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Lophanthera lactescens

Lophanthera lactescens - 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 UUID644047d260e2d928048209
Scientific name Lophanthera lactescens
Authority Ducke
First published in Arch. Jard. Bot. Rio de Janeiro 4: 103 (1925)

Description Top

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Synonyms Top

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Common names Top

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Language Common/alternative name
Portuguese chuva-de-ouro
Portuguese lanterneira
Portuguese lofantera-da-amazônia

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001076166
Tropicos 19500002
KEW urn:lsid:ipni.org:names:143553-2
The Plant List tro-19500002
Open Tree Of Life 406020
NCBI Taxonomy 151846
IUCN Red List 191125694
IPNI 143553-2
iNaturalist 344931
GBIF 5634534
EOL 5492846
USDA GRIN 22663

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
Therapeutic Interventions for Countering Leishmaniasis and Chagas’s Disease: From Traditional Sources to Nanotechnological Systems Souto EB, Dias-Ferreira J, Craveiro SA, Severino P, Sanchez-Lopez E, Garcia ML, Silva AM, Souto SB, Mahant S Pathogens 01-Aug-2019
PMCID:PMC6789685
doi:10.3390/pathogens8030119
PMID:31374930
The Role of Natural Products in Drug Discovery and Development against Neglected Tropical Diseases Cheuka PM, Mayoka G, Mutai P, Chibale K Molecules 31-Dec-2016
PMCID:PMC6155950
doi:10.3390/molecules22010058
PMID:28042865
Natural Products: Insights into Leishmaniasis Inflammatory Response Rodrigues IA, Mazotto AM, Cardoso V, Alves RL, Amaral AC, Silva JR, Pinheiro AS, Vermelho AB Mediators Inflamm 11-Oct-2015
PMCID:PMC4619978
doi:10.1155/2015/835910
PMID:26538837
Leishmanicidal effect of LLD-3 (1), a nor-triterpene isolated from Lophanthera lactescens. Danelli MG, Soares DC, Abreu HS, Peçanha LM, Saraiva EM Phytochemistry 01-Mar-2009
doi:10.1016/J.PHYTOCHEM.2009.03.009
PMID:19359020
A nor-triterpenoid from Lophanthera lactescens Heber Dos S. Abreu, Raimundo Braz Fo, Hugo E. Gottlieb, James N. Shoolery Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(90)83048-6

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
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4aS,6aR,6bS,8aR,12aR,14aS,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-2,4a,5,6,7,8,9,10,12,12a,14,14a-dodecahydro-1H-picen-3-one 38359273 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1)C)C)C 424.70 unknown https://doi.org/10.1016/0031-9422(90)83048-6
4,4,6a,6b,8a,11,11,14b-Octamethyl-1,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,14,14a,14b-octadecahydro-2H-picen-3-one 612782 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1)C)C)C 424.70 unknown https://doi.org/10.1016/0031-9422(90)83048-6
beta-Amyrone 12306160 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1)C)C)C 424.70 unknown https://doi.org/10.1016/0031-9422(90)83048-6
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(17R)-17-[(2R,5S)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 101613936 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown https://doi.org/10.1016/0031-9422(90)83048-6
(24S)-Ergost-4-en-3-one 14537343 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C 398.70 unknown https://doi.org/10.1016/0031-9422(90)83048-6
(3R,8S,9S,10R,13R,14S,17R)-17-[(2R,5S)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 12358798 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown https://doi.org/10.1016/0031-9422(90)83048-6
17-(5,6-Dimethylheptan-2-yl)-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one 14537342 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C 398.70 unknown https://doi.org/10.1016/0031-9422(90)83048-6
5-Cholestene-3-ol, 24-methyl- 312822 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown https://doi.org/10.1016/0031-9422(90)83048-6
Ergost-5-en-3-ol 18660356 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown https://doi.org/10.1016/0031-9422(90)83048-6
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids
methyl (1S,2R,3S,4R,5R,6S,8R,11R,12R,15S,16S,21R,22R,23R,24S)-3,4,23,24-tetraacetyloxy-22-(acetyloxymethyl)-11-hydroxy-2,5,15,21-tetramethyl-9-methylidene-19-oxo-7,20-dioxahexacyclo[13.9.0.02,12.05,11.06,8.016,22]tetracos-17-ene-6-carboxylate 162846818 Click to see CC1C2(C(C=CC(=O)O1)C3(CCC4C(C3C(C2OC(=O)C)OC(=O)C)(C(C(C5(C4(CC(=C)C6C5(O6)C(=O)OC)O)C)OC(=O)C)OC(=O)C)C)C)COC(=O)C 788.80 unknown https://doi.org/10.1016/0031-9422(90)83048-6
Methyl 3,4,23,24-tetraacetyloxy-22-(acetyloxymethyl)-11-hydroxy-2,5,15,21-tetramethyl-9-methylidene-19-oxo-7,20-dioxahexacyclo[13.9.0.02,12.05,11.06,8.016,22]tetracos-17-ene-6-carboxylate 14633165 Click to see CC1C2(C(C=CC(=O)O1)C3(CCC4C(C3C(C2OC(=O)C)OC(=O)C)(C(C(C5(C4(CC(=C)C6C5(O6)C(=O)OC)O)C)OC(=O)C)OC(=O)C)C)C)COC(=O)C 788.80 unknown https://doi.org/10.1016/0031-9422(90)83048-6
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-Ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one 255607 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C 410.70 unknown https://doi.org/10.1016/0031-9422(90)83048-6
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 122544 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/0031-9422(90)83048-6
Stigmasta-4,22-dien-3-one 6442194 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C 410.70 unknown https://doi.org/10.1016/0031-9422(90)83048-6
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/0031-9422(90)83048-6
> Organic acids and derivatives / Carboxylic acids and derivatives / Hexacarboxylic acids and derivatives
methyl (1S,2R,3S,4R,5R,6S,8R,11R,12R,15S,16S,21R,22R,23R,24S)-3,4,23,24-tetraacetyloxy-22-(acetyloxymethyl)-11-hydroxy-2,5,15,21-tetramethyl-9,19-dimethylidene-7,20-dioxahexacyclo[13.9.0.02,12.05,11.06,8.016,22]tetracos-17-ene-6-carboxylate 101470671 Click to see CC1C2(C(C=CC(=C)O1)C3(CCC4C(C3C(C2OC(=O)C)OC(=O)C)(C(C(C5(C4(CC(=C)C6C5(O6)C(=O)OC)O)C)OC(=O)C)OC(=O)C)C)C)COC(=O)C 786.90 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.03.009
Methyl 3,4,23,24-tetraacetyloxy-22-(acetyloxymethyl)-11-hydroxy-2,5,15,21-tetramethyl-9,19-dimethylidene-7,20-dioxahexacyclo[13.9.0.02,12.05,11.06,8.016,22]tetracos-17-ene-6-carboxylate 162882820 Click to see CC1C2(C(C=CC(=C)O1)C3(CCC4C(C3C(C2OC(=O)C)OC(=O)C)(C(C(C5(C4(CC(=C)C6C5(O6)C(=O)OC)O)C)OC(=O)C)OC(=O)C)C)C)COC(=O)C 786.90 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.03.009

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