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Murraya alata

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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 UUID6440557c9a74a278478555
Scientific name Murraya alata
Authority Drake
First published in J. Bot. (Morot) 6: 276 (1892)

Description Top

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Synonyms Top

Scientific name Authority First published in
Chalcas alata Tanaka Stud. Citrol. 2: 21 (1928)
Murraya alata var. hainanensis Swingle J. Wash. Acad. Sci. 32: 26 1942

Common names Top

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Language Common/alternative name
Arabic مورايا جناحية
Chinese 翼叶九里香

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001242531
KEW urn:lsid:ipni.org:names:774412-1
The Plant List tro-50119313
Open Tree Of Life 5233072
NCBI Taxonomy 1224772
IPNI 774412-1
iNaturalist 940184
GBIF 5594671
EOL 2907542
USDA GRIN 314268
CMAUP NPO33003

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
Syntheses of Minutuminolate and Related Coumarin Natural Products and Evaluation of Their TNF-α Inhibitory Activities Choo MZ, Khaw LW, Chai CL ACS Omega 23-Oct-2023
PMCID:PMC10633832
doi:10.1021/acsomega.3c06361
PMID:37970054
Application of Zebrafish as a Model for Anti-Cancer Activity Evaluation and Toxicity Testing of Natural Products Shen Y, Sheng R, Guo R Pharmaceuticals (Basel) 01-Jun-2023
PMCID:PMC10305033
doi:10.3390/ph16060827
PMID:37375774
Natural Coumarin Derivatives Activating Nrf2 Signaling Pathway as Lead Compounds for the Design and Synthesis of Intestinal Anti-Inflammatory Drugs Di Stasi LC Pharmaceuticals (Basel) 30-Mar-2023
PMCID:PMC10142712
doi:10.3390/ph16040511
PMID:37111267
Molecular differentiation of the Murraya paniculata Complex (Rutaceae: Aurantioideae: Aurantieae) Nguyen CH, Beattie GA, Haigh AM, Astuti IP, Mabberley DJ, Weston PH, Holford P BMC Evol Biol 30-Dec-2019
PMCID:PMC6937641
doi:10.1186/s12862-019-1555-4
PMID:31888450
Selective Activation of Nociceptor TRPV1 Channel and Reversal of Inflammatory Pain in Mice by a Novel Coumarin Derivative Muralatin L from Murraya alata Wei NN, Lv HN, Wu Y, Yang SL, Sun XY, Lai R, Jiang Y, Wang K J Biol Chem 29-Oct-2015
PMCID:PMC4705384
doi:10.1074/jbc.M115.654392
PMID:26515068
A chemotaxonomic division of Murraya based on the distribution of the alkaloids yuehchukene and girinimbine Yun-Cheung Kong, Kin-Fai Cheng, Kam-Hung Ng, Paul Pui-Hay But, Qian-Li, Si-Xao Yu, Hung-Ta Chang, Richard C. Cambie, T. Kinoshita, Wei-song Kan, Peter G. Waterman Elsevier BV 10-Feb-2003
doi:10.1016/0305-1978(86)90008-6

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
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives
5,7-dimethoxy-8-[(E)-3-oxobut-1-enyl]chromen-2-one 101893838 Click to see CC(=O)C=CC1=C(C=C(C2=C1OC(=O)C=C2)OC)OC 274.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
2H-1-Benzopyran-2-one, 8-((2S)-2-hydroxy-3-methyl-3-butenyl)-5,7-dimethoxy- 157112 Click to see CC(=C)C(CC1=C(C=C(C2=C1OC(=O)C=C2)OC)OC)O 290.31 unknown via CMAUP database
5,7-Dimethoxy-8-(3-methyl-2-oxo-butyl)chromen-2-one 5316871 Click to see CC(C)C(=O)CC1=C(C=C(C2=C1OC(=O)C=C2)OC)OC 290.31 unknown via CMAUP database
5,7-Dimethoxy-8-[(z)-3-methylbut-1,3-dienyl]-coumarin 10612228 Click to see CC(=C)C=CC1=C(C=C(C2=C1OC(=O)C=C2)OC)OC 272.29 unknown via CMAUP database
7-Methoxycoumarin 10748 Click to see COC1=CC2=C(C=C1)C=CC(=O)O2 176.17 unknown via CMAUP database
8-(1-Hydroxy-3-methyl-2-oxobutyl)-7-methoxychromen-2-one 5319956 Click to see CC(C)C(=O)C(C1=C(C=CC2=C1OC(=O)C=C2)OC)O 276.28 unknown via CMAUP database
8-(2,3-Dihydroxy-3-methylbutyl)-5,6,7-trimethoxychromen-2-one 101311688 Click to see CC(C)(C(CC1=C(C(=C(C2=C1OC(=O)C=C2)OC)OC)OC)O)O 338.40 unknown via CMAUP database
8-[(2R)-2,3-dihydroxy-3-methylbutyl]-5,7-dimethoxychromen-2-one 176970 Click to see CC(C)(C(CC1=C(C=C(C2=C1OC(=O)C=C2)OC)OC)O)O 308.33 unknown via CMAUP database
8-[[(2S)-3,3-Dimethyloxiran-2-yl]methyl]-5,7-dimethoxychromen-2-one 12315527 Click to see CC1(C(O1)CC2=C(C=C(C3=C2OC(=O)C=C3)OC)OC)C 290.31 unknown https://doi.org/10.1016/0305-1978(86)90008-6
Coumurrayin 176911 Click to see CC(=CCC1=C(C=C(C2=C1OC(=O)C=C2)OC)OC)C 274.31 unknown via CMAUP database
Murralongin 179620 Click to see CC(=C(C=O)C1=C(C=CC2=C1OC(=O)C=C2)OC)C 258.27 unknown via CMAUP database
Murrangatin 181514 Click to see CC(=C)C(C(C1=C(C=CC2=C1OC(=O)C=C2)OC)O)O 276.28 unknown via CMAUP database
Murraxocin 188750 Click to see CCOC(C1=C(C=CC2=C1OC(=O)C=C2)OC)C(C(=C)C)O 304.34 unknown via CMAUP database
Osthol 10228 Click to see CC(=CCC1=C(C=CC2=C1OC(=O)C=C2)OC)C 244.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
5-Methoxyseselin 290897 Click to see CC1(C=CC2=C3C(=C(C=C2O1)OC)C=CC(=O)O3)C 258.27 unknown via CMAUP database
8,8-Dimethyl-6-(3-methylbut-2-enyl)pyrano[2,3-f]chromen-2-one 44556806 Click to see CC(=CCC1=C2C(=C3C(=C1)C=CC(=O)O3)C=CC(O2)(C)C)C 296.40 unknown via CMAUP database

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Contributors Top

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Collections Top

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