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Internal ID UUID643fd69272da5536373451
Scientific name Mimosa zimapanensis
Authority Britton & Rose

Ethnobotanical Use Top

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General Uses Top

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Scientific and model-organism use:
Sequenced reference genome available (NCBI BioProject PRJNA794498), enabling comparative legume genomics, nodulation gene studies, and drought-adaptation research. Maintained in ex situ collections (e.g., national herbaria and botanic garden networks) for long-term conservation and voucher specimens supporting taxonomic and ecological research. Used in field and greenhouse experiments to test seed dormancy, germination, and seedling establishment in semi-arid habitats, with data contributed to databases and community resources focused on dryland restoration and plant-trait phenotyping.

Properties relevant to use:
Genomic and physiological data indicate capacity for nitrogen fixation, water-use efficiency, and rapid post-disturbance growth, supporting applications in restoration trials, erosion control, and land rehabilitation studies in temperate xeric and montane regions.

Sustainability and sourcing:
Populations occur across central Mexico, with occurrence in the Sierra Madre Oriental. Codes of practice for seed collection and ex situ conservation (e.g., national botanical garden standards, BGCI guidelines) apply; post-2020 IUCN Red List assessments are not available; commercial use is not documented. If procurement for research occurs, follow regional conservation policies and permit requirements.

Synonyms Top

No known synonyms.

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Subspecies (abbr. subsp./ssp.) 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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000169866
Tropicos 13016627
KEW urn:lsid:ipni.org:names:162076-2
The Plant List ild-16170
IPNI 162076-2
iNaturalist 279343
GBIF 2970296
EOL 639179
Open Tree Of Life 530242

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)!
Title Authors Publication Released IDs
Two diterpene rhamnosides, mimosasides B and C, from Mimosa hostilis. Ohsaki A, Yokoyama R, Miyatake H, Fukuyama Y Chem Pharm Bull (Tokyo) 01-Dec-2006
doi:10.1248/CPB.54.1728
PMID:17139112
Effects of saponins from <i>Mimosa tenuiflora</i> on lymphoma cells and lymphocytes Yulin Jiang, Bernard Weniger, Micheline Haag‐Berrurier, Robert Anton, Jean‐Paul Beck, Liliane Italiano Wiley 18-Oct-2006
doi:10.1002/PTR.2650060606
Structure of a New Saponin from the Bark of Mimosa tenuiflora Yulin Jiang, Micheline Haag-Berrurier, Robert Anton, Georges Massiot, Catherine Lavaud, Jean-Marie Teulon, Christophe Guéchot American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50077A002
Tenuiflorins A-C: new 2-phenoxychromones from the leaves of Mimosa tenuiflora. León L, Maldonado E, Cruz A, Ortega A Planta Med 01-Jun-2004
doi:10.1055/S-2004-827154
PMID:15229805
Pharmacognosy of Mimosa tenuiflora (Willd.) Poiret. Anton R, Jiang Y, Weniger B, Beck JP, Rivier L J Ethnopharmacol 01-Mar-1993
doi:10.1016/0378-8741(93)90010-3
PMID:8510463
Triterpenoid glycosides from the bark of Mimosa tenuiflora. Jiang YL, Massiot G, Lavaud C, Teulon JM, Guéchot C, Haag-Berrurier M, Anton R Phytochemistry 01-Jan-1991
doi:10.1016/0031-9422(91)83648-5
PMID:1367651

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 / Terpene glycosides / Triterpene glycosides / Triterpene saponins
Mimonoside A 164386 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(C(OC(C3O)OC4C(C(C(OC4OC5CCC6(C(C5(C)C)CCC7(C6CC=C8C7(CCC9(C8CC(CC9)(C)C)C(=O)OC1C(C(C(C(O1)C)O)O)O)C)C)C)CO)OC1C(C(C(CO1)O)O)O)O)C1C(C(C(CO1)O)O)O)O)CO)O)O)O)O)O 1469.60 unknown https://doi.org/10.1016/0378-8741(93)90010-3
https://doi.org/10.1016/0031-9422(91)83648-5
https://doi.org/10.1002/PTR.2650060606
Mimonoside B 164387 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(C(OC(C3O)OC4C(C(C(OC4OC5CCC6(C(C5(C)C)CCC7(C6CC=C8C7(CCC9(C8CC(CC9)(C)C)C(=O)O)C)C)C)CO)OC1C(C(C(CO1)O)O)O)O)C1C(C(C(CO1)O)O)O)O)CO)O)O)O)O)O 1323.50 unknown https://doi.org/10.1016/0378-8741(93)90010-3
https://doi.org/10.1002/PTR.2650060606
https://doi.org/10.1016/0031-9422(91)83648-5
Mimonoside C 178435 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(COC(C3O)OC4C(C(C(OC4OC5CCC6(C(C5(C)C)CCC7(C6CC=C8C7(CCC9(C8CC(C(C9)O)(C)C)C(=O)OC1C(C(C(C(O1)C)O)O)O)C)C)C)CO)OC1C(C(C(CO1)O)O)O)O)OC1C(C(C(CO1)O)O)O)CO)O)O)O)O)O 1485.60 unknown https://doi.org/10.1021/NP50077A002
https://doi.org/10.1002/PTR.2650060606
https://doi.org/10.1016/0378-8741(93)90010-3
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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/10.1016/0378-8741(93)90010-3
https://doi.org/10.1016/0031-9422(91)83648-5
Stigmasterol Glucoside 6602508 Click to see 574.80 unknown https://doi.org/10.1016/0378-8741(93)90010-3
https://doi.org/10.1016/0031-9422(91)83648-5
> Phenylpropanoids and polyketides / Coumarins and derivatives
4H-1-Benzopyran-4-one, 5,7-dihydroxy-2-(4-methoxyphenoxy)- 5316512 Click to see 300.26 unknown https://doi.org/10.1055/S-2004-827154
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-4H-chromen-4-one 667495 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown https://doi.org/10.1248/CPB.54.1728
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown https://doi.org/10.1248/CPB.54.1728
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
(R)-Isosakuranetin 1149877 Click to see 286.28 unknown https://doi.org/10.1248/CPB.54.1728
2,3-Dihydro-5,7-dihydroxy-2-(4-methoxyphenyl)-4H-1-benzopyran-4-one 5118250 Click to see 286.28 unknown https://doi.org/10.1248/CPB.54.1728
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
4'-5-Dihydroxy-7-methoxyflavanone, 7-O-Methylnaringenin, Naringenin 7-O-methyl ether 348130 Click to see 286.28 unknown https://doi.org/10.1248/CPB.54.1728
Artocarpanone 15298902 Click to see 302.28 unknown https://doi.org/10.1248/CPB.54.1728
Genkwanin 5281617 Click to see 284.26 unknown https://doi.org/10.1248/CPB.54.1728
Isoflavone, 2',4',5-trihydroxy-7-methoxy- 12000157 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=C(C=C(C=C3)O)O)O 302.28 unknown https://doi.org/10.1248/CPB.54.1728
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
4'-Hydroxywogonin 5322078 Click to see COC1=C(C=C(C2=C1OC(=CC2=O)C3=CC=C(C=C3)O)O)O 300.26 unknown https://doi.org/10.1248/CPB.54.1728
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
(2E)-1-(2,5-dihydroxyphenyl)-3-(4-hydroxyphenyl)prop-2-en-1-one 5980988 Click to see 256.25 unknown https://doi.org/10.1248/CPB.54.1728
(2E)-1-(2,6-Dihydroxy-4-methoxyphenyl)-3-(4-methoxyphenyl)-2-propen-1-one 6438580 Click to see 300.30 unknown https://doi.org/10.1248/CPB.54.1728
1-(2,6-Dihydroxy-4-methoxyphenyl)-3-(4-methoxyphenyl)prop-2-en-1-one 125157 Click to see 300.30 unknown https://doi.org/10.1248/CPB.54.1728
2',4'-Dihydroxy-4-methoxychalcone 5711223 Click to see COC1=CC=C(C=C1)C=CC(=O)C2=C(C=C(C=C2)O)O 270.28 unknown https://doi.org/10.1248/CPB.54.1728
2a(2),4a(2)-Dihydroxy-4-methoxychalcone 166795 Click to see 270.28 unknown https://doi.org/10.1248/CPB.54.1728

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