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Lonchocarpus costaricensis

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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 UUID643fd5a740b4c597413269
Scientific name Lonchocarpus costaricensis
Authority (Donn.Sm.) Pittier
First published in Contr. U.S. Natl. Herb.20: 58 (1917)

Description Top

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Synonyms Top

Scientific name Authority First published in
Derris costaricensis Donn.Sm. Bot. Gaz.44: 110 (1907)

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-0000164467
Tropicos 13002908
KEW urn:lsid:ipni.org:names:143254-2
The Plant List ild-10897
Open Tree Of Life 379571
NCBI Taxonomy 1127057
IUCN Red List 151999698
IPNI 143254-2
GBIF 2969071
EOL 417891

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
Identifying potential monkeypox virus inhibitors: an in silico study targeting the A42R protein Ashley CN, Broni E, Wood CM, Okuneye T, Ojukwu MP, Dong Q, Gallagher C, Miller WA III Front Cell Infect Microbiol 04-Mar-2024
PMCID:PMC10945028
doi:10.3389/fcimb.2024.1351737
PMID:38500508
Exploring the Potential of Chemical Inhibitors for Targeting Post-translational Glycosylation of Coronavirus (SARS-CoV-2) Tripathi N, Goel B, Bhardwaj N, Vishwakarma RA, Jain SK ACS Omega 28-Jul-2022
PMCID:PMC9344791
doi:10.1021/acsomega.2c02345
PMID:35937682
Howler monkey foraging ecology suggests convergent evolution of routine trichromacy as an adaptation for folivory Melin AD, Khetpal V, Matsushita Y, Zhou K, Campos FA, Welker B, Kawamura S Ecol Evol 04-Feb-2017
PMCID:PMC5330884
doi:10.1002/ece3.2716
PMID:28261454
Flavonoids from the seeds of Lonchocarpus costaricensis Peter G. Waterman, Elhadi N. Mahmoud Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)80768-2
Erythro-γ-hydroxyhomo-?-arginine: An amino acid from seed of Lonchocarpus costaricensis, and its preferential interaction with borate S Evans Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)81117-6

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
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
2-Amino-6-guanidino-4-hydroxyhexanoic acid 4479244 Click to see C(CN=C(N)N)C(CC(C(=O)O)N)O 204.23 unknown https://doi.org/10.1016/S0031-9422(00)81117-6
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / D-alpha-amino acids
(2R,4R)-2-amino-6-(diaminomethylideneamino)-4-hydroxyhexanoic acid 5318222 Click to see C(CN=C(N)N)C(CC(C(=O)O)N)O 204.23 unknown https://doi.org/10.1016/S0031-9422(00)81117-6
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(2R)-5-methoxy-7-(3-methylbut-2-enoxy)-8-(3-methylbut-2-enyl)-2-phenyl-2,3-dihydrochromen-4-one 162843968 Click to see CC(=CCC1=C2C(=C(C=C1OCC=C(C)C)OC)C(=O)CC(O2)C3=CC=CC=C3)C 406.50 unknown https://doi.org/10.1016/S0031-9422(00)80768-2
8-Prenyl-5,7-dimethoxyflavanone 14033978 Click to see CC(=CCC1=C2C(=C(C=C1OC)OC)C(=O)CC(O2)C3=CC=CC=C3)C 352.40 unknown https://doi.org/10.1016/S0031-9422(00)80768-2
Candidone 157102 Click to see CC(=CCC1=C2C(=C(C=C1OC)OC)C(=O)CC(O2)C3=CC=CC=C3)C 352.40 unknown https://doi.org/10.1016/S0031-9422(00)80768-2
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2R)-8-[(E)-3-hydroxy-3-methylbut-1-enyl]-7-(3-methylbut-2-enoxy)-2-phenyl-2,3-dihydrochromen-4-one 162928636 Click to see CC(=CCOC1=C(C2=C(C=C1)C(=O)CC(O2)C3=CC=CC=C3)C=CC(C)(C)O)C 392.50 unknown https://doi.org/10.1016/S0031-9422(00)80768-2
(2S)-8-[(E)-3-hydroxy-3-methylbut-1-enyl]-7-(3-methylbut-2-enoxy)-2-phenyl-2,3-dihydrochromen-4-one 163190754 Click to see CC(=CCOC1=C(C2=C(C=C1)C(=O)CC(O2)C3=CC=CC=C3)C=CC(C)(C)O)C 392.50 unknown https://doi.org/10.1016/S0031-9422(00)80768-2
8-(3-Hydroxy-3-methylbut-1-enyl)-7-(3-methylbut-2-enoxy)-2-phenyl-2,3-dihydrochromen-4-one 74819330 Click to see CC(=CCOC1=C(C2=C(C=C1)C(=O)CC(O2)C3=CC=CC=C3)C=CC(C)(C)O)C 392.50 unknown https://doi.org/10.1016/S0031-9422(00)80768-2
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
4H,8H-Benzo(1,2-b:3,4-b')dipyran-4-one, 2,3-dihydro-5-methoxy-8,8-dimethyl-2-phenyl-, (S)- 155236 Click to see CC1(C=CC2=C3C(=C(C=C2O1)OC)C(=O)CC(O3)C4=CC=CC=C4)C 336.40 unknown https://doi.org/10.1016/S0031-9422(00)80768-2
Isopongaflavone 10958572 Click to see CC1(C=CC2=C3C(=C(C=C2O1)OC)C(=O)C=C(O3)C4=CC=CC=C4)C 334.40 unknown https://doi.org/10.1016/S0031-9422(00)80768-2
Obovatin methyl ether 2729164 Click to see CC1(C=CC2=C3C(=C(C=C2O1)OC)C(=O)CC(O3)C4=CC=CC=C4)C 336.40 unknown https://doi.org/10.1016/S0031-9422(00)80768-2
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
3-Hydroxy-1-(5-hydroxy-7-methoxy-2,2-dimethylchromen-6-yl)-3-phenylprop-2-en-1-one 85080286 Click to see CC1(C=CC2=C(C(=C(C=C2O1)OC)C(=O)C=C(C3=CC=CC=C3)O)O)C 352.40 unknown https://doi.org/10.1016/S0031-9422(00)80768-2
Demethylpraecanson B 9975280 Click to see CC1(C=CC2=C(C(=C(C=C2O1)OC)C(=O)C=C(C3=CC=CC=C3)O)O)C 352.40 unknown https://doi.org/10.1016/S0031-9422(00)80768-2
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 3-prenylated chalcones
Ovalichalcone 14033977 Click to see CC(=CCC1=C(C(=C(C=C1OC)OC)C(=O)C=CC2=CC=CC=C2)O)C 352.40 unknown https://doi.org/10.1016/S0031-9422(00)80768-2

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