Zingiber spectabile - Unknown
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Internal ID UUID6440131bc7ad6711103691
Scientific name Zingiber spectabile
Authority Griff.
First published in Not. Pl. Asiat. 3:413. (1851); Lectotypified in: Gard. Bull. Singapore 48. (1998)

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Synonyms Top

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Common names Top

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Language Common/alternative name
Japanese オオヤマショウガ
Thai กะทือพิลาส
Chinese 蜂巢姜

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-tropical
    • Indo-China
      • Andaman Islands
      • Nicobar Nicobar
      • Thailand
    • Malesia
      • Jawa
      • Malaya

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000617878
Tropicos 34500332
INPN 447937
KEW urn:lsid:ipni.org:names:798388-1
The Plant List kew-273408
Open Tree Of Life 268566
NCBI Taxonomy 188518
IUCN Red List 117469019
IPNI 798388-1
iNaturalist 372652
GBIF 2757200
Freebase /m/0ys_pyg
EOL 987085
USDA GRIN 454980
Wikipedia Zingiber_spectabile
CMAUP NPO33471

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
Antimicrobial Action Mechanisms of Natural Compounds Isolated from Endophytic Microorganisms Eshboev F, Mamadalieva N, Nazarov PA, Hussain H, Katanaev V, Egamberdieva D, Azimova S Antibiotics (Basel) 18-Mar-2024
PMCID:PMC10967585
doi:10.3390/antibiotics13030271
PMID:38534706
Differing structures of galactoglucomannan in eudicots and non-eudicot angiosperms Ishida K, Ohba Y, Yoshimi Y, Wilson LF, Echevarría-Poza A, Yu L, Iwai H, Dupree P PLoS One 21-Dec-2023
PMCID:PMC10735049
doi:10.1371/journal.pone.0289581
PMID:38127933
The complete chloroplast genome sequence of Zingiber teres S. Q. Tong & Y. M. Xia (Zingiberaceae) Wang X, Tian S, Wang H, Yang L, Zou X, Baskaran XR, Li Q, Xing H, Li HL Mitochondrial DNA B Resour 25-Jun-2023
PMCID:PMC10294729
doi:10.1080/23802359.2023.2226256
PMID:37383606
Antimicrobial potentials of natural products against multidrug resistance pathogens: a comprehensive review Elmaidomy AH, Shady NH, Abdeljawad KM, Elzamkan MB, Helmy HH, Tarshan EA, Adly AN, Hussien YH, Sayed NG, Zayed A, Abdelmohsen UR RSC Adv 13-Oct-2022
PMCID:PMC9558262
doi:10.1039/d2ra04884a
PMID:36320761
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
New plastome structural rearrangements discovered in core Tillandsioideae (Bromeliaceae) support recently adopted taxonomy Vera-Paz SI, Díaz Contreras Díaz DD, Jost M, Wanke S, Rossado AJ, Hernández-Gutiérrez R, Salazar GA, Magallón S, Gouda EJ, Ramírez-Morillo IM, Donadío S, Granados Mendoza C Front Plant Sci 01-Aug-2022
PMCID:PMC9378858
doi:10.3389/fpls.2022.924922
PMID:35982706
Clonal Propagation of Valeriana jatamansi Retains the Essential Oil Profile of Mother Plants: An Approach Toward Generating Homogenous Grade of Essential Oil for Industrial Use Gautam RD, Kumar A, Kumar R, Chauhan R, Singh S, Kumar M, Kumar D, Kumar A, Singh S Front Plant Sci 14-Oct-2021
PMCID:PMC8551450
doi:10.3389/fpls.2021.738247
PMID:34721465
Phylogenetic analysis and development of molecular markers for five medicinal Alpinia species based on complete plastome sequences Yang H, Wang L, Chen H, Jiang M, Wu W, Liu S, Wang J, Liu C BMC Plant Biol 22-Sep-2021
PMCID:PMC8456601
doi:10.1186/s12870-021-03204-1
PMID:34551721
Biodiversity of Secondary Metabolites Compounds Isolated from Phylum Actinobacteria and Its Therapeutic Applications Al-shaibani MM, Radin Mohamed RM, Sidik NM, Enshasy HA, Al-Gheethi A, Noman E, Al-Mekhlafi NA, Zin NM Molecules 26-Jul-2021
PMCID:PMC8347454
doi:10.3390/molecules26154504
PMID:34361657
Population genetic structure and connectivity of a riparian selfing herb Caulokaempferia coenobialis at a fine-scale geographic level in subtropical monsoon forest Fu Q, Deng J, Chen M, Zhong Y, Lu GH, Wang YQ BMC Plant Biol 08-Jul-2021
PMCID:PMC8265151
doi:10.1186/s12870-021-03101-7
PMID:34238223
Enhanced Pharmaceutically Active Compounds Productivity from Streptomyces SUK 25: Optimization, Characterization, Mechanism and Techno-Economic Analysis Al-Shaibani MM, Radin Mohamed RM, Zin NM, Al-Gheethi A, Al-Sahari M, El Enshasy HA Molecules 25-Apr-2021
PMCID:PMC8123281
doi:10.3390/molecules26092510
PMID:33923072
Complete chloroplast genome of Zingiber mioga by de novo sequencing Jiang P, Huang R, Sun T, Chen C, Zuo R, Taoa Y Mitochondrial DNA B Resour 26-Mar-2021
PMCID:PMC8008884
doi:10.1080/23802359.2021.1904799
PMID:33829093
Medicinal plants as a fight against murine blood-stage malaria Dkhil MA, Al-Quraishy S, Al-Shaebi EM, Abdel-Gaber R, Thagfan FA, Qasem MA Saudi J Biol Sci 19-Dec-2020
PMCID:PMC7938113
doi:10.1016/j.sjbs.2020.12.014
PMID:33732056
Complete chloroplast genomes of Zingiber montanum and Zingiber zerumbet: Genome structure, comparative and phylogenetic analyses Li DM, Ye YJ, Xu YC, Liu JM, Zhu GF PLoS One 31-Jul-2020
PMCID:PMC7394419
doi:10.1371/journal.pone.0236590
PMID:32735595
The Complete Chloroplast Genome Sequences of 14 Curcuma Species: Insights Into Genome Evolution and Phylogenetic Relationships Within Zingiberales Liang H, Zhang Y, Deng J, Gao G, Ding C, Zhang L, Yang R Front Genet 23-Jul-2020
PMCID:PMC7396571
doi:10.3389/fgene.2020.00802
PMID:32849804

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 / Diterpenoids / Colensane and clerodane diterpenoids
3-[2-[(4aR,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]ethenyl]furan 138113847 Click to see CC1(CCCC2(C1CCC(=C)C2C=CC3=COC=C3)C)C 284.40 unknown https://doi.org/10.1016/S0031-9422(00)89800-3
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids / Curcuminoids
(1E,4Z,6E)-5-hydroxy-1,7-bis(4-hydroxy-3-methoxyphenyl)hepta-1,4,6-trien-3-one 5281767 Click to see COC1=C(C=CC(=C1)C=CC(=CC(=O)C=CC2=CC(=C(C=C2)O)OC)O)O 368.40 unknown https://doi.org/10.1016/J.BMCL.2012.02.064
Curcumin 969516 Click to see COC1=C(C=CC(=C1)C=CC(=O)CC(=O)C=CC2=CC(=C(C=C2)O)OC)O 368.40 unknown https://doi.org/10.1016/J.BMCL.2012.02.064
p-Hydroxy-curucumin 5324476 Click to see COC1=C(C=CC(=C1)C=CC(=CC(=O)C=CC2=CC=C(C=C2)O)O)O 338.40 unknown https://doi.org/10.1016/J.BMCL.2012.02.064
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
spectaflavoside A 70690358 Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C2=O)C(=C(C(=C3)O)C4=C(C=C(C5=C4OC(=C(C5=O)OC6C(C(C(C(O6)C)OC(=O)C)O)O)C7=CC=C(C=C7)O)O)O)O)C8=CC=C(C=C8)O)O)O)OC(=O)C 946.80 unknown https://doi.org/10.1016/J.BMCL.2012.02.064
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1016/J.BMCL.2012.02.064
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
5,7-Dihydroxy-2-(4-Hydroxyphenyl)-4-Oxo-4h-Chromen-3-Yl 3,4-Di-O-Acetyl-6-Deoxy-Alpha-L-Mannopyranoside 10459196 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)OC(=O)C)OC(=O)C 516.40 unknown https://doi.org/10.1016/J.BMCL.2012.02.064
kaempferol-3-O-(2,3-di-O-acetyl-alpha-L-rhamnopyranoside) 11203112 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)OC(=O)C)OC(=O)C)O 516.40 unknown https://doi.org/10.1016/J.BMCL.2012.02.064
kaempferol-3-O-(2,4-di-O-acetyl-alpha-L-rhamnopyranoside) 14825858 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)OC(=O)C)O)OC(=O)C 516.40 unknown https://doi.org/10.1016/J.BMCL.2012.02.064
kaempferol-3-O-(4-O-acetyl-alpha-L-rhamnopyranoside) 10624340 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)OC(=O)C 474.40 unknown https://doi.org/10.1016/J.BMCL.2012.02.064

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