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Monechma ciliatum

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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 UUID643ff53d59552062858274
Scientific name Monechma ciliatum
Authority (Jacq.) Milne-Redh.
First published in Bull. Misc. Inform. Kew 1934: 304 (1934)

Description Top

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Synonyms Top

Scientific name Authority First published in
Justicia togoensis Lindau Bot. Jahrb. Syst. 20: 72 (1894)
Justicia ciliata Jacq. Hort. Bot. Vindob. 2: 47. [1772-1773]
Justicia buettneri Lindau Bot. Jahrb. Syst. 20(1-2): 68. 1894 [16 Nov 1894]
Monechma hispidum Hochst. Flora 24(1): 375. 1841
Schwabea ciliaris Nees Prodr. [A. P. de Candolle] 11: 384. 1847 [25 Nov 1847]
Schwabea modesta Endl. Nov. Stirp. Dec. : 81 (1839)
Beloperone ciliata Nees Prodr. [A. P. de Candolle] 11: 422. 1847 [25 Nov 1847]
Dianthera ciliata Medik. Bot. Beob. 1782 : 9 (1783)
Dianthera setacea (Kuntze) Voss Vilm. Blumengärtn. ed. 3 , 1: 809 (1895)
Dicliptera ciliaris Willd. ex Nees Prodr. [A. P. de Candolle] 11: 384. 1847 [25 Nov 1847]
Ecbolium setaceum Kuntze Revis. Gen. Pl. 2: 979 (1891)
Hygrophila lutea T.Anderson J. Proc. Linn. Soc., Bot. 7: 22 (1863)

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
  • Africa
    • East Tropical Africa
      • Tanzania
      • Uganda
    • Northeast Tropical Africa
      • Chad
      • Ethiopia
      • Sudan
    • South Tropical Africa
      • Malawi
      • Mozambique
      • Zambia
    • West Tropical Africa
      • Benin
      • Burkina
      • Gambia
      • Ghana
      • Guinea
      • Guinea-Bissau
      • Ivory Coast
      • Mali
      • Mauritania
      • Niger
      • Nigeria
      • Senegal
      • Sierra Leone
      • Togo
    • West-central Tropical Africa
      • Burundi
      • Cameroon
      • Central African Republic
      • Rwanda
      • Zaïre

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000370998
Tropicos 103176
KEW urn:lsid:ipni.org:names:52491-1
The Plant List kew-2362459
NCBI Taxonomy 2739801
IPNI 52491-1
iNaturalist 505736
GBIF 3770207
EPPO MHMCI
CMAUP NPO16896

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
Profiling of primary and phytonutrients in edible mahlab cherry (Prunus mahaleb L.) seeds in the context of its different cultivars and roasting as analyzed using molecular networking and chemometric tools Mostafa MM, Farag MA PeerJ 30-Aug-2023
PMCID:PMC10474835
doi:10.7717/peerj.15908
PMID:37663279
Chemistry and Biological Activities of Naturally Occurring and Structurally Modified Podophyllotoxins Jin L, Song Z, Cai F, Ruan L, Jiang R Molecules 30-Dec-2022
PMCID:PMC9822336
doi:10.3390/molecules28010302
PMID:36615496
Sorghum Flour Application in Bread: Technological Challenges and Opportunities Ari Akin P, Demirkesen I, Bean SR, Aramouni F, Boyaci IH Foods 16-Aug-2022
PMCID:PMC9407531
doi:10.3390/foods11162466
PMID:36010465
Profiling of Primary Metabolites and Volatile Determinants in Mahlab Cherry (Prunus mahaleb L.) Seeds in the Context of Its Different Varieties and Roasting as Analyzed Using Chemometric Tools Farag MA, Khattab AR, Shamma S, Afifi SM Foods 30-Mar-2021
PMCID:PMC8066072
doi:10.3390/foods10040728
PMID:33808142
Spatial Distribution of Heavy Metals and Pollution of Environmental Media Around a Used Lead-acid Battery Recycling Center in Ibadan, Nigeria Oloruntoba E, Gurusa O, Omokhodion F, Fobil J, Basu N, Arko-Mensah J, Robin T J Health Pollut 02-Mar-2021
PMCID:PMC8009648
doi:10.5696/2156-9614-11.29.210304
PMID:33815902
Potential Anticancer Agents Characterized from Selected Tropical Plants Ren Y, Carcache de Blanco EJ, Fuchs JR, Soejarto DD, Burdette JE, Swanson SM, Kinghorn AD J Nat Prod 04-Mar-2019
PMCID:PMC6441492
doi:10.1021/acs.jnatprod.9b00018
PMID:30830783
Breeders’ knowledge on cattle fodder species preference in rangelands of Benin Ouachinou JM, Dassou GH, Azihou AF, Adomou AC, Yédomonhan H J Ethnobiol Ethnomed 08-Nov-2018
PMCID:PMC6225710
doi:10.1186/s13002-018-0264-1
PMID:30409166
Potent Cytotoxic Arylnaphthalene Lignan Lactones from Phyllanthus poilanei Ren Y, Lantvit DD, Deng Y, Kanagasabai R, Gallucci JC, Ninh TN, Chai HB, Soejarto DD, Fuchs JR, Yalowich JC, Yu J, Swanson SM, Kinghorn AD J Nat Prod 12-Jun-2014
PMCID:PMC4073661
doi:10.1021/np5002785
PMID:24937209
Phytochemical screening and evaluation of Monechma ciliatum (black mahlab) seed extracts as antimicrobial agents Ahmed Oshi M, Mohmmed Abdelkarim A Avicenna J Phytomed 01-Mar-2013
PMCID:PMC4075707
PMID:25050266
Field experiments of Anopheles gambiae attraction to local fruits/seedpods and flowering plants in Mali to optimize strategies for malaria vector control in Africa using attractive toxic sugar bait methods Müller GC, Beier JC, Traore SF, Toure MB, Traore MM, Bah S, Doumbia S, Schlein Y Malar J 20-Sep-2010
PMCID:PMC2949744
doi:10.1186/1475-2875-9-262
PMID:20854666
Uterotonic Plants and their Bioactive Constituents Gruber CW, O’Brien M Planta Med 15-Sep-2010
PMCID:PMC3407953
doi:10.1055/s-0030-1250317
PMID:20845261
Antifertility effect of aqueous and ethanol extracts of the leaves and roots of Asparagus africanus in rats Tafesse G, Mekonnen Y, Makonnen E Afr Health Sci 01-Jun-2006
PMCID:PMC2567240
PMID:16916296
NMR Spectral Analysis of Tetrahydro‐2‐( 3,4 ‐dimethoxyphenyl)‐4‐[(3,4‐dimethoxyphenyl)methyl]‐3‐furanmethanol, a Dimethyl Ether of Lariciresinol, from <i>Monechma ciliaturn</i> L. Maat, J. A. Peters, J. T. M. Linders, S. M. Hussein Ayoub Wiley 28-May-2005
doi:10.1002/MRC.1260230520

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
> Lignans, neolignans and related compounds / Arylnaphthalene lignans
9-(3,4-dimethoxyphenyl)-5-hydroxy-6H-[2]benzofuro[5,6-f][1,3]benzodioxol-8-one 332529 Click to see COC1=C(C=C(C=C1)C2=C3C(=C(C4=CC5=C(C=C42)OCO5)O)COC3=O)OC 380.30 unknown via CMAUP database
9-(4-hydroxy-3-methoxyphenyl)-4,6,7-trimethoxy-3H-benzo[f][2]benzofuran-1-one 10023637 Click to see COC1=C(C=CC(=C1)C2=C3C(=C(C4=CC(=C(C=C42)OC)OC)OC)COC3=O)O 396.40 unknown via CMAUP database
Chinensinaphthol methyl ether 5315828 Click to see COC1=C(C=C(C=C1)C2=C3C(=C(C4=CC5=C(C=C42)OCO5)OC)COC3=O)OC 394.40 unknown via CMAUP database
Cilinaphthalide B 10476659 Click to see COC1=C(C=C(C=C1)C2=C3C(=C(C4=CC(=C(C=C42)OC)OC)OC)COC3=O)OC 410.40 unknown via CMAUP database
Justicidin A 159982 Click to see COC1=C(C=C2C(=C1)C(=C3C(=C2OC)COC3=O)C4=CC5=C(C=C4)OCO5)OC 394.40 unknown via CMAUP database
Justicidin C 493173 Click to see COC1=C(C=C2C(=C1)C(=C3COC(=O)C3=C2OC)C4=CC5=C(C=C4)OCO5)OC 394.40 unknown via CMAUP database
Justicidin F 11740369 Click to see COC1=C2COC(=O)C2=C(C3=CC4=C(C=C31)OCO4)C5=CC6=C(C=C5)OCO6 378.30 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
[(2S,3R,4R)-2-(3,4-dimethoxyphenyl)-4-[(3,4-dimethoxyphenyl)methyl]oxolan-3-yl]methanol 181325 Click to see COC1=C(C=C(C=C1)CC2COC(C2CO)C3=CC(=C(C=C3)OC)OC)OC 388.50 unknown https://doi.org/10.1002/MRC.1260230520
> Lignans, neolignans and related compounds / Lignan glycosides
Ciliatoside A 10462924 Click to see COC1=C(C=C2C(=C1)C(=C3C(=C2OC4C(C(CO4)(COC5C(C(C(CO5)O)O)O)O)OC6C(C(C(CO6)O)O)O)COC3=O)C7=CC8=C(C=C7)OCO8)OC 776.70 unknown via CMAUP database
Ciliatoside B 10557698 Click to see COC1=C(C=C2C(=C1)C(=C3C(=C2OC4C(C(CO4)(COC5C(C(C(CO5)O)O)O)O)OC6C(C(C(CO6)O)OC7C(C(CO7)(CO)O)O)O)COC3=O)C8=CC9=C(C=C8)OCO9)OC 908.80 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Cianidanol 9064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown via CMAUP database
> 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 via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Vitexin 5280441 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
Trifolin 5282149 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
7-(alpha-D-Glucopyranosyloxy)-5-hydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one 12304095 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Santin 5281695 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC 344.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
5-Hydroxyauranetin 11079623 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)OC 388.40 unknown via CMAUP database

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