Anisodus luridus - Unknown
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Internal ID UUID644040ef52430996375510
Scientific name Anisodus luridus
Authority Link & Otto
First published in Icon. Pl. Select. 77. 1825 [Jul-Dec 1825]

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Synonyms Top

Scientific name Authority First published in
Anisodus fischerianus Pascher Repert. Spec. Nov. Regni Veg. 7: 226. 1909
Anisodus luridus var. fischeranus (Pascher) C.Y.Wu & C.Chen Acta Phytotax. Sin. 15(2): 62. 1977.
Anisodus mairei (H.Lév.) C.Y.Wu & C.Chen Acta Phytotax. Sin. 15(2): 64. 1977.
Anisodus stramonifolius G.Don Hort. Brit. [Loudon] 61. 1830
Nicandra anomala Link & Otto Icon. Pl. Select. 77, t. 35. 1825 [Jul-Dec 1825]
Physalis stramoniifolia Wall. Fl. Ind. (Carey & Wallich ed.) 2: 242. 1824
Scopolia anomala (Link & Otto) Airy Shaw J. Bot. 75: 195. 1937
Scopolia mairei H.Lév. Acta Phytotax. Sin. 15(2): 64. 1977.
Scopolia straminifolia (Wall.) Shrestha Bull. Dep. Med. Pl., 2 (Fl. Phulchoki & Godawari): 81. 1969
Scopolina stramonifolia (Wall.) Kuntze Revis. Gen. Pl. 2: 452. 1891.
Whitleya stramonifolia (Wall.) Sweet News Lit. and Fashion 3: 108. 1825.
Anisodus anomalus (Link & Otto) V.S.Kumar Nelumbo 55: 209. 2013

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Language Common/alternative name
Chinese 搜山虎
Chinese 三分三
Chinese 东莨菪
Chinese 丽山莨菪(变种)
Chinese 铃铛子
Chinese 铃铛子(丽江山莨菪)
Chinese 唐冲那薄
Chinese 喜马拉雅东莨菪
Chinese 山箊
Chinese 藏茄
Chinese 丽江山莨菪

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Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001019290
Tropicos 29604680
KEW urn:lsid:ipni.org:names:60459144-2
The Plant List kew-2640218
Open Tree Of Life 100843
NCBI Taxonomy 258458
IPNI 60459144-2
GBIF 7300207
EOL 2894377

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)!
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Title Authors Publication Released IDs
Metabolic Effects of Elicitors on the Biosynthesis of Tropane Alkaloids in Medicinal Plants Wen Y, Liao Y, Tang Y, Zhang H, Zhang J, Liao Z Plants (Basel) 24-Aug-2023
PMCID:PMC10490125
doi:10.3390/plants12173050
PMID:37687296
Transcriptome Analysis Reveals an Essential Role of Exogenous Brassinolide on the Alkaloid Biosynthesis Pathway in Pinellia Ternata Guo C, Chen Y, Wu D, Du Y, Wang M, Liu C, Chu J, Yao X Int J Mol Sci 17-Sep-2022
PMCID:PMC9501358
doi:10.3390/ijms231810898
PMID:36142812
Beauty of the beast: anticholinergic tropane alkaloids in therapeutics Shim KH, Kang MJ, Sharma N, An SS Nat Prod Bioprospect 16-Sep-2022
PMCID:PMC9478010
doi:10.1007/s13659-022-00357-w
PMID:36109439
Biotic Elicitors in Adventitious and Hairy Root Cultures: A Review from 2010 to 2022 Alcalde MA, Perez-Matas E, Escrich A, Cusido RM, Palazon J, Bonfill M Molecules 17-Aug-2022
PMCID:PMC9416168
doi:10.3390/molecules27165253
PMID:36014492
Biotechnological Approaches on Engineering Medicinal Tropane Alkaloid Production in Plants Gong H, He P, Lan X, Zeng L, Liao Z Front Plant Sci 02-Jun-2022
PMCID:PMC9201383
doi:10.3389/fpls.2022.924413
PMID:35720595
Application of metabolic engineering to enhance the content of alkaloids in medicinal plants Mora-Vásquez S, Wells-Abascal GG, Espinosa-Leal C, Cardineau GA, García-Lara S Metab Eng Commun 16-Feb-2022
PMCID:PMC8881666
doi:10.1016/j.mec.2022.e00194
PMID:35242556
Persistent calyces increase floral longevity and female fitness in Salvia miltiorrhiza (Lamiaceae) Li DF, Yu Y, Yang HJ, Yan XC AoB Plants 27-Jan-2022
PMCID:PMC8903887
doi:10.1093/aobpla/plac004
PMID:35273787
Effects of Light on Secondary Metabolite Biosynthesis in Medicinal Plants Zhang S, Zhang L, Zou H, Qiu L, Zheng Y, Yang D, Wang Y Front Plant Sci 10-Dec-2021
PMCID:PMC8702564
doi:10.3389/fpls.2021.781236
PMID:34956277
Development of CE-C4D Method for Determination Tropane Alkaloids Gołąb M, Przybyłowska M, Kubáň P, Itterheimová P, Woźniakiewicz M Molecules 22-Sep-2021
PMCID:PMC8510007
doi:10.3390/molecules26195749
PMID:34641293
Wild plants used by the Lhoba people in Douyu Village, characterized by high mountains and valleys, in southeastern Tibet, China Chen WY, Yang T, Yang J, Qiu ZC, Ding XY, Wang YH, Wang YH J Ethnobiol Ethnomed 23-Jul-2021
PMCID:PMC8305498
doi:10.1186/s13002-021-00472-x
PMID:34301287
Development of Atropa belladonna L. Plants with High-Yield Hyoscyamine and without Its Derivatives Using the CRISPR/Cas9 System Zeng L, Zhang Q, Jiang C, Zheng Y, Zuo Y, Qin J, Liao Z, Deng H Int J Mol Sci 09-Feb-2021
PMCID:PMC7915368
doi:10.3390/ijms22041731
PMID:33572199
Plant tissue culture as a perpetual source for production of industrially important bioactive compounds Chandran H, Meena M, Barupal T, Sharma K Biotechnol Rep (Amst) 20-Apr-2020
PMCID:PMC7193120
doi:10.1016/j.btre.2020.e00450
PMID:32373483
Establishment of in vitro culture system for Codonopsis pilosula transgenic hairy roots Yang J, Yang X, Li B, Lu X, Kang J, Cao X 3 Biotech 24-Feb-2020
PMCID:PMC7040125
doi:10.1007/s13205-020-2130-9
PMID:32158633
Elicitation: A biotechnological tool for enhanced production of secondary metabolites in hairy root cultures Halder M, Sarkar S, Jha S Eng Life Sci 25-Jul-2019
PMCID:PMC6999060
doi:10.1002/elsc.201900058
PMID:32624980
Corolla retention after pollination facilitates the development of fertilized ovules in Fritillaria delavayi (Liliaceae) Gao Y, Wang C, Song B, Du F Sci Rep 24-Jan-2019
PMCID:PMC6345895
doi:10.1038/s41598-018-37358-0
PMID:30679717

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 / Tropane alkaloids
Atropine sulfate 3661 Click to see CN1C2CCC1CC(C2)OC(=O)C(CO)C3=CC=CC=C3 289.40 unknown https://doi.org/10.1002/ARDP.18902280210
> Organic oxygen compounds / Organooxygen compounds / Ethers / Acetals / Ketals
Nigericin 34230 Click to see CC1CCC(OC1C(C)C(=O)O)CC2CC(C(C3(O2)C(CC(O3)(C)C4CCC(O4)(C)C5C(CC(O5)C6C(CC(C(O6)(CO)O)C)C)C)C)C)OC 725.00 unknown https://doi.org/10.1002/ARDP.18902280210
https://doi.org/10.1002/ARDP.18902280209
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 51402807 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/S0305-1978(00)00053-3
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1016/S0305-1978(00)00053-3
Kaempferol-3-O-rutinoside 5318767 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O)O)O 594.50 unknown https://doi.org/10.1016/S0305-1978(00)00053-3
Rutin 5280805 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1016/S0305-1978(00)00053-3

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