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Lonchocarpus guatemalensis

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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 UUID643fd73e97f18693023485
Scientific name Lonchocarpus guatemalensis
Authority Benth.
First published in J. Proc. Linn. Soc., Bot.4(Suppl.): 87 (1860)

Description Top

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Synonyms Top

Scientific name Authority First published in
Lonchocarpus guatemalensis var. proteranthus (Pittier) F.J.Herm. J. Washington Acad. Sci.38: 312 (1949)
Lonchocarpus mexicanus Pittier Contr. U.S. Natl. Herb.20: 71 (1917)
Lonchocarpus proteranthus Pittier Contr. U.S. Natl. Herb.20: 63 (1917)
Lonchocarpus xuul Lundell Bull. Torrey Bot. Club69: 391 (1942)
Lonchocarpus darienensis Pittier Contr. U.S. Natl. Herb.20: 69 (1917)
Lonchocarpus dumetorum Brandegee Univ. Calif. Publ. Bot.10: 181 (1922)
Lonchocarpus megalanthus Pittier Contr. U.S. Natl. Herb.20: 70 (1917)
Lonchocarpus guatemalensis var. megalanthus (Pittier) F.J.Herm. J. Washington Acad. Sci.39: 312 (1949)
Lonchocarpus guatemalensis var. guatemalensis Benth.
Lonchocarpus guatemalensis var. jurgenseni Benth. J. Proc. Linn. Soc., Bot.4(Suppl.): 88 (1860)
Lonchocarpus guatemalensis var. mexicanus (Pittier) F.J.Herm. J. Washington Acad. Sci.39: 312 (1949)

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
  • Northern America
    • Mexico
      • Mexico Central
      • Mexico Gulf
      • Mexico Northeast
      • Mexico Northwest
      • Mexico Southeast
      • Mexico Southwest
  • Southern America
    • Central America
      • Belize
      • Costa Rica
      • El Salvador
      • Guatemala
      • Honduras
      • Nicaragua
      • Panamá

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000173718
Tropicos 13021974
KEW urn:lsid:ipni.org:names:502966-1
The Plant List ild-19857
Open Tree Of Life 379585
Observations.org 233072
NCBI Taxonomy 1127059
IUCN Red List 62513
IPNI 502966-1
iNaturalist 118508
GBIF 2969021
EOL 639940
Elurikkus 343786

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
Ecological quality as a coffee quality enhancer. A review Torrez V, Benavides-Frias C, Jacobi J, Speranza CI Agron Sustain Dev 02-Feb-2023
PMCID:PMC9894527
doi:10.1007/s13593-023-00874-z
PMID:36748099
Pharmacological Properties of Chalcones: A Review of Preclinical Including Molecular Mechanisms and Clinical Evidence Salehi B, Quispe C, Chamkhi I, El Omari N, Balahbib A, Sharifi-Rad J, Bouyahya A, Akram M, Iqbal M, Docea AO, Caruntu C, Leyva-Gómez G, Dey A, Martorell M, Calina D, López V, Les F Front Pharmacol 18-Jan-2021
PMCID:PMC7849684
doi:10.3389/fphar.2020.592654
PMID:33536909
Secondary Succession under invasive species (Pteridium aquilinum) conditions in a seasonal dry tropical forest in southeastern Mexico Jean Baptiste A, Macario PA, Islebe GA, Vargas-Larreta B, Pool L, Valdez-Hernández M, López-Martínez JO PeerJ 28-May-2019
PMCID:PMC6544012
doi:10.7717/peerj.6974
PMID:31179179
Major Flavanones from Lonchocarpus guatamalensis John L. Ingham, Satoshi Tahara, Stanley Dziedzic Walter de Gruyter GmbH 02-Aug-2018
doi:10.1515/ZNC-1988-11-1205
Additional flavonoids from Lonchocarpus yucatanensis and L. xuul Rocío Borges-Argáez, Maria Esther Poot Díaz, Peter G. Waterman, Luis M. Peña-Rodríguez FapUNIFESP (SciELO) 09-Jan-2006
doi:10.1590/S0103-50532005000600028
Flavonoids from two Lonchocarpus species of the Yucatan Peninsula. Borges-Argáez R, Peña-Rodríguez LM, Waterman PG Phytochemistry 01-Jul-2002
doi:10.1016/S0031-9422(02)00131-0
PMID:12052520
Flavonoids from the stem bark of Lonchocarpus xuul. Borges-Argáez R, Peñia-Rodríguez LM, Waterman PG Phytochemistry 01-Jul-2000
doi:10.1016/S0031-9422(00)00170-9
PMID:10963455

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 / Proline and derivatives
4-Hydroxy-methylprolin 11499239 Click to see CN1CC(CC1C(=O)O)O 145.16 unknown https://doi.org/10.1590/S0103-50532005000600028
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(7S,8R)-5-hydroxy-8-(4-hydroxyphenyl)-7-methoxy-2,2-dimethyl-10-(3-methylbut-2-enyl)-7,8-dihydropyrano[3,2-g]chromen-6-one 163106855 Click to see CC(=CCC1=C2C(=C(C3=C1OC(C(C3=O)OC)C4=CC=C(C=C4)O)O)C=CC(O2)(C)C)C 436.50 unknown https://doi.org/10.1515/ZNC-1988-11-1205
(S)-2,3-Dihydro-5,7-dihydroxy-2-phenyl-6,8-diprenyl-4H-1-benzopyran-4-one 25775471 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=CC=CC=C3)CC=C(C)C)O)C 392.50 unknown https://doi.org/10.1016/S0031-9422(00)00170-9
5-Hydroxy-8-(4-hydroxyphenyl)-7-methoxy-2,2-dimethyl-10-(3-methylbut-2-enyl)-7,8-dihydropyrano[3,2-g]chromen-6-one 163106854 Click to see CC(=CCC1=C2C(=C(C3=C1OC(C(C3=O)OC)C4=CC=C(C=C4)O)O)C=CC(O2)(C)C)C 436.50 unknown https://doi.org/10.1515/ZNC-1988-11-1205
5,7-Dihydroxy-6,8-di-C-prenylflavanone 11143677 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=CC=CC=C3)CC=C(C)C)O)C 392.50 unknown https://doi.org/10.1016/S0031-9422(00)00170-9
Lupinifolin 10250777 Click to see CC(=CCC1=C2C(=C(C3=C1OC(CC3=O)C4=CC=C(C=C4)O)O)C=CC(O2)(C)C)C 406.50 unknown https://doi.org/10.1515/ZNC-1988-11-1205
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
(6R,8R)-5,6-dimethoxy-2,2-dimethyl-8-phenyl-7,8-dihydro-6H-pyrano[3,2-g]chromene 162941837 Click to see CC1(C=CC2=C(C3=C(C=C2O1)OC(CC3OC)C4=CC=CC=C4)OC)C 352.40 unknown https://doi.org/10.1016/S0031-9422(00)00170-9
(6S,7S,8R)-5-methoxy-2,2-dimethyl-8-phenyl-7,8-dihydro-6H-pyrano[3,2-g]chromene-6,7-diol 11100309 Click to see CC1(C=CC2=C(C3=C(C=C2O1)OC(C(C3O)O)C4=CC=CC=C4)OC)C 354.40 unknown https://doi.org/10.1016/S0031-9422(02)00131-0
(8R)-5-methoxy-2,2-dimethyl-8-phenyl-8H-pyrano[3,2-g]chromene-6,7-diol 101803955 Click to see CC1(C=CC2=C(C3=C(C=C2O1)OC(C(=C3O)O)C4=CC=CC=C4)OC)C 352.40 unknown https://doi.org/10.1016/S0031-9422(00)00170-9
2alpha-Phenyl-8,8-dimethyl-4beta-ethoxy-5-methoxy-3,4-dihydro-2H,8H-benzo[1,2-b:5,4-b']dipyran 12016631 Click to see CCOC1CC(OC2=C1C(=C3C=CC(OC3=C2)(C)C)OC)C4=CC=CC=C4 366.40 unknown https://doi.org/10.1016/S0031-9422(00)00170-9
3beta-Methoxyxuulanin 10475006 Click to see CC1(C=CC2=C(C3=C(C=C2O1)OC(C(C3OC)OC)C4=CC=CC=C4)OC)C 382.40 unknown https://doi.org/10.1016/S0031-9422(00)00170-9
https://doi.org/10.1016/S0031-9422(02)00131-0
4-(5,6,7-trimethoxy-2,2-dimethyl-7,8-dihydro-6H-pyrano[3,2-g]chromen-8-yl)phenol 22297334 Click to see CC1(C=CC2=C(C3=C(C=C2O1)OC(C(C3OC)OC)C4=CC=C(C=C4)O)OC)C 398.40 unknown https://doi.org/10.1016/S0031-9422(02)00131-0
5-Hydroxy-8-(4-hydroxy-3-methoxyphenyl)-2,2-dimethyl-2H,6H-benzo[1,2-b:5,4-b']dipyran-6-one 10915521 Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C=C(O3)C4=CC(=C(C=C4)O)OC)C 366.40 unknown https://doi.org/10.1016/S0031-9422(02)00131-0
5-methoxy-2,2-dimethyl-8-phenyl-7,8-dihydro-6H-pyrano[3,2-g]chromene-6,7-diol 85398796 Click to see CC1(C=CC2=C(C3=C(C=C2O1)OC(C(C3O)O)C4=CC=CC=C4)OC)C 354.40 unknown https://doi.org/10.1016/S0031-9422(02)00131-0
5,6-dimethoxy-2,2-dimethyl-8-phenyl-7,8-dihydro-6H-pyrano[3,2-g]chromen-7-ol 85366894 Click to see CC1(C=CC2=C(C3=C(C=C2O1)OC(C(C3OC)O)C4=CC=CC=C4)OC)C 368.40 unknown https://doi.org/10.1016/S0031-9422(02)00131-0
5,6-dimethoxy-2,2-dimethyl-8-phenyl-7,8-dihydro-6H-pyrano[3,2-g]chromene 74977193 Click to see CC1(C=CC2=C(C3=C(C=C2O1)OC(CC3OC)C4=CC=CC=C4)OC)C 352.40 unknown https://doi.org/10.1016/S0031-9422(00)00170-9
5,6,7-trimethoxy-2,2-dimethyl-8-phenyl-7,8-dihydro-6H-pyrano[3,2-g]chromene 85153237 Click to see CC1(C=CC2=C(C3=C(C=C2O1)OC(C(C3OC)OC)C4=CC=CC=C4)OC)C 382.40 unknown https://doi.org/10.1016/S0031-9422(00)00170-9
https://doi.org/10.1016/S0031-9422(02)00131-0
6-ethoxy-5-methoxy-2,2-dimethyl-8-phenyl-7,8-dihydro-6H-pyrano[3,2-g]chromene 162853636 Click to see CCOC1CC(OC2=C1C(=C3C=CC(OC3=C2)(C)C)OC)C4=CC=CC=C4 366.40 unknown https://doi.org/10.1016/S0031-9422(00)00170-9
Carpachromene 10449654 Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C=C(O3)C4=CC=C(C=C4)O)C 336.30 unknown https://doi.org/10.1016/S0031-9422(02)00131-0
Carpachromene dimethyl ether 14607844 Click to see CC1(C=CC2=C(O1)C=C3C(=C2OC)C(=O)C=C(O3)C4=CC=C(C=C4)OC)C 364.40 unknown https://doi.org/10.1016/S0031-9422(02)00131-0
Xuulanin 44257134 Click to see CC1(C=CC2=C(C3=C(C=C2O1)OC(CC3OC)C4=CC=CC=C4)OC)C 352.40 unknown https://doi.org/10.1016/S0031-9422(00)00170-9
Xuuranin 10247444 Click to see CC1(C=CC2=C(C3=C(C=C2O1)OC(CC3OC)C4=CC=CC=C4)OC)C 352.40 unknown https://doi.org/10.1016/S0031-9422(00)00170-9
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
1-(5-Hydroxy-7-methoxy-2,2-dimethylchromen-6-yl)-3-(4-methoxyphenyl)prop-2-en-1-one 73189671 Click to see CC1(C=CC2=C(C(=C(C=C2O1)OC)C(=O)C=CC3=CC=C(C=C3)OC)O)C 366.40 unknown https://doi.org/10.1016/S0031-9422(02)00131-0
Glychalcone A 15230651 Click to see CC1(C=CC2=C(C(=C(C=C2O1)OC)C(=O)C=CC3=CC=C(C=C3)OC)O)C 366.40 unknown https://doi.org/10.1016/S0031-9422(02)00131-0
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 3-prenylated chalcones
1-[2,4-Dihydroxy-3-(3-methylbut-2-enyl)phenyl]-3-phenylprop-2-en-1-one 321234 Click to see CC(=CCC1=C(C=CC(=C1O)C(=O)C=CC2=CC=CC=C2)O)C 308.40 unknown https://doi.org/10.1016/S0031-9422(02)00131-0
Isocordoin 6251270 Click to see CC(=CCC1=C(C=CC(=C1O)C(=O)C=CC2=CC=CC=C2)O)C 308.40 unknown https://doi.org/10.1016/S0031-9422(02)00131-0

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