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Potalia amara

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID6440479ef3f1b206111775
Scientific name Potalia amara
Authority Aubl.
First published in Hist. Pl. Guiane : 394 (1775)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Nicandra amara (Aubl.) J.F.Gmel. Syst. Nat., ed. 13[bis]. : 677 (1791)

Common names Top

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Language Common/alternative name
Arabic بوطاليا مرة
Dutch anabi
Portuguese anabi

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
    • Central America
      • Nicaragua
      • Panamá
    • Northern South America
      • French Guiana
      • Suriname
    • Western South America
      • Ecuador
      • Peru

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001074057
Tropicos 19000568
INPN 733366
KEW urn:lsid:ipni.org:names:546882-1
The Plant List tro-19000568
Open Tree Of Life 435049
NCBI Taxonomy 84951
IUCN Red List 145496805
IPNI 546882-1
GBIF 7289373
EPPO PQJAM
EOL 5346480

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
Medicinal Plants for the Treatment of Local Tissue Damage Induced by Snake Venoms: An Overview from Traditional Use to Pharmacological Evidence Félix-Silva J, Silva-Junior AA, Zucolotto SM, Fernandes-Pedrosa MD Evid Based Complement Alternat Med 21-Aug-2017
PMCID:PMC5585606
doi:10.1155/2017/5748256
PMID:28904556
Dietary restrictions in healing among speakers of Iquito, an endangered language of the Peruvian Amazon Jernigan KA J Ethnobiol Ethnomed 11-Jul-2011
PMCID:PMC3148960
doi:10.1186/1746-4269-7-20
PMID:21745400
Phenolic glycosides from Potalia amara. Li XC, ElSohly HN, Walker LA, Clark AM Planta Med 01-Oct-2005
doi:10.1055/S-2005-871233
PMID:16254836
Morphological and Ultrastructural Diversity of Orbicules in Gentianaceae VINCKIER S, SMETS E Ann Bot 01-Nov-2003
PMCID:PMC4244851
doi:10.1093/aob/mcg187
PMID:14500324

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 oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(-)-Sweroside 161036 Click to see 358.34 unknown https://doi.org/10.1055/S-2005-871233
(3S,4R,4aS)-4-ethenyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-8-one 354447 Click to see 358.34 unknown https://doi.org/10.1055/S-2005-871233
4-ethenyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-8-one 581257 Click to see 358.34 unknown https://doi.org/10.1055/S-2005-871233
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[4-(hydroxymethyl)-2,6-dimethoxyphenoxy]oxan-2-yl]methoxy]oxane-3,4,5-triol 162977597 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)COC3C(C(C(C(O3)CO)O)O)O)O)O)O)OC)CO 508.50 unknown https://doi.org/10.1055/S-2005-871233
(2S,3R,4S,5S,6R)-2-[4-(hydroxymethyl)-2,6-dimethoxyphenoxy]-6-[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxane-3,4,5-triol 101565910 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)COC3C(C(C(CO3)O)O)O)O)O)O)OC)CO 478.40 unknown https://doi.org/10.1055/S-2005-871233
2-(4-Hydroxy-2,6-dimethoxyphenoxy)-6-(hydroxymethyl)oxane-3,4,5-triol 14237625 Click to see 332.30 unknown https://doi.org/10.1055/S-2005-871233
2-(Hydroxymethyl)-6-[[3,4,5-trihydroxy-6-[4-(hydroxymethyl)-2,6-dimethoxyphenoxy]oxan-2-yl]methoxy]oxane-3,4,5-triol 162977596 Click to see 508.50 unknown https://doi.org/10.1055/S-2005-871233
2-(Hydroxymethyl)-6-[4-(hydroxymethyl)-2,6-dimethoxyphenoxy]oxane-3,4,5-triol 13965334 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)CO 346.33 unknown https://doi.org/10.1055/S-2005-871233
2-[4-(Hydroxymethyl)-2,6-dimethoxyphenoxy]-6-[(3,4,5-trihydroxyoxan-2-yl)oxymethyl]oxane-3,4,5-triol 162885109 Click to see 478.40 unknown https://doi.org/10.1055/S-2005-871233
Di-O-Methylcrenatin 10736338 Click to see 346.33 unknown https://doi.org/10.1055/S-2005-871233
Leonuriside 14237626 Click to see 332.30 unknown https://doi.org/10.1055/S-2005-871233

Gallery Top

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Contributors Top

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Collections Top

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