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Clusia multiflora

Clusia multiflora - 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 UUID6440122d1509c695083214
Scientific name Clusia multiflora
Authority Kunth
First published in Nov. Gen. Sp. 5: 200 (1822)

Description Top

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Synonyms Top

No known synonyms.

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 West-central
    • Central America
      • Costa Rica
      • Honduras
      • Nicaragua
      • Panamá
    • Northern South America
      • Venezuela
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000612333
Tropicos 7800183
KEW urn:lsid:ipni.org:names:427594-1
The Plant List kew-2728497
Open Tree Of Life 47590
NCBI Taxonomy 156472
IUCN Red List 151980211
IPNI 427594-1
iNaturalist 154532
GBIF 7330264
CMAUP NPO16244

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
The Triprenylated Anthranoid Ferruginin A, a Promising Scaffold for the Development of Novel Antibiotics against Gram-Positive Bacteria Casciaro B, Ghirga F, Cappiello F, Vergine V, Loffredo MR, Cammarone S, Puglisi E, Tortora C, Quaglio D, Mori M, Botta B, Mangoni ML Antibiotics (Basel) 11-Jan-2022
PMCID:PMC8773144
doi:10.3390/antibiotics11010084
PMID:35052961
Seeing the wood despite the trees: Exploring human disturbance impact on plant diversity, community structure, and standing biomass in fragmented high Andean forests Calbi M, Fajardo‐Gutiérrez F, Posada JM, Lücking R, Brokamp G, Borsch T Ecol Evol 01-Feb-2021
PMCID:PMC7920791
doi:10.1002/ece3.7182
PMID:33717446
A Phytosociological Study on Andean Rainforests of Peru, and a Comparison with the Surrounding Countries Galán-de-Mera A, Campos-de-la-Cruz J, Linares-Perea E, Montoya-Quino J, Torres-Marquina I, Vicente-Orellana JA Plants (Basel) 26-Nov-2020
PMCID:PMC7761437
doi:10.3390/plants9121654
PMID:33256180
Leaf cuticle analyses: implications for the existence of cutan/non-ester cutin and its biosynthetic origin Leide J, Nierop KG, Deininger AC, Staiger S, Riederer M, de Leeuw JW Ann Bot 28-Mar-2020
PMCID:PMC7304474
doi:10.1093/aob/mcaa056
PMID:32222770
Recent advances in the synthesis of gem-dimethylcyclobutane natural products Hancock EN, Wiest JM, Brown MK Nat Prod Rep 16-Oct-2019
PMCID:PMC6739199
doi:10.1039/c8np00083b
PMID:30855044
Astonishing diversity—the medicinal plant markets of Bogotá, Colombia Bussmann RW, Paniagua Zambrana NY, Romero C, Hart RE J Ethnobiol Ethnomed 20-Jun-2018
PMCID:PMC6011411
doi:10.1186/s13002-018-0241-8
PMID:29925407
Leaf Spectra and Weight of Species in Canopy, Subcanopy, and Understory Layers in a Venezuelan Andean Cloud Forest Acevedo MF, Ataroff M Scientifica (Cairo) 23-May-2012
PMCID:PMC3820457
doi:10.6064/2012/839584
PMID:24278746
Ability of crassulacean acid metabolism plants to overcome interacting stresses in tropical environments Lüttge U AoB Plants 13-May-2010
PMCID:PMC3000696
doi:10.1093/aobpla/plq005
PMID:22476063
Crassulacean acid metabolism and fitness under water deficit stress: if not for carbon gain, what is facultative CAM good for? Herrera A Ann Bot 17-Aug-2008
PMCID:PMC2707347
doi:10.1093/aob/mcn145
PMID:18708641
Ecophysiology of Crassulacean Acid Metabolism (CAM) LÜTTGE U Ann Bot 01-Jun-2004
PMCID:PMC4242292
doi:10.1093/aob/mch087
PMID:15150072
Expression of Phosphoenolpyruvate Carboxylase and Phosphoenolpyruvate Carboxylase Kinase Genes. Implications for Genotypic Capacity and Phenotypic Plasticity in the Expression of Crassulacean Acid Metabolism Taybi T, Nimmo HG, Borland AM Plant Physiol 01-May-2004
PMCID:PMC429420
doi:10.1104/pp.103.036962
PMID:15133148
Citrans and cyclols from Clusia multiflora☆ Jaime Gonzalez Gonzalez, Eduardo Martinez Olivares, Franco Delle Monache Elsevier BV 01-May-2003
doi:10.1016/0031-9422(94)00642-7

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
> Benzenoids / Benzene and substituted derivatives / Benzophenones
(3,5-Dihydroxy-9,13,13-trimethyl-8-oxatetracyclo[7.4.1.02,7.012,14]tetradeca-2(7),3,5-trien-6-yl)-phenylmethanone 73232507 Click to see CC1(C2CCC3(C2C1C4=C(O3)C(=C(C=C4O)O)C(=O)C5=CC=CC=C5)C)C 364.40 unknown https://doi.org/10.1016/0031-9422(94)00642-7
(9-Hydroxy-1,5,5-trimethyl-6,15-dioxatetracyclo[9.3.1.04,13.07,12]pentadeca-7(12),8,10-trien-10-yl)-phenylmethanone 101915968 Click to see CC1(C2CCC3(CC2C4=C(O1)C=C(C(=C4O3)C(=O)C5=CC=CC=C5)O)C)C 364.40 unknown https://doi.org/10.1016/0031-9422(94)00642-7
[(1R,4S,13R)-9-hydroxy-1,5,5-trimethyl-6,15-dioxatetracyclo[9.3.1.04,13.07,12]pentadeca-7,9,11-trien-8-yl]-phenylmethanone 26303713 Click to see CC1(C2CCC3(CC2C4=C(O3)C=C(C(=C4O1)C(=O)C5=CC=CC=C5)O)C)C 364.40 unknown https://doi.org/10.1016/0031-9422(94)00642-7
[(1S,4R,13S)-9-hydroxy-1,5,5-trimethyl-6,15-dioxatetracyclo[9.3.1.04,13.07,12]pentadeca-7(12),8,10-trien-10-yl]-phenylmethanone 163187913 Click to see CC1(C2CCC3(CC2C4=C(O1)C=C(C(=C4O3)C(=O)C5=CC=CC=C5)O)C)C 364.40 unknown https://doi.org/10.1016/0031-9422(94)00642-7
[(1S,9S,12R,14S)-3,5-dihydroxy-9,13,13-trimethyl-8-oxatetracyclo[7.4.1.02,7.012,14]tetradeca-2(7),3,5-trien-4-yl]-phenylmethanone 51521299 Click to see CC1(C2CCC3(C2C1C4=C(O3)C=C(C(=C4O)C(=O)C5=CC=CC=C5)O)C)C 364.40 unknown https://doi.org/10.1016/0031-9422(94)00642-7
[(1S,9S,12R,14S)-3,5-dihydroxy-9,13,13-trimethyl-8-oxatetracyclo[7.4.1.02,7.012,14]tetradeca-2(7),3,5-trien-6-yl]-phenylmethanone 16070715 Click to see CC1(C2CCC3(C2C1C4=C(O3)C(=C(C=C4O)O)C(=O)C5=CC=CC=C5)C)C 364.40 unknown https://doi.org/10.1016/0031-9422(94)00642-7
[(2R)-5,7-dihydroxy-2-methyl-2-(4-methylpent-3-enyl)chromen-8-yl]-phenylmethanone 25765598 Click to see CC(=CCCC1(C=CC2=C(O1)C(=C(C=C2O)O)C(=O)C3=CC=CC=C3)C)C 364.40 unknown https://doi.org/10.1016/0031-9422(94)00642-7
[5,7-Dihydroxy-2-methyl-2-(4-methylpent-3-enyl)chromen-8-yl]-phenylmethanone 16070714 Click to see CC(=CCCC1(C=CC2=C(O1)C(=C(C=C2O)O)C(=O)C3=CC=CC=C3)C)C 364.40 unknown https://doi.org/10.1016/0031-9422(94)00642-7
Clusiacitran A 45359597 Click to see CC1(C2CCC3(CC2C4=C(O3)C=C(C(=C4O1)C(=O)C5=CC=CC=C5)O)C)C 364.40 unknown https://doi.org/10.1016/0031-9422(94)00642-7
Clusiacyclol A 23955805 Click to see CC1(C2CCC3(C2C1C4=C(O3)C=C(C(=C4O)C(=O)C5=CC=CC=C5)O)C)C 364.40 unknown https://doi.org/10.1016/0031-9422(94)00642-7
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Tetracosanoic acid 11197 Click to see CCCCCCCCCCCCCCCCCCCCCCCC(=O)O 368.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
(1R,3R,5R,6S,7R,8Z)-7-hydroxy-8-[hydroxy(phenyl)methylidene]-6-methyl-1,3,5-tris(3-methylbut-2-enyl)tricyclo[4.3.1.03,7]decane-2,9-dione 163188375 Click to see CC(=CCC1CC2(C(=O)C3(CC1(C2(C(=C(C4=CC=CC=C4)O)C3=O)O)C)CC=C(C)C)CC=C(C)C)C 502.70 unknown https://doi.org/10.1016/0031-9422(94)00642-7
7-Hydroxy-8-[hydroxy(phenyl)methylidene]-6-methyl-1,3,5-tris(3-methylbut-2-enyl)tricyclo[4.3.1.03,7]decane-2,9-dione 162898558 Click to see CC(=CCC1CC2(C(=O)C3(CC1(C2(C(=C(C4=CC=CC=C4)O)C3=O)O)C)CC=C(C)C)CC=C(C)C)C 502.70 unknown https://doi.org/10.1016/0031-9422(94)00642-7
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Euphol 441678 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC3=C2CCC4C3(CCC(C4(C)C)O)C)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(94)00642-7
Friedelin 91472 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(94)00642-7
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Cianidanol 9064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Galangin 3-methyl ether 5281946 Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 284.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
[(2R,3R,4S,5R,6S)-6-hydroxy-4,5-bis[(3,4,5-trihydroxybenzoyl)oxy]-2-[(3,4,5-trihydroxybenzoyl)oxymethyl]oxan-3-yl] 3,4,5-trihydroxy-2-[[(10R,11S,12R,13S,15R)-3,4,5,22,23-pentahydroxy-8,18-dioxo-11,12,13-tris[(3,4,5-trihydroxybenzoyl)oxy]-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-21-yl]oxy]benzoate 16157969 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)OC8=C(C(=C(C=C8C(=O)OC9C(OC(C(C9OC(=O)C1=CC(=C(C(=C1)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)O)COC(=O)C1=CC(=C(C(=C1)O)O)O)O)O)O)O)O)O)O)O 1725.20 unknown via CMAUP database
alpha-Pedunculagin 13834142 Click to see C1C2C(C3C(C(O2)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O3)O)O)O)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)O)O)O)O)O)O 784.50 unknown via CMAUP database
beta-Pedunculagin 5320441 Click to see C1C2C(C3C(C(O2)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O3)O)O)O)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)O)O)O)O)O)O 784.50 unknown via CMAUP database
Casuarictin 73644 Click to see C1C2C(C3C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O3)O)O)O)O)O)O)OC(=O)C7=CC(=C(C(=C7C8=C(C(=C(C=C8C(=O)O1)O)O)O)O)O)O 936.60 unknown via CMAUP database
CID 12302513 12302513 Click to see C1C2C(C3C4C(C5=C(C(=C(C(=C5C(=O)O4)C6=C(C(=C(C(=C6C(=O)O3)C7=C(C(=C(C=C7C(=O)O2)O)O)O)O)O)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O1)O)O)O)O)O)O 934.60 unknown via CMAUP database
Ellagic Acid 5281855 Click to see C1=C2C3=C(C(=C1O)O)OC(=O)C4=CC(=C(C(=C43)OC2=O)O)O 302.19 unknown via CMAUP database
Eugeniin 442679 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)O)O)O)O)O)O 938.70 unknown via CMAUP database
Phyllyraeoidin 16170028 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)OC8=C(C(=C(C=C8C(=O)OC9C(OC(C(C9OC(=O)C1=CC(=C(C(=C1)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)COC(=O)C1=CC(=C(C(=C1)O)O)O)O)O)O)O)O)O)O)O 1877.30 unknown via CMAUP database

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