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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Filter by language:

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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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 click to expand
- China
  - China South-central
  - China Southeast
  - Hainan

Asia-tropical click to expand
- 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

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

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

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

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
> Benzenoids / Benzene and substituted derivatives / Biphenols
Randaiol	13337243	Click to see C=CCC1=CC(=C(C=C1)O)C2=C(C=CC(=C2)O)O	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 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
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 CC1C(OC(C(O1)C)C2=CC(=C(C=C2)O)C3=C(C=CC(=C3)CC=C)O)C4=CC(=C(C=C4)O)C5=C(C=CC(=C5)CC=C)O	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/10.1016/J.BMCL.2013.01.046 https://doi.org/10.1002/MRC.2186
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/10.1002/MRC.2186 https://doi.org/10.1016/J.BMCL.2013.01.046
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/10.1016/J.BMCL.2013.01.046 https://doi.org/10.1002/MRC.2186
Strebluslignanol	71717736	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 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 C=CCC1=CC=C(C=C1)OC2=C(C=C(C=C2)C=O)O	254.28	unknown	https://doi.org/10.1016/J.BMCL.2013.01.046
Isostrebluslignanaldehyde	71580866	Click to see C=CCC1=CC(=C(C=C1)OC2=CC=C(C=C2)C=CC=O)O	280.30	unknown	https://doi.org/10.1016/J.BMCL.2013.01.046
Obovatol	100771	Click to see C=CCC1=CC=C(C=C1)OC2=CC(=CC(=C2O)O)CC=C	282.30	unknown	https://doi.org/10.1016/J.BMCL.2013.01.046
Phenol, 4-(2-propenyl)-2-(4-(2-propenyl)phenoxy)-	159137	Click to see C=CCC1=CC=C(C=C1)OC2=C(C=CC(=C2)CC=C)O	266.30	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 COC1=C(C=C2C(C(C(CC2=C1)CO)CO)C3=CC(=C(C=C3)O)OC)O	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 CC1C(C(C(C(O1)OC2CCC3(C(C2)CCC4C3CCC5(C4(CCC5C6=CC(=O)OC6)O)C)C=O)OC)OC)O	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 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-(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 CC1C(C(C(C(O1)OC2CCC3(C(C2)CCC4C3CCC5(C4(CCC5C6=CC(=O)OC6)O)C)C=O)OC)OC)O	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 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-[(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 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-[(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 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-[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 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-[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
3-[3,4-dimethoxy-6-methyl-5-[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	199567	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
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 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
Mansonin	15560101	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/10.1021/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/10.1021/NP50042A019 https://doi.org/10.1002/DDR.430260106
Strophalloside	23618277	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/10.1055/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 CC(=O)C1CCC2(C1(CCC3C2CCC4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)OC)O)C)C)O	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 CC(=O)C1CCC2(C1(CCC3C2CCC4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)OC)O)C)C)O	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/10.1055/S-2007-969509 https://doi.org/10.1002/DDR.430260106
> 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 C=CCC1=CC(=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O)C3=C(C=CC(=C3)CC(CO)O)O	462.50	unknown	https://doi.org/10.1002/MRC.2186
magnolignan A-2-O-beta-D-glucopyranoside	71720154	Click to see C=CCC1=CC(=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O)C3=C(C=CC(=C3)CC(CO)O)O	462.50	unknown	https://doi.org/10.1016/J.BMCL.2013.01.046 https://doi.org/10.1002/MRC.2186
> 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
Dihydrodehydrodiconiferyl alcohol	384679	Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)CCCO	360.40	unknown	https://doi.org/10.1016/J.BMCL.2013.01.046
Glycosmisic Acid	38356809	Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)C=CC(=O)O	372.40	unknown	https://doi.org/10.1016/J.BMCL.2013.01.046

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Streblus asper

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