Southern America click to expand
- 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

Wood density is related to aboveground biomass and productivity along a successional gradient in upper Andean tropical forests

Castillo-Figueroa D, González-Melo A, Posada JM

Front Plant Sci

09-Nov-2023

PMCID:	PMC10665531
doi:	10.3389/fpls.2023.1276424
PMID:	38023915

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

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

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

Add a new one!

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
> 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
Lignoceric 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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Clusia multiflora

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

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