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Lonchocarpus salvadorensis

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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 UUID643fd5f696745134173125
Scientific name Lonchocarpus salvadorensis
Authority Pittier
First published in Contr. U.S. Natl. Herb.20: 80 (1917)

Description Top

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Synonyms Top

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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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Northern America
    • Mexico
      • Mexico Northeast
      • Mexico Southeast
      • Mexico Southwest
  • Southern America
    • Central America
      • Costa Rica
      • El Salvador
      • Guatemala
      • Honduras

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000165958
Tropicos 13009911
KEW urn:lsid:ipni.org:names:143371-2
The Plant List ild-12382
Open Tree Of Life 3920416
IUCN Red List 144263574
IPNI 143371-2
iNaturalist 290381
GBIF 2968989
Freebase /m/0fp_hbp
EOL 416226
Wikipedia Lonchocarpus_salvadorensis
CMAUP NPO25289

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
Rotenoids of Lonchocarpus salvadorensis: Their effectiveness in protecting seeds against bruchid predation Nicholas Birch, Leslie Crombie, W.Mary Crombie Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(85)80019-4

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
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
3-Hydroxylup-20(29)-en-28-amide 10161414 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)N 455.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
Coumarin 323 Click to see C1=CC=C2C(=C1)C=CC(=O)O2 146.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
7-hydroxy-8-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one 22524175 Click to see C1=CC(=C(C2=C1C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O)O 340.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-methoxypsoralens
Bergapten 2355 Click to see COC1=C2C=CC(=O)OC2=CC3=C1C=CO3 216.19 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-methoxypsoralens
Methoxsalen 4114 Click to see COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2 216.19 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7,8-dihydroxycoumarins
Daphnetin 5280569 Click to see C1=CC(=C(C2=C1C=CC(=O)O2)O)O 178.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Rotenoids / Rotenones
(-)-Deguelin;(-)-cis-Deguelin 606171 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC)C 394.40 unknown https://doi.org/10.1016/0031-9422(85)80019-4
5'beta-Rotenone 5102 Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC 394.40 unknown https://doi.org/10.1016/0031-9422(85)80019-4
6-Hydroxy-9,10-dimethoxy-3,3-dimethyl-13,13a-dihydro-3H,7aH-pyrano[2,3-c:6,5-f']dichromen-7-one 243723 Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC)O)C 410.40 unknown https://doi.org/10.1016/0031-9422(85)80019-4
alpha-Toxicarol 442826 Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC)O)C 410.40 unknown https://doi.org/10.1016/0031-9422(85)80019-4
Deguelin 107935 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC)C 394.40 unknown https://doi.org/10.1016/0031-9422(85)80019-4
Derride 13846199 Click to see COC1=C(C=C2C(=C1)C3C(CO2)OC4=C(C3=O)C=CC5=C4C=CO5)OC 352.30 unknown https://doi.org/10.1016/0031-9422(85)80019-4
Elliptone 160477 Click to see COC1=C(C=C2C(=C1)C3C(CO2)OC4=C(C3=O)C=CC5=C4C=CO5)OC 352.30 unknown https://doi.org/10.1016/0031-9422(85)80019-4
Rotenone 6758 Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC 394.40 unknown https://doi.org/10.1016/0031-9422(85)80019-4

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