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Rauia resinosa

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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 UUID64404d8586196243669718
Scientific name Rauia resinosa
Authority Nees & Mart.
First published in Nova Acta Phys.-Med. Acad. Caes. Leop.-Carol. Nat. Cur. 11: 169 (1823)

Description Top

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Synonyms Top

Scientific name Authority First published in
Angostura resinosa (Nees & Mart.) Gereau Candollea 45: 368 (1990)
Bonplandia resinosa Spreng. Syst. Veg., ed. 16 [Sprengel] 1: 780. 1824 [dated 1825; publ. in late 1824]
Esenbeckia lucida Rusby Bull. New York Bot. Gard. 8: 98 (1912)
Galipea lucida (Rusby) Kaastra Acta Bot. Neerl. 26: 487 (1977)
Galipea resinosa St.Hil. ex DC. Prodr. 1: 731 (1824)

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
      • Brazil Southeast
    • Western South America
      • Bolivia
      • Peru

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001132931
Tropicos 28100611
INPN 1013507
KEW urn:lsid:ipni.org:names:774999-1
The Plant List tro-28100611
Open Tree Of Life 6126588
NCBI Taxonomy 2321334
IUCN Red List 180078063
IPNI 774999-1
GBIF 6040873
EOL 5621046

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)!
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Title Authors Publication Released IDs
Cumarinas e alcaloides de Rauia resinosa (rutaceae) Tatiane Regina Albarici, Paulo Cezar Vieira, João Batista Fernandes, Maria Fátima das Graças Fernandes d Silva, José Rubens Pirani FapUNIFESP (SciELO) 20-Dec-2010
doi:10.1590/S0100-40422010001000024
Rauianin, A New Coumarin from<i>Rauia Resinosa</i> Eudes S. Velozo, Davi J. Oliveira, Alberto C. Arruda, Paulo C. Vieira, João B. Fernandes, M. Fátima Das, G. F. Da Silva, Inez Caracelli, J. Zukerman-schpector Informa UK Limited 07-Jul-2007
doi:10.1080/10575639708043633

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 / Quinolines and derivatives / Dihydrofuranoquinolines
(2S,3S)-2-(2-hydroxypropan-2-yl)-4-methoxy-2,3-dihydrofuro[2,3-b]quinolin-3-ol 163024601 Click to see CC(C)(C1C(C2=C(C3=CC=CC=C3N=C2O1)OC)O)O 275.30 unknown https://doi.org/10.1590/S0100-40422010001000024
2-(2-Hydroxypropan-2-yl)-4-methoxy-2,3-dihydrofuro[2,3-b]quinolin-3-ol 21769979 Click to see CC(C)(C1C(C2=C(C3=CC=CC=C3N=C2O1)OC)O)O 275.30 unknown https://doi.org/10.1590/S0100-40422010001000024
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Pyranoquinolines
(3R,4S)-3,4-dihydroxy-7-methoxy-2,2-dimethyl-4,6-dihydro-3H-pyrano[3,2-c]quinolin-5-one 163096920 Click to see CC1(C(C(C2=C(O1)C3=C(C(=CC=C3)OC)NC2=O)O)O)C 291.30 unknown https://doi.org/10.1590/S0100-40422010001000024
3,4-dihydroxy-7-methoxy-2,2-dimethyl-4,6-dihydro-3H-pyrano[3,2-c]quinolin-5-one 163096919 Click to see CC1(C(C(C2=C(O1)C3=C(C(=CC=C3)OC)NC2=O)O)O)C 291.30 unknown https://doi.org/10.1590/S0100-40422010001000024
7-Hydroxy-2,2,6-trimethylpyrano[3,2-c]quinolin-5-one 85741561 Click to see CC1(C=CC2=C(O1)C3=C(C(=CC=C3)O)N(C2=O)C)C 257.28 unknown https://doi.org/10.1590/S0100-40422010001000024
8-Hydroxy-7-methoxy-2,2,6-trimethylpyrano[3,2-c]quinolin-5-one 162902219 Click to see CC1(C=CC2=C(O1)C3=C(C(=C(C=C3)O)OC)N(C2=O)C)C 287.31 unknown https://doi.org/10.1590/S0100-40422010001000024
Rel-zanthodioline 5315424 Click to see CC1(C(C(C2=C(O1)C3=C(C(=CC=C3)OC)N(C2=O)C)O)O)C 305.32 unknown https://doi.org/10.1590/S0100-40422010001000024
Veprisine 338941 Click to see CC1(C=CC2=C(O1)C3=C(C(=C(C=C3)OC)OC)N(C2=O)C)C 301.34 unknown https://doi.org/10.1590/S0100-40422010001000024
> Phenylpropanoids and polyketides / Coumarins and derivatives
(7-Methoxy-8-(1,2-dihydroxy-3-methyl-3-butenyl))coumarin 13917407 Click to see CC(=C)C(C(C1=C(C=CC2=C1OC(=O)C=C2)OC)O)O 276.28 unknown https://doi.org/10.1590/S0100-40422010001000024
[(1S,2R)-2-acetyloxy-1-(7-methoxy-2-oxochromen-8-yl)-3-methylbut-3-enyl] acetate 131854581 Click to see CC(=C)C(C(C1=C(C=CC2=C1OC(=O)C=C2)OC)OC(=O)C)OC(=O)C 360.40 unknown https://doi.org/10.1590/S0100-40422010001000024
2-(7-Methoxy-2-oxochromen-8-yl)-3-methylbut-2-enal 179620 Click to see CC(=C(C=O)C1=C(C=CC2=C1OC(=O)C=C2)OC)C 258.27 unknown https://doi.org/10.1590/S0100-40422010001000024
2H-1-Benzopyran-2-one, 8-((1S,2S)-1,2-dihydroxy-3-methyl-3-butenyl)-7-methoxy- 6426907 Click to see CC(=C)C(C(C1=C(C=CC2=C1OC(=O)C=C2)OC)O)O 276.28 unknown https://doi.org/10.1590/S0100-40422010001000024
8-(1,2-Dihydroxy-3-methylbut-3-enyl)chromen-2-one 5319844 Click to see CC(=C)C(C(C1=CC=CC2=C1OC(=O)C=C2)O)O 246.26 unknown https://doi.org/10.1590/S0100-40422010001000024
Minumicrolin 389002 Click to see CC(=C)C(C(C1=C(C=CC2=C1OC(=O)C=C2)OC)O)O 276.28 unknown https://doi.org/10.1590/S0100-40422010001000024
Murrangatin diacetate 389004 Click to see CC(=C)C(C(C1=C(C=CC2=C1OC(=O)C=C2)OC)OC(=O)C)OC(=O)C 360.40 unknown https://doi.org/10.1590/S0100-40422010001000024
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
16-Methyl-3,11,14-trioxatetracyclo[8.7.0.02,7.013,17]heptadeca-1(10),2(7),5,8,16-pentaene-4,15-dione 44309997 Click to see CC1=C2C(COC3=C2C4=C(C=C3)C=CC(=O)O4)OC1=O 270.24 unknown https://doi.org/10.1590/S0100-40422010001000024
https://doi.org/10.1080/10575639708043633
5-Ethyl-16-methyl-3,11,14-trioxatetracyclo[8.7.0.02,7.013,17]heptadeca-1(10),2(7),5,8,16-pentaene-4,15-dione 162820588 Click to see CCC1=CC2=C(C3=C(C=C2)OCC4C3=C(C(=O)O4)C)OC1=O 298.29 unknown https://doi.org/10.1590/S0100-40422010001000024

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