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Swartzia laevicarpa

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 UUID643fd8e60158a592227970
Scientific name Swartzia laevicarpa
Authority Amshoff
First published in Meded. Bot. Mus. Herb. Rijks Univ. Utrecht52: 37 (1939)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

No known synonyms.

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
  • Southern America
    • Brazil
      • Brazil North
    • Northern South America
      • Guyana
      • Suriname

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000182091
Tropicos 13001730
INPN 735461
KEW urn:lsid:ipni.org:names:246668-2
The Plant List ild-28188
Open Tree Of Life 91609
NCBI Taxonomy 450079
IPNI 246668-2
GBIF 5352099
EOL 642669
USDA GRIN 437177

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
Constituintes químicos de Tovomita brasiliensis () Raimundo Braz Filho, , Carlos A. S. Miranda, Otto R. Gottlieb, Mauro T. Magalhães, , , FapUNIFESP (SciELO) 29-Oct-2016
doi:10.1590/1809-43921982124801
Submerged in darkness: adaptations to prolonged submergence by woody species of the Amazonian floodplains Parolin P Ann Bot 10-Nov-2008
PMCID:PMC2707320
doi:10.1093/aob/mcn216
PMID:19001429
Pterocarpans from Swartzia laevicarpa Raimundo Braz Filho, Miguel P.L. De Moraes, Otto R. Gottlieb Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(80)83022-6

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
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
5-Hydroxy-7,8-dimethoxy-2-methylchromon 85529857 Click to see 236.22 unknown https://doi.org/10.1016/0031-9422(80)83022-6
> Organoheterocyclic compounds / Benzopyrans / 2-benzopyrans
(3S)-8-hydroxy-3,5-dimethyl-3,4-dihydroisochromen-1-one 130638185 Click to see 192.21 unknown https://doi.org/10.1016/0031-9422(80)83022-6
3,4-Dihydro-8-hydroxy-3,5-dimethylisocoumarin 10330203 Click to see CC1CC2=C(C=CC(=C2C(=O)O1)O)C 192.21 unknown https://doi.org/10.1590/1809-43921982124801
https://doi.org/10.1016/0031-9422(80)83022-6
> Phenylpropanoids and polyketides / Isocoumarins and derivatives
5-Chloro-8-hydroxy-6-methoxy-3-methyl-1H-2-benzopyran-1-one 5376985 Click to see 240.64 unknown https://doi.org/10.1016/0031-9422(80)83022-6
7-Chloro-8-hydroxy-6-methoxy-3-methylisocoumarin 91664839 Click to see 240.64 unknown https://doi.org/10.1590/1809-43921982124801
https://doi.org/10.1016/0031-9422(80)83022-6
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
(6aR,11aR)-3,4,9,10-tetramethoxy-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromen-8-ol 162852583 Click to see 360.40 unknown https://doi.org/10.1016/0031-9422(80)83022-6
(6aR,11aR)-3,4,9,10-tetramethoxy-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-2,8-diol 162982023 Click to see COC1=C(C=C2C3COC4=C(C(=C(C=C4C3OC2=C1OC)O)OC)OC)O 376.40 unknown https://doi.org/10.1016/0031-9422(80)83022-6
(6aR,11aR)-3,9-dimethoxy-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-2,8-diol 162871019 Click to see COC1=C(C=C2C3COC4=CC(=C(C=C4C3OC2=C1)O)OC)O 316.30 unknown https://doi.org/10.1016/0031-9422(80)83022-6
(6aR,11aR)-3,9,10-trimethoxy-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-2,8-diol 163034974 Click to see 346.30 unknown https://doi.org/10.1016/0031-9422(80)83022-6
2,8-Dihydroxy-3,4,9,10-tetramethoxypterocarpan 44257465 Click to see COC1=C(C=C2C3COC4=C(C(=C(C=C4C3OC2=C1OC)O)OC)OC)O 376.40 unknown https://doi.org/10.1016/0031-9422(80)83022-6
2,8-Dihydroxy-3,9-dimethoxypterocarpan 44257453 Click to see 316.30 unknown https://doi.org/10.1016/0031-9422(80)83022-6
2,8-Dihydroxy-3,9,10-trimethoxypterocarpan 44257455 Click to see 346.30 unknown https://doi.org/10.1016/0031-9422(80)83022-6
8-Hydroxy-3,4,9,10-tetramethoxypterocarpan 44257463 Click to see COC1=C(C2=C(C=C1)C3C(CO2)C4=CC(=C(C(=C4O3)OC)OC)O)OC 360.40 unknown https://doi.org/10.1016/0031-9422(80)83022-6

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