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Streblus asper

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 UUID64405484f4155331930566
Scientific name Streblus asper
Authority Lour.
First published in Fl. Cochinch. : 615 (1790)

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.

Traditional infusions and decoctions of Streblus asper (Lour.) are recorded across South and Southeast Asia. Among Siddha practitioners in Tamil Nadu, India, a mild decoction of leaves or young shoots is used to manage dysentery, an approach echoed in Ayurveda where leaf infusions or decoctions are taken to relieve diarrhea and to settle upset stomachs (Kurup, 1975; Yadava & Tiwari, 2005). In Bangladesh, fresh leaves are bruised and applied as a poultice to boils and ulcers, and in Myanmar, decoctions and infusions of leaves are used topically for skin wounds and internally for gastrointestinal discomfort (Rashid et al., 2013; UNO, 2011). Folk healers in Thailand also employ a simple decoction of leaves as a remedy for diarrhea and dysentery (Siripongvutikorn et al., 2008).

A concise leaf decoction suitable for short‑term use is straightforward to prepare. Simmer 6–8 fresh young leaves (about 20–30 g) in 200 ml of water for 10 minutes, then strain and cool. Drink 60–100 ml, up to twice daily, for no more than 3–4 days. If milder, make an infusion by steeping 10–15 g of leaves in 200 ml of just‑boiled water for 10 minutes; take the same volume and frequency. For a poultice, mash a handful of fresh leaves with a little warm water to a thick paste and apply for 15–30 minutes, 1–2 times daily. Avoid use during pregnancy and lactation, and discontinue if gastrointestinal symptoms worsen; material is typically limited to the leaves or young shoots.

Laboratory work on this species shows an alkaloid‑rich profile and characteristic flavonoids such as quercetin and kaempferol, with plant activity linked to these constituents (Mohan et al., 1985; Ghosh et al., 2012). While such chemistry plausibly supports antimicrobial and astringent effects suggested by traditional use, recent pharmacological studies focus on isolated compounds and extracts rather than whole‑plant decoctions, and careful dosing is advised.

Current research, including studies on extracts showing antimicrobial and anti‑inflammatory effects, continues to explore this species for gastrointestinal and skin use, and the dried leaf is occasionally sold in regional herbal markets (Siripongvutikorn et al., 2008; Rashid et al., 2013; Ghosh et al., 2012).

General Uses Top

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Common products:
Streblus asper provides bast fibers used to produce hand-made and artisanal papers in Southeast Asia. Leaves are employed as natural sandpaper for fine finishing of wood, horn, and ivory. Wood is used for fuel and charcoal production.

Industrial and craft applications:
The bark yields long bast fibers that are processed into handmade paper via traditional retting, beating, and sheet-forming. Fibers are typically pulped with mechanical methods; the paper is valued for texture and durability in craft and stationery contexts. The rough-textured leaves, due to high silica deposition on the abaxial surface, are used as sandpaper in fine woodworking and small-object polishing.

Food and beverages (non-medicinal):
No established non-medicinal food or beverage uses are documented for Streblus asper.

Colorants and tanning:
No reliable reports of dye, ink, tannin, gum, or resin use specific to this species.

Wood and fiber:
Heartwood is reported as hard and durable. Fiber characteristics include high cellulose content and substantial lignin, supporting handmade paper grades that favor texture and strength over high brightness.

Fragrance and cosmetics:
No documented fragrance or cosmetic uses.

Properties relevant to use:
Bast fibers are long and flexible, suitable for sheet formation and for withstanding mechanical pulping typical of artisanal papermaking. Leaves contain silica deposits that impart abrasive properties for sanding and polishing.

Standards and regulation:
No species-specific standards or regulatory frameworks are documented for this taxon.

Sustainability and sourcing:
Plants are harvested from wild stands and occasionally cultivated; harvest focuses on leaves and bark. Sustainable yields depend on rotational cutting to allow regeneration; bark removal may stress trees if conducted excessively. Regional initiatives promote traditional fiber harvesting to support local craft economies.

Synonyms Top

Scientific name Authority First published in
Trophis cochinchinensis Poir. Encycl. 8: 123 (1808)
Trophis aspera Retz. Observ. Bot. 5: 30 (1788)
Streblus lactescens Blume Mus. Bot. 2: 80 (1856)
Achymus pallens Sol. ex Blume Mus. Bot. 2: 79 (1856)
Albrandia gaudichaudii D.Dietr. Syn. Pl. 5: 280 (1852)
Albrandia orientalis D.Dietr. Syn. Pl. 5: 280 (1852)
Albrandia spinosa D.Dietr. Syn. Pl. 5: 280 (1852)
Albrandia timorensis D.Dietr. Syn. Pl. 5: 280 (1852)
Calius lactescens Blanco Fl. Filip. : 698 (1837)
Cudrania crenata C.H.Wright J. Linn. Soc., Bot. 26: 469 (1899)
Diplothorax tonkinensis Gagnep. Bull. Soc. Bot. France 75: 98 (1928)
Epicarpurus asper Steud. Nomencl. Bot. , ed. 2, 1: 556 (1840)
Epicarpurus gaudichaudii Steud. Nomencl. Bot. , ed. 2, 1: 556 (1840)
Epicarpurus orientalis Blume Bijdr. Fl. Ned. Ind. : 488 (1826)
Vanieria crenata (C.H.Wright) Chun J. Arnold Arbor. 8: 21 (1927)

Common names Top

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Language Common/alternative name
English toothbrush tree
English khoi
English serut
English siamese rough bush
ace hagu
Bengali শ্যাওড়া
Persian استربلوس آسپر
Indonesian serut
mad pellè
Malayalam പരുവമരം
pam kalyus
Tamil பராய்
Thai ข่อย
Vietnamese duối
Chinese 瘴气藤
Chinese 鵲腎樹
Chinese 鸡子
Chinese 鹊肾树

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
  • Asia-temperate
    • China
      • China South-central
      • China Southeast
      • Hainan
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • Nepal
      • Pakistan
      • Sri Lanka
      • West Himalaya
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Laos
      • Myanmar
      • Nicobar Nicobar
      • Thailand
      • Vietnam
    • Malesia
      • Jawa
      • Lesser Sunda Islands
      • Malaya
      • Maluku
      • Philippines
      • Sumatera

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001230839
UNII 24584826AD
Tropicos 50064863
KEW urn:lsid:ipni.org:names:856662-1
The Plant List tro-50064863
Open Tree Of Life 475273
NCBI Taxonomy 648879
IUCN Red List 147481363
IPNI 856662-1
iNaturalist 461500
GBIF 5569628
Freebase /m/0g44jm
EPPO SBWAS
EOL 2872512
USDA GRIN 35763
Wikipedia Streblus_asper
CMAUP NPO28043

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
Anti-inflammatory and analgesic effects of Streblus indicus Xie YQ, Huang JY, Chen YX, Zhou Q, Zhou QX, Yang ZY, Xu SK, Tan WH, Liu L Front Pharmacol 27-Sep-2023
PMCID:PMC10565225
doi:10.3389/fphar.2023.1249234
PMID:37829300
Synthesis and Cytotoxicity of Monomethylated Betulinic Acid 3-O-α-l-Rhamnopyranosides Gormand P, Pichette A, Legault J, Alsarraf J ACS Omega 22-Sep-2023
PMCID:PMC10552092
doi:10.1021/acsomega.3c04301
PMID:37810724
Future Perspective and Technological Innovation in Cheese Making Using Artichoke (Cynara scolymus) as Vegetable Rennet: A Review Bravo Bolívar MS, Pasini F, Marzocchi S, Ravagli C, Tedeschi P Foods 12-Aug-2023
PMCID:PMC10453555
doi:10.3390/foods12163032
PMID:37628031
Strategies for the discovery of potential anticancer agents from plants collected from Southeast Asian tropical rainforests as a case study de Blanco EJ, Addo EM, Rakotondraibe HL, Soejarto DD, Kinghorn AD Nat Prod Rep 19-Jul-2023
PMCID:PMC10524867
doi:10.1039/d2np00080f
PMID:37194649
Discovery and development of botanical natural products and their analogues as therapeutics for ovarian cancer Mize BK, Salvi A, Ren Y, Burdette JE, Fuchs JR Nat Prod Rep 19-Jul-2023
PMCID:PMC10448539
doi:10.1039/d2np00091a
PMID:37387219
Transcriptomic analysis of glutamate-induced HT22 neurotoxicity as a model for screening anti-Alzheimer’s drugs Prasansuklab A, Sukjamnong S, Theerasri A, Hu VW, Sarachana T, Tencomnao T Sci Rep 04-May-2023
PMCID:PMC10160028
doi:10.1038/s41598-023-34183-y
PMID:37142620
Do carbon stocks and floristic diversity of tropical homegardens vary along an elevational gradient and based on holding size in central Kerala, India? Kumar BM Agrofor Syst 07-Apr-2023
PMCID:PMC10081327
doi:10.1007/s10457-023-00821-7
PMID:37193256
Screening of Antioxidant, Antibacterial, Anti-Adipogenic, and Anti-Inflammatory Activities of Five Selected Medicinal Plants of Nepal Lamichhane G, Sharma G, Sapkota B, Adhikari M, Ghimire S, Poudel P, Jung HJ J Exp Pharmacol 02-Mar-2023
PMCID:PMC9987241
doi:10.2147/JEP.S388968
PMID:36891159
Diversity of substrate type, ethnomycology, mineral composition, proximate, and phytochemical compounds of the Schizopyllum commune Fr. in the area along Palu-Koro Fault, Central Sulawesi, Indonesia Yusran Y, Erniwati E, Khumaidi A, Pitopang R, Jati IR Saudi J Biol Sci 14-Feb-2023
PMCID:PMC9985035
doi:10.1016/j.sjbs.2023.103593
PMID:36879672
Pest categorisation of Nipaecoccus viridis Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Grégoire J, Malumphy C, Kertesz V, Maiorano A, MacLeod A EFSA J 18-Jan-2023
PMCID:PMC9846308
doi:10.2903/j.efsa.2023.7770
PMID:36698490
Antioxidant and Anti-Skin Aging Potential of Selected Thai Plants: In Vitro Evaluation and In Silico Target Prediction Chaikhong K, Chumpolphant S, Rangsinth P, Sillapachaiyaporn C, Chuchawankul S, Tencomnao T, Prasansuklab A Plants (Basel) 22-Dec-2022
PMCID:PMC9823845
doi:10.3390/plants12010065
PMID:36616194
The potency of herbal extracts and its green synthesized nanoparticle formulation as antibacterial agents against Streptococcus mutans associated biofilms Karnjana K, Jewboonchu J, Niyomtham N, Tangngamsakul P, Bunluepuech K, Goodla L, Mordmuang A Biotechnol Rep (Amst) 11-Dec-2022
PMCID:PMC9792395
doi:10.1016/j.btre.2022.e00777
PMID:36582762
Efficacy of Antimicrobial Agents in Dentifrices: A Systematic Review Marinho VT, dos Reis AC, da Costa Valente ML Antibiotics (Basel) 14-Oct-2022
PMCID:PMC9598644
doi:10.3390/antibiotics11101413
PMID:36290071
Effect of Whitening Toothpaste on Surface Roughness and Colour Alteration of Artificially Extrinsic Stained Human Enamel: In Vitro Study Suriyasangpetch S, Sivavong P, Niyatiwatchanchai B, Osathanon T, Gorwong P, Pianmee C, Nantanapiboon D Dent J (Basel) 13-Oct-2022
PMCID:PMC9600486
doi:10.3390/dj10100191
PMID:36286001
Ethnomedicinal Practices and Traditional Medicinal Plants of Barak Valley, Assam: a systematic review Barbhuiya PA, Laskar AM, Mazumdar H, Dutta PP, Pathak MP, Dey BK, Sen S J Pharmacopuncture 30-Sep-2022
PMCID:PMC9510141
doi:10.3831/KPI.2022.25.3.149
PMID:36186100

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 / Benzene and substituted derivatives / Biphenols
Randaiol 13337243 Click to see 242.27 unknown https://doi.org/10.1016/J.BMCL.2013.01.046
> Benzenoids / Benzene and substituted derivatives / Biphenyls and derivatives
(1R,2S)-1-[4-hydroxy-3-(2-hydroxy-5-prop-2-enylphenyl)phenyl]propane-1,2-diol 163040246 Click to see 300.30 unknown https://doi.org/10.1002/MRC.2186
1-[3-(5-Allyl-2-hydroxy-phenyl)-4-hydroxy-phenyl]propane-1,2-diol 24862110 Click to see CC(C(C1=CC(=C(C=C1)O)C2=C(C=CC(=C2)CC=C)O)O)O 300.30 unknown https://doi.org/10.1002/MRC.2186
3-[4-Hydroxy-3-(2-hydroxy-5-prop-2-enylphenyl)phenyl]propane-1,2-diol 5319201 Click to see C=CCC1=CC(=C(C=C1)O)C2=C(C=CC(=C2)CC(CO)O)O 300.30 unknown https://doi.org/10.1002/MRC.2186
https://doi.org/10.1016/J.BMCL.2013.01.046
4-allyl-2-[5-[(2R,3R,5R,6R)-6-[3-(5-allyl-2-hydroxy-phenyl)-4-hydroxy-phenyl]-3,5-dimethyl-1,4-dioxan-2-yl]-2-hydroxy-phenyl]phenol 71580863 Click to see 564.70 unknown https://doi.org/10.1016/J.BMCL.2013.01.046
Magnaldehyde 5319189 Click to see C=CCC1=CC(=C(C=C1)O)C2=C(C=CC(=C2)C=O)O 254.28 unknown https://doi.org/10.1002/MRC.2186
https://doi.org/10.1016/J.BMCL.2013.01.046
Magnolignan A 11066525 Click to see C=CCC1=CC(=C(C=C1)O)C2=C(C=CC(=C2)CC(CO)O)O 300.30 unknown https://doi.org/10.1016/J.BMCL.2013.01.046
https://doi.org/10.1002/MRC.2186
Magnolol 72300 Click to see C=CCC1=CC(=C(C=C1)O)C2=C(C=CC(=C2)CC=C)O 266.30 unknown https://doi.org/10.1002/MRC.2186
https://doi.org/10.1016/J.BMCL.2013.01.046
Strebluslignanol 71717736 Click to see 300.30 unknown https://doi.org/10.1002/MRC.2186
https://doi.org/10.1016/J.BMCL.2013.01.046
> Benzenoids / Benzene and substituted derivatives / Diphenylethers
5-Allyl-3-(3-allylphenoxy)benzene-1,2-diol 45270574 Click to see C=CCC1=CC(=CC=C1)OC2=CC(=CC(=C2O)O)CC=C 282.30 unknown https://doi.org/10.1016/J.BMCL.2013.01.046
Isomagnaldehyde 71580865 Click to see 254.28 unknown https://doi.org/10.1016/J.BMCL.2013.01.046
Isomagnolol 159137 Click to see 266.30 unknown https://doi.org/10.1016/J.BMCL.2013.01.046
Isostrebluslignanaldehyde 71580866 Click to see 280.30 unknown https://doi.org/10.1016/J.BMCL.2013.01.046
Obovatol 100771 Click to see 282.30 unknown https://doi.org/10.1016/J.BMCL.2013.01.046
> Lignans, neolignans and related compounds / Aryltetralin lignans / 9,9p-dihydroxyaryltetralin lignans
(+)-Isolariciresinol 160521 Click to see 360.40 unknown https://doi.org/10.1016/J.BMCL.2013.01.046
> Lignans, neolignans and related compounds / Furanoid lignans
(+)-Eudesmin 73117 Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC)OC)OC 386.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Lignan glycosides
(2R,3R,4S,5R)-2-[[(2R,3R)-7-hydroxy-1-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-6-methoxy-1,2,3,4-tetrahydronaphthalen-2-yl]methoxy]oxane-3,4,5-triol 71718945 Click to see COC1=C(C=C2C(C(C(CC2=C1)CO)COC3C(C(C(CO3)O)O)O)C4=CC(=C(C=C4)O)OC)O 492.50 unknown https://doi.org/10.1016/J.BMCL.2013.01.046
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Cardenolides and derivatives / Cardenolide glycosides and derivatives
(3S,5R,8R,9S,10R,13R,14S,17R)-14-hydroxy-3-[(2R,3R,4S,5S,6R)-5-hydroxy-3,4-dimethoxy-6-methyloxan-2-yl]oxy-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 162882272 Click to see 562.70 unknown https://doi.org/10.3987/COM-02-S86
(3S,5S,8R,9S,10S,13R,14S,17R)-3-[(2R,3R,4S,5S,6R)-3,4-dimethoxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5,14-dihydroxy-13-methyl-17-(5-oxo-2H-furan-3-yl)-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-10-carbaldehyde 163004802 Click to see CC1C(C(C(C(O1)OC2CCC3(C4CCC5(C(CCC5(C4CCC3(C2)O)O)C6=CC(=O)OC6)C)C=O)OC)OC)OC7C(C(C(C(O7)CO)O)O)O 740.80 unknown https://doi.org/10.1002/HLCA.19640470822
[(3S,5S,8S,9S,10S,13R,14S,16S,17S)-14-hydroxy-3-[(2R,3R,4S,5R,6R)-6-(hydroxymethyl)-3,4-dimethoxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-10,13-dimethyl-17-(5-oxo-2H-furan-3-yl)-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-16-yl] acetate 162937854 Click to see CC(=O)OC1CC2(C3CCC4CC(CCC4(C3CCC2(C1C5=CC(=O)OC5)C)C)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)CO)O)O)O)OC)OC)O 784.90 unknown https://doi.org/10.1002/HLCA.19640470822
[14-hydroxy-3-[6-(hydroxymethyl)-3,4-dimethoxy-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-10,13-dimethyl-17-(5-oxo-2H-furan-3-yl)-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-16-yl] acetate 162937853 Click to see 784.90 unknown https://doi.org/10.1002/HLCA.19640470822
14-hydroxy-3-(5-hydroxy-3,4-dimethoxy-6-methyloxan-2-yl)oxy-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 162882271 Click to see 562.70 unknown https://doi.org/10.3987/COM-02-S86
3-[(3R,5R,8S,9R,10S,13R,14S,16R,17R)-14,16-dihydroxy-3-[(2S,3S,4S,5R,6R)-6-(hydroxymethyl)-3,4-dimethoxy-5-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl]-2H-furan-5-one 163195674 Click to see 742.80 unknown https://doi.org/10.1002/HLCA.19640470822
3-[(3S,5R,8R,9S,10R,11R,13R,14S,17R)-3-[(2R,3R,4S,5R,6R)-3,5-dihydroxy-6-(hydroxymethyl)-4-methoxyoxan-2-yl]oxy-11,14-dihydroxy-10-(hydroxymethyl)-13-methyl-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl]-2H-furan-5-one 21633941 Click to see CC12CC(C3C(C1(CCC2C4=CC(=O)OC4)O)CCC5C3(CCC(C5)OC6C(C(C(C(O6)CO)O)OC)O)CO)O 582.70 unknown https://doi.org/10.3987/COM-02-S86
3-[(3S,5R,8R,9S,10R,13R,14S,17S)-14-hydroxy-3-[(2R,3R,4S,5R,6R)-5-hydroxy-6-(hydroxymethyl)-3,4-dimethoxyoxan-2-yl]oxy-10-(hydroxymethyl)-13-methyl-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl]-2H-furan-5-one 163034092 Click to see CC12CCC3C(C1(CCC2C4=CC(=O)OC4)O)CCC5C3(CCC(C5)OC6C(C(C(C(O6)CO)O)OC)OC)CO 580.70 unknown https://doi.org/10.1002/HLCA.19640470822
3-[(3S,5R,8R,9S,10S,11R,13R,14S,17R)-3-[(2R,3R,4S,5R,6R)-3,5-dihydroxy-6-(hydroxymethyl)-4-methoxyoxan-2-yl]oxy-11,14-dihydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl]-2H-furan-5-one 101233455 Click to see 566.70 unknown https://doi.org/10.3987/COM-02-S86
3-[(3S,5R,8R,9S,10S,13R,14S,17R)-14-hydroxy-3-[(2R,3R,4S,5R,6R)-5-hydroxy-6-(hydroxymethyl)-3,4-dimethoxyoxan-2-yl]oxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl]-2H-furan-5-one 12308689 Click to see CC12CCC(CC1CCC3C2CCC4(C3(CCC4C5=CC(=O)OC5)O)C)OC6C(C(C(C(O6)CO)O)OC)OC 564.70 unknown https://doi.org/10.3987/COM-02-S86
3-[(3S,5R,8R,9S,10S,13R,14S,17R)-3-[(2R,3R,4S,5R,6R)-3,5-dihydroxy-6-(hydroxymethyl)-4-methoxyoxan-2-yl]oxy-14-hydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl]-2H-furan-5-one 21633940 Click to see CC12CCC(CC1CCC3C2CCC4(C3(CCC4C5=CC(=O)OC5)O)C)OC6C(C(C(C(O6)CO)O)OC)O 550.70 unknown https://doi.org/10.3987/COM-02-S86
3-[(3S,5S,8R,9S,10R,13R,14S,17R)-3-[(2S,3S,4R,5R,6R)-3,4-dimethoxy-6-methyl-5-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5,14-dihydroxy-10,13-dimethyl-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]-2H-furan-5-one 162857730 Click to see CC1C(C(C(C(O1)OC2CCC3(C4CCC5(C(CCC5(C4CCC3(C2)O)O)C6=CC(=O)OC6)C)C)OC)OC)OC7C(C(C(C(O7)CO)O)O)O 726.80 unknown https://doi.org/10.1002/HLCA.19640470822
3-[(3S,5S,8R,9S,10R,13R,14S,17R)-5,14-dihydroxy-10-(hydroxymethyl)-13-methyl-3-[(2R,3R,4R,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]-2H-furan-5-one 25058059 Click to see CC1C(C(C(C(O1)OC2CCC3(C4CCC5(C(CCC5(C4CCC3(C2)O)O)C6=CC(=O)OC6)C)CO)O)O)O 552.70 unknown https://doi.org/10.1002/HLCA.19640470822
3-[14-hydroxy-3-[5-hydroxy-6-(hydroxymethyl)-3,4-dimethoxyoxan-2-yl]oxy-10-(hydroxymethyl)-13-methyl-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl]-2H-furan-5-one 163034091 Click to see 580.70 unknown https://doi.org/10.1002/HLCA.19640470822
3-[14-hydroxy-3-[5-hydroxy-6-(hydroxymethyl)-3,4-dimethoxyoxan-2-yl]oxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl]-2H-furan-5-one 12308688 Click to see 564.70 unknown https://doi.org/10.3987/COM-02-S86
3-[14,16-dihydroxy-3-[6-(hydroxymethyl)-3,4-dimethoxy-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl]-2H-furan-5-one 162892530 Click to see CC12CCC(CC1CCC3C2CCC4(C3(CC(C4C5=CC(=O)OC5)O)O)C)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)CO)O)O)O)OC)OC 742.80 unknown https://doi.org/10.1002/HLCA.19640470822
3-[3-[3,4-dimethoxy-6-methyl-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5,14-dihydroxy-10,13-dimethyl-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]-2H-furan-5-one 162857729 Click to see CC1C(C(C(C(O1)OC2CCC3(C4CCC5(C(CCC5(C4CCC3(C2)O)O)C6=CC(=O)OC6)C)C)OC)OC)OC7C(C(C(C(O7)CO)O)O)O 726.80 unknown https://doi.org/10.1002/HLCA.19640470822
3-[3-[3,5-dihydroxy-6-(hydroxymethyl)-4-methoxyoxan-2-yl]oxy-11,14-dihydroxy-10-(hydroxymethyl)-13-methyl-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl]-2H-furan-5-one 73816544 Click to see CC12CC(C3C(C1(CCC2C4=CC(=O)OC4)O)CCC5C3(CCC(C5)OC6C(C(C(C(O6)CO)O)OC)O)CO)O 582.70 unknown https://doi.org/10.3987/COM-02-S86
3-[3-[3,5-dihydroxy-6-(hydroxymethyl)-4-methoxyoxan-2-yl]oxy-11,14-dihydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl]-2H-furan-5-one 162906340 Click to see CC12CCC(CC1CCC3C2C(CC4(C3(CCC4C5=CC(=O)OC5)O)C)O)OC6C(C(C(C(O6)CO)O)OC)O 566.70 unknown https://doi.org/10.3987/COM-02-S86
3-[3-[3,5-dihydroxy-6-(hydroxymethyl)-4-methoxyoxan-2-yl]oxy-14-hydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl]-2H-furan-5-one 73816543 Click to see CC12CCC(CC1CCC3C2CCC4(C3(CCC4C5=CC(=O)OC5)O)C)OC6C(C(C(C(O6)CO)O)OC)O 550.70 unknown https://doi.org/10.3987/COM-02-S86
Desglucocheirotoxin 2862 Click to see CC1C(C(C(C(O1)OC2CCC3(C4CCC5(C(CCC5(C4CCC3(C2)O)O)C6=CC(=O)OC6)C)C=O)O)O)O 550.60 unknown https://doi.org/10.1002/HLCA.19640470822
Desglucocheirotoxol 12309172 Click to see 552.70 unknown https://doi.org/10.1002/HLCA.19640470822
Glucostrebloside 199567 Click to see 740.80 unknown https://doi.org/10.1002/HLCA.19640470822
Mansonin 15560101 Click to see 578.70 unknown https://doi.org/10.1021/NP50042A019
Strebloside 21123718 Click to see CC1C(C(C(C(O1)OC2CCC3(C4CCC5(C(CCC5(C4CCC3(C2)O)O)C6=CC(=O)OC6)C)C=O)OC)OC)O 578.70 unknown https://doi.org/10.1002/DDR.430260106
https://doi.org/10.1021/NP50042A019
Strophalloside 23618277 Click to see 550.60 unknown https://doi.org/10.1055/S-2007-969509
https://doi.org/10.1002/HLCA.19640470822
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
1-[(3S,5R,8R,9S,10S,13R,14S,17S)-3-[(2R,3R,4S,5R,6R)-3,5-dihydroxy-6-(hydroxymethyl)-4-methoxyoxan-2-yl]oxy-14-hydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl]ethanone 162924525 Click to see 510.70 unknown https://doi.org/10.1016/0031-9422(92)80075-P
1-[3-[3,5-Dihydroxy-6-(hydroxymethyl)-4-methoxyoxan-2-yl]oxy-14-hydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl]ethanone 162924524 Click to see 510.70 unknown https://doi.org/10.1016/0031-9422(92)80075-P
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
Asperosid 3085030 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)C)OC8C(C(C(C(O8)C)O)O)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)OC1(CCC(C)COC1C(C(C(C(O1)CO)O)O)O)O 1195.30 unknown https://doi.org/10.1002/DDR.430260106
https://doi.org/10.1055/S-2007-969509
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
2-[2-[5-(2,3-Dihydroxypropyl)-2-hydroxyphenyl]-4-prop-2-enylphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 74336680 Click to see 462.50 unknown https://doi.org/10.1002/MRC.2186
Magnolignan A-2-O-Beta-D-Glucopyranoside 71720154 Click to see 462.50 unknown https://doi.org/10.1002/MRC.2186
https://doi.org/10.1016/J.BMCL.2013.01.046
> Organic oxygen compounds / Organooxygen compounds / Ethers / Diarylethers
(7'R,8'S,7"R,8"S)-erythro-strebluslignanol G 71580864 Click to see CC(C(C1=CC2=C(C=C1)OC3=C(C=C(C=C3)CC=C)C4=C(C=CC(=C4)C(C(C)O)O)OC5=C2C=C(C=C5)CC=C)O)O 564.70 unknown https://doi.org/10.1016/J.BMCL.2013.01.046
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(7S,8R)-Dihydrodehydrodiconiferyl Alcohol 384679 Click to see 360.40 unknown https://doi.org/10.1016/J.BMCL.2013.01.046
Glycosmisic Acid 38356809 Click to see 372.40 unknown https://doi.org/10.1016/J.BMCL.2013.01.046

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