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Mimosa hamata

Mimosa hamata - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID643fd99b0905f060552756
Scientific name Mimosa hamata
Authority Willd.
First published in Sp. Pl., ed. 4, 4: 1033 (1806)

Description Top

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Synonyms Top

Scientific name Authority First published in
Mimosa hemata Willd.
Mimosa armata Rottler ex Spreng. Syst. Veg. ed. 16, 2: 206 (1825)

Common names Top

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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
  • Asia-tropical
    • Indian Subcontinent
      • India
      • Pakistan
    • Indo-China
      • Andaman Islands

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000186329
Tropicos 13065554
KEW urn:lsid:ipni.org:names:508092-1
The Plant List ild-32771
Open Tree Of Life 20231
NCBI Taxonomy 648363
IPNI 508092-1
GBIF 2969258
Freebase /m/09ghw6_
EOL 643932
USDA GRIN 70447
Wikipedia Mimosa_hamata

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
Biogenic Synthesis of Copper Nanoparticles: A Systematic Review of Their Features and Main Applications Luque-Jacobo CM, Cespedes-Loayza AL, Echegaray-Ugarte TS, Cruz-Loayza JL, Cruz I, de Carvalho JC, Goyzueta-Mamani LD Molecules 18-Jun-2023
PMCID:PMC10301071
doi:10.3390/molecules28124838
PMID:37375393
Phytochemistry and Diverse Pharmacology of Genus Mimosa: A Review Rizwan K, Majeed I, Bilal M, Rasheed T, Shakeel A, Iqbal S Biomolecules 05-Jan-2022
PMCID:PMC8773851
doi:10.3390/biom12010083
PMID:35053231
A Comprehensive Review of the Ethnotraditional Uses and Biological and Pharmacological Potential of the Genus Mimosa Majeed I, Rizwan K, Ashar A, Rasheed T, Amarowicz R, Kausar H, Zia-Ul-Haq M, Marceanu LG Int J Mol Sci 12-Jul-2021
PMCID:PMC8307580
doi:10.3390/ijms22147463
PMID:34299082
Important Flavonoids and Their Role as a Therapeutic Agent Ullah A, Munir S, Badshah SL, Khan N, Ghani L, Poulson BG, Emwas AH, Jaremko M Molecules 11-Nov-2020
PMCID:PMC7697716
doi:10.3390/molecules25225243
PMID:33187049
Specificity in Legume-Rhizobia Symbioses Andrews M, Andrews ME Int J Mol Sci 26-Mar-2017
PMCID:PMC5412291
doi:10.3390/ijms18040705
PMID:28346361
Multifunctional oxidosqualene cyclases and cytochrome P450 involved in the biosynthesis of apple fruit triterpenic acids Andre CM, Legay S, Deleruelle A, Nieuwenhuizen N, Punter M, Brendolise C, Cooney JM, Lateur M, Hausman J, Larondelle Y, Laing WA New Phytol 23-May-2016
PMCID:PMC5089662
doi:10.1111/nph.13996
PMID:27214242
Genome sequence of Ensifer sp. TW10; a Tephrosia wallichii (Biyani) microsymbiont native to the Indian Thar Desert Tak N, Gehlot HS, Kaushik M, Choudhary S, Tiwari R, Tian R, Hill Y, Bräu L, Goodwin L, Han J, Liolios K, Huntemann M, Palaniappan K, Pati A, Mavromatis K, Ivanova N, Markowitz V, Woyke T, Kyrpides N, Reeve W Stand Genomic Sci 15-Dec-2013
PMCID:PMC4062627
doi:10.4056/sigs.4598281
PMID:24976887
An invasive Mimosa in India does not adopt the symbionts of its native relatives Gehlot HS, Tak N, Kaushik M, Mitra S, Chen WM, Poweleit N, Panwar D, Poonar N, Parihar R, Tak A, Sankhla IS, Ojha A, Rao SR, Simon MF, dos Reis Junior FB, Perigolo N, Tripathi AK, Sprent JI, Young JP, James EK, Gyaneshwar P Ann Bot 26-May-2013
PMCID:PMC3690997
doi:10.1093/aob/mct112
PMID:23712450
Monocyclic Phenolic Acids; Hydroxy- and Polyhydroxybenzoic Acids: Occurrence and Recent Bioactivity Studies Khadem S, Marles RJ Molecules 08-Nov-2010
PMCID:PMC6259451
doi:10.3390/molecules15117985
PMID:21060304
ChemInform Abstract: Saponins from the Roots of Mimosa hamata Willd. R. JAIN, R. ARORA, S. C. JAIN Wiley 06-Aug-2010
doi:10.1002/CHIN.199740223
4-Ethylgallic acid from two Mimosa species B.K. Mehta, Km. Savita Sharma, Avinash Dubey Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(88)80713-1
Antimicrobial principles in Mimosa hamata. Hussain N, Modan MH, Shabbir SG, Zaidi SA J Nat Prod 01-Sep-1979
doi:10.1021/NP50005A014
PMID:521821

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 / Gallic acids
Gallic Acid 370 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)O 170.12 unknown https://doi.org/10.1021/NP50005A014
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
Methyl gallate 7428 Click to see COC(=O)C1=CC(=C(C(=C1)O)O)O 184.15 unknown https://doi.org/10.1021/NP50005A014
> 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/10.1002/CHIN.199740223
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/10.1002/CHIN.199740223
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/10.1002/CHIN.199740223
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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/10.1002/CHIN.199740223
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
4-Ethyl-3,4,5-trihydroxycyclohexa-1,5-diene-1-carboxylic acid 163192760 Click to see CCC1(C(C=C(C=C1O)C(=O)O)O)O 200.19 unknown https://doi.org/10.1016/0031-9422(88)80713-1

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