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Bourreria pulchra

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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
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Details Top

Internal ID UUID64400da3f01a4252543915
Scientific name Bourreria pulchra
Authority Millsp.
First published in Publ. Field Columb. Mus., Bot. Ser. 2: 338 (1912)

Description Top

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Synonyms Top

Scientific name Authority First published in
Cordia pulchra Millsp. Beibl. Bot. Jahrb. Syst. 80: 24 (1905)

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000570004
Tropicos 4002067
KEW urn:lsid:ipni.org:names:35516-2
The Plant List kew-2680870
Open Tree Of Life 5512885
NCBI Taxonomy 1443952
IUCN Red List 136813766
IPNI 35516-2
iNaturalist 283130
GBIF 4062820

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
SARs for the Antiparasitic Plant Metabolite Pulchrol. 3. Combinations of New Substituents in A/B-Rings and A/C-Rings Terrazas P, Salamanca E, Dávila M, Manner S, Gimenez A, Sterner O Molecules 28-Jun-2021
PMCID:PMC8271509
doi:10.3390/molecules26133944
PMID:34203527
SARs for the Antiparasitic Plant Metabolite Pulchrol. Part 2: B- and C-Ring Substituents Terrazas P, Manner S, Sterner O, Dávila M, Giménez A, Salamanca E Molecules 01-Oct-2020
PMCID:PMC7582507
doi:10.3390/molecules25194510
PMID:33019678
SAR:s for the Antiparasitic Plant Metabolite Pulchrol. 1. The Benzyl Alcohol Functionality Terrazas P, Salamanca E, Dávila M, Manner S, Giménez A, Sterner O Molecules 04-Jul-2020
PMCID:PMC7412453
doi:10.3390/molecules25133058
PMID:32635469
Simpler intake estimation using direct observation in small ruminants: grouping bites by plant structure and morphology González-Pech PG, Torres-Acosta JF, Sandoval-Castro CA BMC Res Notes 11-Jul-2018
PMCID:PMC6042344
doi:10.1186/s13104-018-3570-8
PMID:29996923
Benzochromenes from the roots of Bourreria pulchra Gilda J. Erosa-Rejón, Alejandro Yam-Puc, Manuel J. Chan-Bacab, Alberto Giménez-Turbax, Efraín Salamanca, Luis M. Peña-Rodríguez, Olov Sterner Elsevier BV 31-Oct-2009
doi:10.1016/J.PHYTOL.2009.10.002

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
Physcione 10639 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)OC 284.26 unknown https://doi.org/10.1016/J.PHYTOL.2009.10.002
> Lignans, neolignans and related compounds
(2R,3R)-1,4-Diphenyl-2,3-butanediol 11983937 Click to see C1=CC=C(C=C1)CC(C(CC2=CC=CC=C2)O)O 242.31 unknown https://doi.org/10.1016/J.PHYTOL.2009.10.002
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4aS,6aR,6aS,6bR,8aR,10R,12aR,14bS)-10-acetyloxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 37888803 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C(=O)O)C)C)C 498.70 unknown https://doi.org/10.1016/J.PHYTOL.2009.10.002
(8a-Formyl-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl) acetate 14829105 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C=O)C)C)C 482.70 unknown https://doi.org/10.1016/J.PHYTOL.2009.10.002
[(3R,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-8a-formyl-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl] acetate 162976800 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C=O)C)C)C 482.70 unknown https://doi.org/10.1016/J.PHYTOL.2009.10.002
10-Acetyloxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 619165 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C(=O)O)C)C)C 498.70 unknown https://doi.org/10.1016/J.PHYTOL.2009.10.002
> 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/J.PHYTOL.2009.10.002
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/J.PHYTOL.2009.10.002
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
2,5-Dihydroxybenzaldehyde 70949 Click to see C1=CC(=C(C=C1O)C=O)O 138.12 unknown https://doi.org/10.1016/J.PHYTOL.2009.10.002
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
2H-1-Benzopyran-6-ol, 2,2-dimethyl- 177039 Click to see CC1(C=CC2=C(O1)C=CC(=C2)O)C 176.21 unknown https://doi.org/10.1016/J.PHYTOL.2009.10.002
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Dibenzopyrans
2-Methoxy-6,6-dimethyl-6H-dibenzo[b,d]pyran-9-methanol 102367661 Click to see CC1(C2=C(C=C(C=C2)CO)C3=C(O1)C=CC(=C3)OC)C 270.32 unknown https://doi.org/10.1016/J.PHYTOL.2009.10.002
2-Methoxy-6,6-dimethylbenzo[c]chromene-9-carbaldehyde 102367662 Click to see CC1(C2=C(C=C(C=C2)C=O)C3=C(O1)C=CC(=C3)OC)C 268.31 unknown https://doi.org/10.1016/J.PHYTOL.2009.10.002
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Methyl 3-(3,4-dihydroxyphenyl)-2-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]propanoate 76511959 Click to see COC(=O)C(CC1=CC(=C(C=C1)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O 374.30 unknown https://doi.org/10.1016/J.PHYTOL.2009.10.002
Methyl rosmarinate 6479915 Click to see COC(=O)C(CC1=CC(=C(C=C1)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O 374.30 unknown https://doi.org/10.1016/J.PHYTOL.2009.10.002

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