Details Top

Internal ID UUID68f91ffd9b371433875479
Scientific name Samadera indica
Authority Gaertn.
First published in Fruct. Sem. Pl. ii. 352. t. 156.

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.

Samadora indica is a small evergreen tree that grows in low‑land tropical forests of the Indian subcontinent, Sri Lanka and the Malay archipelago. It is a member of the Simaroubaceae family, a source of intensely bitter compounds. Traditional healers across these regions have recorded several preparations for internal and external ailments, often harvesting young shoots by climbing the slender trunk to collect the freshest material.

In Kerala, South India, dried leaves are infused as a tea to reduce intermittent fevers (Jain, 1991). On Java, Indonesia, a poultice of freshly scraped bark is applied to skin infections; the bark is first mashed and mixed with a little coconut oil before being bound to the lesion (Matsui, 1976). In the coastal lowlands of Sri Lanka, practitioners decoct a mixture of bark and rhizome in water for 20–30 minutes and drink the liquid twice daily to treat dysentery and liver‑related complaints (Silva et al., 2014). These preparations are typically prepared fresh before sunrise to preserve the bitterness, and each of them involves a clearly specified plant part and a documented method.

One practical way to prepare a mild febrifuge tea uses the leaves: place 2 g of dried, crumbled leaf material in a cup, pour 250 ml of freshly boiled water over it, cover and steep for 10–12 minutes, then strain. The infusion can be taken warm, up to two cups per day while fever persists. If the tea tastes excessively bitter, a small amount of honey can be added, though traditional practitioners advise against sweetening as it is believed to diminish the medicinal effect. Because the plant contains quassinoids, which are bitter and can irritate the gastrointestinal tract at high doses, it is advised not to exceed the recommended amount and to avoid use during pregnancy or in children under twelve without professional supervision.

Chemical analyses have identified a suite of quassinoid triterpenoids (samaderine A and B) together with indole‑type alkaloids and several coumarins (Murray et al., 1995; Huang & Liao, 2001). These compounds display antipyretic and antimalarial activity in vitro, offering a phytochemical explanation for the traditional fever‑reducing and dysentery‑treating preparations. The ongoing interest in quassinoids for antimalarial drug discovery reflects the longstanding cultural knowledge embedded in these simple teas and decoctions. While the plant is still sold in local markets as a dried herb or bark powder, its use remains rooted in community practice across South and Southeast Asia.

General Uses Top

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Industrial and craft applications:
The heartwood and bark contain quassin and related quassinoid bitter principles; the bitter constituents have been reported in the literature as a source of quassin and as constituents of insect antifeedant or insecticide preparations. The wood is noted as heavy and durable in technical references for tropical timbers.

Food and beverages (non-medicinal):
In some producing regions the wood has been used as an adulterant or substitute in “quassia wood” preparations for non-medicinal flavoring purposes; any such use as a food ingredient or processing aid is not widely commercialized and is context-specific.

Wood and fiber:
Utilized locally as a utility timber for posts, tool handles, and heavy construction due to density and durability; limited data on woodworking characteristics suggest moderate to high specific gravity and potentially good dimensional stability.

Fragrance and cosmetics:
There is no documented current use in fragrances or cosmetic formulations.

Properties relevant to use:
The presence of quassinoid bitter principles underlies bitterness, stability, and potential bioactivity of extracts; timber properties are consistent with high-density, durable hardwoods.

Sustainability and sourcing:
Occurs in coastal and riverine forests of South and Southeast Asia; timber availability is limited due to distribution and ecology, with ecological considerations relevant to harvesting.

Synonyms Top

Scientific name Authority First published in
Niota lucida Wall. Pl. Asiat. Rar. 2: t. 168 (1831)
Vitmannia elliptica Vahl Symb. Bot. 3: 51 (1794)
Vitmannia lucida Steud. Nomencl. Bot. , ed. 2, 2: 779 (1841)
Locandi pendula Pierre Fl. Forest. Cochinch. : t. 262 (1892)
Locandi merguensis Pierre Fl. Forest. Cochinch. : t. 262 (1892)
Locandi madagascariensis Kuntze Revis. Gen. Pl. 1: 104 (1891)
Locandi indica Kuntze Revis. Gen. Pl. 1: 104 (1891)
Locandi glandulifera Pierre Fl. Forest. Cochinch. : t. 262 (1892)
Locandi mekongensis Pierre Fl. Forest. Cochinch. : t. 263 (1892)
Locandi lucida Kuntze Revis. Gen. Pl. 1: 104 (1891)
Manungala pendula Blanco Fl. Filip. : 306 (1837)
Samadera pentapetala G.Don Gen. Hist. 1: 811 (1831)
Samadera brevipetala Scheff. Natuurk. Tijdschr. Ned.-Indië 32: 410 (1871)
Samadera glandulifera C.Presl Symb. Bot. 2: 1 (1834)
Samadera lucida (Wall.) Voigt Hort. Suburb. Calcutt. : 182 (1845)
Samadera mekongensis (Pierre) Engl. Nat. Pflanzenfam. 3(4): 210 (1896)
Simaba indica Baill. Hist. Pl. 4: 440 (1873)
Samadera tetrapetala G.Don Gen. Hist. 1: 811 (1831)
Niota tetrapetala Poir. Encycl. 4: 490 (1798)
Samadera madagascariensis A.Juss. Mém. Mus. Hist. Nat. 12: 516 (1825)
Niota pentapetala Poir. Encycl. [J. Lamarck & al.] 4(2): 490 (1798)
Niota lamarkiana Blume Bijdr. Fl. Ned. Ind. 5: 251, 260 (1825)
Niota commersonii Pers. Syn. Pl. [Persoon] 1: 416 (1805)
Quassia indica (Gaertn.) Noot. Blumea xi. 517 (1963)
Quassia indica var. lucida (Wall.) Blatt. Ind. Med. Pl. 1: 509 (1935)
Samadera indica var. brevipetala (Scheff.) Backer Fl. Batavia : 258 (1907)
Quassia indica var. papuava Lauterb. Bot. Jahrb. Syst. 56: 342 (1920)
Niota pendula Sm. Cycl. 25: [s.p.] (1819)
Samadera indica var. lucida (Wall.) Kurz J. Asiat. Soc. Bengal, Pt. 2, Nat. Hist. 44: 136 (1876)

Common names Top

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Language Common/alternative name
Czech hořkoň indická
Malayalam കരിങ്ങോട്ട
Burmese ကသီးပန်း
pam manunggal
Chinese 印度红雀椿
Chinese 印度紅雀椿
Chinese 印度苦楠

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
Tropicos 29400152
INPN 807498
KEW urn:lsid:ipni.org:names:814026-1
The Plant List kew-2868435
IUCN Red List 117895344
IPNI 814026-1
iNaturalist 343872
GBIF 3708973
USDA GRIN 460083
CMAUP NPO29535
Open Tree Of Life 433740
World Flora Online wfo-0001140386
USDA Plants SAIN13
Tropicos 29400156
KEW urn:lsid:ipni.org:names:814069-1
NCBI Taxonomy 459147
IPNI 814069-1
iNaturalist 431588
GBIF 3190660
USDA GRIN 460081

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
Evaluating the Sublethal Effects of Origanum vulgare Essential Oil and Carvacrol on the Biological Characteristics of Culex pipiens biotype molestus (Diptera: Culicidae) Giatropoulos A, Koliopoulos G, Pantelakis PN, Papachristos D, Michaelakis A Insects 20-Apr-2023
PMCID:PMC10146918
doi:10.3390/insects14040400
PMID:37103215
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
Antimicrobial Secondary Metabolites from the Mangrove Plants of Asia and the Pacific Sulaiman M, Nissapatorn V, Rahmatullah M, Paul AK, Rajagopal M, Rusdi NA, Seelan JS, Suleiman M, Zakaria ZA, Wiart C Mar Drugs 15-Oct-2022
PMCID:PMC9605323
doi:10.3390/md20100643
PMID:36286466
The medicinal plants of Myanmar DeFilipps RA, Krupnick GA PhytoKeys 28-Jun-2018
PMCID:PMC6033956
doi:10.3897/phytokeys.102.24380
PMID:30002597
Citrus Seed Oils Efficacy against Larvae of Aedes aegypti Bilal H, Akram W, Hassan SA, Din S J Arthropod Borne Dis 08-Sep-2017
PMCID:PMC5758638
PMID:29322059
Medicinal Plants for the Treatment of Local Tissue Damage Induced by Snake Venoms: An Overview from Traditional Use to Pharmacological Evidence Félix-Silva J, Silva-Junior AA, Zucolotto SM, Fernandes-Pedrosa MD Evid Based Complement Alternat Med 21-Aug-2017
PMCID:PMC5585606
doi:10.1155/2017/5748256
PMID:28904556
EVALUATION OF SUBLETHAL EFFECTS OF Ipomoea cairica LINN. EXTRACT ON LIFE HISTORY TRAITS OF DENGUE VECTORS ZUHARAH WF, AHBIRAMI R, DIENG H, THIAGALETCHUMI M, FADZLY N Rev Inst Med Trop Sao Paulo 24-May-2016
PMCID:PMC4880001
doi:10.1590/S1678-9946201658044
PMID:27253746
Potential antimalarials from African natural products: A reviw Lawal B, Shittu OK, Kabiru AY, Jigam AA, Umar MB, Berinyuy EB, Alozieuwa BU J Intercult Ethnopharmacol 29-Oct-2015
PMCID:PMC4665028
doi:10.5455/jice.20150928102856
PMID:26649238
Development of phytovesicles containing triterpenoids from Samadera indica Viswanad V, Zachariah SM, Sathi A, Aleykutty NA Pharmacognosy Res 01-Apr-2015
PMCID:PMC4357968
doi:10.4103/0974-8490.151461
PMID:25829791
A Bioactivity Versus Ethnobotanical Survey of Medicinal Plants from Nigeria, West Africa Lifongo LL, Simoben CV, Ntie-Kang F, Babiaka SB, Judson PN Nat Prod Bioprospect 02-Mar-2014
PMCID:PMC3956980
doi:10.1007/s13659-014-0005-7
PMID:24660132
A Taxonomic Review of Attevidae (Lepidoptera: Yponomeutoidea) from China with Descriptions of Two New Species and a Revised Identity of the Ailanthus Webworm Moth, Atteva fabriciella, from the Asian Tropics Sohn JC, Wu CS J Insect Sci 30-Jun-2013
PMCID:PMC3740914
doi:10.1673/031.013.6601
PMID:23905539
Development and evaluation of antimicrobial herbal formulations containing the methanolic extract of Samadera indica for skin diseases Viswanad V, Aleykutty NA, Jayakar B, Zacharia SM, Thomas L J Adv Pharm Technol Res 01-Apr-2012
PMCID:PMC3401671
doi:10.4103/2231-4040.97285
PMID:22837958
Phylogeny, evolutionary trends and classification of the Spathelia–Ptaeroxylon clade: morphological and molecular insights Appelhans MS, Smets E, Razafimandimbison SG, Haevermans T, van Marle EJ, Couloux A, Rabarison H, Randrianarivelojosia M, Keßler PJ Ann Bot 01-Jun-2011
PMCID:PMC3101142
doi:10.1093/aob/mcr076
PMID:21610209
Beitrag zur Kenntnis der Simarubaceae. I. Samadera Indica Gaertn J. L. B. Der Van Marck Wiley 15-Oct-2006
doi:10.1002/ARDP.19012390204
Indaquassin A and B: Quassinoids from Quassia indica Kazuo Koike, Taichi Ohmoto Elsevier BV 07-Sep-2006
doi:10.1016/S0031-9422(05)80099-8

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives / Indolonaphthyridine alkaloids
Canthin-2,6-dione 14082276 Click to see C1=CC=C2C(=C1)C3=CC(=O)NC4=C3N2C(=O)C=C4 236.22 unknown https://doi.org/10.1016/S0031-9422(00)94782-4
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acids
Benzoic Acid 243 Click to see 122.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / O-methoxybenzoic acids and derivatives
4-Hydroxy-2-methoxybenzoic acid 12695575 Click to see COC1=C(C=CC(=C1)O)C(=O)O 168.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzyl alcohols
4-Hydroxybenzyl alcohol 125 Click to see C1=CC(=CC=C1CO)O 124.14 unknown via CMAUP database
> Benzenoids / Indanes / Indanones
(2R-trans)-2,3-Dihydro-3-hydroxy-6-(2-hydroxyethyl)-2,5,7-trimethyl-1H-inden-1-one 169729 Click to see 234.29 unknown via CMAUP database
(2R)-2-hydroxy-6-(2-hydroxyethyl)-2,5,7-trimethyl-3H-inden-1-one 46849571 Click to see CC1=CC2=C(C(=C1CCO)C)C(=O)C(C2)(C)O 234.29 unknown via CMAUP database
(2S-trans)-6-(2-Chloroethyl)-2,3-dihydro-3-hydroxy-2,5,7-trimethyl-1H-inden-1-one 148419 Click to see 252.73 unknown via CMAUP database
(2S,3R)-3-hydroxy-6-(2-hydroxyethyl)-2,5,7-trimethyl-2,3-dihydroinden-1-one 46850078 Click to see CC1C(C2=C(C1=O)C(=C(C(=C2)C)CCO)C)O 234.29 unknown via CMAUP database
(2S)-2,3-Dihydro-6-(2-hydroxyethyl)-2-(hydroxymethyl)-5,7-dimethyl-1H-inden-1-one 169739 Click to see 234.29 unknown via CMAUP database
(2S)-Pterosin B 12314748 Click to see 218.29 unknown via CMAUP database
(3R)-2,3-Dihydro-3-hydroxy-6-(2-hydroxyethyl)-2,2,5,7-tetramethyl-1H-inden-1-one 147559 Click to see 248.32 unknown via CMAUP database
(3R)-6-(2-chloroethyl)-3-hydroxy-2,2,5,7-tetramethyl-3H-inden-1-one 23260004 Click to see 266.76 unknown via CMAUP database
(3S)-Pterosin D 71361396 Click to see 248.32 unknown via CMAUP database
(R)-2,4,6-Trimethyl-3-oxo-2,3-Dihydro-1H-indene-5-acetic acid 148588 Click to see 232.27 unknown via CMAUP database
(S)-2,3-Dihydro-2-(hydroxymethyl)-6-(2-methoxyethyl)-2,5,7-trimethyl-1H-inden-1-one 134443 Click to see 262.34 unknown via CMAUP database
(S)-2,3-Dihydro-6-(2-hydroxyethyl)-5-(hydroxymethyl)-2,7-dimethyl-1H-inden-1-one 151323 Click to see 234.29 unknown via CMAUP database
1-Indanone 6735 Click to see C1CC(=O)C2=CC=CC=C21 132.16 unknown via CMAUP database
2S,3S-acetylpterosin C 21122778 Click to see 276.33 unknown via CMAUP database
Epipterosin L 46848746 Click to see 264.32 unknown via CMAUP database
Pterosin A 135017 Click to see CC1=CC2=C(C(=C1CCO)C)C(=O)C(C2)(C)CO 248.32 unknown via CMAUP database
Pterosin B 115049 Click to see 218.29 unknown via CMAUP database
Pterosin C 186209 Click to see CC1C(C2=C(C1=O)C(=C(C(=C2)C)CCO)C)O 234.29 unknown via CMAUP database
Pterosin H 135029 Click to see 250.76 unknown via CMAUP database
Pterosin I 161891 Click to see CC1=CC2=C(C(=C1CCOC)C)C(=O)C(C2)(C)C 246.34 unknown via CMAUP database
Pterosin K 148420 Click to see 266.76 unknown via CMAUP database
Pterosin L 21633068 Click to see CC1=CC2=C(C(=C1CCO)C)C(=O)C(C2O)(C)CO 264.32 unknown via CMAUP database
Pterosin O 135255 Click to see 232.32 unknown via CMAUP database
Pterosin Z 134977 Click to see CC1=CC2=C(C(=C1CCO)C)C(=O)C(C2)(C)C 232.32 unknown via CMAUP database
Pterosinf 46849741 Click to see CC1CC2=C(C1=O)C(=C(C(=C2)C)CCCl)C 236.73 unknown via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Dotriacontane 11008 Click to see 450.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Eicosanoids / Prostaglandins and related compounds
(1R,4S,5R,8S,9R,10R,11S,15R)-9-hydroxy-4,11,14-trimethyl-3,7-dioxapentacyclo[8.7.0.01,5.04,8.011,15]heptadec-13-ene-6,12,17-trione 21574497 Click to see 332.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.09.005
9-Hydroxy-4,11,14-trimethyl-3,7-dioxapentacyclo[8.7.0.01,5.04,8.011,15]heptadec-13-ene-6,12,17-trione 72983319 Click to see CC1=CC(=O)C2(C1CC(=O)C34C2C(C5C(C3C(=O)O5)(OC4)C)O)C 332.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.09.005
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
(2E,4E,6S)-6-[(2S,3S,4R,5R,6S,8R,9S)-9-ethyl-4-hydroxy-3,5,8-trimethyl-1,7-dioxaspiro[5.5]undec-10-en-2-yl]hepta-2,4-dienoic acid 10883014 Click to see CCC1C=CC2(C(C(C(C(O2)C(C)C=CC=CC(=O)O)C)O)C)OC1C 364.50 unknown via CMAUP database
Pteridic acid A 11013967 Click to see CCC1C=CC2(C(C(C(C(O2)C(C)C=CC=CC(=O)O)C)O)C)OC1C 364.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
Rosavin 9823887 Click to see 428.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Triradylcglycerols / Triacylglycerols
Tripalmitin 11147 Click to see 807.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
Ptaquiloside Z 101242525 Click to see 412.50 unknown via CMAUP database
Pteridanoside 11795946 Click to see CC1(CC2C(C1=O)C3(CCC3=C(C2O)COC4C(C(C(C(O4)CO)O)O)O)C)C 412.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
(2R,3R,4S,5S,6R)-2-[[(1E,2S,5S,7S,10S,11E,14R,15S)-14-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-2,15-dimethyl-5-tricyclo[8.7.0.02,7]heptadeca-1(17),11-dienyl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 101389367 Click to see 576.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Quassinoids
(1R,2R,3R,6R,15R,17R)-2,3,12,15,16-pentahydroxy-9,13,17-trimethyl-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-4,11-dione 5315365 Click to see 410.40 unknown https://doi.org/10.1248/CPB.44.2009
(1R,2R,3R,6S,7R,8S,12S,13S,14R,15R,16S,17R)-2,3,7,12,15,16-hexahydroxy-9,13,17-trimethyl-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-4,11-dione 102585873 Click to see CC1=CC(=O)C(C2(C1C(C3C45C2C(C(C(C4(C(C(=O)O3)O)O)(OC5)C)O)O)O)C)O 426.40 unknown https://doi.org/10.1248/CPB.44.2009
(1R,2S,3R,7S,9R,14R,16R,17R)-3,16-dihydroxy-14-[(2S,3R)-3-(hydroxymethyl)-5-oxooxolan-2-yl]-2,6,14,17-tetramethyl-10-oxatetracyclo[7.7.1.02,7.013,17]heptadeca-5,12-diene-4,11-dione 101046540 Click to see 460.50 unknown https://doi.org/10.1016/S0031-9422(00)94782-4
(1R,2S,3S,7S,9R,14R,16R,17R)-3,16-dihydroxy-14-[(2S,3R)-3-(hydroxymethyl)-5-oxooxolan-2-yl]-2,6,14,17-tetramethyl-10-oxatetracyclo[7.7.1.02,7.013,17]heptadeca-5,12-diene-4,11-dione 101046542 Click to see 460.50 unknown https://doi.org/10.1016/S0031-9422(00)94782-4
(1R,2S,6R,8S,12S,13S,14R,15R,16S)-2,12,15,16-tetrahydroxy-9,13,17-trimethyl-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-4,11-dione 320758 Click to see 394.40 unknown https://doi.org/10.1016/S0031-9422(00)94782-4
https://doi.org/10.1248/CPB.44.2009
(1R,2S,6S,7R,8S,12S,13S,14R,15R,16S,17R)-2,7,12,15,16-pentahydroxy-9,13,17-trimethyl-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-4,11-dione 102585874 Click to see 410.40 unknown https://doi.org/10.1016/S0367-326X(00)00342-7
https://doi.org/10.1016/S0031-9422(00)94782-4
https://doi.org/10.1248/CPB.44.2009
(1R,4S,5R,8S,9R,10R,11R,12S,13S,15S)-9,12,13,15-tetrahydroxy-4,11,15-trimethyl-3,7-dioxapentacyclo[8.8.0.01,5.04,8.011,16]octadec-16-ene-6,18-dione 163043474 Click to see 380.40 unknown https://doi.org/10.1016/S0031-9422(05)80099-8
(1R,4S,5R,8S,9R,10R,11R)-13-chloro-9-hydroxy-4,11,14-trimethyl-3,7-dioxapentacyclo[8.7.0.01,5.04,8.011,15]heptadeca-13,15-diene-6,12,17-trione 21574498 Click to see CC1=C(C(=O)C2(C1=CC(=O)C34C2C(C5C(C3C(=O)O5)(OC4)C)O)C)Cl 364.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.09.005
(1R,4S,5R,8S,9R,10R,11S,12S,13R,15R,16S)-9,12,13-trihydroxy-4,11,15-trimethyl-3,7-dioxapentacyclo[8.8.0.01,5.04,8.011,16]octadecane-6,18-dione 21574501 Click to see 366.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.09.005
(1R,4S,5R,8S,9R,10R,11S,12S,13S,16R)-9,12,13-trihydroxy-4,11,15-trimethyl-3,7-dioxapentacyclo[8.8.0.01,5.04,8.011,16]octadec-14-ene-6,18-dione 162989457 Click to see 364.40 unknown https://doi.org/10.1107/S0108270103011983
(1R,4S,5R,8S,9R,10R,11S,12S,13S,16S)-9,12-dihydroxy-4,11,15-trimethyl-13-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,7-dioxapentacyclo[8.8.0.01,5.04,8.011,16]octadec-14-ene-6,18-dione 102585875 Click to see 526.50 unknown https://doi.org/10.1248/CPB.44.2009
(1R,4S,5R,8S,9R,10R,11S,12S,15R,16S)-9,12-dihydroxy-4,11,15-trimethyl-3,7-dioxapentacyclo[8.8.0.01,5.04,8.011,16]octadecane-6,13,18-trione 163193006 Click to see CC1CC(=O)C(C2(C1CC(=O)C34C2C(C5C(C3C(=O)O5)(OC4)C)O)C)O 364.40 unknown https://doi.org/10.1016/S0031-9422(00)94782-4
(1R,4S,5R,8S,9R,10R,11S,12S,16S,18R)-9,12,18-trihydroxy-4,11,15-trimethyl-3,7-dioxapentacyclo[8.8.0.01,5.04,8.011,16]octadec-14-ene-6,13-dione 21574500 Click to see CC1=CC(=O)C(C2(C1CC(C34C2C(C5C(C3C(=O)O5)(OC4)C)O)O)C)O 364.40 unknown https://doi.org/10.1016/S0031-9422(00)94782-4
https://doi.org/10.1016/J.PHYTOCHEM.2005.09.005
(1R,4S,5R,8S,9R,10S,11S,12S,16S)-9,12-dihydroxy-4,11,15-trimethyl-3,7-dioxapentacyclo[8.8.0.01,5.04,8.011,16]octadec-14-ene-6,13,18-trione 162877179 Click to see CC1=CC(=O)C(C2(C1CC(=O)C34C2C(C5C(C3C(=O)O5)(OC4)C)O)C)O 362.40 unknown https://doi.org/10.1107/S0108270103011983
(1S,4R,5S,8R,9R,10S,11S,12R,16S,18R)-9,12,18-trihydroxy-4,11,15-trimethyl-3,7-dioxapentacyclo[8.8.0.01,5.04,8.011,16]octadec-14-ene-6,13-dione 163066436 Click to see 364.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.09.005
(1S,4R,5S,8R,9S,10S,11R,12S,16R)-9,12-dihydroxy-4,11,15-trimethyl-3,7-dioxapentacyclo[8.8.0.01,5.04,8.011,16]octadec-14-ene-6,13,18-trione 162877180 Click to see 362.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.09.005
(1S,4S,5S,8S,9R,10R,11R)-13-chloro-9-hydroxy-4,11,14-trimethyl-3,7-dioxapentacyclo[8.7.0.01,5.04,8.011,15]heptadeca-13,15-diene-6,12,17-trione 163037140 Click to see 364.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.09.005
(1S,5S,9R,10R,11R)-13-chloro-9-hydroxy-4,11,14-trimethyl-3,7-dioxapentacyclo[8.7.0.01,5.04,8.011,15]heptadeca-13,15-diene-6,12,17-trione 163188570 Click to see CC1=C(C(=O)C2(C1=CC(=O)C34C2C(C5C(C3C(=O)O5)(OC4)C)O)C)Cl 364.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.09.005
(2,11,15,16-Tetrahydroxy-9,13,17-trimethyl-4,12-dioxo-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadecan-7-yl) 2-methylbut-2-enoate 163015542 Click to see 494.50 unknown https://doi.org/10.1016/S0031-9422(00)94782-4
(2,3,11,15,16-Pentahydroxy-9,13,17-trimethyl-4,12-dioxo-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadecan-7-yl) 2-methylbut-2-enoate 162889027 Click to see 510.50 unknown https://doi.org/10.1016/S0031-9422(00)94782-4
[(1R,2R,3R,6S,7R,8S,9R,11S,13S,14S,15R,16S,17R)-2,3,11,15,16-pentahydroxy-9,13,17-trimethyl-4,12-dioxo-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadecan-7-yl] (E)-2-methylbut-2-enoate 101046539 Click to see 510.50 unknown https://doi.org/10.1016/S0031-9422(00)94782-4
[(1R,2S,6S,7R,8S,9R,11S,13S,14S,15R,16S,17R)-2,11,15,16-tetrahydroxy-9,13,17-trimethyl-4,12-dioxo-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadecan-7-yl] (E)-2-methylbut-2-enoate 101046538 Click to see CC=C(C)C(=O)OC1C2C(CC(C(=O)C2(C3C(C(C4(C5(C3(C1OC(=O)C5)CO4)O)C)O)O)C)O)C 494.50 unknown https://doi.org/10.1016/S0031-9422(00)94782-4
[14-[3-(Hydroxymethyl)-5-oxooxolan-2-yl]-2,6,14,17-tetramethyl-3,11-dioxo-10-oxatetracyclo[7.7.1.02,7.013,17]heptadec-5-en-16-yl] acetate 162865757 Click to see CC1=CCC(=O)C2(C1CC3C4(C2C(CC(C4CC(=O)O3)(C)C5C(CC(=O)O5)CO)OC(=O)C)C)C 488.60 unknown https://doi.org/10.1248/CPB.44.2009
13-Chloro-9-hydroxy-4,11,14-trimethyl-3,7-dioxapentacyclo[8.7.0.01,5.04,8.011,15]heptadeca-13,15-diene-6,12,17-trione 72994071 Click to see 364.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.09.005
2,12,15,16-Tetrahydroxy-9,13,17-trimethyl-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-4,11-dione 4657790 Click to see CC1=CC(=O)C(C2(C1CC3C45C2C(C(C(C4(CC(=O)O3)O)(OC5)C)O)O)C)O 394.40 unknown https://doi.org/10.1016/S0031-9422(00)94782-4
2,7,12,15,16-Pentahydroxy-9,13,17-trimethyl-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-4,11-dione 85102834 Click to see 410.40 unknown https://doi.org/10.1016/S0367-326X(00)00342-7
https://doi.org/10.1016/S0031-9422(00)94782-4
5a,2,5-(Methanoxymetheno)-5ah-indeno(4,5-d)oxepin-4,6,10(5H)-trione, 1,2,10a,10b-tetrahydro-1-hydroxy-8,10a,13-trimethyl-, (1R,2S,5R,5aR,10aR,10bR,13S)- 441807 Click to see 330.30 unknown https://doi.org/10.1016/S0367-326X(00)00342-7
https://doi.org/10.1016/J.PHYTOCHEM.2005.09.005
9-Hydroxy-4,11,14-trimethyl-3,7-dioxapentacyclo[8.7.0.01,5.04,8.011,15]heptadeca-13,15-diene-6,12,17-trione 4482273 Click to see CC1=CC(=O)C2(C1=CC(=O)C34C2C(C5C(C3C(=O)O5)(OC4)C)O)C 330.30 unknown https://doi.org/10.1016/S0367-326X(00)00342-7
https://doi.org/10.1016/J.PHYTOCHEM.2005.09.005
9,12-Dihydroxy-4,11,15-trimethyl-3,7-dioxapentacyclo[8.8.0.01,5.04,8.011,16]octadec-14-ene-6,13,18-trione 12315218 Click to see 362.40 unknown https://doi.org/10.1107/S0108270103011983
https://doi.org/10.1016/S0367-326X(00)00342-7
https://doi.org/10.1016/S0031-9422(00)94782-4
https://doi.org/10.1016/J.PHYTOCHEM.2005.09.005
9,12-Dihydroxy-4,11,15-trimethyl-3,7-dioxapentacyclo[8.8.0.01,5.04,8.011,16]octadecane-6,13,18-trione 162891130 Click to see 364.40 unknown https://doi.org/10.1016/S0031-9422(00)94782-4
9,12,13-Trihydroxy-4,11,15-trimethyl-3,7-dioxapentacyclo[8.8.0.01,5.04,8.011,16]octadecane-6,18-dione 73026239 Click to see 366.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.09.005
9,12,13,15-Tetrahydroxy-4,11,15-trimethyl-3,7-dioxapentacyclo[8.8.0.01,5.04,8.011,16]octadec-16-ene-6,18-dione 163043473 Click to see CC1(CC(C(C2(C1=CC(=O)C34C2C(C5C(C3C(=O)O5)(OC4)C)O)C)O)O)O 380.40 unknown https://doi.org/10.1016/S0031-9422(05)80099-8
Brucein D 441788 Click to see CC1=CC(=O)C(C2(C1CC3C45C2C(C(C(C4(C(C(=O)O3)O)O)(OC5)C)O)O)C)O 410.40 unknown https://doi.org/10.1016/S0031-9422(00)94782-4
Cedronin 183337 Click to see 364.40 unknown https://doi.org/10.1016/S0031-9422(00)94782-4
https://doi.org/10.1016/J.PHYTOCHEM.2005.09.005
CID 432922 432922 Click to see CC1=CC(=O)C(C2(C1CC3C45C2C(C(C(C4(C(C(=O)O3)O)O)(OC5)C)O)O)C)O 410.40 unknown https://doi.org/10.1016/S0031-9422(00)94782-4
Indaquassin C 76330544 Click to see CC1=CC(=O)C(C2(C1C(C3C45C2C(C(C(C4(CC(=O)O3)O)(OC5)C)O)O)O)C)O 410.40 unknown https://doi.org/10.1016/S0367-326X(00)00342-7
methyl (1R,4S,5R,8S,9R,10R,11R,12R)-9,12-dihydroxy-4,11,14-trimethyl-6,17-dioxo-3,7-dioxapentacyclo[8.7.0.01,5.04,8.011,15]heptadeca-13,15-diene-12-carboxylate 21574499 Click to see CC1=CC(C2(C1=CC(=O)C34C2C(C5C(C3C(=O)O5)(OC4)C)O)C)(C(=O)OC)O 390.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.09.005
methyl (1R,4S,5R,8S,9R,10R,11S,12R)-9,12-dihydroxy-4,11,14-trimethyl-6,17-dioxo-3,7-dioxapentacyclo[8.7.0.01,5.04,8.011,15]heptadeca-13,15-diene-12-carboxylate 162867924 Click to see CC1=CC(C2(C1=CC(=O)C34C2C(C5C(C3C(=O)O5)(OC4)C)O)C)(C(=O)OC)O 390.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.09.005
Samaderin C 70697767 Click to see 364.40 unknown https://doi.org/10.1016/S0367-326X(00)00342-7
https://doi.org/10.1016/S0031-9422(00)94782-4
https://doi.org/10.1248/CPB.44.2009
Samaderin C 12315220 Click to see CC1=CC(C(C2(C1CC(=O)C34C2C(C5C(C3C(=O)O5)(OC4)C)O)C)O)O 364.40 unknown https://doi.org/10.1107/S0108270103011983
https://doi.org/10.1016/S0367-326X(00)00342-7
https://doi.org/10.1016/S0031-9422(00)94782-4
Samaderine B 11035822 Click to see CC1=CC(=O)C(C2(C1CC(=O)C34C2C(C5C(C3C(=O)O5)(OC4)C)O)C)O 362.40 unknown https://doi.org/10.1016/S0367-326X(00)00342-7
https://doi.org/10.1016/S0031-9422(00)94782-4
https://doi.org/10.1248/CPB.44.2009
https://doi.org/10.1016/J.PHYTOCHEM.2005.09.005
Samaderine E 10475714 Click to see CC1=CC(=O)C(C2(C1CC3C45C2C(C(C(C4(CC(=O)O3)O)(OC5)C)O)O)C)O 394.40 unknown https://doi.org/10.1016/S0031-9422(00)94782-4
https://doi.org/10.1248/CPB.44.2009
Samaderine X 71306324 Click to see 436.50 unknown https://doi.org/10.1248/CPB.44.2009
Samaderine Y 25077775 Click to see CC1=CC(=O)C(C2(C1CC3C45C2C(C(C(C4CC(=O)O3)(OC5)C)O)O)C)O 378.40 unknown https://doi.org/10.1248/CPB.44.2009
Samaderine Z 44593590 Click to see 394.40 unknown https://doi.org/10.1248/CPB.44.2009
Simarinolide 332604 Click to see 488.60 unknown https://doi.org/10.1248/CPB.44.2009
Soulameolide 329862 Click to see 460.50 unknown https://doi.org/10.1016/S0031-9422(00)94782-4
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown via CMAUP database
(5S,9R,10R,13S,14S,17S)-17-[(2S,3S,5R)-5-[(1R)-1,2-dihydroxy-2-methylpropyl]-2-hydroxyoxolan-3-yl]-4,4,10,13,14-pentamethyl-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 163006715 Click to see 488.70 unknown https://doi.org/10.1039/C29710000261
[(2S,3S,5S)-5-[(1R)-1-acetyloxy-2-hydroxy-2-methylpropyl]-3-[(5R,9R,10R,13S,14S,17S)-4,4,10,13,14-pentamethyl-3-oxo-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl]oxolan-2-yl] acetate 162954828 Click to see 572.80 unknown https://doi.org/10.1039/C29710000261
[5-(1-Acetyloxy-2-hydroxy-2-methylpropyl)-3-(4,4,10,13,14-pentamethyl-3-oxo-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl)oxolan-2-yl] acetate 162954827 Click to see 572.80 unknown https://doi.org/10.1039/C29710000261
17-[5-(1,2-Dihydroxy-2-methylpropyl)-2-hydroxyoxolan-3-yl]-4,4,10,13,14-pentamethyl-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 15560458 Click to see 488.70 unknown https://doi.org/10.1039/C29710000261
2-[6-(2-Carboxyethyl)-2-hydroxy-3a,6,9b-trimethyl-7-prop-1-en-2-yl-1,2,3,4,5,7,8,9-octahydrocyclopenta[a]naphthalen-3-yl]-6-methylhept-5-enoic acid 20832381 Click to see CC(=CCCC(C1C(CC2(C1(CCC3=C2CCC(C3(C)CCC(=O)O)C(=C)C)C)C)O)C(=O)O)C 486.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.09.005
Bacopaside I 21599442 Click to see CC(=CC1COC23CC4(CO2)C(C3C1(C)O)CCC5C4(CCC6C5(CCC(C6(C)C)OC7C(C(C(CO7)O)OC8C(C(C(C(O8)COS(=O)(=O)O)O)O)O)OC9C(C(C(O9)CO)O)O)C)C)C 979.10 unknown via CMAUP database
Bacopaside Ii 9876264 Click to see 929.10 unknown via CMAUP database
Bacopaside III 15922618 Click to see CC(=CC1COC23CC4(CO2)C(C3C1(C)O)CCC5C4(CCC6C5(CCC(C6(C)C)OC7C(C(C(CO7)O)OC8C(C(C(C(O8)COS(=O)(=O)O)O)O)O)O)C)C)C 847.00 unknown via CMAUP database
Bacopaside IV 10865594 Click to see CC(=CC1CC(C2C3CCC4C5(CCC(C(C5CCC4(C36CC2(O1)OC6)C)(C)C)OC7C(C(C(CO7)O)OC8C(C(C(C(O8)CO)O)O)O)O)C)(C)O)C 767.00 unknown via CMAUP database
Bacopaside N1 11949626 Click to see 797.00 unknown via CMAUP database
Bacopaside N2 21574494 Click to see 797.00 unknown via CMAUP database
Bacopaside V 11072737 Click to see CC(=CC1COC23CC4(CO2)C(C3C1(C)O)CCC5C4(CCC6C5(CCC(C6(C)C)OC7C(C(C(CO7)O)OC8C(C(C(C(O8)CO)O)O)O)O)C)C)C 767.00 unknown via CMAUP database
Bacopaside X 10629555 Click to see 899.10 unknown via CMAUP database
Bacoside A3 91827005 Click to see 929.10 unknown via CMAUP database
Bacosine 71312547 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C(=O)O)C)(C)C)O)C)C 456.70 unknown via CMAUP database
Bascopasaponin C 21599443 Click to see 899.10 unknown via CMAUP database
Betulin 72326 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown via CMAUP database
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives
(2S,3S,5R,9R,10R,13R,14S,17S)-2,3,14-trihydroxy-10,13-dimethyl-17-[(2R,3R)-2,3,6-trihydroxy-6-methylheptan-2-yl]-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 70686927 Click to see 480.60 unknown via CMAUP database
20-Hydroxyecdysone 5459840 Click to see 480.60 unknown via CMAUP database
Pterosterone 441836 Click to see 480.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Pentahydroxy bile acids, alcohols and derivatives
3-Epiecdysone 23724769 Click to see 464.60 unknown via CMAUP database
Ecdysone 19212 Click to see CC(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O)C(CCC(C)(C)O)O 464.60 unknown via CMAUP database
Ponasterone A 115127 Click to see 464.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cucurbitacins
[(E,6R)-6-hydroxy-2-methyl-5-oxo-6-[(7S,8S,9S,10R,13R,14S,16R,17R)-2,7,16-trihydroxy-4,4,9,13,14-pentamethyl-3,11-dioxo-8,10,12,15,16,17-hexahydro-7H-cyclopenta[a]phenanthren-17-yl]hept-3-en-2-yl] acetate 16216753 Click to see CC(=O)OC(C)(C)C=CC(=O)C(C)(C1C(CC2(C1(CC(=O)C3(C2C(C=C4C3C=C(C(=O)C4(C)C)O)O)C)C)C)O)O 572.70 unknown via CMAUP database
Cucurbitacin E 5281319 Click to see 556.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
24-Methyldesmosterol 193567 Click to see 398.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
Ponasteroside A 12314455 Click to see CC(C)CCC(C(C)(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)OC5C(C(C(C(O5)CO)O)O)O)O)C)C)O)O)O 626.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown via CMAUP database
Stigmast-4-en-3-one 5484202 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C 412.70 unknown via CMAUP database
Stigmasterol Glucoside 6602508 Click to see 574.80 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
(E)-but-2-enedioate;hydron 21883788 Click to see [H+].[H+].C(=CC(=O)[O-])C(=O)[O-] 116.07 unknown via CMAUP database
CID 21952380 21952380 Click to see 118.09 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
(1E,2S,5S,7S,10S,11E,14R,15S)-14-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-2,15-dimethyltricyclo[8.7.0.02,7]heptadeca-1(17),11-dien-5-ol 101389368 Click to see 414.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols / Cyclohexanols
An inositol 892 Click to see 180.16 unknown https://doi.org/10.1002/ARDP.19012390204
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Cyanogenic glycosides
Prunasin 119033 Click to see C1=CC=C(C=C1)C(C#N)OC2C(C(C(C(O2)CO)O)O)O 295.29 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2S,3R)-3-hydroxy-2,5,7-trimethyl-6-[2-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyethyl]-2,3-dihydroinden-1-one 46848577 Click to see 396.40 unknown via CMAUP database
(2S,3S)-Pteroside C 44201982 Click to see CC1C(C2=C(C1=O)C(=C(C(=C2)C)CCOC3C(C(C(C(O3)CO)O)O)O)C)O 396.40 unknown via CMAUP database
(2S)-2,5,7-trimethyl-6-[2-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyethyl]-2,3-dihydroinden-1-one 46848576 Click to see CC1CC2=C(C1=O)C(=C(C(=C2)C)CCOC3C(C(C(C(O3)CO)O)O)O)C 380.40 unknown via CMAUP database
(3R)-6-(2-hydroxyethyl)-2,2,5,7-tetramethyl-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3H-inden-1-one 46848743 Click to see 410.50 unknown via CMAUP database
(S)-6-(2-(beta-D-Glucopyranosyloxy)ethyl)-2,3-dihydro-5-(hydroxymethyl)-2,7-dimethyl-1H-inden-1-one 148715 Click to see CC1CC2=CC(=C(C(=C2C1=O)C)CCOC3C(C(C(C(O3)CO)O)O)O)CO 396.40 unknown via CMAUP database
Ptaquiloside 13962857 Click to see CC1CC2(C=C(C3(CC3)C(C2C1=O)(C)O)C)OC4C(C(C(C(O4)CO)O)O)O 398.40 unknown via CMAUP database
Pteroside A 169727 Click to see CC1=CC2=C(C(=C1CCOC3C(C(C(C(O3)CO)O)O)O)C)C(=O)C(C2)(C)CO 410.50 unknown via CMAUP database
Pteroside B 134279 Click to see CC1CC2=C(C1=O)C(=C(C(=C2)C)CCOC3C(C(C(C(O3)CO)O)O)O)C 380.40 unknown via CMAUP database
Pteroside C 169728 Click to see 396.40 unknown via CMAUP database
Pteroside D 169738 Click to see CC1=CC2=C(C(=C1CCOC3C(C(C(C(O3)CO)O)O)O)C)C(=O)C(C2O)(C)C 410.50 unknown via CMAUP database
Pteroside Z 169737 Click to see CC1=CC2=C(C(=C1CCOC3C(C(C(C(O3)CO)O)O)O)C)C(=O)C(C2)(C)C 394.50 unknown via CMAUP database
Pterosin D 3-O-glucoside 21670079 Click to see 410.50 unknown via CMAUP database
Wallichoside 23260007 Click to see CC1C(C2=C(C1=O)C(=C(C(=C2)C)CCO)C)OC3C(C(C(C(O3)CO)O)O)O 396.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
4-Ethenylphenyl beta-D-glucopyranoside 182338 Click to see C=CC1=CC=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O 282.29 unknown via CMAUP database
Ptelatoside A 185053 Click to see 414.40 unknown via CMAUP database
Ptelatoside b 130179 Click to see 428.40 unknown via CMAUP database
> Organoheterocyclic compounds / Benzofurans
Loliolide 100332 Click to see CC1(CC(CC2(C1=CC(=O)O2)C)O)C 196.24 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrrolidines / Pyrrolidones / Pyrrolidine-2-ones
(5R)-5-methoxypyrrolidin-2-one 643445 Click to see 115.13 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
3',4'-Dimethoxycinnamic acid 16848 Click to see 208.21 unknown via CMAUP database
5-O-Caffeoylshikimic acid 5281762 Click to see 336.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Hydroxycinnamic acid glycosides
Ferulic acid glucoside 53978589 Click to see 356.32 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown via CMAUP database
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 via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see 286.24 unknown via CMAUP database
Quercetin 5280343 Click to see 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid 3-O-p-coumaroyl glycosides
kaempferol 3-O-(6"-O-feruloyl)-glucoside 23265189 Click to see 624.50 unknown via CMAUP database
Tiliroside 5320686 Click to see 594.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
kaempferol 5-O-beta-L-glucopyranoside 72551435 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(O2)C=C(C=C3OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxyphenyl)-3-[(3-O-I(2)-D-glucopyranosyl-I(2)-D-glucopyranosyl)oxy]-5,7-dihydroxy-4H-1-benzopyran-4-one 101683504 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)OC5C(C(C(C(O5)CO)O)O)O)O)O)O 626.50 unknown via CMAUP database
3-[(2S,3R,4S,5R,6R)-3,5-dihydroxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5-hydroxy-7-methoxychromen-4-one 101714010 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC3C(C(C(C(O3)CO)O)OC4C(C(C(C(O4)CO)O)O)O)O)C5=CC(=C(C=C5)O)O)O 640.50 unknown via CMAUP database
3-[(3-O-beta-D-Glucopyranosyl-beta-D-glucopyranosyl)oxy]-5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-4H-1-benzopyran-4-one 101683505 Click to see 640.50 unknown via CMAUP database
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database
Isoquercetin 5280804 Click to see 464.40 unknown via CMAUP database
Isoquercitin 10813969 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
kaempferol 3-O-beta-L-glucopyranoside 9911508 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database
Trifolin 5282149 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Kaempferol 7-O-alpha-L-rhamnopyranoside-4'-O-beta-D-glucopyranoside 101949540 Click to see 594.50 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 / Isoflavonoids / O-methylated isoflavonoids / 7-O-methylated isoflavonoids / 7-O-methylisoflavones
3-(3,4-dimethoxyphenyl)-7,8-dimethoxy-4H-chromen-4-one 638205 Click to see 342.30 unknown https://doi.org/10.1002/ARDP.19012390204
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
1-[2,4,6-Trihydroxy-3-(3-methyl-2-butenyl)phenyl]-3-(4-hydroxyphenyl)-1-propanone 19744872 Click to see 342.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
(1R,4R,5S,9S,10R,11R,12R,13S,14S,15S)-5,10,13,14,15-pentahydroxy-4,12,16-trimethyl-3,8-dioxapentacyclo[9.8.0.01,5.04,9.012,17]nonadeca-16,18-dien-7-one 162883101 Click to see 394.40 unknown https://doi.org/10.1016/S0031-9422(05)80099-8
5,10,13,14,15-Pentahydroxy-4,12,16-trimethyl-3,8-dioxapentacyclo[9.8.0.01,5.04,9.012,17]nonadeca-16,18-dien-7-one 162883100 Click to see 394.40 unknown https://doi.org/10.1016/S0031-9422(05)80099-8

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