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Micranthemum umbrosum

Micranthemum umbrosum - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Micranthemum umbrosum - 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 UUID643ffe281b052890215511
Scientific name Micranthemum umbrosum
Authority (J.F.Gmel.) S.F.Blake
First published in Rhodora 17: 131. 1915 Based on Anonymos umbrosus Walt. (invalid)

Description Top

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Synonyms Top

Scientific name Authority First published in
Anonymos umbrosa Walter Fl. 63.
Micranthemum pilosum Ernst Flora 57: 215 (1874)
Micranthemum orbiculatum Michx. Fl. Bor.-Amer. 1: 10 (1803)
Pinarda repens Vell. Fl. Flumin. 23. 1829 [1825 publ. 7 Sep-28 Nov 1829] ; see also Fl. Flumin. Icon. 1: t. 52. 1831. [1827 publ. 29 Oct 1831]
Globifera umbrosa J.F.Gmel. Syst. Nat., ed. 13[bis]. 2(1): 32. 1791 [late Sep-Nov 1791]
Micranthemum emarginatum Elliott Sketch Bot. S. Carolina 1: 18 (1816)
Micranthemum tweediei Benth. Prodr. 10: 423 (1846)
Micranthemum orbiculatum var. tweediei (Benth.) J.A.Schmidt Fl. Bras. 8(1): 288 (1862)
Micranthemum orbiculatum var. emarginatum C.Mohr Bull. Torrey Bot. Club 24(1): 26. 1897 [28 Jan 1897]

Common names Top

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Language Common/alternative name
English shade mudflower
Polish mikrantemum okrągłolistne
Chinese 矮婴泪草
Chinese 微花草
Chinese 矮小泥花草

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000450924
Flora of Alabama 3478
USDA Plants MIUM
Tropicos 29201062
INPN 630161
KEW urn:lsid:ipni.org:names:805826-1
The Plant List kew-2506433
Open Tree Of Life 1067215
NCBI Taxonomy 69918
Nature Serve 2.136384
IPNI 160014-2
iNaturalist 165372
GBIF 3172187
Freebase /m/0l8pcrf
EPPO MJCUM
EOL 578802
USDA GRIN 433118
CMAUP NPO2333

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
Diverse traits of aquatic plants cannot individually explain their consumption by the generalist gastropod Biomphalairia glabrata Pereira RC, Nocchi N, Konno TU, Soares AR PeerJ 20-Sep-2021
PMCID:PMC8459730
doi:10.7717/peerj.12031
PMID:34616600
Phytoremediation of Cadmium: Physiological, Biochemical, and Molecular Mechanisms Raza A, Habib M, Kakavand SN, Zahid Z, Zahra N, Sharif R, Hasanuzzaman M Biology (Basel) 21-Jul-2020
PMCID:PMC7407403
doi:10.3390/biology9070177
PMID:32708065
Microbial and plant-assisted heavy metal remediation in aquatic ecosystems: a comprehensive review Haldar S, Ghosh A 3 Biotech 20-Apr-2020
PMCID:PMC7171024
doi:10.1007/s13205-020-02195-4
PMID:32328403
Microbial and Plant-Assisted Bioremediation of Heavy Metal Polluted Environments: A Review Ojuederie OB, Babalola OO Int J Environ Res Public Health 04-Dec-2017
PMCID:PMC5750922
doi:10.3390/ijerph14121504
PMID:29207531
Methyl Eugenol: Its Occurrence, Distribution, and Role in Nature, Especially in Relation to Insect Behavior and Pollination Tan KH, Nishida R J Insect Sci 24-Apr-2012
PMCID:PMC3500151
doi:10.1673/031.012.5601
PMID:22963669
Towards resolving Lamiales relationships: insights from rapidly evolving chloroplast sequences Schäferhoff B, Fleischmann A, Fischer E, Albach DC, Borsch T, Heubl G, Müller KF BMC Evol Biol 12-Nov-2010
PMCID:PMC2992528
doi:10.1186/1471-2148-10-352
PMID:21073690
Structure-activity relationship of chemical defenses from the freshwater plant Micranthemum umbrosum. Lane AL, Kubanek J Phytochemistry 01-Jun-2006
doi:10.1016/J.PHYTOCHEM.2006.05.007
PMID:16793072
Chemical defenses promote persistence of the aquatic plant Micranthemum umbrosum. Parker JD, Collins DO, Kubanek J, Sullards MC, Bostwick D, Hay ME J Chem Ecol 01-Apr-2006
doi:10.1007/S10886-006-9038-7
PMID:16586032

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Benzyloxycarbonyls
bis[(4-hydroxyphenyl)methyl] (2S)-2-[(2S)-butan-2-yl]-2-hydroxybutanedioate 163106516 Click to see CCC(C)C(CC(=O)OCC1=CC=C(C=C1)O)(C(=O)OCC2=CC=C(C=C2)O)O 402.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.007
> Benzenoids / Benzene and substituted derivatives / Diphenylmethanes
bis(4-hydroxyphenyl)methyl (2R)-2-ethyl-2-hydroxy-4-methylpentanoate 100989770 Click to see CCC(CC(C)C)(C(=O)OC(C1=CC=C(C=C1)O)C2=CC=C(C=C2)O)O 358.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.007
> Benzenoids / Phenol ethers / Anisoles
Elemicin 10248 Click to see COC1=CC(=CC(=C1OC)OC)CC=C 208.25 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.007
https://doi.org/10.1007/S10886-006-9038-7
> Lignans, neolignans and related compounds / Dibenzylbutane lignans
(-)-Dihydroguaiaretic acid 11602375 Click to see CC(CC1=CC(=C(C=C1)O)OC)C(C)CC2=CC(=C(C=C2)O)OC 330.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.007
Sauriol A 15965507 Click to see CC(CC1=CC(=C(C(=C1)OC)O)O)C(C)CC2=CC(=C(C(=C2)OC)O)O 362.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.007
Sauriol B 15965508 Click to see CC(CC1=CC(=C(C(=C1)OC)O)O)C(C)CC2=CC(=C(C(=C2)OC)O)OC 376.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.007
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,7-epoxylignans
(1R,2S)-1-(3,4-dimethoxyphenyl)-2-[4-[(2S,3R,4S,5R)-5-(3,4-dimethoxyphenyl)-3,4-dimethyloxolan-2-yl]-2-methoxyphenoxy]propan-1-ol 163011447 Click to see CC1C(C(OC1C2=CC(=C(C=C2)OC)OC)C3=CC(=C(C=C3)OC(C)C(C4=CC(=C(C=C4)OC)OC)O)OC)C 552.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.007
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
(3S,4R)-3-[(S)-1,3-benzodioxol-5-yl(hydroxy)methyl]-4-[(3,4-dimethoxyphenyl)methyl]oxolan-2-one 163066875 Click to see COC1=C(C=C(C=C1)CC2COC(=O)C2C(C3=CC4=C(C=C3)OCO4)O)OC 386.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.007
https://doi.org/10.1007/S10886-006-9038-7
3-[1,3-Benzodioxol-5-yl(hydroxy)methyl]-4-[(3,4-dimethoxyphenyl)methyl]oxolan-2-one 163066874 Click to see COC1=C(C=C(C=C1)CC2COC(=O)C2C(C3=CC4=C(C=C3)OCO4)O)OC 386.40 unknown https://doi.org/10.1007/S10886-006-9038-7
4-(1,3-Benzodioxol-5-ylmethyl)-3-(1,3-benzodioxol-5-ylmethylidene)oxolan-2-one 98946 Click to see C1C(C(=CC2=CC3=C(C=C2)OCO3)C(=O)O1)CC4=CC5=C(C=C4)OCO5 352.30 unknown https://doi.org/10.1007/S10886-006-9038-7
Savinin 5281867 Click to see C1C(C(=CC2=CC3=C(C=C2)OCO3)C(=O)O1)CC4=CC5=C(C=C4)OCO5 352.30 unknown https://doi.org/10.1007/S10886-006-9038-7
https://doi.org/10.1016/J.PHYTOCHEM.2006.05.007
> Lignans, neolignans and related compounds / Lignan lactones / Podophyllotoxins
(5R,5aR,8aR,9S)-5-hydroxy-9-(3,4,5-trimethoxyphenyl)-5a,6,8a,9-tetrahydro-5H-[2]benzofuro[5,6-f][1,3]benzodioxol-8-one 11047943 Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(COC3=O)C(C4=CC5=C(C=C24)OCO5)O 414.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.007
Podofilox 10607 Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(COC3=O)C(C4=CC5=C(C=C24)OCO5)O 414.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.007
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
Phytol 5280435 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-alpha-Terpineol 442501 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Betulin 72326 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown via CMAUP database
Betulinic Acid 64971 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown via CMAUP database
Canophyllal 12302400 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C=O)C)C)C)C 440.70 unknown via CMAUP database
Epifriedelin 15559350 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown via CMAUP database
Friedelin 91472 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown via CMAUP database
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown via CMAUP database
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthofurans / Furanonaphthodioxoles
(5S)-5-(3,4,5-trimethoxyphenyl)-8,9-dihydro-5H-[2]benzofuro[5,6-f][1,3]benzodioxol-6-one 5319572 Click to see COC1=CC(=CC(=C1OC)OC)C2C3=CC4=C(C=C3CC5=C2C(=O)OC5)OCO4 396.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.007
5-(3,4,5-trimethoxyphenyl)-8,9-dihydro-5H-[2]benzofuro[5,6-f][1,3]benzodioxol-6-one 10408428 Click to see COC1=CC(=CC(=C1OC)OC)C2C3=CC4=C(C=C3CC5=C2C(=O)OC5)OCO4 396.40 unknown https://doi.org/10.1007/S10886-006-9038-7
https://doi.org/10.1016/J.PHYTOCHEM.2006.05.007
beta-Apopicropodophyllin 6452099 Click to see COC1=CC(=CC(=C1OC)OC)C2C3=CC4=C(C=C3CC5=C2C(=O)OC5)OCO4 396.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.007
https://doi.org/10.1007/S10886-006-9038-7
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
Licarin A 5281836 Click to see CC=CC1=CC2=C(C(=C1)OC)OC(C2C)C3=CC(=C(C=C3)O)OC 326.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.007

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