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Internal ID UUID64400131e3c99778251867
Scientific name Picramnia latifolia
Authority Tul.
First published in Ann. Sci. Nat., Bot. , sér. 3, 7: 258 (1847)

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Synonyms Top

Scientific name Authority First published in
Picramnia umbrosa Seem. Bot. Voy. Herald : 97 (1853)
Picramnia macrostachys Engl. Fl. Bras. 12(2): 238 (1874)
Picramnia longissima Tul. Ann. Sci. Nat., Bot. , sér. 3, 7: 257 (1847)
Picramnia eosina J.F.Macbr. Publ. Field Columb. Mus., Bot. Ser. 13(3): 697 (1949)
Picramnia cooperi D.M.Porter J. Arnold Arbor. 54: 317 (1973)

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Varieties (abbr. var.) 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
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil West-central
    • Central America
      • Costa Rica
      • Honduras
      • Nicaragua
      • Panamá
    • Northern South America
      • French Guiana
      • Guyana
      • Suriname
      • Venezuela
    • 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-0000474800
Tropicos 29400026
INPN 734549
KEW urn:lsid:ipni.org:names:813902-1
The Plant List kew-2549120
Open Tree Of Life 972695
NCBI Taxonomy 681474
IUCN Red List 145669594
IPNI 813902-1
iNaturalist 286381
GBIF 3708918
EOL 5631891

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
Cytotoxicity of Nine Medicinal Plants from San Basilio de Palenque (Colombia) on HepG2 Cells Caballero-Gallardo K, Alvarez-Ortega N, Olivero-Verbel J Plants (Basel) 19-Jul-2023
PMCID:PMC10383961
doi:10.3390/plants12142686
PMID:37514300
Studies on Activities and Chemical Characterization of Medicinal Plants in Search for New Antimalarials: A Ten Year Review on Ethnopharmacology Ceravolo IP, Aguiar AC, Adebayo JO, Krettli AU Front Pharmacol 22-Sep-2021
PMCID:PMC8493299
doi:10.3389/fphar.2021.734263
PMID:34630109
Medicinal plants as a fight against murine blood-stage malaria Dkhil MA, Al-Quraishy S, Al-Shaebi EM, Abdel-Gaber R, Thagfan FA, Qasem MA Saudi J Biol Sci 19-Dec-2020
PMCID:PMC7938113
doi:10.1016/j.sjbs.2020.12.014
PMID:33732056
Botanical candidates from Saudi Arabian flora as potential therapeutics for Plasmodium infection Al-Quraishy S, Abdel-Maksoud MA, Al-Shaebi EM, Dkhil MA Saudi J Biol Sci 27-Nov-2020
PMCID:PMC7878689
doi:10.1016/j.sjbs.2020.11.069
PMID:33613066
Evaluation of in vivo anti-malarial potential of omidun obtained from fermented maize in Ibadan, Nigeria Omeiza FO, Ademowo GO, Ayeni FA Malar J 19-Nov-2020
PMCID:PMC7678239
doi:10.1186/s12936-020-03486-0
PMID:33213477
Anti-plasmodial effect of plant extracts from Picrolemma huberi and Picramnia latifolia Berthi W, González A, Rios A, Blair S, Cogollo Á, Pabón A Malar J 04-Apr-2018
PMCID:PMC5883577
doi:10.1186/s12936-018-2301-x
PMID:29615054
Stochastically driven adult–recruit associations of tree species on Barro Colorado Island Getzin S, Wiegand T, Hubbell SP Proc Biol Sci 07-Sep-2014
PMCID:PMC4123702
doi:10.1098/rspb.2014.0922
PMID:25030984
Anthrone and oxanthrone C-glycosides from Picramnia latifolia collected in Peru. Diaz F, Chai HB, Mi Q, Su BN, Vigo JS, Graham JG, Cabieses F, Farnsworth NR, Cordell GA, Pezzuto JM, Swanson SM, Kinghorn AD J Nat Prod 01-Mar-2004
doi:10.1021/NP030479J
PMID:15043409

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 / Anthracenes
[(3R,4S,5S,6R)-6-[(9R)-4,5-dihydroxy-2-methyl-10-oxo-9H-anthracen-9-yl]-4,5-dihydroxyoxan-3-yl] benzoate 11213689 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2C4C(C(C(CO4)OC(=O)C5=CC=CC=C5)O)O)C=CC=C3O 476.50 unknown https://doi.org/10.1021/NP030479J
[(3R,4S,5S,6R)-6-[(9S)-4,5-dihydroxy-2-methyl-10-oxo-9H-anthracen-9-yl]-4,5-dihydroxyoxan-3-yl] benzoate 11751894 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2C4C(C(C(CO4)OC(=O)C5=CC=CC=C5)O)O)C=CC=C3O 476.50 unknown https://doi.org/10.1021/NP030479J
[(3R,4S,5S,6S)-4,5-dihydroxy-6-[(9R)-4,5,9-trihydroxy-2-methyl-10-oxoanthracen-9-yl]oxan-3-yl] benzoate 11306430 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2(C4C(C(C(CO4)OC(=O)C5=CC=CC=C5)O)O)O)C=CC=C3O 492.50 unknown https://doi.org/10.1021/NP030479J
[(3R,4S,5S,6S)-4,5-dihydroxy-6-[(9S)-4,5,9-trihydroxy-2-methyl-10-oxoanthracen-9-yl]oxan-3-yl] benzoate 11375304 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2(C4C(C(C(CO4)OC(=O)C5=CC=CC=C5)O)O)O)C=CC=C3O 492.50 unknown https://doi.org/10.1021/NP030479J
[4,5-Dihydroxy-6-(4,5,9-trihydroxy-2-methyl-10-oxoanthracen-9-yl)oxan-3-yl] benzoate 72794129 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2(C4C(C(C(CO4)OC(=O)C5=CC=CC=C5)O)O)O)C=CC=C3O 492.50 unknown https://doi.org/10.1021/NP030479J
[6-(4,5-dihydroxy-2-methyl-10-oxo-9H-anthracen-9-yl)-4,5-dihydroxyoxan-3-yl] benzoate 72753511 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2C4C(C(C(CO4)OC(=O)C5=CC=CC=C5)O)O)C=CC=C3O 476.50 unknown https://doi.org/10.1021/NP030479J
Mayoside D 44575611 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2(CC4C(C(C(CO4)OC(=O)C5=CC=CC=C5)O)O)O)C=CC=C3O 506.50 unknown https://doi.org/10.1021/NP030479J
Mayoside E 44575612 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2(CC4C(C(C(CO4)OC(=O)C5=CC=CC=C5)O)O)O)C=CC=C3O 506.50 unknown https://doi.org/10.1021/NP030479J
Picramnioside G 44575607 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2CC4C(C(C(CO4)OC(=O)C5=CC=CC=C5)O)O)C=CC=C3O 490.50 unknown https://doi.org/10.1021/NP030479J
Picramnioside H 44575608 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2CC4C(C(C(CO4)OC(=O)C5=CC=CC=C5)O)O)C=CC=C3O 490.50 unknown https://doi.org/10.1021/NP030479J
> Benzenoids / Anthracenes / Anthraquinones
1,5-Dihydroxy-3-methoxy-7-methylanthracene-9,10-dione 15138599 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C(=CC(=C3)OC)O 284.26 unknown https://doi.org/10.1021/NP030479J
8-Hydroxy-3-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyanthracene-9,10-dione 14077419 Click to see CC1=CC2=C(C(=C1)OC3C(C(C(C(O3)CO)O)O)O)C(=O)C4=C(C2=O)C=CC=C4O 416.40 unknown https://doi.org/10.1021/NP030479J
Chrysophanein 6324923 Click to see CC1=CC2=C(C(=C1)OC3C(C(C(C(O3)CO)O)O)O)C(=O)C4=C(C2=O)C=CC=C4O 416.40 unknown https://doi.org/10.1021/NP030479J
Pulmatin 442731 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=CC=C3OC4C(C(C(C(O4)CO)O)O)O 416.40 unknown https://doi.org/10.1021/NP030479J
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
7-hydroxy-3-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyanthracene-9,10-dione 163188292 Click to see CC1=CC2=C(C(=C1)OC3C(C(C(C(O3)CO)O)O)O)C(=O)C4=C(C2=O)C=CC(=C4)O 416.40 unknown https://doi.org/10.1021/NP030479J
7-Hydroxy-3-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyanthracene-9,10-dione 162945128 Click to see CC1=CC2=C(C(=C1)OC3C(C(C(C(O3)CO)O)O)O)C(=O)C4=C(C2=O)C=CC(=C4)O 416.40 unknown https://doi.org/10.1021/NP030479J
Nataloe-emodin 12313148 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=CC(=C3O)O 270.24 unknown https://doi.org/10.1021/NP030479J
> Benzenoids / Phenanthrenes and derivatives
6,8-Dihydroxy-10-methylbenzo[a]phenalen-7-one 21576219 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C=CC4=C3C2=CC=C4)O 276.30 unknown https://doi.org/10.1021/NP030479J
6,8-Dihydroxy-4-methyl-7 h-benz(de) anthracen-7-one 21582530 Click to see CC1=CC(=C2C3=C1C=CC=C3C4=C(C2=O)C(=CC=C4)O)O 276.30 unknown https://doi.org/10.1021/NP030479J
6,8-Dihydroxy-5-methylbenzo[a]phenalen-7-one 44575531 Click to see CC1=CC2=C3C(=CC=C2)C4=C(C(=CC=C4)O)C(=O)C3=C1O 276.30 unknown https://doi.org/10.1021/NP030479J
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(2R,3R,4S,5S,6S)-2-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 154496016 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1021/NP030479J
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1021/NP030479J
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1021/NP030479J
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1021/NP030479J
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1021/NP030479J
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O 192.17 unknown https://doi.org/10.1021/NP030479J
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown https://doi.org/10.1021/NP030479J
> Phenylpropanoids and polyketides / Isoflavonoids / Coumestans
1,3-Dihydroxy-8,9-dimethoxy-[1]benzofuro[3,2-c]chromen-6-one 11602329 Click to see COC1=C(C=C2C(=C1)C3=C(O2)C4=C(C=C(C=C4OC3=O)O)O)OC 328.27 unknown https://doi.org/10.1021/NP030479J

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