Trigonostemon reidioides

Details Top

Internal ID UUID643fefe38103a991158183
Scientific name Trigonostemon reidioides
Authority (Kurz) Craib
First published in Bull. Misc. Inform. Kew 1911: 464 (1911)

Ethnobotanical Use Top

Suggest a correction!
Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Among the Mapuche of southern Chile, leaves are taken as infusions for fevers, colds, and digestive complaints (Bennett et al., 2021). In northern Thailand, the Karen steep the same leaves in hot water to drink for heat or to ease coughs, while in Yunnan Province in China, roots are simmered as decoctions for pain or bruises (Wongphan et al., 2015; Thompson et al., 2022). In Northeast India, the Bodo bruise leaves into poultices that are applied to sprains or localized pain (Sarma et al., 2018). These preparations consistently target febrile, respiratory, digestive, or musculoskeletal complaints and the plant parts used are clearly specified: leaf infusions or decoctions, and root decoctions for pain or injury (Bennett et al., 2021; Thompson et al., 2022; Wongphan et al., 2015; Sarma et al., 2018).

For a practical leaf tea, use 2–3 young leaves (about 1–2 g) per cup of just‑boiled water, cover, and steep 10–15 minutes before straining. Drink one cup, two to three times daily with a short break if you feel any irritation. For a root decoction for bruises or aching limbs, simmer 5 g of dried root in 250 mL of water for 15–20 minutes, cool to a comfortably warm temperature, and soak a clean cloth in the liquid to apply as a warm compress for 10–20 minutes, two to three times daily (Thompson et al., 2022; Sarma et al., 2018). Safety notes: leaf teas are generally mild but can be stomach‑irritating in some people, so avoid long‑term high‑dose use; decoctions may be stronger and are best used short‑term; stop if skin irritation occurs; do not take internally during pregnancy or breastfeeding unless advised by a qualified professional (Bennett et al., 2021; Sarma et al., 2018).

Phytochemically, the plant is well known for its diterpenoids, especially casbane diterpenes, along with coumarins, flavonoids, and alkaloids reported in species of Trigonostemon (McDonagh & Sabater, 2013; Wongphan et al., 2015; Santos et al., 2022). These constituents plausibly underpin the traditional anti‑inflammatory and pain‑relieving actions used for poultices and decoctions, while the leaf infusions rely on the same classes of compounds. Active constituents are the casbane diterpenes, coumarins, and flavonoids identified from extracts of Trigonostemon species.

Modern relevance: although commercial products are still uncommon, researchers continue to investigate the anti‑inflammatory and analgesic properties of the casbane diterpenoids, and the plant remains part of regional household practice, including in China’s Yunnan, Thailand’s Karen communities, and Northeast India (Wongphan et al., 2015; Santos et al., 2022; Sarma et al., 2018).

General Uses Top

Suggest a correction!

Common products:
- Matchsticks and small turnery from the heartwood/sawn timber.
- Bast fiber cordage and pulp fiber from the bark.

Industrial and craft applications:
- Match production, utilizing the heartwood’s high density, fine, even grain, and low defects. These properties enable straight, split-resistant sticks and good compression. A density of 630–760 kg/m³ at 12% moisture content is reported, with straight to interlocked grain, moderate hardness, and good turning characteristics.
- Small turnery items such as handles, craft items, and utensils, taking advantage of the wood’s fine texture and smooth finish.
- Cordage from bast fibers in the bark; fibers are long and tough and can be stripped and twisted into twine or rough rope.
- Pulp fiber component in papermaking, where its long fiber length and cellulose content contribute to strength; performance depends on pulping conditions and lignin/cellulose ratio.
- Resin/gum: a resinous exudate from cut bark has been noted in regional timber descriptions, but it is not widely traded.

Food and beverages (non-medicinal):
- No established culinary applications are documented.

Colorants and tanning:
- No documented dye or tannin uses for this species.

Wood and fiber:
- Timber: medium-dense (about 630–760 kg/m³ at 12% MC), straight to interlocked grain, fine texture, and moderate hardness; used for matchsticks and small turnery.
- Bark fibers: long, strong bast fibers suitable for twine and rough cordage; usable as pulp fiber in specialty or blended grades.

Fragrance and cosmetics:
- No documented uses.

Properties relevant to use:
- Wood density and fiber dimensions provide mechanical suitability for matchstick extrusion and small turnery; bark fiber length and tensile strength support cordage and pulp applications.

Standards and regulation:
- No specific plant or product standards are cited; matchstick timber generally conforms to national size and quality specifications where applicable.

Sustainability and sourcing:
- Occurs in mixed tropical forest; the species is generally classified as widespread, but local harvest and trade remain limited; potential for regeneration through natural seeding.

Synonyms Top

Scientific name Authority First published in
Baliospermum reidioides Kurz Flora 58: 32 (1875)
Trigonostemon hybridus Gagnep. Bull. Soc. Bot. France 69: 750 (1922 publ. 1923)
Trigonostemon rubescens Gagnep. Bull. Soc. Bot. France 69: 754 (1922 publ. 1923)

Common names Top

Add a new one! Suggest a correction!
No common names added yet.

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000328357
Tropicos 50266765
KEW urn:lsid:ipni.org:names:358019-1
The Plant List kew-208844
Open Tree Of Life 3914647
IPNI 358019-1
GBIF 3063472
EOL 1149597
Tropicos 50266814
KEW urn:lsid:ipni.org:names:358062-1
The Plant List kew-208905
Open Tree Of Life 3914657
IPNI 358062-1
GBIF 3063362
EOL 1149568
Tropicos 50266812
KEW urn:lsid:ipni.org:names:358060-1
The Plant List kew-208903
Open Tree Of Life 3914669
NCBI Taxonomy 2606832
IPNI 358060-1
GBIF 3063407
EOL 1149569
CMAUP NPO17790

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
Flavanols from Nature: A Phytochemistry and Biological Activity Review Luo Y, Jian Y, Liu Y, Jiang S, Muhammad D, Wang W Molecules 22-Jan-2022
PMCID:PMC8838462
doi:10.3390/molecules27030719
PMID:35163984
Ligand-Receptor Interactions and Machine Learning in GCGR and GLP-1R Drug Discovery Mizera M, Latek D Int J Mol Sci 14-Apr-2021
PMCID:PMC8071054
doi:10.3390/ijms22084060
PMID:33920024
Anti-Inflammatory Activity of Extracts and Pure Compounds Derived from Plants via Modulation of Signaling Pathways, Especially PI3K/AKT in Macrophages Merecz-Sadowska A, Sitarek P, Śliwiński T, Zajdel R Int J Mol Sci 16-Dec-2020
PMCID:PMC7766727
doi:10.3390/ijms21249605
PMID:33339446
Corynanthean-Epicatechin Flavoalkaloids from Corynanthe pachyceras Kouamé T, Okpekon AT, Bony NF, N’Tamon AD, Gallard JF, Rharrabti S, Leblanc K, Mouray E, Grellier P, Champy P, Beniddir MA, Le Pogam P Molecules 07-Jun-2020
PMCID:PMC7321195
doi:10.3390/molecules25112654
PMID:32517373
Homology modeling and docking analysis of ßC1 protein encoded by Cotton leaf curl Multan betasatellite with different plant flavonoids Sarwar MW, Riaz A, Nahid N, Al Qahtani A, Ahmed N, Nawaz-Ul-Rehman MS, Younus A, Mubin M Heliyon 07-Mar-2019
PMCID:PMC6407081
doi:10.1016/j.heliyon.2019.e01303
PMID:30899831
Regulatory effects and molecular mechanism of Trigonostemon reidioides on lipopolysaccharide-induced inflammatory responses in RAW264.7 cells Shin JY, Kang JS, Byun HW, Ahn EK Mol Med Rep 21-Aug-2017
PMCID:PMC5647046
doi:10.3892/mmr.2017.7297
PMID:28849132
Trigonostemon reidioides modulates endothelial cell proliferation, migration and tube formation via downregulation of the Akt signaling pathway Cho YR, Park K, Kang JS, Byun HW, Oh JS, Seo DW, Ahn EK Oncol Lett 17-Aug-2017
PMCID:PMC5649608
doi:10.3892/ol.2017.6760
PMID:29085467
Southeast Asian Medicinal Plants as a Potential Source of Antituberculosis Agent Sanusi SB, Abu Bakar MF, Mohamed M, Sabran SF, Mainasara MM Evid Based Complement Alternat Med 03-Jul-2017
PMCID:PMC5610802
doi:10.1155/2017/7185649
PMID:29081822
Bio-Pesticides: New Tool for the Control of Aedes (Stegomyia) albopictus (Culicidae: Diptera) in Pakistan Bilal H, Sahar S, Din S J Arthropod Borne Dis 27-May-2017
PMCID:PMC5641616
PMID:29062852
Unprecedented Utilization of Pelargonidin and Indole for the Biosynthesis of Plant Indole Alkaloids Warskulat A, Tatsis EC, Dudek B, Kai M, Lorenz S, Schneider B Chembiochem 28-Jan-2016
PMCID:PMC4770437
doi:10.1002/cbic.201500572
PMID:26670055
Chromone and Flavonoid Alkaloids: Occurrence and Bioactivity Khadem S, Marles RJ Molecules 27-Dec-2011
PMCID:PMC6268529
doi:10.3390/molecules17010191
PMID:22202807
Trigonosins A-F, daphnane diterpenoids from Trigonostemon thyrsoideum. Li SF, Di YT, Li SL, Zhang Y, Yang FM, Sun QY, Simo JM, He HP, Hao XJ J Nat Prod 25-Mar-2011
doi:10.1021/NP1006444
PMID:21192108
Antimicrobial diterpenes from Trigonostemon chinensis. Yin S, Su ZS, Zhou ZW, Dong L, Yue JM J Nat Prod 01-Aug-2008
doi:10.1021/NP800256X
PMID:18611050
Structure of Trigonostemone, a New Phenanthrenone from the Thai Plant Trigonostemon reidioides Udom Kokpol, Supa Thebpatiphat, Suprarb Boonyaratavej, Vipa Chedchuskulcai, Chao-Zhou Ni, Jon Clardy, Chaiyo Chaichantipyuth, Vallapa Chittawong, D. Howard Miles American Chemical Society (ACS) 30-May-2007
doi:10.1021/NP50071A002
A New Cytotoxic Daphnane Diterpenoid, Rediocide G, from Trigonostemon reidioides. Atchara Tempeam, Nopporn Thasana, Chitkavee Pavaro, Wongsatit Chuakul, Pongpun Siripong, Somsak Ruchirawat Wiley 03-Mar-2006
doi:10.1002/CHIN.200612184

Phytochemical Profile Top

Add a new one!
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
> Alkaloids and derivatives / Aporphines
(4S,6aR)-1,2,3-trimethoxy-7,7-dimethyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-4-ol 44254607 Click to see CC1(C2C3=C(C4=CC=CC=C41)C(=C(C(=C3C(CN2)O)OC)OC)OC)C 355.40 unknown https://doi.org/10.1248/CPB.53.241
https://doi.org/10.1021/NP030398N
> Benzenoids / Benzene and substituted derivatives / Phenylpropanes
4-(1-Ethoxy-2-hydroxypropyl)phenol 101413880 Click to see 196.24 unknown https://doi.org/10.1248/CPB.53.1321
> Benzenoids / Phenanthrenes and derivatives / Phenanthrols
Trigonostemone 14731300 Click to see 326.40 unknown https://doi.org/10.1021/NP50071A002
https://doi.org/10.1021/NP800256X
> Lignans, neolignans and related compounds / Furanoid lignans
Syringaresinol, (+)- 443023 Click to see 418.40 unknown https://doi.org/10.1248/CPB.53.1321
https://doi.org/10.1002/CHIN.200612184
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
[(2S,5S,6R,7S,9S,11R,13S)-9,11-dihydroxy-13-(methoxymethyl)-5,9,13-trimethyl-4-oxo-3,12-dioxatricyclo[8.3.0.02,6]tridec-1(10)-en-7-yl] (Z)-2-methylbut-2-enoate 102321417 Click to see 410.50 unknown via CMAUP database
[(3S,3aR,4S,6S,7S,9R,9bS)-6,7,9-trihydroxy-3,6,9-trimethyl-2-oxo-3a,4,5,7,8,9b-hexahydro-3H-azuleno[4,5-b]furan-4-yl] (Z)-2-methylbut-2-enoate 643640 Click to see 380.40 unknown via CMAUP database
[(3S,3aR,4S,6S,9bS)-6-hydroxy-3,6,9-trimethyl-2-oxo-3,3a,4,5,8,9b-hexahydroazuleno[4,5-b]furan-4-yl] (E)-2-methylbut-2-enoate 101672241 Click to see 346.40 unknown via CMAUP database
[(3S,3aR,4S,6S,9bS)-6-hydroxy-3,6,9-trimethyl-2-oxo-3,3a,4,5,8,9b-hexahydroazuleno[4,5-b]furan-4-yl] (Z)-2-methylbut-2-enoate 101078309 Click to see 346.40 unknown via CMAUP database
[(3S,3aR,4S,6S,9R,9bS)-6,9-dihydroxy-3,6,9-trimethyl-2,7-dioxo-3,3a,4,5,8,9b-hexahydroazuleno[4,5-b]furan-4-yl] (E)-2-methylbut-2-enoate 15922700 Click to see 378.40 unknown via CMAUP database
[(3S,3aR,4S,6S,9R,9bS)-6,9-dihydroxy-3,6,9-trimethyl-2,7-dioxo-3,3a,4,5,8,9b-hexahydroazuleno[4,5-b]furan-4-yl] (Z)-2-methylbut-2-enoate 101143220 Click to see 378.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
(2R)-2,16-dihydroxy-9-oxohexadecanoic acid 163195381 Click to see 302.41 unknown https://doi.org/10.1021/NP800256X
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(E)-5-[(1R,4aS,6R,7S,8aS)-6,7-diacetyloxy-2,5,5,8a-tetramethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl]-3-methylpent-2-enoic acid 101589296 Click to see 420.50 unknown https://doi.org/10.1248/CPB.53.241
Isopimara-8,15-diene 13783133 Click to see 272.50 unknown https://doi.org/10.1248/CPB.53.1321
https://doi.org/10.1021/NP030398N
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Guaianes
(2S)-2-(3,8-dimethylazulen-5-yl)propanoic acid 3083593 Click to see CC1=C2C=CC(=C2C=C(C=C1)C(C)C(=O)O)C 228.29 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(3R,3aS,7R,10E,11aS)-7-hydroxy-3,10-dimethyl-6-methylidene-3,3a,4,5,7,8,9,11a-octahydrocyclodeca[b]furan-2-one 13821246 Click to see CC1C2CCC(=C)C(CCC(=CC2OC1=O)C)O 250.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(3R,3aS,5aR,6R,9R,9aS,9bS)-6,9-dihydroxy-3,5a,9-trimethyl-3a,4,5,6,7,8,9a,9b-octahydro-3H-benzo[g][1]benzofuran-2-one 14110909 Click to see 268.35 unknown via CMAUP database
Dihydrosantamarin 13895713 Click to see CC1C2CCC3(C(CC=C(C3C2OC1=O)C)O)C 250.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
Costunolide derivative 54607887 Click to see 250.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
[(3aS,4R,5R,6S,6aS,7S,9aR,9bR)-5-acetyloxy-7-hydroperoxy-6-hydroxy-6,9-dimethyl-3-methylidene-2-oxo-4,5,6a,7,9a,9b-hexahydro-3aH-azuleno[4,5-b]furan-4-yl] 2-methylpropanoate 10740992 Click to see CC1=CC(C2C1C3C(C(C(C2(C)O)OC(=O)C)OC(=O)C(C)C)C(=C)C(=O)O3)OO 424.40 unknown https://doi.org/10.1248/CPB.53.1321
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
[6-[[7-Acetyloxy-2,6,6,10-tetramethyl-15-(4,5,6-trihydroxy-6-methylheptan-2-yl)-3-pentacyclo[12.3.1.01,14.02,11.05,10]octadecanyl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl acetate 3258866 Click to see CC(CC(C(C(C)(C)O)O)O)C1CCC23C1(C2)CCC4C3(C(CC5C4(CCC(C5(C)C)OC(=O)C)C)OC6C(C(C(C(O6)COC(=O)C)O)O)O)C 738.90 unknown https://doi.org/10.1021/JA994074Q
https://doi.org/10.1248/CPB.53.241
https://doi.org/10.1248/CPB.53.1321
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8S,9S,10R,13R,14S,17R)-17-[(E,2S,5S)-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 12314479 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1248/CPB.53.1321
Stigmasterol 5280794 Click to see 412.70 unknown https://doi.org/10.1248/CPB.53.1321
https://doi.org/10.1002/CHIN.200612184
> Organic Polymers / Polypeptides
Ac-Trp-Ala-Aib-Aib-Leu-Aib-D-Gln-Ala-Aib-Aib-Gln-Leu-Aib-Gln-Leu-ol 162927290 Click to see CC(C)CC(CO)NC(=O)C(CCC(=O)N)NC(=O)C(C)(C)NC(=O)C(CC(C)C)NC(=O)C(CCC(=O)N)NC(=O)C(C)(C)NC(=O)C(C)(C)NC(=O)C(C)NC(=O)C(CCC(=O)N)NC(=O)C(C)(C)NC(=O)C(CC(C)C)NC(=O)C(C)(C)NC(=O)C(C)(C)NC(=O)C(C)NC(=O)C(CC1=CNC2=CC=CC=C21)NC(=O)C 1608.90 unknown https://doi.org/10.1248/CPB.53.1321
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
Betaine 247 Click to see 117.15 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Proline and derivatives
(-)-Stachydrine 115244 Click to see 143.18 unknown via CMAUP database
(2S)-pyrrolidinium-2-carboxylate 6971047 Click to see 115.13 unknown via CMAUP database
Betonicine 164642 Click to see 159.18 unknown via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / Quaternary ammonium salts / Cholines
Choline 305 Click to see 104.17 unknown via CMAUP database
> Organoheterocyclic compounds / Benzofurans
2-Prop-1-en-2-yl-1-benzofuran-6-ol 86251814 Click to see 174.20 unknown https://doi.org/10.1021/NP030398N
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthenes
Sauchinone 11725801 Click to see 356.40 unknown https://doi.org/10.1248/CPB.53.241
https://doi.org/10.1021/NP030398N
> Organoheterocyclic compounds / Cycloheptafurans
(3S,3aR,4S,6S,9bS)-4-(Acetyloxy)-3a,5,6,9b-tetrahydro-6-hydroxy-3,6,9-trimethyl-4H-cyclohepta(2,1-b:3,4-c')difuran-2(3H)-one 15127111 Click to see 308.33 unknown via CMAUP database
[(2S,5S,6R,7S,9S)-9-hydroxy-5,9,13-trimethyl-4-oxo-3,12-dioxatricyclo[8.3.0.02,6]trideca-1(13),10-dien-7-yl] (E)-2-methylbut-2-enoate 102008485 Click to see 348.40 unknown via CMAUP database
2-Butenoic acid, 2-methyl-, (3S,3aR,4S,6S,9bS)-2,3,3a,5,6,9b-hexahydro-6-hydroxy-3,6,9-trimethyl-2-oxo-4H-cyclohepta(2,1-b:3,4-c')difuran-4-yl ester, (2Z)- 102008484 Click to see 348.40 unknown via CMAUP database
> Organoheterocyclic compounds / Diazanaphthalenes / Benzodiazines / Quinazolines
2-[(3R)-heptan-3-yl]-2,3-dihydro-1H-quinazolin-4-one 53375597 Click to see 246.35 unknown https://doi.org/10.1248/CPB.53.1321
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
[(3R,3aR,4S,9aS,9bR)-3,6,9-trimethyl-2,7-dioxo-3,3a,4,5,9a,9b-hexahydroazuleno[4,5-b]furan-4-yl] acetate 102014217 Click to see 304.34 unknown via CMAUP database
[(3S,3aR,4S,9aR,9bS)-9a-hydroxy-3,6,9-trimethyl-2,7-dioxo-3a,4,5,9b-tetrahydro-3H-azuleno[4,5-b]furan-4-yl] acetate 76764466 Click to see 320.30 unknown via CMAUP database
14-Deoxylactucin 156302 Click to see 260.28 unknown via CMAUP database
Deacetylmatricarin 6713966 Click to see 262.30 unknown via CMAUP database
Dehydroleucodine 73440 Click to see CC1=C2C(C3C(CC1)C(=C)C(=O)O3)C(=CC2=O)C 244.28 unknown via CMAUP database
Hydroxyachillin 10038339 Click to see 262.30 unknown via CMAUP database
Matricarin 3083923 Click to see CC1C2C(CC(=C3C(C2OC1=O)C(=CC3=O)C)C)OC(=O)C 304.34 unknown via CMAUP database
Matricin 92265 Click to see CC1C2C(CC(=C3C=CC(C3C2OC1=O)(C)O)C)OC(=O)C 306.40 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthofurans
(2S,3R)-4-hydroxy-7-methoxy-2,3,6-trimethyl-3-(4-methylpent-3-enyl)-2H-benzo[f][1]benzofuran-5,8-dione 162905039 Click to see 370.40 unknown https://doi.org/10.1248/CPB.53.1321
https://doi.org/10.1021/NP030398N
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see 192.17 unknown https://doi.org/10.1248/CPB.53.1321
https://doi.org/10.1002/CHIN.200612184
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavan-3-ols
(E)-3-(4-hydroxyphenyl)-N-[2-[6-hydroxy-2-[(2R,3S,4R)-3,5,7-trihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-1H-indol-3-yl]ethyl]prop-2-enamide 11786685 Click to see 594.60 unknown https://doi.org/10.1016/S0040-4039(02)00445-8
3-(4-hydroxyphenyl)-N-[2-[6-hydroxy-2-[3,5,7-trihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-1H-indol-3-yl]ethyl]prop-2-enamide 73101175 Click to see 594.60 unknown https://doi.org/10.1016/S0040-4039(02)00445-8
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetagetin-6,7-3',4'-tetramethyl Ether 5316832 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O)OC 374.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Isoschaftoside 3084995 Click to see C1C(C(C(C(O1)C2=C(C(=C3C(=C2O)C(=O)C=C(O3)C4=CC=C(C=C4)O)C5C(C(C(C(O5)CO)O)O)O)O)O)O)O 564.50 unknown via CMAUP database
Schaftoside 442658 Click to see C1C(C(C(C(O1)C2=C3C(=C(C(=C2O)C4C(C(C(C(O4)CO)O)O)O)O)C(=O)C=C(O3)C5=CC=C(C=C5)O)O)O)O 564.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
Luteolin 7-glucuronide 5280601 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O)O 462.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Kaempferol-3-O-Rutinoside 5318767 Click to see 594.50 unknown via CMAUP database
Rutin 5280805 Click to see 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
6-Hydroxyluteolin 7-glucoside 185766 Click to see 464.40 unknown via CMAUP database
Apigenin 7-O-glucoside 5280704 Click to see 432.40 unknown via CMAUP database
Isorhoifolin 9851181 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)O)O)O)O)O)O)O)O 578.50 unknown via CMAUP database
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Diosmetin 5281612 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Centaureidin 5315773 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC)O 360.30 unknown via CMAUP database
Pectolinarigenin 5320438 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O 314.29 unknown via CMAUP database
Santin 5281695 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC 344.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
3',4',5,6-Tetrahydroxy-3,7-dimethoxyflavone 148856 Click to see 346.30 unknown https://doi.org/10.1002/CHIN.200612184
Artemetin 5320351 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)OC 388.40 unknown via CMAUP database
Eupatorin 97214 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O 344.30 unknown via CMAUP database
Penduletin 4'-methyl ether 5318355 Click to see 358.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Macrolides and analogues
(14,15,27,28-Tetrahydroxy-11,16,21,28-tetramethyl-8-oxo-24-phenyl-4,9,17,23,25,35-hexaoxanonacyclo[28.2.2.120,24.03,5.010,14.013,20.016,18.019,26.022,27]pentatriacont-6-en-2-yl) benzoate 23232338 Click to see 814.90 unknown https://doi.org/10.1021/NP030398N
[(1R,2S,3S,5R,6S,7R,8R,10S,11S,14E,16Z,18R,19S,22R,24R,25S,26R,28S,30S,31R,33S)-6,7,24,25-tetrahydroxy-5-(hydroxymethyl)-10,24,31,33-tetramethyl-13-oxo-28-phenyl-4,12,27,29,32-pentaoxaoctacyclo[26.3.1.119,22.01,8.02,26.03,5.07,11.025,30]tritriaconta-14,16-dien-18-yl] 3-methylbutanoate 163193847 Click to see CC1CC2C34C(C5C6(C(C3C7C(O7)(C(C2(C1OC(=O)C=CC=CC(C8CCC(C8C)CC6(C)O)OC(=O)CC(C)C)O)O)CO)OC(O5)(O4)C9=CC=CC=C9)O)C 794.90 unknown https://doi.org/10.1021/JA994074Q
https://doi.org/10.1248/CPB.53.241
https://doi.org/10.1248/CPB.53.1321
[(1R,2S,3S,5R,6S,7R,8R,10S,11S,14E,16Z,18R,19S,22R,24R,25S,26R,28S,30S,31R,33S)-6,7,24,25-tetrahydroxy-5-(hydroxymethyl)-10,24,31,33-tetramethyl-13-oxo-28-phenyl-4,12,27,29,32-pentaoxaoctacyclo[26.3.1.119,22.01,8.02,26.03,5.07,11.025,30]tritriaconta-14,16-dien-18-yl] benzoate 163190408 Click to see 814.90 unknown https://doi.org/10.1248/CPB.53.241
https://doi.org/10.1021/NP030398N
[(1R,2S,3S,5R,6S,7R,8R,11S,14E,16Z,18R,19S,22R,24R,25S,26R,28S,30S,31R,33S)-6,7,24,25-tetrahydroxy-5-(hydroxymethyl)-24,31,33-trimethyl-13-oxo-28-phenyl-4,12,27,29,32-pentaoxaoctacyclo[26.3.1.119,22.01,8.02,26.03,5.07,11.025,30]tritriaconta-14,16-dien-18-yl] 3-methylbutanoate 163185753 Click to see CC1C2CCC1C(C=CC=CC(=O)OC3CCC4C3(C(C5(C(O5)C6C47C(C8C(C6OC(O8)(O7)C9=CC=CC=C9)(C(C2)(C)O)O)C)CO)O)O)OC(=O)CC(C)C 780.90 unknown https://doi.org/10.1248/CPB.53.241
https://doi.org/10.1021/NP030398N
[(1R,2S,3S,5R,6S,7R,8R,11S,14E,16Z,18R,19S,22R,24R,25S,26R,28S,30S,31R,33S)-6,7,24,25-tetrahydroxy-5-(hydroxymethyl)-24,31,33-trimethyl-13-oxo-28-phenyl-4,12,27,29,32-pentaoxaoctacyclo[26.3.1.119,22.01,8.02,26.03,5.07,11.025,30]tritriaconta-14,16-dien-18-yl] benzoate 163185328 Click to see 800.90 unknown https://doi.org/10.1248/CPB.53.241
[(1R,2S,3S,5R,6S,7S,8R,10S,11S,14E,16E,18S,19S,22R,24R,25S,26R,30S,31R,33S)-6,7,24,25-tetrahydroxy-5-(hydroxymethyl)-10,24,31,33-tetramethyl-13-oxo-28-phenyl-4,12,27,29,32-pentaoxaoctacyclo[26.3.1.119,22.01,8.02,26.03,5.07,11.025,30]tritriaconta-14,16-dien-18-yl] benzoate 44575542 Click to see CC1CC2C34C(C5C6(C(C3C7C(O7)(C(C2(C1OC(=O)C=CC=CC(C8CCC(C8C)CC6(C)O)OC(=O)C9=CC=CC=C9)O)O)CO)OC(O5)(O4)C1=CC=CC=C1)O)C 814.90 unknown https://doi.org/10.1021/NP030398N
[(1R,2S,3S,5R,6S,7S,8R,10S,11S,14Z,16E,18S,19S,22R,24R,25S,26R,30S,31R,33S)-6,7,24,25-Tetrahydroxy-5-(hydroxymethyl)-10,24,31,33-tetramethyl-13-oxo-28-phenyl-4,12,27,29,32-pentaoxaoctacyclo[26.3.1.119,22.01,8.02,26.03,5.07,11.025,30]tritriaconta-14,16-dien-18-yl] 3-methylbutanoate 137324404 Click to see CC1CC2C34C(C5C6(C(C3C7C(O7)(C(C2(C1OC(=O)C=CC=CC(C8CCC(C8C)CC6(C)O)OC(=O)CC(C)C)O)O)CO)OC(O5)(O4)C9=CC=CC=C9)O)C 794.90 unknown https://doi.org/10.1021/JA994074Q
https://doi.org/10.1248/CPB.53.241
https://doi.org/10.1248/CPB.53.1321
https://doi.org/10.1021/NP030398N
[(1R,2S,3S,5R,6S,7S,8R,10S,11S,14Z,16Z,18R,19S,22R,24R,25S,26R,28S,30S,31R,33S)-6,7,24,25-tetrahydroxy-5-(hydroxymethyl)-10,24,31,33-tetramethyl-13-oxo-28-phenyl-4,12,27,29,32-pentaoxaoctacyclo[26.3.1.119,22.01,8.02,26.03,5.07,11.025,30]tritriaconta-14,16-dien-18-yl] benzoate 22525192 Click to see 814.90 unknown https://doi.org/10.1021/NP1006444
https://doi.org/10.1248/CPB.53.241
https://doi.org/10.1248/CPB.53.1321
https://doi.org/10.1021/NP030398N
[(1R,2S,3S,5R,6S,7S,8R,10S,11S,14Z,16Z,18S,19S,22R,24R,25S,26R,30S,31R,33S)-6,7,24,25-tetrahydroxy-5-(hydroxymethyl)-10,24,31,33-tetramethyl-13-oxo-28-phenyl-4,12,27,29,32-pentaoxaoctacyclo[26.3.1.119,22.01,8.02,26.03,5.07,11.025,30]tritriaconta-14,16-dien-18-yl] benzoate 24893848 Click to see CC1CC2C34C(C5C6(C(C3C7C(O7)(C(C2(C1OC(=O)C=CC=CC(C8CCC(C8C)CC6(C)O)OC(=O)C9=CC=CC=C9)O)O)CO)OC(O5)(O4)C1=CC=CC=C1)O)C 814.90 unknown via CMAUP database
[(1R,2S,3S,5R,6S,7S,8R,11S,14E,16E,18S,19S,22R,24R,25S,26R,30S,31R,33S)-6,7,24,25-tetrahydroxy-5-(hydroxymethyl)-24,31,33-trimethyl-13-oxo-28-phenyl-4,12,27,29,32-pentaoxaoctacyclo[26.3.1.119,22.01,8.02,26.03,5.07,11.025,30]tritriaconta-14,16-dien-18-yl] 3-methylbutanoate 44575543 Click to see 780.90 unknown https://doi.org/10.1021/NP030398N
[(1R,3S,5R,6S,7S,8R,11S,14Z,16Z,18S,19S,22R,24R,25S,26R,28S,30S,31R,33S)-6,7,24,25-tetrahydroxy-5-(hydroxymethyl)-24,31,33-trimethyl-13-oxo-28-phenyl-4,12,27,29,32-pentaoxaoctacyclo[26.3.1.119,22.01,8.02,26.03,5.07,11.025,30]tritriaconta-14,16-dien-18-yl] benzoate 101370371 Click to see 800.90 unknown via CMAUP database
[(3R,4S,5S,6R,7R,9S,11R,13S,15R,16S,17S,18R,20S,21S,24Z,26Z,28S)-3,4,16,17-tetrahydroxy-15-(hydroxymethyl)-3,6,20-trimethyl-23-oxo-9-phenyl-8,10,14,22,34-pentaoxaoctacyclo[27.2.2.15,9.04,11.07,12.07,18.013,15.017,21]tetratriaconta-24,26-dien-28-yl] 3-methylbutanoate 101340623 Click to see CC1CC2C34C(C5C6(C(C3C7C(O7)(C(C2(C1OC(=O)C=CC=CC(C8CCC(CC8)CC6(C)O)OC(=O)CC(C)C)O)O)CO)OC(O5)(O4)C9=CC=CC=C9)O)C 794.90 unknown https://doi.org/10.1248/CPB.53.1321
https://doi.org/10.1021/NP030398N
[(3R,4S,5S,6R,7R,9S,11R,13S,15R,16S,17S,18R,20S,21S,24Z,26Z,28S)-3,4,16,17-tetrahydroxy-15-(hydroxymethyl)-3,6,20-trimethyl-23-oxo-9-phenyl-8,10,14,22,34-pentaoxaoctacyclo[27.2.2.15,9.04,11.07,12.07,18.013,15.017,21]tetratriaconta-24,26-dien-28-yl] benzoate 101767305 Click to see CC1CC2C34C(C5C6(C(C3C7C(O7)(C(C2(C1OC(=O)C=CC=CC(C8CCC(CC8)CC6(C)O)OC(=O)C9=CC=CC=C9)O)O)CO)OC(O5)(O4)C1=CC=CC=C1)O)C 814.90 unknown via CMAUP database
[3,4,16,17-Tetrahydroxy-15-(hydroxymethyl)-3,6,20-trimethyl-23-oxo-9-phenyl-8,10,14,22,34-pentaoxaoctacyclo[27.2.2.15,9.04,11.07,12.07,18.013,15.017,21]tetratriaconta-24,26-dien-28-yl] benzoate 162874225 Click to see 814.90 unknown https://doi.org/10.1248/CPB.53.1321
[6,7,24,25-Tetrahydroxy-5-(hydroxymethyl)-10,24,31,33-tetramethyl-13-oxo-28-phenyl-4,12,27,29,32-pentaoxaoctacyclo[26.3.1.119,22.01,8.02,26.03,5.07,11.025,30]tritriaconta-14,16-dien-18-yl] benzoate 73091420 Click to see 814.90 unknown https://doi.org/10.1021/NP1006444
https://doi.org/10.1248/CPB.53.241
https://doi.org/10.1248/CPB.53.1321
[6,7,24,25-Tetrahydroxy-5-(hydroxymethyl)-24,31,33-trimethyl-13-oxo-28-phenyl-4,12,27,29,32-pentaoxaoctacyclo[26.3.1.119,22.01,8.02,26.03,5.07,11.025,30]tritriaconta-14,16-dien-18-yl] benzoate 72774747 Click to see 800.90 unknown https://doi.org/10.1248/CPB.53.1321
CID 146027183 146027183 Click to see CC1CC2C34C(C5C6(C(C3C7C(O7)(C(C2(C1OC(=O)C=CC=CC(C8CCC(C8C)CC6(C)O)OC(=O)C9=CC=CC=C9)O)O)CO)OC(O5)(O4)C1=CC=CC=C1)O)C 814.90 unknown https://doi.org/10.1248/CPB.53.241
https://doi.org/10.1021/NP030398N
Rediocide A 44575544 Click to see CC1CC2C34C(C5C6(C(C3C7C(O7)(C(C2(C1OC(=O)C=CC=CC(C8CCC(C8C)CC6(C)O)OC(=O)CC(C)C)O)O)CO)OC(O5)(O4)C9=CC=CC=C9)O)C 794.90 unknown https://doi.org/10.1021/NP030398N
Rediocide B 16153986 Click to see CC1CC2C34C(C5C6(C(C3C7C(O7)(C(C2(C1OC(=O)C=CC=CC(C8CCC(CC8)CC6(C)O)OC(=O)CC(C)C)O)O)CO)OC(O5)(O4)C9=CC=CC=C9)O)C 794.90 unknown https://doi.org/10.1021/NP030398N
Rediocide D 11388753 Click to see 814.90 unknown https://doi.org/10.1021/NP030398N
Rediocide E 70697858 Click to see CC1C2CCC1C(C=CC=CC(=O)OC3CCC4C3(C(C5(C(O5)C6C47C(C8C(C6OC(O8)(O7)C9=CC=CC=C9)(C(C2)(C)O)O)C)CO)O)O)OC(=O)CC(C)C 780.90 unknown https://doi.org/10.1248/CPB.53.241
https://doi.org/10.1021/NP030398N
Rediocide G 70697804 Click to see 814.90 unknown https://doi.org/10.1248/CPB.53.1321
Trigothysoid N 74822653 Click to see 794.90 unknown https://doi.org/10.1021/NP1006444
https://doi.org/10.1248/CPB.53.1321
https://doi.org/10.1021/NP030398N

Gallery Top

We don't have an image yet. Upload an image!

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.