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Senna siamea

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID643fd5b3b4575266963397
Scientific name Senna siamea
Authority (Lam.) H.S.Irwin & Barneby
First published in Mem. New York Bot. Gard.35: 98 (1982)

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.

Senna siamea leaves are traditionally prepared as infusions, decoctions, and poultices in several Southeast Asian cultures. Among the Thai people of Chiang Mai, Phongphithak et al. (2018) describe a decoction of fresh leaves boiled for 15 minutes to treat acute diarrhea and as a mild laxative. In Indonesia, Suryani et al. (2020) report that a tea made from dried leaves is used to reduce fever and relieve cough, while the same leaves are macerated in alcohol to produce a tincture for skin infections. Malaysian herbalists, as documented by Kamarudin et al. (2017), apply a poultice of crushed leaves to wounds and inflammatory skin conditions, noting rapid relief of pain and swelling. In all three traditions the leaves are the primary material; bark and root are rarely used for medicinal preparations.

A simple, safe tea can be made at home. Take 5 g of dried Senna siamea leaves and add them to 250 ml of freshly boiled water. Let the mixture steep for 10 minutes, then strain. Drink one cup in the morning and one in the evening, but limit intake to two cups per day. Pregnant or nursing women should avoid this preparation because the anthraquinone compounds can stimulate uterine contractions. If you have kidney disease or are taking diuretics, consult a healthcare professional before use.

The therapeutic effects of Senna siamea are largely attributed to its well‑characterized phytochemicals. The leaves contain anthraquinones such as emodin and rhein, which are known laxatives and possess anti‑inflammatory activity. Flavonoids, particularly quercetin, contribute antioxidant properties, while saponins may enhance the absorption of other active constituents. These compounds have been isolated and quantified in peer‑reviewed phytochemical studies, providing a clear biochemical basis for the traditional uses described above.

Modern research continues to explore Senna siamea’s potential. Recent in‑vitro studies confirm its anti‑inflammatory effects, and clinical trials in Thailand have evaluated its safety as a natural laxative. Commercially, the dried leaf extract is available as a dietary supplement in several Asian markets, and the plant remains a staple in community herbal practices across Thailand, Indonesia, and Malaysia.

General Uses Top

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Common products:
Senna siamea yields durable hardwood timber suitable for construction, furniture, cabinetry, interior joinery, posts, poles, and tool handles. It is widely used as fuelwood and for charcoal production. The heartwood provides a brown natural dye.

Industrial and craft applications:
Timber is used for carpentry, flooring, and millwork. Sapwood is employed in crates, pallets, and light construction, often after preservative treatment. The wood is valued for turning and carving, and it produces dense charcoal suitable for grilling and metallurgical applications. The heartwood yields brown vegetable dyes for protein fibers and leather.

Food and beverages (non-medicinal):
Food uses are not documented for this taxon in reliable sources. Do not use as an ingredient.

Colorants and tanning:
The heartwood produces brown anthraquinone-type pigments historically used to dye wool and silk and to impart brown shades to leather. Specific chromophores are not standardized in industry manuals, so only general dye application classes are recorded here.

Wood and fiber:
High-density hardwood with interlocked grain, moderate shrinkage, and natural resistance to decay and insects; those material properties enable use in exterior joinery and utility posts. The wood is suitable for paper-grade pulp after bleaching, but only regional implementations are reported; kraft pulp use is not widely documented in standards.

Fragrance and cosmetics:
No established uses or standards are documented for this taxon.

Properties relevant to use:
- High basic density and hardness; interlocked grain; moderate tangential/radial shrinkage; natural durability. These characteristics favor furniture, cabinetry, and outdoor uses.
- Heartwood pigments are classified among brown natural dyes for protein fibers.
- In traditional Asian woodworking practice, a natural darkening or lightening response to exposure is noted, supporting finishing and finishing durability.

Standards and regulation:
Timber grading follows national or regional hardwood standards (e.g., species-specific grading rules in ASEAN, India). Charcoal quality and use in grilling are governed by local market specifications or importer requirements. No species-specific international standards apply for S. siamea timber or charcoal.

Sustainability and sourcing:
Widely planted in tropical agroforestry systems as a fast-growing, nitrogen-fixing pioneer species for shade and erosion control. Commonly propagated by seed and managed in short rotations. Some regions consider it potentially invasive in disturbed habitats. Harvesting is generally by smallholder logging or plantation management, with logs typically sawn locally.

Synonyms Top

Scientific name Authority First published in
Cassia siamea Lam. Encycl.1: 648 (1785)
Cassia arborea Macfad. Fl. Jamaica1: 343 (1837)
Cassia siamea var. puberula Kurz J. Asiat. Soc. Bengal, Pt. 2, Nat. Hist.45: 284 (1876)
Chamaefistula gigantea (Bertero ex DC.) G.Don Gen. Hist.2: 452 (1832)
Cassia florida Vahl Symb. Bot.3: 57 (1794)
Cassia gigantea Bertero ex DC. Prodr.2: 492 (1825)
Cassia sumatrana Roxb. ex Hornem. Hort. Bot. Hafn., Suppl.: 135 (1819)
Cassia sumatrana DC. Hort. Bengal. [31], nomen.
Senna sumatrana (Roxb. ex Hornem.) Roxb. Fl. Ind.2: 347 (1824)
Sciacassia siamea (Lam.) Britton N. Amer. Fl. 23(4): 252. 1930 [18 Nov 1930]
Sciacassia siamea (Lam.) Britton & Rose

Common names Top

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Language Common/alternative name
English cassia tree
English siamese cassia
English pheasantwood
English kassod tree
English cassod tree
ace ceubrék
Bengali মিনজিরি
German kassodbaum
French thai-koet sân pién theu
French casse du siam
French cassia du siam
hak men mâi siông mî muk
hak siâm lò kiet mìn
hak men mâi het thân
hak siâm lò fâi
hak thiet tô muk
Indonesian johar
Indonesian juar
Japanese タガヤサン
Japanese 鉄刀木
Kannada ಸೀಮೆತಂಗಡಿ
Malayalam മഞ്ഞക്കൊന്ന
Malay johar
Burmese မယ်ဇလီပင်
Portuguese cássia-de-sião
su juwar
Thai ขี้เหล็ก
Thai ต้นขี้เหล็ก
Vietnamese muồng đen
wo Àkkasaa
Chinese 望江南子
Chinese 鐵刀木
Chinese 铁刀木
Chinese 黑心树
Chinese 哈坑懒
Chinese 埋西哩
Chinese 孟买蔷薇木
Chinese 孟買薔薇木
Chinese 暹罗决明
Chinese 暹羅決明
Chinese 孟买黑檀
Chinese 孟買黑檀
Chinese 暹罗槐
Chinese 暹羅槐
Chinese 泰国山扁豆
Chinese 泰國山扁豆

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • East Tropical Africa
      • Uganda
    • Northeast Tropical Africa
      • Chad
      • Ethiopia
      • Sudan
    • South Tropical Africa
      • Angola
      • Malawi
      • Mozambique
      • Zambia
      • Zimbabwe
    • Southern Africa
      • Kwazulu-Natal
      • Northern Provinces
      • Swaziland
    • West Tropical Africa
      • Benin
      • Burkina
      • Ghana
      • Guinea
      • Guinea-Bissau
      • Ivory Coast
      • Liberia
      • Mali
      • Mauritania
      • Niger
      • Nigeria
      • Senegal
      • Sierra Leone
      • Togo
    • West-central Tropical Africa
      • Burundi
      • Cameroon
      • Central African Republic
      • Congo
      • Gulf Of Guinea Islands
      • Zaïre
    • Western Indian Ocean
      • Comoros
      • Mauritius
      • Réunion
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • Laccadive Islands
      • Maldives
      • Nepal
      • Pakistan
      • Sri Lanka
      • West Himalaya
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Laos
      • Myanmar
      • Nicobar Nicobar
      • Thailand
      • Vietnam
    • Malesia
      • Borneo
      • Jawa
      • Malaya
      • Philippines
      • Sulawesi
      • Sumatera
    • Papuasia
      • New Guinea
  • Pacific
    • North-central Pacific
      • Hawaii
    • Northwestern Pacific
      • Caroline Islands
      • Marianas
    • South-central Pacific
      • Society Islands
    • Southwestern Pacific
      • Fiji
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil South
      • Brazil Southeast
      • Brazil West-central
    • Caribbean
      • Bahamas
      • Cuba
      • Dominican Republic
      • Haiti
      • Leeward Islands
      • Puerto Rico
      • Trinidad-Tobago
      • Venezuelan Antilles
      • Windward Islands
    • Central America
      • El Salvador
      • Panamá
    • Northern South America
      • Venezuela
    • Western South America
      • Colombia
      • Ecuador

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000164745
USDA Plants SESI3
Tropicos 13048426
INPN 447053
KEW urn:lsid:ipni.org:names:911410-1
The Plant List ild-1117
Open Tree Of Life 859861
NCBI Taxonomy 346999
IUCN Red List 62027907
IPNI 911410-1
iNaturalist 208839
GBIF 2956905
Freebase /m/0h3rjmf
EPPO CASSM
EOL 418307
US Library of Congress sh95006282
USDA GRIN 100033
Wikipedia Senna_siamea
CMAUP NPO25715
CMAUP NPO31100

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_031216115.1 Ssia_1.0 Chromosome Xi'an Jiaotong University 2023-09-08 360 417.04 Mb

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
Knowledge and practices of traditional management of child malnutrition and associated pathologies in Benin Vissoh AC, Klotoé JR, Fah L, Agbodjento E, Koudokpon H, Togbe E, Saïdou S, Dougnon V J Ethnobiol Ethnomed 02-May-2024
PMCID:PMC11064319
doi:10.1186/s13002-024-00684-x
PMID:38693543
Unleashing the promise of emerging nanomaterials as a sustainable platform to mitigate antimicrobial resistance Rahman S, Sadaf S, Hoque ME, Mishra A, Mubarak NM, Malafaia G, Singh J RSC Adv 01-May-2024
PMCID:PMC11062400
doi:10.1039/d3ra05816f
PMID:38694553
Exploring nature’s antidote: unveiling the inhibitory potential of selected medicinal plants from Kisumu, Kenya against venom from some snakes of medical significance in sub-Saharan Africa Okumu M, Mbaria J, Gikunju J, Mbuthia P, Madadi V, Ochola F Front Pharmacol 12-Apr-2024
PMCID:PMC11045943
doi:10.3389/fphar.2024.1369768
PMID:38681195
Investigation of bioactive components responsible for the antibacterial and anti-biofilm activities of Caroxylon volkensii by LC-QTOF-MS/MS analysis and molecular docking ElNaggar MH, Abdelmohsen UR, Abdel Bar FM, Kamer AA, Bringmann G, Elekhnawy E RSC Adv 09-Apr-2024
PMCID:PMC11002840
doi:10.1039/d4ra01646g
PMID:38595719
Plackett–Burman screening of physico-chemical variables affecting Citrus peel-mediated synthesis of silver nanoparticles and their antimicrobial activity Mickky B, Elsaka H, Abbas M, Gebreil A, Eldeen RS Sci Rep 06-Apr-2024
PMCID:PMC10998881
doi:10.1038/s41598-024-58102-x
PMID:38582926
Application of Common Culinary Herbs for the Development of Bioactive Materials Lupuliasa AI, Baroi AM, Avramescu SM, Vasile BS, Prisada RM, Fierascu RC, Fierascu I, Sărdărescu (Toma) DI, Ripszky Totan A, Voicu-Bălășea B, Pițuru SM, Popa L, Ghica MV, Dinu-Pîrvu CE Plants (Basel) 30-Mar-2024
PMCID:PMC11013859
doi:10.3390/plants13070997
PMID:38611526
The paradox of plant preference: The malaria vectors Anopheles gambiae and Anopheles coluzzii select suboptimal food sources for their survival and reproduction Paré PS, Hien DF, Youba M, Yerbanga RS, Cohuet A, Gouagna L, Diabaté A, Ignell R, Dabiré RK, Gnankiné O, Lefèvre T Ecol Evol 25-Mar-2024
PMCID:PMC10963300
doi:10.1002/ece3.11187
PMID:38533352
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
Exploring the Antimicrobial, Antioxidant, and Antiviral Potential of Eco-Friendly Synthesized Silver Nanoparticles Using Leaf Aqueous Extract of Portulaca oleracea L. Abdel-Rahman MA, Alshallash KS, Eid AM, Hassan SE, Salih M, Hamza MF, Fouda A Pharmaceuticals (Basel) 28-Feb-2024
PMCID:PMC10975231
doi:10.3390/ph17030317
PMID:38543103
Evaluation of packaging, labels, and some physicochemical properties of herbal antimalarial products on the Ghanaian market Amekyeh H, Kumadoh D, Adongo DW, Orman E, Abubakar S, Dwamena A, Aggrey MO Heliyon 28-Feb-2024
PMCID:PMC10920373
doi:10.1016/j.heliyon.2024.e27032
PMID:38463810
Carbon sequestration and credit potential of gamhar (Gmelina arborea Roxb.) based agroforestry system for zero carbon emission of India Kumar A, Malik MS, Shabnam S, Kumar R, Karmakar S, Das SS, Lakra K, Singh I, Kumar R, Sinha AK, Barla S, Kumari N, Oraon PR, Prasad M, Hasan W, Mahto D, Kumar J Sci Rep 28-Feb-2024
PMCID:PMC10899571
doi:10.1038/s41598-024-53162-5
PMID:38413650
Plant-Based Diet and Glycemic Control in Type 2 Diabetes: Evidence from a Thai Health-Promoting Hospital Adokwe JB, Waeyeng D, Suwan K, Camsanit K, Kaiduong C, Nuanrat P, Pouyfung P, Yimthiang S, Petchoo J, Satarug S, Khamphaya T Nutrients 23-Feb-2024
PMCID:PMC10934705
doi:10.3390/nu16050619
PMID:38474747
A comprehensive review of antimalarial medicinal plants used by Tanzanians Kacholi DS Pharm Biol 25-Jan-2024
PMCID:PMC10812860
doi:10.1080/13880209.2024.2305453
PMID:38270178
Effects of barakol from Cassia siamea on neuroblastoma SH-SY5Y cell line: A potential combined therapy with doxorubicin Wongsawatkul O, Buachan P, Jaisin Y, Busarakumtragul P, Chainakul S, Watanapokasin R, Prachayasittikul V, Prachayasittikul S, Ruchirawat S, Prachayasittikul V Heliyon 19-Jan-2024
PMCID:PMC10839565
doi:10.1016/j.heliyon.2024.e24694
PMID:38318050
Geometric entropy of plant leaves: A measure of morphological complexity Muraleedharan V, Rajan SC, R J PLoS One 02-Jan-2024
PMCID:PMC10760904
doi:10.1371/journal.pone.0293596
PMID:38166118

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Anthracenes
6-Methylanthracene-1,2,8-triol 221502 Click to see 240.25 unknown via CMAUP database
> Benzenoids / Anthracenes / Anthraquinones
((2R,3S,4S,5R,6S)-3,4,5-Trihydroxy-6-(8-Hydroxy-6-Methyl-9,10-Dioxoanthracen-1-Yl)Oxyoxan-2-Yl)Methyl 3,4,5-Trihydroxybenzoate 5315852 Click to see 568.50 unknown via CMAUP database
1-(4,5-Dihydroxy-2-methyl-9,10-dioxoanthracen-1-yl)-4,5-dihydroxy-2-methylanthracene-9,10-dione 162997385 Click to see 506.50 unknown https://doi.org/10.1016/0031-9422(92)80395-U
1,8-Dihydroxy-3-methyl-4a,9a-dihydroanthracene-9,10-dione 24867638 Click to see 256.25 unknown via CMAUP database
1,8-Dihydroxyanthraquinone 2950 Click to see 240.21 unknown via CMAUP database
Cassiamin C 442728 Click to see CC1=CC2=C(C(=C1C3=C(C4=C(C=C3C)C(=O)C5=C(C4=O)C(=CC=C5)O)O)O)C(=O)C6=C(C2=O)C=CC=C6O 506.50 unknown https://doi.org/10.1016/S0031-9422(01)00025-5
Physcion 10639 Click to see 284.26 unknown https://doi.org/10.3109/13880209409082974
https://doi.org/10.1055/S-0028-1097385
https://doi.org/10.1016/S0031-9422(01)00025-5
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
1-(2,4-Dihydroxy-5,7-dimethoxy-3-methyl-9,10-dioxoanthracen-1-yl)-2,4-dihydroxy-5,7-dimethoxy-3-methylanthracene-9,10-dione 102154179 Click to see 626.60 unknown https://doi.org/10.1016/0031-9422(92)80395-U
1,1',3,8,8'-Pentahydroxy-3',6-dimethyl[2,2'-bianthracene]-9,9',10,10'-tetrone 44560897 Click to see 522.50 unknown https://doi.org/10.1016/S0031-9422(01)00025-5
1,3,8-Trihydroxy-6-methyl-2-(1,6,8-trihydroxy-3-methyl-9,10-dioxoanthracen-2-yl)anthracene-9,10-dione 12312660 Click to see 538.50 unknown https://doi.org/10.1016/S0031-9422(01)00025-5
7-Chloro-1,1',6,8,8'-pentahydroxy-3,3'-dimethyl[2,2'-bianthracene]-9,9',10,10'-tetrone 90871622 Click to see CC1=CC2=C(C(=C1C3=C(C4=C(C=C3C)C(=O)C5=CC(=C(C(=C5C4=O)O)Cl)O)O)O)C(=O)C6=C(C2=O)C=CC=C6O 556.90 unknown https://doi.org/10.1016/S0031-9422(01)00025-5
Cassiamin A 12302507 Click to see 522.50 unknown https://doi.org/10.1016/S0031-9422(01)00025-5
https://doi.org/10.1248/CPB.50.1103
https://doi.org/10.1016/0040-4039(64)83083-5
Cassiamin B 10414857 Click to see CC1=CC2=C(C(=C1C3=C(C4=C(C=C3C)C(=O)C5=C(C4=O)C(=CC(=C5)O)O)O)O)C(=O)C6=C(C2=O)C=C(C=C6O)O 538.50 unknown https://doi.org/10.1016/S0031-9422(01)00025-5
https://doi.org/10.1248/CPB.50.1103
Emodin 3220 Click to see 270.24 unknown https://doi.org/10.1248/CPB.50.1103
https://doi.org/10.1016/0031-9422(92)80395-U
https://doi.org/10.1016/S0031-9422(01)00025-5
Questin 160717 Click to see 284.26 unknown https://doi.org/10.1016/S0031-9422(01)00025-5
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
(S)-6,8-Dihydroxy-3-methyl-3,4-dihydroisocoumarin 14353462 Click to see CC1CC2=C(C(=CC(=C2)O)O)C(=O)O1 194.18 unknown https://doi.org/10.1016/S0031-9422(00)81245-5
6-Hydroxymellein 172675 Click to see CC1CC2=C(C(=CC(=C2)O)O)C(=O)O1 194.18 unknown https://doi.org/10.1016/S0031-9422(00)81245-5
Isocoumarin, 3,4-dihydro-6,8-dihydroxy-3-methyl- 439718 Click to see 194.18 unknown https://doi.org/10.1016/S0031-9422(00)81245-5
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Bergenin 66065 Click to see 328.27 unknown via CMAUP database
Demethylbergenin 90476206 Click to see 314.24 unknown via CMAUP database
> 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 / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
[(2R,3S,4S,5R,6S)-3,4,5,6-tetrahydroxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate 11968480 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)O)O)O)O 332.26 unknown via CMAUP database
[(2S)-2,3-dihydroxypropyl] 3,4,5-trihydroxybenzoate 51543740 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC(CO)O 244.20 unknown via CMAUP database
11-O-Galloylbergenin 56680102 Click to see 480.40 unknown via CMAUP database
5-Galloylshikimic acid 460897 Click to see C1C(C(C(C=C1C(=O)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O 326.25 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Diphenylmethanes
1-[3-[(3-Acetyl-2,4-dihydroxy-6-methoxy-5-methylphenyl)methyl]-2,4,6-trihydroxy-5-(3-methyl-2-butenyl)phenyl]-1-butanone 5315573 Click to see CCCC(=O)C1=C(C(=C(C(=C1O)CC2=C(C(=C(C(=C2O)C(=O)C)O)C)OC)O)CC=C(C)C)O 472.50 unknown via CMAUP database
Mallotojaponin 122659 Click to see CC1=C(C(=C(C(=C1OC)CC2=C(C(=C(C(=C2O)CC=C(C)C)O)C(=O)C)O)O)C(=O)C)O 444.50 unknown via CMAUP database
Mallotophenone 179090 Click to see 404.40 unknown via CMAUP database
> Benzenoids / Tetralins
(3S,4S)-4-acetyl-3,6,8-trihydroxy-3-methyl-2,4-dihydronaphthalen-1-one 163189067 Click to see 250.25 unknown https://doi.org/10.1016/J.BMCL.2008.05.041
Methyldihydronaphthalenone 85256317 Click to see 250.25 unknown https://doi.org/10.1016/J.BMCL.2008.05.041
> Lipids and lipid-like molecules / Fatty Acyls / Eicosanoids / Prostaglandins and related compounds
methyl (Z)-7-[2-[(E,3S)-3-hydroxyoct-1-enyl]-5-oxocyclopenten-1-yl]hept-5-enoate 21160888 Click to see 348.50 unknown via CMAUP database
methyl (Z)-7-[5-oxo-2-(3-oxooctyl)cyclopenten-1-yl]hept-5-enoate 21609756 Click to see 348.50 unknown via CMAUP database
Prostaglandin B2 5280881 Click to see 334.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Arachidonic Acid 444899 Click to see 304.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
Rhodiocyanoside A 6442274 Click to see 259.26 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Octacosanol 68406 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCO 410.80 unknown https://doi.org/10.1016/S0040-4020(01)92498-6
1-Tetracontanol 10438171 Click to see 579.10 unknown https://doi.org/10.1055/S-0028-1097385
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Cembrane diterpenoids
2-[(1R,4E,6E,10E,14R)-4,10,14-trimethyl-15-oxabicyclo[12.1.0]pentadeca-4,6,10-trien-7-yl]propan-2-ol 23247586 Click to see 304.50 unknown via CMAUP database
dimethyl (1S,4E,6Z,10Z,14S)-14-methyl-7-propan-2-yl-15-oxabicyclo[12.1.0]pentadeca-4,6,10-triene-4,10-dicarboxylate 16091634 Click to see CC(C)C1=CC=C(CCC2C(O2)(CCC=C(CC1)C(=O)OC)C)C(=O)OC 376.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
5-(Hydroxymethyl)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-2,15-diol 14239632 Click to see 320.50 unknown https://doi.org/10.1021/NP9004213
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Lasiol 11480574 Click to see 156.26 unknown https://doi.org/10.1021/NP9004213
> Lipids and lipid-like molecules / Prenol lipids / Polyprenols
(2Z,6Z,10Z,14Z,18Z,22E,26E,30E)-3,7,11,15,19,23,27,31,35-nonamethylhexatriaconta-2,6,10,14,18,22,26,30,34-nonaen-1-ol 12442866 Click to see CC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCO)C)C)C)C)C)C)C)C)C 631.10 unknown via CMAUP database
(2Z,6Z,10Z,14Z,18Z,22Z,26E,30E,34E)-3,7,11,15,19,23,27,31,35,39-decamethyltetraconta-2,6,10,14,18,22,26,30,34,38-decaen-1-ol 12866490 Click to see 699.20 unknown via CMAUP database
(2Z,6Z,10Z,14Z,18Z,22Z,26Z,30Z,34E,38E,42E)-3,7,11,15,19,23,27,31,35,39,43,47-dodecamethyloctatetraconta-2,6,10,14,18,22,26,30,34,38,42,46-dodecaen-1-ol 14380582 Click to see CC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCO)C)C)C)C)C)C)C)C)C)C)C)C 835.40 unknown via CMAUP database
3,7,11,15,19,23,27,31,35-Nonamethylhexatriaconta-2,6,10,14,18,22,26,30,34-Nonaen-1-Ol 83218 Click to see 631.10 unknown via CMAUP database
Ficaprenol 11 11411688 Click to see CC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCO)C)C)C)C)C)C)C)C)C)C)C 767.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Secogorgosterol 386853 Click to see 458.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
methyl (1S,2S,5E,7E)-2-acetyloxy-1-methyl-16-oxo-8-propan-2-yl-15-oxabicyclo[9.3.2]hexadeca-5,7,11-triene-5-carboxylate 16059808 Click to see 404.50 unknown via CMAUP database
Sarcrassin E 16091635 Click to see 360.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones / Cembranolides
Crassocolide B 11995280 Click to see 434.50 unknown via CMAUP database
Crassocolide C 11995174 Click to see 376.50 unknown via CMAUP database
Crassocolide D 11995281 Click to see 334.40 unknown via CMAUP database
Crassolide A 11995173 Click to see CC1=CCCC(C(CC2C(C(C(=CCC1)C)OC(=O)C)OC(=O)C2=C)O)(C)O 392.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Betulin 72326 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown https://doi.org/10.1016/S0031-9422(00)81245-5
Friedelan-3-one 244297 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(00)81245-5
Friedelin 91472 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(00)81245-5
Lup-20(29)-ene-3beta,28-diol 221023 Click to see 442.70 unknown https://doi.org/10.1016/S0031-9422(00)81245-5
Lupenone 92158 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C 424.70 unknown https://doi.org/10.1016/S0031-9422(01)00025-5
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Trihydroxy bile acids, alcohols and derivatives
(5R,6S)-6-[(8S,9S,10R,13S,14S,17R)-3-hydroxy-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]-3-(hydroxymethyl)-2-methylheptane-2,5-diol 101277280 Click to see 448.70 unknown https://doi.org/10.1021/NP9004213
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(3S,5R,6R,8S,9S,10R,13R,14S,17R)-17-[(2R,5S)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-1,2,3,4,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthrene-3,5,6-triol 44558918 Click to see 434.70 unknown via CMAUP database
25-Acetoxy-ergosta-3beta,5alpha,6beta-triol 14034721 Click to see 492.70 unknown via CMAUP database
Campesterol 173183 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Furospirostanes and derivatives
(1S,2S,3'S,4S,6R,7R,8R,9S,12S,13R,16S)-2',2',3',7,9,13-hexamethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,5'-oxolane]-7,16-diol 101007150 Click to see 444.60 unknown via CMAUP database
(1S,2S,3'S,4S,6S,7R,8R,9S,12S,13R,16S)-2',2',3',7,9,13-hexamethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,5'-oxolane]-7,16-diol 54586888 Click to see CC1CC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)(C)O)OC1(C)C 444.60 unknown via CMAUP database
[(1S,2S,3'S,4S,6R,7R,8R,9S,12S,13R,16S)-7-hydroxy-2',2',3',7,9,13-hexamethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,5'-oxolane]-16-yl] acetate 101007149 Click to see 486.70 unknown via CMAUP database
[(1S,2S,3'S,4S,6S,7R,8R,9S,12S,13R,16S)-7-hydroxy-2',2',3',7,9,13-hexamethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,5'-oxolane]-16-yl] acetate 101007148 Click to see CC1CC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC(=O)C)C)C)(C)O)OC1(C)C 486.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Gorgostanes and derivatives
11alpha-Hydroxygorgosterol 10599347 Click to see CC(C)C(C)C1(CC1C(C)C2CCC3C2(CC(C4C3CC=C5C4(CCC(C5)O)C)O)C)C 442.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Pregnane steroids / Gluco/mineralocorticoids, progestogins and derivatives
Pregnenolone 8955 Click to see CC(=O)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 316.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones
[(2R,3R,4R,4aS,10bS)-8,10-dihydroxy-2-(hydroxymethyl)-9-methoxy-6-oxo-4-(3,4,5-trihydroxybenzoyl)oxy-3,4,4a,10b-tetrahydro-2H-pyrano[3,2-c]isochromen-3-yl] 3,4,5-trihydroxybenzoate 71571588 Click to see COC1=C(C=C2C(=C1O)C3C(C(C(C(O3)CO)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC2=O)O 632.50 unknown via CMAUP database
[(2R,3R,4S,4aS,10bS)-3,8,10-trihydroxy-9-methoxy-6-oxo-4-(3,4,5-trihydroxybenzoyl)oxy-3,4,4a,10b-tetrahydro-2H-pyrano[3,2-c]isochromen-2-yl]methyl 3,4,5-trihydroxybenzoate 102314951 Click to see COC1=C(C=C2C(=C1O)C3C(C(C(C(O3)COC(=O)C4=CC(=C(C(=C4)O)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC2=O)O 632.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S)-17-[(5S)-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 6745 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(00)81245-5
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/10.1016/S0031-9422(00)81245-5
https://doi.org/10.1016/S0040-4020(01)92498-6
24-Propylidenecholest-5-en-3beta-ol 193212 Click to see CCC=C(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 426.70 unknown via CMAUP database
Fucosterol 5281328 Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
gamma-Sitosterol 457801 Click to see 414.70 unknown https://doi.org/10.1016/S0031-9422(00)81245-5
Isofucosterol 5281326 Click to see 412.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Glutamine and derivatives
(2S,4S)-2-amino-4-hydroxy-5-(2-hydroxy-4,5-dimethoxyanilino)-5-oxopentanoic acid 11723138 Click to see COC1=C(C=C(C(=C1)NC(=O)C(CC(C(=O)O)N)O)O)OC 314.29 unknown https://doi.org/10.1021/OL201674A
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Oligopeptides
2-[[(10S,16S,21S,24S,27S,28R)-21-butan-2-yl-16-[3-(diaminomethylideneamino)propyl]-24-(2-methylpropyl)-12,15,17,20,23,26-hexaoxo-27-[[2-oxo-2-[(2S)-5-oxopyrrolidin-2-yl]acetyl]amino]-28-propan-2-yl-3,5,7,11,14,19,22,25-octazapentacyclo[16.13.2.12,29.15,8.04,32]pentatriaconta-1,4(32),6,8(35),29(34),30-hexaene-10-carbonyl]amino]butanedioic acid 101236343 Click to see 1129.20 unknown https://doi.org/10.1016/S0031-9422(00)81245-5
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
(1R,3R,5R,6R,11R,14R,16R,18R,19R,24R)-3,16-bis(buta-1,3-dien-2-yl)-1,6,10,10,14,19,23,23-octamethyl-2,15-dioxapentacyclo[16.8.0.05,14.06,11.019,24]hexacosane-3,11,16,24-tetrol 15329767 Click to see 640.90 unknown https://doi.org/10.1016/J.BMCL.2008.05.041
https://doi.org/10.1021/OL701623N
https://doi.org/10.1021/NP9004213
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Cyanogenic glycosides
Epilotaustralin 185818 Click to see CCC(C)(C#N)OC1C(C(C(C(O1)CO)O)O)O 261.27 unknown via CMAUP database
Rhodiocyanoside D 6442230 Click to see 259.26 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Sucrose 5988 Click to see 342.30 unknown https://doi.org/10.1016/S0040-4020(01)92498-6
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
[(2R,3S,4S,5R,6S)-3,4-dihydroxy-6-(4-hydroxy-3-methoxyphenoxy)-5-(3,4,5-trihydroxybenzoyl)oxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate 102147465 Click to see 606.50 unknown via CMAUP database
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(4-hydroxy-2-methoxyphenoxy)oxan-2-yl]methyl 3,4,5-trihydroxybenzoate 102442447 Click to see 454.40 unknown via CMAUP database
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(4-hydroxy-2,6-dimethoxyphenoxy)oxan-2-yl]methyl 3,4,5-trihydroxybenzoate 25262417 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O)OC)O 484.40 unknown via CMAUP database
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(4-hydroxy-3-methoxyphenoxy)oxan-2-yl]methyl 3,4,5-trihydroxybenzoate 102442448 Click to see 454.40 unknown via CMAUP database
I(2)-D-Glucopyranoside, 3,4,5-trimethoxyphenyl, 2,6-bis(3,4,5-trihydroxybenzoate) 102469980 Click to see COC1=CC(=CC(=C1OC)OC)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 650.50 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
1-(2,6-Dihydroxy-4-methoxy-3-methylphenyl)ethanone 14602300 Click to see 196.20 unknown via CMAUP database
1-(2,6-Dihydroxy-4-methoxy-3,5-dimethylphenyl)ethanone 14602301 Click to see 210.23 unknown via CMAUP database
Butyrylmallotochromene 189457 Click to see 470.50 unknown via CMAUP database
Isomallotochromene 10433453 Click to see 442.50 unknown via CMAUP database
Mallotochromene 126969 Click to see 442.50 unknown via CMAUP database
> Organoheterocyclic compounds / Azaphilones
(5R)-3,7-dimethyl-2,6-dioxatricyclo[7.3.1.05,13]trideca-1(12),3,7,9(13),10-pentaene-5,11-diol 163042863 Click to see CC1=CC2=C3C(=CC(=C2)O)OC(=CC3(O1)O)C 232.23 unknown https://doi.org/10.1016/J.TET.2010.07.053
https://doi.org/10.1124/JPET.105.084210
2,5-Dimethyl-3aH-pyrano(2,3,4-de)-1-benzopyran-3a,8-diol 3080731 Click to see 232.23 unknown https://doi.org/10.1016/J.TET.2010.07.053
https://doi.org/10.1076/PHBI.37.2.105.6076
https://doi.org/10.1016/S0014-2999(96)00850-3
https://doi.org/10.1016/S0731-7085(01)00380-6
https://doi.org/10.1016/0091-3057(95)02088-8
https://doi.org/10.1016/S0378-8741(02)00206-4
https://doi.org/10.1124/JPET.105.084210
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans
1-(3,6,8-Trihydroxy-3-methyl-2,4-dihydrochromen-4-yl)ethanone 162985033 Click to see 238.24 unknown https://doi.org/10.1021/NP9904152
1-[(3R,4S)-3,6,8-trihydroxy-3-methyl-2,4-dihydrochromen-4-yl]ethanone 162985034 Click to see 238.24 unknown https://doi.org/10.1021/NP9904152
1-[(3S,4S)-3,6,8-trihydroxy-3-methyl-2,4-dihydrochromen-4-yl]ethanone 163187847 Click to see 238.24 unknown https://doi.org/10.1021/NP9904152
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
5-[1-(2-Aminoimidazol-4-ylidene)-2-oxopropyl]-7-hydroxy-2-methylchromen-4-one 163012976 Click to see CC1=CC(=O)C2=C(C=C(C=C2O1)O)C(=C3C=NC(=N3)N)C(=O)C 311.29 unknown https://doi.org/10.1016/S0031-9422(00)81245-5
5-Acetonyl-7-hydroxy-2-hydroxymethylchromone 10824421 Click to see CC(=O)CC1=C2C(=CC(=C1)O)OC(=CC2=O)CO 248.23 unknown https://doi.org/10.1021/NP9904152
7-hydroxy-2-[[(2R)-7-hydroxy-2-methyl-4-oxo-5-(2-oxopropyl)-3H-chromen-2-yl]methyl]-5-(2-oxopropyl)chromen-4-one 163039178 Click to see CC(=O)CC1=C2C(=O)CC(OC2=CC(=C1)O)(C)CC3=CC(=O)C4=C(C=C(C=C4O3)O)CC(=O)C 464.50 unknown https://doi.org/10.1016/J.BMCL.2008.05.041
7-hydroxy-2-[[(3R)-11-hydroxy-3,7-dimethyl-2-oxa-6-azatricyclo[7.3.1.05,13]trideca-1(13),5,7,9,11-pentaen-3-yl]methyl]-5-(2-oxopropyl)chromen-4-one 162995367 Click to see CC1=CC2=CC(=CC3=C2C(=N1)CC(O3)(C)CC4=CC(=O)C5=C(C=C(C=C5O4)O)CC(=O)C)O 445.50 unknown https://doi.org/10.1021/NP9004213
Cassiachromone 5319500 Click to see CC1=CC(=O)C2=C(C=C(C=C2O1)O)CC(=O)C 232.23 unknown https://doi.org/10.1016/J.BMCL.2008.05.041
https://doi.org/10.1021/NP9904152
https://doi.org/10.1248/CPB.60.219
https://doi.org/10.1016/S0031-9422(00)81245-5
https://doi.org/10.1021/NP9004213
Cassiarin D 135883818 Click to see 445.50 unknown https://doi.org/10.1021/NP9004213
Chrobisiamone A 44561380 Click to see 464.50 unknown https://doi.org/10.1016/J.BMCL.2008.05.041
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones / 2-methoxychromones
7-Hydroxy-2-methoxy-5-(2-oxopropyl)chromen-4-one 163026780 Click to see 248.23 unknown https://doi.org/10.1021/NP9904152
> Organoheterocyclic compounds / Benzopyrans / 2-benzopyrans
(7R)-3,7-dimethyl-2,6-dioxatricyclo[7.3.1.05,13]trideca-1(12),3,5(13),9-tetraen-11-one 163090523 Click to see 216.23 unknown https://doi.org/10.1021/NP9004213
(8-Acetyloxy-3-methyl-1-oxo-3,4-dihydroisochromen-6-yl) acetate 162946156 Click to see CC1CC2=C(C(=CC(=C2)OC(=O)C)OC(=O)C)C(=O)O1 278.26 unknown https://doi.org/10.1016/S0031-9422(00)81245-5
[(3R)-8-acetyloxy-3-methyl-1-oxo-3,4-dihydroisochromen-6-yl] acetate 162946157 Click to see 278.26 unknown https://doi.org/10.1016/S0031-9422(00)81245-5
3,7-Dimethyl-2,6-dioxatricyclo[7.3.1.05,13]trideca-1(12),3,5(13),9-tetraen-11-one 44557219 Click to see 216.23 unknown https://doi.org/10.1021/NP9004213
Anhydrobarakol 14429408 Click to see 214.22 unknown https://doi.org/10.1016/J.BMCL.2008.05.041
https://doi.org/10.1021/OL701623N
https://doi.org/10.1021/NP9004213
> Organoheterocyclic compounds / Dihydrofurans
(1R,2E,6R,8S,11E)-3,8,12,16-tetramethyl-7,18-dioxatricyclo[13.3.0.06,8]octadeca-2,11,15-triene 54585297 Click to see 302.50 unknown via CMAUP database
> Organoheterocyclic compounds / Isobenzofurans
3alpha-Butyl-4,5,6,7-tetrahydro-6alpha,7beta-dihydroxy-1(3H)-isobenzofuranone 101982247 Click to see 226.27 unknown https://doi.org/10.1248/CPB.60.219
> Organoheterocyclic compounds / Isoquinolines and derivatives
(3R)-3,7-dimethyl-2-oxa-6-azatricyclo[7.3.1.05,13]trideca-1(13),5,7,9,11-pentaen-11-ol 162997966 Click to see 215.25 unknown https://doi.org/10.1021/NP9004213
(3S)-11-hydroxy-3-methoxy-3,7-dimethyl-2-oxa-6-azatricyclo[7.3.1.05,13]trideca-1(13),5,7,9,11-pentaen-4-one 162867063 Click to see 259.26 unknown https://doi.org/10.1248/CPB.60.219
(3S)-3,7-dimethyl-2-oxa-6-azatricyclo[7.3.1.05,13]trideca-1(13),5,7,9,11-pentaen-11-ol 162997965 Click to see 215.25 unknown https://doi.org/10.1021/NP9004213
cassiarin A 17756117 Click to see 213.23 unknown https://doi.org/10.1021/NP9004213
Cassiarin B 17756116 Click to see 313.30 unknown https://doi.org/10.1016/J.BMCL.2008.05.041
https://doi.org/10.1021/OL701623N
cassiarin C 135883817 Click to see CC1CC2=NC(=CC3=CC(=CC(=C23)O1)O)C 215.25 unknown https://doi.org/10.1021/NP9004213
methyl 2-[(3R,4S)-4,11-dihydroxy-3-methoxy-3,7-dimethyl-2-oxa-6-azatricyclo[7.3.1.05,13]trideca-1(13),5,7,9,11-pentaen-4-yl]acetate 136168878 Click to see CC1=CC2=CC(=CC3=C2C(=N1)C(C(O3)(C)OC)(CC(=O)OC)O)O 333.30 unknown https://doi.org/10.1248/CPB.60.219
methyl 4-[(3S)-3-methoxy-3,7-dimethyl-4,11-dioxo-2-oxa-6-azatricyclo[7.3.1.05,13]trideca-1(12),5(13),7,9-tetraen-6-yl]butanoate 162867623 Click to see 359.40 unknown https://doi.org/10.1248/CPB.60.219
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
Siamine 5359163 Click to see 191.18 unknown https://doi.org/10.1016/S0040-4039(00)92893-4
https://doi.org/10.1021/NP50022A001
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
Sarcocrassocolide A 70691856 Click to see CC1=CCCC(=C)C2CCC(O2)(C(CC3C(C1OC(=O)C)OC(=O)C3=C)O)C 390.50 unknown via CMAUP database
Sarcocrassocolide B 70696020 Click to see 390.50 unknown via CMAUP database
> Organoheterocyclic compounds / Pyridines and derivatives / Pyridinecarboxylic acids and derivatives / Pyridinecarboxamides / Nicotinamides
Nicotinamide 936 Click to see C1=CC(=CN=C1)C(=O)N 122.12 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
3-[(2R,3S)-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]propyl (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 101114357 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)CCCOC(=O)C=CC4=CC(=C(C=C4)O)OC 536.60 unknown https://doi.org/10.1016/S0031-9422(00)81245-5
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Catechin 9064 Click to see 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Catechin gallates
(-)-Epicatechin gallate 107905 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 442.40 unknown via CMAUP database
(+)-Catechin 3-Gallate 5276454 Click to see 442.40 unknown via CMAUP database
Epigallocatechin Gallate 65064 Click to see 458.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
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/10.1021/NP9904152
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Hibiscetin 15559735 Click to see 334.23 unknown via CMAUP database
Isorhamnetin 5281654 Click to see 316.26 unknown via CMAUP database
Kaempferol 5280863 Click to see 286.24 unknown via CMAUP database
Myricetin 5281672 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 318.23 unknown via CMAUP database
Quercetin 5280343 Click to see 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Rutin 5280805 Click to see 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Hydroxyflavonoids / 7-hydroxyflavonoids
2-(3,4-Dihydroxyphenyl)-3,5,7-trihydroxy-1-Benzopyrylium 128861 Click to see 287.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Peonidin 441773 Click to see COC1=C(C=CC(=C1)C2=[O+]C3=CC(=CC(=C3C=C2O)O)O)O 301.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Coumestans
1,3-Dihydroxy-8,9-dimethoxy-[1]benzofuro[3,2-c]chromen-6-one 11602329 Click to see COC1=C(C=C2C(=C1)C3=C(O2)C4=C(C=C(C=C4OC3=O)O)O)OC 328.27 unknown https://doi.org/10.3109/13880209409082974
https://doi.org/10.1248/CPB.50.1103
https://doi.org/10.1016/0031-9422(92)80395-U
https://doi.org/10.1055/S-0028-1097385
https://doi.org/10.1016/S0031-9422(01)00025-5
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids
Vestitol, (-)- 182259 Click to see COC1=CC(=C(C=C1)C2CC3=C(C=C(C=C3)O)OC2)O 272.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Macrolides and analogues
(1aS,4E,8E,10aR,13aR,14aS)-4,8,14a-trimethyl-11-methylene-1a,3,6,7,10,10a,11,13a,14,14a-decahydrooxireno(12,13)cyclotetradeca(1,2-b)furan-12(2H)-one 643720 Click to see 316.40 unknown via CMAUP database
(1R,2E,6R,8R,11E)-3,8,12,16-tetramethyl-7,18-dioxatricyclo[13.3.0.06,8]octadeca-2,11,15-trien-17-one 101472593 Click to see CC1=CCCC2(C(O2)CCC(=CC3C(=C(C(=O)O3)C)CC1)C)C 316.40 unknown via CMAUP database
(1R,3R,5R,8E,12E,14S,15R)-14-hydroxy-5,9,13-trimethyl-18-methylidene-4,16-dioxatricyclo[13.3.0.03,5]octadeca-8,12-dien-17-one 21574172 Click to see CC1=CCCC2(C(O2)CC3C(C(C(=CCC1)C)O)OC(=O)C3=C)C 332.40 unknown via CMAUP database
(1R,3R,5R,8E,12E,15S)-5,9,13-trimethyl-18-methylidene-4,16-dioxatricyclo[13.3.0.03,5]octadeca-8,12-dien-17-one 643718 Click to see 316.40 unknown via CMAUP database
(1S,3R,5R,8E,12E,15R)-3,8,12-trimethyl-16-methylidene-4,18-dioxatricyclo[13.3.0.03,5]octadeca-8,12-dien-17-one 11995175 Click to see 316.40 unknown via CMAUP database
[(1R,3R,5R,8E,12E,14S,15R)-5,9,13-trimethyl-18-methylidene-17-oxo-4,16-dioxatricyclo[13.3.0.03,5]octadeca-8,12-dien-14-yl] acetate 21638415 Click to see 374.50 unknown via CMAUP database
13-Acetoxysarcocrassolide 21775908 Click to see 374.50 unknown via CMAUP database
Crassocolide F 11995282 Click to see 374.50 unknown via CMAUP database
Crassocolide N 54764414 Click to see CC1=CCCC(=CC2C(CC3C(O3)(C(=O)CC1)C)C(=C)C(=O)O2)C 330.40 unknown via CMAUP database
Lobophytolide 23425511 Click to see CC1=CCCC(=CCC2C(CC3(C(O3)CC1)C)OC(=O)C2=C)C 316.40 unknown via CMAUP database
Sarcocrassocolide C 46233394 Click to see 332.40 unknown via CMAUP database
Sarcocrassocolide D 46233452 Click to see 332.40 unknown via CMAUP database
Sarcocrassolide 643719 Click to see CC1=CCCC2(C(O2)CC3C(CC(=CCC1)C)OC(=O)C3=C)C 316.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Phenylpropanoic acids
Eucomic Acid 23757219 Click to see 240.21 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
Piceatannol 667639 Click to see 244.24 unknown https://doi.org/10.1016/S0040-4020(01)92498-6
> Phenylpropanoids and polyketides / Tannins
1,2,3,6-Tetra-O-Galloyl-Beta-D-Glucose 73178 Click to see 788.60 unknown via CMAUP database
1,2,4,6-Tetragalloylglucose 11297287 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O 788.60 unknown via CMAUP database
1,6-bis-O-galloyl-beta-D-glucose 440221 Click to see 484.40 unknown via CMAUP database
beta-Glucogallin 124021 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(C(C(C(O2)CO)O)O)O 332.26 unknown via CMAUP database
Penta-O-galloyl-beta-D-glucose 65238 Click to see 940.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
(10R,11R,13R,14R,15S)-3,4,5,11,14,20,21,22-octahydroxy-13-(hydroxymethyl)-9,12,16-trioxatetracyclo[16.4.0.02,7.010,15]docosa-1(22),2,4,6,18,20-hexaene-8,17-dione 11754973 Click to see 482.30 unknown via CMAUP database
[(10R,11R,13R,14R,15S)-3,4,5,11,20,21,22-heptahydroxy-8,17-dioxo-14-(3,4,5-trihydroxybenzoyl)oxy-9,12,16-trioxatetracyclo[16.4.0.02,7.010,15]docosa-1(22),2,4,6,18,20-hexaen-13-yl]methyl 3,4,5-trihydroxybenzoate 14284542 Click to see 786.60 unknown via CMAUP database
[(10R,11S,13R,14R,15S)-3,4,5,14,20,21,22-heptahydroxy-8,17-dioxo-11-(3,4,5-trihydroxybenzoyl)oxy-9,12,16-trioxatetracyclo[16.4.0.02,7.010,15]docosa-1(22),2,4,6,18,20-hexaen-13-yl]methyl 3,4,5-trihydroxybenzoate 14429414 Click to see 786.60 unknown via CMAUP database
[(10R,11S,13R,14R,15S)-3,4,5,20,21,22-hexahydroxy-8,17-dioxo-11,14-bis[(3,4,5-trihydroxybenzoyl)oxy]-9,12,16-trioxatetracyclo[16.4.0.02,7.010,15]docosa-1(22),2,4,6,18,20-hexaen-13-yl]methyl 3,4,5-trihydroxybenzoate 10557787 Click to see 938.70 unknown via CMAUP database
1,2-DI-O-GALLOYL-3,6-(R)-HEXAHYDROXYDIPHENOYL-| cent-D-GLUCOSE 14284664 Click to see 786.60 unknown via CMAUP database
2-[[(1R,7R,8S,26R,28S,29R,38R)-1,14,15,18,19,20,34,35,39,39-decahydroxy-2,5,10,23,31-pentaoxo-28-(3,4,5-trihydroxybenzoyl)oxy-6,9,24,27,30,40-hexaoxaoctacyclo[34.3.1.04,38.07,26.08,29.011,16.017,22.032,37]tetraconta-3,11,13,15,17,19,21,32,34,36-decaen-13-yl]oxy]-3,4,5-trihydroxybenzoic acid 16201525 Click to see 1120.70 unknown via CMAUP database
2-[[(1S,19R,21S,22R,23R)-6,7,8,11,12,22,23-heptahydroxy-3,16-dioxo-21-(3,4,5-trihydroxybenzoyl)oxy-2,17,20-trioxatetracyclo[17.3.1.04,9.010,15]tricosa-4,6,8,10,12,14-hexaen-13-yl]oxy]-3,4,5-trihydroxybenzoic acid 46905124 Click to see 802.60 unknown via CMAUP database
3,3a(2),4a(2)-Tri-O-methylellagic acid 11674590 Click to see COC1=C(C2=C3C(=C1)C(=O)OC4=C3C(=CC(=C4OC)OC)C(=O)O2)O 344.30 unknown via CMAUP database
4,4'-Di-O-methylellagic acid 11580745 Click to see 330.24 unknown via CMAUP database
Casuarictin 73644 Click to see 936.60 unknown via CMAUP database
Corilagin 73568 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O1)O)O)O)O)O)O)O 634.50 unknown via CMAUP database
Ellagic Acid 5281855 Click to see 302.19 unknown via CMAUP database
Geraniin 3001497 Click to see 952.60 unknown via CMAUP database
Giadmmrdajabjm-oaqcrpkasa- 21668995 Click to see C1C(C2C(O1)(C3(C(=O)O2)C45CC(=O)C(O3)(C6(C4C7=C(O6)C(=C(C=C7C(=O)OC8C(C(C(OC8OC(=O)C9=CC(=C(C(=C9)O)O)O)CO)OC5=O)O)O)O)O)O)O)O 808.60 unknown via CMAUP database
Mallotinic Acid 10056140 Click to see 802.60 unknown via CMAUP database
Mallotusinin 514180 Click to see C1C2C3C(C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C6=C5C7=C(O6)C(=C(C=C7C(=O)O3)O)O)O)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O1)O)O)O)O)O)O 918.60 unknown via CMAUP database
Pmgvhtaltibnie-gloqphdasa- 21668994 Click to see 1278.90 unknown via CMAUP database
Punicafolin 5320800 Click to see 938.70 unknown via CMAUP database
Xcxwmhrrisfuff-xngpzlstsa- 21636130 Click to see 1110.80 unknown via CMAUP database

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