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Zanthoxylum piasezkii

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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID64405436e8188968374843
Scientific name Zanthoxylum piasezkii
Authority Maxim.
First published in Trudy Imp. S.-Peterburgsk. Bot. Sada 11: 93 (1889)

Description Top

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Synonyms Top

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Common names Top

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Language Common/alternative name
Chinese 川陕花椒
Chinese 山花椒

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
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • China Southeast

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001226755
Tropicos 50049621
KEW urn:lsid:ipni.org:names:775944-1
The Plant List tro-50049621
Open Tree Of Life 6125726
NCBI Taxonomy 1752150
IUCN Red List 152839582
IPNI 775944-1
GBIF 3835358
EOL 2888555
Wikipedia Zanthoxylum_piasezkii

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
The complete chloroplast genome sequence of Zanthoxylum ailanthoides Sieb. et. Zucc (Rutaceae): an important medicinal plant Liang YN, Cui N, Liang XB, Huang XY, Zhang W, Li H Mitochondrial DNA B Resour 12-Apr-2024
PMCID:PMC11018064
doi:10.1080/23802359.2024.2338260
PMID:38623176
Preliminary Study on Insecticidal Potential and Chemical Composition of Five Rutaceae Essential Oils against Thrips flavus (Thysanoptera: Thripidae) Pei TH, Zhao YJ, Wang SY, Li XF, Sun CQ, Shi SS, Xu ML, Gao Y Molecules 28-Mar-2023
PMCID:PMC10095842
doi:10.3390/molecules28072998
PMID:37049761
Comparative metabolomics analysis of pericarp from four varieties of Zanthoxylum bungeanum Maxim Cao Y, Ren M, Yang J, Guo L, Lin Y, Wu H, Wang B, Lv R, Zhang C, Gong X, Wang H Bioengineered 23-Oct-2022
PMCID:PMC9601549
doi:10.1080/21655979.2022.2108632
PMID:36274249
The complete chloroplast genome of Zanthoxylum piasezkii Maxim. (Rutaceae) and its phylogenetic analysis Sun C, Liu X, Dong P, Kuang M, Chen Z Mitochondrial DNA B Resour 05-Feb-2021
PMCID:PMC7872585
doi:10.1080/23802359.2020.1866458
PMID:33659657
Transcriptome and metabolome analyses reveal the regulation of peel coloration in green, red Chinese prickly ash (Zanthoxylum L.) Zheng T, Zhang Q, Su KX, Liu SM Food Chem (Oxf) 22-Oct-2020
PMCID:PMC8991852
doi:10.1016/j.fochms.2020.100004
PMID:35415618
Chemical Constituents of Zanthoxylum armatum. I Tao Guo, Tong-tong Song, Xiao-feng Tang, Su-bei Tan, Ya Wang, Yin-Quan Wang Springer Science and Business Media LLC 16-Sep-2018
doi:10.1007/S10600-018-2544-3

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 / Indolonaphthyridine alkaloids
Canthin-6-one 97176 Click to see C1=CC=C2C(=C1)C3=C4N2C(=O)C=CC4=NC=C3 220.23 unknown https://doi.org/10.1007/S10600-018-2544-3
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1007/S10600-018-2544-3
> 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/10.1007/S10600-018-2544-3
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1007/S10600-018-2544-3
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1007/S10600-018-2544-3
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1007/S10600-018-2544-3
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
Xanthoxylin 66654 Click to see CC(=O)C1=C(C=C(C=C1OC)OC)O 196.20 unknown https://doi.org/10.1007/S10600-018-2544-3
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Angular furanocoumarins
(-)-Columbianetin 442104 Click to see CC(C)(C1CC2=C(O1)C=CC3=C2OC(=O)C=C3)O 246.26 unknown https://doi.org/10.1007/S10600-018-2544-3
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
Marmesin 334704 Click to see CC(C)(C1CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)O 246.26 unknown https://doi.org/10.1007/S10600-018-2544-3
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
Esculetin 5281416 Click to see C1=CC(=O)OC2=CC(=C(C=C21)O)O 178.14 unknown https://doi.org/10.1007/S10600-018-2544-3

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