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Leptospermum polygalifolium

Leptospermum polygalifolium - 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 UUID643fe12a3227f534602965
Scientific name Leptospermum polygalifolium
Authority Salisb.
First published in Prodr. Stirp. Chap. Allerton : 350 (1796)

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Malay pokok china maki
Malay pokok cina maki
Malay pokok gelam bukit
Russian Тонкосемянник истодолистный
Chinese 澳洲茶
Chinese 细子树
Chinese 远志叶松红梅

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Leptospermum polygalifolium subsp. cismontanum Joy Thomps. Telopea 3: 400 (1989)
Leptospermum polygalifolium subsp. polygalifolium Unknown

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
  • Australasia
    • Australia
      • New South Wales
      • Norfolk Island
      • Queensland

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000226708
Tropicos 100214696
KEW urn:lsid:ipni.org:names:597483-1
The Plant List kew-111429
Open Tree Of Life 1010674
NCBI Taxonomy 106055
IPNI 597483-1
iNaturalist 83602
GBIF 3181788
Freebase /m/0h3xgg_
USDA GRIN 403638
Wikipedia Leptospermum_polygalifolium

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
Comparison of In Vitro Bacterial Susceptibility to Common and Novel Equine Wound Care Dressings Simpson M, Hendrickson DA, Hyatt DR, Rao S Animals (Basel) 01-Mar-2024
PMCID:PMC10931437
doi:10.3390/ani14050776
PMID:38473161
Leptospermum extract (QV0) suppresses pleural mesothelioma tumor growth in vitro and in vivo by mitochondrial dysfunction associated apoptosis Shi H, Zhang L, Yu TK, Zhuang L, Ke H, Johnson B, Rath E, Lee K, Klebe S, Kao S, Qin KL, Pham HN, Vuong Q, Cheng YY Front Oncol 05-Jul-2023
PMCID:PMC10354640
doi:10.3389/fonc.2023.1162027
PMID:37476375
Honey: An Advanced Antimicrobial and Wound Healing Biomaterial for Tissue Engineering Applications Yupanqui Mieles J, Vyas C, Aslan E, Humphreys G, Diver C, Bartolo P Pharmaceutics 10-Aug-2022
PMCID:PMC9414000
doi:10.3390/pharmaceutics14081663
PMID:36015289
A Review of Commonly Used Methodologies for Assessing the Antibacterial Activity of Honey and Honey Products Hossain ML, Lim LY, Hammer K, Hettiarachchi D, Locher C Antibiotics (Basel) 20-Jul-2022
PMCID:PMC9312033
doi:10.3390/antibiotics11070975
PMID:35884229
A Comprehensive Survey of Phenolic Constituents Reported in Monofloral Honeys around the Globe Lawag IL, Lim LY, Joshi R, Hammer KA, Locher C Foods 15-Apr-2022
PMCID:PMC9025093
doi:10.3390/foods11081152
PMID:35454742
Shifting season of fire and its interaction with fire severity: Impacts on reproductive effort in resprouting plants Thomsen AM, Ooi MK Ecol Evol 18-Mar-2022
PMCID:PMC8931712
doi:10.1002/ece3.8717
PMID:35342578
Monofloral Honeys as a Potential Source of Natural Antioxidants, Minerals and Medicine Mărgăoan R, Topal E, Balkanska R, Yücel B, Oravecz T, Cornea-Cipcigan M, Vodnar DC Antioxidants (Basel) 25-Jun-2021
PMCID:PMC8300703
doi:10.3390/antiox10071023
PMID:34202118
Honey: Another Alternative in the Fight against Antibiotic-Resistant Bacteria? Combarros-Fuertes P, Fresno JM, Estevinho MM, Sousa-Pimenta M, Tornadijo ME, Estevinho LM Antibiotics (Basel) 04-Nov-2020
PMCID:PMC7694208
doi:10.3390/antibiotics9110774
PMID:33158063
Agastache honey has superior antifungal activity in comparison with important commercial honeys Anand S, Deighton M, Livanos G, Pang EC, Mantri N Sci Rep 03-Dec-2019
PMCID:PMC6890684
doi:10.1038/s41598-019-54679-w
PMID:31796803
Antimicrobial Activity of Agastache Honey and Characterization of Its Bioactive Compounds in Comparison With Important Commercial Honeys Anand S, Deighton M, Livanos G, Morrison PD, Pang EC, Mantri N Front Microbiol 25-Feb-2019
PMCID:PMC6397887
doi:10.3389/fmicb.2019.00263
PMID:30858831
Characterization of Physico-Chemical Properties and Antioxidant Capacities of Bioactive Honey Produced from Australian Grown Agastache rugosa and its Correlation with Colour and Poly-Phenol Content Anand S, Pang E, Livanos G, Mantri N Molecules 05-Jan-2018
PMCID:PMC6017773
doi:10.3390/molecules23010108
PMID:29304019
The Antibacterial Activity of Australian Leptospermum Honey Correlates with Methylglyoxal Levels Cokcetin NN, Pappalardo M, Campbell LT, Brooks P, Carter DA, Blair SE, Harry EJ PLoS One 28-Dec-2016
PMCID:PMC5193333
doi:10.1371/journal.pone.0167780
PMID:28030589
Bumble bee parasite strains vary in resistance to phytochemicals Palmer-Young EC, Sadd BM, Stevenson PC, Irwin RE, Adler LS Sci Rep 24-Nov-2016
PMCID:PMC5121629
doi:10.1038/srep37087
PMID:27883009
Therapeutic Manuka Honey: No Longer So Alternative Carter DA, Blair SE, Cokcetin NN, Bouzo D, Brooks P, Schothauer R, Harry EJ Front Microbiol 20-Apr-2016
PMCID:PMC4837971
doi:10.3389/fmicb.2016.00569
PMID:27148246
Impact of floral sources and processing on the antimicrobial activities of different unifloral honeys Elbanna K, Attalla K, Elbadry M, Abdeltawab A, Gamal-Eldin H, Ramadan MF Asian Pac J Trop Dis 01-Jun-2014
PMCID:PMC4032034
doi:10.1016/S2222-1808(14)60504-1

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
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Monocyclic monoterpenoids
Flavesone 15800949 Click to see CC(C)C(=O)C1C(=O)C(C(=O)C(C1=O)(C)C)(C)C 252.31 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.09.006
Isoleptospermone 59518515 Click to see CCC(C)C(=O)C1C(=O)C(C(=O)C(C1=O)(C)C)(C)C 266.33 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.09.006
Leptospermone 3083632 Click to see CC(C)CC(=O)C1C(=O)C(C(=O)C(C1=O)(C)C)(C)C 266.33 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.09.006
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.09.006
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzoquinones / M-benzoquinones
5-Hydroxy-2,2,6,6-tetramethyl-4-(2-methylbutanoyl)cyclohex-4-ene-1,3-dione 6482356 Click to see CCC(C)C(=O)C1=C(C(C(=O)C(C1=O)(C)C)(C)C)O 266.33 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.09.006
5-Hydroxy-2,2,6,6-tetramethyl-4-(2-methylpropanoyl)cyclohex-4-ene-1,3-dione 5325550 Click to see CC(C)C(=O)C1=C(C(C(=O)C(C1=O)(C)C)(C)C)O 252.31 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.09.006
5-Hydroxy-2,2,6,6-tetramethyl-4-(3-methylbutanoyl)cyclohex-4-ene-1,3-dione 6428441 Click to see CC(C)CC(=O)C1=C(C(C(=O)C(C1=O)(C)C)(C)C)O 266.33 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.09.006
5-hydroxy-2,2,6,6-tetramethyl-4-[(2R)-2-methylbutanoyl]cyclohex-4-ene-1,3-dione 163078248 Click to see CCC(C)C(=O)C1=C(C(C(=O)C(C1=O)(C)C)(C)C)O 266.33 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.09.006
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(2R)-2,5-dihydroxy-7-methoxy-8-methyl-2-phenyl-3H-chromen-4-one 163032589 Click to see CC1=C(C=C(C2=C1OC(CC2=O)(C3=CC=CC=C3)O)O)OC 300.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.09.006
(2S)-2,5-dihydroxy-7-methoxy-6-methyl-2-phenyl-3H-chromen-4-one 102062189 Click to see CC1=C(C=C2C(=C1O)C(=O)CC(O2)(C3=CC=CC=C3)O)OC 300.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.09.006
2,5-Dihydroxy-7-methoxy-6-methylflavanone 12116707 Click to see CC1=C(C=C2C(=C1O)C(=O)CC(O2)(C3=CC=CC=C3)O)OC 300.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.09.006
2,5-Dihydroxy-7-methoxy-8-methylflavanone 12116708 Click to see CC1=C(C=C(C2=C1OC(CC2=O)(C3=CC=CC=C3)O)O)OC 300.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.09.006
4H-1-Benzopyran-4-one, 5-hydroxy-7-methoxy-8-methyl-2-phenyl- 12094473 Click to see CC1=C(C=C(C2=C1OC(=CC2=O)C3=CC=CC=C3)O)OC 282.29 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.09.006
5-Hydroxy-7-methoxy-6-methylflavone 369599 Click to see CC1=C(C=C2C(=C1O)C(=O)C=C(O2)C3=CC=CC=C3)OC 282.29 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.09.006

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