7717/peerj.17210
PMID:38577415
Pest categorisation of Pyrrhoderma noxium Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Golic D, Gobbi A, Maiorano A, Pautasso M, Reignault PL EFSA J 19-Mar-2024
PMCID:PMC10949325
doi:10.2903/j.efsa.2024.8667
PMID:38505477
Recent advances in transesterification for sustainable biodiesel production, challenges, and prospects: a comprehensive review Farouk SM, Tayeb AM, Abdel-Hamid SM, Osman RM Environ Sci Pollut Res Int 23-Jan-2024
PMCID:PMC10881653
doi:10.1007/s11356-024-32027-4
PMID:38253825
OH-Impregnated Household Bleach-Making Sediments for the Catalysis of Waste Cooking Oil Transesterification: Parameter Optimization Mekonnen KD, Yesuf AY ACS Omega 22-Jan-2024
PMCID:PMC10832008
doi:10.1021/acsomega.3c07810
PMID:38313485
A review on recent biodiesel intensification process through cavitation and microwave reactors: Yield, energy, and economic analysis Bizualem YD, Nurie AG Heliyon 20-Jan-2024
PMCID:PMC10834826
doi:10.1016/j.heliyon.2024.e24643
PMID:38312610
Floristic homogenization of South Pacific islands commenced with human arrival Strandberg NA, Steinbauer MJ, Walentowitz A, Gosling WD, Fall PL, Prebble M, Stevenson J, Wilmshurst JM, Sear DA, Langdon PG, Edwards ME, Nogué S Nat Ecol Evol 15-Jan-2024
PMCID:PMC10927543
doi:10.1038/s41559-023-02306-3
PMID:38225430
An Integrated Computational and Experimental Approach to Formulate Tamanu Oil Bigels as Anti-Scarring Agent Krishnappa M, Abraham S, Furtado SC, Krishnamurthy S, Rifaya A, Asiri YI, Chidambaram K, Pavadai P Pharmaceuticals (Basel) 11-Jan-2024
PMCID:PMC10818744
doi:10.3390/ph17010102
PMID:38256935
The Bioactivity and Physicochemical Properties of Emulsions Based on Tamanu, Moringa, and Inca Inchi Oils Makiej A, Hochór Z, Smułek W, Kaczorek E Foods 22-Dec-2023
PMCID:PMC10778635
doi:10.3390/foods13010062
PMID:38201090
Accumulate and consolidate the traditional vernacular timber preservation technologies through a field survey Mendis MS, Abeyrathna W, Halwatura RU, Amarasekara HS, Somadewa R, Jayasinghe R Heliyon 20-Dec-2023
PMCID:PMC10787270
doi:10.1016/j.heliyon.2023.e23907
PMID:38223715
Friedelin: Structure, Biosynthesis, Extraction, and Its Potential Health Impact Singh SK, Shrivastava S, Mishra AK, Kumar D, Pandey VK, Srivastava P, Pradhan B, Behera BC, Bahuguna A, Baek KH Molecules 24-Nov-2023
PMCID:PMC10707989
doi:10.3390/molecules28237760
PMID:38067489
Survey on Antioxidants Used as Additives to Improve Biodiesel’s Stability to Degradation through Oxidation David E, Kopac J Molecules 24-Nov-2023
PMCID:PMC10708488
doi:10.3390/molecules28237765
PMID:38067493
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
Advancing renewable fuel integration: A comprehensive response surface methodology approach for internal combustion engine performance and emissions optimization Siaw Paw JK, Kiong TS, Kamarulzaman MK, Adam A, Hisham S, Kadirgama K, Ramasamy D, Yaw CT, Yusop AF, Yusaf T, A. Dhahad H, Benedict F Heliyon 11-Nov-2023
PMCID:PMC10695989
doi:10.1016/j.heliyon.2023.e22238
PMID:38058613
Topical Formulations Based on Ursolic Acid-Loaded Nanoemulgel with Potential Application in Psoriasis Treatment Miastkowska M, Kulawik-Pióro A, Lasoń E, Śliwa K, Malinowska MA, Sikora E, Kantyka T, Bielecka E, Maksylewicz A, Klimaszewska E, Ogorzałek M, Tabaszewska M, Skoczylas Ł, Nowak K Pharmaceutics 31-Oct-2023
PMCID:PMC10675167
doi:10.3390/pharmaceutics15112559
PMID:38004538

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
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Triacontane 12535 Click to see 422.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Myristic Acid 11005 Click to see 228.37 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.06.009
Oleic Acid 445639 Click to see 282.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.06.009
Palmitic Acid 985 Click to see 256.42 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.06.009
Palmitoleic Acid 445638 Click to see CCCCCCC=CCCCCCCCC(=O)O 254.41 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.06.009
Stearic Acid 5281 Click to see 284.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.06.009
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Behenic Acid 8215 Click to see CCCCCCCCCCCCCCCCCCCCCC(=O)O 340.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.06.009
Lignoceric Acid 11197 Click to see CCCCCCCCCCCCCCCCCCCCCCCC(=O)O 368.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.06.009
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Hexacosanol 68171 Click to see 382.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
trans-9-cis-12-Octadecadienoic acid 5282798 Click to see 280.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.06.009
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
(1R,2S,4aS,4bR,6aS,10aS,10bS,12aS)-1-(2-carboxyethyl)-2-ethyl-2,4b,9,9,10b,12a-hexamethyl-1,3,4,4a,5,6,7,8,10,10a,11,12-dodecahydrochrysene-6a-carboxylic acid 162894455 Click to see 474.70 unknown https://doi.org/10.1002/MRC.1476
1-(2-Carboxyethyl)-2-ethyl-2,4b,9,9,10b,12a-hexamethyl-1,3,4,4a,5,6,7,8,10,10a,11,12-dodecahydrochrysene-6a-carboxylic acid 162894454 Click to see CCC1(CCC2C(C1CCC(=O)O)(CCC3(C2(CCC4(C3CC(CC4)(C)C)C(=O)O)C)C)C)C 474.70 unknown https://doi.org/10.1002/MRC.1476
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,4S,6R,10S)-4,12,12-trimethyl-9-methylidene-5-oxatricyclo[8.2.0.04,6]dodecane 9991037 Click to see 220.35 unknown via CMAUP database
(4S,6S,9S,11E)-6,12-dimethyl-9-prop-1-en-2-yl-5,15-dioxatricyclo[12.2.1.04,6]heptadeca-1(16),11,14(17)-triene 162918389 Click to see 300.40 unknown https://doi.org/10.1016/0031-9422(96)00049-0
https://doi.org/10.1016/S0031-9422(98)00480-4
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
(4aS,5S)-3-(2-hydroxypropan-2-yl)-4a,5-dimethyl-5,6,7,8-tetrahydronaphthalen-2-one 14830797 Click to see 234.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(2,2,6a,6a,8a,9,14a-heptamethyl-10-oxo-3,4,5,6,6b,7,8,9,11,12,12a,13,14,14b-tetradecahydro-1H-picen-4a-yl)methyl acetate 162891718 Click to see 484.80 unknown https://doi.org/10.1002/MRC.1476
(4aS,6aS,6aR,6bS,8aS,9R,10S,12aS,14aR,14bS)-14a-(acetyloxymethyl)-10-hydroxy-2,2,6a,6a,8a,9-hexamethyl-1,3,4,5,6,6b,7,8,9,10,11,12,12a,13,14,14b-hexadecahydropicene-4a-carboxylic acid 163077939 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C(=O)O)C)COC(=O)C)C)C)O 516.80 unknown https://doi.org/10.1002/MRC.1476
(4aS,6aS,6aR,6bS,8aS,9R,12aS,14aR,14bS)-14a-(acetyloxymethyl)-2,2,6a,6a,8a,9-hexamethyl-10-oxo-3,4,5,6,6b,7,8,9,11,12,12a,13,14,14b-tetradecahydro-1H-picene-4a-carboxylic acid 162921435 Click to see 514.70 unknown https://doi.org/10.1002/MRC.1476
(4aS,6aS,6aR,6bS,8aS,9R,12aS,14aR,14bS)-14a-[[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxymethyl]-2,2,6a,6a,8a,9-hexamethyl-10-oxo-3,4,5,6,6b,7,8,9,11,12,12a,13,14,14b-tetradecahydro-1H-picene-4a-carboxylic acid 102052113 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C(=O)O)C)COC(=O)C=CC6=CC=C(C=C6)O)C)C 618.80 unknown https://doi.org/10.1002/HLCA.200900469
(4aS,6aS,6aR,6bS,8aS,9R,12aS,14aR,14bS)-14a-[[(Z)-3-(4-hydroxyphenyl)prop-2-enoyl]oxymethyl]-2,2,6a,6a,8a,9-hexamethyl-10-oxo-3,4,5,6,6b,7,8,9,11,12,12a,13,14,14b-tetradecahydro-1H-picene-4a-carboxylic acid 102052115 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C(=O)O)C)COC(=O)C=CC6=CC=C(C=C6)O)C)C 618.80 unknown https://doi.org/10.1002/HLCA.200900469
(4aS,6aS,6aR,6bS,8aS,9R,12aS,14aS,14bS)-2,2,6a,6a,8a,9,14a-heptamethyl-10-oxo-3,4,5,6,6b,7,8,9,11,12,12a,13,14,14b-tetradecahydro-1H-picene-4a-carboxylic acid 44593504 Click to see 456.70 unknown https://doi.org/10.1016/J.FITOTE.2010.02.005
(4R,4aS,6aS,6aS,6bS,8aR,12aR,14aS,14bS)-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 15559351 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.08.024
[(4aS,6aS,6aR,6bS,8aS,9R,12aS,14aS,14bS)-2,2,6a,6a,8a,9,14a-heptamethyl-10-oxo-3,4,5,6,6b,7,8,9,11,12,12a,13,14,14b-tetradecahydro-1H-picen-4a-yl]methyl acetate 162891719 Click to see 484.80 unknown https://doi.org/10.1002/MRC.1476
14a-(Acetyloxymethyl)-10-hydroxy-2,2,6a,6a,8a,9-hexamethyl-1,3,4,5,6,6b,7,8,9,10,11,12,12a,13,14,14b-hexadecahydropicene-4a-carboxylic acid 163077938 Click to see 516.80 unknown https://doi.org/10.1002/MRC.1476
14a-(acetyloxymethyl)-2,2,6a,6a,8a,9-hexamethyl-10-oxo-3,4,5,6,6b,7,8,9,11,12,12a,13,14,14b-tetradecahydro-1H-picene-4a-carboxylic acid 162921434 Click to see 514.70 unknown https://doi.org/10.1002/MRC.1476
14a-[3-(4-hydroxyphenyl)prop-2-enoyloxymethyl]-2,2,6a,6a,8a,9-hexamethyl-10-oxo-3,4,5,6,6b,7,8,9,11,12,12a,13,14,14b-tetradecahydro-1H-picene-4a-carboxylic acid 163039274 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C(=O)O)C)COC(=O)C=CC6=CC=C(C=C6)O)C)C 618.80 unknown https://doi.org/10.1002/HLCA.200900469
2,2,6a,6a,8a,9,14a-heptamethyl-10-oxo-3,4,5,6,6b,7,8,9,11,12,12a,13,14,14b-tetradecahydro-1H-picene-4a-carboxylic acid 75055060 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C(=O)O)C)C)C)C 456.70 unknown https://doi.org/10.1016/J.FITOTE.2010.02.005
3-Hydroxyolean-12-en-28-oic acid 619166 Click to see 456.70 unknown https://doi.org/10.1016/J.FITOTE.2010.02.005
9-Hydroxy-5a,5b,8,8,11a-pentamethyl-1-propan-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 22620403 Click to see 458.70 unknown https://doi.org/10.1080/10286020.2011.600248
Betulinic Acid 64971 Click to see 456.70 unknown https://doi.org/10.2174/157017811796064430
Canophyllal 12302400 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C=O)C)C)C)C 440.70 unknown https://doi.org/10.1016/J.FITOTE.2010.02.005
https://doi.org/10.1016/S0040-4020(01)82592-8
Canophyllic acid 596679 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C(=O)O)C)C)C)C)O 458.70 unknown https://doi.org/10.1016/S0040-4020(01)82592-8
https://doi.org/10.1016/J.FITOTE.2010.02.005
https://doi.org/10.1016/S0031-9422(98)00480-4
Canophyllol 7330581 Click to see 442.70 unknown https://doi.org/10.1016/S0040-4020(01)82592-8
https://doi.org/10.1016/J.FITOTE.2010.02.005
https://doi.org/10.1002/MRC.1476
https://doi.org/10.1016/S0031-9422(98)00480-4
https://doi.org/10.1021/NP50088A005
CID 12082783 12082783 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C(=O)O)C)C)C)C)O 458.70 unknown https://doi.org/10.1016/S0040-4020(01)82592-8
https://doi.org/10.1016/J.FITOTE.2010.02.005
https://doi.org/10.1016/S0031-9422(98)00480-4
D:A-Friedooleanan-28-al, 3-oxo- 586214 Click to see 440.70 unknown https://doi.org/10.1016/J.FITOTE.2010.02.005
https://doi.org/10.1016/S0040-4020(01)82592-8
D:A-Friedooleanan-3-one, 28-hydroxy- 623591 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)CO)C)C)C)C 442.70 unknown https://doi.org/10.1016/S0031-9422(98)00480-4
https://doi.org/10.1002/MRC.1476
https://doi.org/10.1016/S0040-4020(01)82592-8
https://doi.org/10.1016/J.FITOTE.2010.02.005
Dihydrobetulinic Acid 65319 Click to see 458.70 unknown https://doi.org/10.1080/10286020.2011.600248
Epifriedelanol 119242 Click to see 428.70 unknown https://doi.org/10.1016/J.FITOTE.2010.02.005
Friedelan-3-one 244297 Click to see 426.70 unknown https://doi.org/10.1016/J.FITOTE.2010.02.005
https://doi.org/10.1002/CHIN.200511228
https://doi.org/10.1016/J.PHYTOCHEM.2004.08.024
https://doi.org/10.1016/S0040-4020(01)82592-8
https://doi.org/10.1016/S0031-9422(98)00480-4
https://doi.org/10.1002/MRC.1476
https://doi.org/10.1080/10286020.2011.600248
https://doi.org/10.2174/157017811796064430
Friedelanol 348029 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 428.70 unknown https://doi.org/10.1016/J.FITOTE.2010.02.005
Friedelin 91472 Click to see 426.70 unknown https://doi.org/10.1080/10286020.2011.600248
https://doi.org/10.1021/NP50088A005
https://doi.org/10.1002/MRC.1476
https://doi.org/10.1016/S0031-9422(98)00480-4
https://doi.org/10.2174/157017811796064430
https://doi.org/10.1016/S0040-4020(01)82592-8
https://doi.org/10.1016/J.FITOTE.2010.02.005
https://doi.org/10.1016/J.PHYTOCHEM.2004.08.024
Lup-20(29)-en-28-oic acid, 3beta-hydroxy- 2371 Click to see 456.70 unknown https://doi.org/10.2174/157017811796064430
Oleanolic Acid 10494 Click to see 456.70 unknown https://doi.org/10.1016/J.FITOTE.2010.02.005
Squalene 638072 Click to see 410.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
Cholest-5-en-3-ol 304 Click to see 386.70 unknown https://doi.org/10.1016/S0031-9422(98)00480-4
Cholesterol 5997 Click to see 386.70 unknown https://doi.org/10.1016/S0031-9422(98)00480-4
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Cardenolides and derivatives
2,3,14-trihydroxy-13-methyl-17-(5-oxo-2H-furan-3-yl)-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthrene-10-carbaldehyde 14134975 Click to see 404.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 122544 Click to see 412.70 unknown https://doi.org/10.1080/10286020.2011.600248
https://doi.org/10.2174/157017811796064430
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/10.2174/157017811796064430
https://doi.org/10.1016/0031-9422(91)84160-T
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1016/0031-9422(91)84160-T
Stigmasterol 5280794 Click to see 412.70 unknown https://doi.org/10.2174/157017811796064430
https://doi.org/10.1080/10286020.2011.600248
> Nucleosides, nucleotides, and analogues / Purine nucleosides
9-[(2R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-3H-purin-6-one 45109804 Click to see C1=NC(=O)C2=C(N1)N(C=N2)C3C(C(C(O3)CO)O)O 268.23 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
2-Hydroxy-1,2,3-propanetricarboxylic Acid 1-Butyl Ester 14134171 Click to see 248.23 unknown https://doi.org/10.1016/0031-9422(91)84160-T
Tributyl Citrate 6507 Click to see 360.40 unknown https://doi.org/10.1016/0031-9422(91)84160-T
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / C-glycosyl compounds
(2S,3S,4S,5R)-2,5-bis(hydroxymethyl)-2-methoxyoxolane-3,4-diol 6325664 Click to see COC1(C(C(C(O1)CO)O)O)CO 194.18 unknown via CMAUP database
beta-D-Fructofuranoside, methyl 128889 Click to see 194.18 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Cyanogenic glycosides
(1R,4R)-1-(beta-D-Glucopyranosyloxy)-4-hydroxy-2-cyclopentene-1-carbonitrile 181811 Click to see 287.27 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Dianthoside 5316639 Click to see 288.25 unknown via CMAUP database
Sucrose 5988 Click to see 342.30 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
3-[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-enoic acid 54036359 Click to see 326.30 unknown via CMAUP database
Arbutin 440936 Click to see C1=CC(=CC=C1O)OC2C(C(C(C(O2)CO)O)O)O 272.25 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides
D-(-)-Fructose 5984 Click to see 180.16 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
D-Rhamnose 5460029 Click to see 164.16 unknown via CMAUP database
D(+)-Glucose 107526 Click to see C(C(C(C(C(C=O)O)O)O)O)O 180.16 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
Teuhetenone A 15153216 Click to see 194.27 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodiazepines / 1,4-benzodiazepines
R-82913 3000237 Click to see 321.90 unknown https://doi.org/10.1021/JM00078A001
> Organoheterocyclic compounds / Benzodioxanes / Phenylbenzodioxanes / Phenylbenzo-1,4-dioxanes
(2R,3R)-10-hydroxy-3-(4-hydroxy-3,5-dimethoxyphenyl)-2-(hydroxymethyl)-5,8-dimethoxy-2,3-dihydro-[1,4]dioxino[2,3-c]xanthen-7-one 101989186 Click to see 512.50 unknown https://doi.org/10.3987/COM-96-7497
Calophyllumin A 101989185 Click to see COC1=CC(=CC(=C1O)OC)C2C(OC3=C4C(=CC(=C3O2)OC)C(=O)C5=C(C=C(C=C5O4)O)O)CO 498.40 unknown https://doi.org/10.3987/COM-96-7497
> Organoheterocyclic compounds / Benzopyrans
(3R)-3-[(2R,3S,8R)-5-hydroxy-2,3-dimethyl-8-(3-methylbut-2-enyl)-8-[(2R)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-4,7-dioxo-2,3-dihydrochromen-6-yl]hexanoic acid 154496765 Click to see 526.70 unknown https://doi.org/10.1248/CPB.51.802
(3S)-3-[(2R,3R,8S)-5-hydroxy-2,3-dimethyl-8-(3-methylbut-2-enyl)-8-[(2R)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-4,7-dioxo-2,3-dihydrochromen-6-yl]hexanoic acid 162993043 Click to see 526.70 unknown https://doi.org/10.1248/CPB.51.802
3-[(2R,3R)-5-hydroxy-2,3-dimethyl-8-(3-methylbut-2-enyl)-8-(5-methyl-2-prop-1-en-2-ylhex-4-enyl)-4,7-dioxo-2,3-dihydrochromen-6-yl]hexanoic acid 11135173 Click to see 526.70 unknown https://doi.org/10.1002/CHIN.200349225
3-[5-Hydroxy-2,3-dimethyl-8-(3-methylbut-2-enyl)-8-(5-methyl-2-prop-1-en-2-ylhex-4-enyl)-4,7-dioxo-2,3-dihydrochromen-6-yl]hexanoic acid 12314665 Click to see CCCC(CC(=O)O)C1=C(C2=C(C(C1=O)(CC=C(C)C)CC(CC=C(C)C)C(=C)C)OC(C(C2=O)C)C)O 526.70 unknown https://doi.org/10.1248/CPB.51.802
3-[6-[(2,2-Dimethyl-3-prop-1-en-2-ylcyclobutyl)methyl]-7-hydroxy-2,3-dimethyl-6-(3-methylbut-2-enyl)-4,5-dioxo-2,3-dihydrochromen-8-yl]hexanoic acid 71436710 Click to see 526.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.08.024
3-[7-Hydroxy-2,3-dimethyl-6-(3-methylbut-2-enyl)-6-(5-methyl-2-prop-1-en-2-ylhex-5-enyl)-4,5-dioxo-2,3-dihydrochromen-8-yl]hexanoic acid 71436711 Click to see CCCC(CC(=O)O)C1=C(C(C(=O)C2=C1OC(C(C2=O)C)C)(CC=C(C)C)CC(CCC(=C)C)C(=C)C)O 526.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.08.024
methyl (3S)-3-[(2R,3R,8R)-5-hydroxy-2,3-dimethyl-8-(3-methylbut-2-enyl)-8-[(2R)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-4,7-dioxo-2,3-dihydrochromen-6-yl]-3-phenylpropanoate 163075335 Click to see CC1C(OC2=C(C1=O)C(=C(C(=O)C2(CC=C(C)C)CC(CC=C(C)C)C(=C)C)C(CC(=O)OC)C3=CC=CC=C3)O)C 574.70 unknown https://doi.org/10.1248/CPB.51.802
methyl (3S)-3-[(2R,3R,8S)-5-hydroxy-2,3-dimethyl-8-(3-methylbut-2-enyl)-8-[(2R)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-4,7-dioxo-2,3-dihydrochromen-6-yl]hexanoate 163194411 Click to see 540.70 unknown https://doi.org/10.1248/CPB.51.802
Methyl 3-[5-hydroxy-2,3-dimethyl-8-(3-methylbut-2-enyl)-8-(5-methyl-2-prop-1-en-2-ylhex-4-enyl)-4,7-dioxo-2,3-dihydrochromen-6-yl]-3-phenylpropanoate 85368304 Click to see 574.70 unknown https://doi.org/10.1248/CPB.51.802
Methyl 3-[5-hydroxy-2,3-dimethyl-8-(3-methylbut-2-enyl)-8-(5-methyl-2-prop-1-en-2-ylhex-4-enyl)-4,7-dioxo-2,3-dihydrochromen-6-yl]hexanoate 85372340 Click to see 540.70 unknown https://doi.org/10.1248/CPB.51.802
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
3-[7-Hydroxy-5-Methoxy-2,2-Dimethyl-6-(2-Methyl-But-2-Enoyl)-2H-Chromen-8-Yl]-3-Phenyl-Acrylic Acid 44354054 Click to see 434.50 unknown https://doi.org/10.1021/JM00078A001
3-[7-Hydroxy-5-methoxy-2,2-dimethyl-6-(2-methylbut-2-enoyl)chromen-8-yl]-3-phenylprop-2-enoic acid 455247 Click to see 434.50 unknown https://doi.org/10.1021/JM00078A001
Callophyllolide 6473846 Click to see CC=C(C)C(=O)C1=C(C2=C(C(=C1O)C(=CC(=O)O)C3=CC=CC=C3)OC(C=C2)(C)C)OC 434.50 unknown https://doi.org/10.1021/JM00078A001
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Pyranochromenes
(2R,3R)-5-hydroxy-2,3,8,8-tetramethyl-6-(1-phenylethenyl)-2,3-dihydropyrano[2,3-h]chromen-4-one 5318443 Click to see 376.40 unknown https://doi.org/10.1016/S0031-9422(98)00480-4
https://doi.org/10.1016/0031-9422(96)00049-0
(2R,3S)-5-hydroxy-2,3,8,8-tetramethyl-6-(1-phenylethenyl)-2,3-dihydropyrano[2,3-h]chromen-4-one 5318576 Click to see 376.40 unknown https://doi.org/10.1016/S0031-9422(98)00480-4
(2S,3R)-5-hydroxy-2,3,8,8-tetramethyl-6-(1-phenylethenyl)-2,3-dihydropyrano[2,3-h]chromen-4-one 101992979 Click to see 376.40 unknown https://doi.org/10.1016/0031-9422(96)00049-0
[Z,(-)]-3-(3,4-Dihydro-5-hydroxy-2,3,8,8-tetramethyl-4-oxo-2H,8H-benzo[1,2-b 54322117 Click to see 420.50 unknown https://doi.org/10.1002/HLCA.200900469
https://doi.org/10.1021/JM00078A001
3-(5-Hydroxy-2,3,8,8-tetramethyl-4-oxo-3,4-dihydro-2H,8H-pyrano[2,3-f]chromen-6-yl)-3-phenyl-acrylic acid 6473847 Click to see CC1C(OC2=C3C=CC(OC3=C(C(=C2C1=O)O)C(=CC(=O)O)C4=CC=CC=C4)(C)C)C 420.50 unknown https://doi.org/10.3987/COM-96-7497
https://doi.org/10.1002/HLCA.200900469
https://doi.org/10.1021/JM00078A001
Calophyllic acid 44257564 Click to see 420.50 unknown https://doi.org/10.3987/COM-96-7497
https://doi.org/10.1021/JM00078A001
Isocalophyllic acid 6473848 Click to see CC1C(OC2=C3C=CC(OC3=C(C(=C2C1=O)O)C(=CC(=O)O)C4=CC=CC=C4)(C)C)C 420.50 unknown https://doi.org/10.1002/HLCA.200900469
https://doi.org/10.1016/S0304-3835(01)00521-3
https://doi.org/10.1021/JM00078A001
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
(2R)-5,9-dihydroxy-10-methoxy-1,1,2-trimethyl-6-oxo-2H-[1]benzofuro[4,5-b]chromene-7-carboxylic acid 53343361 Click to see 386.40 unknown https://doi.org/10.1080/10286020.2010.550884
(2S)-5,9,10-trihydroxy-1,1,2-trimethyl-2H-furo[2,3-c]xanthen-6-one 163021269 Click to see 328.30 unknown https://doi.org/10.1080/10286020.2010.550884
1,3,5,6-Tetrahydroxy-7-methoxyxanthen-9-one 86180520 Click to see 290.22 unknown https://doi.org/10.1016/0031-9422(94)00733-A
1,3,6-Trihydroxy-2-methoxyxanthen-9-one 15380736 Click to see 274.22 unknown https://doi.org/10.1016/0031-9422(94)00733-A
1,3,8-Trihydroxy-7-methoxyxanthone 14839957 Click to see 274.22 unknown https://doi.org/10.1016/0031-9422(94)00733-A
1,5-Dihydroxyxanthone 5480299 Click to see C1=CC2=C(C(=C1)O)OC3=CC=CC(=C3C2=O)O 228.20 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.08.024
https://doi.org/10.1016/S0031-9422(00)94795-2
1,5,6-Trihydroxyxanthone 5281652 Click to see C1=CC(=C2C(=C1)OC3=C(C2=O)C=CC(=C3O)O)O 244.20 unknown via CMAUP database
2-Hydroxy-1-methoxyxanthone 10399460 Click to see COC1=C(C=CC2=C1C(=O)C3=CC=CC=C3O2)O 242.23 unknown https://doi.org/10.3987/COM-93-S70
4-Hydroxyxanthone 611428 Click to see C1=CC=C2C(=C1)C(=O)C3=C(O2)C(=CC=C3)O 212.20 unknown https://doi.org/10.1080/10286020.2011.600248
https://doi.org/10.3987/COM-93-S70
5,9,10-trihydroxy-1,1,2-trimethyl-2H-furo[2,3-c]xanthen-6-one 10336602 Click to see CC1C(C2=C(O1)C=C(C3=C2OC4=C(C3=O)C=CC(=C4O)O)O)(C)C 328.30 unknown https://doi.org/10.1080/10286020.2010.550884
6-(3,3-Dimethylallyl)-1,5-dihydroxyxanthone 5281624 Click to see CC(=CCC1=C(C2=C(C=C1)C(=O)C3=C(C=CC=C3O2)O)O)C 296.30 unknown https://doi.org/10.1016/S0031-9422(00)88888-3
6-Hydroxy-1,2-dimethoxyxanthen-9-one 101916324 Click to see 272.25 unknown https://doi.org/10.1016/0031-9422(94)00733-A
8-Hydroxy-7-methoxyxanthone 5464636 Click to see COC1=C(C2=C(C=C1)OC3=CC=CC=C3C2=O)O 242.23 unknown https://doi.org/10.3987/COM-93-S70
Buchanaxanthone 5481840 Click to see 258.23 unknown via CMAUP database
Dimethoxyxanthone 14189053 Click to see COC1=C(C2=C(C=C1)OC3=CC=CC=C3C2=O)OC 256.25 unknown https://doi.org/10.3987/COM-93-S70
Euxanthone 5281631 Click to see 228.20 unknown https://doi.org/10.1016/S0040-4020(01)82592-8
Swertinin 5491517 Click to see 288.25 unknown https://doi.org/10.1016/0031-9422(94)00733-A
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 2-prenylated xanthones
2-(3-Hydroxy-3-methylbutyl)-1,3,5,6-tetrahydroxyxanthone 14804158 Click to see 346.30 unknown https://doi.org/10.1016/0031-9422(91)84160-T
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 4-prenylated xanthones
11,22-Dihydroxy-7,7,19,19-tetramethyl-4-(3-methylbut-2-enyl)-2,6,20-trioxapentacyclo[12.8.0.03,12.05,10.016,21]docosa-1(14),3(12),4,8,10,15,17,21-octaen-13-one 15292596 Click to see 460.50 unknown via CMAUP database
22-Hydroxy-6,6,18,18-tetramethyl-15-(3-methylbut-2-enyl)-5,13,17-trioxapentacyclo[12.8.0.03,12.04,9.016,21]docosa-1(14),3(12),4(9),7,10,15,19,21-octaen-2-one 162866749 Click to see CC(=CCC1=C2C(=C(C3=C1OC4=C(C3=O)C5=C(C=C4)C=CC(O5)(C)C)O)C=CC(O2)(C)C)C 444.50 unknown https://doi.org/10.2174/157017811796064430
5,8,9-Trihydroxy-2,2-dimethyl-10-(3-methylbut-2-enyl)pyrano[3,2-b]xanthen-6-one 10046140 Click to see CC(=CCC1=C2C(=CC(=C1O)O)C(=O)C3=C(C4=C(C=C3O2)OC(C=C4)(C)C)O)C 394.40 unknown https://doi.org/10.1111/J.2042-7158.1996.TB03988.X
https://doi.org/10.1016/S0031-9422(00)94795-2
https://doi.org/10.1016/J.PHYTOCHEM.2004.08.024
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 8-prenylated xanthones
(2S)-5,9-dihydroxy-10-methoxy-1,1,2-trimethyl-7-(3-methylbut-2-enyl)-2H-furo[2,3-c]xanthen-6-one 162874198 Click to see 410.50 unknown https://doi.org/10.1016/S0031-9422(00)94795-2
https://doi.org/10.1016/J.PHYTOCHEM.2004.08.024
https://doi.org/10.2174/157017811796064430
5,9-Dihydroxy-7-(2-hydroxy-3-methylbut-3-enyl)-10-methoxy-1,1,2,2-tetramethylfuro[2,3-c]xanthen-6-one 163042273 Click to see 440.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257128/
5,9-dihydroxy-7-[(2S)-2-hydroxy-3-methylbut-3-enyl]-10-methoxy-1,1,2,2-tetramethylfuro[2,3-c]xanthen-6-one 163042274 Click to see 440.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257128/
7-(2,3-Dihydroxy-3-methylbutyl)-5,9-dihydroxy-10-methoxy-1,1,2,2-tetramethylfuro[2,3-c]xanthen-6-one 163089978 Click to see 458.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257128/
7-[(2S)-2,3-dihydroxy-3-methylbutyl]-5,9-dihydroxy-10-methoxy-1,1,2,2-tetramethylfuro[2,3-c]xanthen-6-one 163089979 Click to see CC1(C2=C(C=C(C3=C2OC4=C(C3=O)C(=CC(=C4OC)O)CC(C(C)(C)O)O)O)OC1(C)C)C 458.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257128/
Npc310735 102066908 Click to see 410.50 unknown https://doi.org/10.1016/S0031-9422(00)94795-2
https://doi.org/10.1016/J.PHYTOCHEM.2004.08.024
https://doi.org/10.2174/157017811796064430
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / Pyranoxanthones
(5S,6S)-5,9,14-trihydroxy-6-(2-hydroxypropan-2-yl)-18,18-dimethyl-2,7,19-trioxapentacyclo[11.8.0.03,11.04,8.015,20]henicosa-1(21),3,8,10,13,15(20),16-heptaen-12-one 162947371 Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C4=CC(=C5C(=C4O3)C(C(O5)C(C)(C)O)O)O)C 426.40 unknown https://doi.org/10.1016/0031-9422(94)00733-A
5,9,14-Trihydroxy-6-(2-hydroxypropan-2-yl)-18,18-dimethyl-2,7,19-trioxapentacyclo[11.8.0.03,11.04,8.015,20]henicosa-1(21),3,8,10,13,15(20),16-heptaen-12-one 101916325 Click to see 426.40 unknown https://doi.org/10.1016/0031-9422(94)00733-A
6-Deoxyjacareubin 5281629 Click to see 310.30 unknown https://doi.org/10.1016/0031-9422(91)84160-T
https://doi.org/10.1080/10286020.2010.550884
https://doi.org/10.3987/COM-93-S70
https://doi.org/10.1016/S0040-4020(01)82592-8
6,11-Dihydroxy-3,3-dimethyl-5-(2-methylbut-3-en-2-yl)pyrano[2,3-c]xanthen-7-one 163073804 Click to see 378.40 unknown https://doi.org/10.1080/10286020.2011.600248
https://doi.org/10.2174/157017811796064430
Blancoxanthone 11703574 Click to see CC1(C=CC2=C(C3=C(C(=C2O1)C(C)(C)C=C)OC4=C(C3=O)C=CC=C4O)O)C 378.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.08.024
https://doi.org/10.3987/COM-93-S70
https://doi.org/10.1248/CPB.53.244
Brasilixanthone B 5324261 Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C4=C(O3)C=C(C5=C4C=CC(O5)(C)C)O)C 392.40 unknown https://doi.org/10.2174/157017811796064430
Jacareubin 5281644 Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C4=C(O3)C(=C(C=C4)O)O)C 326.30 unknown https://doi.org/10.1016/0031-9422(91)84160-T
https://doi.org/10.1080/10286020.2010.550884
Macluraxanthone 5281646 Click to see 394.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.08.024
https://doi.org/10.1111/J.2042-7158.1996.TB03988.X
https://doi.org/10.1080/10286020.2011.600248
https://doi.org/10.1002/CHIN.200511228
https://doi.org/10.1016/S0031-9422(00)94795-2
Pyranojacareubin 15307925 Click to see 392.40 unknown https://doi.org/10.1080/10286020.2011.600248
> Organoheterocyclic compounds / Indoles and derivatives / Indolines
3-[(1E)-3-Methyl-2-butene-1-ylidene]-2,3-dihydro-1H-indole-2-one 5319526 Click to see CC(=CC=C1C2=CC=CC=C2NC1=O)C 199.25 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives / Dihydropyranones
(2R,7S,16R,17R)-10,10,16,17-tetramethyl-6-phenyl-3,9,15-trioxatetracyclo[12.4.0.02,7.08,13]octadeca-1(14),5,8(13),11-tetraene-4,18-dione 163187877 Click to see 404.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.08.024
(2R,7S,16R,17S)-10,10,16,17-tetramethyl-6-phenyl-3,9,15-trioxatetracyclo[12.4.0.02,7.08,13]octadeca-1(14),5,8(13),11-tetraene-4,18-dione 163186212 Click to see 404.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.08.024
10,10,16,17-Tetramethyl-6-phenyl-3,9,15-trioxatetracyclo[12.4.0.02,7.08,13]octadeca-1(14),5,8(13),11-tetraene-4,18-dione 163005461 Click to see CC1C(OC2=C(C1=O)C3C(C(=CC(=O)O3)C4=CC=CC=C4)C5=C2C=CC(O5)(C)C)C 404.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.08.024
> Organoheterocyclic compounds / Quinolizidines
(1R,14R,16S,20S)-4,14-dimethyl-24,26-diazaheptacyclo[14.6.2.12,6.12,12.013,23.020,24.010,26]hexacos-13(23)-ene 100917538 Click to see 380.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.08.024
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid esters
[4-Acetyloxy-8-formyl-14-(furan-3-yl)-6,6,9,13-tetramethyl-18-methylidene-10,16-dioxo-2,7,15-trioxatetracyclo[9.6.1.01,13.03,9]octadecan-5-yl] 3-phenylprop-2-enoate 163022693 Click to see 646.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.08.024
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
(16R,17R,18R)-6-[(2R)-butan-2-yl]-18-hydroxy-10,10,16,17-tetramethyl-3,9,15-trioxatetracyclo[12.4.0.02,7.08,13]octadeca-1(14),2(7),5,8(13),11-pentaen-4-one 162933700 Click to see CCC(C)C1=CC(=O)OC2=C1C3=C(C=CC(O3)(C)C)C4=C2C(C(C(O4)C)C)O 384.50 unknown https://doi.org/10.1002/MRC.2482
(16R,17S,18R)-6-[(2R)-butan-2-yl]-18-hydroxy-10,10,16,17-tetramethyl-3,9,15-trioxatetracyclo[12.4.0.02,7.08,13]octadeca-1(14),2(7),5,8(13),11-pentaen-4-one 162933701 Click to see CCC(C)C1=CC(=O)OC2=C1C3=C(C=CC(O3)(C)C)C4=C2C(C(C(O4)C)C)O 384.50 unknown https://doi.org/10.1002/MRC.2482
10-[(2R)-butan-2-yl]-5-methoxy-2,2-dimethyl-6-[(E)-2-methylbut-2-enoyl]pyrano[2,3-f]chromen-8-one 163189313 Click to see CCC(C)C1=CC(=O)OC2=C1C3=C(C=CC(O3)(C)C)C(=C2C(=O)C(=CC)C)OC 396.50 unknown https://doi.org/10.1002/MRC.2482
10-Butan-2-yl-5-methoxy-2,2-dimethyl-6-(2-methylbut-2-enoyl)pyrano[2,3-f]chromen-8-one 162903441 Click to see 396.50 unknown https://doi.org/10.1002/MRC.2482
6-Butan-2-yl-18-hydroxy-10,10,16,17-tetramethyl-3,9,15-trioxatetracyclo[12.4.0.02,7.08,13]octadeca-1(14),2(7),5,8(13),11-pentaen-4-one 162933699 Click to see 384.50 unknown https://doi.org/10.1002/MRC.2482
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
10-[5-(5,7-Dihydroxy-4-oxochromen-2-yl)-2-hydroxyphenyl]-5-hydroxy-8-(4-hydroxyphenyl)-2,2-dimethylpyrano[3,2-g]chromen-6-one 21582613 Click to see CC1(C=CC2=C(C3=C(C(=C2O1)C4=C(C=CC(=C4)C5=CC(=O)C6=C(C=C(C=C6O5)O)O)O)OC(=CC3=O)C7=CC=C(C=C7)O)O)C 604.60 unknown https://doi.org/10.1021/NP50088A005
Amentoflavone 5281600 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4=C(C=CC(=C4)C5=CC(=O)C6=C(C=C(C=C6O5)O)O)O)O 538.50 unknown https://doi.org/10.3987/COM-96-7497
https://doi.org/10.1021/NP50088A005
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,5,7-triol 1203 Click to see 290.27 unknown https://doi.org/10.1016/S0031-9422(00)94795-2
Epicatechin 72276 Click to see 290.27 unknown https://doi.org/10.1016/S0031-9422(00)94795-2
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Pinocembrin 68071 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
8-C-(2-Rhamnosyl-6-deoxyhexopyranosulyl)luteolin 102040777 Click to see 576.50 unknown via CMAUP database
Luteolin 8-C-E-propenoic acid 16109839 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C(=C3O2)C=CC(=O)O)O)O)O)O 356.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin 5280343 Click to see 302.23 unknown https://doi.org/10.3987/COM-96-7497
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
(1S)-1,5-anhydro-2-O-(6-deoxy-beta-L-mannopyranosyl)-1-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxo-4H-chromen-8-yl]-D-glucitol 86289611 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2C3=C(C=C(C4=C3OC(=CC4=O)C5=CC=C(C=C5)O)O)O)CO)O)O)O)O)O 578.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
Mesuein 42607965 Click to see CC1C(C(C(C(O1)OC2=C(C(=CC(=C2)C3CC(=O)C4=C(C=C(C=C4O3)O)O)C)O)O)O)OC5C(C(C(C(O5)CO)O)O)O 610.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxy-5-methoxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 102401707 Click to see 656.50 unknown via CMAUP database
5,7-dihydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 16109838 Click to see 670.60 unknown via CMAUP database
Quercetin 3-O-gentiobioside 5320834 Click to see 626.50 unknown via CMAUP database
Quercitrin 5280459 Click to see 448.40 unknown https://doi.org/10.3987/COM-96-7497
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
[(2R,3S,4R,5R,6S)-4,5-dihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxy-2-(hydroxymethyl)oxan-3-yl] (Z)-3-(4-hydroxyphenyl)prop-2-enoate 16109840 Click to see 578.50 unknown via CMAUP database
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxyoxan-2-yl]methyl (Z)-3-(4-hydroxyphenyl)prop-2-enoate 16109837 Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)O)O)O)O)O)O 578.50 unknown via CMAUP database
7-O-Beta-D-Glucopyranoside 11294177 Click to see 462.40 unknown via CMAUP database
Apigenin 7-O-glucoside 5280704 Click to see 432.40 unknown via CMAUP database
Apigenin-7-O-(6''-O-4-coumaroyl)-beta-glucopyranoside 6439941 Click to see 578.50 unknown via CMAUP database
Echinaticin 101321313 Click to see C1=CC(=CC=C1C=CC(=O)OC2C(OC(C(C2O)O)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)O)O)CO)O 578.50 unknown via CMAUP database
Tricin 7-glucoside 5322022 Click to see COC1=CC(=CC(=C1O)OC)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O 492.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Acacetin 5280442 Click to see 284.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
5-Hydroxy-7,4'-dimethoxyflavone 5281601 Click to see 298.29 unknown via CMAUP database
Velutin 5464381 Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C=C3)O)OC)O 314.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Neoflavonoids / Prenylated neoflavonoids
(16R,17R,18S)-18-(4-bromobenzoyl)-10,10,16,17-tetramethyl-6-phenyl-3,9,15-trioxatetracyclo[12.4.0.02,7.08,13]octadeca-1(14),2(7),5,8(13),11-pentaen-4-one 455256 Click to see 571.50 unknown https://doi.org/10.1021/JM00078A001
(16R,17S,18R)-18-butoxy-10,10,16,17-tetramethyl-6-phenyl-3,9,15-trioxatetracyclo[12.4.0.02,7.08,13]octadeca-1(14),2(7),5,8(13),11-pentaen-4-one 102052114 Click to see 460.60 unknown https://doi.org/10.1002/HLCA.200900469
(16R,17S,18R)-18-ethoxy-10,10,16,17-tetramethyl-6-phenyl-3,9,15-trioxatetracyclo[12.4.0.02,7.08,13]octadeca-1(14),2(7),5,8(13),11-pentaen-4-one 102052112 Click to see CCOC1C(C(OC2=C1C3=C(C(=CC(=O)O3)C4=CC=CC=C4)C5=C2C=CC(O5)(C)C)C)C 432.50 unknown https://doi.org/10.1002/HLCA.200900469
(16R,17S)-10,10,16,17-tetramethyl-6-phenyl-3,9,15-trioxatetracyclo[12.4.0.02,7.08,13]octadeca-1(14),2(7),5,8(13),11-pentaene-4,18-dione 455251 Click to see 402.40 unknown https://doi.org/10.1021/JM00078A001
https://doi.org/10.1016/S0304-3835(01)00521-3
https://doi.org/10.1016/J.PHYTOCHEM.2004.08.024
https://doi.org/10.1016/S0960-894X(98)00628-3
https://doi.org/10.1002/HLCA.200900469
https://doi.org/10.1002/CHIN.200511228
(16S,17S)-10,10,16,17-tetramethyl-6-phenyl-3,9,15-trioxatetracyclo[12.4.0.02,7.08,13]octadeca-1(14),2(7),5,8(13),11-pentaene-4,18-dione 5352084 Click to see 402.40 unknown via CMAUP database
(7R,8R)-5-hydroxy-7,8-dimethyl-10-(3-methylbut-2-enyl)-4-phenyl-7,8-dihydropyrano[3,2-g]chromene-2,6-dione 21579151 Click to see 404.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.08.024
(7S,8R)-5-hydroxy-7,8-dimethyl-10-(3-methylbut-2-enyl)-4-phenyl-7,8-dihydropyrano[3,2-g]chromene-2,6-dione 159309136 Click to see 404.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.08.024
11,12-Anhydroinophyllum P 455259 Click to see 386.40 unknown https://doi.org/10.1021/JM00078A001
12-O-Methylinophyllum D 15817181 Click to see 418.50 unknown https://doi.org/10.1002/HLCA.200900469
18-Butoxy-10,10,16,17-tetramethyl-6-phenyl-3,9,15-trioxatetracyclo[12.4.0.02,7.08,13]octadeca-1(14),2(7),5,8(13),11-pentaen-4-one 162963281 Click to see 460.60 unknown https://doi.org/10.1002/HLCA.200900469
18-Ethoxy-10,10,16,17-tetramethyl-6-phenyl-3,9,15-trioxatetracyclo[12.4.0.02,7.08,13]octadeca-1(14),2(7),5,8(13),11-pentaen-4-one 163030867 Click to see 432.50 unknown https://doi.org/10.1002/HLCA.200900469
18-Methoxy-10,10,16,17-tetramethyl-6-phenyl-3,9,15-trioxatetracyclo[12.4.0.02,7.08,13]octadeca-1(14),2(7),5,8(13),11-pentaen-4-one 85217621 Click to see 418.50 unknown https://doi.org/10.1002/HLCA.200900469
5-Hydroxy-2,2-dimethyl-6-(2-methylbutanoyl)-10-phenylpyrano[2,3-f]chromen-8-one 12314461 Click to see 404.50 unknown via CMAUP database
5-hydroxy-2,2-dimethyl-6-[(E)-2-methylbut-2-enoyl]-10-phenyl-pyrano[2,3-f]chromen-8-one 6475630 Click to see 402.40 unknown via CMAUP database
5-Hydroxy-7,8-dimethyl-10-(3-methylbut-2-enyl)-4-phenyl-7,8-dihydropyrano[3,2-g]chromene-2,6-dione 73803897 Click to see 404.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.08.024
5-Hydroxy-8,9-dimethyl-6-(3-methylbut-2-enyl)-4-phenyl-8,9-dihydropyrano[2,3-f]chromene-2,10-dione 73112696 Click to see CC1C(OC2=C(C1=O)C3=C(C(=CC(=O)O3)C4=CC=CC=C4)C(=C2CC=C(C)C)O)C 404.50 unknown https://doi.org/10.1016/S0304-3835(01)00521-3
5-Methoxy-2,2-dimethyl-10-(2-methylbut-2-enoyl)-6-phenylpyrano[3,2-g]chromen-8-one 162997360 Click to see CC=C(C)C(=O)C1=C2C(=C(C3=C1OC(C=C3)(C)C)OC)C(=CC(=O)O2)C4=CC=CC=C4 416.50 unknown https://doi.org/10.1002/HLCA.200900469
5-methoxy-2,2-dimethyl-10-[(E)-2-methylbut-2-enoyl]-6-phenylpyrano[3,2-g]chromen-8-one 102052119 Click to see 416.50 unknown https://doi.org/10.1016/S0304-3835(01)00521-3
https://doi.org/10.1002/HLCA.200900469
5-Methoxy-2,2-dimethyl-6-(2-methylbut-2-enoyl)-10-phenylpyrano[2,3-f]chromen-8-one 196983 Click to see 416.50 unknown https://doi.org/10.1002/HLCA.200900469
https://doi.org/10.1016/J.PHYTOCHEM.2004.08.024
Calophyllolide 5281392 Click to see 416.50 unknown https://doi.org/10.1002/CHIN.200349225
https://doi.org/10.1021/JM00078A001
https://doi.org/10.1016/S0304-3835(01)00521-3
https://doi.org/10.1016/J.PHYTOCHEM.2004.08.024
https://doi.org/10.1016/S0960-894X(98)00628-3
https://doi.org/10.1002/HLCA.200900469
https://doi.org/10.1002/CHIN.200511228
Inophyllolide chromanol 15223670 Click to see CC1C(OC2=C(C1O)C3=C(C(=CC(=O)O3)C4=CC=CC=C4)C5=C2C=CC(O5)(C)C)C 404.50 unknown https://doi.org/10.1002/HLCA.200900469
https://doi.org/10.1021/JM00078A001
Inophyllum A 455248 Click to see 404.50 unknown https://doi.org/10.1016/S0304-3835(01)00521-3
https://doi.org/10.1002/HLCA.200900469
https://doi.org/10.1021/JM00078A001
Inophyllum B 72412 Click to see CC1C(OC2=C(C1O)C3=C(C(=CC(=O)O3)C4=CC=CC=C4)C5=C2C=CC(O5)(C)C)C 404.50 unknown https://doi.org/10.1021/JM00078A001
https://doi.org/10.1016/S0960-894X(98)00628-3
Inophyllum B acetate 455258 Click to see CC1C(OC2=C(C1OC(=O)C)C3=C(C(=CC(=O)O3)C4=CC=CC=C4)C5=C2C=CC(O5)(C)C)C 446.50 unknown https://doi.org/10.1021/JM00078A001
Inophyllum C 455252 Click to see 402.40 unknown https://doi.org/10.1021/JM00078A001
https://doi.org/10.1016/S0304-3835(01)00521-3
https://doi.org/10.1016/J.PHYTOCHEM.2004.08.024
https://doi.org/10.1016/S0960-894X(98)00628-3
https://doi.org/10.1002/HLCA.200900469
https://doi.org/10.1002/CHIN.200511228
Inophyllum D 455250 Click to see 404.50 unknown https://doi.org/10.1016/S0040-4039(00)61999-8
https://doi.org/10.1016/S0304-3835(01)00521-3
https://doi.org/10.1021/JM00078A001
Inophyllum E 5254 Click to see CC1C(OC2=C(C1=O)C3=C(C(=CC(=O)O3)C4=CC=CC=C4)C5=C2C=CC(O5)(C)C)C 402.40 unknown https://doi.org/10.1021/JM00078A001
https://doi.org/10.1016/S0304-3835(01)00521-3
https://doi.org/10.1016/J.PHYTOCHEM.2004.08.024
https://doi.org/10.1016/S0960-894X(98)00628-3
https://doi.org/10.1002/HLCA.200900469
Inophyllum P 455249 Click to see CC1C(OC2=C(C1O)C3=C(C(=CC(=O)O3)C4=CC=CC=C4)C5=C2C=CC(O5)(C)C)C 404.50 unknown https://doi.org/10.1002/HLCA.200900469
https://doi.org/10.1021/JM00078A001
https://doi.org/10.1016/S0960-894X(98)00628-3
Inophyllum P acetate 455257 Click to see 446.50 unknown https://doi.org/10.1021/JM00078A001
> Phenylpropanoids and polyketides / Neoflavonoids / Pyranoneoflavonoids
(3R,5S,15R,16R,17R)-15-hydroxy-4,4,16,17-tetramethyl-9-phenyl-6,12,18-trioxapentacyclo[12.4.0.02,7.03,5.08,13]octadeca-1(14),2(7),8(13),9-tetraen-11-one 163005482 Click to see CC1C(OC2=C(C1O)C3=C(C(=CC(=O)O3)C4=CC=CC=C4)C5=C2C6C(C6(C)C)O5)C 404.50 unknown https://doi.org/10.1002/HLCA.200900469
(3R,5S,17R)-4,4,16,17-tetramethyl-9-phenyl-6,12,18-trioxapentacyclo[12.4.0.02,7.03,5.08,13]octadeca-1,7,9,13,15-pentaen-11-one 163023641 Click to see 386.40 unknown https://doi.org/10.1002/HLCA.200900469
15-Hydroxy-4,4,16,17-tetramethyl-9-phenyl-6,12,18-trioxapentacyclo[12.4.0.02,7.03,5.08,13]octadeca-1(14),2(7),8(13),9-tetraen-11-one 78185855 Click to see CC1C(OC2=C(C1O)C3=C(C(=CC(=O)O3)C4=CC=CC=C4)C5=C2C6C(C6(C)C)O5)C 404.50 unknown https://doi.org/10.1002/HLCA.200900469
https://doi.org/10.1021/JM00078A001
4,4,16,17-Tetramethyl-9-phenyl-6,12,18-trioxapentacyclo[12.4.0.02,7.03,5.08,13]octadeca-1,7,9,13,15-pentaen-11-one 102052118 Click to see 386.40 unknown https://doi.org/10.1002/HLCA.200900469
4,4,16,17-Tetramethyl-9-phenyl-6,12,18-trioxapentacyclo[12.4.0.02,7.03,5.08,13]octadeca-1(14),2(7),8(13),9-tetraene-11,15-dione 163192304 Click to see CC1C(OC2=C(C1=O)C3=C(C(=CC(=O)O3)C4=CC=CC=C4)C5=C2C6C(C6(C)C)O5)C 402.40 unknown https://doi.org/10.1016/S0304-3835(01)00521-3
8-methoxy-5,5-dimethyl-9-[(E)-2-methylbut-2-enoyl]-14-phenyl-3,11-dioxatetracyclo[8.4.0.02,7.04,6]tetradeca-1(10),2(7),8,13-tetraen-12-one 102193576 Click to see CC=C(C)C(=O)C1=C(C2=C(C3=C1OC(=O)C=C3C4=CC=CC=C4)OC5C2C5(C)C)OC 416.50 unknown https://doi.org/10.1016/S0304-3835(01)00521-3
Inophyllum G-1 455254 Click to see 404.50 unknown https://doi.org/10.1021/JM00078A001
Ndjilohyahlipo-ctklgvqlsa- 10319040 Click to see 404.50 unknown https://doi.org/10.1021/JM00078A001
Ndjilohyahlipo-ovtdjojusa- 455255 Click to see 404.50 unknown https://doi.org/10.1021/JM00078A001
> Phenylpropanoids and polyketides / Phenylpropanoic acids
(3R)-3-[(2R,3R,8S)-5-hydroxy-2,3-dimethyl-8-(3-methylbut-2-enyl)-8-[(2R)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-4,7-dioxo-2,3-dihydrochromen-6-yl]-3-phenylpropanoic acid 162884315 Click to see 560.70 unknown https://doi.org/10.1248/CPB.51.802
https://doi.org/10.1016/J.PHYTOCHEM.2004.08.024
(3S)-3-[(2R,3S,8S)-5-hydroxy-2,3-dimethyl-8-(3-methylbut-2-enyl)-8-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-4,7-dioxo-2,3-dihydrochromen-6-yl]-3-phenylpropanoic acid 154496764 Click to see 560.70 unknown https://doi.org/10.1248/CPB.51.802
3-[(2R,3R)-5-hydroxy-2,3-dimethyl-8-(3-methylbut-2-enyl)-8-(5-methyl-2-prop-1-en-2-ylhex-4-enyl)-4,7-dioxo-2,3-dihydrochromen-6-yl]-3-phenylpropanoic acid 10984572 Click to see 560.70 unknown https://doi.org/10.1002/CHIN.200349225
3-[5-Hydroxy-2,3-dimethyl-8-(3-methylbut-2-enyl)-8-(5-methyl-2-prop-1-en-2-ylhex-4-enyl)-4,7-dioxo-2,3-dihydrochromen-6-yl]-3-phenylpropanoic acid 12302262 Click to see 560.70 unknown https://doi.org/10.1248/CPB.51.802
https://doi.org/10.1016/J.PHYTOCHEM.2004.08.024

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