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Tovomita brevistaminea

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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 UUID643ff90dc9fa8323172670
Scientific name Tovomita brevistaminea
Authority Engl.
First published in Fl. Bras. 12(1): 446 (1888)

Description Top

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Synonyms Top

Scientific name Authority First published in
Tovomita triflora Huber Bol. Mus. Paraense Hist. Nat. Ethnogr. 3: 436 (1902)
Tovomita jenmanii Engl. Fl. Bras. 12(1): 447 (1888)

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
      • Brazil Northeast
    • Northern South America
      • French Guiana
      • Guyana
      • Suriname
      • Venezuela
    • Western South America
      • Colombia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000407097
Tropicos 7801007
INPN 733028
KEW urn:lsid:ipni.org:names:255606-2
The Plant List kew-2431710
Open Tree Of Life 6099549
NCBI Taxonomy 1937628
IUCN Red List 128036028
IPNI 255606-2
GBIF 3711807

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
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
Two New Xanthones from Calophyllum nodusum (Guttiferae) Nasir NM, Rahmani M, Shaari K, Cheng Lian Ee G, Go R, Kassim NK, Muhamad SN, Iskandar MJ Molecules 25-Oct-2011
PMCID:PMC6264213
doi:10.3390/molecules16118973
PMID:22027953
Cytotoxic constituents from the roots of Tovomita brevistaminea. Seo EK, Wall ME, Wani MC, Navarro H, Mukherjee R, Farnsworth NR, Kinghorn AD Phytochemistry 01-Oct-1999
doi:10.1016/S0031-9422(99)00274-5
PMID:10570828

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 / Benzophenones
[(2R)-6-hydroxy-2-(2-hydroxypropan-2-yl)-4-methoxy-5-[(2S)-5-methyl-2-prop-1-en-2-ylhex-5-enyl]-2,3-dihydro-1-benzofuran-7-yl]-(3-hydroxyphenyl)methanone 162990444 Click to see CC(=C)CCC(CC1=C(C2=C(C(=C1O)C(=O)C3=CC(=CC=C3)O)OC(C2)C(C)(C)O)OC)C(=C)C 480.60 unknown https://doi.org/10.1016/S0031-9422(99)00274-5
[(2S)-6-hydroxy-2-(2-hydroxypropan-2-yl)-4-methoxy-5-[(2R)-5-methyl-2-prop-1-en-2-ylhex-5-enyl]-2,3-dihydro-1-benzofuran-7-yl]-(3-hydroxyphenyl)methanone 162990443 Click to see CC(=C)CCC(CC1=C(C2=C(C(=C1O)C(=O)C3=CC(=CC=C3)O)OC(C2)C(C)(C)O)OC)C(=C)C 480.60 unknown https://doi.org/10.1016/S0031-9422(99)00274-5
[(3R)-3,7-dihydroxy-5-methoxy-2,2-dimethyl-6-[(2R)-5-methyl-2-prop-1-en-2-ylhex-5-enyl]-3,4-dihydrochromen-8-yl]-(3-hydroxyphenyl)methanone 163029123 Click to see CC(=C)CCC(CC1=C(C2=C(C(=C1O)C(=O)C3=CC(=CC=C3)O)OC(C(C2)O)(C)C)OC)C(=C)C 480.60 unknown https://doi.org/10.1016/S0031-9422(99)00274-5
[(3S)-3,7-dihydroxy-5-methoxy-2,2-dimethyl-6-[(2S)-5-methyl-2-prop-1-en-2-ylhex-5-enyl]-3,4-dihydrochromen-8-yl]-(3-hydroxyphenyl)methanone 163029124 Click to see CC(=C)CCC(CC1=C(C2=C(C(=C1O)C(=O)C3=CC(=CC=C3)O)OC(C(C2)O)(C)C)OC)C(=C)C 480.60 unknown https://doi.org/10.1016/S0031-9422(99)00274-5
[2,6-Dihydroxy-4-methoxy-3-(3-methyl-2-butenyl)-5-[5-methyl-2-(1-methylethenyl)-5-hexenyl]phenyl](3-hydroxyphenyl)methanone 100943937 Click to see CC(=CCC1=C(C(=C(C(=C1OC)CC(CCC(=C)C)C(=C)C)O)C(=O)C2=CC(=CC=C2)O)O)C 464.60 unknown https://doi.org/10.1016/S0031-9422(99)00274-5
[2,6-dihydroxy-4-methoxy-3-(3-methylbut-2-enyl)-5-[(2R)-5-methyl-2-prop-1-en-2-ylhex-5-enyl]phenyl]-(3-hydroxyphenyl)methanone 162874468 Click to see CC(=CCC1=C(C(=C(C(=C1OC)CC(CCC(=C)C)C(=C)C)O)C(=O)C2=CC(=CC=C2)O)O)C 464.60 unknown https://doi.org/10.1016/S0031-9422(99)00274-5
[2,6-dihydroxy-4-methoxy-3-(3-methylbut-2-enyl)-5-[(2S)-5-methyl-2-prop-1-en-2-ylhex-5-enyl]phenyl]-(3-hydroxyphenyl)methanone 162874469 Click to see CC(=CCC1=C(C(=C(C(=C1OC)CC(CCC(=C)C)C(=C)C)O)C(=O)C2=CC(=CC=C2)O)O)C 464.60 unknown https://doi.org/10.1016/S0031-9422(99)00274-5
[3,7-Dihydroxy-5-methoxy-2,2-dimethyl-6-(5-methyl-2-prop-1-en-2-ylhex-5-enyl)-3,4-dihydrochromen-8-yl]-(3-hydroxyphenyl)methanone 100943938 Click to see CC(=C)CCC(CC1=C(C2=C(C(=C1O)C(=O)C3=CC(=CC=C3)O)OC(C(C2)O)(C)C)OC)C(=C)C 480.60 unknown https://doi.org/10.1016/S0031-9422(99)00274-5
[6-Hydroxy-2-(2-hydroxypropan-2-yl)-4-methoxy-5-(5-methyl-2-prop-1-en-2-ylhex-5-enyl)-2,3-dihydro-1-benzofuran-7-yl]-(3-hydroxyphenyl)methanone 100943936 Click to see CC(=C)CCC(CC1=C(C2=C(C(=C1O)C(=O)C3=CC(=CC=C3)O)OC(C2)C(C)(C)O)OC)C(=C)C 480.60 unknown https://doi.org/10.1016/S0031-9422(99)00274-5
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
9-Hydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 2371 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown https://doi.org/10.1016/S0031-9422(99)00274-5
Betulinic Acid 64971 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown https://doi.org/10.1016/S0031-9422(99)00274-5
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 4-prenylated xanthones
Manglexanthone 10001484 Click to see CC(=CCC1=C2C(=CC(=C1OC)O)C(=O)C3=C(C4=C(C=C3O2)OC(C=C4)(C)C)O)C 408.40 unknown https://doi.org/10.1016/S0031-9422(99)00274-5
Trapezifolixanthone 188341 Click to see CC(=CCC1=C2C(=C(C3=C1OC4=C(C3=O)C=CC=C4O)O)C=CC(O2)(C)C)C 378.40 unknown https://doi.org/10.1016/S0031-9422(99)00274-5

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