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Neoraputia paraensis

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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 UUID643ff65ad47f7225915914
Scientific name Neoraputia paraensis
Authority (Ducke) Emmerich
First published in Rodriguésia no. 45: 243. 1978

Description Top

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Synonyms Top

Scientific name Authority First published in
Neoraputia cowanii Emmerich Rodriguésia 30(45): 259, without type. 1978
Raputia paraensis Ducke Arch. Jard. Bot. Rio de Janeiro 3: 184 (1922)

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000380611
Tropicos 28101434
INPN 734950
KEW urn:lsid:ipni.org:names:77101137-1
The Plant List kew-2381600
Open Tree Of Life 6126505
IUCN Red List 180069168
IPNI 168986-2
GBIF 3836285

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
Anti-African trypanocidal and antimalarial activity of natural flavonoids, dibenzoylmethanes and synthetic analogues. dos Santos DA, de C Braga PA, da Silva MF, Fernandes JB, Vieira PC, Magalhães AF, Magalhães EG, Marsaioli AJ, de S Moraes VR, Rattray L, Croft SL J Pharm Pharmacol 01-Feb-2009
doi:10.1211/JPP/61.02.0017
PMID:19178775
Enzymatic inhibition studies of selected flavonoids and chemosystematic significance of polymethoxylated flavonoids and quinoline alkaloids in Neoraputia (Rutaceae) Valéria R. de S. Moraes, Daniela M. Tomazela, Ricardo J. Ferracin, Cleverson F. Garcia, Míriam Sannomiya, M. del Pilar C. Soriano, M. Fátima das G. F. da Silva, Paulo C. Vieira, João B. Fernandes, Edson Rodrigues Filho, Eva G. Magalhães, Aderbal F. Magalhães, Eli F. Pimenta, Dulce H. F. de Souza, Glaucius Oliva FapUNIFESP (SciELO) 25-Apr-2005
doi:10.1590/S0103-50532003000300007
A pyrano chalcone and a flavanone from Neoraputia magnifica Edna A.P. Passador, M.Fátima das G.F. da Silva, Edson Rodrigues Fo, João B. Fernandes, Paulo C. Vieira, José R. Pirani Elsevier BV 04-Mar-2003
doi:10.1016/S0031-9422(97)00140-4
Prenylated flavones from Neoraputia paraensis José Pio I. de Souza, Alberto C. Arruda, Gaspar D. Muñoz, Mara S.P. Arruda, Adolfo H. Müller Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(99)00197-1
C-glycosylflavones fromRaputia paraensis Amri Bakhtiar, Jacqueline Gleye, Claude Moulis, Isabelle Fouraste Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(91)80133-L
Pyrano chalcones and a flavone from Neoraputia magnifica and their Trypanosoma cruzi glycosomal glyceraldehyde-3-phosphate dehydrogenase-inhibitory activities. Tomazela DM, Pupo MT, Passador EA, da Silva MF, Vieira PC, Fernandes JB, Fo ER, Oliva G, Pirani JR Phytochemistry 01-Nov-2000
doi:10.1016/S0031-9422(00)00248-X
PMID:11130676

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 / Quinolones and derivatives / Pyranoquinolines
Flindersine 68230 Click to see CC1(C=CC2=C(O1)C3=CC=CC=C3NC2=O)C 227.26 unknown https://doi.org/10.1590/S0103-50532003000300007
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
5,7-Dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-8-(3,4,5-trihydroxyoxan-2-yl)chromen-4-one 74977687 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)C4C(C(C(CO4)O)O)O)O)C5C(C(C(C(O5)CO)O)O)O)O)O 594.50 unknown https://doi.org/10.1016/0031-9422(91)80133-L
5,7-Dihydroxy-2-(4-Hydroxyphenyl)-6-(3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-Yl)-8-(3,4,5-Trihydroxyoxan-2-Yl)Chromen-4-One 3550102 Click to see C1C(C(C(C(O1)C2=C3C(=C(C(=C2O)C4C(C(C(C(O4)CO)O)O)O)O)C(=O)C=C(O3)C5=CC=C(C=C5)O)O)O)O 564.50 unknown https://doi.org/10.1016/0031-9422(91)80133-L
5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[(3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-8-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]chromen-4-one 138454316 Click to see C1C(C(C(C(O1)C2=C3C(=C(C(=C2O)C4C(C(C(C(O4)CO)O)O)O)O)C(=O)C=C(O3)C5=CC=C(C=C5)O)O)O)O 564.50 unknown https://doi.org/10.1016/0031-9422(91)80133-L
5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2S,4R,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-6-[(2S,4S,5R)-3,4,5-trihydroxyoxan-2-yl]chromen-4-one 44257662 Click to see C1C(C(C(C(O1)C2=C(C(=C3C(=C2O)C(=O)C=C(O3)C4=CC=C(C=C4)O)C5C(C(C(C(O5)CO)O)O)O)O)O)O)O 564.50 unknown https://doi.org/10.1016/0031-9422(91)80133-L
Corymboside 13644660 Click to see C1C(C(C(C(O1)C2=C(C(=C3C(=C2O)C(=O)C=C(O3)C4=CC=C(C=C4)O)C5C(C(C(C(O5)CO)O)O)O)O)O)O)O 564.50 unknown https://doi.org/10.1016/0031-9422(91)80133-L
Schaftoside 442658 Click to see C1C(C(C(C(O1)C2=C3C(=C(C(=C2O)C4C(C(C(C(O4)CO)O)O)O)O)C(=O)C=C(O3)C5=CC=C(C=C5)O)O)O)O 564.50 unknown https://doi.org/10.1016/0031-9422(91)80133-L
Vicenin-1 13644663 Click to see C1C(C(C(C(O1)C2=C(C(=C3C(=C2O)C(=O)C=C(O3)C4=CC=C(C=C4)O)C5C(C(C(C(O5)CO)O)O)O)O)O)O)O 564.50 unknown https://doi.org/10.1016/0031-9422(91)80133-L
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
5-Hydroxy-3',4',6,7-tetramethoxyflavone 152430 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC 358.30 unknown https://doi.org/10.1590/S0103-50532003000300007
5,6,7-Trimethoxy-2-(7-methoxy-1,3-benzodioxol-5-yl)chromen-4-one 184922 Click to see COC1=CC(=CC2=C1OCO2)C3=CC(=O)C4=C(C(=C(C=C4O3)OC)OC)OC 386.40 unknown https://doi.org/10.1016/S0031-9422(00)00248-X
5,6,7,3',4',5'-Hexamethoxyflavone 185670 Click to see COC1=CC(=CC(=C1OC)OC)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)OC 402.40 unknown https://doi.org/10.1016/S0031-9422(97)00140-4
Ageconyflavone A 10089586 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC4=C(C=C3)OCO4)OC)OC 356.30 unknown https://doi.org/10.1016/S0031-9422(00)00248-X
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
5-Hydroxy-8-(4-hydroxy-3,5-dimethoxyphenyl)-2,2-dimethyl-2H,6H-benzo[1,2-b:5,4-b']dipyran-6-one 15486955 Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C=C(O3)C4=CC(=C(C(=C4)OC)O)OC)C 396.40 unknown https://doi.org/10.1016/S0031-9422(99)00197-1
7,8,3',4'-Tetramethoxy-6'',6''-dimethylpyrano[2'',3'':5,6]flavone 44258614 Click to see CC1(C=CC2=C(O1)C3=C(C(=C2OC)OC)OC(=CC3=O)C4=CC(=C(C=C4)OC)OC)C 424.40 unknown https://doi.org/10.1211/JPP/61.02.0017

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