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Myristica cinnamomea

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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 UUID643ffdea6ad79417172518
Scientific name Myristica cinnamomea
Authority King
First published in Ann. Roy. Bot. Gard. (Calcutta) 3(3): 292 (1891)

Description Top

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Synonyms Top

No known synonyms.

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
    • Indo-China
      • Thailand
    • Malesia
      • Borneo
      • Malaya
      • Philippines
      • Sumatera

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000448154
KEW urn:lsid:ipni.org:names:586016-1
Open Tree Of Life 5700107
NCBI Taxonomy 1504465
IUCN Red List 33278
IPNI 586016-1
iNaturalist 440910
GBIF 5564454
Freebase /m/02xbtcl
Wikipedia Myristica_cinnamomea

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
A review on antimicrobial strategies in mitigating biofilm-associated infections on medical implants Kadirvelu L, Sivaramalingam SS, Jothivel D, Chithiraiselvan DD, Karaiyagowder Govindarajan D, Kandaswamy K Curr Res Microb Sci 07-Mar-2024
PMCID:PMC10951465
doi:10.1016/j.crmicr.2024.100231
PMID:38510214
Acylphenols and Dimeric Acylphenols from the Genus Myristica: A Review of Their Phytochemistry and Pharmacology Othman MA, Sivasothy Y Plants (Basel) 09-Apr-2023
PMCID:PMC10143527
doi:10.3390/plants12081589
PMID:37111813
Anti-quorum sensing evaluation of methyleugenol, the principal bioactive component, from the Melaleuca bracteata leaf oil Wang W, Lin X, Yang H, Huang X, Pan L, Wu S, Yang C, Zhang L, Li Y Front Microbiol 22-Aug-2022
PMCID:PMC9477228
doi:10.3389/fmicb.2022.970520
PMID:36118239
Non-Alkaloid Cholinesterase Inhibitory Compounds from Natural Sources Tamfu AN, Kucukaydin S, Yeskaliyeva B, Ozturk M, Dinica RM Molecules 14-Sep-2021
PMCID:PMC8472022
doi:10.3390/molecules26185582
PMID:34577053
Quorum Sensing and NF-κB Inhibition of Synthetic Coumaperine Derivatives from Piper nigrum Kadosh Y, Muthuraman S, Yaniv K, Baruch Y, Gopas J, Kushmaro A, Kumar RS Molecules 15-Apr-2021
PMCID:PMC8071387
doi:10.3390/molecules26082293
PMID:33921056
Anti-Helicobacter pylori, Anti-Inflammatory, Cytotoxic, and Antioxidant Activities of Mace Extracts from Myristica fragrans Suthisamphat N, Dechayont B, Phuaklee P, Prajuabjinda O, Vilaichone RK, Itharat A, Mokmued K, Prommee N Evid Based Complement Alternat Med 29-Mar-2020
PMCID:PMC7146089
doi:10.1155/2020/7576818
PMID:32308716
Malabaricone C Attenuates Nonsteroidal Anti-Inflammatory Drug-Induced Gastric Ulceration by Decreasing Oxidative/Nitrative Stress and Inflammation and Promoting Angiogenic Autohealing Basak M, Mahata T, Chakraborti S, Kumar P, Bhattacharya B, Bandyopadhyay SK, Das M, Stewart A, Saha S, Maity B Antioxid Redox Signal 04-Mar-2020
PMCID:PMC7071091
doi:10.1089/ars.2019.7781
PMID:31830804
Bioautography and GC-MS based identification of piperine and trichostachine as the active quorum quenching compounds in black pepper Vázquez-Martínez J, Buitemea-Cantúa GV, Gutierrez-Villagomez JM, García-González JP, Ramírez-Chávez E, Molina-Torres J Heliyon 02-Jan-2020
PMCID:PMC6948270
doi:10.1016/j.heliyon.2019.e03137
PMID:31922049
Malabaricone C as Natural Sphingomyelin Synthase Inhibitor against Diet-Induced Obesity and Its Lipid Metabolism in Mice Othman MA, Yuyama K, Murai Y, Igarashi Y, Mikami D, Sivasothy Y, Awang K, Monde K ACS Med Chem Lett 03-Jul-2019
PMCID:PMC6691482
doi:10.1021/acsmedchemlett.9b00171
PMID:31413799
Quorum sensing inimical activity of Tribulus terrestris against gram negative bacterial pathogens by signalling interference Vadakkan K, Vijayanand S, Hemapriya J, Gunasekaran R 3 Biotech 01-Apr-2019
PMCID:PMC6443769
doi:10.1007/s13205-019-1695-7
PMID:30944810
The Effects of Chinese Herbal Medicines on the Quorum Sensing-Regulated Virulence in Pseudomonas aeruginosa PAO1 Chong YM, How KY, Yin WF, Chan KG Molecules 21-Apr-2018
PMCID:PMC6017394
doi:10.3390/molecules23040972
PMID:29690523
Anti-Quorum Sensing Natural Compounds Asfour HZ J Microsc Ultrastruct 01-Jan-2018
PMCID:PMC6014249
doi:10.4103/JMAU.JMAU_10_18
PMID:30023261
Heme Oxygenases in Cardiovascular Health and Disease Ayer A, Zarjou A, Agarwal A, Stocker R Physiol Rev 07-Sep-2016
PMCID:PMC5504454
doi:10.1152/physrev.00003.2016
PMID:27604527
Quorum quenching: Signal jamming in dental plaque biofilms Basavaraju M, Sisnity VS, Palaparthy R, Addanki PK J Dent Sci 11-Apr-2016
PMCID:PMC6395279
doi:10.1016/j.jds.2016.02.002
PMID:30894996
Quorum Sensing Inhibitory Activity of Giganteone A from Myristica cinnamomea King against Escherichia coli Biosensors Sivasothy Y, Krishnan T, Chan KG, Abdul Wahab SM, Othman MA, Litaudon M, Awang K Molecules 21-Mar-2016
PMCID:PMC6273857
doi:10.3390/molecules21030391
PMID:27102164

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
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
Hinokinin 442879 Click to see C1C(C(C(=O)O1)CC2=CC3=C(C=C2)OCO3)CC4=CC5=C(C=C4)OCO5 354.40 unknown https://doi.org/10.1021/JO020045D
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
1-(2,4,6-Trihydroxyphenyl)dodecan-1-one 11771258 Click to see CCCCCCCCCCCC(=O)C1=C(C=C(C=C1O)O)O 308.40 unknown https://doi.org/10.1021/JO020045D
> Phenylpropanoids and polyketides / Flavonoids / Hydroxyflavonoids / 7-hydroxyflavonoids
(+)-Myristinin A 497359 Click to see CCCCCCCCCCCC(=O)C1=C(C=C(C(=C1O)C2CC(OC3=C2C=CC(=C3)O)C4=CC=C(C=C4)O)O)O 548.70 unknown https://doi.org/10.1021/JO020045D
(+)-Myristinin D 497362 Click to see C1C(C2=C(C=C(C=C2)O)OC1C3=CC=C(C=C3)O)C4=C(C(=C(C=C4O)O)C(=O)CCCCCCCCC5=CC=CC=C5)O 582.70 unknown https://doi.org/10.1021/JO020045D
9-phenyl-1-[2,4,6-trihydroxy-3-[(2R,4R)-7-hydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]phenyl]nonan-1-one 10054015 Click to see C1C(C2=C(C=C(C=C2)O)OC1C3=CC=C(C=C3)O)C4=C(C(=C(C=C4O)O)C(=O)CCCCCCCCC5=CC=CC=C5)O 582.70 unknown https://doi.org/10.1021/JO020045D
Myristinin B 497361 Click to see CCCCCCCCCCCC(=O)C1=C(C=C(C(=C1O)C2CC(OC3=C2C=CC(=C3)O)C4=CC=C(C=C4)O)O)O 548.70 unknown https://doi.org/10.1021/JO020045D

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