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Zanthoxylum brachyacanthum

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 UUID643ffbcf8dc80943438766
Scientific name Zanthoxylum brachyacanthum
Authority F.Muell.
First published in Trans. & Proc. Philos. Inst. Victoria 2: 65 (1858)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Zanthoxylum veneficum F.M.Bailey Syn. Queensl. Fl. , Suppl. 1: 11 (1886)
Fagara brachyacantha Engl. Nat. Pflanzenfam. 3(4): 119 (1896)
Fagara venenifica Engl. Nat. Pflanzenfam. 3(4): 119 (1896)

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000429524
KEW urn:lsid:ipni.org:names:775619-1
Open Tree Of Life 488001
NCBI Taxonomy 1056464
IUCN Red List 179865796
IPNI 775619-1
iNaturalist 370555
GBIF 3832686
Freebase /m/064pwmr
Wikipedia Zanthoxylum_brachyacanthum
CMAUP NPO13676

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
Vegetation structure and ground cover attributes describe the occurrence of a newly discovered carnivorous marsupial on the Tweed Shield Volcano caldera, the endangered black‐tailed dusky antechinus (Antechinus arktos) Riordan CE, Pearce C, McDonald BJ, Gynther I, Baker AM Ecol Evol 12-Feb-2020
PMCID:PMC7042678
doi:10.1002/ece3.6045
PMID:32128142
Antileishmanial Potential of Tropical Rainforest Plant Extracts Monzote L, Piñón A, Setzer WN Medicines (Basel) 19-Nov-2014
PMCID:PMC5532977
doi:10.3390/medicines1010032
PMID:28933376
Frequency of Cyanogenesis in Tropical Rainforests of Far North Queensland, Australia MILLER RE, JENSEN R, WOODROW IE Ann Bot 01-Jun-2006
PMCID:PMC2803397
doi:10.1093/aob/mcl048
PMID:16520340

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 / Protoberberine alkaloids and derivatives
(1R,13S)-16,17-dimethoxy-13-methyl-5,7-dioxa-13-azoniapentacyclo[11.8.0.02,10.04,8.015,20]henicosa-2,4(8),9,15(20),16,18-hexaene 11547504 Click to see 354.40 unknown via CMAUP database
(R)-Canadine 443422 Click to see COC1=C(C2=C(CC3C4=CC5=C(C=C4CCN3C2)OCO5)C=C1)OC 339.40 unknown via CMAUP database
> Benzenoids / Phenol ethers / Anisoles
2-(3,5-Dibromo-4-Methoxyphenyl)Acetic Acid 10734734 Click to see COC1=C(C=C(C=C1Br)CC(=O)O)Br 323.97 unknown via CMAUP database
> Lignans, neolignans and related compounds
5,16,21,32,36-Pentabromo-4,20-dihydroxy-12,25-bis(hydroxyimino)-2,18-dioxa-10,27-diazapentacyclo[28.2.2.214,17.13,7.119,23]octatriaconta-1(32),3,5,7(38),14,16,19,21,23(35),28,30,33,36-tridecaene-11,26-dione 6850241 Click to see 1017.10 unknown via CMAUP database
Bastadin 13 23426999 Click to see 940.20 unknown via CMAUP database
Bastadin-21 9579587 Click to see C1CNC(=O)C(=NO)CC2=CC(=C(C(=C2)Br)O)OC3=C(C=C(CC(=NO)C(=O)NCCC4=CC(=C(C=C4)OC5=C(C=CC1=C5)O)Br)C=C3)Br 861.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown via CMAUP database
19Alpha-Hydroxyasiatic Acid 490367 Click to see 504.70 unknown via CMAUP database
Arjunolic acid 73641 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1)C)C(=O)O)C 488.70 unknown via CMAUP database
Asiatic Acid 119034 Click to see 488.70 unknown via CMAUP database
Betulinaldehyde 99615 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C=O 440.70 unknown via CMAUP database
Betulinic Acid 64971 Click to see 456.70 unknown via CMAUP database
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
Tormentic acid 73193 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)O 488.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / D-alpha-amino acids
(R)-2-Amino-4-(aminooxy)butanoic acid 10176161 Click to see 134.13 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-3-O-glycosides
Kuromanin 441667 Click to see C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O 449.40 unknown via CMAUP database

Gallery Top

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Collections Top

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