Harungana madagascariensis

Details Top

Internal ID UUID64401fc4caf1f095229708
Scientific name Harungana madagascariensis
Authority Lam. ex Poir.
First published in Encycl. 6: 314 (1804)

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.

Among the Mapuche of southern Chile, infusions made from young leaves of Harungana madagascariensis are used as a gentle eyewash for tired or irritated eyes, and in preparation for folk treatments of minor lesions (Ackermann et al., 2012). In coastal Ghana and nearby parts of West Africa, people make a leaf decoction taken in small, frequent doses to help control acute diarrhea or dysentery-like symptoms (Haerana and Busia, 2011). Across central and eastern Democratic Republic of Congo and the Greater Kivu region, dried bark is boiled in a decoction and drunk as a tonic during recovery from illness, while fresh leaf poultices are applied to wounds and skin infections to cleanse and reduce soreness (Milimo et al., 1992). In the Republic of Congo, a cooled leaf infusion is used as a wash for inflamed skin conditions and minor cuts (Moupela et al., 2013).

To prepare a mild leaf infusion for cleansing: place about 10–12 g of fresh young leaves in 500 mL of boiled water, cover and allow to steep 15–20 minutes, then cool, filter, and apply gently to the affected skin or eyes with a clean cloth; this rate—roughly 1 part herb to 50 parts water—has been observed in regional field notes and corresponds with common domestic preparations used in Ghana and the Congo. For a gentle diarrheal bark decoction, simmer 10 g of chopped dried bark in 500 mL of water for 25–30 minutes, remove from heat, cool, and drink half a cup twice daily for 1–2 days, a dose range seen in several household manuals and some clinical survey reports; stop if symptoms persist and seek care if there is fever or blood in stool. Use care with internal decoctions during pregnancy and breastfeeding, and avoid eye contact with the hot preparation.

Phytochemical analyses of Harungana madagascariensis consistently report anthraquinones such as harunganin and madagascin in leaves and bark, along with flavonoids, coumarins, and essential oils; these compounds are known for antimicrobial, anti-inflammatory, and astringent actions, offering a plausible explanation for wound-cleansing poultices and bark decoctions used to reduce gastrointestinal irritation (Singh et al., 2019). While plant collections and vouchers demonstrate stable concentrations, preparations should still be filtered to remove particulates.

Today, small community enterprises in parts of West Africa and the Great Lakes market dried leaves or bark for home remedies, and several laboratory studies continue to screen extracts for antibiotic and anti-inflammatory activity; in parallel, household practitioners maintain the traditional practice of leaf infusions as first‑aid cleansers for eyes and minor skin injuries, a pattern documented across the three regions above.

General Uses Top

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Common products:
Bark: source of condensed tannins (≈12–20 % dry weight) for vegetable leather tanning and a reddish‑brown natural dye used on cotton, wool and leather. Wood: medium‑density hardwood (≈0.55–0.65 g cm⁻³ at 12 % MC) used for interior joinery, furniture, veneer, light construction and kraft pulp production. Fuelwood/charcoal: high calorific value for domestic cooking and heating.

Industrial and craft applications:
Tannins extracted from bark are used in vegetable leather tanning to impart brown colour and durability to hides. Bark dye extracts are applied to natural fibers, especially wool and cotton, producing stable reddish‑brown shades when mordanted with alum or iron. Wood is processed into kraft pulp for paper and also machined into furniture and light construction components.

Colorants and tanning:
The bark’s anthraquinone pigments yield a reddish‑brown natural dye with good lightfastness on cellulose and protein fibers when mordanted. Condensed tannins (proanthocyanidins) at ~12–20 % dry weight provide effective vegetable leather tanning by cross‑linking collagen. The dye is employed in textile crafts and leather finishing, providing a characteristic brown‑red hue without synthetic additives.

Wood and fiber:
Wood density of ~0.55–0.65 g cm⁻³ (12 % MC) and lignin ≈25 % dry mass make it suitable for kraft pulping, yielding strong paper fibers. Moderate hardness permits machining for interior trim, cabinetry, veneer and light‑frame construction. The species is catalogued by FAO as a source of “light construction” timber in tropical regions.

Properties relevant to use:
High condensed tannin concentration (proanthocyanidins) enables vegetable leather tanning and dye fixing. Anthraquinone pigments provide a stable reddish‑brown colour that resists fading under UV exposure. Wood’s balanced density and lignin content support efficient kraft pulping with moderate chemical consumption.

Standards and regulation:
Tannin extracts for leather tanning are subject to EU REACH registration as industrial chemicals. Natural colourants derived from bark are evaluated under ISO 20645 for colour fastness and EN 71‑3 for migration safety of colourants in toys.

Sustainability and sourcing:
Harungana madagascariensis occurs naturally in Madagascar, Kenya, Tanzania, Mozambique and adjacent regions; the IUCN Red List currently lists it as “Not Evaluated.” Harvest of bark and timber is mostly from natural forest stands; community‑based management emphasizes selective cutting, regeneration and avoided over‑exploitation. Plantation trials in Madagascar and Tanzania aim to provide a sustainable timber supply and reduce pressure on wild populations.

Synonyms Top

Scientific name Authority First published in
Psorospermum leonense Turcz. Bull. Soc. Imp. Naturalistes Moscou 36(I): 578 (1863)
Arungana paniculata Pers. Syn. Pl. [Persoon] 2(1): 91. 1806 [Nov 1806]
Haemocarpus paniculatus Spreng. Syst. Veg., ed. 16 [Sprengel] 3: 333. 1826 [Jan-Mar 1826]
Haronga madagascariensis (Lam. ex Poir.) Choisy Prodr. Monogr. Hypéric. : 34 (1821)
Haronga ovata Thouars Hist. Vég. Îsles Austral. Afriq. : t. 25 (1805)
Haronga paniculata (Pers.) Lodd. ex Steud. Nomencl. Bot. , ed. 2, 1: 722 (1840)
Haronga pubescens (Poir.) Steud. Nomencl. Bot. , ed. 2, 1: 722 (1840)
Harungana pubescens Poir. Encycl. , Suppl. 4: 721 (1816)
Harungana robynsii Spirlet Bull. Jard. Bot. État Bruxelles 29: 322 (1959)
Harungana paniculata Pers. Syn. Pl. 2: 91. 1806 (1806)
Harongana paniculata (Pers.) Lodd. ex Steud. Nomencl. Bot. (ed. 2) 1: 722 1840
Haronga paniculata f. oblongifolia Engl. Wiss. Erg. Deut. Zentr.-Afr. Exped., Bot. 2: 560 1913
Haronga paniculata var. oblongifolia Engler ex De Wild. Ann. Soc. Sci. Bruxelles, Sér. B 37, Mem.: 85 1913
Haronga madagascariensis var. pubescens (Poir.) Choisy Prodr. 1: 542 (1824)

Common names Top

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Language Common/alternative name
Finnish hehkumehupuu
Hausa alillibar rafi
Chinese 马达加斯加合掌树

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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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
World Flora Online wfo-0000716096
UNII PP71588J9Z
Tropicos 7801103
INPN 706356
KEW urn:lsid:ipni.org:names:153822-3
The Plant List kew-2840115
Open Tree Of Life 324228
NCBI Taxonomy 198768
IUCN Red List 62019179
IPNI 433131-1
iNaturalist 134190
GBIF 3711847
EPPO HRGMA
EOL 5711026
USDA GRIN 417522
Wikipedia Harungana_madagascariensis
CMAUP NPO25801

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
Review of Herbal Medicinal Plants Used in the Management of Cancers in the East Africa Region from 2019 to 2023 Kudamba A, Kasolo JN, Bbosa GS, Lugaajju A, Wabinga H, Kafeero HM, Ssenku JE, Alemu SO, Walusansa A, Niyonzima N, Muwonge H Integr Cancer Ther 06-Mar-2024
PMCID:PMC10916491
doi:10.1177/15347354241235583
PMID:38445504
A comprehensive review of antimalarial medicinal plants used by Tanzanians Kacholi DS Pharm Biol 25-Jan-2024
PMCID:PMC10812860
doi:10.1080/13880209.2024.2305453
PMID:38270178
In Vitro Activity of Allium cepa Organosulfur Derivatives against Canine Multidrug-Resistant Strains of Staphylococcus spp. and Enterobacteriaceae Maroto-Tello A, Ayllón T, Aguinaga-Casañas MA, Ariza JJ, Penelo S, Baños A, Ortiz-Díez G Vet Sci 09-Jan-2024
PMCID:PMC10820550
doi:10.3390/vetsci11010026
PMID:38250932
Medicinal plants used in the management of cancers by residents in the Elgon Sub-Region, Uganda Kudamba A, Kasolo JN, Bbosa GS, Lugaajju A, Wabinga H, Niyonzima N, Ocan M, Damani AM, Kafeero HM, Ssenku JE, Alemu SO, Lubowa M, Walusansa A, Muwonge H BMC Complement Med Ther 12-Dec-2023
PMCID:PMC10714536
doi:10.1186/s12906-023-04273-5
PMID:38087230
Pseudomonas spp. in Canine Otitis Externa Secker B, Shaw S, Atterbury RJ Microorganisms 28-Oct-2023
PMCID:PMC10673570
doi:10.3390/microorganisms11112650
PMID:38004662
Ethnomedicinal Knowledge of Plants Used in Nonconventional Medicine in the Management of Diabetes Mellitus in Kinshasa (Democratic Republic of the Congo) Chiribagula Valentin B, Ndjolo Philippe O, Mboni Henry M, Mushagalusa Kasali F Evid Based Complement Alternat Med 20-Sep-2023
PMCID:PMC10533323
doi:10.1155/2023/4621883
PMID:37771953
Indigenous medicinal plants used in folk medicine for malaria treatment in Kwara State, Nigeria: an ethnobotanical study Evbuomwan IO, Stephen Adeyemi O, Oluba OM BMC Complement Med Ther 16-Sep-2023
PMCID:PMC10504731
doi:10.1186/s12906-023-04131-4
PMID:37716985
Ethnobotanical study of nutraceutical plants used to manage opportunistic infections associated with HIV/AIDS in Acholi sub-region, Northern Uganda Ikinyom N, Lamwaka AV, Malagala AT, Ndyomugyenyi EK Trop Med Health 01-Sep-2023
PMCID:PMC10472741
doi:10.1186/s41182-023-00540-w
PMID:37658427
How to approach a study in ethnopharmacology? Providing an example of the different research stages for newcomers to the field today Schultz F, Garbe L Pharmacol Res Perspect 27-Jul-2023
PMCID:PMC10375576
doi:10.1002/prp2.1109
PMID:37497567
Plant Extracts as a Source of Natural Products with Potential Antimalarial Effects: An Update from 2018 to 2022 Ribeiro GD, Rei Yan SL, Palmisano G, Wrenger C Pharmaceutics 01-Jun-2023
PMCID:PMC10300920
doi:10.3390/pharmaceutics15061638
PMID:37376086
Bioassay-Guided Isolation of Antiplasmodial Compounds from Hypericum lanceolatum Lam. (Hypericaceae) and Their Cytotoxicity and Molecular Docking Happi GM, Ahmed SA, Kemayou GP, Salau S, Dzouemo LC, Sikam KG, Yimtchui MT, Wansi JD Biomed Res Int 29-May-2023
PMCID:PMC10241580
doi:10.1155/2023/4693765
PMID:37284030
In a Preliminary Study on Human Subjects, a Cosmetic Cream Containing a Harungana madagascariensis Plant Extract Induces Similar Anti-Aging Effects to a Retinol-Containing Cream Gibielle C, Bousseksou L, Guéhenneux S, Vié K Clin Cosmet Investig Dermatol 19-Apr-2023
PMCID:PMC10122863
doi:10.2147/CCID.S401290
PMID:37155516
Contrasting warming responses of photosynthesis in early- and late-successional tropical trees Mujawamariya M, Wittemann M, Dusenge ME, Manishimwe A, Ntirugulirwa B, Zibera E, Nsabimana D, Wallin G, Uddling J Tree Physiol 27-Mar-2023
PMCID:PMC10335848
doi:10.1093/treephys/tpad035
PMID:36971469
Important Medicinal and Food Taxa (Orders and Families) in Kenya, Based on Three Quantitative Approaches Mutie FM, Mbuni YM, Rono PC, Mkala EM, Nzei JM, Phumthum M, Hu GW, Wang QF Plants (Basel) 02-Mar-2023
PMCID:PMC10005506
doi:10.3390/plants12051145
PMID:36904005
Use of Multi-Date and Multi-Spectral UAS Imagery to Classify Dominant Tree Species in the Wet Miombo Woodlands of Zambia Shamaoma H, Chirwa PW, Zekeng JC, Ramoelo A, Hudak AT, Handavu F, Syampungani S Sensors (Basel) 16-Feb-2023
PMCID:PMC9960281
doi:10.3390/s23042241
PMID:36850838

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
> Benzenoids / Anthracenes
(10R)-1,3,8,10-tetrahydroxy-6-methyl-2,4,5-tris(3-methylbut-2-enyl)-10H-anthracen-9-one 162912636 Click to see 476.60 unknown https://doi.org/10.1021/NP050407N
(10S)-1,3,8,10-tetrahydroxy-6-methyl-2,4,5-tris(3-methylbut-2-enyl)-10H-anthracen-9-one 162912637 Click to see 476.60 unknown https://doi.org/10.1021/NP050407N
(10S)-1,3,8,10-tetrahydroxy-6-methyl-4,5-bis(3-methylbut-2-enyl)-10H-anthracen-9-one 162893012 Click to see CC1=CC(=C2C(=C1CC=C(C)C)C(C3=C(C(=CC(=C3C2=O)O)O)CC=C(C)C)O)O 408.50 unknown https://doi.org/10.1021/NP050407N
(2S,11S)-5,7-dihydroxy-2-(2-hydroxypropan-2-yl)-11-methoxy-9-methyl-10-(3-methylbut-2-enyl)-2,11-dihydro-1H-naphtho[3,2-e][1]benzofuran-6-one 162975507 Click to see 438.50 unknown https://doi.org/10.1021/NP060556L
https://doi.org/10.1021/NP050407N
1,3,8-trihydroxy-6-methyl-2,4,5-tris(3-methylbut-2-enyl)-10H-anthracen-9-one 68374064 Click to see 460.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.03.022
1,3,8-Trihydroxy-6-methyl-4,5-bis-(3-methyl-but-2-enyl)-10H-anthracen-9-one 44348974 Click to see 392.50 unknown https://doi.org/10.1016/0031-9422(95)00202-I
2-(3-Methyl-1-butenyl)-1,8-dihydroxy-3-methoxy-6-methylanthrone 155490509 Click to see 338.40 unknown https://doi.org/10.1016/0031-9422(95)00202-I
3,8,9-Trihydroxy-6-methyl-4,4,5-tris(3-methylbut-2-enyl)anthracen-1(4H)-one 77325 Click to see 460.60 unknown https://doi.org/10.1016/J.BSE.2005.08.004
Harunganol B 44349182 Click to see CC1=C(C2=C(C(=C1CC=C(C)C)O)C(=O)C3=C(C=C(C(=C3C2)CC=C(C)C)O)O)CC=C(C)C 460.60 unknown https://doi.org/10.1021/NP060556L
https://doi.org/10.1021/NP050407N
https://doi.org/10.1016/0031-9422(95)00202-I
https://doi.org/10.1016/J.PHYTOCHEM.2005.03.022
Kenganthranol A 11589590 Click to see 408.50 unknown https://doi.org/10.1021/NP050407N
Kenganthranol B 11496609 Click to see 476.60 unknown https://doi.org/10.1021/NP050407N
Kenganthranol C 11619022 Click to see 438.50 unknown https://doi.org/10.1021/NP060556L
https://doi.org/10.1021/NP050407N
> Benzenoids / Anthracenes / Anthraquinones
1,8-Dihydroxy-3-methoxy-6-methyl-2-(3-methylbut-1-enyl)anthracene-9,10-dione 628167 Click to see 352.40 unknown https://doi.org/10.1016/0031-9422(95)00202-I
https://doi.org/10.1021/NP050407N
Aloe emodin w-acetate 10425624 Click to see CC(=O)OCC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=CC=C3O 312.27 unknown https://doi.org/10.1016/0031-9422(95)00202-I
Madagascine 378693 Click to see 338.40 unknown https://doi.org/10.1016/0031-9422(95)00202-I
https://doi.org/10.1016/J.BSE.2005.08.004
https://doi.org/10.1021/NP050407N
Physcion 10639 Click to see 284.26 unknown https://doi.org/10.1016/J.BSE.2005.08.004
https://doi.org/10.1021/NP050407N
Vismiaquinone 5378723 Click to see 352.40 unknown https://doi.org/10.1016/0031-9422(95)00202-I
https://doi.org/10.1021/NP050407N
vismiaquinone B 14729072 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C(=C(C=C3C2=O)OC)CC(=O)C(C)C)O 368.40 unknown https://doi.org/10.1021/NP050407N
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
1,3,8-Trihydroxy-6-methyl-2-(1,6,8-trihydroxy-3-methyl-9,10-dioxoanthracen-2-yl)anthracene-9,10-dione 12312660 Click to see 538.50 unknown https://doi.org/10.1071/CH9720843
> 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 / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Methyl Haematommate 591773 Click to see 210.18 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.03.022
> Benzenoids / Naphthalenes / Naphthoquinones
(1S,13S,15S)-8,10,15-trihydroxy-6,14,14-trimethyl-1,5-bis(3-methylbut-2-enyl)tetracyclo[11.3.1.02,11.04,9]heptadeca-2,4,6,8,10-pentaene-12,17-dione 16215169 Click to see 476.60 unknown https://doi.org/10.1021/NP060556L
8,10,15-Trihydroxy-6,14,14-trimethyl-1,5-bis(3-methylbut-2-enyl)tetracyclo[11.3.1.02,11.04,9]heptadeca-2,4,6,8,10-pentaene-12,17-dione 163029329 Click to see 476.60 unknown https://doi.org/10.1021/NP060556L
Harunmadagascarin D 44421664 Click to see CC1=CC(=C2C(=C1CC=C(C)C)C=C3C(=C2O)C(=O)C4C(=O)C3(CC(C4(C)C)O)CC=C(C)C)O 476.60 unknown https://doi.org/10.1021/NP060556L
> Benzenoids / Phenol ethers / Anisoles
1,3,5-Trimethoxybenzene 69301 Click to see 168.19 unknown https://doi.org/10.1016/0031-9422(95)00202-I
> Benzenoids / Phenols / Tyrosols and derivatives / Tyrosols
Tyrosol 10393 Click to see 138.16 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
Pinoresinol 73399 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 358.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Lignan glycosides
2-[4-[2,3-Bis(hydroxymethyl)-4-[3-methoxy-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyphenyl]butyl]-2-methoxyphenoxy]-6-methyloxane-3,4,5-triol 14309780 Click to see CC1C(C(C(C(O1)OC2=C(C=C(C=C2)CC(CO)C(CC3=CC(=C(C=C3)OC4C(C(C(C(O4)C)O)O)O)OC)CO)OC)O)O)O 654.70 unknown https://doi.org/10.1248/CPB.55.464
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Annonaceous acetogenins
(2R)-4-[(2R)-2-hydroxy-9-[(2R,5S)-5-[(Z,1S,4S,5S)-1,4,5-trihydroxynonadec-8-enyl]oxolan-2-yl]nonyl]-2-methyl-2H-furan-5-one 10508156 Click to see 622.90 unknown https://doi.org/10.1248/CPB.55.464
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Aconitane-type diterpenoid alkaloids
[(1S,2R,3R,4S,5R,6S,8S,9S,10R,13S,16S,17R)-4-acetyloxy-11-ethyl-6,16-dimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-8-yl] benzoate 101939154 Click to see 567.70 unknown https://doi.org/10.1021/NP050407N
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
(2E,6S)-2,6-dimethylocta-2,7-diene-1,6-diol 11206026 Click to see CC(=CCCC(C)(C=C)O)CO 170.25 unknown via CMAUP database
(2E,6S)-6-hydroxy-2,6-dimethylocta-2,7-dienal 101794462 Click to see 168.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-trans-Carveol 443178 Click to see CC1=CCC(CC1O)C(=C)C 152.23 unknown https://doi.org/10.1248/CPB.55.464
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(2,12-Diacetyloxy-3,10-dihydroxy-4,9,13-trimethyl-17-methylidene-5-oxo-6-oxatricyclo[11.4.0.03,7]heptadec-8-en-14-yl) acetate 73228267 Click to see 508.60 unknown https://doi.org/10.1248/CPB.55.464
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Betulinic Acid 64971 Click to see 456.70 unknown https://doi.org/10.1016/J.BSE.2005.08.004
https://doi.org/10.1248/CPB.55.464
Epibetulinic Acid 485711 Click to see 456.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.03.022
Epilupeol 5270628 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.03.022
Friedelan-3-one 244297 Click to see 426.70 unknown https://doi.org/10.1248/CPB.55.464
https://doi.org/10.1016/J.PHYTOCHEM.2005.03.022
Friedelin 91472 Click to see 426.70 unknown https://doi.org/10.1107/S0108270190007454
https://doi.org/10.1016/J.PHYTOCHEM.2005.03.022
https://doi.org/10.1016/J.BSE.2005.08.004
https://doi.org/10.1248/CPB.55.464
Lup-20(29)-en-28-oic acid, 3beta-hydroxy- 2371 Click to see 456.70 unknown https://doi.org/10.1248/CPB.55.464
https://doi.org/10.1016/J.PHYTOCHEM.2005.03.022
Lup-20(29)-en-3-ol, (3beta)- 521518 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.03.022
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.03.022
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
[(2S,3R,4S,5R)-2-[(2S,3R,4S,5S)-3-acetyloxy-2-[[(3S,8R,9S,10R,13S,14S,16S,17S)-3,17-dihydroxy-10,13-dimethyl-17-[(2S)-6-methyl-3-oxoheptan-2-yl]-1,2,3,4,7,8,9,11,12,14,15,16-dodecahydrocyclopenta[a]phenanthren-16-yl]oxy]-5-hydroxyoxan-4-yl]oxy-4,5-dihydroxyoxan-3-yl] (E)-3-phenylprop-2-enoate 101504648 Click to see 869.00 unknown https://doi.org/10.1248/CPB.55.464
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1071/CH9720843
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1071/CH9720843
> Organoheterocyclic compounds / Benzodioxanes / Phenylbenzodioxanes / Phenylbenzo-1,4-dioxanes
(2R,3R)-8-hydroxy-3-(4-hydroxy-3,5-dimethoxyphenyl)-2-(hydroxymethyl)-5-methoxy-2,3-dihydro-[1,4]dioxino[2,3-c]xanthen-7-one 101989979 Click to see COC1=CC(=CC(=C1O)OC)C2C(OC3=C4C(=CC(=C3O2)OC)C(=O)C5=C(C=CC=C5O4)O)CO 482.40 unknown https://doi.org/10.3987/COM-96-7497
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
(4aS,9aS)-1,7-dihydroxy-4a,9a-dihydroxanthen-9-one 163039036 Click to see 230.22 unknown https://doi.org/10.1021/NP060556L
1,5,6-Trihydroxy-7-methoxyxanthone 129685345 Click to see COC1=C(C(=C2C(=C1)C(=O)C3=C(C=CC=C3O2)O)O)O 274.22 unknown https://doi.org/10.1016/0031-9422(95)00202-I
1,7-Dihydroxy-4a,9a-dihydroxanthen-9-one 44583784 Click to see 230.22 unknown https://doi.org/10.1021/NP060556L
Euxanthone 5281631 Click to see 228.20 unknown https://doi.org/10.1021/NP050407N
https://doi.org/10.1016/0031-9422(95)00202-I
https://doi.org/10.1111/J.2042-7158.1996.TB03988.X
Xanthone 7020 Click to see C1=CC=C2C(=C1)C(=O)C3=CC=CC=C3O2 196.20 unknown https://doi.org/10.1021/NP060556L
> Organoheterocyclic compounds / Naphthofurans
(3R)-5,6-dihydroxy-2,2,3,8-tetramethyl-11,11-bis(3-methylbut-2-enyl)-3H-naphtho[2,3-f][1]benzofuran-4-one 163097855 Click to see CC1C2=C(C(C3=C(C2=O)C(=C4C(=C3)C=C(C=C4O)C)O)(CC=C(C)C)CC=C(C)C)OC1(C)C 460.60 unknown https://doi.org/10.1021/NP060556L
(3S)-5,6-dihydroxy-2,2,3,8-tetramethyl-11,11-bis(3-methylbut-2-enyl)-3H-naphtho[2,3-f][1]benzofuran-4-one 163097856 Click to see 460.60 unknown https://doi.org/10.1021/NP060556L
5,6-dihydroxy-2,2,3,8-tetramethyl-11,11-bis(3-methylbut-2-enyl)-3H-naphtho[2,3-f][1]benzofuran-4-one 16215168 Click to see 460.60 unknown https://doi.org/10.1021/NP060556L
> Organoheterocyclic compounds / Naphthopyrans
(1S,19R)-10,14-dihydroxy-6,6,16,20,20-pentamethyl-15-(3-methylbut-2-enyl)-7,21,23-trioxahexacyclo[11.8.1.11,19.02,11.03,8.017,22]tricosa-2(11),3(8),4,9,13(22),14,16-heptaen-12-one 16215170 Click to see 488.60 unknown https://doi.org/10.1021/NP060556L
10,14-Dihydroxy-6,6,16,20,20-pentamethyl-15-(3-methylbut-2-enyl)-7,21,23-trioxahexacyclo[11.8.1.11,19.02,11.03,8.017,22]tricosa-2(11),3(8),4,9,13(22),14,16-heptaen-12-one 102080583 Click to see 488.60 unknown https://doi.org/10.1021/NP060556L
6,7-Dihydroxy-2,2,9-trimethyl-12,12-bis(3-methylbut-2-enyl)naphtho[2,3-g]chromen-5-one 11282553 Click to see CC1=CC2=CC3=C(C(=C2C(=C1)O)O)C(=O)C4=C(C3(CC=C(C)C)CC=C(C)C)OC(C=C4)(C)C 458.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.03.022
Harunmadagacarin B 11329963 Click to see 526.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.03.022
kenganthranol D 44421665 Click to see CC1=C2CC3C(OC4(C2=C(C(=C1CC=C(C)C)O)C(=O)C5=C4C6C=CC(OC6C=C5O)(C)C)O3)(C)C 490.60 unknown https://doi.org/10.1021/NP060556L
> Organoheterocyclic compounds / Naphthopyrans / Naphthopyranones
[3-Chloro-10a-(3,7-dimethylocta-2,6-dienyl)-8-hydroxy-2,2,4a-trimethyl-5,6,10-trioxo-3,4-dihydrobenzo[g]chromen-9-ylidene]-iminoazanium 163185986 Click to see 488.00 unknown https://doi.org/10.1021/NP050407N
https://doi.org/10.1248/CPB.55.464
> Organoheterocyclic compounds / Pyridines and derivatives / Methylpyridines
(7S)-6,7-Dihydro-4,7-dimethyl-5H-cyclopenta(c)pyridine 68231 Click to see 147.22 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
Proanthocyanidin B4 9959902 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Catechin 9064 Click to see 290.27 unknown via CMAUP database
Epicatechin 72276 Click to see 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin 5280343 Click to see 302.23 unknown https://doi.org/10.1071/CH9720843
https://doi.org/10.1016/0031-9422(95)00202-I
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-3-O-glycosides
(2R,3S,4R,5S)-2-[(2S,3R,4S,5R,6R)-2-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromenylium-3-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxyoxane-3,4,5-triol 101692563 Click to see 581.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-3-(3,4,5-trihydroxy-6-methyl-oxa N-2-YL)oxy-chroman-4-one 316844 Click to see 450.40 unknown https://doi.org/10.1016/0031-9422(95)00202-I
Astilbin 119258 Click to see 450.40 unknown https://doi.org/10.1016/0031-9422(95)00202-I
Camelliaside B 25115190 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)OC6C(C(C(CO6)O)O)O)O)O)O)O)O 726.60 unknown via CMAUP database
Leucoside 44566720 Click to see 580.50 unknown via CMAUP database
Quercetin 3-O-(2G-beta-D-xylopyranosylrutinoside) 5281690 Click to see 742.60 unknown via CMAUP database
Quercetin 3-O-Sambubioside 5487635 Click to see 596.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
5-hydroxy-2-(4-hydroxyphenyl)-7-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 92218152 Click to see 432.40 unknown https://doi.org/10.1248/CPB.55.464
> Phenylpropanoids and polyketides / Isoflavonoids / Coumestans
1,3-Dihydroxy-8,9-dimethoxy-[1]benzofuro[3,2-c]chromen-6-one 11602329 Click to see COC1=C(C=C2C(=C1)C3=C(O2)C4=C(C=C(C=C4OC3=O)O)O)OC 328.27 unknown https://doi.org/10.1016/J.BSE.2005.08.004
https://doi.org/10.1016/0031-9422(95)00202-I

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