Dendrocnide moroides - Unknown
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Internal ID UUID6440164376ace938904364
Scientific name Dendrocnide moroides
Authority (Wedd.) Chew
First published in Gard. Bull. Singapore 21: 204 (1965)

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Synonyms Top

Scientific name Authority First published in
Urticastrum morodes Kuntze Revis. Gen. Pl. 2: 635 (1891)
Laportea moroides Wedd. Nouv. Arch. Mus. Hist. Nat. 9: 142 (1856)

Common names Top

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Language Common/alternative name
English mulberry-leaved stinger
English stinging bush
English gympie gympie
English stinging tree
Arabic جيمبي جيمبي
Bengali ডেনড্রোকনাইড মোরয়েডস
Czech kopřivák morušovitý
German australische brennnessel
Estonian valu-nõgespuu
Persian گیاه خودکشی
Hebrew גימפי גימפי
Croatian gympie-gympie
Indonesian gympie-gympie
Japanese ギンピ・ギンピ
Korean 짐피짐피
mo urzica australiană
Portuguese gympie ferrão
Romanian urzica australiană
Russian Жалящее дерево
Swedish nässelträd
Swedish gympie gympie
Tamil ஜிம்பி ஜிம்பி
Tamil கொட்டு புதர்
Tamil கொட்டு மரம்
Tamil டெண்ட்ரோக்னைடு மொராய்ட்ஸ்
Telugu జిమ్పి జిమ్పి చెట్టు

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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-0000641039
Tropicos 50218632
KEW urn:lsid:ipni.org:names:851456-1
The Plant List kew-2760700
Open Tree Of Life 5922341
NCBI Taxonomy 1842752
IPNI 851456-1
iNaturalist 129503
GBIF 4098695
Freebase /m/0fz2h2
EOL 5726734
Wikipedia Dendrocnide_moroides

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
Neurotoxic and cytotoxic peptides underlie the painful stings of the tree nettle Urtica ferox Xie J, Robinson SD, Gilding EK, Jami S, Deuis JR, Rehm FB, Yap K, Ragnarsson L, Chan LY, Hamilton BR, Harvey PJ, Craik DJ, Vetter I, Durek T J Biol Chem 30-Jun-2022
PMCID:PMC9352542
doi:10.1016/j.jbc.2022.102218
PMID:35780839
Strengthening Structures in the Petiole–Lamina Junction of Peltate Leaves Wunnenberg J, Rjosk A, Neinhuis C, Lautenschläger T Biomimetics (Basel) 02-Apr-2021
PMCID:PMC8167582
doi:10.3390/biomimetics6020025
PMID:33918405
Distribution, Ecology, Chemistry and Toxicology of Plant Stinging Hairs Ensikat HJ, Wessely H, Engeser M, Weigend M Toxins (Basel) 13-Feb-2021
PMCID:PMC7918447
doi:10.3390/toxins13020141
PMID:33668609
The use of antimalarial plants as traditional treatment in Papua Island, Indonesia Budiarti M, Maruzy A, Mujahid R, Sari AN, Jokopriyambodo W, Widayat T, Wahyono S Heliyon 14-Dec-2020
PMCID:PMC7736719
doi:10.1016/j.heliyon.2020.e05562
PMID:33344788
Leaf Life Span Plasticity in Tropical Seedlings Grown under Contrasting Light Regimes VINCENT G Ann Bot 01-Feb-2006
PMCID:PMC2803358
doi:10.1093/aob/mcj023
PMID:16299004
Computer-assisted structure determination. Structure of the peptide moroidin from Laportea moroides S. D. Kahn, P. M. Booth, J. P. Waltho, D. H. Williams American Chemical Society (ACS) 12-Mar-2005
doi:10.1021/JO00269A028
Structural studies on the peptide moroidin from laportea moroides T-W Christina Leung, Dudley H Williams, Jennifer C J Barna, Salvatore Foti, Peter B.Oelrichs Elsevier BV 25-Jul-2002
doi:10.1016/S0040-4020(01)87397-X

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
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Cyclic peptides
(8R,9S,12S,15S,18R,21S,27S)-21-[3-(diaminomethylideneamino)propyl]-12-(2-methylpropyl)-10,13,16,19,22,25-hexaoxo-9-[[(2S)-5-oxopyrrolidine-2-carbonyl]amino]-8,15-di(propan-2-yl)-2,11,14,17,20,23,26,30,32-nonazapentacyclo[16.14.2.13,7.129,32.04,33]hexatriaconta-1(33),3,5,7(36),29(35),30-hexaene-27-carboxylic acid 163193580 Click to see CC(C)CC1C(=O)NC(C(=O)NC2CC3=C(NC4=C3C=CC(=C4)C(C(C(=O)N1)NC(=O)C5CCC(=O)N5)C(C)C)N6C=C(CC(NC(=O)CNC(=O)C(NC2=O)CCCN=C(N)N)C(=O)O)N=C6)C(C)C 987.10 unknown https://doi.org/10.1016/S0040-4020(01)87397-X
21-[3-(Diaminomethylideneamino)propyl]-12-(2-methylpropyl)-10,13,16,19,22,25-hexaoxo-9-[(5-oxopyrrolidine-2-carbonyl)amino]-8,15-di(propan-2-yl)-2,11,14,17,20,23,26,30,32-nonazapentacyclo[16.14.2.13,7.129,32.04,33]hexatriaconta-1(33),3,5,7(36),29(35),30-hexaene-27-carboxylic acid 14311393 Click to see CC(C)CC1C(=O)NC(C(=O)NC2CC3=C(NC4=C3C=CC(=C4)C(C(C(=O)N1)NC(=O)C5CCC(=O)N5)C(C)C)N6C=C(CC(NC(=O)CNC(=O)C(NC2=O)CCCN=C(N)N)C(=O)O)N=C6)C(C)C 987.10 unknown https://doi.org/10.1016/S0040-4020(01)87397-X
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Oligopeptides
Moroidin 23247762 Click to see CC(C)CC1C(=O)NC(C(=O)NC2CC3=C(NC4=C3C=CC(=C4)C(C(C(=O)N1)NC(=O)C5CCC(=O)N5)C(C)C)N6C=C(CC(NC(=O)CNC(=O)C(NC2=O)CCCN=C(N)N)C(=O)O)N=C6)C(C)C 987.10 unknown https://doi.org/10.1016/S0040-4020(01)87397-X
https://doi.org/10.1021/JO00269A028

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