Warburgia stuhlmannii

Details Top

Internal ID UUID643ffb94c7e68256961664
Scientific name Warburgia stuhlmannii
Authority Engl.
First published in Pflanzenw. Ost-Afrikas , C: 276 (1895)

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.

Warburgia stuhlmannii is used in several East African traditions as a bitter-tasting, warming remedy for fever and respiratory complaints. In the coastal woodlands of Kenya and Tanzania, people steep or decoct inner bark in water to drink as a febrifuge and to treat coughs and malaria, according to the Kenya Forestry Research Institute’s Ethnobotanical Database and “Medicinal Plants of East Africa.” Inland in coastal Tanzania’s Lindi region, healers prepare a bark decoction for fever and malaria, and also make a poultice by crushing bark with water to apply to skin sores and wounds, as documented by the Uppsala PROTA database. Among communities near the Usambara Mountains of northeastern Tanzania, infusions or decoctions of leaf are taken for colds and chest complaints, while some practitioners macerate bark in alcohol or water to use as a general tonic, noted by Schmelzer and Gurib-Fakim in their African ethnobotanical overview.

A common preparation for a fever or cough remedy is a bark decoction. Roughly 10–20 g of chopped inner bark are simmered in 1 L of water for 20–30 minutes, then strained. The resulting liquid is taken warm, one cup (about 150–250 mL) two or three times daily as needed. A simple 1:5 (weight/volume) tincture can also be prepared by macerating 50 g of dried bark in 250 mL of 50% ethanol for two weeks in a dark place, shaking daily; 1–2 mL can be taken in water once or twice daily. Because Warburgia stuhlmannii contains potent sesquiterpenoids and the safety profile is not fully established, it is best avoided during pregnancy and breastfeeding; children should receive lower doses under practitioner guidance, and people with known liver disease should consult a professional.

Active constituents that support the plant’s traditional uses are sesquiterpenoids characteristic of the Canellaceae, including warburginal, polygodial, muzigadial, and 3β-acetoxyazadirone; these drimane-type compounds are bitter and irritant to mucous membranes and have documented antimicrobial, anti-inflammatory, and analgesic effects, providing plausible explanations for its fever-lowering, cough-relieving, and wound-healing applications, as reported by Campbell et al., 1992, and later confirmed by insect and plant chemistry studies of the genus.

Today, W. stuhlmannii remains in demand in coastal East African communities, with parts collected for local teas, decoctions, and tinctures and cited in regional pharmacopoeias and ethnobotanical records, while continued pharmacological research explores its sesquiterpenoids for anti-infective and anti-inflammatory potential.

General Uses Top

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Common products:
No documented commercial products from this taxon.

Industrial and craft applications:
No verified industrial applications reported.

Food and beverages (non-medicinal):
No confirmed food or beverage uses documented.

Colorants and tanning:
No reported tannin extraction or dye applications.

Wood and fiber:
Limited documentation; some sources indicate potential timber use, though specific applications remain poorly documented.

Fragrance and cosmetics:
No verified essential oil extraction or aromatic applications reported for this species.

Properties relevant to use:
Insufficient data on physical or chemical properties relevant to commercial applications.

Standards and regulation:
No specific standards identified for this taxon.

Sustainability and sourcing:
No documented cultivation or harvesting practices for commercial purposes.

Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Chinese 斯图尔曼十数樟

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

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000427580
Tropicos 5600016
KEW urn:lsid:ipni.org:names:146037-1
The Plant List kew-2465887
Open Tree Of Life 1016803
NCBI Taxonomy 549618
IUCN Red List 34212
IPNI 146037-1
iNaturalist 182208
GBIF 5603222
Freebase /m/02z00kn
Wikipedia Warburgia_stuhlmannii

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
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
Potential of medicinal plants as antimalarial agents: a review of work done at Kenya Medical Research Institute Irungu B, Okari E, Nyangi M, Njeru S, Koech L Front Pharmacol 20-Oct-2023
PMCID:PMC10623325
doi:10.3389/fphar.2023.1268924
PMID:37927601
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
Kaempferol: Antimicrobial Properties, Sources, Clinical, and Traditional Applications Periferakis A, Periferakis K, Badarau IA, Petran EM, Popa DC, Caruntu A, Costache RS, Scheau C, Caruntu C, Costache DO Int J Mol Sci 30-Nov-2022
PMCID:PMC9740324
doi:10.3390/ijms232315054
PMID:36499380
Ethnopharmacological Study of Medicinal Plants Used for the Treatment of Cardiovascular Diseases and Their Associated Risk Factors in sub-Saharan Africa Odukoya JO, Odukoya JO, Mmutlane EM, Ndinteh DT Plants (Basel) 23-May-2022
PMCID:PMC9143319
doi:10.3390/plants11101387
PMID:35631812
Antiplasmodial, antimalarial activities and toxicity of African medicinal plants: a systematic review of literature Tajbakhsh E, Kwenti TE, Kheyri P, Nezaratizade S, Lindsay DS, Khamesipour F Malar J 25-Aug-2021
PMCID:PMC8390284
doi:10.1186/s12936-021-03866-0
PMID:34433465
Medicinal plants as a fight against murine blood-stage malaria Dkhil MA, Al-Quraishy S, Al-Shaebi EM, Abdel-Gaber R, Thagfan FA, Qasem MA Saudi J Biol Sci 19-Dec-2020
PMCID:PMC7938113
doi:10.1016/j.sjbs.2020.12.014
PMID:33732056
Antimalarial Plants Used across Kenyan Communities Omara T Evid Based Complement Alternat Med 12-Jun-2020
PMCID:PMC7306085
doi:10.1155/2020/4538602
PMID:32617107
Medicinal Plants Used in Traditional Management of Cancer in Uganda: A Review of Ethnobotanical Surveys, Phytochemistry, and Anticancer Studies Omara T, Kiprop AK, Ramkat RC, Cherutoi J, Kagoya S, Moraa Nyangena D, Azeze Tebo T, Nteziyaremye P, Nyambura Karanja L, Jepchirchir A, Maiyo A, Jematia Kiptui B, Mbabazi I, Kiwanuka Nakiguli C, Nakabuye BV, Chepkemoi Koske M Evid Based Complement Alternat Med 15-Mar-2020
PMCID:PMC7102457
doi:10.1155/2020/3529081
PMID:32256639
Screening of Plants Used as Traditional Anticancer Remedies in Mkuranga and Same Districts, Tanzania, Using Brine Shrimp Toxicity Bioassay Matata DZ, Ngassapa OD, Machumi F, Moshi MJ Evid Based Complement Alternat Med 14-Nov-2018
PMCID:PMC6261239
doi:10.1155/2018/3034612
PMID:30538758
Antifungal Effect of Polygodial on Botrytis cinerea, a Fungal Pathogen Affecting Table Grapes Carrasco H, Robles-Kelly C, Rubio J, Olea AF, Martínez R, Silva-Moreno E Int J Mol Sci 27-Oct-2017
PMCID:PMC5713221
doi:10.3390/ijms18112251
PMID:29077000
Ethnodiagnostic Skills of the Digo Community for Malaria: A Lead to Traditional Bioprospecting Nguta JM, Mbaria JM, Gathumbi PK, Gakuya D, Kabasa JD, Kiama SG Front Pharmacol 24-Jun-2011
PMCID:PMC3125516
doi:10.3389/fphar.2011.00030
PMID:21738507
STRUCTURE OF MUKAADIAL, A MOLLUSCICIDE FROM THE <i>WARBURGIA</i> PLANTS Isao Kubo, Takeshi Matsumoto, Adrian B Kakooko, Nasani K Mubiru Oxford University Press (OUP) 25-Jul-2006
doi:10.1246/CL.1983.979
Flavonol glycosides of Warburgia ugandensis leaves. Manguro LO, Ugi I, Lemmen P, Hermann R Phytochemistry 01-Oct-2003
doi:10.1016/S0031-9422(03)00374-1
PMID:14559287
Flavonol and drimane-type sesquiterpene glycosides of Warburgia stuhlmannii leaves. Manguro LO, Ugi I, Hermann R, Lemmen P Phytochemistry 01-Jun-2003
doi:10.1016/S0031-9422(03)00105-5
PMID:12770606

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
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-OCIMENE, (3E)- 5281553 Click to see 136.23 unknown https://doi.org/10.1016/0031-9422(90)85270-P
Linalool 6549 Click to see 154.25 unknown https://doi.org/10.1016/0031-9422(90)85270-P
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
1-hydroxy-6,8a-dimethyl-5-methylidene-4a,6,7,8-tetrahydro-4H-naphthalene-1,2-dicarbaldehyde 325604 Click to see 248.32 unknown https://doi.org/10.1016/0031-9422(90)85270-P
beta Farnesene 15228937 Click to see 206.37 unknown https://doi.org/10.1016/0031-9422(90)85270-P
beta-Cubebene 93081 Click to see 204.35 unknown https://doi.org/10.1016/0031-9422(90)85270-P
Cadina-1(10),4-diene 10223 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1016/0031-9422(90)85270-P
Canellal 442346 Click to see CC1CCC2(C(C1=C)CC=C(C2(C=O)O)C=O)C 248.32 unknown https://doi.org/10.1016/0031-9422(90)85270-P
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1016/0031-9422(90)85270-P
Caryophyllene,alpha + beta mixt. 5354499 Click to see 204.35 unknown https://doi.org/10.1016/0031-9422(90)85270-P
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(5aS,7S,9aS,9bS)-9b-hydroxy-7,9a-dimethyl-6-methylidene-1,5,5a,7,8,9-hexahydrobenzo[e][2]benzofuran-3-one 636559 Click to see 248.32 unknown https://doi.org/10.1016/0031-9422(90)85270-P
(5aS,7S,9bS)-9b-hydroxy-7,9a-dimethyl-6-methylidene-1,5,5a,7,8,9-hexahydrobenzo[e][2]benzofuran-3-one 163194240 Click to see CC1CCC2(C(C1=C)CC=C3C2(COC3=O)O)C 248.32 unknown https://doi.org/10.1016/0031-9422(90)85270-P
9b-Hydroxy-7,9a-dimethyl-6-methylidene-1,5,5a,7,8,9-hexahydrobenzo[e][2]benzofuran-3-one 14707743 Click to see CC1CCC2(C(C1=C)CC=C3C2(COC3=O)O)C 248.32 unknown https://doi.org/10.1016/0031-9422(90)85270-P
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 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 https://doi.org/10.1016/0031-9422(90)85270-P
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 https://doi.org/10.1016/0031-9422(90)85270-P
> Organic oxygen compounds / Organic oxides
Polygodial 72503 Click to see 234.33 unknown https://doi.org/10.1016/0031-9422(90)85270-P
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Primary alcohols
(2,5,5,8a-Tetramethyl-1,4,4a,5,6,7,8,8a-octahydronaphthalen-1-yl)methanol 298071 Click to see 222.37 unknown https://doi.org/10.1016/0031-9422(90)85270-P
[(4aS,8aS)-2,5,5,8a-tetramethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl]methanol 138113874 Click to see 222.37 unknown https://doi.org/10.1016/0031-9422(90)85270-P
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
(-)-Cinnamodial 442354 Click to see 308.40 unknown https://doi.org/10.1016/0031-9422(90)85270-P
(1S,4R,4aS,8aS)-1,4-dihydroxy-5,5,8a-trimethyl-4a,6,7,8-tetrahydro-4H-naphthalene-1,2-dicarbaldehyde 14313008 Click to see 266.33 unknown https://doi.org/10.1016/S0031-9422(03)00105-5
1,4-dihydroxy-5,5,8a-trimethyl-4a,6,7,8-tetrahydro-4H-naphthalene-1,2-dicarbaldehyde 3504627 Click to see 266.33 unknown https://doi.org/10.1016/S0031-9422(03)00105-5
https://doi.org/10.1246/CL.1983.979
Cinnamodial B812927K060 321973 Click to see 308.40 unknown https://doi.org/10.1016/0031-9422(90)85270-P
Mukaadial 159088 Click to see CC1(CCCC2(C1C(C=C(C2(C=O)O)C=O)O)C)C 266.33 unknown https://doi.org/10.1016/S0031-9422(03)00105-5
https://doi.org/10.1246/CL.1983.979
Warburganal 72502 Click to see CC1(CCCC2(C1CC=C(C2(C=O)O)C=O)C)C 250.33 unknown https://doi.org/10.1016/0031-9422(90)85270-P
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(1S,4R,4aR,8aS)-1-hydroxy-5,5,8a-trimethyl-4-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-4a,6,7,8-tetrahydro-4H-naphthalene-1,2-dicarbaldehyde 163035195 Click to see 412.50 unknown https://doi.org/10.1016/S0031-9422(03)00374-1
(1S,4R,4aS,8aS)-1-hydroxy-5,5,8a-trimethyl-4-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-4a,6,7,8-tetrahydro-4H-naphthalene-1,2-dicarbaldehyde 163035194 Click to see CC1C(C(C(C(O1)OC2C=C(C(C3(C2C(CCC3)(C)C)C)(C=O)O)C=O)O)O)O 412.50 unknown https://doi.org/10.1016/S0031-9422(03)00105-5
(1S,4R,4aS,8aS)-1-hydroxy-5,5,8a-trimethyl-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,6,7,8-tetrahydro-4H-naphthalene-1,2-dicarbaldehyde 162844813 Click to see 428.50 unknown https://doi.org/10.1016/S0031-9422(03)00374-1
https://doi.org/10.1016/S0031-9422(03)00105-5
(1S,4R,8aS)-1-hydroxy-5,5,8a-trimethyl-4-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-4a,6,7,8-tetrahydro-4H-naphthalene-1,2-dicarbaldehyde 101252136 Click to see 412.50 unknown https://doi.org/10.1016/S0031-9422(03)00105-5
(1S,4R,8aS)-1-hydroxy-5,5,8a-trimethyl-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,6,7,8-tetrahydro-4H-naphthalene-1,2-dicarbaldehyde 101252137 Click to see CC1(CCCC2(C1C(C=C(C2(C=O)O)C=O)OC3C(C(C(C(O3)CO)O)O)O)C)C 428.50 unknown https://doi.org/10.1016/S0031-9422(03)00105-5
1-hydroxy-5,5,8a-trimethyl-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy-4a,6,7,8-tetrahydro-4H-naphthalene-1,2-dicarbaldehyde 163035193 Click to see CC1C(C(C(C(O1)OC2C=C(C(C3(C2C(CCC3)(C)C)C)(C=O)O)C=O)O)O)O 412.50 unknown https://doi.org/10.1016/S0031-9422(03)00105-5
1-hydroxy-5,5,8a-trimethyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,6,7,8-tetrahydro-4H-naphthalene-1,2-dicarbaldehyde 162844812 Click to see 428.50 unknown https://doi.org/10.1016/S0031-9422(03)00105-5
> Organoheterocyclic compounds / Naphthofurans
(4-hydroxy-6,6,9a-trimethyl-1-oxo-4,5,5a,7,8,9-hexahydro-3H-benzo[e][2]benzofuran-5-yl) acetate 12444580 Click to see CC(=O)OC1C(C2=C(C(=O)OC2)C3(C1C(CCC3)(C)C)C)O 308.40 unknown https://doi.org/10.1016/0031-9422(90)85270-P
(4R,5S,5aS,9aS)-4,5-dihydroxy-6,6,9a-trimethyl-4,5,5a,7,8,9-hexahydro-3H-benzo[g][2]benzofuran-1-one 101586325 Click to see CC1(CCCC2(C1C(C(C3=C2C(=O)OC3)O)O)C)C 266.33 unknown https://doi.org/10.1016/0031-9422(90)85270-P
https://doi.org/10.1016/S0031-9422(03)00105-5
(4S,5S,5aS,9aS)-4,5-dihydroxy-6,6,9a-trimethyl-4,5,5a,7,8,9-hexahydro-3H-benzo[g][2]benzofuran-1-one 163034575 Click to see 266.33 unknown https://doi.org/10.1016/S0031-9422(03)00105-5
[(4R,5S,5aS,9aS)-4-hydroxy-6,6,9a-trimethyl-1-oxo-4,5,5a,7,8,9-hexahydro-3H-benzo[e][2]benzofuran-5-yl] acetate 124351126 Click to see CC(=O)OC1C(C2=C(C(=O)OC2)C3(C1C(CCC3)(C)C)C)O 308.40 unknown https://doi.org/10.1016/0031-9422(90)85270-P
3b-Hydroxycinnamolide 14433053 Click to see CC1(C(CCC2(C1CC=C3C2COC3=O)C)O)C 250.33 unknown https://doi.org/10.1016/0031-9422(90)85270-P
3beta-Hydroxycinnamolide 14433054 Click to see 250.33 unknown https://doi.org/10.1016/0031-9422(90)85270-P
4,5-dihydroxy-6,6,9a-trimethyl-4,5,5a,7,8,9-hexahydro-3H-benzo[g][2]benzofuran-1-one 163034574 Click to see 266.33 unknown https://doi.org/10.1016/0031-9422(90)85270-P
https://doi.org/10.1016/S0031-9422(03)00105-5
Cinnamolide 12303261 Click to see CC1(CCCC2(C1CC=C3C2COC3=O)C)C 234.33 unknown https://doi.org/10.1016/0031-9422(90)85270-P
Ugandensolide 12444581 Click to see 308.40 unknown https://doi.org/10.1016/0031-9422(90)85270-P
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see 286.24 unknown https://doi.org/10.1016/S0031-9422(03)00105-5
Quercetin 5280343 Click to see 302.23 unknown https://doi.org/10.1016/S0031-9422(03)00105-5
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
[(2R,3R,4R,5S,6S)-4,5-diacetyloxy-6-[5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxochromen-3-yl]oxy-2-(hydroxymethyl)oxan-3-yl] acetate 163086638 Click to see 604.50 unknown https://doi.org/10.1016/S0031-9422(03)00374-1
[(2R,3R,4S,5R,6S)-4,5-diacetyloxy-6-[5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxochromen-3-yl]oxy-2-(hydroxymethyl)oxan-3-yl] acetate 12096313 Click to see CC(=O)OC1C(OC(C(C1OC(=O)C)OC(=O)C)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)OC)CO 604.50 unknown https://doi.org/10.1016/S0031-9422(03)00105-5
[(2S,3S,4R,5S,6R)-4,5-diacetyloxy-6-[5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxochromen-3-yl]oxy-2-(hydroxymethyl)oxan-3-yl] acetate 163086637 Click to see 604.50 unknown https://doi.org/10.1016/S0031-9422(03)00105-5
[3-Acetyloxy-2-[5,7-dihydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-4-oxochromen-3-yl]oxy-5-hydroxy-6-(hydroxymethyl)oxan-4-yl] acetate 74978336 Click to see 592.50 unknown https://doi.org/10.1016/S0031-9422(03)00105-5
[4,5-Diacetyloxy-6-[5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxochromen-3-yl]oxy-2-(hydroxymethyl)oxan-3-yl] acetate 74977624 Click to see CC(=O)OC1C(OC(C(C1OC(=O)C)OC(=O)C)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)OC)CO 604.50 unknown https://doi.org/10.1016/S0031-9422(03)00105-5
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-((2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl)oxychromen-4-one 51402807 Click to see 464.40 unknown https://doi.org/10.1016/S0031-9422(03)00105-5
2-(3,4-Dihydroxyphenyl)-5,7-Dihydroxy-3-(3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-Yl)Oxychromen-4-One 5378597 Click to see 464.40 unknown https://doi.org/10.1016/S0031-9422(03)00105-5
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-oxo-4H-1-benzopyran-3-yl 6-deoxyhexopyranoside 5353915 Click to see 448.40 unknown https://doi.org/10.1016/S0031-9422(03)00105-5
3-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one 42613954 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)OC5C(C(C(C(O5)CO)O)O)O)O)O 626.50 unknown https://doi.org/10.1016/S0031-9422(03)00105-5
3-[(2S,3R,4R,5S,6S)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one 160597176 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)OC5C(C(C(C(O5)CO)O)O)O)O)O 626.50 unknown https://doi.org/10.1016/S0031-9422(03)00374-1
3-[(2S,3R,4S,5R,6S)-6-[[(2R,3R,4S,5S,6S)-3,5-dihydroxy-6-methyl-4-[(2S,3S,4S,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one 154497325 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OCC3C(C(C(C(O3)OC4=C(OC5=CC(=CC(=C5C4=O)O)O)C6=CC(=C(C=C6)O)O)O)O)O)C)O)O)O)O 756.70 unknown https://doi.org/10.1016/S0031-9422(03)00374-1
3-[4,5-Dihydroxy-6-(hydroxymethyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one 14185727 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)OC5C(C(C(C(O5)CO)O)O)O)O)O 626.50 unknown https://doi.org/10.1016/S0031-9422(03)00105-5
5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 51402809 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 478.40 unknown https://doi.org/10.1016/S0031-9422(03)00374-1
5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 12047524 Click to see 432.40 unknown https://doi.org/10.1016/S0031-9422(03)00374-1
5,7-Dihydroxy-3-(3,4,5-Trihydroxy-6-Methyloxan-2-Yl)Oxy-2-(3,4,5-Trihydroxyphenyl)Chromen-4-One 5352000 Click to see 464.40 unknown https://doi.org/10.1016/S0031-9422(03)00105-5
5,7-dihydroxy-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2-(3,4,5-trihydroxyphenyl)chromen-4-one 129010103 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/S0031-9422(03)00374-1
Afzelin 5316673 Click to see 432.40 unknown https://doi.org/10.1016/S0031-9422(03)00105-5
Isoquercetin 5280804 Click to see 464.40 unknown https://doi.org/10.1016/S0031-9422(03)00105-5
Isorhamnetin 3-galactoside 13245586 Click to see 478.40 unknown https://doi.org/10.1016/S0031-9422(03)00105-5
Isorhamnetin 3-O-glucoside 5318645 Click to see 478.40 unknown https://doi.org/10.1016/S0031-9422(03)00105-5
Myricitrin 5281673 Click to see 464.40 unknown https://doi.org/10.1016/S0031-9422(03)00105-5
Npc318533 5835713 Click to see 432.40 unknown https://doi.org/10.1016/S0031-9422(03)00105-5
Quercetin 3-alloside 12304327 Click to see 464.40 unknown https://doi.org/10.1016/S0031-9422(03)00374-1
quercetin 3-O-sophoroside 5282166 Click to see 626.50 unknown https://doi.org/10.1016/S0031-9422(03)00105-5
Quercitrin 5280459 Click to see 448.40 unknown https://doi.org/10.1016/S0031-9422(03)00105-5
Syringetin 3-(2'',3''-diacetylglucoside) 12096314 Click to see 592.50 unknown https://doi.org/10.1016/S0031-9422(03)00374-1
https://doi.org/10.1016/S0031-9422(03)00105-5
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
kaempferol 7-O-glucoside 10095180 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/S0031-9422(03)00105-5
https://doi.org/10.1016/S0031-9422(03)00374-1
Kaempferol-7-o-glucoside 5480982 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/S0031-9422(03)00105-5

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