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Hedychium gardnerianum

Hedychium gardnerianum - Unknown
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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 UUID643ffcbbf059b807729055
Scientific name Hedychium gardnerianum
Authority Sheppard ex Ker Gawl.
First published in Bot. Reg. 9, pl.774. (1824)

Description Top

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Synonyms Top

Scientific name Authority First published in
Renealmia grandiflora R.Br. Prodr. Fl. Nov. Holl. 591 1810
Hedychium gardnerianum var. fasciatum K.Koch Index seminum [B, Berolinensis] App. 1 5

Common names Top

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Language Common/alternative name
English kahila garland-lily
Finnish tuoksuinkivääri
French longose
Portuguese conteira
Chinese 红丝姜花
Chinese 紅絲薑花

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Name Authority First published in
Hedychium gardnerianum var. pallidum (Regel) Baker Fl. Brit. India 230

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

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000435987
USDA Plants HEGA
Tropicos 100201790
KEW urn:lsid:ipni.org:names:69077-3
The Plant List kew-248143
Open Tree Of Life 207486
NCBI Taxonomy 4647
Nature Serve 2.160086
IPNI 60474165-2
iNaturalist 52495
GBIF 2758700
Freebase /m/07tyx_
EPPO HEYGA
EOL 1118152
USDA GRIN 18582
Wikipedia Hedychium_gardnerianum

Genomes (via NCBI) Top

Below is displayed the reference genome only!
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Accession Assembly
Name Level Submitter Released Coverage Size
GCA_038050645.1 ASM3805064v1 Scaffold Iridian Genomes 2024-04-10 60.0x 787.56 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
Macaronesian Plants as Promising Biopesticides against the Crop Pest Ceratitis capitata Tavares WR, Jiménez IA, Oliveira L, Kuhtinskaja M, Vaher M, Rosa JS, Seca AM, Bazzocchi IL, Barreto MD Plants (Basel) 10-Dec-2023
PMCID:PMC10747946
doi:10.3390/plants12244122
PMID:38140449
Functional and ecological diversification of underground organs in Solanum Gagnon E, Baldaszti L, Moonlight P, Knapp S, Lehmann CE, Särkinen T Front Genet 10-Oct-2023
PMCID:PMC10597785
doi:10.3389/fgene.2023.1231413
PMID:37886686
Strategies for the Management of Aggressive Invasive Plant Species Lorenzo P, Morais MC Plants (Basel) 28-Jun-2023
PMCID:PMC10346621
doi:10.3390/plants12132482
PMID:37447043
Human Settlement and Landscape Anthropization of Remote Oceanic Islands: A Comparison between Rapa Nui (Pacific Ocean) and the Azores (Atlantic Ocean) Rull V Plants (Basel) 24-May-2023
PMCID:PMC10255592
doi:10.3390/plants12112089
PMID:37299069
A Comprehensive Review on Pharmacologically Active Phyto-Constituents from Hedychium species Singh AP, Chitme H, Sharma RK, Kandpal J, Behera A, Abdel-Wahab BA, Orabi MA, Khateeb MM, Shafiuddin Habeeb M, Bakir MB Molecules 06-Apr-2023
PMCID:PMC10096824
doi:10.3390/molecules28073278
PMID:37050042
Invasion by an ecosystem engineer changes biotic interactions between native and non‐native taxa Holmquist AJ, Adams SA, Gillespie RG Ecol Evol 22-Feb-2023
PMCID:PMC9943940
doi:10.1002/ece3.9820
PMID:36844666
Xanthones: Biosynthesis and Trafficking in Plants, Fungi and Lichens Badiali C, Petruccelli V, Brasili E, Pasqua G Plants (Basel) 04-Feb-2023
PMCID:PMC9967055
doi:10.3390/plants12040694
PMID:36840041
Bioprospecting essential oils of exotic species as potential mitigations of ruminant enteric methanogenesis Nunes HP, Maduro Dias CS, Borba AE Heliyon 02-Jan-2023
PMCID:PMC9850177
doi:10.1016/j.heliyon.2022.e12786
PMID:36685396
Alternative Forages as Roughage for Ruminant: Nutritional Characteristics and Digestibility of Six Exotic Plants in Azores Archipelago Nunes HP, Teixeira S, Maduro Dias CS, Borba AE Animals (Basel) 19-Dec-2022
PMCID:PMC9774218
doi:10.3390/ani12243587
PMID:36552506
Functional bioactive compounds in ginger, turmeric, and garlic Ajanaku CO, Ademosun OT, Atohengbe PO, Ajayi SO, Obafemi YD, Owolabi OA, Akinduti PA, Ajanaku KO Front Nutr 08-Dec-2022
PMCID:PMC9773837
doi:10.3389/fnut.2022.1012023
PMID:36570131
Plant-Associated Bacteria as Sources for the Development of Bioherbicides Fang W, Liu F, Wu Z, Zhang Z, Wang K Plants (Basel) 06-Dec-2022
PMCID:PMC9737584
doi:10.3390/plants11233404
PMID:36501441
Cytotoxic Labdane Diterpenes, Norlabdane Diterpenes and Bis-Labdanic Diterpenes from the Zingiberaceae: A Systematic Review Voon KJ, Sivasothy Y, Sundralingam U, Lalmahomed A, Goh AP Pharmaceuticals (Basel) 05-Dec-2022
PMCID:PMC9783331
doi:10.3390/ph15121517
PMID:36558968
Tissue Culture in Ornamentals: Cultivation Factors, Propagation Techniques, and Its Application Mehbub H, Akter A, Akter MA, Mandal MS, Hoque MA, Tuleja M, Mehraj H Plants (Basel) 23-Nov-2022
PMCID:PMC9736077
doi:10.3390/plants11233208
PMID:36501247
Multi-Target Mechanisms of Phytochemicals in Alzheimer’s Disease: Effects on Oxidative Stress, Neuroinflammation and Protein Aggregation Sharifi-Rad J, Rapposelli S, Sestito S, Herrera-Bravo J, Arancibia-Diaz A, Salazar LA, Yeskaliyeva B, Beyatli A, Leyva-Gómez G, González-Contreras C, Gürer ES, Martorell M, Calina D J Pers Med 15-Sep-2022
PMCID:PMC9500804
doi:10.3390/jpm12091515
PMID:36143299
Coronarin A modulated hepatic glycogen synthesis and gluconeogenesis via inhibiting mTORC1/S6K1 signaling and ameliorated glucose homeostasis of diabetic mice Huang SL, Xie W, Ye YL, Liu J, Qu H, Shen Y, Xu TF, Zhao ZH, Shi Y, Shen JH, Leng Y Acta Pharmacol Sin 09-Sep-2022
PMCID:PMC9958036
doi:10.1038/s41401-022-00985-5
PMID:36085523

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Salicylic acid and derivatives / Salicylic acids
Salicylic Acid 338 Click to see C1=CC=C(C(=C1)C(=O)O)O 138.12 unknown https://doi.org/10.1080/1478641031000118906
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
(2S)-4-[(E)-2-(furan-3-yl)ethenyl]-4a,8,8-trimethyl-3-methylidene-2,4,5,6,7,8a-hexahydro-1H-naphthalen-2-ol 5316079 Click to see CC1(CCCC2(C1CC(C(=C)C2C=CC3=COC=C3)O)C)C 300.40 unknown https://doi.org/10.1002/PTR.3057
3-[2-(5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl)ethenyl]furan 85079076 Click to see CC1(CCCC2(C1CCC(=C)C2C=CC3=COC=C3)C)C 284.40 unknown https://doi.org/10.1002/PTR.3057
4-[2-(furan-3-yl)ethenyl]-4a,8,8-trimethyl-3-methylidene-2,4,5,6,7,8a-hexahydro-1H-naphthalen-1-ol 72780923 Click to see CC1(CCCC2(C1C(CC(=C)C2C=CC3=COC=C3)O)C)C 300.40 unknown https://doi.org/10.1002/PTR.3057
4-[2-(furan-3-yl)ethenyl]-4a,8,8-trimethyl-3-methylidene-2,4,5,6,7,8a-hexahydro-1H-naphthalen-2-ol 74333099 Click to see CC1(CCCC2(C1CC(C(=C)C2C=CC3=COC=C3)O)C)C 300.40 unknown https://doi.org/10.1002/PTR.3057
Coronarin A 24851535 Click to see CC1(CCCC2(C1CC(C(=C)C2C=CC3=COC=C3)O)C)C 300.40 unknown https://doi.org/10.1002/PTR.3057
Coronarin E 9971144 Click to see CC1(CCCC2(C1CCC(=C)C2C=CC3=COC=C3)C)C 284.40 unknown https://doi.org/10.1002/PTR.3057
Yunnancoronarin A 12187319 Click to see CC1(CCCC2(C1C(CC(=C)C2C=CC3=COC=C3)O)C)C 300.40 unknown https://doi.org/10.1002/PTR.3057
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
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/10.1080/1478641031000118906
Oplopanone 10466745 Click to see CC(C)C1CCC(C2C1C(CC2)C(=O)C)(C)O 238.37 unknown https://doi.org/10.1080/1478641031000118906
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(2S)-3-[(E)-2-[(1R,3S,4aS,8aS)-3-hydroxy-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]ethenyl]-2-hydroxy-2H-furan-5-one 163185135 Click to see CC1(CCCC2(C1CC(C(=C)C2C=CC3=CC(=O)OC3O)O)C)C 332.40 unknown https://doi.org/10.1002/PTR.3057
(2S)-3-[2-[(1R,3S,4aS,8aS)-3-hydroxy-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]ethenyl]-2-hydroxy-2H-furan-5-one 163075075 Click to see CC1(CCCC2(C1CC(C(=C)C2C=CC3=CC(=O)OC3O)O)C)C 332.40 unknown https://doi.org/10.1002/PTR.3057
4-[(E)-2-[(1R,3S,4aS,8aS)-3-hydroxy-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]ethenyl]-2H-furan-5-one 12068804 Click to see CC1(CCCC2(C1CC(C(=C)C2C=CC3=CCOC3=O)O)C)C 316.40 unknown https://doi.org/10.1002/PTR.3057
4-[2-(4-hydroxy-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl)ethenyl]-2H-furan-5-one 74322364 Click to see CC1(CCCC2(C1C(CC(=C)C2C=CC3=CCOC3=O)O)C)C 316.40 unknown https://doi.org/10.1002/PTR.3057
4-[2-(5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl)ethenyl]-2H-furan-5-one 73315303 Click to see CC1(CCCC2(C1CCC(=C)C2C=CC3=CCOC3=O)C)C 300.40 unknown https://doi.org/10.1002/PTR.3057
4-[2-[(1R,3S,4aS,8aS)-3-hydroxy-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]ethenyl]-2H-furan-5-one 162868160 Click to see CC1(CCCC2(C1CC(C(=C)C2C=CC3=CCOC3=O)O)C)C 316.40 unknown https://doi.org/10.1002/PTR.3057
Villosin 16733738 Click to see CC1(CCCC2(C1CCC(=C)C2C=CC3=CCOC3=O)C)C 300.40 unknown https://doi.org/10.1002/PTR.3057
Yunnancoronarin B 101457894 Click to see CC1(CCCC2(C1C(CC(=C)C2C=CC3=CCOC3=O)O)C)C 316.40 unknown https://doi.org/10.1002/PTR.3057
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
1-Hydroxyxanthone 5376036 Click to see C1=CC=C2C(=C1)C(=O)C3=C(C=CC=C3O2)O 212.20 unknown https://doi.org/10.1080/1478641031000118906
3-(2-Hydroxyethoxy)-9H-xanthen-9-one 71379467 Click to see C1=CC=C2C(=C1)C(=O)C3=C(O2)C=C(C=C3)OCCO 256.25 unknown https://doi.org/10.1080/1478641031000118906
> Phenylpropanoids and polyketides / Isoflavonoids / Rotenoids / Rotenones
6-Hydroxysumatrol 14427376 Click to see CC(=C)C1CC2=C(O1)C=C(C3=C2OC4C(C3=O)C5=CC(=C(C=C5OC4O)OC)OC)O 426.40 unknown https://doi.org/10.1002/PTR.3057

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Collections Top

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