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Zanthoxylum syncarpum

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID643ffbcd06ea3555334076
Scientific name Zanthoxylum syncarpum
Authority Tul.
First published in Index Kew. 2: 1248 (1895)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Perijea syncarpa (Tul.) Tul. Ann. Sci. Nat., Bot. , sér. 3, 7: 279 (1847)
Fagara syncarpa Engl. Nat. Pflanzenfam. 3(4): 116 (1896)
Fagara valenciana Pittier Trab. Mus. Comercial Venezuela (Bol. Minist. Relac. Exter. Nos. 8-12), 277 (1929).

Common names Top

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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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Southern America
    • Brazil
      • Brazil Northeast
      • Brazil Southeast
    • Northern South America
      • Venezuela

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000429458
Tropicos 28100304
KEW urn:lsid:ipni.org:names:776047-1
The Plant List kew-2469197
Open Tree Of Life 6125759
IPNI 776047-1
iNaturalist 1070753
GBIF 3833922
EOL 5304510
CMAUP NPO27680

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)!
Title Authors Publication Released IDs
Alkamides from the leaves of Zanthoxylum syncarpum. Ross SA, Al-Azeib MA, Krishnaveni KS, Fronczek FR, Burandt CL J Nat Prod 01-Aug-2005
doi:10.1021/NP0580558
PMID:16124784
Syncarpamide, a new antiplasmodial (+)-norepinephrine derivative from Zanthoxylum syncarpum. Ross SA, Sultana GN, Burandt CL, ElSohly MA, Marais JP, Ferreira D J Nat Prod 01-Jan-2004
doi:10.1021/NP030417T
PMID:14738394

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 / Benzene and substituted derivatives / Benzyloxycarbonyls
[(1R)-1-(3,4-dimethoxyphenyl)-2-[[(E)-3-phenylprop-2-enoyl]amino]ethyl] acetate 162900177 Click to see 369.40 unknown https://doi.org/10.1021/NP0580558
[1-(3,4-Dimethoxyphenyl)-2-(3-phenylprop-2-enoylamino)ethyl] acetate 73038414 Click to see CC(=O)OC(CNC(=O)C=CC1=CC=CC=C1)C2=CC(=C(C=C2)OC)OC 369.40 unknown https://doi.org/10.1021/NP0580558
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Celastrol 122724 Click to see CC1=C(C(=O)C=C2C1=CC=C3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C(=O)O)C)C)C)C)O 450.60 unknown via CMAUP database
Epifriedelanol 119242 Click to see 428.70 unknown via CMAUP database
Friedelin 91472 Click to see 426.70 unknown via CMAUP database
Pristimerin 159516 Click to see 464.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 3-hydroxysteroids
Netzahualcoyene 21636463 Click to see 462.60 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
Tingenin B 73147 Click to see CC1CC2C(CCC3(C2(CCC4(C3=CC=C5C4=CC(=O)C(=C5C)O)C)C)C)(C(C1=O)O)C 436.60 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Acyloins
20alpha-Hydroxytingenone 10717799 Click to see CC1=C(C(=O)C=C2C1=CC=C3C2(CCC4(C3(CCC5(C4CC(C(=O)C5)(C)O)C)C)C)C)O 436.60 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
Tingenone 101520 Click to see 420.60 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
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/10.1021/NP030417T
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid amides
(E)-N-[(2R)-2-(3,4-dimethoxyphenyl)-2-hydroxyethyl]-3-phenylprop-2-enamide 93475860 Click to see COC1=C(C=C(C=C1)C(CNC(=O)C=CC2=CC=CC=C2)O)OC 327.40 unknown https://doi.org/10.1021/NP0580558
(E)-N-[(E,2R)-2-(3,4-dimethoxyphenyl)-3-oxo-5-phenylpent-4-enyl]-3-phenylprop-2-enamide 44559210 Click to see 441.50 unknown https://doi.org/10.1021/NP0580558
N-[2-(3,4-dimethoxyphenyl)-2-hydroxyethyl]-3-phenylprop-2-enamide 73045413 Click to see COC1=C(C=C(C=C1)C(CNC(=O)C=CC2=CC=CC=C2)O)OC 327.40 unknown https://doi.org/10.1021/NP0580558
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid esters
[(1R)-1-(3,4-dimethoxyphenyl)-2-[[(E)-3-phenylprop-2-enoyl]amino]ethyl] (E)-3-phenylprop-2-enoate 138523232 Click to see 457.50 unknown https://doi.org/10.1021/NP0580558
[1-(3,4-Dimethoxyphenyl)-2-(3-phenylprop-2-enoylamino)ethyl] 3-phenylprop-2-enoate 73029211 Click to see COC1=C(C=C(C=C1)C(CNC(=O)C=CC2=CC=CC=C2)OC(=O)C=CC3=CC=CC=C3)OC 457.50 unknown https://doi.org/10.1021/NP0580558
https://doi.org/10.1021/NP030417T
Syncarpamide 11753871 Click to see 457.50 unknown https://doi.org/10.1021/NP030417T
https://doi.org/10.1021/NP0580558
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
2-(2-Hydroxypropan-2-yl)-2,3-dihydrofuro(3,2-g)chromen-7-one 604512 Click to see 246.26 unknown https://doi.org/10.1021/NP030417T
Marmesin 334704 Click to see CC(C)(C1CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)O 246.26 unknown https://doi.org/10.1021/NP030417T

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