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Homalomena aromatica

Homalomena aromatica - 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 UUID64403e61b074c534756218
Scientific name Homalomena aromatica
Authority Schott
First published in Melet. Bot. : 20 (1832)

Description Top

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Synonyms Top

Scientific name Authority First published in
Zantedeschia aromatica Spreng. Syst. Veg. 3: 765 (1826)
Zantedeschia foetida K.Koch Index Seminum (B, Berolinensis) 1854(App.): 9 (1855)
Calla aromatica Roxb. Fl. Ind. ed. 1832 , 3: 513 (1832)

Common names Top

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Language Common/alternative name
Chinese 芬芳千年健

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000983059
Tropicos 2102825
KEW urn:lsid:ipni.org:names:87159-1
The Plant List kew-99903
Open Tree Of Life 4000469
NCBI Taxonomy 1804071
GBIF 2868616
EOL 1099878
IPNI 87159-1

Genomes (via NCBI) Top

Below is displayed the reference genome only!
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Accession Assembly
Name Level Submitter Released Coverage Size
GCA_040966555.1 ASM4096655v1 Scaffold Iridian Genomes 2024-07-30 60.0x 672.72 Mb

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
Ethnomedicinal Practices and Traditional Medicinal Plants of Barak Valley, Assam: a systematic review Barbhuiya PA, Laskar AM, Mazumdar H, Dutta PP, Pathak MP, Dey BK, Sen S J Pharmacopuncture 30-Sep-2022
PMCID:PMC9510141
doi:10.3831/KPI.2022.25.3.149
PMID:36186100
A Review: Natural and Synthetic Compounds Targeting Entamoeba histolytica and Its Biological Membrane Jasni N, Saidin S, Arifin N, Azman DK, Shin LN, Othman N Membranes (Basel) 01-Apr-2022
PMCID:PMC9024486
doi:10.3390/membranes12040396
PMID:35448367
Exploring the Roles of Dietary Herbal Essential Oils in Aquaculture: A Review Dawood MA, El Basuini MF, Yilmaz S, Abdel-Latif HM, Alagawany M, Kari ZA, Abdul Razab MK, Hamid NK, Moonmanee T, Van Doan H Animals (Basel) 24-Mar-2022
PMCID:PMC8996993
doi:10.3390/ani12070823
PMID:35405814
Section 1: 5th IUPHAR WCP-NP, 2019 INDIA N/A Indian J Pharmacol 01-Dec-2021
PMCID:PMC9045588
Insight into the antifungals used to address human infection due to Trichosporon spp.: a scoping review Malacrida AM, Salci TP, Negri M, Svidzinski TI Future Microbiol 25-Oct-2021
PMCID:PMC8544482
doi:10.2217/fmb-2021-0048
PMID:34689610
Status and consolidated list of threatened medicinal plants of India Gowthami R, Sharma N, Pandey R, Agrawal A Genet Resour Crop Evol 25-May-2021
PMCID:PMC8148398
doi:10.1007/s10722-021-01199-0
PMID:34054223
Investigation of Potential Antioxidant, Thrombolytic and Neuropharmacological Activities of Homalomena aromatica Leaves Using Experimental and In Silico Approaches Ali MS, Sayem SA, Habibullah, Quah Y, Lee EB, Birhanu BT, Suk K, Park SC Molecules 12-Feb-2021
PMCID:PMC7918836
doi:10.3390/molecules26040975
PMID:33673167
Bigger Data Approach to Analysis of Essential Oils and Their Antifungal Activity against Aspergillus niger, Candida albicans, and Cryptococcus neoformans Powers CN, Satyal P, Mayo JA, McFeeters H, McFeeters RL Molecules 07-Aug-2019
PMCID:PMC6718987
doi:10.3390/molecules24162868
PMID:31394798
Medicinal Plants for the Treatment of Local Tissue Damage Induced by Snake Venoms: An Overview from Traditional Use to Pharmacological Evidence Félix-Silva J, Silva-Junior AA, Zucolotto SM, Fernandes-Pedrosa MD Evid Based Complement Alternat Med 21-Aug-2017
PMCID:PMC5585606
doi:10.1155/2017/5748256
PMID:28904556
Asymmetric syntheses of 8-oxabicyclo[3,2,1]octane and 11-oxatricyclo[5.3.1.0]undecane from glycals Liao H, Leng WL, Le Mai Hoang K, Yao H, He J, Voo AY, Liu XW Chem Sci 07-Aug-2017
PMCID:PMC5625258
doi:10.1039/c7sc02625k
PMID:28989693
Hypoglycaemic activity of Mathurameha, a Thai traditional herbal formula aqueous extract, and its effect on biochemical profiles of streptozotocin-nicotinamide-induced diabetic rats Chayarop K, Peungvicha P, Temsiririrkkul R, Wongkrajang Y, Chuakul W, Rojsanga P BMC Complement Altern Med 29-Jun-2017
PMCID:PMC5492915
doi:10.1186/s12906-017-1851-8
PMID:28662699
Bio-Pesticides: New Tool for the Control of Aedes (Stegomyia) albopictus (Culicidae: Diptera) in Pakistan Bilal H, Sahar S, Din S J Arthropod Borne Dis 27-May-2017
PMCID:PMC5641616
PMID:29062852
Biomaterials and Nanotherapeutics for Enhancing Skin Wound Healing Das S, Baker AB Front Bioeng Biotechnol 31-Oct-2016
PMCID:PMC5087310
doi:10.3389/fbioe.2016.00082
PMID:27843895
Ethnopharmacological Survey of Medicinal Plants Used by Traditional Healers and Indigenous People in Chittagong Hill Tracts, Bangladesh, for the Treatment of Snakebite Kadir MF, Karmoker JR, Alam MR, Jahan SR, Mahbub S, Mia MM Evid Based Complement Alternat Med 23-Mar-2015
PMCID:PMC4386694
doi:10.1155/2015/871675
PMID:25878719
In vitro propagation of Homalomena aromatica Schott., an endangered aromatic medicinal herb of Northeast India Raomai S, Kumaria S, Tandon P Physiol Mol Biol Plants 21-Feb-2013
PMCID:PMC3656179
doi:10.1007/s12298-013-0168-4
PMID:24431499

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
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Linalool, (+/-)- 6549 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown https://doi.org/10.1002/FFJ.2730030409
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-Bullatantriol 71430886 Click to see CC12CCC(C1C(CCC2O)(C)O)CC(C)(C)O 256.38 unknown https://doi.org/10.1016/0031-9422(92)83719-F
(1S,4R,4aS,8aS)-4,8a-dimethyl-6-propan-2-yl-1,2,3,4a,5,8-hexahydronaphthalene-1,4-diol 133561762 Click to see CC(C)C1=CCC2(C(CCC(C2C1)(C)O)O)C 238.37 unknown https://doi.org/10.1016/0031-9422(92)83719-F
2,8-Dimethyl-5-propan-2-yl-11-oxatricyclo[5.3.1.02,6]undecan-8-ol 162899174 Click to see CC(C)C1CCC2(C1C3C(CCC2O3)(C)O)C 238.37 unknown https://doi.org/10.1016/0031-9422(92)83123-G
2,8-Dimethyl-5-propan-2-yl-11-oxatricyclo[5.3.1.02,6]undecane-1,8-diol 163007589 Click to see CC(C)C1CCC2(C1C3C(CCC2(O3)O)(C)O)C 254.36 unknown https://doi.org/10.1016/0031-9422(92)83123-G
3-(2-Hydroxy-2-methylpropyl)-4,7a-dimethyl-2,3,3a,5,6,7-hexahydro-1H-indene-4,7-diol 78069537 Click to see CC12CCC(C1C(CCC2O)(C)O)CC(C)(C)O 256.38 unknown https://doi.org/10.1016/0031-9422(92)83719-F
4-Isopropyl-1,6-dimethyl-1,2,3,4,4a,7,8,8a-octahydro-1-naphthalenol 519662 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1016/0031-9422(92)83123-G
4,7a-dimethyl-3-(2-methylprop-1-enyl)-2,3,3a,5,6,7-hexahydro-1H-indene-4,7-diol 85401441 Click to see CC(=CC1CCC2(C1C(CCC2O)(C)O)C)C 238.37 unknown https://doi.org/10.1016/0031-9422(92)83719-F
4,7a-dimethyl-3-(2-methylprop-2-enyl)-2,3,3a,5,6,7-hexahydro-1H-indene-4,7-diol 85381822 Click to see CC(=C)CC1CCC2(C1C(CCC2O)(C)O)C 238.37 unknown https://doi.org/10.1016/0031-9422(92)83719-F
7-Acetyl-2-hydroxy-2-methyl-5-isopropylbicyclo[4.3.0]nonane 539857 Click to see CC(C)C1CCC(C2C1C(CC2)C(=O)C)(C)O 238.37 unknown https://doi.org/10.1016/0031-9422(92)83719-F
7,10-Dihydroxy-1,7-dimethyl-4-isopropylbicyclo[4.4.0]dec-3-ene 12313755 Click to see CC(C)C1=CCC2(C(CCC(C2C1)(C)O)O)C 238.37 unknown https://doi.org/10.1016/0031-9422(92)83719-F
alpha-Cadinol 10398656 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1016/0031-9422(92)83123-G
Homalomenol A 91884956 Click to see CC(=CC1CCC2(C1C(CCC2O)(C)O)C)C 238.37 unknown https://doi.org/10.1016/0031-9422(92)83719-F
Homalomenol B 101634633 Click to see CC(=C)CC1CCC2(C1C(CCC2O)(C)O)C 238.37 unknown https://doi.org/10.1016/0031-9422(92)83719-F
Homalomenol D 101712280 Click to see CC(C)C1CCC2(C1C3C(CCC2O3)(C)O)C 238.37 unknown https://doi.org/10.1016/0031-9422(92)83123-G
Oplodiol 12313756 Click to see CC(C)C1=CCC2(C(CCC(C2C1)(C)O)O)C 238.37 unknown https://doi.org/10.1016/0031-9422(92)83719-F
Oplopanone 10466745 Click to see CC(C)C1CCC(C2C1C(CC2)C(=O)C)(C)O 238.37 unknown https://doi.org/10.1016/0031-9422(92)83719-F
rel-(1R,2S,5R,6R,7R,8R)-5-isopropyl-2,8-dimethyl-11-oxatricyclo[5.3.1.0(2,6)]undecane-1,8-diol 121596197 Click to see CC(C)C1CCC2(C1C3C(CCC2(O3)O)(C)O)C 254.36 unknown https://doi.org/10.1016/0031-9422(92)83123-G
T-Muurolol 3084331 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1016/J.MYCMED.2011.10.007
https://doi.org/10.1016/0031-9422(92)83123-G
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
1,4,7-Eudesmanetriol 101634632 Click to see CC(C)C1(CCC2(C(CCC(C2C1)(C)O)O)C)O 256.38 unknown https://doi.org/10.1016/0031-9422(92)83719-F
4,8a-dimethyl-6-propan-2-yl-2,3,4a,5,7,8-hexahydro-1H-naphthalene-1,4,6-triol 73323499 Click to see CC(C)C1(CCC2(C(CCC(C2C1)(C)O)O)C)O 256.38 unknown https://doi.org/10.1016/0031-9422(92)83719-F

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