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Murraya caloxylon

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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 UUID644042932c92e030111600
Scientific name Murraya caloxylon
Authority Ridl.
First published in J. Straits Branch Roy. Asiat. Soc. 50: 113 (1908)

Description Top

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Synonyms Top

Scientific name Authority First published in
Merrillia caloxylon (Ridl.) Swingle Philipp. J. Sci., C 13: 333 (1918)

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

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001039028
Tropicos 100363287
KEW urn:lsid:ipni.org:names:774418-1
NCBI Taxonomy 159055
IPNI 774418-1
iNaturalist 866645
GBIF 5594651
USDA GRIN 24700

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
Plastome evolution and phylogeny of the tribe Ruteae (Rutaceae) Liu Q, Gao Y, Dong W, Zhao L Ecol Evol 09-Feb-2023
PMCID:PMC9911629
doi:10.1002/ece3.9821
PMID:36789335
α-Glucosidase inhibitory activity of compounds isolated from the twig and leaf extracts of Desmos dumosus Suthiphasilp V, Maneerat T, Andersen RJ, Patrick BO, Pyne SG, Laphookhieo S Heliyon 15-Feb-2021
PMCID:PMC7900706
doi:10.1016/j.heliyon.2021.e06180
PMID:33665411
Pest categorisation of Diaphorina citri Bragard C, Dehnen‐Schmutz K, Di Serio F, Gonthier P, Jacques M, Jaques Miret JA, Justesen AF, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Kertesz V, Streissl F, MacLeod A EFSA J 06-Jan-2021
PMCID:PMC7786542
doi:10.2903/j.efsa.2021.6357
PMID:33437319
Complete chloroplast genome sequence of Murraya paniculata (Rutaceae): a widely used folk medicinal herb Liu H, Zhao Y, Zhou J, Ma Q, Wang X, Hua Z Mitochondrial DNA B Resour 11-Nov-2020
PMCID:PMC7671698
doi:10.1080/23802359.2020.1829518
PMID:33367064
Complete chloroplast genome sequence of Peganum harmala, an important medicinal plant Zha X, Zhao P, Gao F, Zhou Y Mitochondrial DNA B Resour 16-Jan-2020
PMCID:PMC7748625
doi:10.1080/23802359.2019.1711230
PMID:33366688
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
Complete plastome sequence of Atalantia kwangtungensis (Rutaceae): an endemic “near threatened” shrub in South China Zhu ZX, Wang JH, Sun XZ, Zhao KK, Wang HF Mitochondrial DNA B Resour 03-Jul-2018
PMCID:PMC7800406
doi:10.1080/23802359.2018.1483764
PMID:33474301
Complete plastome sequencing from Toona (Meliaceae) and phylogenomic analyses within Sapindales Lin N, Moore MJ, Deng T, Sun H, Yang L, Sun Y, Wang H Appl Plant Sci 27-Apr-2018
PMCID:PMC5947613
doi:10.1002/aps3.1040
PMID:30131882
Phylogenetic Relationships of Citrus and Its Relatives Based on matK Gene Sequences Penjor T, Yamamoto M, Uehara M, Ide M, Matsumoto N, Matsumoto R, Nagano Y PLoS One 25-Apr-2013
PMCID:PMC3636227
doi:10.1371/journal.pone.0062574
PMID:23638116
The biochemical systematics of Merrillia; in relation to Murraya, the clauseneae and the aurantioideae Yun-Cheung Kong, Paul Pui-Hay But, Kam-Hung Ng, Kin-Fai Cheng, Kiaw-Lan Chang, Khoon Meng Wonga, Alexander I. Gray, Peter G. Waterman Elsevier BV 10-Feb-2003
doi:10.1016/0305-1978(88)90116-0
Coumarins of Merrillia caloxylon Muhamad Bin Zakaria, Isao Saito, Teruo Matsuura Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(89)80080-9
Flavonoids from Merrillia caloxylon Alan W. Fraser, John R. Lewis Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(74)80328-6
Eupatorin, a constituent of Merrillia caloxylon. Adams JH, Lewis JR Planta Med 01-Aug-1977
doi:10.1055/S-0028-1097564
PMID:905420

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
> Organoheterocyclic compounds / Indoles and derivatives / Indoles / 3-alkylindoles
Yuehchukene 126009 Click to see CC1=CC2C(C(C3=C2C4=CC=CC=C4N3)C5=CNC6=CC=CC=C65)C(C1)(C)C 366.50 unknown https://doi.org/10.1016/0305-1978(88)90116-0
> Phenylpropanoids and polyketides / Coumarins and derivatives
(7-Methoxy-8-(1,2-dihydroxy-3-methyl-3-butenyl))coumarin 13917407 Click to see CC(=C)C(C(C1=C(C=CC2=C1OC(=O)C=C2)OC)O)O 276.28 unknown https://doi.org/10.1016/0031-9422(89)80080-9
7-Methoxy-8-(3-prop-1-en-2-yloxiran-2-yl)chromen-2-one 5320515 Click to see CC(=C)C1C(O1)C2=C(C=CC3=C2OC(=O)C=C3)OC 258.27 unknown https://doi.org/10.1016/0031-9422(89)80080-9
8-(1,2-Dihydroxy-3-methylbutyl)-7-methoxychromen-2-one 14185878 Click to see CC(C)C(C(C1=C(C=CC2=C1OC(=O)C=C2)OC)O)O 278.30 unknown https://doi.org/10.1016/0031-9422(89)80080-9
8-[(1R,2S)-1,2-dihydroxy-3-methylbutyl]-7-methoxychromen-2-one 14185879 Click to see CC(C)C(C(C1=C(C=CC2=C1OC(=O)C=C2)OC)O)O 278.30 unknown https://doi.org/10.1016/0031-9422(89)80080-9
8-[(1S,2R)-1,2-dihydroxy-3-methylbutyl]-7-methoxychromen-2-one 163012008 Click to see CC(C)C(C(C1=C(C=CC2=C1OC(=O)C=C2)OC)O)O 278.30 unknown https://doi.org/10.1016/0031-9422(89)80080-9
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 https://doi.org/10.1016/0031-9422(89)80080-9
8-[[(2R)-3,3-dimethyloxiran-2-yl]methyl]-5,7-dimethoxychromen-2-one 176971 Click to see CC1(C(O1)CC2=C(C=C(C3=C2OC(=O)C=C3)OC)OC)C 290.31 unknown https://doi.org/10.1016/0031-9422(89)80080-9
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(88)90116-0
https://doi.org/10.1016/0031-9422(89)80080-9
CID 13917405 13917405 Click to see CC(=C)C1C(O1)C2=C(C=CC3=C2OC(=O)C=C3)OC 258.27 unknown https://doi.org/10.1016/0031-9422(89)80080-9
Isomexoticin 4465807 Click to see CC(C)(C(CC1=C(C=C(C2=C1OC(=O)C=C2)OC)OC)O)O 308.33 unknown https://doi.org/10.1016/0031-9422(89)80080-9
Minumicrolin 389002 Click to see CC(=C)C(C(C1=C(C=CC2=C1OC(=O)C=C2)OC)O)O 276.28 unknown https://doi.org/10.1016/0031-9422(89)80080-9
Murrangatin 181514 Click to see CC(=C)C(C(C1=C(C=CC2=C1OC(=O)C=C2)OC)O)O 276.28 unknown https://doi.org/10.1016/0031-9422(89)80080-9
Phebalosin 188300 Click to see CC(=C)C1C(O1)C2=C(C=CC3=C2OC(=O)C=C3)OC 258.27 unknown https://doi.org/10.1016/0305-1978(88)90116-0
https://doi.org/10.1016/0031-9422(89)80080-9
Sibiricin 12315526 Click to see CC1(C(O1)CC2=C(C=C(C3=C2OC(=O)C=C3)OC)OC)C 290.31 unknown https://doi.org/10.1016/0031-9422(89)80080-9
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
4H-1-Benzopyran-4-one, 6,7-dihydroxy-2-(3,4,5-trimethoxyphenyl)- 5488683 Click to see COC1=CC(=CC(=C1OC)OC)C2=CC(=O)C3=CC(=C(C=C3O2)O)O 344.30 unknown https://doi.org/10.1016/0031-9422(74)80328-6
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Eupatorin 97214 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O 344.30 unknown https://doi.org/10.1016/0305-1978(88)90116-0
https://doi.org/10.1055/S-0028-1097564
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
1-(2-Hydroxy-4,6-dimethoxyphenyl)-3-(3-hydroxy-4-methoxyphenyl)prop-2-en-1-one 148236 Click to see COC1=C(C=C(C=C1)C=CC(=O)C2=C(C=C(C=C2OC)OC)O)O 330.30 unknown https://doi.org/10.1016/0031-9422(74)80328-6
2'-Hydroxy-3,4,4',5,6'-pentamethoxychalcone 5374858 Click to see COC1=CC(=C(C(=C1)OC)C(=O)C=CC2=CC(=C(C(=C2)OC)OC)OC)O 374.40 unknown https://doi.org/10.1016/0031-9422(74)80328-6
2'-Hydroxy-3,4,4',6'-tetramethoxychalcone 5373259 Click to see COC1=C(C=C(C=C1)C=CC(=O)C2=C(C=C(C=C2OC)OC)O)OC 344.40 unknown https://doi.org/10.1016/0031-9422(74)80328-6
2'-Hydroxy-4',6',3,4,5-pentamethoxychalcone 602639 Click to see COC1=CC(=C(C(=C1)OC)C(=O)C=CC2=CC(=C(C(=C2)OC)OC)OC)O 374.40 unknown https://doi.org/10.1016/0031-9422(74)80328-6
2',3-Dihydroxy-4,4',6'-trimethoxychalcone 5379071 Click to see COC1=C(C=C(C=C1)C=CC(=O)C2=C(C=C(C=C2OC)OC)O)O 330.30 unknown https://doi.org/10.1016/0031-9422(74)80328-6
3-(3,4-Dimethoxyphenyl)-1-(2-hydroxy-4,6-dimethoxyphenyl)prop-2-en-1-one 592132 Click to see COC1=C(C=C(C=C1)C=CC(=O)C2=C(C=C(C=C2OC)OC)O)OC 344.40 unknown https://doi.org/10.1016/0031-9422(74)80328-6

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