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Clusia rosea

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID64401235dea52366411050
Scientific name Clusia rosea
Authority Jacq.
First published in Enum. Syst. Pl. : 34 (1760)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Clusia retusa Poir. Encycl. 5: 183 (1804)
Clusia silvicola Britton Bull. Torrey Bot. Club 37: 354 (1910)
Elwertia retusa Raf. Sylva Tellur. : 163 (1838)
Firkea rosea Raf. Sylva Tellur. : 163 (1838)

Common names Top

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Language Common/alternative name
English scotch attorney
Finnish klusia
Finnish kuristajaklusia
Tamil ஆட்டோகிராப் மரம்
Tamil குளூசியா ரோசியா
Chinese 粉红香果树
Chinese 書帶木

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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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
  • Northern America
    • Mexico
      • Mexico Gulf
      • Mexico Southeast
      • Mexico Southwest
    • Southeastern U.S.A.
      • Florida
  • Southern America
    • Brazil
      • Brazil Northeast
    • Caribbean
      • Aruba
      • Bahamas
      • Cayman Islands
      • Cuba
      • Dominican Republic
      • Haiti
      • Jamaica
      • Leeward Islands
      • Netherlands Antilles
      • Puerto Rico
      • Trinidad-Tobago
      • Turks-caicos Islands
      • Venezuelan Antilles
      • Windward Islands
    • Central America
      • Belize
      • Central American Pacific
      • Costa Rica
      • El Salvador
      • Guatemala
      • Honduras
      • Nicaragua
      • Panamá
    • Northern South America
      • French Guiana
      • Guyana
      • Suriname
      • Venezuela
    • Western South America
      • Colombia
      • Ecuador

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000612436
Florida Plant Atlas 2180
USDA Plants CLRO
Tropicos 7800689
INPN 629374
KEW urn:lsid:ipni.org:names:61583-2
The Plant List kew-2728591
Plantarium 123122
Observations.org 198927
NCBI Taxonomy 156476
Nature Serve 2.160463
IUCN Red List 136312479
IPNI 61583-2
iNaturalist 160760
GBIF 5421060
Freebase /m/0cc7psd
EPPO CUFRO
Elurikkus 537019
USDA GRIN 10952
Wikipedia Clusia_rosea
Open Tree Of Life 47595

Genomes (via NCBI) Top

Below is displayed the reference genome only!
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Accession Assembly
Name Level Submitter Released Coverage Size
GCA_056149645.1 CroV1.0_contigs Contig University of Vienna 2026-03-19 50 3.06 Gb

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
Plasticity of Plantago lanceolata L. in Adaptation to Extreme Environmental Conditions Miszalski Z, Kaszycki P, Śliwa-Cebula M, Kaczmarczyk A, Gieniec M, Supel P, Kornaś A Int J Mol Sci 02-Sep-2023
PMCID:PMC10487448
doi:10.3390/ijms241713605
PMID:37686411
Different routes for the construction of biologically active diversely functionalized bicyclo[3.3.1]nonanes: an exploration of new perspectives for anticancer chemotherapeutics Roy N, Das R, Paira R, Paira P RSC Adv 25-Jul-2023
PMCID:PMC10369265
doi:10.1039/d3ra02003g
PMID:37501776
Klaus Winter – the indefatigable CAM experimentalist Holtum JA Ann Bot 03-Apr-2023
PMCID:PMC10799999
doi:10.1093/aob/mcad028
PMID:37010384
Forty years of research into crassulacean acid metabolism in the genus Clusia: anatomy, ecophysiology and evolution Luján M, Leverett A, Winter K Ann Bot 09-Mar-2023
PMCID:PMC10799992
doi:10.1093/aob/mcad039
PMID:36891814
Molecular Mechanisms of Nemorosone-Induced Ferroptosis in Cancer Cells Fernández-Acosta R, Hassannia B, Caroen J, Wiernicki B, Alvarez-Alminaque D, Verstraeten B, Van der Eycken J, Vandenabeele P, Vanden Berghe T, Pardo-Andreu GL Cells 24-Feb-2023
PMCID:PMC10000521
doi:10.3390/cells12050735
PMID:36899871
Leaf vein density correlates with crassulacean acid metabolism, but not hydraulic capacitance, in the genus Clusia Leverett A, Ferguson K, Winter K, Borland AM Ann Bot 23-Feb-2023
PMCID:PMC10799986
doi:10.1093/aob/mcad035
PMID:36821473
Submerged leaves of live indoor foliage plants adsorb H1N1 influenza virus from suspension Song HJ, Yang SW, Jo JW, Choi YK, Lee IS, Lee BU, Lee SH, Kim HH, Kim KJ, Kim HJ Plant Signal Behav 12-Jan-2023
PMCID:PMC9851199
doi:10.1080/15592324.2022.2163869
PMID:36635991
Improving productivity in rabbits by using some natural feed additives under hot environmental conditions — A review Abdelsalam M, Fathi M Anim Biosci 11-Jan-2023
PMCID:PMC9996268
doi:10.5713/ab.22.0354
PMID:36634656
Plants: Sources of Diversity in Propolis Properties Bobiş O Plants (Basel) 02-Sep-2022
PMCID:PMC9460479
doi:10.3390/plants11172298
PMID:36079680
Propolis: An update on its chemistry and pharmacological applications Hossain R, Quispe C, Khan RA, Saikat AS, Ray P, Ongalbek D, Yeskaliyeva B, Jain D, Smeriglio A, Trombetta D, Kiani R, Kobarfard F, Mojgani N, Saffarian P, Ayatollahi SA, Sarkar C, Islam MT, Keriman D, Uçar A, Martorell M, Sureda A, Pintus G, Butnariu M, Sharifi-Rad J, Cho WC Chin Med 26-Aug-2022
PMCID:PMC9412804
doi:10.1186/s13020-022-00651-2
PMID:36028892
Pest categorisation of Pulvinaria psidii Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Grégoire J, Malumphy C, Akrivou A, Kertesz V, Maiorano A, Papachristos D, MacLeod A EFSA J 12-Aug-2022
PMCID:PMC9372818
doi:10.2903/j.efsa.2022.7526
PMID:35978619
Pest categorisation of Russellaspis pustulans 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, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Grégoire J, Malumphy C, Kertesz V, Maiorano A, MacLeod A EFSA J 03-Jun-2022
PMCID:PMC9164144
doi:10.2903/j.efsa.2022.7335
PMID:35662805
Propolis: chemical diversity and challenges in quality control Kasote D, Bankova V, Viljoen AM Phytochem Rev 24-May-2022
PMCID:PMC9128321
doi:10.1007/s11101-022-09816-1
PMID:35645656
An Overview of the Isoprenoid Emissions From Tropical Plant Species Mu Z, Llusià J, Zeng J, Zhang Y, Asensio D, Yang K, Yi Z, Wang X, Peñuelas J Front Plant Sci 20-May-2022
PMCID:PMC9163954
doi:10.3389/fpls.2022.833030
PMID:35668805
Commodity risk assessment of Acer palmatum plants grafted on Acer davidii from China Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Gonthier P EFSA J 12-May-2022
PMCID:PMC9096882
doi:10.2903/j.efsa.2022.7298
PMID:35592020

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
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters
Methyl Stearate 8201 Click to see CCCCCCCCCCCCCCCCCC(=O)OC 298.50 unknown https://doi.org/10.1016/S0031-9422(00)00292-2
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(1R,3Z,5S,7S)-3-[(3,4-dihydroxyphenyl)-hydroxy-methylene]-1-[(2R)-2-isopropenyl-5-methyl-hex-5-enyl]-6,6-dimethyl-5,7-bis(3-methylbut-2-enyl)bicyclo[3.3.1]nonane-2,4,9-trione 5281574 Click to see 602.80 unknown https://doi.org/10.1016/S0040-4020(01)89039-6
(1R,5S,7R)-3-[(3,4-dihydroxyphenyl)-hydroxymethylidene]-6,6-dimethyl-5,7-bis(3-methylbut-2-enyl)-1-[(2R)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]bicyclo[3.3.1]nonane-2,4,9-trione 102461074 Click to see 602.80 unknown https://doi.org/10.1016/S0040-4020(01)89039-6
(1R,5S,7R)-3-[(3,4-dihydroxyphenyl)-hydroxymethylidene]-6,6-dimethyl-5,7-bis(3-methylbut-2-enyl)-1-[(2R)-5-methyl-2-prop-1-en-2-ylhex-5-enyl]bicyclo[3.3.1]nonane-2,4,9-trione 101688705 Click to see 602.80 unknown https://doi.org/10.1016/S0040-4020(01)89039-6
Guttiferone E 5352088 Click to see 602.80 unknown https://doi.org/10.1016/S0040-4020(01)89039-6
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(18|A)-Oleanolic acid 7048528 Click to see 456.70 unknown https://doi.org/10.1016/S0031-9422(00)90127-4
(3S,4R,4aS,6aS,6aR,6bR,8aR,12aR,14aS,14bR)-4,4a,6a,6b,8a,11,11,14a-octamethyl-1,2,3,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-hexadecahydropicen-3-ol 162967132 Click to see 428.70 unknown https://doi.org/10.1016/S0031-9422(00)90127-4
(4S,4aS,6aS,6aS,6bR,8aR,12aS,14aS,14bS)-4,4a,6a,6b,8a,11,11,14a-octamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-3-one 162968771 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(00)90127-4
3-Hydroxyolean-12-en-28-oic acid 619166 Click to see 456.70 unknown https://doi.org/10.1016/S0031-9422(00)90127-4
Friedelan-3-one 244297 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(00)90127-4
Friedelanol 348029 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 428.70 unknown https://doi.org/10.1016/S0031-9422(00)90127-4
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8R,9R,10R,13R,14R,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 11870456 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(00)90127-4
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(00)90127-4
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
(1S,5S,7R)-1-benzoyl-4-methoxy-8,8-dimethyl-3,5,7-tris(3-methylbut-2-enyl)bicyclo[3.3.1]non-3-ene-2,9-dione 162965983 Click to see CC(=CCC1CC2(C(=C(C(=O)C(C2=O)(C1(C)C)C(=O)C3=CC=CC=C3)CC=C(C)C)OC)CC=C(C)C)C 516.70 unknown https://doi.org/10.1016/S0031-9422(98)00476-2
1-Benzoyl-4-methoxy-8,8-dimethyl-3,5,7-tris(3-methylbut-2-enyl)bicyclo[3.3.1]non-3-ene-2,9-dione 58740983 Click to see CC(=CCC1CC2(C(=C(C(=O)C(C2=O)(C1(C)C)C(=O)C3=CC=CC=C3)CC=C(C)C)OC)CC=C(C)C)C 516.70 unknown https://doi.org/10.1016/S0031-9422(98)00476-2
Nemorosone 637105 Click to see CC(=CCC1CC2(C(=C(C(=O)C(C2=O)(C1(C)C)C(=O)C3=CC=CC=C3)CC=C(C)C)O)CC=C(C)C)C 502.70 unknown https://doi.org/10.1016/0040-4039(96)00656-9
https://doi.org/10.1016/S0031-9422(00)00510-0

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