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Barbacenia flava

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 UUID6440253c890a6516691710
Scientific name Barbacenia flava
Authority Mart. ex Steud.
First published in Syst. Veg., ed. 15 bis 7: 286 (1829)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Barbacenia bishopii L.B.Sm. Bradea 4: 157 (1985)
Barbacenia sellowii Goethart & Henrard Blumea 2: 359 (1937)
Barbacenia flava var. minor L.B.Sm. Contr. U.S. Natl. Herb. 35: 279 (1962)

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000761157
Tropicos 33600022
KEW urn:lsid:ipni.org:names:63160-1
The Plant List kew-300163
Open Tree Of Life 575233
NCBI Taxonomy 1051457
IPNI 63160-1
iNaturalist 570465
GBIF 2863857
EOL 1086049
CMAUP NPO11441

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
Accelerated diversification and functional trait evolution in Velloziaceae reveal new insights into the origins of the campos rupestres’ exceptional floristic richness Alcantara S, Ree RH, Mello-Silva R Ann Bot 23-May-2018
PMCID:PMC6025242
doi:10.1093/aob/mcy063
PMID:29800276
Evaluation of the Effects of Some Brazilian Medicinal Plants on the Production of TNF-α and CCL2 by THP-1 Cells Gusman GS, Campana PR, Castro LC, Castilho RO, Teixeira MM, Braga FC Evid Based Complement Alternat Med 23-Mar-2015
PMCID:PMC4386292
doi:10.1155/2015/497123
PMID:25878716
Five vicarious genera from Gondwana: the Velloziaceae as shown by molecules and morphology Mello-Silva R, Santos DY, Salatino ML, Motta LB, Cattai MB, Sasaki D, Lovo J, Pita PB, Rocini C, Rodrigues CD, Zarrei M, Chase MW Ann Bot 01-Jan-2011
PMCID:PMC3119618
doi:10.1093/aob/mcr107
PMID:21693665
Barbacenic acid, a bisnorditerpene with a novel skeleton from Barcacenia flava Angelo C. Pinto, Maria do Carmo Frechiani, Bernard Tinant, Jean-Paul Declercq, Maurice Van Meerssche Royal Society of Chemistry (RSC) 30-Mar-2004
doi:10.1039/C39850000446
Bisnorditerpenes with a barbacenane skeleton from Barbacenia flava Angelo C. Pinto, Maria Do Carmo Frechiani, Anibal L. Pereira Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(88)83044-9

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 / Fatty Acyls / Eicosanoids / Prostaglandins and related compounds
2-(3a-hydroxy-6,9a,9b-trimethyl-3,7-dioxo-2,4,5,5a,8,9-hexahydro-1H-cyclopenta[a]naphthalen-6-yl)acetic acid 14191489 Click to see CC12CCC(=O)C(C1CCC3(C2(CCC3=O)C)O)(C)CC(=O)O 322.40 unknown https://doi.org/10.1016/0031-9422(88)83044-9
2-(6,9a,9b-Trimethyl-3,7-dioxo-1,2,3a,4,5,5a,8,9-octahydrocyclopenta[a]naphthalen-6-yl)acetic acid 14191486 Click to see 306.40 unknown https://doi.org/10.1016/0031-9422(88)83044-9
2-[(3aR,5aS,6R,9aR,9bR)-6,9a,9b-trimethyl-3,7-dioxo-1,2,3a,4,5,5a,8,9-octahydrocyclopenta[a]naphthalen-6-yl]acetic acid 163042606 Click to see 306.40 unknown https://doi.org/10.1016/0031-9422(88)83044-9
Barbacenic acid 11151421 Click to see 322.40 unknown https://doi.org/10.1039/C39850000446
https://doi.org/10.1016/0031-9422(88)83044-9
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Carbocyclic fatty acids
3-[(1S,4aS,5R,8aR)-5-(carboxymethyl)-1,5,8a-trimethyl-2,6-dioxo-4,4a,7,8-tetrahydro-3H-naphthalen-1-yl]propanoic acid 14191494 Click to see CC12CCC(=O)C(C1CCC(=O)C2(C)CCC(=O)O)(C)CC(=O)O 338.40 unknown https://doi.org/10.1016/0031-9422(88)83044-9
3-[5-(carboxymethyl)-1,5,8a-trimethyl-2,6-dioxo-4,4a,7,8-tetrahydro-3H-naphthalen-1-yl]propanoic acid 14191493 Click to see CC12CCC(=O)C(C1CCC(=O)C2(C)CCC(=O)O)(C)CC(=O)O 338.40 unknown https://doi.org/10.1016/0031-9422(88)83044-9
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
Phytol 5280435 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Alpha-Amyrin 73170 Click to see 426.70 unknown via CMAUP database
Pomolic Acid 382831 Click to see 472.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
Isoorientin 114776 Click to see 448.40 unknown via CMAUP database
Isovitexin 162350 Click to see 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Orientin 5281675 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O)O 448.40 unknown via CMAUP database

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