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Euxylophora paraensis

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 UUID64401bfda1fe3547172485
Scientific name Euxylophora paraensis
Authority Huber
First published in Bol. Mus. Goeldi Hist. Nat. Ethnogr. 6: 85 (1910)

Ethnobotanical Use Top

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General Uses Top

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Common products:
The principal commercial product is timber (sawn wood, veneer) marketed under the trade name “pau-amarelo.”

Wood and fiber:
The wood is used for high-grade furniture, cabinetry, interior joinery, fine flooring, and specialty items such as musical instruments and turned pieces. The grain is fine to very fine and generally straight; the natural durability of the heartwood supports applications in interior joinery and flooring without preservative treatment. The wood is dense and strong with silica content that can dull cutting edges, a property relevant to machining and tooling choices in industrial processing. These physical characteristics enable precision surfacing and finishing in craft and industrial contexts.

Properties relevant to use:
The dense, fine-grained structure underpins dimensional stability and surface quality demanded in fine cabinetry and flooring. Natural decay resistance of the heartwood reduces the need for preservative treatments in interior service classes.

Sustainability and sourcing:
The species occurs in Brazil and has a limited natural distribution; consequently, supply is intermittent and the timber is classed as scarce in trade. No international trade restrictions are reported under CITES; exports are subject to Brazilian forestry regulations and applicable permits. Sustainable management requires regulation of harvest volumes and attention to in situ regeneration due to the species’ restricted occurrence.

Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Portuguese pau-amarelo
Portuguese amarelão

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

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

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000683742
Tropicos 28100113
KEW urn:lsid:ipni.org:names:102485-2
The Plant List kew-2805566
Open Tree Of Life 6126323
IUCN Red List 61958701
IPNI 102485-2
iNaturalist 1195334
GBIF 3834762
EOL 5624064
USDA GRIN 465386

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)!
Title Authors Publication Released IDs
Fitoquímica e quimiossistemática de Euxylophora paraensis (Rutaceae) Marsele Machado Isidoro, Maria Fátima das Graças Fernandes d Silva, João Batista Fernandes, Paulo Cezar Vieira, Alberto C. Arruda, Sebastião da Cruz Silva FapUNIFESP (SciELO) 05-Dec-2012
doi:10.1590/S0100-40422012001100004
New quinolinone and bis-quinolinone alkaloids from Euxylophora paraensis L Jurd, M Benson, RY Wong CSIRO Publishing 02-Sep-2010
doi:10.1071/CH9830759
The structures of paraensidimerin A and C, two bisquinolinone alkaloids from Euxylophora paraensis L Jurd, RY Wong, M Benson CSIRO Publishing 02-Sep-2010
doi:10.1071/CH9822505
New quinolinone alkaloids from the heartwood of, Euxylophora paraensis L Jurd, RY Wong CSIRO Publishing 02-Sep-2010
doi:10.1071/CH9811625
Structures of paraensidimerins B, E, F, and G, four new dimeric quinolinone alkaloids from Euxylophora paraensis Leonard Jurd, Mabry Benson Royal Society of Chemistry (RSC) 30-Mar-2004
doi:10.1039/C39830000092
New indolopyridoquinazoline alkaloids from Euxylophora paraënsis B. Danieli, P. Manitto, F. Ronchetti, G. Russo, G. Ferrari Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(72)85046-5
A new indolopyridoquinazoline in the bark of Euxylophora paraënsis Bruno Danieli, Carlo Farachi, Giovanni Palmisano Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)84427-1
Minor indolopyridoquinazoline alkaloids from Euxylophora paraënsis Bruno Danieli, Giovanni Palmisano, Giovanni Russo, Giorgio Ferrari Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(73)80468-6
1-Hydroxyrutaecarpine from Euxylophora paraënsis Bruno Danieli, Giovanni Palmisano, Guglielmo Rainoldi, Giovanni Russo Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(74)80336-5
Paraensine, a new indolopyridoquinazoline alkaloid from euxylophora paraënsis hub. Danieli B, Manitto P, Ronchetti F, Russo G, Ferrari G Experientia 15-Mar-1972
doi:10.1007/BF01928667
PMID:5026416
New quinazolinocarboline alkaloids from Euxylophora paraënsis Hub. Canonica L, Danieli B, Manitto P, Russo G Tetrahedron Lett 01-Jan-1970
doi:10.1016/S0040-4039(00)72778-X
PMID:5681780

Phytochemical Profile Top

Add a new one!
Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
4,5-Dimethoxyanthranilic acid 79736 Click to see 197.19 unknown https://doi.org/10.1016/S0040-4039(00)72778-X
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3R,3aR,5aR,5bS,7aS,11aS,11bR,13aS,13bR)-3a,5a,7a,11b,13a-pentamethyl-3-propan-2-yl-1,2,3,4,5,5b,6,7,10,11,11a,12,13,13b-tetradecahydrocyclopenta[a]chrysene-8-carbaldehyde 101596938 Click to see CC(C)C1CCC2C1(CCC3(C2(CCC4(C3CCC5(C4CCC=C5C=O)C)C)C)C)C 424.70 unknown https://doi.org/10.1071/CH9830759
https://doi.org/10.1039/C39830000092
https://doi.org/10.1071/CH9811625
https://doi.org/10.1071/CH9822505
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
Sericine hydrochlride 4311469 Click to see 367.40 unknown https://doi.org/10.1071/CH9811625
Spectabiline 73414 Click to see CC1C(=O)OC2CCN3C2C(=CC3)COC(=O)C(C1(C)OC(=O)C)(C)O 367.40 unknown https://doi.org/10.1071/CH9811625
Trachyspic acid 9909587 Click to see CCCCCCCCCC1=COC2(C1=O)CC(C(O2)(CC(=O)O)C(=O)O)C(=O)O 412.40 unknown https://doi.org/10.1071/CH9830759
https://doi.org/10.1039/C39830000092
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
1-Hydroxyrutaecarpine 10447696 Click to see C1CN2C(=NC3=C(C2=O)C=CC=C3O)C4=C1C5=CC=CC=C5N4 303.30 unknown https://doi.org/10.1016/0031-9422(74)80336-5
10-Methoxy-7,7-dimethyl-8-oxa-2,14,24-triazahexacyclo[12.11.0.03,12.04,9.017,25.018,23]pentacosa-1,3,5,9,11,17(25),18,20,22-nonaen-13-one 21769551 Click to see 399.40 unknown https://doi.org/10.1071/CH9830759
17,18-Dimethoxy-3,13,21-triazapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-1(21),2(10),4,6,8,15,17,19-octaen-14-one 136026475 Click to see 347.40 unknown https://doi.org/10.1016/S0040-4039(00)72778-X
18-Hydroxy-17-methoxy-3,13,21-triazapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-1(21),2(10),4,6,8,15,17,19-octaen-14-one 135778998 Click to see COC1=C(C=C2C(=C1)C(=O)N3CCC4=C(C3=N2)NC5=CC=CC=C45)O 333.30 unknown https://doi.org/10.1016/S0031-9422(00)84427-1
18,20-Dioxa-3,13,24-triazahexacyclo[11.11.0.02,10.04,9.015,23.017,21]tetracosa-1(24),2(10),4,6,8,15,17(21),22-octaen-14-one 135778996 Click to see C1CN2C(=NC3=CC4=C(C=C3C2=O)OCO4)C5=C1C6=CC=CC=C6N5 331.30 unknown https://doi.org/10.1016/0031-9422(72)85046-5
2,3-Dimethoxy-14-methylindolo[2',3':3,4]pyrido[2,1-b]quinazolin-5(14h)-one 91799094 Click to see 359.40 unknown https://doi.org/10.1016/0031-9422(72)85046-5
7,17,18-Trimethoxy-21-methyl-3,13,21-triazapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-1,3,5,7,9,11,15,17,19-nonaen-14-one 162929875 Click to see CN1C2=CC(=C(C=C2C(=O)N3C1=C4C(=C5C=C(C=CC5=N4)OC)C=C3)OC)OC 389.40 unknown https://doi.org/10.1016/0031-9422(73)80468-6
7,17,18-Trimethoxy-3,13,21-triazapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-1(21),2(10),4(9),5,7,11,15,17,19-nonaen-14-one 136738243 Click to see COC1=CC2=C(C=C1)NC3=C2C=CN4C3=NC5=CC(=C(C=C5C4=O)OC)OC 375.40 unknown https://doi.org/10.1016/0031-9422(73)80468-6
7,17,18-Trimethoxy-3,13,21-triazapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-1(21),2(10),4(9),5,7,15,17,19-octaen-14-one 135778997 Click to see COC1=CC2=C(C=C1)NC3=C2CCN4C3=NC5=CC(=C(C=C5C4=O)OC)OC 377.40 unknown https://doi.org/10.1016/0031-9422(73)80468-6
7,7-Dimethyl-8-oxa-2,14,24-triazahexacyclo[12.11.0.03,12.04,9.017,25.018,23]pentacosa-1,3(12),4(9),5,10,17(25),18,20,22-nonaen-13-one 163040104 Click to see CC1(C=CC2=C(O1)C=CC3=C2N=C4C5=C(CCN4C3=O)C6=CC=CC=C6N5)C 369.40 unknown https://doi.org/10.1007/BF01928667
> Organoheterocyclic compounds / Pyridopyrimidines
17,18-Dimethoxy-21-methyl-3,13,21-triazapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-1,3,5,7,9,15,17,19-octaen-14-one 15559186 Click to see 361.40 unknown https://doi.org/10.1016/S0040-4039(00)72778-X
7,17,18-Trimethoxy-21-methyl-3,13,21-triazapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-1,3,5,7,9,15,17,19-octaen-14-one 163009104 Click to see 391.40 unknown https://doi.org/10.1016/0031-9422(73)80468-6
> Organoheterocyclic compounds / Quinolines and derivatives / Dihydrofuranoquinolines
(2R)-2,3,3-trimethyl-2,5-dihydrofuro[3,2-c]quinolin-4-one 163189051 Click to see 229.27 unknown https://doi.org/10.1071/CH9830759
(2R)-2,3,3,5-tetramethyl-2H-furo[3,2-c]quinolin-4-one 163193047 Click to see 243.30 unknown https://doi.org/10.1071/CH9830759
(3S)-2,2,3,9-tetramethyl-3H-furo[2,3-b]quinolin-4-one 162938621 Click to see 243.30 unknown https://doi.org/10.1071/CH9811625
2,3,3-Trimethyl-2,5-dihydrofuro[3,2-c]quinolin-4-one 162850260 Click to see 229.27 unknown https://doi.org/10.1071/CH9830759
2,3,3,5-tetramethyl-2H-furo[3,2-c]quinolin-4-one 86077303 Click to see CC1C(C2=C(O1)C3=CC=CC=C3N(C2=O)C)(C)C 243.30 unknown https://doi.org/10.1071/CH9830759
Lemobiline 442917 Click to see CC1C2=C(N(C3=CC=CC=C3C2=O)C)OC1(C)C 243.30 unknown https://doi.org/10.1071/CH9811625
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
Skimmianine 6760 Click to see COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC 259.26 unknown https://doi.org/10.1071/CH9811625
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroquinolones
4-(2,3-Dihydroxy-3-methylbutoxy)-1-methylquinolin-2-one 162850037 Click to see 277.31 unknown https://doi.org/10.1071/CH9811625
4-[(2S)-2,3-dihydroxy-3-methylbutoxy]-1-methylquinolin-2-one 162850038 Click to see CC(C)(C(COC1=CC(=O)N(C2=CC=CC=C21)C)O)O 277.31 unknown https://doi.org/10.1071/CH9811625
4-Hydroxy-3-(3-hydroxy-3-methylbutan-2-yl)-1-methylquinolin-2-one 54696163 Click to see 261.32 unknown https://doi.org/10.1071/CH9830759
4-hydroxy-3-[(2R)-3-hydroxy-3-methylbutan-2-yl]-1-methylquinolin-2-one 162977467 Click to see 261.32 unknown https://doi.org/10.1071/CH9830759
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Pyranoquinolines
(1R,14R,15S)-4,13,13,18-tetramethyl-15-(2-methylprop-1-enyl)-12,26-dioxa-4,18-diazahexacyclo[12.12.0.02,11.05,10.016,25.019,24]hexacosa-2(11),5,7,9,16(25),19,21,23-octaene-3,17-dione 92340639 Click to see 482.60 unknown https://doi.org/10.1071/CH9811625
(1R,14S,15S)-4,13,13,18-tetramethyl-15-(2-methylprop-1-enyl)-12,26-dioxa-4,18-diazahexacyclo[12.12.0.02,11.05,10.016,25.019,24]hexacosa-2(11),5,7,9,16(25),19,21,23-octaene-3,17-dione 335878 Click to see 482.60 unknown https://doi.org/10.1071/CH9811625
(1R,2R,15R,17S)-3,3,12,17,26-pentamethyl-4,18-dioxa-12,26-diazaheptacyclo[15.11.1.02,15.05,14.06,11.019,28.020,25]nonacosa-5(14),6,8,10,19(28),20,22,24-octaene-13,27-dione 21770540 Click to see 482.60 unknown https://doi.org/10.1071/CH9811625
https://doi.org/10.1071/CH9822505
https://doi.org/10.1071/CH9830759
(1R,2S,15R,17R)-3,3,12,17,26-pentamethyl-4,18-dioxa-12,26-diazaheptacyclo[15.11.1.02,15.05,14.06,11.019,28.020,25]nonacosa-5(14),6,8,10,19(28),20,22,24-octaene-13,27-dione 14378598 Click to see 482.60 unknown https://doi.org/10.1071/CH9822505
https://doi.org/10.1071/CH9830759
(1R,2S,15R,17S)-3,3,12,17,26-pentamethyl-4,18-dioxa-12,26-diazaheptacyclo[15.11.1.02,15.05,14.06,11.019,28.020,25]nonacosa-5(14),6,8,10,19(28),20,22,24-octaene-13,27-dione 21770543 Click to see 482.60 unknown https://doi.org/10.1039/C39830000092
https://doi.org/10.1071/CH9830759
(1R,2S,17S)-3,3,12,17,26-pentamethyl-4,18-dioxa-12,26-diazaheptacyclo[15.11.1.02,15.05,14.06,11.019,28.020,25]nonacosa-5(14),6,8,10,15,19(28),20,22,24-nonaene-13,27-dione 21770544 Click to see 480.60 unknown https://doi.org/10.1039/C39830000092
(1S,14R,15R)-15-(2-hydroxy-2-methylpropyl)-4,13,13,18-tetramethyl-12,26-dioxa-4,18-diazahexacyclo[12.12.0.02,11.05,10.016,25.019,24]hexacosa-2(11),5,7,9,16(25),19,21,23-octaene-3,17-dione 162932255 Click to see CC1(C2C(C3=C(C4=CC=CC=C4N(C3=O)C)OC2C5=C(O1)C6=CC=CC=C6N(C5=O)C)CC(C)(C)O)C 500.60 unknown https://doi.org/10.1039/C39830000092
https://doi.org/10.1071/CH9830759
(1S,2R,15R,17R)-3,3,12,17,26-pentamethyl-4,18-dioxa-12,26-diazaheptacyclo[15.11.1.02,15.05,14.06,11.019,28.020,25]nonacosa-5(14),6,8,10,19(28),20,22,24-octaene-13,27-dione 162958671 Click to see 482.60 unknown https://doi.org/10.1039/C39830000092
(1S,2R,15S,17R)-3,3,12,17,26-pentamethyl-4,18-dioxa-12,26-diazaheptacyclo[15.11.1.02,15.05,14.06,11.019,28.020,25]nonacosa-5(14),6,8,10,19(28),20,22,24-octaene-13,27-dione 162958672 Click to see 482.60 unknown https://doi.org/10.1039/C39830000092
(1S,2R,17R)-3,3,12,17,26-pentamethyl-4,18-dioxa-12,26-diazaheptacyclo[15.11.1.02,15.05,14.06,11.019,28.020,25]nonacosa-5(14),6,8,10,15,19(28),20,22,24-nonaene-13,27-dione 162844130 Click to see 480.60 unknown https://doi.org/10.1071/CH9830759
(1S,2S,15S,17S)-3,3,12,17,26-pentamethyl-4,18-dioxa-12,26-diazaheptacyclo[15.11.1.02,15.05,14.06,11.019,28.020,25]nonacosa-5(14),6,8,10,19(28),20,22,24-octaene-13,27-dione 14378600 Click to see CC1(C2C(CC3(CC2C4=C(O3)C5=CC=CC=C5N(C4=O)C)C)C6=C(O1)C7=CC=CC=C7N(C6=O)C)C 482.60 unknown https://doi.org/10.1071/CH9822505
(4R)-4-hydroxy-2,2,6-trimethyl-3,4-dihydropyrano[3,2-c]quinolin-5-one 163041792 Click to see CC1(CC(C2=C(O1)C3=CC=CC=C3N(C2=O)C)O)C 259.30 unknown https://doi.org/10.1071/CH9811625
15-(2-Hydroxy-2-methylpropyl)-4,13,13,18-tetramethyl-12,26-dioxa-4,18-diazahexacyclo[12.12.0.02,11.05,10.016,25.019,24]hexacosa-2(11),5,7,9,16(25),19,21,23-octaene-3,17-dione 73834407 Click to see 500.60 unknown https://doi.org/10.1071/CH9830759
https://doi.org/10.1071/CH9811625
https://doi.org/10.1039/C39830000092
4-Hydroxy-2,2,6-trimethyl-3,4-dihydropyrano[3,2-c]quinolin-5-one 163041791 Click to see CC1(CC(C2=C(O1)C3=CC=CC=C3N(C2=O)C)O)C 259.30 unknown https://doi.org/10.1071/CH9811625
4,13,13,18-Tetramethyl-15-(2-methylprop-1-enyl)-12,26-dioxa-4,18-diazahexacyclo[12.12.0.02,11.05,10.016,25.019,24]hexacosa-2(11),5,7,9,16(25),19,21,23-octaene-3,17-dione 4031614 Click to see CC(=CC1C2C(C3=C(C4=CC=CC=C4N(C3=O)C)OC2(C)C)OC5=C1C(=O)N(C6=CC=CC=C65)C)C 482.60 unknown https://doi.org/10.1071/CH9811625
https://doi.org/10.1071/CH9830759
N-Methylflindersine 72819 Click to see 241.28 unknown https://doi.org/10.1071/CH9811625
https://doi.org/10.1071/CH9830759
Paraensidimerin C 21770541 Click to see CC1(C2C(CC3(CC2C4=C(O3)C5=CC=CC=C5N(C4=O)C)C)C6=C(O1)C7=CC=CC=C7N(C6=O)C)C 482.60 unknown https://doi.org/10.1071/CH9822505
https://doi.org/10.1071/CH9811625
https://doi.org/10.1071/CH9830759
Veprisine 338941 Click to see 301.34 unknown https://doi.org/10.1071/CH9811625
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
(7-Oxofuro[3,2-g]chromen-4-yl) 3-methylbutanoate 162820499 Click to see CC(C)CC(=O)OC1=C2C=CC(=O)OC2=CC3=C1C=CO3 286.28 unknown https://doi.org/10.1590/S0100-40422012001100004
2-(2-Hydroxypropan-2-yl)-9-methoxy-2,3-dihydrofuro(3,2-g)chromen-7-one 180058 Click to see 276.28 unknown https://doi.org/10.1590/S0100-40422012001100004
4-(2,3-Dihydroxy-3-methylbutoxy)furo(3,2-g)chromen-7-one 483513 Click to see 304.29 unknown https://doi.org/10.1590/S0100-40422012001100004
Isooxypeucedanin 625383 Click to see 286.28 unknown https://doi.org/10.1590/S0100-40422012001100004
Methoxy rutaretin 139069891 Click to see CC(C)(C1CC2=C(O1)C(=C3C(=C2)C=CC(=O)O3)OC)O 276.28 unknown https://doi.org/10.1590/S0100-40422012001100004
Oxypeucedanin hydrate 17536 Click to see CC(C)(C(COC1=C2C=CC(=O)OC2=CC3=C1C=CO3)O)O 304.29 unknown https://doi.org/10.1590/S0100-40422012001100004
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 12314853 Click to see 448.40 unknown https://doi.org/10.1590/S0100-40422012001100004
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-oxo-4H-1-benzopyran-3-yl 6-deoxyhexopyranoside 5353915 Click to see 448.40 unknown https://doi.org/10.1590/S0100-40422012001100004
5,7-Dihydroxy-3-(3,4,5-Trihydroxy-6-Methyloxan-2-Yl)Oxy-2-(3,4,5-Trihydroxyphenyl)Chromen-4-One 5352000 Click to see 464.40 unknown https://doi.org/10.1590/S0100-40422012001100004
5,7-dihydroxy-3-[(3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2-(3,4,5-trihydroxyphenyl)chromen-4-one 12313050 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)O)O)O)O)O 464.40 unknown https://doi.org/10.1590/S0100-40422012001100004
Myricitrin 5281673 Click to see 464.40 unknown https://doi.org/10.1590/S0100-40422012001100004
Quercitrin 5280459 Click to see 448.40 unknown https://doi.org/10.1590/S0100-40422012001100004

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