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Gynochthodes umbellata

Gynochthodes umbellata - Unknown
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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 UUID644043256d0d2400495953
Scientific name Gynochthodes umbellata
Authority (L.) Razafim. & B.Bremer
First published in Adansonia , sér. 3, 33: 296 (2011)

Description Top

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Synonyms Top

Scientific name Authority First published in
Morinda padavara Juss. Gen. Pl. : 206 (1789)
Morinda scandens Roxb. Fl. Ind. 2: 202 (1824)
Morinda tetrandra Jack Malayan Misc. 1(5): 13 (1820)
Morinda umbellata L. Sp. Pl. : 176 (1753)
Morinda umbellata var. archboldiana Fosberg Sargentia 1: 123. 1942
Morinda umbellata subsp. obovata Y.Z.Ruan Fl. Reipubl. Popularis Sin. 71(2): 325 (1999)
Morinda umbellata var. papuana Valeton Nova Guinea 8: 515. 1911
Stigmanthus cymosus Lour. Fl. Cochinch. : 146 (1790)
Morinda umbellata var. tonkinensis Pit. Fl. Indo-Chine 3: 423. 1924
Morinda umbellata var. acuminatissima Valeton Bot. Jahrb. Syst. 61: 153. 1927
Guttenbergia umbellata Zoll. & Moritzi Natuur- Geneesk. Arch. Ned.-Indië 2: 3 (1845)

Common names Top

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Language Common/alternative name
Malay mengkudu akar

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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No forms added yet.

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-temperate
    • China
      • China South-central
      • China Southeast
      • Hainan
    • Eastern Asia
      • Japan
      • Nansei-shoto
      • Taiwan
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • India
      • Sri Lanka
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Laos
      • Thailand
      • Vietnam
    • Malesia
      • Borneo
      • Jawa
      • Malaya
      • Philippines
      • Sumatera
    • Papuasia
      • Bismarck Archipelago
      • New Guinea
      • Solomon Islands
  • Pacific
    • Northwestern Pacific
      • Marianas
    • Southwestern Pacific
      • Samoa

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001043056
Tropicos 100376397
KEW urn:lsid:ipni.org:names:77117618-1
The Plant List tro-100376397
Open Tree Of Life 116375
NCBI Taxonomy 268745
IPNI 77117618-1
GBIF 7533157
CMAUP NPO30535
CMAUP NPO4192

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
Review on melanosis coli and anthraquinone-containing traditional Chinese herbs that cause melanosis coli Zhang R, Huang C, Wu F, Fang K, Jiang S, Zhao Y, Chen G, Dong R Front Pharmacol 04-May-2023
PMCID:PMC10193150
doi:10.3389/fphar.2023.1160480
PMID:37214441
Stem cambial variants of Taiwan lianas Yang SZ, Chen PH, Chen JJ Bot Stud 24-Sep-2022
PMCID:PMC9509506
doi:10.1186/s40529-022-00358-5
PMID:36153445
Morinda umbellata active fraction inhibits lipopolysaccharide induced proinflammatory cytokines by downregulating NF-κB activation Krishnakumar NM, Manikantan K, Suja SN, Latha PG, Ceasar SA Toxicol Res (Camb) 08-Sep-2022
PMCID:PMC9618104
doi:10.1093/toxres/tfac063
PMID:36337241
Antioxidant and Anticancer Potential of Bioactive Compounds from Rhinacanthus nasutus Cell Suspension Culture Songserm P, Klanrit P, Klanrit P, Phetcharaburanin J, Thanonkeo P, Apiraksakorn J, Phomphrai K, Klanrit P Plants (Basel) 30-Jul-2022
PMCID:PMC9370634
doi:10.3390/plants11151994
PMID:35956472
Comparative phytochemistry, antioxidant, antidiabetic, and anti-inflammatory activities of traditionally used Ocimum basilicum L. Ocimum gratissimum L., and Ocimum tenuiflorum L. Sharma AD, Kaur I, Angish S, Thakur A, Sania S, Singh A BioTechnologia (Pozn) 29-Jun-2022
PMCID:PMC9642949
doi:10.5114/bta.2022.116206
PMID:36606068
Is the High Proportion of Males in a Population of the Self-Incompatible Fraxinus platypoda (Oleaceae) Indicative of True Androdioecy or Cryptic-Dioecy? Sakio H, Nirei T Plants (Basel) 11-Mar-2022
PMCID:PMC8951091
doi:10.3390/plants11060753
PMID:35336635
Chemistry, Biosynthesis, Physicochemical and Biological Properties of Rubiadin: A Promising Natural Anthraquinone for New Drug Discovery and Development Watroly MN, Sekar M, Fuloria S, Gan SH, Jeyabalan S, Wu YS, Subramaniyan V, Sathasivam KV, Ravi S, Mat Rani NN, Lum PT, Vaijanathappa J, Meenakshi DU, Mani S, Fuloria NK Drug Des Devel Ther 03-Nov-2021
PMCID:PMC8576757
doi:10.2147/DDDT.S338548
PMID:34764636
Impacts of growth form and phylogenetic relatedness on seed germination: A large‐scale analysis of a subtropical regional flora Wang J, Xu G, Chen W, Ma Y, Qi W, Zhang C, Cui X Ecol Evol 07-Jan-2021
PMCID:PMC7863672
doi:10.1002/ece3.7132
PMID:33598130
Pest categorisation of non‐EU Monochamus spp. Bragard C, Dehnen‐Schmutz K, Di Serio F, Gonthier P, Jacques M, Jaques Miret JA, Fejer Justesen A, MacLeod A, Magnusson CS, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Grégoire J, Kertész V, Milonas P EFSA J 19-Nov-2018
PMCID:PMC7009674
doi:10.2903/j.efsa.2018.5435
PMID:32625739
Anti-Diabetic Potential of Noni: The Yin and the Yang Nerurkar PV, Hwang PW, Saksa E Molecules 25-Sep-2015
PMCID:PMC6331903
doi:10.3390/molecules201017684
PMID:26404212
Secondary Metabolites from Rubiaceae Species Martins D, Nunez CV Molecules 22-Jul-2015
PMCID:PMC6331836
doi:10.3390/molecules200713422
PMID:26205062
Functional Androdioecy in Critically Endangered Gymnocladus assamicus (Leguminosae) in the Eastern Himalayan Region of Northeast India Choudhury BI, Khan ML, Dayanandan S PLoS One 28-Feb-2014
PMCID:PMC3938411
doi:10.1371/journal.pone.0087287
PMID:24586267
Frequency of Cyanogenesis in Tropical Rainforests of Far North Queensland, Australia MILLER RE, JENSEN R, WOODROW IE Ann Bot 01-Jun-2006
PMCID:PMC2803397
doi:10.1093/aob/mcl048
PMID:16520340

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 / Anthracenes / Anthracenecarboxylic acids and derivatives / Anthracenecarboxylic acids
2-Carboxy-3-hydroxy-9,10-dioxoanthracen-1-olate 54740334 Click to see C1=CC=C2C(=C1)C(=O)C3=CC(=C(C(=C3C2=O)[O-])C(=O)O)O 283.21 unknown via CMAUP database
> Benzenoids / Anthracenes / Anthraquinones
1-Hydroxy-2-methoxyanthraquinone 80103 Click to see COC1=C(C2=C(C=C1)C(=O)C3=CC=CC=C3C2=O)O 254.24 unknown via CMAUP database
1-Hydroxy-2-methylanthraquinone 160817 Click to see CC1=C(C2=C(C=C1)C(=O)C3=CC=CC=C3C2=O)O 238.24 unknown via CMAUP database
1-Methoxy-2-methyl-anthraquinone 3534338 Click to see CC1=C(C2=C(C=C1)C(=O)C3=CC=CC=C3C2=O)OC 252.26 unknown via CMAUP database
2-Methylanthraquinone 6773 Click to see CC1=CC2=C(C=C1)C(=O)C3=CC=CC=C3C2=O 222.24 unknown via CMAUP database
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
1,3-Dihydroxyanthraquinone 196978 Click to see C1=CC=C2C(=C1)C(=O)C3=C(C2=O)C(=CC(=C3)O)O 240.21 unknown via CMAUP database
2-Hydroxyanthraquinone 11796 Click to see C1=CC=C2C(=C1)C(=O)C3=C(C2=O)C=C(C=C3)O 224.21 unknown via CMAUP database
Alizarin 6293 Click to see C1=CC=C2C(=C1)C(=O)C3=C(C2=O)C(=C(C=C3)O)O 240.21 unknown via CMAUP database
Alizarin 1-methyl ether 80309 Click to see COC1=C(C=CC2=C1C(=O)C3=CC=CC=C3C2=O)O 254.24 unknown via CMAUP database
Lucidin 10163 Click to see C1=CC=C2C(=C1)C(=O)C3=CC(=C(C(=C3C2=O)O)CO)O 270.24 unknown via CMAUP database
Rubiadin 124062 Click to see CC1=C(C=C2C(=C1O)C(=O)C3=CC=CC=C3C2=O)O 254.24 unknown via CMAUP database
Rubiadin 1-methyl ether 96191 Click to see CC1=C(C=C2C(=C1OC)C(=O)C3=CC=CC=C3C2=O)O 268.26 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Ethyl arachidonate 5367369 Click to see CCCCCC=CCC=CCC=CCC=CCCCC(=O)OCC 332.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Monoradylglycerols / Monoalkylglycerols
Batilol, (R)- 10831326 Click to see CCCCCCCCCCCCCCCCCCOCC(CO)O 344.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Cembrane diterpenoids
Grandilobatin E 44585761 Click to see CC1CCC(=CC=C(CCCC(=CC(=O)C1)C)C)C(C)(C)O 304.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Taxanes and derivatives
[(2R,3R,5S,7S,8S,9R,10R)-7,9,10-triacetyloxy-5-hydroxy-8,12,15,15-tetramethyl-4-methylidene-2-tricyclo[9.3.1.03,8]pentadec-11-enyl] 2-methylbutanoate 5318282 Click to see CCC(C)C(=O)OC1C2CCC(=C(C2(C)C)C(C(C3(C1C(=C)C(CC3OC(=O)C)O)C)OC(=O)C)OC(=O)C)C 562.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(5aR,6R,9R)-6,9-dihydroxy-5a,9-dimethyl-3-methylidene-3a,4,5,6,7,8,9a,9b-octahydrobenzo[g][1]benzofuran-2-one 5318148 Click to see CC12CCC3C(C1C(CCC2O)(C)O)OC(=O)C3=C 266.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
11-(hydroxymethyl)-4,4,6a,6b,8a,11,14b-heptamethyl-2,4a,5,6,7,8,9,10,12,12a,14,14a-dodecahydro-1H-picen-3-one 5319945 Click to see CC1(C2CCC3(C(C2(CCC1=O)C)CC=C4C3(CCC5(C4CC(CC5)(C)CO)C)C)C)C 440.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids
(2S,3S,4R,5R)-2-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5S)-6-hydroxy-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]oxane-3,4,5-triol 21597411 Click to see CC(CCC(C)C(C)(C)O)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(CO5)O)O)O)C)C 548.80 unknown via CMAUP database
Sinugrandisterol C 16656588 Click to see CC(C)C(=C)CCC(C)C1CCC2C1(CCC3C2C(C4C5(C3(C(CC(C5)O)O)C)O4)O)C 446.70 unknown via CMAUP database
Sinugrandisterol D 16656567 Click to see CC(C)C(=C)C=CC(C)C1CCC2C1(CCC3C2C(C4C5(C3(C(CC(C5)O)O)C)O4)O)C 444.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5S)-6-hydroxy-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 14632863 Click to see CC(CCC(C)C(C)(C)O)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 416.70 unknown via CMAUP database
Sinugrandisterol A 16656568 Click to see CC(C)C(=C)CCC(C)C1CCC2C1(CCC3C2C(C=C4C3(C(CC(C4)O)O)C)O)C 430.70 unknown via CMAUP database
Sinugrandisterol B 16656566 Click to see CC(C)C(=C)C=CC(C)C1CCC2C1(CCC3C2C(C=C4C3(C(CC(C4)O)O)C)O)C 428.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Pregnane steroids / Gluco/mineralocorticoids, progestogins and derivatives
Pregnenolone 8955 Click to see CC(=O)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 316.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3R,8R,9R,10S,13R,14R,17R)-17-[(E,2R,5R)-5-ethyl-6-methylhept-3-en-2-yl]-3,10,13-trimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene 50930798 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)C)C)C)C(C)C 410.70 unknown via CMAUP database

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