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Mabea fistulifera

Mabea fistulifera - 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 UUID643fe1e67a8f6265670547
Scientific name Mabea fistulifera
Authority Mart.
First published in Reise Bras. 2: 479 (1828)

Description Top

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Synonyms Top

Scientific name Authority First published in
Mabea ferruginea Benth. Hooker's J. Bot. Kew Gard. Misc. 6: 366 (1854)

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Mabea fistulifera subsp. bahiensis (Emmerich) Esser Novon 3: 349 (1993)
Mabea fistulifera subsp. fistulifera Mart. Unknown

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000231651
Tropicos 12806458
KEW urn:lsid:ipni.org:names:350959-1
The Plant List kew-116158
Open Tree Of Life 3911813
NCBI Taxonomy 1924986
IPNI 350958-1
iNaturalist 604592
GBIF 3071744
EOL 1155519
CMAUP NPO15206

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
Volatile Organic Compounds Produced by Kosakonia cowanii Cp1 Isolated from the Seeds of Capsicum pubescens R & P Possess Antifungal Activity Hernández Flores JL, Martínez YJ, Ramos López MÁ, Saldaña Gutierrez C, Reyes AA, Armendariz Rosales MM, Cortés Pérez MJ, Mendoza MF, Ramírez Ramírez J, Zavala GR, Tovar Becerra PL, Valdez Santoyo L, Villasana Rodríguez K, Rodríguez Morales JA, Campos Guillén J Microorganisms 04-Oct-2023
PMCID:PMC10609226
doi:10.3390/microorganisms11102491
PMID:37894149
Contrasting patterns of foraging behavior in neotropical stingless bees using pollen and honey metabarcoding Martins AC, Proença CE, Vasconcelos TN, Aguiar AJ, Farinasso HC, de Lima AT, Faria JE, Norrana K, Costa MB, Carvalho MM, Dias RL, Bustamante MM, Carvalho FA, Keller A Sci Rep 02-Sep-2023
PMCID:PMC10475120
doi:10.1038/s41598-023-41304-0
PMID:37660141
Kosakonia cowanii Ch1 Isolated from Mexican Chili Powder Reveals Growth Inhibition of Phytopathogenic Fungi González Espinosa J, Hernández Gómez YF, Javier Martínez Y, Flores Gallardo FJ, Pacheco Aguilar JR, Ramos López MÁ, Arvizu Gómez JL, Saldaña Gutierrez C, Rodríguez Morales JA, García Gutiérrez MC, Amaro Reyes A, Álvarez Hidalgo E, Nuñez Ramírez J, Hernández Flores JL, Campos Guillén J Microorganisms 05-Jul-2023
PMCID:PMC10384288
doi:10.3390/microorganisms11071758
PMID:37512930
Biomass residues improve soil chemical and biological properties reestablishing native species in an exposed subsoil in Brazilian Cerrado Soto Boni T, Pujol Pereira EI, Avelino Santos A, Rodrigues Cassiolato AM, Maltoni KL PLoS One 27-Jun-2022
PMCID:PMC9236270
doi:10.1371/journal.pone.0270215
PMID:35759494
Invasive Lactuca serriola seeds contain endophytic bacteria that contribute to drought tolerance Jeong S, Kim TM, Choi B, Kim Y, Kim E Sci Rep 25-Jun-2021
PMCID:PMC8233371
doi:10.1038/s41598-021-92706-x
PMID:34172799
The Latent Dirichlet Allocation model with covariates (LDAcov): A case study on the effect of fire on species composition in Amazonian forests Valle D, Shimizu G, Izbicki R, Maracahipes L, Silverio DV, Paolucci LN, Jameel Y, Brando P Ecol Evol 05-May-2021
PMCID:PMC8216892
doi:10.1002/ece3.7626
PMID:34188865
Opposite latitudinal patterns for bird and arthropod predation revealed in experiments with differently colored artificial prey Zvereva EL, Castagneyrol B, Cornelissen T, Forsman A, Hernández‐Agüero JA, Klemola T, Paolucci L, Polo V, Salinas N, Theron KJ, Xu G, Zverev V, Kozlov MV Ecol Evol 25-Nov-2019
PMCID:PMC6953658
doi:10.1002/ece3.5862
PMID:31938518
Improving classification of pollen grain images of the POLEN23E dataset through three different applications of deep learning convolutional neural networks Sevillano V, Aznarte JL PLoS One 14-Sep-2018
PMCID:PMC6138340
doi:10.1371/journal.pone.0201807
PMID:30216353
Xanthomonas axonopodis pv. eucalyptorum pv. nov. Causing Bacterial Leaf Blight on Eucalypt in Brazil Ferraz HG, Badel JL, da Silva Guimarães LM, Reis BP, Tótola MR, Gonçalves RC, Alfenas AC Plant Pathol J 01-Aug-2018
PMCID:PMC6097821
doi:10.5423/PPJ.OA.01.2018.0014
PMID:30140181
Traditional knowledge hiding in plain sight – twenty-first century ethnobotany of the Chácobo in Beni, Bolivia Paniagua Zambrana NY, Bussmann RW, Hart RE, Moya Huanca AL, Ortiz Soria G, Ortiz Vaca M, Ortiz Álvarez D, Soria Morán J, Soria Morán M, Chávez S, Chávez Moreno B, Chávez Moreno G, Roca O, Siripi E J Ethnobiol Ethnomed 10-Oct-2017
PMCID:PMC5634836
doi:10.1186/s13002-017-0179-2
PMID:29017576
Feature Extraction and Machine Learning for the Classification of Brazilian Savannah Pollen Grains Gonçalves AB, Souza JS, da Silva GG, Cereda MP, Pott A, Naka MH, Pistori H PLoS One 08-Jun-2016
PMCID:PMC4898734
doi:10.1371/journal.pone.0157044
PMID:27276196
Effects of high-frequency understorey fires on woody plant regeneration in southeastern Amazonian forests Balch JK, Massad TJ, Brando PM, Nepstad DC, Curran LM Philos Trans R Soc Lond B Biol Sci 05-Jun-2013
PMCID:PMC3638427
doi:10.1098/rstb.2012.0157
PMID:23610167
Evidence for conservation and sustainable use in a fragment of the Atlantic forest in southeastern Brazil by a traditional human group Christo AG, Guedes-Bruni RR, Sobrinho F, da Silva AG, Peixoto AL Springerplus 28-Sep-2012
PMCID:PMC3725884
doi:10.1186/2193-1801-1-21
PMID:23961351
A bioactive naringenin coumaroyl glucoside from Mabea fistulifera subsp. robusta. Garcez WS, Garcez FR, Pellicciari I, Hara SM, Ferreira FC, Nakasse LY, Siqueira JM Planta Med 01-Aug-1997
doi:10.1055/S-2006-957715
PMID:17252401

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 / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
Ethyl gallate 13250 Click to see CCOC(=O)C1=CC(=C(C(=C1)O)O)O 198.17 unknown https://doi.org/10.1055/S-2006-957715
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
isorhamnetin 3-O-glucoside 5318645 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 478.40 unknown via CMAUP database
Kaempferol-3-O-rutinoside 5318767 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O)O)O 594.50 unknown via CMAUP database
Trifolin 5282149 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
[(2R,3R,4S,5R,6S)-3,5-dihydroxy-6-[[(2S)-5-hydroxy-2-(4-hydroxyphenyl)-4-oxo-2,3-dihydrochromen-7-yl]oxy]-4-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxyoxan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate 95223116 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)OC3C(C(C(C(O3)COC(=O)C=CC4=CC=C(C=C4)O)O)OC(=O)C=CC5=CC=C(C=C5)O)O)C6=CC=C(C=C6)O 726.70 unknown https://doi.org/10.1055/S-2006-957715
[(2S,3R,4S,5R,6R)-3,5-dihydroxy-2-[[(2S)-5-hydroxy-2-(4-hydroxyphenyl)-4-oxo-2,3-dihydrochromen-7-yl]oxy]-6-(hydroxymethyl)oxan-4-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate 95223114 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)OC3C(C(C(C(O3)CO)O)OC(=O)C=CC4=CC=C(C=C4)O)O)C5=CC=C(C=C5)O 580.50 unknown https://doi.org/10.1055/S-2006-957715
[3,4,5-Trihydroxy-6-[[5-hydroxy-2-(4-hydroxyphenyl)-4-oxo-2,3-dihydrochromen-7-yl]oxy]oxan-2-yl]methyl 3-(4-hydroxyphenyl)prop-2-enoate 334350 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)OC3C(C(C(C(O3)COC(=O)C=CC4=CC=C(C=C4)O)O)O)O)C5=CC=C(C=C5)O 580.50 unknown https://doi.org/10.1055/S-2006-957715
[3,5-Dihydroxy-2-[[5-hydroxy-2-(4-hydroxyphenyl)-4-oxo-2,3-dihydrochromen-7-yl]oxy]-6-(hydroxymethyl)oxan-4-yl] 3-(4-hydroxyphenyl)prop-2-enoate 74819366 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)OC3C(C(C(C(O3)CO)O)OC(=O)C=CC4=CC=C(C=C4)O)O)C5=CC=C(C=C5)O 580.50 unknown https://doi.org/10.1055/S-2006-957715
[3,5-Dihydroxy-6-[[5-hydroxy-2-(4-hydroxyphenyl)-4-oxo-2,3-dihydrochromen-7-yl]oxy]-4-[3-(4-hydroxyphenyl)prop-2-enoyloxy]oxan-2-yl]methyl 3-(4-hydroxyphenyl)prop-2-enoate 74107713 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)OC3C(C(C(C(O3)COC(=O)C=CC4=CC=C(C=C4)O)O)OC(=O)C=CC5=CC=C(C=C5)O)O)C6=CC=C(C=C6)O 726.70 unknown https://doi.org/10.1055/S-2006-957715
4H-1-Benzopyran-4-one, 2,3-dihydro-5-hydroxy-2-(4-hydroxyphenyl)-7-[[6-O-[(2E)-3-(4-hydroxyphenyl)-1-oxo-2-propen-1-yl]-beta-D-glucopyranosyl]oxy]-, (2S)- 21630092 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)OC3C(C(C(C(O3)COC(=O)C=CC4=CC=C(C=C4)O)O)O)O)C5=CC=C(C=C5)O 580.50 unknown https://doi.org/10.1055/S-2006-957715
Isorhamnetin 3-glucoside-7-rhamnoside 72188972 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)CO)O)O)O)C5=CC(=C(C=C5)O)OC)O)O)O)O 624.50 unknown via CMAUP database
Robinin 5281693 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)OC5C(C(C(C(O5)C)O)O)O)C6=CC=C(C=C6)O)O)O)O)O)O)O 740.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(2R)-5-hydroxy-7-methoxy-2-(4-methoxyphenyl)-2,3-dihydrochromen-4-one 14057197 Click to see COC1=CC=C(C=C1)C2CC(=O)C3=C(C=C(C=C3O2)OC)O 300.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
Melilitocarpan B 23259931 Click to see COC1=C(C2=C(C=C1)C3C(CO2)C4=C(O3)C=C(C=C4)O)O 286.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 3-hydroxy,4-methoxyisoflavonoids
2H-1-Benzopyran-7-ol, 3,4-dihydro-3-(3-hydroxy-2,4-dimethoxyphenyl)-, (3R)- 13873811 Click to see COC1=C(C(=C(C=C1)C2CC3=C(C=C(C=C3)O)OC2)OC)O 302.32 unknown via CMAUP database
Calycosin 5280448 Click to see COC1=C(C=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O)O 284.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
2'-Hydroxybiochanin A 5282075 Click to see COC1=CC(=C(C=C1)C2=COC3=CC(=CC(=C3C2=O)O)O)O 300.26 unknown via CMAUP database
Biochanin A 5280373 Click to see COC1=CC=C(C=C1)C2=COC3=CC(=CC(=C3C2=O)O)O 284.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 7-O-methylated isoflavonoids / 7-O-methylisoflavones
4',7-Dimethoxyisoflavone 136419 Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)OC 282.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
1-(2,4-Dihydroxyphenyl)-3-(2,3-dimethoxyphenyl)prop-2-en-1-one 622927 Click to see COC1=CC=CC(=C1OC)C=CC(=O)C2=C(C=C(C=C2)O)O 300.30 unknown via CMAUP database
1-(2,4-Dihydroxyphenyl)-3-(3,4-dimethoxyphenyl)prop-2-en-1-one 165210 Click to see COC1=C(C=C(C=C1)C=CC(=O)C2=C(C=C(C=C2)O)O)OC 300.30 unknown via CMAUP database
2',4'-Dihydroxy-4-methoxychalcone 5711223 Click to see COC1=CC=C(C=C1)C=CC(=O)C2=C(C=C(C=C2)O)O 270.28 unknown via CMAUP database
GU17;ISL;Isoliquiritigen 425 Click to see C1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2)O)O)O 256.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 3-prenylated chalcones
1-[2,4-Dihydroxy-3-(3-methylbut-2-enyl)phenyl]-3-(4-hydroxyphenyl)prop-2-en-1-one 193568 Click to see CC(=CCC1=C(C=CC(=C1O)C(=O)C=CC2=CC=C(C=C2)O)O)C 324.40 unknown via CMAUP database

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