Zanthoxylum gilletii

Details Top

Internal ID UUID643ffbce92221170470854
Scientific name Zanthoxylum gilletii
Authority (De Wild.) P.G.Waterman
First published in Taxon 23: 363 (1975)

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.

For the past several months we’ve been asked to report only on documented, verifiable uses of the exact taxon Zanthoxylum gilletii, and after reviewing ethnobotanical monographs and peer‑reviewed sources as requested (e.g., Schmelzer & Gurib-Fakim 2008; Harinantenaina et al. 2012; Klein et al. 2021), there is no reliable record of its use as tea, decoction, tincture, maceration, or poultice.

General Uses Top

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Wood and fiber:
The timber of Zanthoxylum gilletii is used locally in West and Central Africa for light construction, tool handles, furniture, flooring, and general carpentry. The wood is generally light to medium in density and exhibits good workability with hand and machine tools, allowing sawing, planing, turning, and finishing for interior joinery and utility items. It is also employed for agricultural implements and occasionally for fuelwood and charcoal.

Food and beverages (non-medicinal):
The mature fruits are harvested and used as a condiment and spice, valued for their aromatic, pepper-like flavor. Fruit are commonly dried and ground for flavoring dishes; in some regions they are similarly processed to Piper guineense for local cuisine. Roots and leaves have been noted as flavorants in seasoning blends, though the primary commercial spice use derives from the fruit.

Fragrance and cosmetics:
The fruits yield an essential oil by steam distillation. The oil contains limonene and linalool as major constituents and smaller amounts of sabinene, terpinen-4-ol, and α-terpineol. It is used by local food and fragrance industries as a flavor and fragrance ingredient; concentration in finished goods is typically low due to sensory and regulatory considerations.

Properties relevant to use:
Heartwood is generally pale brown with good dimensional stability; the oil composition is characteristic of Zanthoxylum fruits with a citrus–peppery aroma profile. Density classes are typically medium (around 550–750 kg/m³ air-dry), allowing a balance of strength and workability suitable for light structural and joinery applications. Essential oil content of the fruit commonly ranges around 1–3% by dry weight.

Standards and regulation:
Wood suitable for internal joinery and furniture is graded per national timber standards and export specifications in supplier countries. Flavoring and essential oils derived from the fruit are handled under regional food and fragrance regulations that stipulate maximum permissible levels and permissible flavoring categories for food and beverages.

Sustainability and sourcing:
The species occurs naturally in lowland and secondary forests and is also cultivated as an orchard tree for its fruit. Sustainable management involves selective harvesting of mature stems, planting in agroforestry systems, and maintaining sufficient regeneration. Local initiatives prioritize mixed plantings and seed supply to balance spice production with timber supply and forest integrity.

Synonyms Top

Scientific name Authority First published in
Zanthoxylum melanorhachis (Hoyle) Little Phytologia 6: 506 (1959)
Zanthoxylum tessmannii (Engl.) Ayafor Pl. Med. (Stuttgart) 50: 210 (1984)
Fagara amaniensis Engl. Bot. Jahrb. Syst. 54: 301 (1917)
Fagara annobonensis Mildbr. Notizbl. Bot. Gart. Berlin-Dahlem 13: 700 (1937)
Fagara discolor Engl. Bot. Jahrb. Syst. 54: 302 (1917)
Fagara gilletii De Wild. Ann. Mus. Congo Belge, Bot. , sér. 5, 1: 271 (1906)
Fagara inaequalis Engl. Bot. Jahrb. Syst. 54: 303 (1917)
Fagara iturensis Engl. Wiss. Erg. Deut. Zentr.-Afr. Exped., Bot. 2: 423 (1912)
Fagara kivuensis Lebrun ex Gilbert Bull. Jard. Bot. État Bruxelles 28: 379 (1958)
Fagara macrophylla Engl. Nat. Pflanzenfam. 3(4): 118 (1896)
Fagara melanorhachis Hoyle Bull. Misc. Inform. Kew 1933: 174 (1933)
Fagara obliquefoliolata Engl. Nat. Pflanzenfam. ed. 2 , 19a: 222 (1931)
Fagara rigidifolia Engl. Bot. Jahrb. Syst. 54(4): 303. 1917 [13 Mar 1917]
Fagara tessmannii Engl. Bot. Jahrb. Syst. 46: 406 (1911)
Fagara gilletii var. cordata G.C.C.Gilbert
Fagara macrophylla var. preussii Engl. ex De Wild.
Zanthoxylum macrophyllum Oliv. Fl. Trop. Afr. 1: 304 (1868)

Common names Top

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Language Common/alternative name
Chinese 非洲花椒

Subspecies (abbr. subsp./ssp.) Top

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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
  • Africa
    • East Tropical Africa
      • Kenya
      • Tanzania
      • Uganda
    • Northeast Tropical Africa
      • Ethiopia
      • Sudan
    • South Tropical Africa
      • Angola
      • Zambia
      • Zimbabwe
    • West Tropical Africa
      • Benin
      • Ghana
      • Guinea
      • Ivory Coast
      • Liberia
      • Nigeria
      • Sierra Leone
    • West-central Tropical Africa
      • Cabinda
      • Cameroon
      • Central African Republic
      • Congo
      • Gabon
      • Gulf Of Guinea Islands
      • Rwanda
      • Zaïre

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000429498
Tropicos 28101651
KEW urn:lsid:ipni.org:names:775746-1
The Plant List kew-2469299
Open Tree Of Life 4728649
NCBI Taxonomy 1291627
IUCN Red List 61958923
IPNI 775746-1
iNaturalist 133504
GBIF 3838162
Freebase /m/0vsgch9
EOL 5620483
Wikipedia Zanthoxylum_gilletii

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
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
Traditional knowledge of plants used in hunting and fishing practices among Baka hunter-gatherers of eastern Cameroon Fongnzossie EF, Ngansop MT, Oishi T, Biwole AB, Biye EH, Ichikawa M J Ethnobiol Ethnomed 03-Jan-2023
PMCID:PMC9808952
doi:10.1186/s13002-022-00571-3
PMID:36597154
Improved wood species identification based on multi-view imagery of the three anatomical planes Rosa da Silva N, Deklerck V, Baetens JM, Van den Bulcke J, De Ridder M, Rousseau M, Bruno OM, Beeckman H, Van Acker J, De Baets B, Verwaeren J Plant Methods 11-Jun-2022
PMCID:PMC9188236
doi:10.1186/s13007-022-00910-1
PMID:35690828
Phytochemical and Functional Characterization of Different Parts of the Garcinia xanthochymus Fruit Prakash J, Sallaram S, Martin A, Veeranna RP, Peddha MS ACS Omega 09-Jun-2022
PMCID:PMC9219070
doi:10.1021/acsomega.2c01966
PMID:35755390
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
Determination of Anti-Alzheimer’s Disease Activity of Selected Plant Ingredients Tuzimski T, Petruczynik A Molecules 18-May-2022
PMCID:PMC9147832
doi:10.3390/molecules27103222
PMID:35630702
Influence of scattered trees in grazing areas on soil properties in the Piedmont region of the Colombian Amazon Álvarez F, Casanoves F, Suárez JC PLoS One 29-Dec-2021
PMCID:PMC8716041
doi:10.1371/journal.pone.0261612
PMID:34965264
Wandering through southwestern Nigeria: An inventory of Yoruba useful angiosperm plants Ajao AA, Mukaila YO, Sabiu S Heliyon 25-Dec-2021
PMCID:PMC8733184
doi:10.1016/j.heliyon.2021.e08668
PMID:35024488
Phenolics from Medicinal and Aromatic Plants: Characterisation and Potential as Biostimulants and Bioprotectants Kisiriko M, Anastasiadi M, Terry LA, Yasri A, Beale MH, Ward JL Molecules 20-Oct-2021
PMCID:PMC8588183
doi:10.3390/molecules26216343
PMID:34770752
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
Structure, composition and diversity of restored forest ecosystems on mine-spoils in South-Western Ghana Nero BF PLoS One 14-Jun-2021
PMCID:PMC8202926
doi:10.1371/journal.pone.0252371
PMID:34125836
Traditional knowledge, use and conservation of plants by the communities of Tharaka-Nithi County, Kenya Kathambi V, Mutie FM, Rono PC, Wei N, Munyao JN, Kamau P, Gituru RW, Hu GW, Wang QF Plant Divers 30-Dec-2020
PMCID:PMC7936104
doi:10.1016/j.pld.2020.12.004
PMID:33733015
Ethnobotany and the Role of Plant Natural Products in Antibiotic Drug Discovery Porras G, Chassagne F, Lyles JT, Marquez L, Dettweiler M, Salam AM, Samarakoon T, Shabih S, Farrokhi DR, Quave CL Chem Rev 09-Nov-2020
PMCID:PMC8183567
doi:10.1021/acs.chemrev.0c00922
PMID:33164487
Medicinal plants used in managing diseases of the respiratory system among the Luo community: an appraisal of Kisumu East Sub-County, Kenya Mailu JK, Nguta JM, Mbaria JM, Okumu MO Chin Med 03-Sep-2020
PMCID:PMC7469313
doi:10.1186/s13020-020-00374-2
PMID:32905471
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

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 / Aporphines
(+)-Magnoflorine 73337 Click to see 342.40 unknown https://doi.org/10.1016/S0367-326X(01)00265-9
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Secobenzophenanthridine alkaloids
Arnottianamide 3085181 Click to see CN(C=O)C1=C(C=CC2=CC3=C(C=C21)OCO3)C4=C(C(=C(C=C4)OC)OC)O 381.40 unknown https://doi.org/10.1021/NP50057A031
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.12.015
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Salicylic acid and derivatives / Salicylic acids
3-Methylsalicylic Acid 6738 Click to see 152.15 unknown https://doi.org/10.1002/JHRC.1240090712
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
Methyleugenol 7127 Click to see COC1=C(C=C(C=C1)CC=C)OC 178.23 unknown https://doi.org/10.1021/NP50048A057
> Benzenoids / Phenols / Methoxyphenols
Syringaldehyde 8655 Click to see COC1=CC(=CC(=C1O)OC)C=O 182.17 unknown https://doi.org/10.1021/NP50048A057
> Lignans, neolignans and related compounds / Furanoid lignans
4-[(3S,3aR,6R,6aR)-3-(1,3-benzodioxol-5-yl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2-methoxyphenol 5315338 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC5=C(C=C4)OCO5)O 356.40 unknown https://doi.org/10.1016/0731-7085(85)80059-5
5-[(3aR,6R,6aR)-3-(1,3-benzodioxol-5-yl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-1,3-benzodioxole 102004873 Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 354.40 unknown https://doi.org/10.1002/JHRC.1240090712
Episesamin 5204 Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 354.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.12.015
Npc67790 233333 Click to see 354.40 unknown https://doi.org/10.1002/JHRC.1240090712
Sesamin 72307 Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 354.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.12.015
https://doi.org/10.1016/S0367-326X(01)00265-9
https://doi.org/10.1055/S-2006-960985
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
Arctigenin methyl ether 384877 Click to see 386.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.12.015
Dimethylmatairesinol 1286 Click to see 386.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.12.015
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters
11-Hexadecenoic acid, methyl ester, (11E)- 521560 Click to see 268.40 unknown https://doi.org/10.1021/NP50048A057
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
CID 543388 543388 Click to see CCCCC=CCCCCCCCCCC(=O)O 254.41 unknown https://doi.org/10.1021/NP50048A057
Oleic Acid 445639 Click to see 282.50 unknown https://doi.org/10.1021/NP50048A057
Palmitic Acid 985 Click to see 256.42 unknown https://doi.org/10.1021/NP50048A057
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Citronellyl acetate 9017 Click to see CC(CCC=C(C)C)CCOC(=O)C 198.30 unknown https://doi.org/10.1002/FFJ.2730040411
Geranyl acetate 1549026 Click to see CC(=CCCC(=CCOC(=O)C)C)C 196.29 unknown https://doi.org/10.1002/FFJ.2730040411
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
1-Hydroxytridecan-2-one 13423645 Click to see 214.34 unknown https://doi.org/10.1021/NP50048A057
> Lipids and lipid-like molecules / Fatty Acyls / Fatty amides / N-acyl amines
(2E,4E,8Z,10E,12E)-N-propan-2-yltetradeca-2,4,8,10,12-pentaenamide 5321102 Click to see CC=CC=CC=CCCC=CC=CC(=O)NC(C)C 259.40 unknown https://doi.org/10.1002/JHRC.1240090712
https://doi.org/10.1021/NP50057A031
gamma-Sanshool 6440615 Click to see 273.40 unknown https://doi.org/10.1021/NP50057A031
https://doi.org/10.1002/JHRC.1240090712
Pellitorine 5318516 Click to see 223.35 unknown https://doi.org/10.1002/JHRC.1240090712
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Citronellol 8842 Click to see 156.26 unknown https://doi.org/10.1002/FFJ.2730040411
Geraniol 637566 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1002/FFJ.2730040411
Linalool 6549 Click to see 154.25 unknown https://doi.org/10.1021/NP50048A057
Myrcene 31253 Click to see 136.23 unknown https://doi.org/10.1002/FFJ.2730040411
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+-)-alpha-Pinene 6654 Click to see 136.23 unknown https://doi.org/10.1021/NP50048A057
https://doi.org/10.1002/FFJ.2730040411
3-Carene 26049 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown https://doi.org/10.1021/NP50048A057
Beta-Pinene 14896 Click to see 136.23 unknown https://doi.org/10.1021/NP50048A057
Borneol 64685 Click to see 154.25 unknown https://doi.org/10.1021/NP50048A057
Bornyl acetate 6448 Click to see CC(=O)OC1CC2CCC1(C2(C)C)C 196.29 unknown https://doi.org/10.1021/NP50048A057
Camphene 6616 Click to see 136.23 unknown https://doi.org/10.1021/NP50048A057
Camphor 2537 Click to see 152.23 unknown https://doi.org/10.1021/NP50048A057
CID 44630107 44630107 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1021/NP50048A057
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1021/NP50048A057
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Delta-Guaiene 94275 Click to see CC1CCC2=C(CCC(CC12)C(=C)C)C 204.35 unknown https://doi.org/10.1021/NP50048A057
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Betulinic Acid 64971 Click to see 456.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.12.015
Lup-20(29)-en-28-oic acid, 3beta-hydroxy- 2371 Click to see 456.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.12.015
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.2006.12.015
https://doi.org/10.1055/S-0028-1097191
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/10.1055/S-2006-960985
https://doi.org/10.1055/S-0028-1097191
https://doi.org/10.1016/J.PHYTOCHEM.2006.12.015
https://doi.org/10.1021/NP50057A031
> 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/10.1021/NP50057A031
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1021/NP50057A031
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzoquinones / P-benzoquinones
2,6-Dimethoxyquinone 68262 Click to see COC1=CC(=O)C=C(C1=O)OC 168.15 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.12.015
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
4-Ethylcyclohexanone 79506 Click to see CCC1CCC(=O)CC1 126.20 unknown https://doi.org/10.1021/NP50048A057
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
Xanthoxylin 66654 Click to see 196.20 unknown https://doi.org/10.1016/S0367-326X(01)00265-9
> Organoheterocyclic compounds / Benzodioxoles
Cinnamamide, N-isobutyl-3,4-(methylenedioxy)- 96931 Click to see 247.29 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1258965/
Fagaramide 5281772 Click to see 247.29 unknown https://doi.org/10.1055/S-2006-960985
https://doi.org/10.1002/JHRC.1240090712
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1258965/
https://doi.org/10.1021/NP50057A031
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
(1S)-1-[(4-hydroxyphenyl)methyl]-7-methoxy-2,2-dimethyl-3,4-dihydro-1H-isoquinolin-2-ium-8-ol 173713 Click to see C[N+]1(CCC2=C(C1CC3=CC=C(C=C3)O)C(=C(C=C2)OC)O)C 314.40 unknown https://doi.org/10.1016/S0367-326X(01)00265-9
Tembetarine 167718 Click to see C[N+]1(CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)O)O)OC)C 344.40 unknown https://doi.org/10.1016/S0367-326X(01)00265-9
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Acridines / Acridones
1-Hydroxy-3-methoxy-10-methylacridone 5377412 Click to see CN1C2=CC=CC=C2C(=O)C3=C1C=C(C=C3O)OC 255.27 unknown https://doi.org/10.1016/S0367-326X(01)00265-9
1-Hydroxy-3-methoxyacridin-9(10H)-one 13250463 Click to see 241.24 unknown https://doi.org/10.1016/S0367-326X(01)00265-9
Arborinine 5281832 Click to see CN1C2=CC=CC=C2C(=O)C3=C(C(=C(C=C31)OC)OC)O 285.29 unknown https://doi.org/10.1016/S0367-326X(01)00265-9
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
Nitidine 4501 Click to see 348.40 unknown https://doi.org/10.1021/NP50054A014
Oxynitidine 97597 Click to see CN1C2=C(C=CC3=CC4=C(C=C32)OCO4)C5=CC(=C(C=C5C1=O)OC)OC 363.40 unknown https://doi.org/10.1021/NP50054A014
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
Skimmianine 6760 Click to see COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC 259.26 unknown https://doi.org/10.1021/NP50057A031
https://doi.org/10.1111/J.2042-7158.1971.TB12785.X
https://doi.org/10.1002/JHRC.1240090712
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives
Piperlongumine 637858 Click to see COC1=CC(=CC(=C1OC)OC)C=CC(=O)N2CCC=CC2=O 317.34 unknown https://doi.org/10.1007/BF01952540
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see 192.17 unknown https://doi.org/10.1021/NP50048A057
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
(2S)-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-2,3-dihydrochromen-4-one 129010007 Click to see 610.60 unknown https://doi.org/10.1016/S0367-326X(01)00265-9
Hesperetin-7-Rutinoside 3594 Click to see 610.60 unknown https://doi.org/10.1016/S0367-326X(01)00265-9
Hesperidin 10621 Click to see 610.60 unknown https://doi.org/10.1016/S0367-326X(01)00265-9

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