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Jacaranda glabra

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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 UUID6440273d9bca0158106038
Scientific name Jacaranda glabra
Authority (DC.) Bureau & K.Schum.
First published in Fl. Bras. 8(2): 394 (1897)

Description Top

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Synonyms Top

Scientific name Authority First published in
Jacaranda longiflora Britton ex Rusby Bull. Torrey Bot. Club 27: 73. 1900
Jacaranda rachidoptera Bureau & K.Schum. Fl. Bras. 8(2): 374 (1897)
Jacaranda cauliflora Bureau & K.Schum. Fl. Bras. 8(2): 373 (1897)
Jacaranda atropurpurea Rusby Mem. New York Bot. Gard. 7: 357 (1927)
Pteropodium glabrum DC. Prodr. 9: 239 (1845)

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
  • Southern America
    • Brazil
      • Brazil North
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador
      • Peru

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000778769
Tropicos 3701026
KEW urn:lsid:ipni.org:names:130921-2
The Plant List kew-317319
Open Tree Of Life 6080571
NCBI Taxonomy 1835392
IUCN Red List 194012027
IPNI 130921-2
iNaturalist 874098
GBIF 4094115

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)!
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Title Authors Publication Released IDs
Ethnobotanical inventory of medicinal plants used by Cashinahua (Huni Kuin) herbalists in Purus Province, Peruvian Amazon Horackova J, Chuspe Zans ME, Kokoska L, Sulaiman N, Clavo Peralta ZM, Bortl L, Polesny Z J Ethnobiol Ethnomed 12-May-2023
PMCID:PMC10176740
doi:10.1186/s13002-023-00586-4
PMID:37170108
Antileishmanial Activities of Medicinal Herbs and Phytochemicals In Vitro and In Vivo: An Update for the Years 2015 to 2021 Hassan AA, Khalid HE, Abdalla AH, Mukhtar MM, Osman WJ, Efferth T Molecules 04-Nov-2022
PMCID:PMC9656935
doi:10.3390/molecules27217579
PMID:36364404
Jacaranone Derivatives with Antiproliferative Activity from Crepis pulchra and Relevance of This Group of Plant Metabolites Dávid CZ, Kúsz N, Pinke G, Kulmány Á, Zupkó I, Hohmann J, Vasas A Plants (Basel) 16-Mar-2022
PMCID:PMC8955310
doi:10.3390/plants11060782
PMID:35336664
The Potential of Traditional Knowledge to Develop Effective Medicines for the Treatment of Leishmaniasis Passero LF, Brunelli ED, Sauini T, Amorim Pavani TF, Jesus JA, Rodrigues E Front Pharmacol 08-Jun-2021
PMCID:PMC8248671
doi:10.3389/fphar.2021.690432
PMID:34220515
Antiplasmodial natural products: an update Tajuddeen N, Van Heerden FR Malar J 05-Dec-2019
PMCID:PMC6896759
doi:10.1186/s12936-019-3026-1
PMID:31805944
Antiplasmodial Natural Products Nogueira CR, Lopes LM Molecules 04-Mar-2011
PMCID:PMC6259672
doi:10.3390/molecules16032146
Jacaranone-derived glucosidic esters from Jacaranda glabra and their activity against Plasmodium falciparum. Gachet MS, Kunert O, Kaiser M, Brun R, Muñoz RA, Bauer R, Schühly W J Nat Prod 23-Apr-2010
doi:10.1021/NP900528M
PMID:20307077

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 / Benzene and substituted derivatives
Phenylacetic Acid 999 Click to see C1=CC=C(C=C1)CC(=O)O 136.15 unknown https://doi.org/10.1021/NP900528M
> Lipids and lipid-like molecules / Saccharolipids
[(2S,3R,4S,5R,6R)-5-hydroxy-2-[2-(1-hydroxy-4-oxocyclohexa-2,5-dien-1-yl)acetyl]oxy-6-[[2-(1-hydroxy-4-oxocyclohexa-2,5-dien-1-yl)acetyl]oxymethyl]-4-[2-(3-hydroxyphenyl)acetyl]oxyoxan-3-yl] 2-phenylacetate 162909049 Click to see C1=CC=C(C=C1)CC(=O)OC2C(C(C(OC2OC(=O)CC3(C=CC(=O)C=C3)O)COC(=O)CC4(C=CC(=O)C=C4)O)O)OC(=O)CC5=CC(=CC=C5)O 732.70 unknown https://doi.org/10.1021/NP900528M
[4,5-Dihydroxy-2-[2-(1-hydroxy-4-oxocyclohexa-2,5-dien-1-yl)acetyl]oxy-6-[[2-(1-hydroxy-4-oxocyclohexa-2,5-dien-1-yl)acetyl]oxymethyl]oxan-3-yl] 2-phenylacetate 75111192 Click to see C1=CC=C(C=C1)CC(=O)OC2C(C(C(OC2OC(=O)CC3(C=CC(=O)C=C3)O)COC(=O)CC4(C=CC(=O)C=C4)O)O)O 598.50 unknown https://doi.org/10.1021/NP900528M
[5-Hydroxy-2-[2-(1-hydroxy-4-oxocyclohexa-2,5-dien-1-yl)acetyl]oxy-6-[[2-(1-hydroxy-4-oxocyclohexa-2,5-dien-1-yl)acetyl]oxymethyl]-3-(2-phenylacetyl)oxyoxan-4-yl] 2-phenylacetate 75150106 Click to see C1=CC=C(C=C1)CC(=O)OC2C(C(OC(C2OC(=O)CC3=CC=CC=C3)OC(=O)CC4(C=CC(=O)C=C4)O)COC(=O)CC5(C=CC(=O)C=C5)O)O 716.70 unknown https://doi.org/10.1021/NP900528M
[5-Hydroxy-2-[2-(1-hydroxy-4-oxocyclohexa-2,5-dien-1-yl)acetyl]oxy-6-[[2-(1-hydroxy-4-oxocyclohexa-2,5-dien-1-yl)acetyl]oxymethyl]-3-[2-(4-hydroxyphenyl)acetyl]oxyoxan-4-yl] 2-phenylacetate 75150107 Click to see C1=CC=C(C=C1)CC(=O)OC2C(C(OC(C2OC(=O)CC3=CC=C(C=C3)O)OC(=O)CC4(C=CC(=O)C=C4)O)COC(=O)CC5(C=CC(=O)C=C5)O)O 732.70 unknown https://doi.org/10.1021/NP900528M
[5-Hydroxy-2-[2-(1-hydroxy-4-oxocyclohexa-2,5-dien-1-yl)acetyl]oxy-6-[[2-(1-hydroxy-4-oxocyclohexa-2,5-dien-1-yl)acetyl]oxymethyl]-4-[2-(3-hydroxyphenyl)acetyl]oxyoxan-3-yl] 2-phenylacetate 162909048 Click to see C1=CC=C(C=C1)CC(=O)OC2C(C(C(OC2OC(=O)CC3(C=CC(=O)C=C3)O)COC(=O)CC4(C=CC(=O)C=C4)O)O)OC(=O)CC5=CC(=CC=C5)O 732.70 unknown https://doi.org/10.1021/NP900528M
Jacaglabroside A 46211770 Click to see C1=CC=C(C=C1)CC(=O)OC2C(C(OC(C2OC(=O)CC3=CC=CC=C3)OC(=O)CC4(C=CC(=O)C=C4)O)COC(=O)CC5(C=CC(=O)C=C5)O)O 716.70 unknown https://doi.org/10.1021/NP900528M
Jacaglabroside B 45360280 Click to see C1=CC=C(C=C1)CC(=O)OC2C(C(C(OC2OC(=O)CC3(C=CC(=O)C=C3)O)COC(=O)CC4(C=CC(=O)C=C4)O)O)O 598.50 unknown https://doi.org/10.1021/NP900528M
Jacaglabroside C 46211771 Click to see C1=CC=C(C=C1)CC(=O)OC2C(C(OC(C2OC(=O)CC3=CC=C(C=C3)O)OC(=O)CC4(C=CC(=O)C=C4)O)COC(=O)CC5(C=CC(=O)C=C5)O)O 732.70 unknown https://doi.org/10.1021/NP900528M
Jacaglabroside D 46211772 Click to see C1=CC=C(C=C1)CC(=O)OC2C(C(C(OC2OC(=O)CC3(C=CC(=O)C=C3)O)COC(=O)CC4(C=CC(=O)C=C4)O)O)OC(=O)CC5=CC=C(C=C5)O 732.70 unknown https://doi.org/10.1021/NP900528M
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
Jacaranone 73307 Click to see COC(=O)CC1(C=CC(=O)C=C1)O 182.17 unknown https://doi.org/10.1021/NP900528M

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