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Duboisia hopwoodii

Duboisia hopwoodii - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID6440411c5653f401307514
Scientific name Duboisia hopwoodii
Authority F.Muell.
First published in Fragm. (Mueller) 8(69): 232. 1874

Description Top

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Synonyms Top

Scientific name Authority First published in
Anthocercis hopwoodii F.Muell. Fragm. (Mueller) 2(15): 138. 1861

Common names Top

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Language Common/alternative name
English pitchuri thornapple
English pituri

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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No forms added yet.

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
  • Australasia
    • Australia
      • New South Wales
      • Northern Territory
      • Queensland
      • South Australia
      • Western Australia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001021491
USDA Plants DUHO2
Tropicos 29605761
KEW urn:lsid:ipni.org:names:815654-1
The Plant List kew-2778801
Open Tree Of Life 434595
NCBI Taxonomy 540800
IPNI 815654-1
iNaturalist 698942
GBIF 5341762
Freebase /m/0bbv7bp
EOL 486415
USDA GRIN 14732
Wikipedia Duboisia_hopwoodii

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
Moringa oleifera as a Natural Alternative for the Control of Gastrointestinal Parasites in Equines: A Review Elghandour MM, Maggiolino A, Vázquez-Mendoza P, Alvarado-Ramírez ER, Cedillo-Monroy J, De Palo P, Salem AZ Plants (Basel) 08-May-2023
PMCID:PMC10181162
doi:10.3390/plants12091921
PMID:37176979
Rumors of Psychedelics, Psychotropics and Related Derivatives in Vachellia and Senegalia in Contrast with Verified Records in Australian Acacia Sadgrove NJ Plants (Basel) 02-Dec-2022
PMCID:PMC9738376
doi:10.3390/plants11233356
PMID:36501395
Aboriginal medicinal plants of Queensland: ethnopharmacological uses, species diversity, and biodiscovery pathways Turpin G, Ritmejerytė E, Jamie J, Crayn D, Wangchuk P J Ethnobiol Ethnomed 10-Aug-2022
PMCID:PMC9364609
doi:10.1186/s13002-022-00552-6
PMID:35948982
Ortholog genes from cactophilic Drosophila provide insight into human adaptation to hallucinogenic cacti Padró J, De Panis DN, Luisi P, Dopazo H, Szajnman S, Hasson E, Soto IM Sci Rep 01-Aug-2022
PMCID:PMC9343604
doi:10.1038/s41598-022-17118-x
PMID:35915153
Historical and Scientific Evidence for the Origin and Cultural Importance to Australia’s First-Nations Peoples of the Laboratory Accession of Nicotiana benthamiana, a Model for Plant Virology Wylie S, Li H Viruses 08-Apr-2022
PMCID:PMC9027518
doi:10.3390/v14040771
PMID:35458501
Psychedelics as Tools for Belief Transmission. Set, Setting, Suggestibility, and Persuasion in the Ritual Use of Hallucinogens Dupuis D Front Psychol 23-Nov-2021
PMCID:PMC8651242
doi:10.3389/fpsyg.2021.730031
PMID:34887799
Diversity in Chemical Structures and Biological Properties of Plant Alkaloids Bhambhani S, Kondhare KR, Giri AP Molecules 03-Jun-2021
PMCID:PMC8199754
doi:10.3390/molecules26113374
PMID:34204857
Pyridine alkaloids with activity in the central nervous system Lin SX, Curtis MA, Sperry J Bioorg Med Chem 16-Oct-2020
PMCID:PMC7561606
doi:10.1016/j.bmc.2020.115820
PMID:33120080
Brain Ageing, Cognition and Diet: A Review of the Emerging Roles of Food-Based Nootropics in Mitigating Age-Related Memory Decline Onaolapo AY, Obelawo AY, Onaolapo OJ Curr Aging Sci 01-May-2019
PMCID:PMC6971896
doi:10.2174/1874609812666190311160754
PMID:30864515
Systematic review of gastrointestinal nematodes of horses from Australia Saeed MA, Beveridge I, Abbas G, Beasley A, Bauquier J, Wilkes E, Jacobson C, Hughes KJ, El-Hage C, O’Handley R, Hurley J, Cudmore L, Carrigan P, Walter L, Tennent-Brown B, Nielsen MK, Jabbar A Parasit Vectors 29-Apr-2019
PMCID:PMC6489199
doi:10.1186/s13071-019-3445-4
PMID:31036059
Cloning and Characterization of Two Iridoid Synthase Homologs from Swertia Mussotii Xiang B, Li X, Wang Y, Tian X, Yang Z, Ma L, Liu X, Wang Y Molecules 22-Aug-2017
PMCID:PMC6152284
doi:10.3390/molecules22081387
PMID:28829394
Smoking in Pregnancy Among Indigenous Women in High-Income Countries: A Narrative Review Gould GS, Patten C, Glover M, Kira A, Jayasinghe H Nicotine Tob Res 11-Apr-2017
PMCID:PMC5896479
doi:10.1093/ntr/ntw288
PMID:28403465
Diseases of the Nervous System N/A Veterinary Medicine 10-Feb-2017
PMCID:PMC7322266
doi:10.1016/B978-0-7020-5246-0.00014-0
Establishing Natural Nootropics: Recent Molecular Enhancement Influenced by Natural Nootropic Suliman NA, Mat Taib CN, Mohd Moklas MA, Adenan MI, Hidayat Baharuldin MT, Basir R Evid Based Complement Alternat Med 30-Aug-2016
PMCID:PMC5021479
doi:10.1155/2016/4391375
PMID:27656235
Nicotelline: A Proposed Biomarker and Environmental Tracer for Particulate Matter Derived from Tobacco Smoke Jacob P III, Goniewicz ML, Havel C, Schick SF, Benowitz NL Chem Res Toxicol 14-Oct-2013
PMCID:PMC3929594
doi:10.1021/tx400094y
PMID:24125094

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 / Tropane alkaloids
Atropine sulfate 3661 Click to see CN1C2CCC1CC(C2)OC(=O)C(CO)C3=CC=CC=C3 289.40 unknown https://doi.org/10.1016/S0031-9422(00)95286-5
> Organic acids and derivatives / Hydroxy acids and derivatives / Beta hydroxy acids and derivatives
(-)-Scopolamine 5184 Click to see CN1C2CC(CC1C3C2O3)OC(=O)C(CO)C4=CC=CC=C4 303.35 unknown https://doi.org/10.1016/S0031-9422(00)95286-5
Tropic acid ester with scopine 153311 Click to see CN1C2CC(CC1C3C2O3)OC(=O)C(CO)C4=CC=CC=C4 303.35 unknown https://doi.org/10.1016/S0031-9422(00)95286-5
https://doi.org/10.1016/S0031-9422(00)81107-3
> 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/10.1016/S0031-9422(00)95286-5
> Organoheterocyclic compounds / Pyridines and derivatives
3-Buten-1-amine, N-methyl-4-(3-pyridinyl)- 72928 Click to see CNCCC=CC1=CN=CC=C1 162.23 unknown https://doi.org/10.1016/S0031-9422(00)95286-5
Myosmine 442649 Click to see C1CC(=NC1)C2=CN=CC=C2 146.19 unknown https://doi.org/10.1016/S0031-9422(00)95286-5
Rivanicline 5310967 Click to see CNCCC=CC1=CN=CC=C1 162.23 unknown https://doi.org/10.1016/S0031-9422(00)95286-5
> Organoheterocyclic compounds / Pyridines and derivatives / Pyrrolidinylpyridines
(2S)-2-(3-Pyridinyl)-1-pyrrolidinecarboxaldehyde 13945368 Click to see C1CC(N(C1)C=O)C2=CN=CC=C2 176.21 unknown https://doi.org/10.1016/S0031-9422(00)95286-5
(R)-3-(Pyrrolidin-2-yl)pyridine 93047 Click to see C1CC(NC1)C2=CN=CC=C2 148.20 unknown https://doi.org/10.1038/ICB.1935.20
https://doi.org/10.1016/S0031-9422(00)95286-5
https://doi.org/10.1038/ICB.1947.27
https://doi.org/10.1071/CH9510107
3-(1-Methylpyrrolidin-2-yl)pyridine 942 Click to see CN1CCCC1C2=CN=CC=C2 162.23 unknown https://doi.org/10.1016/S0031-9422(00)95286-5
https://doi.org/10.1071/CH9510107
https://doi.org/10.1016/S0031-9422(00)81107-3
Nicotine 89594 Click to see CN1CCCC1C2=CN=CC=C2 162.23 unknown https://doi.org/10.1016/S0031-9422(00)81107-3
https://doi.org/10.1071/CH9510107
https://doi.org/10.1016/S0031-9422(00)95286-5
Nornicotine, N-formyl 528369 Click to see C1CC(N(C1)C=O)C2=CN=CC=C2 176.21 unknown https://doi.org/10.1016/S0031-9422(00)95286-5
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
[(2R,3S,4S,5R,6S)-6-[(2S,3R,4S,5R,6S)-4,5-dihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxo-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-3-yl]oxy-2-methyloxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl (2S)-3-hydroxy-2-methylpropanoate 163030082 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O)C5=CC=C(C=C5)O)O)O)OC6C(C(C(C(O6)COC(=O)C(C)CO)O)O)O 842.70 unknown https://doi.org/10.1016/S0031-9422(00)95286-5
https://doi.org/10.1038/ICB.1935.20
https://doi.org/10.1071/CH9510107
https://doi.org/10.1016/S0031-9422(00)81107-3

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