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Sinningia aggregata

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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 UUID6440468e719bf598431409
Scientific name Sinningia aggregata
Authority (Ker Gawl.) Wiehler
First published in Selbyana 1: 32 (1975)

Description Top

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Synonyms Top

Scientific name Authority First published in
Styrosinia coccinea Raf. Fl. Tellur. 2: 96 (1837)
Corytholoma aggregatum Decne. Rev. Hort. (Paris) , sér. 3, 2: 467 (1848)
Corytholoma pendulinum Decne. Rev. Hort. (Paris) , sér. 3, 2: 467 (1848)
Corytholoma uleanum Fritsch Beibl. Bot. Jahrb. Syst. 65: 22 (1900)
Gesneria aggregata Ker Gawl. Bot. Reg. 4: t. 329 (1818)
Gesneria bulbosa var. lateritia (Lindl.) Klotzsch Verh. Vereins Beförd. Gartenbaues Königl. Preuss. Staaten 16: 160 (1842)
Gesneria lateritia Lindl. Edwards's Bot. Reg. 23: t. 1950 (1837)
Gesneria macrantha Lem. Hort. Universel 6: 127 (1844)
Gesneria pendulina Lindl. Bot. Reg. 12: t. 1032 (1827)
Gesneria selloi hort. ex G.Don Hort. Brit. , ed. 3: 527 (1839)
Gesneria tenella hort. ex Hanst. Fl. Bras. 8(1): 366 (1864)
Gesneria trifoliata Martens Linnaea 18: 165 (1844)
Rechsteineria uleana Fritsch Bot. Jahrb. Syst. 50: 436 (1913)
Rechsteineria aggregata Kuntze Revis. Gen. Pl. 2: 474 (1891)
Rechsteineria pendulina Kuntze Revis. Gen. Pl. 2: 474 (1891)

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 South
      • Brazil Southeast
      • Brazil West-central
    • Southern South America
      • Paraguay

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001064923
Tropicos 14001548
KEW urn:lsid:ipni.org:names:236680-2
The Plant List tro-14001548
Open Tree Of Life 340069
Observations.org 445413
NCBI Taxonomy 188998
IPNI 236680-2
iNaturalist 970753
GBIF 3818724
EOL 5644484
Elurikkus 418519
USDA GRIN 451033

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
Correction: Chen et al. Cytotoxic, Antibacterial, and Antioxidant Activities of the Leaf Extract of Sinningia bullata. Plants 2023, 12, 859 Chen PJ, Lin ES, Su HH, Huang CY Plants (Basel) 13-Oct-2023
PMCID:PMC10609666
doi:10.3390/plants12203557
PMID:37896126
Nectar Guide Patterns on Developmentally Homologous Regions of the Subtribe Ligeriinae (Gesneriaceae) Hsu HC, Kuo YF Front Plant Sci 12-Apr-2021
PMCID:PMC8072120
doi:10.3389/fpls.2021.650836
PMID:33912210
3D revelation of phenotypic variation, evolutionary allometry, and ancestral states of corolla shape: a case study of clade Corytholoma (subtribe Ligeriinae, family Gesneriaceae) Hsu HC, Chou WC, Kuo YF Gigascience 22-Jan-2020
PMCID:PMC6974915
doi:10.1093/gigascience/giz155
PMID:31967295
Antinociceptive Activity of the Ethanolic Extract, Fractions, and Aggregatin D Isolated from Sinningia aggregata Tubers Souza GV, Simas AS, Bastos-Pereira AL, Frois GR, Ribas JL, Verdan MH, Kassuya CA, Stefanello ME, Zampronio AR PLoS One 26-Feb-2015
PMCID:PMC4342217
doi:10.1371/journal.pone.0117501
PMID:25719394
Evaluation of the anti-mycobacterium tuberculosis activity and in vivo acute toxicity of Annona sylvatic Araujo RC, Neves FA, Formagio AS, Kassuya CA, Stefanello ME, Souza VV, Pavan FR, Croda J BMC Complement Altern Med 28-Jun-2014
PMCID:PMC4082671
doi:10.1186/1472-6882-14-209
PMID:24974069
Lactones and quinones from the tubers of Sinningia aggregata. Verdan MH, Barison A, de Sá EL, Salvador MJ, Poliquesi CB, Eberlin MN, Stefanello ME J Nat Prod 27-Aug-2010
doi:10.1021/NP1002466
PMID:20684540

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 / Anthracenes / Anthraquinones
2-Methoxy-7-methylanthracene-9,10-dione 12963549 Click to see CC1=CC2=C(C=C1)C(=O)C3=C(C2=O)C=C(C=C3)OC 252.26 unknown https://doi.org/10.1021/NP1002466
2-Methylanthraquinone 6773 Click to see CC1=CC2=C(C=C1)C(=O)C3=CC=CC=C3C2=O 222.24 unknown https://doi.org/10.1021/NP1002466
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
7-Hydroxy-2-methylanthraquinone 150722 Click to see CC1=CC2=C(C=C1)C(=O)C3=C(C2=O)C=C(C=C3)O 238.24 unknown https://doi.org/10.1021/NP1002466
> Benzenoids / Naphthalenes
(3R,11bS)-3,11b-dihydroxy-3-methyl-6-(3-methylbut-2-enyl)-2H-benzo[i][1]benzoxepin-7-one 46919399 Click to see CC(=CCC1=C2C=CC(COC2(C3=CC=CC=C3C1=O)O)(C)O)C 326.40 unknown https://doi.org/10.1021/NP1002466
3,11b-dihydroxy-3-methyl-6-(3-methylbut-2-enyl)-2H-benzo[i][1]benzoxepin-7-one 75254441 Click to see CC(=CCC1=C2C=CC(COC2(C3=CC=CC=C3C1=O)O)(C)O)C 326.40 unknown https://doi.org/10.1021/NP1002466
> Organoheterocyclic compounds / Benzoxepines
(3S)-7-methoxy-3-methyl-3H-benzo[i][1]benzoxepin-2-one 46919397 Click to see CC1C=CC2=C(C3=CC=CC=C3C(=C2)OC)OC1=O 254.28 unknown https://doi.org/10.1021/NP1002466
(3S)-7,9-dimethoxy-3-methyl-3H-benzo[i][1]benzoxepin-2-one 46919398 Click to see CC1C=CC2=CC(=C3C=C(C=CC3=C2OC1=O)OC)OC 284.31 unknown https://doi.org/10.1021/NP1002466
(3S)-9-hydroxy-7-methoxy-3-methyl-3H-benzo[i][1]benzoxepin-2-one 46919396 Click to see CC1C=CC2=CC(=C3C=C(C=CC3=C2OC1=O)O)OC 270.28 unknown https://doi.org/10.1021/NP1002466
7-methoxy-3-methyl-3H-benzo[i][1]benzoxepin-2-one 75254439 Click to see CC1C=CC2=C(C3=CC=CC=C3C(=C2)OC)OC1=O 254.28 unknown https://doi.org/10.1021/NP1002466
7,9-dimethoxy-3-methyl-3H-benzo[i][1]benzoxepin-2-one 75254440 Click to see CC1C=CC2=CC(=C3C=C(C=CC3=C2OC1=O)OC)OC 284.31 unknown https://doi.org/10.1021/NP1002466
9-hydroxy-7-methoxy-3-methyl-3H-benzo[i][1]benzoxepin-2-one 75254438 Click to see CC1C=CC2=CC(=C3C=C(C=CC3=C2OC1=O)O)OC 270.28 unknown https://doi.org/10.1021/NP1002466

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