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

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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)

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Distribution (via POWO/KEW) Top

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

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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

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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 C[N+]12CCC3=CC4=C(C=C3C1CC5=C(C2)C(=C(C=C5)OC)OC)OCO4 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 C1CNC(=O)C(=NO)CC2=CC(=C(C(=C2)Br)OC3=C(C(=CC(=C3)CC(=NO)C(=O)NC=CC4=CC(=C(C=C4)OC5=C(C(=CC1=C5)Br)O)Br)Br)O)Br 1017.10 unknown via CMAUP database
Bastadin 13 23426999 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=C3Br)Br 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
19Alpha-Hydroxyasiatic Acid 490367 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1(C)O)C)C(=O)O 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 CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1C)C)C(=O)O 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 CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 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
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 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 C(CON)C(C(=O)O)N 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

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