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Bouchea fluminensis

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID68f8f418915ea529414143
Scientific name Bouchea fluminensis
Authority (Vell.) Moldenke
First published in Repert. Spec. Nov. Regni Veg. 48: 25 (1940)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Verbena fluminensis Vell. Fl. Flumin. 1: t. 38, 17 (1829)
Verbena pseudogervao A.St.-Hil. Pl. Usuel. Bras. : t. 40 (1825)
Bouchea fluminensis f. albiflora Moldenke Phytologia 8: 273 (1962)
Bouchea fluminensis var. pilosa Moldenke Phytologia 2: 408 (1948)
Bouchea cipoensis Moldenke Phytologia 3: 261 (1950)
Bouchea pseudogervao (A.St.-Hil.) Cham. Linnaea 7: 252 (1832)

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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Distribution (via POWO/KEW) Top

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Links to other databases Top

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Database ID/link to page
Tropicos 33700101
KEW urn:lsid:ipni.org:names:1200796-2
The Plant List kew-23550
IPNI 1200796-2
iNaturalist 936072
GBIF 4083862
Tropicos 50215577
KEW urn:lsid:ipni.org:names:35421-2
The Plant List kew-23511
Open Tree Of Life 6088982
IPNI 35421-2
iNaturalist 936088
GBIF 4084311
Open Tree Of Life 606453
World Flora Online wfo-0000365375
KEW urn:lsid:ipni.org:names:861178-1
NCBI Taxonomy 42207
IPNI 861178-1
iNaturalist 715207
GBIF 7297089

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
Brazilian medicinal plants with corroborated anti-inflammatory activities: a review Ribeiro VP, Arruda C, Abd El-Salam M, Bastos JK Pharm Biol 12-Apr-2018
PMCID:PMC6130656
doi:10.1080/13880209.2018.1454480
PMID:29648503
Impact of an Educational Hands-on Project on the Antimicrobial, Antitumor and Anti-Inflammatory Properties of Plants on Portuguese Students’ Awareness, Knowledge, and Competences Azevedo MM, Pinheiro C, Dias AC, Pinto-Ribeiro F, Baltazar F Int J Environ Res Public Health 23-Feb-2015
PMCID:PMC4377910
doi:10.3390/ijerph120302437
PMID:25711362
Anti-Inflammatory Iridoids of Botanical Origin Viljoen A, Mncwangi N, Vermaak I Curr Med Chem 01-May-2012
PMCID:PMC3873812
doi:10.2174/092986712800229005
PMID:22414102
Database Survey of Anti-Inflammatory Plants in South America: A Review de Morais Lima GR, de Albuquerque Montenegro C, de Almeida CL, de Athayde-Filho PF, Barbosa-Filho JM, Batista LM Int J Mol Sci 21-Apr-2011
PMCID:PMC3127143
doi:10.3390/ijms12042692
PMID:21731467
Anti-inflammatory activity and lipid peroxidation inhibition of iridoid lamiide isolated from Bouchea fluminensis (Vell.) Mold. (Verbenaceae). Delaporte RH, Sánchez GM, Cuellar AC, Giuliani A, Palazzo de Mello JC J Ethnopharmacol 01-Oct-2002
doi:10.1016/S0378-8741(02)00181-2
PMID:12241987
Iridoid glucosides from Bouchea fluminensis Ivânia T.Albrecht Schuquel, Angela Malheiros, Maria Helena Sarragiotto, Gentil José Vidotti Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(98)00355-0

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 / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
Durantoside II 6443018 Click to see 582.50 unknown https://doi.org/10.1016/S0031-9422(98)00355-0
Lamiide 443327 Click to see 422.40 unknown https://doi.org/10.1016/S0378-8741(02)00181-2
https://doi.org/10.1016/S0031-9422(98)00355-0
Lamiidoside 23815404 Click to see 568.50 unknown https://doi.org/10.1016/S0031-9422(98)00355-0
methyl (1R,4aS,6R,7R,7aR)-4a,7-dihydroxy-6-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy-7-methyl-1-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,5,6,7a-tetrahydrocyclopenta[c]pyran-4-carboxylate 162910485 Click to see 568.50 unknown https://doi.org/10.1016/S0031-9422(98)00355-0
methyl (1R,4aS,6R,7S,7aR)-4a,7-dihydroxy-6-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy-7-methyl-1-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,5,6,7a-tetrahydrocyclopenta[c]pyran-4-carboxylate 133556257 Click to see CC1(C(CC2(C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O)OC(=O)C=CC4=CC=C(C=C4)O)O 568.50 unknown https://doi.org/10.1016/S0031-9422(98)00355-0
methyl (1S,4aR,6S,7R,7aS)-4a,6,7-trihydroxy-7-methyl-1-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,5,6,7a-tetrahydrocyclopenta[c]pyran-4-carboxylate 163063657 Click to see CC1(C(CC2(C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O)O)O 422.40 unknown https://doi.org/10.1016/S0031-9422(98)00355-0
methyl (1S,4aR,6S,7R,7aS)-4a,7-dihydroxy-6-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy-7-methyl-1-[(2R,3S,4R,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,5,6,7a-tetrahydrocyclopenta[c]pyran-4-carboxylate 162910487 Click to see CC1(C(CC2(C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O)OC(=O)C=CC4=CC=C(C=C4)O)O 568.50 unknown https://doi.org/10.1016/S0031-9422(98)00355-0
methyl (1S,4aR,6S,7R,7aS)-4a,7-dihydroxy-6-[(E)-3-(4-methoxyphenyl)prop-2-enoyl]oxy-7-methyl-1-[(2S,3S,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,5,6,7a-tetrahydrocyclopenta[c]pyran-4-carboxylate 154496503 Click to see CC1(C(CC2(C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O)OC(=O)C=CC4=CC=C(C=C4)OC)O 582.50 unknown https://doi.org/10.1016/S0031-9422(98)00355-0
methyl (1S,4aR,6S,7R,7aS)-4a,7-dihydroxy-6-[(Z)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy-7-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,5,6,7a-tetrahydrocyclopenta[c]pyran-4-carboxylate 100955849 Click to see CC1(C(CC2(C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O)OC(=O)C=CC4=CC=C(C=C4)O)O 568.50 unknown https://doi.org/10.1016/S0031-9422(98)00355-0
methyl (1S,4aR,6S,7R,7aS)-4a,7-dihydroxy-6-[(Z)-3-(4-methoxyphenyl)prop-2-enoyl]oxy-7-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,5,6,7a-tetrahydrocyclopenta[c]pyran-4-carboxylate 100955850 Click to see 582.50 unknown https://doi.org/10.1016/S0031-9422(98)00355-0
Methyl 4a,7-dihydroxy-6-[3-(4-hydroxyphenyl)prop-2-enoyloxy]-7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,5,6,7a-tetrahydrocyclopenta[c]pyran-4-carboxylate 74124637 Click to see 568.50 unknown https://doi.org/10.1016/S0031-9422(98)00355-0
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(3S,3aR,4S,6E,10Z,11aR)-4-hydroxy-3-methyl-2-oxo-10-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-3a,4,5,8,9,11a-hexahydro-3H-cyclodeca[b]furan-6-carbaldehyde 162922734 Click to see CC1C2C(CC(=CCCC(=CC2OC1=O)COC3C(C(C(C(O3)CO)O)O)O)C=O)O 442.50 unknown https://doi.org/10.1016/S0031-9422(98)00355-0

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