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Zanthoxylum myriacanthum

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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 UUID6440557adcb8b091145243
Scientific name Zanthoxylum myriacanthum
Authority Wall.
First published in Fl. Brit. India 1: 496 (1875)

Description Top

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Synonyms Top

Scientific name Authority First published in
Fagara diabolica (Elmer) Engl. Nat. Pflanzenfam. ed. 2 , 19a: 220 (1931)
Fagara gigantea Hand.-Mazz. Anz. Akad. Wiss. Wien, Math.-Naturwiss. Kl. 58: 64 (1921)
Fagara myriacantha Engl. Nat. Pflanzenfam. 3(4): 118 (1896)
Fagara odorata (H.Lév.) Hand.-Mazz. Symb. Sin. 7: 623 (1933)
Fagara rhetsoides (Drake) Reeder & S.Y.Cheo J. Arnold Arbor. 32: 69 (1951)
Euodia odorata H.Lév. Repert. Spec. Nov. Regni Veg. 9: 458 (1911)
Zanthoxylum giganteum (Hand.-Mazz.) Rehder J. Arnold Arbor. 8: 151 (1927)
Zanthoxylum odoratum H.Lév. Repert. Spec. Nov. Regni Veg. 13: 266 (1914)
Zanthoxylum rhetsoides Drake J. Bot. (Morot) 6: 275 (1892)
Zanthoxylum diabolicum Elmer Leafl. Philipp. Bot. 2: 477 (1908)

Common names Top

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Language Common/alternative name
Chinese 大叶臭椒
Chinese 大叶臭花椒
Chinese 驱风通
Chinese 刺椿木
Chinese 雷公木
Chinese 大葉臭花椒

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Zanthoxylum myriacanthum var. pubescens (C.C.Huang) C.C.Huang Guihaia 11: 9 (1991)

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 South-central
      • China Southeast
      • Hainan
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • East Himalaya
    • Indo-China
      • Laos
      • Myanmar
      • Vietnam
    • Malesia
      • Malaya
      • Philippines

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001242451
KEW urn:lsid:ipni.org:names:775875-1
The Plant List tro-50118941
Open Tree Of Life 754276
NCBI Taxonomy 1009510
IUCN Red List 146517662
IPNI 775875-1
iNaturalist 632440
GBIF 7269421
EOL 2874934
USDA GRIN 408048
Wikipedia Zanthoxylum_myriacanthum
CMAUP NPO5118

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
Unveiling the Anti-Cholera and Active Diabetic Renoprotective Compounds of Maqian Essential Oil: A Computational and Molecular Dynamics Study Dahab M, Zhang P, Al-Mijalli SH, Abdallah EM Molecules 05-Dec-2023
PMCID:PMC10746104
doi:10.3390/molecules28247954
PMID:38138443
ITRAQ-based proteomics analysis of human ectopic endometrial stromal cells treated by Maqian essential oil Zhang LY, Huang TT, Li LP, Liu DP, Luo Y, Lu W, Huang N, Ma PP, Liu YQ, Zhang P, Yang BC BMC Complement Med Ther 27-Nov-2023
PMCID:PMC10680300
doi:10.1186/s12906-023-04246-8
PMID:38012607
Comparative Analysis of Chemical Composition of Zanthoxylum myriacanthum Branches and Leaves by GC-MS and UPLC-Q-Orbitrap HRMS, and Evaluation of Their Antioxidant Activities Dai W, Zhang L, Dai L, Tian Y, Ye X, Wang S, Li J, Wang Q Molecules 25-Jul-2023
PMCID:PMC10419930
doi:10.3390/molecules28155631
PMID:37570601
Antioxidant and Antimicrobial Properties and GC-MS Chemical Compositions of Makwaen Pepper (Zanthoxylum myriacanthum) Extracted Using Supercritical Carbon Dioxide Nadon S, Leksawasdi N, Jantanasakulwong K, Rachtanapun P, Ruksiriwanich W, Sommano SR, Khaneghah AM, Castagnini JM, Barba FJ, Phimolsiripol Y Plants (Basel) 03-Jun-2023
PMCID:PMC10255492
doi:10.3390/plants12112211
PMID:37299190
Plant Essential Oils as Healthy Functional Ingredients of Nutraceuticals and Diet Supplements: A Review Matera R, Lucchi E, Valgimigli L Molecules 16-Jan-2023
PMCID:PMC9862182
doi:10.3390/molecules28020901
PMID:36677959
Nitidine chloride, a benzophenanthridine alkaloid from Zanthoxylum nitidum (Roxb.) DC., exerts multiple beneficial properties, especially in tumors and inflammation-related diseases Lu Q, Luo S, Shi Z, Yu M, Guo W, Li C Front Pharmacol 24-Nov-2022
PMCID:PMC9729779
doi:10.3389/fphar.2022.1046402
PMID:36506558
Multivariate analysis of chemometric based aroma dynamics in small cardamom (Elettaria cardamomum Maton) during drying Mishra S, Sanwal N, Sharma N, Sahu JK J Food Sci Technol 16-Aug-2022
PMCID:PMC9579224
doi:10.1007/s13197-022-05560-8
PMID:36276529
Evaluation of Phytochemistry and Pharmacological Properties of Alnus nitida Sajid M, Khan MR, Ijaz MU, Ismail H, Bhatti MZ, Shah SA, Ali S, Tareen MU, Alotaibi SS, Albogami SM, Batiha GE Molecules 18-Jul-2022
PMCID:PMC9320741
doi:10.3390/molecules27144582
PMID:35889458
Trunk spines of trees: a physical defence against bark removal and climbing by mammals? Lefebvre T, Charles-Dominique T, Tomlinson KW Ann Bot 24-Feb-2022
PMCID:PMC9007100
doi:10.1093/aob/mcac025
PMID:35199147
Anti-Austerity Activity of Thai Medicinal Plants: Chemical Constituents and Anti-Pancreatic Cancer Activities of Kaempferia parviflora Sun S, Kim MJ, Dibwe DF, Omar AM, Athikomkulchai S, Phrutivorapongkul A, Okada T, Tsuge K, Toyooka N, Awale S Plants (Basel) 25-Jan-2021
PMCID:PMC7911922
doi:10.3390/plants10020229
PMID:33503922
Ethnobotanical study on wild edible plants used by three trans-boundary ethnic groups in Jiangcheng County, Pu’er, Southwest China Cao Y, Li R, Zhou S, Song L, Quan R, Hu H J Ethnobiol Ethnomed 27-Oct-2020
PMCID:PMC7590688
doi:10.1186/s13002-020-00420-1
PMID:33109239
Biologically Active Isoquinoline Alkaloids covering 2014-2018 Shang XF, Yang CJ, Morris-Natschke SL, Li JC, Yin XD, Liu YQ, Guo X, Peng JW, Goto M, Zhang JY, Lee KH Med Res Rev 29-Jul-2020
PMCID:PMC7554109
doi:10.1002/med.21703
PMID:32729169
Antioxidant, Anti-Inflammatory, and Microbial-Modulating Activities of Essential Oils: Implications in Colonic Pathophysiology Spisni E, Petrocelli G, Imbesi V, Spigarelli R, Azzinnari D, Donati Sarti M, Campieri M, Valerii MC Int J Mol Sci 10-Jun-2020
PMCID:PMC7313461
doi:10.3390/ijms21114152
PMID:32532055
Larvicidal activity of Zanthoxylum acanthopodium essential oil against the malaria mosquitoes, Anopheles anthropophagus and Anopheles sinensis He Q, Wang W, Zhu L Malar J 15-May-2018
PMCID:PMC5952513
doi:10.1186/s12936-018-2341-2
PMID:29764438
Chemical constituents and anti-inflammatory activities of Maqian (Zanthoxylum myriacanthum var. pubescens) bark extracts Zhang HL, Gan XQ, Fan QF, Yang JJ, Zhang P, Hu HB, Song QS Sci Rep 06-Apr-2017
PMCID:PMC5382921
doi:10.1038/srep45805
PMID:28383530

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives / Aporphines
Magnoflorine 73337 Click to see C[N+]1(CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)O)OC)C 342.40 unknown https://doi.org/10.1016/0031-9422(75)80395-5
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
3,4-Dihydroxybenzoic acid 72 Click to see C1=CC(=C(C=C1C(=O)O)O)O 154.12 unknown via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Hentriacontane 12410 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC 436.80 unknown https://doi.org/10.1016/J.BSE.2014.02.028
> Lignans, neolignans and related compounds / Furanoid lignans
(+)-Fargesin 5320622 Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC5=C(C=C4)OCO5)OC 370.40 unknown https://doi.org/10.1016/J.JPBA.2016.09.035
https://doi.org/10.1016/J.JPBA.2014.01.028
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6274200/
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(6R,9R)-3-Oxo-alpha-ionol glucoside 9820702 Click to see CC1=CC(=O)CC(C1C=CC(C)OC2C(C(C(C(O2)CO)O)O)O)(C)C 370.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-Camphene 440966 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown via CMAUP database
(-)-Camphor 444294 Click to see CC1(C2CCC1(C(=O)C2)C)C 152.23 unknown via CMAUP database
(+)-Chrysanthenone 11789373 Click to see CC1=CCC2C(=O)C1C2(C)C 150.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Trichothecenes
(1S,2R,7R,9R,10R,11S,12R)-3,10,11-trihydroxy-2-(hydroxymethyl)-1,5-dimethylspiro[8-oxatricyclo[7.2.1.02,7]dodec-5-ene-12,2'-oxirane]-4-one 6325746 Click to see CC1=CC2C(C(C1=O)O)(C3(C(C(C(C34CO4)O2)O)O)C)CO 312.31 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/J.BSE.2014.02.028
> 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/10.1016/J.BSE.2014.02.028
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/10.1016/J.BSE.2014.02.028
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/0031-9422(75)80395-5
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1R,3R,4S,5R)-3-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxycyclohexane-1-carboxylic acid 91492 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
(1S,3R,4R,5R)-3-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxy-cyclohexanecarboxylic acid 9476 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
(1S,3R,4R,5R)-3,4-Bis[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,5-dihydroxycyclohexane-1-carboxylic acid 153946 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O 516.40 unknown via CMAUP database
1,3-Dicaffeoylquinic acid 6474640 Click to see C1C(C(C(CC1(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O)O 516.40 unknown via CMAUP database
3,4-Di-O-caffeoylquinic acid methyl ester 10392218 Click to see COC(=O)C1(CC(C(C(C1)OC(=O)C=CC2=CC(=C(C=C2)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O)O 530.50 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
Protocatechualdehyde 8768 Click to see C1=CC(=C(C=C1C=O)O)O 138.12 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
Dihydronitidine 99641 Click to see CN1CC2=CC(=C(C=C2C3=C1C4=CC5=C(C=C4C=C3)OCO5)OC)OC 349.40 unknown https://doi.org/10.1016/0031-9422(75)80395-5
Nitidine 4501 Click to see C[N+]1=CC2=CC(=C(C=C2C3=C1C4=CC5=C(C=C4C=C3)OCO5)OC)OC 348.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Caffeic acid methyl ester 689075 Click to see COC(=O)C=CC1=CC(=C(C=C1)O)O 194.18 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid 689043 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown via CMAUP database
p-Coumaric acid 637542 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Eriodictyol 440735 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 288.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown via CMAUP database
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown via CMAUP database
Tilianin 5321954 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O 446.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
3'-O-methyltricetin 11267045 Click to see COC1=CC(=CC(=C1O)O)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 316.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
5,7-Dihydroxy-3',4',5'-trimethoxyflavone 5379265 Click to see COC1=CC(=CC(=C1OC)OC)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 344.30 unknown via CMAUP database
Acacetin 5280442 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 284.26 unknown via CMAUP database
Diosmetin 5281612 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
5,7,3'-Trihydroxy-6,4',5'-trimethoxyflavone 5496475 Click to see COC1=CC(=CC(=C1OC)O)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O 360.30 unknown via CMAUP database
6-Methoxytricin 14034284 Click to see COC1=CC(=CC(=C1O)OC)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O 360.30 unknown via CMAUP database
Eupafolin 5317284 Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O 316.26 unknown via CMAUP database
Jaceidin 5464461 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC)O 360.30 unknown via CMAUP database

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