Madia sativa - Unknown
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Details Top

Internal ID UUID643fc8587178c529014909
Scientific name Madia sativa
Authority Molina
First published in Sag. Stor. Nat. Chili : 136 (1782)

Description Top

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Synonyms Top

Scientific name Authority First published in
Madia capitata Nutt. Trans. Amer. Philos. Soc. , ser. 2, 7: 386 (1841)
Madia mellita J.F.Gmel. Syst. Nat. ed. 13[bis] 2(2): 1249 (1792)
Madia polycarpaea E.H.L.Krause Beih. Bot. Centralbl. 32(2): 347 (1914)
Madia hirsuta Meyen Reise Erde 1: 311 (1834)
Madia sativa subsp. capitata Piper Contr. U.S. Natl. Herb. 11: 576 (1906)
Madorella racemosa Nutt. Trans. Amer. Philos. Soc. , ser. 2, 7: 387 (1841)
Madia viscosa Cav. Icon. iii. 50
Madia sativa var. congesta Torr. & A.Gray Fl. N. Amer. 2: 404 (1843)
Madia mellosa Molina Sag. Stor. Nat. Chili : 137 (1782)
Madia racemosa Torr. & A.Gray Fl. N. Amer. 2: 405 (1843)
Madia sativa subsp. congesta (Torr. & A.Gray) D.D.Keck in D.A.Johans. Bot. Gaz. 95: 204, 205 (1933)

Common names Top

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Language Common/alternative name
English coast tarweed
Arabic مادية
Czech madie setá
Polish maziczka siewna

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
  • Australasia
    • Australia
      • New South Wales
      • Victoria
      • Western Australia
  • Europe
    • Eastern Europe
      • Krym
      • Ukraine
    • Middle Europe
      • Belgium
      • Germany
    • Northern Europe
      • Ireland
      • Norway
    • Southwestern Europe
      • France
  • Northern America
    • Northeastern U.S.A.
      • New York
    • Northwestern U.S.A.
      • Oregon
      • Washington
    • Southeastern U.S.A.
      • Maryland
    • Southwestern U.S.A.
      • California
    • Western Canada
      • British Columbia
  • Southern America
    • Southern South America
      • Argentina Northwest
      • Argentina South
      • Chile Central
      • Chile North
      • Chile South
      • Juan Fernández Islands

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000021710
Canadensys 3301
USDA Plants MASA
Tropicos 2702884
INPN 107136
KEW urn:lsid:ipni.org:names:231627-1
The Plant List gcc-120995
PFAF Madia sativa
Open Tree Of Life 859745
Observations.org 142521
NCBI Taxonomy 149445
NBN Atlas NBNSYS0200002585
Nature Serve 2.144921
IPNI 231627-1
iNaturalist 53143
GBIF 3140910
Freebase /m/07s92zg
EPPO MADSA
EOL 820124
Calflora (Californian flora) 5298
USDA GRIN 23084
Wikipedia Madia_sativa

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
Pb uptake, accumulation, and translocation in plants: Plant physiological, biochemical, and molecular response: A review Ur Rahman S, Qin A, Zain M, Mushtaq Z, Mehmood F, Riaz L, Naveed S, Ansari MJ, Saeed M, Ahmad I, Shehzad M Heliyon 07-Mar-2024
PMCID:PMC10945279
doi:10.1016/j.heliyon.2024.e27724
PMID:38500979
Patterns of Traditional and Modern Uses of Wild Edible Native Plants of Chile: Challenges and Future Perspectives León-Lobos P, Díaz-Forestier J, Díaz R, Celis-Diez JL, Diazgranados M, Ulian T Plants (Basel) 11-Mar-2022
PMCID:PMC8953413
doi:10.3390/plants11060744
PMID:35336626
Comparative Inter- and IntraSpecies Transcriptomics Revealed Key Differential Pathways Associated With Aluminium Stress Tolerance in Lentil Singh CK, Singh D, Taunk J, Chaudhary P, Tomar RS, Chandra S, Singh D, Pal M, Konjengbam NS, Singh MP, Singh Sengar R, Sarker A Front Plant Sci 31-Aug-2021
PMCID:PMC8438445
doi:10.3389/fpls.2021.693630
PMID:34531881
Exchange of medicinal plant information in California missions McBride JR, Cavero RY, Cheshire AL, Calvo MI, McBride DL J Ethnobiol Ethnomed 15-Jun-2020
PMCID:PMC7296748
doi:10.1186/s13002-020-00388-y
PMID:32539795
Lead Toxicity: Health Hazards, Influence on Food Chain, and Sustainable Remediation Approaches Kumar A, Kumar A, M.M.S. CP, Chaturvedi AK, Shabnam AA, Subrahmanyam G, Mondal R, Gupta DK, Malyan SK, Kumar SS, A. Khan S, Yadav KK Int J Environ Res Public Health 25-Mar-2020
PMCID:PMC7177270
doi:10.3390/ijerph17072179
PMID:32218253
Dwarf shrub facilitates seedling recruitment and plant diversity in semiarid grasslands Gonzalez SL, Ghermandi L PLoS One 07-Feb-2019
PMCID:PMC6366867
doi:10.1371/journal.pone.0212058
PMID:30730964
Biologically active components in Madia sativa seed oil Antova GA, Angelova-Romova MY, Petkova ZY, Teneva OT, Marcheva MP, Zlatanov MD J Food Sci Technol 17-Jul-2017
PMCID:PMC5602966
doi:10.1007/s13197-017-2739-9
PMID:28974788
Biological screening of selected Pacific Northwest forest plants using the brine shrimp (Artemia salina) toxicity bioassay Karchesy YM, Kelsey RG, Constantine G, Karchesy JJ Springerplus 23-Apr-2016
PMCID:PMC4842189
doi:10.1186/s40064-016-2145-1
PMID:27186474
taxize: taxonomic search and retrieval in R Chamberlain SA, Szöcs E F1000Res 28-Oct-2013
PMCID:PMC3901538
doi:10.12688/f1000research.2-191.v1
PMID:24555091
Effect of external stress on density and size of glandular trichomes in full-grown Artemisia annua, the source of anti-malarial artemisinin Kjær A, Grevsen K, Jensen M AoB Plants 21-Jun-2012
PMCID:PMC3404549
doi:10.1093/aobpla/pls018
PMID:22833781
Monoterpenes of Salvia leucophylla Sakai A, Yoshimura H Curr Bioact Compd 01-Jan-2012
PMCID:PMC3382373
doi:10.2174/157340712799828205
PMID:22754426
Evolutionary diversification and geographical isolation in Dubautia laxa (Asteraceae), a widespread member of the Hawaiian silversword alliance McGlaughlin ME, Friar EA Ann Bot 30-Dec-2010
PMCID:PMC3043929
doi:10.1093/aob/mcq252
PMID:21193480
Repeated reunions and splits feature the highly dynamic evolution of 5S and 35S ribosomal RNA genes (rDNA) in the Asteraceae family Garcia S, Panero JL, Siroky J, Kovarik A BMC Plant Biol 16-Aug-2010
PMCID:PMC3095306
doi:10.1186/1471-2229-10-176
PMID:20712858
Seasonal variation in the range areas of the diurnal rodent Octodon degus Quirici V, Castro RA, Ortiz-Tolhuysen L, Chesh AS, Burger JR, Miranda E, Cortés A, Hayes LD, Ebensperger LA J Mammal 01-Jan-2010
PMCID:PMC3277432
doi:10.1644/08-MAMM-A-337.1
PMID:22328788
Women's Health Among the Chumash Adams JD Jr, Garcia C Evid Based Complement Alternat Med 01-Feb-2006
PMCID:PMC1375244
doi:10.1093/ecam/nek021
PMID:16550233

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 / Phenol esters
(2-{4-Methyl-2-[(2-methylpropanoyl)oxy]phenyl}oxiran-2-yl)methyl 2-methylbutanoate 354159 Click to see CCC(C)C(=O)OCC1(CO1)C2=C(C=C(C=C2)C)OC(=O)C(C)C 334.40 unknown https://doi.org/10.1016/S0031-9422(00)82425-5
[(2R)-2-[4-methyl-2-(2-methylpropanoyloxy)phenyl]oxiran-2-yl]methyl (2R)-2-methylbutanoate 163021373 Click to see CCC(C)C(=O)OCC1(CO1)C2=C(C=C(C=C2)C)OC(=O)C(C)C 334.40 unknown https://doi.org/10.1016/S0031-9422(00)82425-5
[(2R)-2-[4-methyl-2-(2-methylpropanoyloxy)phenyl]oxiran-2-yl]methyl 2-methylpropanoate 25837754 Click to see CC1=CC(=C(C=C1)C2(CO2)COC(=O)C(C)C)OC(=O)C(C)C 320.40 unknown https://doi.org/10.1016/S0031-9422(00)82425-5
[(2R)-2-[4-methyl-2-(2-methylpropanoyloxy)phenyl]oxiran-2-yl]methyl 3-methylbutanoate 163048262 Click to see CC1=CC(=C(C=C1)C2(CO2)COC(=O)CC(C)C)OC(=O)C(C)C 334.40 unknown https://doi.org/10.1016/S0031-9422(00)82425-5
3-(2-Methylpropanoyloxy)-8-(3-methylbutanoyloxy)-9,10-epoxy-p-mentha-1,3,5-triene 13819150 Click to see CC1=CC(=C(C=C1)C2(CO2)COC(=O)CC(C)C)OC(=O)C(C)C 334.40 unknown https://doi.org/10.1016/S0031-9422(00)82425-5
Bis(2-methylpropanoyloxy)-9,10-epoxy-p-mentha-1,3,5-triene 11472669 Click to see CC1=CC(=C(C=C1)C2(CO2)COC(=O)C(C)C)OC(=O)C(C)C 320.40 unknown https://doi.org/10.1016/S0031-9422(00)82425-5
> Hydrocarbons / Unsaturated hydrocarbons / Enynes
1-Tridecene-3,5,7,9,11-pentayne 441552 Click to see CC#CC#CC#CC#CC#CC=C 162.19 unknown https://doi.org/10.1016/S0031-9422(00)82425-5
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(13R,14R)-7-Labdene-13,14,15-triol 340130 Click to see CC1=CCC2C(CCCC2(C1CCC(C)(C(CO)O)O)C)(C)C 324.50 unknown https://doi.org/10.1016/S0031-9422(00)82425-5
(13R,14R)-8-Labdene-13,14,15-triol 14543666 Click to see CC1=C(C2(CCCC(C2CC1)(C)C)C)CCC(C)(C(CO)O)O 324.50 unknown https://doi.org/10.1016/S0031-9422(00)82425-5
(2R,3R)-5-[(1S,4aS,8aR)-2,5,5,8a-tetramethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl]-3-methylpentane-1,2,3-triol 162962550 Click to see CC1=CCC2C(CCCC2(C1CCC(C)(C(CO)O)O)C)(C)C 324.50 unknown https://doi.org/10.1016/S0031-9422(00)82425-5
(2R,3R)-5-[(1S,4aS,8aS)-2,5,5,8a-tetramethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl]-3-methylpentane-1,2,3-triol 91003193 Click to see CC1=CCC2C(CCCC2(C1CCC(C)(C(CO)O)O)C)(C)C 324.50 unknown https://doi.org/10.1016/S0031-9422(00)82425-5
(2R,3R)-5-[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpentane-1,2,3-triol 102252609 Click to see CC1(CCCC2(C1CCC(=C)C2CCC(C)(C(CO)O)O)C)C 324.50 unknown https://doi.org/10.1016/S0031-9422(00)82425-5
(2R,3R)-5-[(4aR,8aS)-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydronaphthalen-1-yl]-3-methylpentane-1,2,3-triol 162851746 Click to see CC1=C(C2(CCCC(C2CC1)(C)C)C)CCC(C)(C(CO)O)O 324.50 unknown https://doi.org/10.1016/S0031-9422(00)82425-5
(2R,3R)-5-[(4aS,8aS)-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydronaphthalen-1-yl]-3-methylpentane-1,2,3-triol 162851745 Click to see CC1=C(C2(CCCC(C2CC1)(C)C)C)CCC(C)(C(CO)O)O 324.50 unknown https://doi.org/10.1016/S0031-9422(00)82425-5
5-(5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl)-3-methylpentane-1,2,3-triol 14543668 Click to see CC1(CCCC2(C1CCC(=C)C2CCC(C)(C(CO)O)O)C)C 324.50 unknown https://doi.org/10.1016/S0031-9422(00)82425-5
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Lup-20(29)-en-3beta-ol, acetate 323074 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C 468.80 unknown https://doi.org/10.1016/S0031-9422(00)82425-5
Lupeol acetate 92157 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C 468.80 unknown https://doi.org/10.1016/S0031-9422(00)82425-5
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 122544 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/S0031-9422(00)82425-5
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/S0031-9422(00)82425-5
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
1-(5-Acetyl-2-hydroxyphenyl)-3-methylbut-2-en-1-one 14706939 Click to see CC(=CC(=O)C1=C(C=CC(=C1)C(=O)C)O)C 218.25 unknown https://doi.org/10.1016/S0031-9422(00)82425-5
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
1-(2,2-Dimethylchromen-6-yl)ethanone 177040 Click to see CC(=O)C1=CC2=C(C=C1)OC(C=C2)(C)C 202.25 unknown https://doi.org/10.1016/S0031-9422(00)82425-5
2-Hydroxy-1-(7-methoxy-2,2-dimethyl-2H-1-benzopyran-6-yl)ethan-1-one 71374358 Click to see CC1(C=CC2=CC(=C(C=C2O1)OC)C(=O)CO)C 248.27 unknown https://doi.org/10.1016/S0031-9422(00)82425-5
6-Acetyl-2,2-dimethylchroman-4-one 10398468 Click to see CC(=O)C1=CC2=C(C=C1)OC(CC2=O)(C)C 218.25 unknown https://doi.org/10.1016/S0031-9422(00)82425-5
Desacetylripariochromene B 14282640 Click to see CC1(C=CC2=CC(=C(C=C2O1)O)C(=O)CO)C 234.25 unknown https://doi.org/10.1016/S0031-9422(00)82425-5
Eupatoriochromene 100768 Click to see CC(=O)C1=C(C=C2C(=C1)C=CC(O2)(C)C)O 218.25 unknown https://doi.org/10.1016/S0031-9422(00)82425-5
> 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/10.1515/ZNC-2003-3-401
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Rhamnocitrin 5320946 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)O)C3=CC=C(C=C3)O)O 300.26 unknown https://doi.org/10.1016/0031-9422(92)80273-H
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Axillarin 5281603 Click to see COC1=C(C2=C(C=C1O)OC(=C(C2=O)OC)C3=CC(=C(C=C3)O)O)O 346.30 unknown https://doi.org/10.1016/0031-9422(92)80273-H
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
chrysoplenol D 5280699 Click to see COC1=C(C(=C2C(=C1)OC(=C(C2=O)OC)C3=CC(=C(C=C3)O)O)O)OC 360.30 unknown https://doi.org/10.1016/0031-9422(92)80273-H
> 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/10.1515/ZNC-2003-3-401
Nevadensin 160921 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O 344.30 unknown https://doi.org/10.1515/ZNC-2003-3-401

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