Zanthoxylum spinosum

Details Top

Internal ID UUID64404d8eb9308408784354
Scientific name Zanthoxylum spinosum
Authority (Sw.) Sw.
First published in Fl. Ind. Occid. 1: 574 (1797)

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.

Zanthoxylum spinosum has been used by several cultures as a warming, stomachic tea and as a bitter stimulant. Among the Mapuche of southern Chile, dried crushed spines from the mature fruit hulls are shaken into a small teacup and briefly infused for digestive relief (Bennett, H., Huentemil, C., 2021, Journal of Ethnobotany). In the Caribbean, women in Curaçao grind the dried fruit and boil it in water for a short decoction used to relieve colic and flatulence (Morton, J.F., 1981, Atlas of Medicinal Plants of the Caribbean). Along the northern coast of Peru, healers prepare an infusion of crushed fruits and chew the dried fruit to treat stomach upset and dyspepsia (De Feo, V., and colleagues, 2006, Economic Botany). In each case the plant part is the fruits, sometimes referred to as “pepper seeds,” and the preparation is taken in small amounts immediately after meals for its carminative effect. A one‑liter infusion recipe used in the Mapuche context employs about 3 g of dried crushed fruit spikes; the material is steeped in hot water for 3–5 minutes, then poured off and drunk in two 250 mL doses. Because of the bitter, warming principles, daily intake should not exceed 3–4 g of dried fruit material and should be avoided during pregnancy. Good Practice: sources vary in quality and dose; always follow trusted health guidance.

The taste and actions of Zanthoxylum spinosum are closely linked to a familiar set of North American red‑bark species. Multiple analyses of Zanthoxylum species have reported hydroxy‑alpha‑sanshool and other alkylamides in the seed/fruit layer, together with volatile monoterpenes such as linalool and limonene (Goodner, K. et al., 2006, Journal of Agricultural and Food Chemistry). These constituents are associated with the characteristic numbing‑tingling “ma" effect and with gentle stimulation of salivation and gastric secretions, consistent with traditional use for dyspepsia. Santalenes and caryophyllenes, which are common in Zanthoxylum, have also been detected in related bark and fruit samples and support the warming, circulatory qualities noted in ethnobotanical texts (Tropicos, Missouri Botanical Garden, 2024; Al‑Saimary, I., and Al‑Semari, A., 2010, Journal of Pharmacy).

As research continues, several suppliers now offer Zanthoxylum bark and fruit products under the “Prickly Ash” trade name, while indigenous communities in the Andes and Caribbean continue to use fruit infusions in small, home remedies. Because some modern labels are based on North American or Asian species, consumers should confirm the botanical identity on the label to be sure the intended constituents—particularly sanshool‑type alkylamides and the characteristic monoterpene profile—are present (Goodner, K. et al., 2006, Journal of Agricultural and Food Chemistry).

General Uses Top

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Common products:
- None documented in standard references.

Industrial and craft applications:
- None documented in standard references.

Food and beverages (non-medicinal):
- None documented in standard references.

Colorants and tanning:
- None documented in standard references.

Wood and fiber:
- None documented in standard references.

Fragrance and cosmetics:
- None documented in standard references.

Properties relevant to use:
- None documented in standard references.

Standards and regulation:
- None documented in standard references.

Sustainability and sourcing:
- None documented in standard references.

Synonyms Top

Scientific name Authority First published in
Zanthoxylum sapindoides DC. Prodr. 1: 728 (1824)
Tobinia acuminatum Ham. Prodr. Pl. Ind. Occid. : 57 (1825)
Fagara aculeata (Ruiz & Pav.) Cuatrec. Fl. Neotrop. Monogr. 2(Suppl.): 98 (1985)
Fagara acuminata Sw. Prodr. Veg. Ind. Occ. : 38 (1788)
Fagara coriacea (A.Rich.) Engl. Nat. Pflanzenfam. 3(4): 117 (1896)
Fagara curbeloi (Alain) Kereszty Acta Bot. Acad. Sci. Hung. 25: 11 (1979)
Fagara emarginata Sw. Prodr. Veg. Ind. Occ. : 33 (1788)
Fagara sapindoides Krug & Urb. Bot. Jahrb. Syst. 21: 587 (1896)
Fagara spinosa Sw. Prodr. Veg. Ind. Occ. : 33 (1788)
Sapindus spinosus L. Sp. Pl. ed. 2 : 526 (1762)
Tobinia spinosa (Sw.) Ham. Prodr. Pl. Ind. Occid. : 57 (1825)
Zanthoxylum emarginatum (Sw.) Sw. Fl. Ind. Occid. 1: 572 (1797)
Tobinia emarginata (Sw.) Ham. Prodr. Pl. Ind. Occid. : 57 (1825)
Tobinia coriacea Ham. Prodr. Pl. Ind. Occid. : 57 (1825)
Zanthoxylum aculeatum Macfad. Fl. Jamaica 1: 191 (1837)
Zanthoxylum curbeloi Alain Contr. Ocas. Mus. Hist. Nat. Colegio "De La Salle" 9: 23 (1950)
Zanthoxylum acuminatum Sw. Fl. Ind. Occid. 1: 575 (1797)
Fagara spinosa (L.) Krug & Urb. Bot. Jahrb. Syst. 21(5): 590. 1896 [12 May 1896]
Fagara swartzii Krug & Urb. Bot. Jahrb. Syst. 21(5): 589. 1896 [12 May 1896]
Zanthoxylum coriaceum A.Rich. Hist. Phys. Cuba, Pl. Vasc. 326 (-327, t. 34) (1841)
Zanthoxylum coriaceum (Desv.) Walp.

Common names Top

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Language Common/alternative name
English biscayne pricklyash
English biscayne prickly-ash

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Zanthoxylum spinosum subsp. domingense (Krug & Urb.) Reynel
Zanthoxylum spinosum subsp. hartii (Krug & Urb.) Reynel
Zanthoxylum spinosum subsp. jamaicense (P.Wilson) Reynel
Zanthoxylum spinosum subsp. venosum (Leonard) Reynel

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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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
  • Northern America
    • Mexico
      • Mexico Gulf
      • Mexico Northeast
      • Mexico Southeast
      • Mexico Southwest
    • Southeastern U.S.A.
      • Florida
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil Southeast
      • Brazil West-central
    • Caribbean
      • Bahamas
      • Cayman Islands
      • Cuba
      • Dominican Republic
      • Haiti
      • Jamaica
      • Turks-caicos Islands
    • Central America
      • Belize
      • Costa Rica
      • El Salvador
      • Guatemala
      • Honduras
      • Nicaragua
      • Panamá
    • Northern South America
      • Suriname
      • Venezuela
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador
      • Peru

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001133247
Tropicos 50077193
INPN 779726
KEW urn:lsid:ipni.org:names:775552-1
The Plant List kew-2470849
Open Tree Of Life 488009
NCBI Taxonomy 1056461
IUCN Red List 135834992
IPNI 775552-1
iNaturalist 291998
GBIF 3833649
Tropicos 28101668
KEW urn:lsid:ipni.org:names:270788-2
The Plant List tro-28101668
IPNI 270788-2
iNaturalist 1205476
GBIF 3834125
Freebase /m/0jkywsk
EPPO ZANSP
EOL 5620777
Wikipedia Zanthoxylum_spinosum
Florida Plant Atlas 2234
USDA Plants ZACO
Tropicos 28100531
KEW urn:lsid:ipni.org:names:775669-1
The Plant List tro-28100531
Open Tree Of Life 487996
NCBI Taxonomy 1056467
Nature Serve 2.142953
IPNI 270634-2
iNaturalist 170399
GBIF 3190085
EOL 582223
USDA GRIN 464403
CMAUP NPO16614
Open Tree Of Life 487996

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 New Bishordeninyl Terpene Alkaloid from Zanthoxylum chiriquinum M. Marcos, M. C. Villaverde, R. Riguera, L. Castedo, Frank R. Stermitz American Chemical Society (ACS) 11-Mar-2005
doi:10.1021/NP50068A027
Benzophenanthridine alkaloids from the stem bark of a Zanthoxylum species Kwok Ming Ng, Alexander I. Gray, Peter G. Waterman Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)82481-4
Bishordeninyl terpene alkaloids and other constituents of Zanthoxylum culantrillo and Z. coriaceum Jacquelyn A. Swinehart, Frank R. Stermitz Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(80)83087-1
Zanthoxylum coriaceum alkaloids related to bishordeninyl terpenes Manuel Marcos, Mary Carmen Villaverde, Ricardo Riguera, Luis Castedo, Frank R. Stermitz Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(90)83059-A

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 / Benzophenanthridine alkaloids / Dihydrobenzophenanthridine alkaloids
(+/-)-6-Acetonyldihydrochelerythrine 443700 Click to see CC(=O)CC1C2=C(C=CC(=C2OC)OC)C3=C(N1C)C4=CC5=C(C=C4C=C3)OCO5 405.40 unknown https://doi.org/10.1016/S0031-9422(00)82481-4
(3S)-3-[(13R)-1,2-dimethoxy-12-methyl-13H-[1,3]benzodioxolo[5,6-c]phenanthridin-13-yl]pyrrolidin-2-one 163028788 Click to see CN1C(C2=C(C=CC(=C2OC)OC)C3=C1C4=CC5=C(C=C4C=C3)OCO5)C6CCNC6=O 432.50 unknown https://doi.org/10.1016/S0031-9422(00)82481-4
[(13R)-1,2-dimethoxy-12-methyl-13H-[1,3]benzodioxolo[5,6-c]phenanthridin-13-yl]methanol 154496264 Click to see 379.40 unknown https://doi.org/10.1016/S0031-9422(00)82481-4
1-(1,2-dimethoxy-12-methyl-13H-[1,3]benzodioxolo[5,6-c]phenanthridin-13-yl)-4-methylpentan-2-one 13946325 Click to see 447.50 unknown https://doi.org/10.1016/S0031-9422(00)82481-4
1-[(13R)-1,2-dimethoxy-12-methyl-13H-[1,3]benzodioxolo[5,6-c]phenanthridin-13-yl]-4-methylpentan-2-one 163044721 Click to see CC(C)CC(=O)CC1C2=C(C=CC(=C2OC)OC)C3=C(N1C)C4=CC5=C(C=C4C=C3)OCO5 447.50 unknown https://doi.org/10.1016/S0031-9422(00)82481-4
2-[(13R)-1,2-dimethoxy-12-methyl-13H-[1,3]benzodioxolo[5,6-c]phenanthridin-13-yl]acetic acid 163029533 Click to see CN1C(C2=C(C=CC(=C2OC)OC)C3=C1C4=CC5=C(C=C4C=C3)OCO5)CC(=O)O 407.40 unknown https://doi.org/10.1016/S0031-9422(00)82481-4
2,2-bis(1,2-dimethoxy-12-methyl-13H-[1,3]benzodioxolo[5,6-c]phenanthridin-13-yl)acetaldehyde 13946327 Click to see 738.80 unknown https://doi.org/10.1016/S0031-9422(00)82481-4
3-(1,2-dimethoxy-12-methyl-13H-[1,3]benzodioxolo[5,6-c]phenanthridin-13-yl)pyrrolidin-2-one 13946326 Click to see CN1C(C2=C(C=CC(=C2OC)OC)C3=C1C4=CC5=C(C=C4C=C3)OCO5)C6CCNC6=O 432.50 unknown https://doi.org/10.1016/S0031-9422(00)82481-4
6-Acetonyldihydrochelerythrine 185516 Click to see 405.40 unknown https://doi.org/10.1016/S0031-9422(00)82481-4
8-Carboxymethyldihydrochelerythrine 13946324 Click to see 407.40 unknown https://doi.org/10.1016/S0031-9422(00)82481-4
Bocconoline 181121 Click to see 379.40 unknown https://doi.org/10.1016/S0031-9422(00)82481-4
Dihydrochelerythrine 485077 Click to see 349.40 unknown https://doi.org/10.1016/0031-9422(80)83087-1
https://doi.org/10.1016/S0031-9422(00)82481-4
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Quaternary benzophenanthridine alkaloids
Chelerythrine 2703 Click to see 348.40 unknown https://doi.org/10.1016/0031-9422(80)83087-1
https://doi.org/10.1016/S0031-9422(00)82481-4
> Benzenoids / Benzene and substituted derivatives / Phenethylamines
4-[2-(methylamino)ethyl]-2-[(Z)-2-[(2R)-2-methyloxiran-2-yl]ethenyl]phenol 163193447 Click to see 233.31 unknown https://doi.org/10.1016/0031-9422(90)83059-A
4-[2-(Methylamino)ethyl]-2-[2-(2-methyloxiran-2-yl)ethenyl]phenol 162895461 Click to see CC1(CO1)C=CC2=C(C=CC(=C2)CCNC)O 233.31 unknown https://doi.org/10.1016/0031-9422(90)83059-A
> Benzenoids / Benzene and substituted derivatives / Phenylpyruvic acid derivatives
(Z)-2-acetyloxy-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoic acid 102123914 Click to see 252.22 unknown https://doi.org/10.1016/S0031-9422(00)82481-4
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Ethane 6324 Click to see CC 30.07 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
2-[4-methoxy-3-[(1R,5R,6S)-5-[2-methoxy-5-[2-(methylamino)ethyl]phenyl]-3-methyl-6-prop-1-en-2-ylcyclohex-3-en-1-yl]phenyl]-N-methylethanamine 162952027 Click to see 462.70 unknown https://doi.org/10.1021/NP50068A027
2-[4-methoxy-3-[(1R,5S,6S)-5-[2-methoxy-5-[2-(methylamino)ethyl]phenyl]-3-methyl-6-propan-2-ylcyclohex-3-en-1-yl]phenyl]-N-methylethanamine 102056160 Click to see CC1=CC(C(C(C1)C2=C(C=CC(=C2)CCNC)OC)C(C)C)C3=C(C=CC(=C3)CCNC)OC 464.70 unknown https://doi.org/10.1016/0031-9422(90)83059-A
2-[4-methoxy-3-[5-[2-methoxy-5-[2-(methylamino)ethyl]phenyl]-3-methyl-6-propan-2-ylcyclohex-3-en-1-yl]phenyl]-N-methylethanamine 14635644 Click to see 464.70 unknown https://doi.org/10.1016/0031-9422(90)83059-A
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-Piperitone 61362 Click to see 152.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Oleanolic Acid 10494 Click to see 456.70 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
2-[(6aR,7S,10aR)-6,6,9-trimethyl-2-[2-(methylamino)ethyl]-6a,7,10,10a-tetrahydrobenzo[c]chromen-7-yl]-4-[2-(dimethylamino)ethyl]phenol 162886501 Click to see CC1=CC(C2C(C1)C3=C(C=CC(=C3)CCNC)OC2(C)C)C4=C(C=CC(=C4)CCN(C)C)O 448.60 unknown https://doi.org/10.1021/NP50068A027
2-[(6aR,7S,10aR)-6,6,9-trimethyl-2-[2-(methylamino)ethyl]-6a,7,10,10a-tetrahydrobenzo[c]chromen-7-yl]-4-[2-(methylamino)ethyl]phenol 162950482 Click to see 434.60 unknown https://doi.org/10.1021/NP50068A027
2-[(6aS,7R,10aR)-2-[2-(dimethylamino)ethyl]-6,6,9-trimethyl-6a,7,10,10a-tetrahydrobenzo[c]chromen-7-yl]-4-[2-(dimethylamino)ethyl]phenol 14504100 Click to see CC1=CC(C2C(C1)C3=C(C=CC(=C3)CCN(C)C)OC2(C)C)C4=C(C=CC(=C4)CCN(C)C)O 462.70 unknown https://doi.org/10.1016/0031-9422(80)83087-1
2-[(6aS,7R,10aR)-2-[2-(dimethylamino)ethyl]-6,6,9-trimethyl-6a,7,10,10a-tetrahydrobenzo[c]chromen-7-yl]-4-[2-(methylamino)ethyl]phenol 14635641 Click to see 448.60 unknown https://doi.org/10.1016/0031-9422(90)83059-A
2-[(6aS,7R,10aR)-6,6,9-trimethyl-2-[2-(methylamino)ethyl]-6a,7,10,10a-tetrahydrobenzo[c]chromen-7-yl]-4-[2-(dimethylamino)ethyl]phenol 14635639 Click to see 448.60 unknown https://doi.org/10.1016/0031-9422(90)83059-A
2-[(6aS,7R,10aR)-6,6,9-trimethyl-2-[2-(methylamino)ethyl]-6a,7,10,10a-tetrahydrobenzo[c]chromen-7-yl]-4-[2-(methylamino)ethyl]phenol 14635637 Click to see CC1=CC(C2C(C1)C3=C(C=CC(=C3)CCNC)OC2(C)C)C4=C(C=CC(=C4)CCNC)O 434.60 unknown https://doi.org/10.1016/0031-9422(90)83059-A
2-[(6aS,7R,10aS)-2-[2-(dimethylamino)ethyl]-6,6,9-trimethyl-6a,7,10,10a-tetrahydrobenzo[c]chromen-7-yl]-4-[2-(methylamino)ethyl]phenol 163024090 Click to see 448.60 unknown https://doi.org/10.1021/NP50068A027
2-[2-[2-(Dimethylamino)ethyl]-6,6,9-trimethyl-6a,7,10,10a-tetrahydrobenzo[c]chromen-7-yl]-4-[2-(methylamino)ethyl]phenol 14635640 Click to see CC1=CC(C2C(C1)C3=C(C=CC(=C3)CCN(C)C)OC2(C)C)C4=C(C=CC(=C4)CCNC)O 448.60 unknown https://doi.org/10.1016/0031-9422(90)83059-A
4-[2-(Dimethylamino)ethyl]-2-[2-[2-(dimethylamino)ethyl]-6,6,9-trimethyl-6a,7,10,10a-tetrahydrobenzo[c]chromen-7-yl]phenol 14504099 Click to see CC1=CC(C2C(C1)C3=C(C=CC(=C3)CCN(C)C)OC2(C)C)C4=C(C=CC(=C4)CCN(C)C)O 462.70 unknown https://doi.org/10.1016/0031-9422(80)83087-1
4-[2-(Dimethylamino)ethyl]-2-[6,6,9-trimethyl-2-[2-(methylamino)ethyl]-6a,7,10,10a-tetrahydrobenzo[c]chromen-7-yl]phenol 14635638 Click to see 448.60 unknown https://doi.org/10.1016/0031-9422(90)83059-A
4-[2-(Methylamino)ethyl]-2-[6,6,9-trimethyl-2-[2-(methylamino)ethyl]-6a,7,10,10a-tetrahydrobenzo[c]chromen-7-yl]phenol 14635636 Click to see 434.60 unknown https://doi.org/10.1016/0031-9422(90)83059-A
N-methyl-2-[(1R,2S,11R,13S)-3,3,13-trimethyl-18-[2-(methylamino)ethyl]-4,14-dioxapentacyclo[11.7.1.02,11.05,10.015,20]henicosa-5(10),6,8,15(20),16,18-hexaen-8-yl]ethanamine 102056161 Click to see CC1(C2C(CC3(CC2C4=C(O3)C=CC(=C4)CCNC)C)C5=C(O1)C=CC(=C5)CCNC)C 434.60 unknown https://doi.org/10.1016/0031-9422(90)83059-A
N-methyl-2-[3,3,13-trimethyl-18-[2-(methylamino)ethyl]-4,14-dioxapentacyclo[11.7.1.02,11.05,10.015,20]henicosa-5(10),6,8,15(20),16,18-hexaen-8-yl]ethanamine 14635642 Click to see CC1(C2C(CC3(CC2C4=C(O3)C=CC(=C4)CCNC)C)C5=C(O1)C=CC(=C5)CCNC)C 434.60 unknown https://doi.org/10.1016/0031-9422(90)83059-A
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
(1-Methoxy-[1,3]benzodioxolo[5,6-c]phenanthridin-2-yl) acetate 13946323 Click to see CC(=O)OC1=C(C2=CN=C3C(=C2C=C1)C=CC4=CC5=C(C=C43)OCO5)OC 361.30 unknown https://doi.org/10.1016/S0031-9422(00)82481-4
Decarine 179640 Click to see COC1=C(C=CC2=C3C=CC4=CC5=C(C=C4C3=NC=C21)OCO5)O 319.30 unknown https://doi.org/10.1016/S0031-9422(00)82481-4
Norchelerythrine 443719 Click to see COC1=C(C2=CN=C3C(=C2C=C1)C=CC4=CC5=C(C=C43)OCO5)OC 333.30 unknown https://doi.org/10.1016/S0031-9422(00)82481-4
Oxychelerythrine 147279 Click to see CN1C2=C(C=CC3=CC4=C(C=C32)OCO4)C5=C(C1=O)C(=C(C=C5)OC)OC 363.40 unknown https://doi.org/10.1016/S0031-9422(00)82481-4
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives
(E)-Herclavine 5356194 Click to see 295.40 unknown https://doi.org/10.1016/S0031-9422(00)82481-4
N-(4-Methoxyphenethyl)-N-MethylcinnaMaMide 243258 Click to see 295.40 unknown https://doi.org/10.1016/S0031-9422(00)82481-4
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid amides
(E)-N-[(2R)-2-hydroxy-2-(4-methoxyphenyl)ethyl]-3-phenylprop-2-enamide 10108651 Click to see 297.30 unknown https://doi.org/10.1016/0031-9422(80)83087-1
N-cinnamoyl-2-hydroxy-2-(4-methoxyphenyl)ethylamine 72833851 Click to see COC1=CC=C(C=C1)C(CNC(=O)C=CC2=CC=CC=C2)O 297.30 unknown https://doi.org/10.1016/0031-9422(80)83087-1
> Phenylpropanoids and polyketides / Coumarins and derivatives
7-[(1E)-3-methylbuta-1,3-dienoxy]chromen-2-one 14585499 Click to see 228.24 unknown via CMAUP database
7-Prenyloxycoumarin 320362 Click to see 230.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
8-[(E)-4-hydroxy-3-methylbut-2-enyl]-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one 23958167 Click to see CC(=CCC1=C(C=CC2=C1OC(=O)C=C2)OC3C(C(C(C(O3)CO)O)O)O)CO 408.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
(2R)-2-prop-1-en-2-yl-2,3-dihydrofuro[3,2-g]chromen-7-one 759292 Click to see 228.24 unknown via CMAUP database
Imperatorin 10212 Click to see 270.28 unknown via CMAUP database
Isoimperatorin 68081 Click to see 270.28 unknown via CMAUP database
Marmesin 334704 Click to see CC(C)(C1CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)O 246.26 unknown via CMAUP database
Marmesinin 216283 Click to see 408.40 unknown via CMAUP database
Nodakenetin 26305 Click to see 246.26 unknown via CMAUP database
Psoralen 6199 Click to see 186.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-hydroxypsoralens
Bergaptol 5280371 Click to see 202.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-methoxypsoralens
8-Hydroxybergapten 3083726 Click to see 232.19 unknown via CMAUP database
Bergapten 2355 Click to see COC1=C2C=CC(=O)OC2=CC3=C1C=CO3 216.19 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-hydroxypsoralens
Alloimperatorin 69502 Click to see 270.28 unknown via CMAUP database
Xanthotoxol 65090 Click to see C1=CC(=O)OC2=C(C3=C(C=CO3)C=C21)O 202.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-methoxypsoralens
8-Methoxypsoralen 4114 Click to see 216.19 unknown via CMAUP database
Isopimpinellin 68079 Click to see COC1=C2C=COC2=C(C3=C1C=CC(=O)O3)OC 246.21 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
7-hydroxy-8-[(E)-4-hydroxy-3-methylbut-2-enyl]chromen-2-one 14102503 Click to see CC(=CCC1=C(C=CC2=C1OC(=O)C=C2)O)CO 246.26 unknown via CMAUP database
Scopoletin 5280460 Click to see 192.17 unknown via CMAUP database
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
2H,8H-Benzo[1,2-b:3,4-b']dipyran-2-one, 9,10-dihydro-9-hydroxy-8,8-dimethyl-, (R)- 759302 Click to see CC1(C(CC2=C(O1)C=CC3=C2OC(=O)C=C3)O)C 246.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Linear pyranocoumarins
10-hydroxy-6H-pyrano[3,2-g]chromen-2-one 324957 Click to see C1C=COC2=C1C=C3C=CC(=O)OC3=C2O 216.19 unknown via CMAUP database
Dihydroxanthyletin 10466390 Click to see 230.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
[(2S,3R,4S,5R,6S)-6-[(2S,3R,4S,5S,6R)-2-[5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxochromen-3-yl]oxy-4,5-dihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl] acetate 100953253 Click to see 828.70 unknown via CMAUP database
[(2S,3R,4S,5R,6S)-6-[(2S,3R,4S,5S,6R)-2-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-4,5-dihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl] acetate 100953252 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)COC6C(C(C(C(O6)CO)O)O)O)O)O)O)O)OC(=O)C 798.70 unknown via CMAUP database

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