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Bagassa guianensis

Bagassa guianensis - 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 UUID64400c0917533091124001
Scientific name Bagassa guianensis
Authority Aubl.
First published in Hist. Pl. Guiane , Suppl.: 15 (1775)

Description Top

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Synonyms Top

Scientific name Authority First published in
Bagassa sagotiana Bureau ex Benth. & Hook.f. Gen. Pl. 3: 362 (1880)
Bagassa tiliifolia Benoist Arch. Bot. Mém. 5(1): 31 (1933)
Piper tiliifolium Desv. ex Ham. Prodr. Pl. Ind. Occid. : 4 (1825)
Laurea tiliifolia Gaudich. Voy. Uranie : 513 (1830)

Common names Top

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Language Common/alternative name
Arabic باجاسا غويانية
Russian Багасса
Chinese 乳桑

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

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000558480
Tropicos 50086767
INPN 734292
KEW urn:lsid:ipni.org:names:850483-1
The Plant List kew-2667845
Open Tree Of Life 192180
NCBI Taxonomy 241862
IUCN Red List 61809223
IPNI 850483-1
iNaturalist 1232538
GBIF 3763926
Freebase /m/06w49zm
EPPO BGSGU
USDA GRIN 435179

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
Coupling remote sensing and eDNA to monitor environmental impact: A pilot to quantify the environmental benefits of sustainable agriculture in the Brazilian Amazon Dyson K, Nicolau AP, Tenneson K, Francesconi W, Daniels A, Andrich G, Caldas B, Castaño S, de Campos N, Dilger J, Guidotti V, Jaques I, McCullough IM, McDevitt AD, Molina L, Nekorchuk DM, Newberry T, Pereira CL, Perez J, Richards-Dimitrie T, Rivera O, Rodriguez B, Sales N, Tello J, Wespestad C, Zutta B, Saah D PLoS One 14-Feb-2024
PMCID:PMC10866516
doi:10.1371/journal.pone.0289437
PMID:38354171
Critical Review on the Use of Extractives of Naturally Durable Woods as Natural Wood Protectants Kirker GT, Hassan B, Mankowski ME, Eller FJ Insects 18-Jan-2024
PMCID:PMC10816604
doi:10.3390/insects15010069
PMID:38249075
The links between wood traits and species demography change during tree development in a lowland tropical rainforest González-Melo A, Posada JM, Beauchêne J, Lehnebach R, Levionnois S, Derroire G, Clair B AoB Plants 27-Dec-2023
PMCID:PMC10799319
doi:10.1093/aobpla/plad090
PMID:38249523
Comparative Histology and Histochemistry of the Parotid Gland and Mandibular Gland in the Lowland Tapir (Tapirus terrestris Perissodactyla) and Aardvark (Orycteropus afer Tubulidentata) Klećkowska-Nawrot J, Barszcz K, Miniajluk JP, Melnyk O, Goździewska-Harłajczuk K Animals (Basel) 18-May-2023
PMCID:PMC10215616
doi:10.3390/ani13101684
PMID:37238113
Structural Characteristics of Reaction Tissue in Plants Liu L, Luan Y, Fang C, Hu J, Chang S, Fei B Plants (Basel) 20-Apr-2023
PMCID:PMC10146549
doi:10.3390/plants12081705
PMID:37111927
Rethinking the nature of intraspecific variability and its consequences on species coexistence Girard‐Tercieux C, Maréchaux I, Clark AT, Clark JS, Courbaud B, Fortunel C, Guillemot J, Künstler G, le Maire G, Pélissier R, Rüger N, Vieilledent G Ecol Evol 07-Mar-2023
PMCID:PMC9992775
doi:10.1002/ece3.9860
PMID:36911314
Antifungal Agents in Wood Protection—A Review Woźniak M Molecules 27-Sep-2022
PMCID:PMC9570806
doi:10.3390/molecules27196392
PMID:36234929
Tatajuba: exploring the distribution of homopolymer tracts de Oliveira Martins L, Bloomfield S, Stoakes E, Grant AJ, Page AJ, Mather AE NAR Genom Bioinform 02-Feb-2022
PMCID:PMC8808543
doi:10.1093/nargab/lqac003
PMID:35118377
Oxyresveratrol: Sources, Productions, Biological Activities, Pharmacokinetics, and Delivery Systems Likhitwitayawuid K Molecules 11-Jul-2021
PMCID:PMC8307110
doi:10.3390/molecules26144212
PMID:34299485
Edible Fruit Plant Species in the Amazon Forest Rely Mostly on Bees and Beetles as Pollinators Paz FS, Pinto CE, de Brito RM, Imperatriz-Fonseca VL, Giannini TC J Econ Entomol 13-Jan-2021
PMCID:PMC8042744
doi:10.1093/jee/toaa284
PMID:33440000
Microstructure of the Surface of the Tongue and Histochemical Study of the Lingual Glands of the Lowland Tapir (Tapirus terrestris Linnaeus, 1758) (Perissodactyla: Tapiridae) Goździewska-Harłajczuk K, Hamouzová P, Klećkowska-Nawrot J, Barszcz K, Čížek P Animals (Basel) 04-Dec-2020
PMCID:PMC7762086
doi:10.3390/ani10122297
PMID:33291801
Paralogs and Off-Target Sequences Improve Phylogenetic Resolution in a Densely Sampled Study of the Breadfruit Genus (Artocarpus, Moraceae) Gardner EM, Johnson MG, Pereira JT, Puad AS, Arifiani D, Sahromi, Wickett NJ, Zerega NJ Syst Biol 24-Sep-2020
PMCID:PMC8048387
doi:10.1093/sysbio/syaa073
PMID:32970819
A reverse chemical ecology approach to explore wood natural durability Thomas P, Guillaume S, Nadine A, Jacques B, Philippe G, Stéphane D, Rodnay S, Mélanie M, Eric G Microb Biotechnol 25-Mar-2020
PMCID:PMC7415366
doi:10.1111/1751-7915.13540
PMID:32212309
Palikur traditional roundwood construction in eastern French Guiana: ethnobotanical and cultural perspectives Ogeron C, Odonne G, Cristinoi A, Engel J, Grenand P, Beauchêne J, Clair B, Davy D J Ethnobiol Ethnomed 24-Apr-2018
PMCID:PMC5916587
doi:10.1186/s13002-018-0226-7
PMID:29690891
Disturbance Regimes Drive The Diversity of Regional Floristic Pools Across Guianan Rainforest Landscapes Guitet S, Sabatier D, Brunaux O, Couteron P, Denis T, Freycon V, Gonzalez S, Hérault B, Jaouen G, Molino JF, Pélissier R, Richard-Hansen C, Vincent G Sci Rep 01-Mar-2018
PMCID:PMC5832822
doi:10.1038/s41598-018-22209-9
PMID:29497098

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 / Phenols / Benzenediols / Resorcinols
Resorcinol 5054 Click to see C1=CC(=CC(=C1)O)O 110.11 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.06.020
> Lignans, neolignans and related compounds / Aryltetralin lignans
(6S,7R,8R)-6,8-bis(2,4-dihydroxyphenyl)-7-(3,5-dihydroxyphenyl)-5,6,7,8-tetrahydronaphthalene-1,3-diol 102048881 Click to see C1C(C(C(C2=C1C=C(C=C2O)O)C3=C(C=C(C=C3)O)O)C4=CC(=CC(=C4)O)O)C5=C(C=C(C=C5)O)O 488.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.06.020
Alboctalol 10696347 Click to see C1C(C(C(C2=C1C=C(C=C2O)O)C3=C(C=C(C=C3)O)O)C4=CC(=CC(=C4)O)O)C5=C(C=C(C=C5)O)O 488.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.06.020
CID 85235974 85235974 Click to see C1C(C(C(C2=C1C=C(C=C2O)O)C3=C(C=C(C=C3)O)O)C4=CC(=CC(=C4)O)O)C5=C(C=C(C=C5)O)O 488.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.06.020
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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/J.PHYTOCHEM.2010.06.020
Beta-Sitosterol 222284 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/J.PHYTOCHEM.2010.06.020
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(-)-Moracin P 25208124 Click to see CC1(C(CC2=C(O1)C=C3C(=C2)C=C(O3)C4=CC(=CC(=C4)O)O)O)C 326.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.06.020
5-(6-Methoxy-1-benzofuran-2-yl)benzene-1,3-diol 102048877 Click to see COC1=CC2=C(C=C1)C=C(O2)C3=CC(=CC(=C3)O)O 256.25 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.06.020
5-[5-(3-Hydroxy-3-methylbutyl)-6-methoxy-1-benzofuran-2-yl]benzene-1,3-diol 102048879 Click to see CC(C)(CCC1=C(C=C2C(=C1)C=C(O2)C3=CC(=CC(=C3)O)O)OC)O 342.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.06.020
5-[6-Methoxy-5-(3-methylbut-2-enyl)-1-benzofuran-2-yl]benzene-1,3-diol 102048878 Click to see CC(=CCC1=C(C=C2C(=C1)C=C(O2)C3=CC(=CC(=C3)O)O)OC)C 324.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.06.020
Moracin M 185848 Click to see C1=CC2=C(C=C1O)OC(=C2)C3=CC(=CC(=C3)O)O 242.23 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.06.020
moracin N 641376 Click to see CC(=CCC1=C(C=C2C(=C1)C=C(O2)C3=CC(=CC(=C3)O)O)O)C 310.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.06.020
Moracin P 14539884 Click to see CC1(C(CC2=C(O1)C=C3C(=C2)C=C(O3)C4=CC(=CC(=C4)O)O)O)C 326.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.06.020
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
4-[(1S)-1-(2,4-dihydroxyphenyl)-2-(3,5-dihydroxyphenyl)ethyl]-6-[(E)-2-(3,5-dihydroxyphenyl)ethenyl]benzene-1,3-diol 154496189 Click to see C1=CC(=C(C=C1O)O)C(CC2=CC(=CC(=C2)O)O)C3=C(C=C(C(=C3)C=CC4=CC(=CC(=C4)O)O)O)O 488.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.06.020
4-[1-(2,4-Dihydroxyphenyl)-2-(3,5-dihydroxyphenyl)ethyl]-6-[2-(3,5-dihydroxyphenyl)ethenyl]benzene-1,3-diol 85399807 Click to see C1=CC(=C(C=C1O)O)C(CC2=CC(=CC(=C2)O)O)C3=C(C=C(C(=C3)C=CC4=CC(=CC(=C4)O)O)O)O 488.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.06.020
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2S)-5,7,2',4'-Tetrahydroxyflavanone 10356745 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=C(C=C(C=C3)O)O 288.25 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.06.020
Steppogenin 21596130 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=C(C=C(C=C3)O)O 288.25 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.06.020
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
2-(2,4-Dihydroxyphenyl)-3,5,7-Trihydroxy-2,3-Dihydrochromen-4-One 362637 Click to see C1=CC(=C(C=C1O)O)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O 304.25 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.06.020
3,5,7-Trihydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one 662 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 288.25 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.06.020
Aromadendrin 122850 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 288.25 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.06.020
Dihydromorin 5458714 Click to see C1=CC(=C(C=C1O)O)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O 304.25 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.06.020
> Phenylpropanoids and polyketides / Stilbenes
1,3-Benzenediol, 5-[(1Z)-2-(4-hydroxyphenyl)ethenyl]- 5056 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)O)O)O 228.24 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.06.020
2-(3-hydroxy-3-methylbutyl)-5-[(E)-2-(4-hydroxyphenyl)ethenyl]benzene-1,3-diol 102048880 Click to see CC(C)(CCC1=C(C=C(C=C1O)C=CC2=CC=C(C=C2)O)O)O 314.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.06.020
2-(3-Hydroxy-3-methylbutyl)-5-[2-(4-hydroxyphenyl)ethenyl]benzene-1,3-diol 162955037 Click to see CC(C)(CCC1=C(C=C(C=C1O)C=CC2=CC=C(C=C2)O)O)O 314.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.06.020
4-Prenylresveratrol 5281725 Click to see CC(=CCC1=C(C=C(C=C1O)C=CC2=CC=C(C=C2)O)O)C 296.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.06.020
5-[2-(4-Hydroxyphenyl)ethenyl]-2-(3-methylbut-2-enyl)benzene-1,3-diol 442718 Click to see CC(=CCC1=C(C=C(C=C1O)C=CC2=CC=C(C=C2)O)O)C 296.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.06.020
CID 73197 73197 Click to see C1=CC(=C(C=C1O)O)C=CC2=CC(=CC(=C2)O)O 244.24 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.06.020
Oxyresveratrol 5281717 Click to see C1=CC(=C(C=C1O)O)C=CC2=CC(=CC(=C2)O)O 244.24 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.06.020
Resveratrol 445154 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)O)O)O 228.24 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.06.020

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