Krameria lappacea - Unknown
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Internal ID UUID6440472d9eced319953924
Scientific name Krameria lappacea
Authority (Dombey) Burdet & B.B.Simpson
First published in Candollea 38: 96 (1983)

Description Top

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Synonyms Top

Scientific name Authority First published in
Krameria illuca Phil. Fl. Atacam. : 9 (1860)
Krameria pentapetala Ruiz & Pav. Fl. Peruv. 1: 62 (1798)
Krameria triandra Ruiz & Pav. Fl. Peruv. 1: 61 (1798)
Krameria triandra var. humboldtiana Chodat Biblioth. Universelle Rev. Suisse , sér. 3, 24: 498 (1890)
Krameria canescens Willd. Mant. 3: 303 (1827)
Landia lappacea Dombey J. Sçavans (Paris, 4) 1784(1): 382. [Jan 1784]

Common names Top

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Language Common/alternative name
Spanish raíz para los dientes
Spanish ratania
Spanish ratania del perú
Spanish ratania del peru
Spanish ratania de payta
Spanish raiz para los dientes
Spanish pumacuchu
Spanish mapato
Spanish landia lappacea
Spanish krameria linearis
Spanish krameria canescens
Spanish krameria pentapetala
Spanish krameria iluca
Spanish krameria triandra
Arabic رطن عقدي
German ratanhia
Finnish punaratania
French ratanhia
Hebrew רתניה פרואנית
Quechua krameria triandria
Quechua pachalluq'i
Quechua krameria triandra
Russian landia lappacea
Russian krameria triandra var. humboldtiana
Russian krameria linearis
Russian krameria pentapetala
Russian krameria triandra

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Southern America
    • Southern South America
      • Argentina Northwest
      • Chile Central
      • Chile North
    • Western South America
      • Bolivia
      • Ecuador
      • Peru

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001069555
UNII 97AC37R8BM
Tropicos 17200083
KEW urn:lsid:ipni.org:names:912741-1
The Plant List tro-17200083
Open Tree Of Life 946864
NCBI Taxonomy 228636
IPNI 912741-1
iNaturalist 704668
GBIF 5687593
Freebase /m/09rw15x
EOL 5491877
USDA GRIN 402605
Wikipedia Krameria_lappacea
CMAUP NPO15400

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
Synthesis of Green Copper Nanoparticles Using Medicinal Plant Krameria sp. Root Extract and Its Applications Alshammari SO, Mahmoud SY, Farrag ES Molecules 08-Jun-2023
PMCID:PMC10301159
doi:10.3390/molecules28124629
PMID:37375184
Chemical Profile and Biological Effects of an Herbal Mixture for the Development of an Oil-in-Water Cream Safta DA, Ielciu I, Șuștic R, Hanganu D, Niculae M, Cenariu M, Pall E, Moldovan ML, Achim M, Bogdan C, Tomuță I Plants (Basel) 05-Jan-2023
PMCID:PMC9861053
doi:10.3390/plants12020248
PMID:36678961
Safety and Efficacy of Medicinal Plants Used to Manufacture Herbal Products with Regulatory Approval in Uganda: A Cross-Sectional Study Kaggwa B, Kyeyune H, Munanura EI, Anywar G, Lutoti S, Aber J, Bagoloire LK, Weisheit A, Tolo CU, Kamba PF, Ogwang PE Evid Based Complement Alternat Med 13-Apr-2022
PMCID:PMC9020950
doi:10.1155/2022/1304839
PMID:35463071
Evaluating Tannins and Flavonoids from Traditionally Used Medicinal Plants with Biofilm Inhibitory Effects against MRGN E. coli Neumann N, Honke M, Povydysh M, Guenther S, Schulze C Molecules 31-Mar-2022
PMCID:PMC9000218
doi:10.3390/molecules27072284
PMID:35408683
Identification of Insulin-Mimetic Plant Extracts: From an In Vitro High-Content Screen to Blood Glucose Reduction in Live Animals Stadlbauer V, Neuhauser C, Aumiller T, Stallinger A, Iken M, Weghuber J Molecules 18-Jul-2021
PMCID:PMC8303208
doi:10.3390/molecules26144346
PMID:34299620
Correction: Genovese et al. In Vitro Antibacterial, Anti-Adhesive and Anti-Biofilm Activities of Krameria lappacea (Dombey) Burdet & B.B. Simpson Root Extract against Methicillin-Resistant Staphylococcus aureus Strains. Antibiotics 2021, 10, 428 Genovese C, D’Angeli F, Bellia F, Distefano A, Spampinato M, Attanasio F, Nicolosi D, Di Salvatore V, Tempera G, Lo Furno D, Mannino G, Milardo F, Li Volti G Antibiotics (Basel) 30-Jun-2021
PMCID:PMC8300609
doi:10.3390/antibiotics10070799
PMID:34209470
Sensitivity of Staphylococcal Biofilm to Selected Compounds of Plant Origin Swolana D, Kępa M, Kabała-Dzik A, Dzik R, Wojtyczka RD Antibiotics (Basel) 20-May-2021
PMCID:PMC8161300
doi:10.3390/antibiotics10050607
PMID:34065384
Sustainability of wild plant use in the Andean Community of South America Kor L, Homewood K, Dawson TP, Diazgranados M Ambio 16-Apr-2021
PMCID:PMC8285437
doi:10.1007/s13280-021-01529-7
PMID:33861399
In Vitro Antibacterial, Anti-Adhesive and Anti-Biofilm Activities of Krameria lappacea (Dombey) Burdet & B.B. Simpson Root Extract against Methicillin-Resistant Staphylococcus aureus Strains Genovese C, D’Angeli F, Bellia F, Distefano A, Spampinato M, Attanasio F, Nicolosi D, Di Salvatore V, Tempera G, Lo Furno D, Mannino G, Milardo F, Li Volti G Antibiotics (Basel) 13-Apr-2021
PMCID:PMC8069196
doi:10.3390/antibiotics10040428
PMID:33924336
Anticancer efficacies of Krameria lappacea extracts against human breast cancer cell line (MCF-7): Role of oxidative stress and ROS generation Al-Oqail MM Saudi Pharm J 10-Feb-2021
PMCID:PMC8084728
doi:10.1016/j.jsps.2021.01.008
PMID:33981173
Structural Features Defining NF-κB Inhibition by Lignan-Inspired Benzofurans and Benzothiophenes Dao-Huy T, Latkolik S, Bräuer J, Pfeil A, Stuppner H, Schnürch M, Dirsch VM, Mihovilovic MD Biomolecules 31-Jul-2020
PMCID:PMC7463992
doi:10.3390/biom10081131
PMID:32751917
How to bridge the gap? European medical plants used for treating oral mucositis: on the search for evidence Buentzel J, Bauer C, Buentzel J J Cancer Res Clin Oncol 18-Jan-2020
PMCID:PMC7085484
doi:10.1007/s00432-020-03124-x
PMID:31955287
ChemInform Abstract: Isolation and Structure Determination of New Active Neolignans and Norneolignans from Ratanhia. A. ARNONE, V. DI MODUGNO, G. NASINI, I. VENTURINI Wiley 24-May-2016
doi:10.1002/CHIN.198913315
Drugs from nature targeting inflammation (DNTI): a successful Austrian interdisciplinary network project Waltenberger B, Atanasov AG, Heiss EH, Bernhard D, Rollinger JM, Breuss JM, Schuster D, Bauer R, Kopp B, Franz C, Bochkov V, Mihovilovic MD, Dirsch VM, Stuppner H Monatsh Chem 25-Feb-2016
PMCID:PMC4785209
doi:10.1007/s00706-015-1653-y
PMID:27069281
Regulation of AMP-activated protein kinase by natural and synthetic activators Grahame Hardie D Acta Pharm Sin B 21-Jul-2015
PMCID:PMC4724661
doi:10.1016/j.apsb.2015.06.002
PMID:26904394

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 / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
3,4-Dihydroxy-5-methoxybenzoic acid 19829 Click to see COC1=CC(=CC(=C1O)O)C(=O)O 184.15 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,7-epoxylignans
(-)-Larreatricin 26389403 Click to see CC1C(C(OC1C2=CC=C(C=C2)O)C3=CC=C(C=C3)O)C 284.30 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3162300/
4-[5-(4-Hydroxyphenyl)-3,4-dimethyloxolan-2-yl]phenol 14213222 Click to see CC1C(C(OC1C2=CC=C(C=C2)O)C3=CC=C(C=C3)O)C 284.30 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3162300/
Meso-3,3'-Didemethoxynectandrin B 14213224 Click to see CC1C(C(OC1C2=CC=C(C=C2)O)C3=CC=C(C=C3)O)C 284.30 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3162300/
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
1,3-Benzenediol, 4-[5-(1-propenyl)-2-benzofuranyl]-, (E)- 54300595 Click to see CC=CC1=CC2=C(C=C1)OC(=C2)C3=C(C=C(C=C3)O)O 266.29 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3162300/
2-(2-Hydroxy-4-methoxyphenyl)-5-(3-hydroxypropyl)benzofuran 14213211 Click to see COC1=CC(=C(C=C1)C2=CC3=C(O2)C=CC(=C3)CCCO)O 298.30 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3162300/
2-(4-hydroxyphenyl)-5-(E)-propenylbenzofuran 53483951 Click to see CC=CC1=CC2=C(C=C1)OC(=C2)C3=CC=C(C=C3)O 250.29 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3162300/
2-(4-Methoxyphenyl)-5-(1-propenyl)benzofuran 91991396 Click to see CC=CC1=CC2=C(C=C1)OC(=C2)C3=CC=C(C=C3)OC 264.30 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3162300/
2-(4-Methoxyphenyl)-5-prop-1-enyl-1-benzofuran 129650689 Click to see CC=CC1=CC2=C(C=C1)OC(=C2)C3=CC=C(C=C3)OC 264.30 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3162300/
4-(3-Methyl-5-prop-1-enyl-1-benzofuran-2-yl)phenol 3001232 Click to see CC=CC1=CC2=C(C=C1)OC(=C2C)C3=CC=C(C=C3)O 264.30 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3162300/
4-(3-Methyl-5-prop-1-enyl-2,3-dihydro-1-benzofuran-2-yl)phenol 70414118 Click to see CC=CC1=CC2=C(C=C1)OC(C2C)C3=CC=C(C=C3)O 266.30 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3162300/
4-(5-Prop-1-enyl-1-benzofuran-2-yl)phenol 76044967 Click to see CC=CC1=CC2=C(C=C1)OC(=C2)C3=CC=C(C=C3)O 250.29 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3162300/
4-[(2S,3R)-3-(hydroxymethyl)-5-[(E)-prop-1-enyl]-2,3-dihydro-1-benzofuran-2-yl]phenol 71460125 Click to see CC=CC1=CC2=C(C=C1)OC(C2CO)C3=CC=C(C=C3)O 282.30 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3162300/
4-[(2S,3R)-3-(hydroxymethyl)-5-prop-1-enyl-2,3-dihydro-1-benzofuran-2-yl]phenol 162896019 Click to see CC=CC1=CC2=C(C=C1)OC(C2CO)C3=CC=C(C=C3)O 282.30 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3162300/
4-{5-[(1E)-prop-1-en-1-yl]-1-benzofuran-2-yl}benzene-1,3-diol 10355545 Click to see CC=CC1=CC2=C(C=C1)OC(=C2)C3=C(C=C(C=C3)O)O 266.29 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3162300/
5-(3-Hydroxypropyl)-2-(2-methoxy-4-hydroxyphenyl)benzofuran 14213209 Click to see COC1=C(C=CC(=C1)O)C2=CC3=C(O2)C=CC(=C3)CCCO 298.30 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3162300/
5-Methoxy-2-(5-prop-1-enyl-1-benzofuran-2-yl)phenol 157488 Click to see CC=CC1=CC2=C(C=C1)OC(=C2)C3=C(C=C(C=C3)OC)O 280.30 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3162300/
Conocarpan 10999992 Click to see CC=CC1=CC2=C(C=C1)OC(C2C)C3=CC=C(C=C3)O 266.30 unknown https://doi.org/10.1002/CHIN.198913315
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3162300/
Eupomatenoid 6 6261723 Click to see CC=CC1=CC2=C(C=C1)OC(=C2C)C3=CC=C(C=C3)O 264.30 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3162300/
https://doi.org/10.1002/CHIN.198913315
Rataniaphenol I 6440631 Click to see CC=CC1=CC2=C(C=C1)OC(=C2)C3=C(C=C(C=C3)OC)O 280.30 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3162300/
https://doi.org/10.1002/CHIN.198913315
Rataniaphenol III 14213215 Click to see CC=CC1=CC2=C(C=C1)OC(=C2)C3=C(C=C(C=C3)O)OC 280.30 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3162300/
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Isoquercetin 5280804 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
kaempferol 3-O-beta-L-glucopyranoside 9911508 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database

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