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Brugmansia sanguinea

Brugmansia sanguinea - Unknown
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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 UUID644040f548cfd328131602
Scientific name Brugmansia sanguinea
Authority (Ruiz & Pav.) D.Don
First published in Brit. Fl. Gard. [Sweet] Ser. 2, 3: t. 272. 1835.

Description Top

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Brugmansia sanguinea, commonly known as the red angel's trumpet, is a species of South American flowering shrub or small tree belonging to the genus Brugmansia in the nightshade family Solanaceae. It is native to the Andes mountains from Colombia to northern Chile and has been cultivated and used as an entheogen for shamanic purposes by the South American Natives for centuries. It can reach up to 10 m (33 ft) in height and has pendent, tubular/trumpet-shaped flowers in shades of brilliant red, yellow, orange and green. All parts of the plant are poisonous, containing tropane alkaloids in varying proportions, with the seeds containing approximately 0.17% alkaloids by mass, of which 78% are scopolomine.

Synonyms Top

Scientific name Authority First published in
Brugmansia bicolor Pers. Syn. Pl. (Persoon) 1: 216. 1805 [1 Apr-15 Jun 1805]
Brugmansia coccinea Poepp. Reise Chile 114. 1835.
Brugmansia lutea Berlèse Jardins de France 20. 1837.
Brugmansia sanguinea var. glabra Marnock Floricult. Mag. 3: 158. 1838.
Datura rosei Saff. J. Wash. Acad. Sci. 11: 188, fig. 3. 1921
Datura coccinea Siebert & Voss S. & Voss, Vilm. Blumengärtn., ed. 3, 1: 727. 1895., 1895.
Elisia mutabilis Milano New Orleans Med. & Surg. Journ. 3: 614-16. 1847 (March 1847)
Datura sanguinea f. coccinea Siebert & Voss

Common names Top

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Language Common/alternative name
English red floripontio
Spanish guamuco
Spanish datura rubella
Spanish datura sanguinea
Spanish datura sanguinea var flava
Spanish datura sanguinea var. flava
Czech durman krvavý
French trompette des anges écarlate
Quechua datura sanguinea
Quechua puka kamapchu
Quechua puka wantuq
Swedish röd änglatrumpet
Tamil புருக்மான்சியா சங்குனியா
Chinese 红花木曼陀罗

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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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
    • New Zealand
      • Chatham Islands
      • New Zealand North
      • New Zealand South
  • Southern America
    • Central America
      • Costa Rica
    • Southern South America
      • Chile North
      • Juan Fernández Islands
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001019777
UNII 4RID533N6U
USDA Plants BRSA3
Tropicos 29605012
INPN 629208
KEW urn:lsid:ipni.org:names:814612-1
The Plant List kew-2684017
Open Tree Of Life 445285
NCBI Taxonomy 540794
IUCN Red List 51247690
IPNI 814612-1
iNaturalist 337796
GBIF 5341760
Freebase /m/0h_c39k
EPPO DATSA
EOL 486431
USDA GRIN 70858
Wikipedia Brugmansia_sanguinea

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
Commodity risk assessment of Petunia spp. and Calibrachoa spp. unrooted cuttings from Kenya Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Reignault PL, Stefani E, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Manda RR, Schulz OM, Akrivou A, Antonatos S, Beris D, Debode J, Kritikos C, Kormpi M, Lacomme C, Manceau C, Papachristos D, Reppa C, Gardi C, Potting R EFSA J 25-Apr-2024
PMCID:PMC11044013
doi:10.2903/j.efsa.2024.8742
PMID:38665158
Unraveling plant-pollinator interactions from a south-west Andean forest in Colombia Becoche-Mosquera JM, Gomez-Bernal LG, Zambrano-Gonzalez G, Angulo-Ortiz D PeerJ 09-Nov-2023
PMCID:PMC10640843
doi:10.7717/peerj.16133
PMID:38025706
Sterol composition in plants is specific to pollen, leaf, pollination and pollinator Furse S, Martel C, Yusuf A, Shearman GC, Koch H, Stevenson PC Phytochemistry 01-Oct-2023
PMCID:PMC10493607
doi:10.1016/j.phytochem.2023.113800
PMID:37532086
Poorly Investigated Ecuadorian Medicinal Plants Armijos C, Ramírez J, Vidari G Plants (Basel) 16-Jun-2022
PMCID:PMC9229133
doi:10.3390/plants11121590
PMID:35736741
D N/A Saunders Comprehensive Veterinary Dictionary 16-Oct-2020
PMCID:PMC9771679
doi:10.1016/B978-0-7020-7463-9.50012-4
Development and validation of a real-time RT-PCR test for screening pepper and tomato seed lots for the presence of pospiviroids Botermans M, Roenhorst JW, Hooftman M, Verhoeven JT, Metz E, van Veen EJ, Geraats BP, Kemper M, Beugelsdijk DC, Koenraadt H, Jodlowska A, Westenberg M PLoS One 24-Sep-2020
PMCID:PMC7514017
doi:10.1371/journal.pone.0232502
PMID:32970706
Biosynthesis of medicinal tropane alkaloids in yeast Srinivasan P, Smolke CD Nature 02-Sep-2020
PMCID:PMC7529995
doi:10.1038/s41586-020-2650-9
PMID:32879484
Effects of Water Availability in the Soil on Tropane Alkaloid Production in Cultivated Datura stramonium Moreno-Pedraza A, Gabriel J, Treutler H, Winkler R, Vergara F Metabolites 03-Jul-2019
PMCID:PMC6680536
doi:10.3390/metabo9070131
PMID:31277288
Tropane Alkaloids: Chemistry, Pharmacology, Biosynthesis and Production Kohnen-Johannsen KL, Kayser O Molecules 22-Feb-2019
PMCID:PMC6412926
doi:10.3390/molecules24040796
PMID:30813289
Range overlap between the sword-billed hummingbird and its guild of long-flowered species: An approach to the study of a coevolutionary mosaic Soteras F, Moré M, Ibañez AC, Iglesias MD, Cocucci AA PLoS One 26-Dec-2018
PMCID:PMC6306261
doi:10.1371/journal.pone.0209742
PMID:30586466
Isolation, expression and biochemical characterization of recombinant hyoscyamine-6β-hydroxylase from Brugmansia sanguinea – tuning the scopolamine production Fischer C, Kwon M, Ro DK, van Belkum MJ, Vederas JC Medchemcomm 02-May-2018
PMCID:PMC6071785
doi:10.1039/c8md00090e
PMID:30108978
Evolution of genes associated with gynoecium patterning and fruit development in Solanaceae Ortiz-Ramírez CI, Plata-Arboleda S, Pabón-Mora N Ann Bot 17-Feb-2018
PMCID:PMC5946927
doi:10.1093/aob/mcy007
PMID:29471367
The relationship between nectaries and floral architecture: a case study in Geraniaceae and Hypseocharitaceae Jeiter J, Hilger HH, Smets EF, Weigend M Ann Bot 14-Sep-2017
PMCID:PMC5691401
doi:10.1093/aob/mcx101
PMID:28961907
The discovery and eradication of potato spindle tuber viroid in Canada Singh RP Virusdisease 02-Dec-2014
PMCID:PMC4262315
doi:10.1007/s13337-014-0225-9
PMID:25674616
Traditional medicine applied by the Saraguro yachakkuna: a preliminary approach to the use of sacred and psychoactive plant species in the southern region of Ecuador Armijos C, Cota I, González S J Ethnobiol Ethnomed 24-Feb-2014
PMCID:PMC3975971
doi:10.1186/1746-4269-10-26
PMID:24565054

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 / Corynanthean-type alkaloids
Methyl 2-(3-ethyl-7a-hydroxy-8-methoxy-2,3,4,6,7,12b-hexahydro-1H-indolo[2,3-a]quinolizin-2-yl)-3-methoxyprop-2-enoate 74987192 Click to see CCC1CN2CCC3(C(=NC4=C3C(=CC=C4)OC)C2CC1C(=COC)C(=O)OC)O 414.50 unknown https://doi.org/10.1039/J39680002775
> Alkaloids and derivatives / Tropane alkaloids
(6,7-Dihydroxy-8-methyl-8-azabicyclo[3.2.1]octan-3-yl) 2-methylbut-2-enoate 4486823 Click to see CC=C(C)C(=O)OC1CC2C(C(C(C1)N2C)O)O 255.31 unknown https://doi.org/10.1039/J39680002775
[(1S,3R,5R,6R,7S)-6-hydroxy-8-methyl-7-[(E)-2-methylbut-2-enoyl]oxy-8-azabicyclo[3.2.1]octan-3-yl] (E)-2-methylbut-2-enoate 129644121 Click to see CC=C(C)C(=O)OC1CC2C(C(C(C1)N2C)OC(=O)C(=CC)C)O 337.40 unknown https://doi.org/10.1039/J39680002775
[(1S,3S,5R,6R,7R)-6-hydroxy-8-methyl-7-(2-methylbut-2-enoyloxy)-8-azabicyclo[3.2.1]octan-3-yl] 2-methylbut-2-enoate 162996034 Click to see CC=C(C)C(=O)OC1CC2C(C(C(C1)N2C)OC(=O)C(=CC)C)O 337.40 unknown https://doi.org/10.1055/S-0028-1100129
[(1S,3S,5R,6R,7R)-6-hydroxy-8-methyl-7-[(Z)-2-methylbut-2-enoyl]oxy-8-azabicyclo[3.2.1]octan-3-yl] (E)-2-methylbut-2-enoate 163192888 Click to see CC=C(C)C(=O)OC1CC2C(C(C(C1)N2C)OC(=O)C(=CC)C)O 337.40 unknown https://doi.org/10.1055/S-0028-1100129
[6-Hydroxy-8-methyl-7-(3-methylbutanoyloxy)-8-azabicyclo[3.2.1]octan-3-yl] 2-methylbut-2-enoate 163028200 Click to see CC=C(C)C(=O)OC1CC2C(C(C(C1)N2C)OC(=O)CC(C)C)O 339.40 unknown https://doi.org/10.1039/J39680002775
3alpha-Tigloyloxy-6beta-isovaleryloxy-7beta-hydroxytropane 91750077 Click to see CC=C(C)C(=O)OC1CC2C(C(C(C1)N2C)OC(=O)CC(C)C)O 339.40 unknown https://doi.org/10.1039/J39680002775
Benzenepropanoic acid, alpha-hydroxy-, 8-methyl-8-azabicyclo[3.2.1]oct-3-yl ester, [3(R)-endo]- 4486822 Click to see CN1C2CCC1CC(C2)OC(=O)C(CC3=CC=CC=C3)O 289.40 unknown https://doi.org/10.1039/J39680002775
L-Hyoscyamine 3661 Click to see CN1C2CCC1CC(C2)OC(=O)C(CO)C3=CC=CC=C3 289.40 unknown https://doi.org/10.1055/S-0028-1100129
Tigloyl pseudotropine; Tiglylpseudotropine; Tiglyssin 443011 Click to see CC=C(C)C(=O)OC1CC2CCC(C1)N2C 223.31 unknown https://doi.org/10.1039/J39680002775
> Lipids and lipid-like molecules / Prenol lipids / Sesquaterpenoids
Bisglaucumlide C 16083075 Click to see CC1=CC2C(=C(CC3C2(CC(=O)C(CC(=O)C(=CCCC(=CC3=O)C)C)C(C)C)C(=O)OC)C)CC(C(C4CCC(C(O4)CC1)(C)O)(C)O)OC(=O)C 738.90 unknown https://doi.org/10.1039/J39680002775
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
methyl 2-[(2R,4aS,7S,8aS)-7,8a-dihydroxy-4a-methyl-8-methylidene-2,3,4,5,6,7-hexahydro-1H-naphthalen-2-yl]prop-2-enoate 13895642 Click to see CC12CCC(CC1(C(=C)C(CC2)O)O)C(=C)C(=O)OC 280.36 unknown https://doi.org/10.1039/J39680002775
> Lipids and lipid-like molecules / Saccharolipids / Acyltrehaloses
CID 85149698 85149698 Click to see CCCCCCCCCCCCCCCCCC(=O)OC1C(C(C(OC1OC2C(C(C(C(O2)CO)O)O)O)COC(=O)C)O)O 650.80 unknown https://doi.org/10.1055/S-0028-1100129
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives
2-Nitrobicyclo[2.2.1]hept-5-ene-2,3-dicarboxylic acid 90472028 Click to see C1C2C=CC1C(C2C(=O)O)(C(=O)O)[N+](=O)[O-] 227.17 unknown https://doi.org/10.1016/S0048-9697(97)84054-5
> 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/10.1055/S-0028-1100129
> Organic acids and derivatives / Peptidomimetics / Hybrid peptides
[NMe-Ser7]MC-RY 146684759 Click to see CC1C(NC(=O)C(NC(=O)C(C(NC(=O)C(NC(=O)C(NC(=O)C(N(C(=O)CCC(NC1=O)C(=O)O)C)CO)C)CCCN=C(N)N)C(=O)O)C)CC2=CC=C(C=C2)O)C=CC(=CC(C)C(CC3=CC=CC=C3)OC)C 1063.20 unknown https://doi.org/10.1055/S-0028-1100129
> Phenylpropanoids and polyketides / Coumarins and derivatives
7-[[(1S,4aS,8aR)-5,5,8a-trimethyl-2-methylidene-6-oxo-1,3,4,4a-tetrahydronaphthalen-1-yl]methoxy]-6,8-dimethoxychromen-2-one 162956913 Click to see CC1(C2CCC(=C)C(C2(C=CC1=O)C)COC3=C(C=C4C=CC(=O)OC4=C3OC)OC)C 438.50 unknown https://doi.org/10.1039/J39680002775

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