Phytolacca tetramera - Unknown
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Internal ID UUID64404a3f8f8af942891186
Scientific name Phytolacca tetramera
Authority Hauman
First published in Apuntes Hist. Nat. 1: 108 (1909)

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

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Database ID/link to page
World Flora Online wfo-0001091525
Tropicos 24800029
KEW urn:lsid:ipni.org:names:195838-2
The Plant List tro-24800029
Open Tree Of Life 5729071
NCBI Taxonomy 1580012
IPNI 195838-2
iNaturalist 823436
GBIF 4192745

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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
The effects of Ziziphus Spina leaves’ Hydro-Alcoholic Extract Vaginal Cream and Clotrimazole on Candida albicans in Wistar Rats Honarmandpour A, Fatahinia M, Masoud Keshavarzzade A, Namjoyan F, Maraghi E, Kamali H Clin Pathol 21-Nov-2022
PMCID:PMC9685217
doi:10.1177/2632010X221138664
PMID:36438542
The anti‐Trypanosoma activities of medicinal plants: A systematic review of the literature Nekoei S, Khamesipour F, Habtemariam S, de Souza W, Mohammadi Pour P, Hosseini SR Vet Med Sci 29-Aug-2022
PMCID:PMC9677405
doi:10.1002/vms3.912
PMID:36037401
Present scenarios and future prospects of herbal nanomedicine for antifungal therapy Yadav R, Pradhan M, Yadav K, Mahalvar A, Yadav H J Drug Deliv Sci Technol 13-May-2022
PMCID:PMC9101776
doi:10.1016/j.jddst.2022.103430
PMID:35582019
Edible Leafy Plants from Mexico as Sources of Antioxidant Compounds, and Their Nutritional, Nutraceutical and Antimicrobial Potential: A Review Mateos-Maces L, Chávez-Servia JL, Vera-Guzmán AM, Aquino-Bolaños EN, Alba-Jiménez JE, Villagómez-González BB Antioxidants (Basel) 20-Jun-2020
PMCID:PMC7346153
doi:10.3390/antiox9060541
PMID:32575671
Early State Research on Antifungal Natural Products Negri M, Salci TP, Shinobu-Mesquita CS, Capoci IR, Svidzinski TI, Seki Kioshima E Molecules 07-Mar-2014
PMCID:PMC6271505
doi:10.3390/molecules19032925
PMID:24609016
Characterization of in vivo anti-rotavirus activities of saponin extracts from Quillaja Saponaria Molina Tam KI, Roner MR Antiviral Res 23-Apr-2011
PMCID:PMC3106224
doi:10.1016/j.antiviral.2011.04.004
PMID:21549151
Evidence for the mechanism of action of the antifungal phytolaccoside B isolated from Phytolacca tetramera Hauman. Escalante A, Gattuso M, Pérez P, Zacchino S J Nat Prod 01-Oct-2008
doi:10.1021/NP070660I
PMID:18816139
Isolation of antifungal saponins from Phytolacca tetramera, an Argentinean species in critic risk. Escalante AM, Santecchia CB, López SN, Gattuso MA, Gutiérrez Ravelo A, Delle Monache F, Gonzalez Sierra M, Zacchino SA J Ethnopharmacol 01-Sep-2002
doi:10.1016/S0378-8741(02)00145-9
PMID:12169402

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
(2S,4aR,6aR,6aS,6bR,8aR,9R,10R,11S,12aR,14bS)-11-hydroxy-9-(hydroxymethyl)-2-methoxycarbonyl-2,6a,6b,9,12a-pentamethyl-10-[(2S,3R,4S,5R)-3,4,5-trihydroxytetrahydropyran-2-yl]oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 118701276 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)OC6C(C(C(CO6)O)O)O)O)C)C)C2C1)C)C(=O)O)C(=O)OC 664.80 unknown https://doi.org/10.1016/S0378-8741(02)00145-9
https://doi.org/10.1021/NP070660I
(2S,4aR,6aR,6aS,6bR,8aR,9R,10R,11S,12aR,14bS)-11-hydroxy-9-(hydroxymethyl)-2-methoxycarbonyl-2,6a,6b,9,12a-pentamethyl-10-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 154496543 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)OC6C(C(C(CO6)O)O)O)O)C)C)C2C1)C)C(=O)O)C(=O)OC 664.80 unknown https://doi.org/10.1021/NP070660I
(2S,4aR,6aR,6aS,6bR,8aR,9R,10S,12aR,14bS)-10-[(2S,3R,4S,5R)-3-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-9-(hydroxymethyl)-2-methoxycarbonyl-2,6a,6b,9,12a-pentamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 101920260 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(C(COC3OC4CCC5(C(C4(C)CO)CCC6(C5CC=C7C6(CCC8(C7CC(CC8)(C)C(=O)OC)C(=O)O)C)C)C)O)O)CO)O)O)O)O)O 957.10 unknown https://doi.org/10.1016/S0378-8741(02)00145-9
(2S,4aS,6aR,6aS,6bR,8aR,9R,10R,11S,12aR,14bS)-10-[(2S,3S,4R,5S)-3,4-dihydroxy-5-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-11-hydroxy-9-(hydroxymethyl)-2-methoxycarbonyl-2,6a,6b,9,12a-pentamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 154497218 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)OC6C(C(C(CO6)OC7C(C(C(C(O7)CO)O)O)O)O)O)O)C)C)C2C1)C)C(=O)O)C(=O)OC 827.00 unknown https://doi.org/10.1021/NP070660I
Esculentoside A 125210 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)OC6COC(C(C6O)O)OC7C(C(C(C(O7)CO)O)O)O)O)C)C)C2C1)C)C(=O)O)C(=O)OC 827.00 unknown https://doi.org/10.1021/NP070660I
https://doi.org/10.1016/S0378-8741(02)00145-9
Phytolaccoside B 5070782 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)OC6C(C(C(CO6)O)O)O)O)C)C)C2C1)C)C(=O)O)C(=O)OC 664.80 unknown https://doi.org/10.1021/NP070660I
Phytolaccoside B 441939 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)OC6C(C(C(CO6)O)O)O)O)C)C)C2C1)C)C(=O)O)C(=O)OC 664.80 unknown https://doi.org/10.1021/NP070660I
https://doi.org/10.1016/S0378-8741(02)00145-9

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