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Backhousia citriodora

Backhousia citriodora - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID643fec4a03739665353912
Scientific name Backhousia citriodora
Authority F.Muell.
First published in Fragm. 1: 78 (1859)

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
English lemon myrtle
English lemon scented ironwood
English lemon scented myrtle
Afrikaans sitroenmirt
Arabic آس الليمون
German zitronenmyrte
Japanese レモンマートル
Chinese 檬香桃

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-0000305828
UNII 2P8IL6SP2R
Tropicos 100151753
KEW urn:lsid:ipni.org:names:591026-1
The Plant List kew-18718
Open Tree Of Life 238737
NCBI Taxonomy 39976
IPNI 591026-1
iNaturalist 122826
GBIF 3185109
Freebase /m/08f1tl
EPPO BKOCI
EOL 3012918
USDA GRIN 6250
Wikipedia Backhousia_citriodora
CMAUP NPO10032

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
Flavonoids: A treasure house of prospective pharmacological potentials Hasnat H, Shompa SA, Islam MM, Alam S, Richi FT, Emon NU, Ashrafi S, Ahmed NU, Chowdhury MN, Fatema N, Hossain MS, Ghosh A, Ahmed F Heliyon 09-Mar-2024
PMCID:PMC10944245
doi:10.1016/j.heliyon.2024.e27533
PMID:38496846
Co-Designing Research for Sustainable Food Systems and Diets with Aboriginal Communities: A Study Protocol Lopes CV, Mihrshahi S, Hunter J, Ronto R, Cawthorne R Int J Environ Res Public Health 04-Mar-2024
PMCID:PMC10970346
doi:10.3390/ijerph21030298
PMID:38541297
Use of Essential Oils to Counteract the Phenomena of Antimicrobial Resistance in Livestock Species Lupia C, Castagna F, Bava R, Naturale MD, Zicarelli L, Marrelli M, Statti G, Tilocca B, Roncada P, Britti D, Palma E Antibiotics (Basel) 07-Feb-2024
PMCID:PMC10885947
doi:10.3390/antibiotics13020163
PMID:38391549
New Insights into the Latest Advancement in α-Amylase Inhibitors of Plant Origin with Anti-Diabetic Effects Kashtoh H, Baek KH Plants (Basel) 14-Aug-2023
PMCID:PMC10458243
doi:10.3390/plants12162944
PMID:37631156
A Comprehensive Review of Pathological Mechanisms and Natural Dietary Ingredients for the Management and Prevention of Sarcopenia Kim J, Lee JY, Kim CY Nutrients 03-Jun-2023
PMCID:PMC10255731
doi:10.3390/nu15112625
PMID:37299588
Drug target of natural products and COVID-19: how far has science progressed? Raman K, Rajagopal K, Ramesh B, Nallasivan PK, Raja MK, Jupudi S, Byran G, Khan SL, Bin Emran T Ann Med Surg (Lond) 19-Apr-2023
PMCID:PMC10289732
doi:10.1097/MS9.0000000000000703
PMID:37363478
Myrtle: a versatile medicinal plant Gorjian H, Khaligh NG 16-Feb-2023
PMCID:PMC9933039
doi:10.1186/s41110-023-00194-y
PMID:38625264
Advancements in nanoparticle-based treatment approaches for skin cancer therapy Zeng L, Gowda BH, Ahmed MG, Abourehab MA, Chen ZS, Zhang C, Li J, Kesharwani P Mol Cancer 12-Jan-2023
PMCID:PMC9835394
doi:10.1186/s12943-022-01708-4
PMID:36635761
Essential Oils against Sarcoptes scabiei Nardoni S, Mancianti F Molecules 19-Dec-2022
PMCID:PMC9788335
doi:10.3390/molecules27249067
PMID:36558200
Drug-Induced Liver Injury from Herbal Liver Detoxification Tea Niazi B, Ahmed K, Ahmed M, Ali S, Song K, Elias S Case Rep Gastroenterol 08-Nov-2022
PMCID:PMC9830300
doi:10.1159/000526311
PMID:36636365
Chemical Composition, Antioxidant, Antibacterial, and Antibiofilm Activities of Backhousia citriodora Essential Oil Lim AC, Tang SG, Zin NM, Maisarah AM, Ariffin IA, Ker PJ, Mahlia TM Molecules 31-Jul-2022
PMCID:PMC9370046
doi:10.3390/molecules27154895
PMID:35956846
Editorial for the Special Issue, “Chemistry of Essential Oils and Food Flavours” Southwell I, Núñez O Foods 22-Jul-2022
PMCID:PMC9330799
doi:10.3390/foods11152182
PMID:35892768
Phytochemical and Safety Evaluations of Finger Lime, Mountain Pepper, and Tamarind in Zebrafish Embryos Cáceres-Vélez PR, Ali A, Fournier-Level A, Dunshea FR, Jusuf PR Antioxidants (Basel) 28-Jun-2022
PMCID:PMC9311898
doi:10.3390/antiox11071280
PMID:35883771
In vitro efficacy of essential oils against Sarcoptes scabiei Andriantsoanirina V, Guillot J, Ratsimbason M, Mekhloufi G, Randriamialinoro F, Ranarivelo L, Ariey F, Durand R Sci Rep 03-May-2022
PMCID:PMC9065015
doi:10.1038/s41598-022-11176-x
PMID:35504935
Review of the Leaf Essential Oils of the Genus Backhousia Sens. Lat. and a Report on the Leaf Essential Oils of B. gundarara and B. tetraptera Bowden BF, Brophy JJ, Jackes BR Plants (Basel) 02-May-2022
PMCID:PMC9103502
doi:10.3390/plants11091231
PMID:35567231

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 / Benzene and substituted derivatives / Benzoic acids and derivatives / Aminobenzoic acids and derivatives / Aminobenzoic acids
2-Amino-3-chlorobenzoic acid 80807 Click to see C1=CC(=C(C(=C1)Cl)N)C(=O)O 171.58 unknown via CMAUP database
> Benzenoids / Phenols / Benzenediols / Resorcinols
Resorstatin 198749 Click to see CCCCCCC1=C(C=C(C=C1O)CCCCC)O 264.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
(R)-(+)-Citronellal 75427 Click to see CC(CCC=C(C)C)CC=O 154.25 unknown https://doi.org/10.1002/FFJ.1003
(Z)-3,7-dimethylocta-3,6-dienal 20837773 Click to see CC(=CCC=C(C)CC=O)C 152.23 unknown https://doi.org/10.1080/10412905.2000.9712204
3,6-Octadienal, 3,7-dimethyl- 6428928 Click to see CC(=CCC=C(C)CC=O)C 152.23 unknown https://doi.org/10.1080/10412905.2000.9712204
3,7-Dimethyl-2,6-octadien-1-al 8843 Click to see CC(=CCCC(=CC=O)C)C 152.23 unknown https://doi.org/10.1080/10412905.2000.9712204
Citral 638011 Click to see CC(=CCCC(=CC=O)C)C 152.23 unknown https://doi.org/10.1080/10412905.2000.9712204
Citronellal 7794 Click to see CC(CCC=C(C)C)CC=O 154.25 unknown https://doi.org/10.1080/10412905.2000.9712204
Linalool, (+/-)- 6549 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown https://doi.org/10.1080/10412905.2000.9712204
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown https://doi.org/10.1080/10412905.2000.9712204
Neral 643779 Click to see CC(=CCCC(=CC=O)C)C 152.23 unknown https://doi.org/10.1080/10412905.2000.9712204
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
6-Methyl-5-hepten-2-one 9862 Click to see CC(=CCCC(=O)C)C 126.20 unknown https://doi.org/10.1080/10412905.2000.9712204
> Organoheterocyclic compounds / Diazanaphthalenes / Benzodiazines / Quinoxalines / Phenazines and derivatives
1-Methoxyphenazine 76137 Click to see COC1=CC=CC2=NC3=CC=CC=C3N=C21 210.23 unknown via CMAUP database
1,6-Phenazinedicarboxylic acid dimethyl ester 10756325 Click to see COC(=O)C1=C2C(=CC=C1)N=C3C(=N2)C=CC=C3C(=O)OC 296.28 unknown via CMAUP database
2-Methoxyphenazine 235279 Click to see COC1=CC2=NC3=CC=CC=C3N=C2C=C1 210.23 unknown via CMAUP database
2,3-Dimethoxy-1-phenazinecarboxylic acid methyl ester 21856883 Click to see COC1=CC2=NC3=CC=CC=C3N=C2C(=C1OC)C(=O)OC 298.29 unknown via CMAUP database
2,3-Dimethoxyphenazine 21679909 Click to see COC1=CC2=NC3=CC=CC=C3N=C2C=C1OC 240.26 unknown via CMAUP database
2,3,7-Trimethoxyphenazine 21856873 Click to see COC1=CC2=NC3=CC(=C(C=C3N=C2C=C1)OC)OC 270.28 unknown via CMAUP database
2,6-Dimethoxy-1-phenazinecarboxylic acid methyl ester 101289916 Click to see COC1=C(C2=NC3=C(C(=CC=C3)OC)N=C2C=C1)C(=O)OC 298.29 unknown via CMAUP database
4-Methoxy-1-phenazinecarboxylic acid methyl ester 21679906 Click to see COC1=CC=C(C2=NC3=CC=CC=C3N=C12)C(=O)OC 268.27 unknown via CMAUP database
6-Methoxy-1-phenazinecarboxylic acid methyl ester 12318570 Click to see COC1=CC=CC2=NC3=C(C=CC=C3N=C21)C(=O)OC 268.27 unknown via CMAUP database
Dimethyl 2,3,7-trimethoxyphenazine-1,6-dicarboxylate 21856884 Click to see COC1=C(C2=NC3=CC(=C(C(=C3N=C2C=C1)C(=O)OC)OC)OC)C(=O)OC 386.40 unknown via CMAUP database
Methyl 2-methoxyphenazine-1-carboxylate 12318580 Click to see COC1=C(C2=NC3=CC=CC=C3N=C2C=C1)C(=O)OC 268.27 unknown via CMAUP database
Methyl 2,3,4-trimethoxyphenazine-1-carboxylate 21856881 Click to see COC1=C(C2=NC3=CC=CC=C3N=C2C(=C1OC)OC)C(=O)OC 328.32 unknown via CMAUP database
Methyl phenazine-1-carboxylate 602126 Click to see COC(=O)C1=CC=CC2=NC3=CC=CC=C3N=C21 238.24 unknown via CMAUP database
Phenazine-1-carboxylic acid 95069 Click to see C1=CC=C2C(=C1)N=C3C=CC=C(C3=N2)C(=O)O 224.21 unknown via CMAUP database
Phenazine-1,6-dicarboxylic acid 193025 Click to see C1=CC(=C2C(=C1)N=C3C(=N2)C=CC=C3C(=O)O)C(=O)O 268.22 unknown via CMAUP database
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
(2R)-4-[(Z)-hex-1-enyl]-2-methyl-2H-furan-5-one 11321306 Click to see CCCCC=CC1=CC(OC1=O)C 180.24 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Indolyl carboxylic acids and derivatives
7-Chloro-indole-1-acetic acid 67082699 Click to see C1=CC2=C(C(=C1)Cl)N(C=C2)CC(=O)O 209.63 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Indolyl carboxylic acids and derivatives / Indole-3-acetic acid derivatives
7-Chloroindole-3-acetic acid 3083739 Click to see C1=CC2=C(C(=C1)Cl)NC=C2CC(=O)O 209.63 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrroles / Substituted pyrroles / Phenylpyrroles
2,3-Dichloro-4-(2-nitro-3-chlorophenyl)pyrrole 367486 Click to see C1=CC(=C(C(=C1)Cl)[N+](=O)[O-])C2=CNC(=C2Cl)Cl 291.50 unknown via CMAUP database
3-Chloro-4-(3-chloro-4-fluoro-2-nitrophenyl)-1H-pyrrole 13024187 Click to see C1=CC(=C(C(=C1C2=CNC=C2Cl)[N+](=O)[O-])Cl)F 275.06 unknown via CMAUP database
4-(2-amino-3-chlorophenyl)-1H-pyrrole-2-carboxylic acid 121223548 Click to see C1=CC(=C(C(=C1)Cl)N)C2=CNC(=C2)C(=O)O 236.65 unknown via CMAUP database
Pyrrolnitrin 13916 Click to see C1=CC(=C(C(=C1)Cl)[N+](=O)[O-])C2=CNC=C2Cl 257.07 unknown via CMAUP database

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