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Etlingera littoralis

Etlingera littoralis - 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 UUID643ffa1358622108300509
Scientific name Etlingera littoralis
Authority (J.Koenig) Giseke
First published in Prael. ord. nat. pl. 209, 229, 251

Description Top

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Etlingera littoralis is a plant belonging to the ginger family, Zingiberaceae. It does not have any subspecies listed in the Catalogue of Life. This plant is typically found in lowland tropical forest floors, specifically in areas with elevations of up to 300 meters. Its natural habitat includes regions such as Hainan, Indo-China, and Malesia.

Synonyms Top

Scientific name Authority First published in
Amomum littorale J.Koenig Observ. bot. 52
Amomum rubroluteum Baker Fl. Brit. India 236
Cardamomum littorale (J.Koenig) Kuntze Revis. gen. pl. 686
Etlingera rubrolutea (Baker) C.K.Lim Folia malaysiana 2:157. (2001)

Common names Top

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Language Common/alternative name
Chinese 红茴砂

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

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
  • Asia-tropical
    • Indo-China
      • Myanmar
      • Thailand
      • Vietnam
    • Malesia
      • Malaya

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000415636
Tropicos 34500559
KEW urn:lsid:ipni.org:names:796614-1
The Plant List kew-244714
Open Tree Of Life 539426
NCBI Taxonomy 188496
IUCN Red List 117234514
IPNI 796614-1
iNaturalist 427622
GBIF 2759996
EOL 1119394
USDA GRIN 409516
Wikipedia Etlingera_littoralis

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
First Report on Wild Ginger (Family: Zingiberaceae) Species Composition with New Records in Limestone Forests of Kelantan, Peninsular Malaysia Appalasamy S, Arumugam N, Zamri NS, Fadhlina A, Kumaran JV, Subramaniam S Trop Life Sci Res 30-Sep-2022
PMCID:PMC9747101
doi:10.21315/tlsr2022.33.3.3
PMID:36545056
Putative Anticancer Compounds from Plant-Derived Endophytic Fungi: A Review Hridoy M, Gorapi MZ, Noor S, Chowdhury NS, Rahman MM, Muscari I, Masia F, Adorisio S, Delfino DV, Mazid MA Molecules 04-Jan-2022
PMCID:PMC8746379
doi:10.3390/molecules27010296
PMID:35011527
Cure lies in nature: medicinal plants and endophytic fungi in curbing cancer Tyagi G, Kapoor N, Chandra G, Gambhir L 3 Biotech 12-May-2021
PMCID:PMC8116431
doi:10.1007/s13205-021-02803-x
PMID:33996375
Assessment of Antimicrobial Activity, Mode of Action and Volatile Compounds of Etlingera pavieana Essential Oil Naksang P, Tongchitpakdee S, Thumanu K, Oruna-Concha MJ, Niranjan K, Rachtanapun C Molecules 16-Jul-2020
PMCID:PMC7397041
doi:10.3390/molecules25143245
PMID:32708709
Endophytic Fungi—Alternative Sources of Cytotoxic Compounds: A Review Uzma F, Mohan CD, Hashem A, Konappa NM, Rangappa S, Kamath PV, Singh BP, Mudili V, Gupta VK, Siddaiah CN, Chowdappa S, Alqarawi AA, Abd_Allah EF Front Pharmacol 26-Apr-2018
PMCID:PMC5932204
doi:10.3389/fphar.2018.00309
PMID:29755344
Chemical Composition and Bioactivities of the Essential Oil from Etlingera yunnanensis against Two Stored Product Insects Guo SS, You CX, Liang JY, Zhang WJ, Geng ZF, Wang CF, Du SS, Lei N Molecules 28-Aug-2015
PMCID:PMC6332329
doi:10.3390/molecules200915735
PMID:26343627
Terpenoids from Endophytic Fungi de Souza JJ, Vieira IJ, Rodrigues-Filho E, Braz-Filho R Molecules 19-Dec-2011
PMCID:PMC6264667
doi:10.3390/molecules161210604
PMID:22183885
Bird Species Diversity in the Padawan Limestone Area, Sarawak Mansor MS, Sah SA, Koon LC, Rahman MA Trop Life Sci Res 01-Dec-2011
PMCID:PMC3819082
PMID:24575218
The First Hydroperoxydihydrochalcone in the Etlingera Genus: Etlinglittoralin from the Rhizomes of Etlingera littoralis Surat Laphookhieo, Chotika Jeerapong, Sarot Cheenpracha, Wisanu Maneerat, Uma Prawat, Thongchai Kruahong The Japan Institute of Heterocyclic Chemistry 14-Mar-2011
doi:10.3987/COM-10-12131
1-(2,6-Dihydr­oxy-4-methoxy­phen­yl)-3-phenyl­propan-1-one Chantrapromma S, Jeerapong J, Kruahong T, Laphookhieo S, Fun HK Acta Crystallogr Sect E Struct Rep Online 21-Apr-2010
PMCID:PMC2979227
doi:10.1107/S1600536810013590
PMID:21579171

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
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
1-(3,6-dihydroxy-1-methoxy-6-methyl-9-propan-2-yl-7,8,9,9a-tetrahydro-5aH-dibenzofuran-4-yl)-3-phenylpropan-1-one 73307027 Click to see CC(C)C1CCC(C2C1C3=C(C=C(C(=C3O2)C(=O)CCC4=CC=CC=C4)O)OC)(C)O 424.50 unknown https://doi.org/10.3987/COM-10-12131
1-[(5aR,6S,9R,9aS)-6-hydroperoxy-3-hydroxy-1-methoxy-6-methyl-9-propan-2-yl-7,8,9,9a-tetrahydro-5aH-dibenzofuran-4-yl]-3-phenylpropan-1-one 53261003 Click to see CC(C)C1CCC(C2C1C3=C(C=C(C(=C3O2)C(=O)CCC4=CC=CC=C4)O)OC)(C)OO 440.50 unknown https://doi.org/10.3987/COM-10-12131
1-[2,6-Dihydroxy-4-methoxy-3-(3-methyl-6-propan-2-ylcyclohex-2-en-1-yl)phenyl]-3-phenylpropan-1-one 14237695 Click to see CC1=CC(C(CC1)C(C)C)C2=C(C=C(C(=C2O)C(=O)CCC3=CC=CC=C3)O)OC 408.50 unknown https://doi.org/10.3987/COM-10-12131
1-[2,6-dihydroxy-4-methoxy-3-[(1S,6S)-3-methyl-6-propan-2-ylcyclohex-2-en-1-yl]phenyl]-3-phenylpropan-1-one 14237696 Click to see CC1=CC(C(CC1)C(C)C)C2=C(C=C(C(=C2O)C(=O)CCC3=CC=CC=C3)O)OC 408.50 unknown https://doi.org/10.3987/COM-10-12131
2',6'-Dihydroxy-4'-methoxydihydrochalcone 169676 Click to see COC1=CC(=C(C(=C1)O)C(=O)CCC2=CC=CC=C2)O 272.29 unknown https://doi.org/10.3987/COM-10-12131
Adunctin E 42607690 Click to see CC(C)C1CCC(C2C1C3=C(C=C(C(=C3O2)C(=O)CCC4=CC=CC=C4)O)OC)(C)O 424.50 unknown https://doi.org/10.3987/COM-10-12131
Asebogenin 442255 Click to see COC1=CC(=C(C(=C1)O)C(=O)CCC2=CC=C(C=C2)O)O 288.29 unknown https://doi.org/10.3987/COM-10-12131
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / Retro-dihydrochalcones
1-Phenyl-3-(2,4,6-trihydroxyphenyl)propan-1-one 57048077 Click to see C1=CC=C(C=C1)C(=O)CCC2=C(C=C(C=C2O)O)O 258.27 unknown https://doi.org/10.3987/COM-10-12131

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Collections Top

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