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Tabebuia ochracea

Tabebuia ochracea - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID644055a61a9c3464249755
Scientific name Tabebuia ochracea
Authority A.H.Gentry
First published in F1. Neotrop. 25 (2):230 1992

Description Top

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Synonyms Top

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Common names Top

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Language Common/alternative name
Spanish tabebuia neochrysantha
Spanish corteza amarilla
Spanish tabebuia chrysatricha
Spanish tabebuia hypodidiction
Spanish tecoma heterotricha
Spanish tecoma ochracea
Arabic تابوبيا مغراء
Portuguese ipê-do-cerrado

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-0001244380
KEW urn:lsid:ipni.org:names:110988-1
The Plant List tro-50128439
IPNI 110988-1
iNaturalist 67514
GBIF 7298479
Freebase /m/02r86hm
USDA GRIN 434882
Wikipedia Tabebuia_ochracea

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
Flavonoids ofBignoniaceae from the “cerrado” and their possible taxonomic significance Cecília T. T. Blatt, Márcia D. dos Santos, Antonio Salatino Springer Science and Business Media LLC 10-Jan-2005
doi:10.1007/BF00985673
Chemical Investigation and in vitro Antimalarial Activity of Tabebuia ochracea ssp. neochrysantha H Pérez, F Díaz, J D Medina Informa UK Limited 02-May-2003
doi:10.1076/PHBI.35.4.227.13306
Furanonaphthoquinones from Tabebuia ochracea Carlos L. Zani, Alaíde B. De Oliveira, Geovane G. De Oliviera(in memoriam) Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(91)83653-3

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 / Naphthalenes / Naphthoquinones
Lapachol 3884 Click to see CC(=CCC1=C(C2=CC=CC=C2C(=O)C1=O)O)C 242.27 unknown https://doi.org/10.1016/0031-9422(91)83653-3
https://doi.org/10.1016/0031-9422(91)83653-3
> Lignans, neolignans and related compounds / Aryltetralin lignans / 9,9p-dihydroxyaryltetralin lignans
4-(4-Hydroxy-3-methoxyphenyl)-2,3-bis(hydroxymethyl)-7-methoxy-1,2,3,4-tetrahydronaphthalene-2,6-diol 235241 Click to see COC1=C(C=C2C(C(C(CC2=C1)(CO)O)CO)C3=CC(=C(C=C3)O)OC)O 376.40 unknown https://doi.org/10.1016/0031-9422(91)83653-3
Isoolivil 5316262 Click to see COC1=C(C=C2C(C(C(CC2=C1)(CO)O)CO)C3=CC(=C(C=C3)O)OC)O 376.40 unknown https://doi.org/10.1016/0031-9422(91)83653-3
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/0031-9422(91)83653-3
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/0031-9422(91)83653-3
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/0031-9422(91)83653-3
> Organoheterocyclic compounds / Naphthofurans
2-(1-Hydroxyethyl)-6-methoxybenzo[f][1]benzofuran-4,9-dione 14861203 Click to see CC(C1=CC2=C(O1)C(=O)C3=C(C2=O)C=C(C=C3)OC)O 272.25 unknown https://doi.org/10.1016/0031-9422(91)83653-3
2-(1-Hydroxyethyl)-7,8-dimethoxybenzo[f][1]benzofuran-4,9-dione 11055756 Click to see CC(C1=CC2=C(O1)C(=O)C3=C(C2=O)C=CC(=C3OC)OC)O 302.28 unknown https://doi.org/10.1016/0031-9422(91)83653-3
2-(1-Hydroxyethyl)-8-methoxybenzo[f][1]benzofuran-4,9-dione 14861205 Click to see CC(C1=CC2=C(O1)C(=O)C3=C(C2=O)C=CC=C3OC)O 272.25 unknown https://doi.org/10.1016/0031-9422(91)83653-3
2-(1-Hydroxyethyl)naphtho(2,3-b)furan-4,9-dione 150068 Click to see CC(C1=CC2=C(O1)C(=O)C3=CC=CC=C3C2=O)O 242.23 unknown https://doi.org/10.1016/0031-9422(91)83653-3
2-[(1R)-1-hydroxyethyl]-6-methoxybenzo[f][1]benzofuran-4,9-dione 162880657 Click to see CC(C1=CC2=C(O1)C(=O)C3=C(C2=O)C=C(C=C3)OC)O 272.25 unknown https://doi.org/10.1016/0031-9422(91)83653-3
2-[(1R)-1-hydroxyethyl]-7,8-dimethoxybenzo[f][1]benzofuran-4,9-dione 162850420 Click to see CC(C1=CC2=C(O1)C(=O)C3=C(C2=O)C=CC(=C3OC)OC)O 302.28 unknown https://doi.org/10.1016/0031-9422(91)83653-3
2-[(1R)-1-hydroxyethyl]-8-methoxybenzo[f][1]benzofuran-4,9-dione 163060540 Click to see CC(C1=CC2=C(O1)C(=O)C3=C(C2=O)C=CC=C3OC)O 272.25 unknown https://doi.org/10.1016/0031-9422(91)83653-3
2-[(1S)-1-hydroxyethyl]benzo[f][1]benzofuran-4,9-dione 156013991 Click to see CC(C1=CC2=C(O1)C(=O)C3=CC=CC=C3C2=O)O 242.23 unknown https://doi.org/10.1016/0031-9422(91)83653-3
2-Acetyl-6-methoxybenzo[f][1]benzofuran-4,9-dione 14861204 Click to see CC(=O)C1=CC2=C(O1)C(=O)C3=C(C2=O)C=C(C=C3)OC 270.24 unknown https://doi.org/10.1016/0031-9422(91)83653-3
2-Acetyl-7,8-dimethoxybenzo[f][1]benzofuran-4,9-dione 11098601 Click to see CC(=O)C1=CC2=C(O1)C(=O)C3=C(C2=O)C=CC(=C3OC)OC 300.26 unknown https://doi.org/10.1016/0031-9422(91)83653-3
2-Acetyl-8-methoxybenzo[f][1]benzofuran-4,9-dione 14861206 Click to see CC(=O)C1=CC2=C(O1)C(=O)C3=C(C2=O)C=CC=C3OC 270.24 unknown https://doi.org/10.1016/0031-9422(91)83653-3
5-Hydroxy-2-(1'-hydroxyethyl)naphtho[2,3-b]furan-4,9-dione 14159819 Click to see CC(C1=CC2=C(O1)C(=O)C3=C(C2=O)C(=CC=C3)O)O 258.23 unknown https://doi.org/10.1076/PHBI.35.4.227.13306
8-Hydroxy-2-(1-hydroxyethyl)benzo[f][1]benzofuran-4,9-dione 4483899 Click to see CC(C1=CC2=C(O1)C(=O)C3=C(C2=O)C=CC=C3O)O 258.23 unknown https://doi.org/10.1076/PHBI.35.4.227.13306
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 51402807 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1007/BF00985673
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1007/BF00985673
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1007/BF00985673
Trifolin 5282149 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1007/BF00985673
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1007/BF00985673

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