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Clusia grandiflora

Clusia grandiflora - 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 UUID6440122581d63963710654
Scientific name Clusia grandiflora
Authority Splitg.
First published in Tijdschr. Natuurl. Gesch. Physiol. 9: 101 (1842)

Description Top

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Synonyms Top

Scientific name Authority First published in
Clusia maxima Rich. ex Planch. & Triana Ann. Sci. Nat., Bot. , sér. 4, 13: 325 (1860)
Clusia petiolata Klotzsch ex Engl. Fl. Bras. (Martius) 12(1): 423. 1888 [1 Apr 1888]

Common names Top

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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
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil Southeast
      • Brazil West-central
    • Northern South America
      • French Guiana
      • Guyana
      • Suriname
      • Venezuela
    • Western South America
      • Colombia
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000612235
Tropicos 7801334
INPN 733006
KEW urn:lsid:ipni.org:names:427524-1
The Plant List kew-2728407
Open Tree Of Life 166592
NCBI Taxonomy 211497
IUCN Red List 147300727
IPNI 427524-1
iNaturalist 465992
GBIF 5556447
EOL 5709647
USDA GRIN 10949

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
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
Host‐tree selection by the ant garden‐initiating arboreal ponerine Neoponera goeldii Dejean A, Rossi V, Azémar F, Compin A, Petitclerc F, Talaga S, Corbara B Ecology 25-Sep-2022
PMCID:PMC10078305
doi:10.1002/ecy.3843
PMID:36156795
How diverse is the chemistry and plant origin of Brazilian propolis? Salatino A, Salatino ML, Negri G Apidologie 01-Oct-2021
PMCID:PMC8485119
doi:10.1007/s13592-021-00889-z
PMID:34611369
Exploration of Long-Chain Vitamin E Metabolites for the Discovery of a Highly Potent, Orally Effective, and Metabolically Stable 5-LOX Inhibitor that Limits Inflammation Neukirch K, Alsabil K, Dinh CP, Bilancia R, Raasch M, Ville A, Cerqua I, Viault G, Bréard D, Pace S, Temml V, Brunner E, Jordan PM, Marques MC, Loeser K, Gollowitzer A, Permann S, Gerstmeier J, Lorkowski S, Stuppner H, Garscha U, Rodrigues T, Bernardes GJ, Schuster D, Séraphin D, Richomme P, Rossi A, Mosig AS, Roviezzo F, Werz O, Helesbeux JJ, Koeberle A J Med Chem 19-Jul-2021
PMCID:PMC8365602
doi:10.1021/acs.jmedchem.1c00806
PMID:34279935
Vascular Epiphytic Medicinal Plants as Sources of Therapeutic Agents: Their Ethnopharmacological Uses, Chemical Composition, and Biological Activities Nugraha AS, Triatmoko B, Wangchuk P, Keller PA Biomolecules 24-Jan-2020
PMCID:PMC7072150
doi:10.3390/biom10020181
PMID:31991657
Natural 6-hydroxy-chromanols and -chromenols: structural diversity, biosynthetic pathways and health implications Birringer M, Siems K, Maxones A, Frank J, Lorkowski S RSC Adv 26-Jan-2018
PMCID:PMC9078042
doi:10.1039/c7ra11819h
PMID:35539527
Species richness, distribution and genetic diversity of Caenorhabditis nematodes in a remote tropical rainforest Félix MA, Jovelin R, Ferrari C, Han S, Cho YR, Andersen EC, Cutter AD, Braendle C BMC Evol Biol 12-Jan-2013
PMCID:PMC3556333
doi:10.1186/1471-2148-13-10
PMID:23311925
Functional Diversity of Photosynthetic Light Use of 16 Vascular Epiphyte Species Under Fluctuating Irradiance in the Canopy of a Giant Virola michelii (Myristicaceae) Tree in the Tropical Lowland Forest of French Guyana Rascher U, Freiberg M, Lüttge U Front Plant Sci 13-Jan-2012
PMCID:PMC3355546
doi:10.3389/fpls.2011.00117
PMID:22629271
Climate Change Impact on Neotropical Social Wasps Dejean A, Céréghino R, Carpenter JM, Corbara B, Hérault B, Rossi V, Leponce M, Orivel J, Bonal D PLoS One 02-Nov-2011
PMCID:PMC3206903
doi:10.1371/journal.pone.0027004
PMID:22073236
Pollination Biology of Jacaranda oxyphylla with an Emphasis on Staminode Function Guimarães E, di Stasi LC, Maimoni-Rodella RD Ann Bot 02-Sep-2008
PMCID:PMC2712375
doi:10.1093/aob/mcn152
PMID:18765441
Ethnomedicines used in Trinidad and Tobago for reproductive problems Lans C J Ethnobiol Ethnomed 15-Mar-2007
PMCID:PMC1838898
doi:10.1186/1746-4269-3-13
PMID:17362507
Floral resins of clusia spp.: Chemical composition and biological function Cecilia M.A. de Oliveira, AndréM. Porto, Volker Bittrich, Ivo Vencato, Anita J. Marsaioli Elsevier BV 26-Jul-2002
doi:10.1016/0040-4039(96)00656-9
Two polyisoprenylated benzophenones from the trunk latex of Clusia grandiflora (Clusiaceae). Lokvam J, Braddock JF, Reichardt PB, Clausen TP Phytochemistry 01-Sep-2000
doi:10.1016/S0031-9422(00)00193-X
PMID:11021641

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
[(2R,3S,4S)-3,4-dimethylheptan-2-yl] butanoate 162885051 Click to see CCCC(C)C(C)C(C)OC(=O)CCC 214.34 unknown https://doi.org/10.1016/S0031-9422(00)00193-X
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
5a,9-Dimethyl-3-methylidene-3a,4,5,9b-tetrahydrobenzo[g][1]benzofuran-2,8-dione 3874468 Click to see CC1=C2C3C(CCC2(C=CC1=O)C)C(=C)C(=O)O3 244.28 unknown https://doi.org/10.1016/S0031-9422(00)00193-X
> Organic acids and derivatives / Peptidomimetics / Depsipeptides / Cyclic depsipeptides
Isariin D 139589091 Click to see CCCCC1CC(=O)NCC(=O)NC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)O1)C)C)CC(C)C)C(C)C 539.70 unknown https://doi.org/10.1016/S0031-9422(00)00193-X
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
Methyl 2-[(3-formyl-4-hydroxyphenyl)methyl]-4-hydroxy-3-(4-hydroxyphenyl)-5-oxofuran-2-carboxylate 134822412 Click to see COC(=O)C1(C(=C(C(=O)O1)O)C2=CC=C(C=C2)O)CC3=CC(=C(C=C3)O)C=O 384.30 unknown https://doi.org/10.1016/0040-4039(96)00656-9
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
Cycloshizukaol A 44240915 Click to see CC1(CC2=C3C=C(C(=O)C(C3(C4C2C4)C)O)C(CC5=C6C=C1C(=O)C(C6(C7C5C7)C)O)(C)C(=O)OC)C(=O)OC 548.60 unknown https://doi.org/10.1016/S0031-9422(00)00193-X
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
(1R,5S,7R)-1-benzoyl-4-hydroxy-8,8-dimethyl-3,5,7-tris(3-methylbut-2-enyl)bicyclo[3.3.1]non-3-ene-2,9-dione 162853620 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/S0031-9422(00)00193-X
(1R,7R)-1-benzoyl-4-hydroxy-8,8-dimethyl-3,5,7-tris(3-methylbut-2-enyl)bicyclo[3.3.1]non-3-ene-2,9-dione 57339900 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/S0031-9422(00)00193-X
(1R,9S,11R)-1-benzoyl-4,4,12,12-tetramethyl-11-(3-methylbut-2-enyl)-9-[(2R)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-3-oxatricyclo[7.3.1.02,7]trideca-2(7),5-diene-8,13-dione 637875 Click to see CC(=CCC1CC2(C(=O)C3=C(C(C2=O)(C1(C)C)C(=O)C4=CC=CC=C4)OC(C=C3)(C)C)CC(CC=C(C)C)C(=C)C)C 568.80 unknown https://doi.org/10.1016/S0031-9422(00)00193-X
(1R,9S,11S)-1-benzoyl-4,4,12,12-tetramethyl-11-(3-methylbut-2-enyl)-9-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-3-oxatricyclo[7.3.1.02,7]trideca-2(7),5-diene-8,13-dione 162963303 Click to see CC(=CCC1CC2(C(=O)C3=C(C(C2=O)(C1(C)C)C(=O)C4=CC=CC=C4)OC(C=C3)(C)C)CC(CC=C(C)C)C(=C)C)C 568.80 unknown https://doi.org/10.1016/S0031-9422(00)00193-X
(1S,5R,7R)-5-benzoyl-4-methoxy-6,6-dimethyl-1,3,7-tris(3-methylbut-2-enyl)bicyclo[3.3.1]non-3-ene-2,9-dione 163065882 Click to see CC(=CCC1CC2(C(=O)C(=C(C(C2=O)(C1(C)C)C(=O)C3=CC=CC=C3)OC)CC=C(C)C)CC=C(C)C)C 516.70 unknown https://doi.org/10.1016/S0031-9422(00)00193-X
(7S)-1-benzoyl-4-hydroxy-8,8-dimethyl-3,7-bis(3-methylbut-2-enyl)-5-(5-methyl-2-prop-1-en-2-ylhex-4-enyl)bicyclo[3.3.1]non-3-ene-2,9-dione 102572074 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(CC=C(C)C)C(=C)C)C 570.80 unknown https://doi.org/10.1016/S0031-9422(00)00193-X
1-Benzoyl-4,4,12,12-tetramethyl-11-(3-methylbut-2-enyl)-9-(5-methyl-2-prop-1-en-2-ylhex-4-enyl)-3-oxatricyclo[7.3.1.02,7]trideca-2(7),5-diene-8,13-dione 22297868 Click to see CC(=CCC1CC2(C(=O)C3=C(C(C2=O)(C1(C)C)C(=O)C4=CC=CC=C4)OC(C=C3)(C)C)CC(CC=C(C)C)C(=C)C)C 568.80 unknown https://doi.org/10.1016/S0031-9422(00)00193-X
5-Benzoyl-4-methoxy-6,6-dimethyl-1,3,7-tris(3-methylbut-2-enyl)bicyclo[3.3.1]non-3-ene-2,9-dione 58740981 Click to see CC(=CCC1CC2(C(=O)C(=C(C(C2=O)(C1(C)C)C(=O)C3=CC=CC=C3)OC)CC=C(C)C)CC=C(C)C)C 516.70 unknown https://doi.org/10.1016/S0031-9422(00)00193-X
> Organoheterocyclic compounds / Naphthopyrans
5,7-Dihydroxy-14-(4-methoxyphenyl)-2,6,6,10-tetramethyl-11,15-dioxatetracyclo[8.8.0.02,7.012,17]octadeca-12(17),13-dien-16-one 85218262 Click to see CC1(C(CCC2(C1(CCC3(C2CC4=C(O3)C=C(OC4=O)C5=CC=C(C=C5)OC)C)O)C)O)C 454.60 unknown https://doi.org/10.1016/S0031-9422(00)00193-X

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