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Allamanda schottii

Allamanda schottii - 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 UUID6440386a5b4b4890785544
Scientific name Allamanda schottii
Authority Pohl
First published in Pl. Bras. Icon. Descr. 1: 73 (1827)

Description Top

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Synonyms Top

Scientific name Authority First published in
Allamanda cathartica var. schottii L.H.Bailey & Raffill in L.H.Bailey Stand. Cycl. Hort. 1: 247 (1914)
Allamanda brasiliensis Schott ex Pohl Pl. Bras. Icon. Descr. 1: 73 (1827)
Allamanda magnifica B.S.Williams Nursery Cat. (B.S.Williams) 1888: 19 (1888)
Allamanda neriifolia Hook. Bot. Mag. 77: t. 4594 (1851)

Common names Top

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Language Common/alternative name
English bush allamanda
Japanese ヒメアリアケカズラ
Malay alamanda anis
Malay alamanda schott
Malay alamanda semak
Malay akar kuning semak
Swedish buskallamanda
Vietnamese huỳnh anh hoa vàng nghệ
Chinese 毛柄短肠蕨
Chinese 黄蝉
Chinese 黄兰蝉
Chinese 硬枝黃蟬
Chinese 硬枝黄蝉
Chinese 黃蟬

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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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 Southeast
      • Hainan
    • Eastern Asia
      • Taiwan
  • Southern America
    • Brazil
      • Brazil South
      • Brazil Southeast
    • Caribbean
      • Puerto Rico
    • Central America
      • Costa Rica
      • Honduras
      • Panamá
    • Northern South America
      • French Guiana
    • Southern South America
      • Argentina Northeast
    • Western South America
      • Galápagos

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000943361
Florida Plant Atlas 4867
USDA Plants ALSC4
Tropicos 1800021
INPN 452487
KEW urn:lsid:ipni.org:names:76487-1
The Plant List kew-6176
Missouri Botanical Garden 254216
Open Tree Of Life 944806
NCBI Taxonomy 403096
IPNI 76487-1
iNaturalist 327732
GBIF 3169838
Freebase /m/02693ph
EPPO ALWSC
EOL 580447
USDA GRIN 2209
Wikipedia Allamanda_schottii

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
The Meaning of Plants' Names: A New Discovering Approach to Its Medicinal and/or Toxic Properties dos Santos Dantas Lima L, Felipe Domingues Passero L, Indriunas A, de Souza Santos I, Francisco Uchôa Coqueiro L, Alexandre Souza da Cruz K, Batista de Almeida A, Carlos Fernandes Galduróz J, Rodrigues E Evid Based Complement Alternat Med 19-Feb-2024
PMCID:PMC10896657
doi:10.1155/2024/6678557
PMID:38410808
Plant Resource Use and Pattern of Usage by the Naturalized Orchid Bee (Euglossa dilemma: Hymenoptera: Apidae) in Florida Pemberton RW Insects 27-Nov-2023
PMCID:PMC10743517
doi:10.3390/insects14120909
PMID:38132583
Characterization of the complete chloroplast genome of Amsonia elliptica (Apocynaceae) Kim Y, Nam BM, Kim I, Deng T, Kim C Mitochondrial DNA B Resour 29-Mar-2023
PMCID:PMC10062215
doi:10.1080/23802359.2023.2192834
PMID:37006955
Perspectives on Nanomaterials and Nanotechnology for Sustainable Bioenergy Generation Markandan K, Chai WS Materials (Basel) 03-Nov-2022
PMCID:PMC9658981
doi:10.3390/ma15217769
PMID:36363361
Secretory Patterns in Colleters of Apocynaceae Ribeiro JC, Tölke ED, Demarco D Plants (Basel) 15-Dec-2021
PMCID:PMC8703501
doi:10.3390/plants10122770
PMID:34961240
Revisiting nature: a review of iridoids as a potential antileishmanial class Arraché Gonçalves G, Eifler-Lima VL, von Poser GL Phytochem Rev 16-Mar-2021
PMCID:PMC7960493
doi:10.1007/s11101-021-09750-8
PMID:33746658
Cellulase immobilized magnetic nanoparticles for green energy production from Allamanda schottii L: Sustainability research in waste recycling Vijayalakshmi S, Govindarajan M, Al-Mulahim N, Ahmed Z, Mahboob S Saudi J Biol Sci 13-Nov-2020
PMCID:PMC7783813
doi:10.1016/j.sjbs.2020.11.034
PMID:33424382
Metabolomic Profiling and Cytotoxic Tetrahydrofurofuran Lignans Investigations from Premna odorata Blanco Elmaidomy AH, Mohammed R, M. Hassan H, I. Owis A, E. Rateb M, A. Khanfar M, Krischke M, J. Mueller M, Ramadan Abdelmohsen U Metabolites 13-Oct-2019
PMCID:PMC6836009
doi:10.3390/metabo9100223
PMID:31614908
Taxonomic and phylogenetic diversity of vascular plants at Ma’anling volcano urban park in tropical Haikou, China: Reponses to soil properties Cheng XL, Yuan LX, Nizamani MM, Zhu ZX, Friedman CR, Wang HF PLoS One 18-Jun-2018
PMCID:PMC6005518
doi:10.1371/journal.pone.0198517
PMID:29912898
Use of rapid fluorescent focus inhibition test (RFFIT) for in vitro evaluation of anti-rabies activity Mehta S, Roy S, Chowdhary A Virusdisease 09-May-2017
PMCID:PMC5510627
doi:10.1007/s13337-017-0371-y
PMID:28770237
Ascertainment of pharmacological activities of Allamanda neriifolia Hook and Aegialitis rotundifolia Roxb used in Bangladesh: An in vitro study Hasan I, Hussain MS, Millat MS, Sen N, Rahman MA, Rahman MA, Islam S, Moghal MM J Tradit Complement Med 26-Apr-2017
PMCID:PMC5755980
doi:10.1016/j.jtcme.2017.03.005
PMID:29321997
Stipules in Apocynaceae: an ontogenetic perspective do Valle Capelli N, Alonso Rodrigues B, Demarco D AoB Plants 10-Feb-2017
PMCID:PMC5499672
doi:10.1093/aobpla/plw083
PMID:28694936
Evaluation of In vitro Antiviral Activity of Datura metel Linn. Against Rabies Virus Roy S, Mukherjee S, Pawar S, Chowdhary A Pharmacognosy Res 01-Oct-2016
PMCID:PMC5004517
doi:10.4103/0974-8490.188874
PMID:27695266
Identification of ethnomedicinal plants (Rauvolfioideae: Apocynaceae) through DNA barcoding from northeast India Mahadani P, Sharma GD, Ghosh SK Pharmacogn Mag 01-Jul-2013
PMCID:PMC3732430
doi:10.4103/0973-1296.113284
PMID:23930011
Evaluation of Antileishmanial Activity of Selected Brazilian Plants and Identification of the Active Principles Filho VC, Meyre-Silva C, Niero R, Bolda Mariano LN, Gomes do Nascimento F, Vicente Farias I, Gazoni VF, dos Santos Silva B, Giménez A, Gutierrez-Yapu D, Salamanca E, Malheiros A Evid Based Complement Alternat Med 09-Jun-2013
PMCID:PMC3690643
doi:10.1155/2013/265025
PMID:23840252

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
> Lignans, neolignans and related compounds / Furanoid lignans
4-[(3aS,6aR)-6-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxyphenol 137705081 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 358.40 unknown https://doi.org/10.1021/NP50056A018
Medioresinol 181681 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC 388.40 unknown https://doi.org/10.1016/0031-9422(88)83144-3
Pinoresinol 73399 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 358.40 unknown https://doi.org/10.1021/NP50056A018
https://doi.org/10.1016/0031-9422(88)83144-3
Syringaresinol, (+)- 443023 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC 418.40 unknown https://doi.org/10.1016/0031-9422(88)83144-3
> Lignans, neolignans and related compounds / Lignan glycosides
(2S,3R,4S,5S,6R)-2-[4-[(3S,3aR,6S,6aR)-3-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2-methoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 486614 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC5C(C(C(C(O5)CO)O)O)O)OC)O 520.50 unknown https://doi.org/10.1016/0031-9422(88)83144-3
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
(1-Hydroxy-4a,8,8,8a-tetramethyl-1,3,3a,4,5,6,7,8b-octahydroindeno[1,2-c]furan-4-yl) 2-methylbut-2-enoate 163041648 Click to see CC=C(C)C(=O)OC1C2COC(C2C3(C1(CCCC3(C)C)C)C)O 336.50 unknown https://doi.org/10.1021/NP50056A018
https://doi.org/10.1248/CPB.32.2947
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
(1S,4aS,7S,7aS)-7-hydroxy-7-methylol-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-methylol-tetrahydropyran-2-yl]oxy-4a,7a-dihydro-1H-cyclopenta[d]pyran-4-carboxylic acid methyl ester 138113473 Click to see COC(=O)C1=COC(C2C1C=CC2(CO)O)OC3C(C(C(C(O3)CO)O)O)O 404.40 unknown https://doi.org/10.1248/CPB.32.2947
Gardenoside 442423 Click to see COC(=O)C1=COC(C2C1C=CC2(CO)O)OC3C(C(C(C(O3)CO)O)O)O 404.40 unknown https://doi.org/10.1248/CPB.32.2947
methyl (1R,4aR,7S,7aR)-5'-oxo-1-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4'-[(1R)-1-[(E)-3-[4-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-enoyl]oxyethyl]spiro[4a,7a-dihydro-1H-cyclopenta[c]pyran-7,2'-furan]-4-carboxylate 133561887 Click to see CC(C1=CC2(C=CC3C2C(OC=C3C(=O)OC)OC4C(C(C(C(O4)CO)O)O)O)OC1=O)OC(=O)C=CC5=CC=C(C=C5)OC6C(C(C(C(O6)CO)O)O)O 778.70 unknown https://doi.org/10.1248/CPB.32.2947
methyl (1S,4R,4aR,7R,7aS)-4'-[(1R)-1-hydroxyethyl]-5'-oxo-1-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyspiro[3,4,4a,7a-tetrahydro-1H-cyclopenta[c]pyran-7,2'-furan]-4-carboxylate 162943489 Click to see CC(C1=CC2(C=CC3C2C(OCC3C(=O)OC)OC4C(C(C(C(O4)CO)O)O)O)OC1=O)O 472.40 unknown https://doi.org/10.1248/CPB.32.2947
methyl 4'-[1-[3-[3-hydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-enoyloxy]ethyl]-5'-oxo-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyspiro[4a,7a-dihydro-1H-cyclopenta[c]pyran-7,2'-furan]-4-carboxylate 163034052 Click to see CC(C1=CC2(C=CC3C2C(OC=C3C(=O)OC)OC4C(C(C(C(O4)CO)O)O)O)OC1=O)OC(=O)C=CC5=CC(=C(C=C5)OC6C(C(C(C(O6)CO)O)O)O)O 794.70 unknown https://doi.org/10.1248/CPB.32.2947
methyl 7-formyl-7-hydroxy-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,7a-dihydro-1H-cyclopenta[c]pyran-4-carboxylate 162963050 Click to see COC(=O)C1=COC(C2C1C=CC2(C=O)O)OC3C(C(C(C(O3)CO)O)O)O 402.30 unknown https://doi.org/10.1248/CPB.32.2947
Plumieride 72319 Click to see CC(C1=CC2(C=CC3C2C(OC=C3C(=O)OC)OC4C(C(C(C(O4)CO)O)O)O)OC1=O)O 470.40 unknown https://doi.org/10.1248/CPB.32.2947
https://doi.org/10.1248/CPB.29.3051
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(1R,4R,6S,8R,10S,11E,14S)-11-ethylidene-6-hydroxy-7,9,13-trioxatetracyclo[6.5.1.01,10.04,14]tetradec-2-en-12-one 134158998 Click to see CC=C1C2C3(C=CC4C3C(O2)OC(C4)O)OC1=O 250.25 unknown https://doi.org/10.1021/NP50056A018
https://doi.org/10.1248/CPB.32.2947
3-O-Methylallamcin 5374090 Click to see CC=C1C2C3(C=CC4C3C(O2)OC(C4)OC)OC1=O 264.27 unknown https://doi.org/10.1248/CPB.32.2947
3,3a,7a,9b-Tetrahydro-3-(1-hydroxyethyl)-2-oxo-2H,4ah-1,4,5-trioxadicyclopent[a,hi]indene-7-carboxylic acid methyl ester 90473101 Click to see CC(C1C2C3(C=CC4C3C(O2)OC(C4C(=O)OC)O)OC1=O)O 326.30 unknown https://doi.org/10.1248/CPB.32.2947
Allamandicin 317838 Click to see CC(C1C2C3(C=CC4C3C(O2)OC=C4C(=O)OC)OC1=O)O 308.28 unknown https://doi.org/10.1248/CPB.32.2947
Allamandin 5281540 Click to see CC=C1C2C3(C=CC4C3C(O2)OC(C4C(=O)OC)O)OC1=O 308.28 unknown https://doi.org/10.1248/CPB.32.2947
https://doi.org/10.1021/NP50056A018
CID 6436806 6436806 Click to see CC=C1C2C3(C=CC4C3C(O2)OC(C4C(=O)OC)O)OC1=O 308.28 unknown https://doi.org/10.1021/NP50056A018
https://doi.org/10.1248/CPB.32.2947
Isoplumericin 5281543 Click to see CC=C1C2C3(C=CC4C3C(O2)OC=C4C(=O)OC)OC1=O 290.27 unknown https://doi.org/10.1021/NP50056A018
https://doi.org/10.1248/CPB.32.2947
methyl (1R,4R,4aR,7R,7aS)-1-hydroxy-4'-[(1R)-1-hydroxyethyl]-5'-oxospiro[3,4,4a,7a-tetrahydro-1H-cyclopenta[c]pyran-7,2'-furan]-4-carboxylate 162905762 Click to see CC(C1=CC2(C=CC3C2C(OCC3C(=O)OC)O)OC1=O)O 310.30 unknown https://doi.org/10.1248/CPB.32.2947
methyl (1R,4S,5S,6S,8R,10S,11S,14S)-6-hydroxy-11-[(1S)-1-hydroxyethyl]-12-oxo-7,9,13-trioxatetracyclo[6.5.1.01,10.04,14]tetradec-2-ene-5-carboxylate 162981234 Click to see CC(C1C2C3(C=CC4C3C(O2)OC(C4C(=O)OC)O)OC1=O)O 326.30 unknown https://doi.org/10.1248/CPB.32.2947
methyl (1R,5S,6S,8R,10S,11S,14S)-6-hydroxy-11-[(1S)-1-hydroxyethyl]-12-oxo-7,9,13-trioxatetracyclo[6.5.1.01,10.04,14]tetradec-2-ene-5-carboxylate 163185896 Click to see CC(C1C2C3(C=CC4C3C(O2)OC(C4C(=O)OC)O)OC1=O)O 326.30 unknown https://doi.org/10.1248/CPB.32.2947
Plumericin 5281545 Click to see CC=C1C2C3(C=CC4C3C(O2)OC=C4C(=O)OC)OC1=O 290.27 unknown https://doi.org/10.1021/NP50056A018
https://doi.org/10.1248/CPB.32.2947
https://doi.org/10.1248/CPB.29.3051
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
methyl (1S,2S,4S,5R,6S,7S)-4'-[(1S)-1-hydroxyethyl]-5'-oxo-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyspiro[3,8-dioxatricyclo[4.4.0.02,4]dec-9-ene-5,2'-furan]-10-carboxylate 101423564 Click to see CC(C1=CC2(C3C(C4C2O4)C(=COC3OC5C(C(C(C(O5)CO)O)O)O)C(=O)OC)OC1=O)O 486.40 unknown https://doi.org/10.1248/CPB.32.2947
> Phenylpropanoids and polyketides / Coumarins and derivatives
Scoparone 8417 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC 206.19 unknown https://doi.org/10.1021/NP50056A018
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O 192.17 unknown https://doi.org/10.1021/NP50056A018

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