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Alpinia intermedia

Alpinia intermedia - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Alpinia intermedia - 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 UUID643ff1878153b083958596
Scientific name Alpinia intermedia
Authority Gagnep.
First published in Bull. Soc. Bot. France 48:LXXXIII. (1901)

Description Top

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Synonyms Top

Scientific name Authority First published in
Alpinia hokutensis Hayata Icon. pl. formosan. 120
Alpinia kelungensis Hayata Icon. pl. formosan. 216
Languas hokutensis (Hayata) Sasaki Trans. Nat. Hist. Soc. Taiwan 14:22. (1924)
Languas intermedia (Gagnep.) Sasaki Trans. Nat. Hist. Soc. Formosa 18:175. (1928)
Languas kelungensis (Hayata) Sasaki Trans. Nat. Hist. Soc. Taiwan 14:23. (1924)

Common names Top

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Language Common/alternative name
Japanese アオノクマタケラン
pwn valjingat
Chinese 小草寇
Chinese 光叶山姜
Chinese 山月桃

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China Southeast
    • Eastern Asia
      • Japan
      • Kazan-retto
      • Nansei-shoto
      • Taiwan
  • Asia-tropical
    • Indo-China
      • Laos
      • Myanmar
      • Thailand
      • Vietnam
    • Malesia
      • Philippines

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000338539
Tropicos 34500597
KEW urn:lsid:ipni.org:names:795301-1
The Plant List kew-218836
Open Tree Of Life 103588
NCBI Taxonomy 105673
IPNI 795301-1
iNaturalist 545106
GBIF 5302174
EPPO AIIIN
EOL 1126873
USDA GRIN 2668

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
Allelopathic Activity of a Novel Compound, Two Known Sesquiterpenes, and a C13 Nor-Isopenoid from the Leave of Croton oblongifolius Roxb. for Weed Control Moh SM, Tojo S, Teruya T, Kato-Noguchi H Plants (Basel) 25-Sep-2023
PMCID:PMC10574435
doi:10.3390/plants12193384
PMID:37836124
Phytochemicals and bioactive compounds effective against acute myeloid leukemia: A systematic review Egbuna C, Patrick‐Iwuanyanwu KC, Onyeike EN, Khan J, Palai S, Patel SB, Parmar VK, Kushwaha G, Singh O, Jeevanandam J, Kumarasamy S, Uche CZ, Narayanan M, Rudrapal M, Odoh U, Chikeokwu I, Găman M, Saravanan K, Ifemeje JC, Ezzat SM, Olisah MC, Chikwendu CJ, Adedokun KA, Imodoye SO, Bello IO, Twinomuhwezi H, Awuchi CG Food Sci Nutr 15-May-2023
PMCID:PMC10345688
doi:10.1002/fsn3.3420
PMID:37457145
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
UHPLC-Q-Orbitrap-MS-Based Metabolomics Reveals Chemical Variations of Two Types of Rhizomes of Polygonatum sibiricum Luo G, Lin J, Cheng W, Liu Z, Yu T, Yang B Molecules 22-Jul-2022
PMCID:PMC9331047
doi:10.3390/molecules27154685
PMID:35897876
Management of Atopic Dermatitis Via Oral and Topical Administration of Herbs in Murine Model: A Systematic Review Mohd Kasim VN, Noble SM, Liew KY, Tan JW, Israf DA, Tham CL Front Pharmacol 24-May-2022
PMCID:PMC9171034
doi:10.3389/fphar.2022.785782
PMID:35685636
Alpinetin: A Review of Its Pharmacology and Pharmacokinetics Zhao G, Tong Y, Luan F, Zhu W, Zhan C, Qin T, An W, Zeng N Front Pharmacol 04-Feb-2022
PMCID:PMC8854656
doi:10.3389/fphar.2022.814370
PMID:35185569
Roosting ecology of endangered plant‐roosting bats on Okinawa Island: Implications for bat‐friendly forestry practices Preble JH, Vincenot CE, Saito K, Ohte N Ecol Evol 17-Sep-2021
PMCID:PMC8525085
doi:10.1002/ece3.8101
PMID:34707831
Germacrene A–A Central Intermediate in Sesquiterpene Biosynthesis Xu H, Dickschat JS Chemistry 30-Sep-2020
PMCID:PMC7821278
doi:10.1002/chem.202002163
PMID:32442350
Can the anatomy of abnormal flowers elucidate relationships of the androecial members in the ginger (Zingiberaceae)? Li X, Fan T, Zou P, Zhang W, Wu X, Zhang Y, Liao J EvoDevo 09-Jun-2020
PMCID:PMC7285767
doi:10.1186/s13227-020-00157-8
PMID:32537122
Complete Chloroplast Genomes of Three Medicinal Alpinia Species: Genome Organization, Comparative Analyses and Phylogenetic Relationships in Family Zingiberaceae Li DM, Zhu GF, Xu YC, Ye YJ, Liu JM Plants (Basel) 24-Feb-2020
PMCID:PMC7076362
doi:10.3390/plants9020286
PMID:32102387
Natural Products and Acute Myeloid Leukemia: A Review Highlighting Mechanisms of Action Hwang D, Kim M, Park H, Jeong MI, Jung W, Kim B Nutrients 03-May-2019
PMCID:PMC6567155
doi:10.3390/nu11051010
PMID:31058874
Amelioration of atopic‐like skin conditions in NC/Tnd mice by topical application with distilled Alpinia intermedia Gagnep extracts Amagai Y, Katsuta C, Nomura Y, Oida K, Matsuda K, Jang H, Ahn G, Hamasaki T, Matsuda H, Tanaka A J Dermatol 16-Aug-2017
PMCID:PMC5697676
doi:10.1111/1346-8138.13995
PMID:28815692
Novel sesquiterpenes from Alpinia intermedia GAGNEP. HIDEJI ITOKAWA, HIROSHI MORITA, TAKESHI KOBAYASHI, KINZO WATANABE, YOICHI IITAKA Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.35.2860

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 / Sesquiterpenoids
(1R,2R,3R,6S,7S)-3,7-dimethyl-10-propan-2-yl-11,12-dioxatricyclo[5.3.2.02,6]dodec-9-en-8-one 13855683 Click to see CC1CCC2C1C3C(=CC(=O)C2(OO3)C)C(C)C 250.33 unknown https://doi.org/10.1248/CPB.35.2860
(1R,2S,5R,6R,7R,8R)-1,5-dimethyl-8-propan-2-yl-11,12-dioxatricyclo[5.3.2.02,6]dodec-9-en-8-ol 21637818 Click to see CC1CCC2C1C3C(C=CC2(OO3)C)(C(C)C)O 252.35 unknown https://doi.org/10.1248/CPB.35.2860
(1S,2R,3R,6S,7R,8S)-3,7-dimethyl-10-propan-2-yl-11,12-dioxatricyclo[5.3.2.02,6]dodec-9-en-8-ol 13855680 Click to see CC1CCC2C1C3C(=CC(C2(OO3)C)O)C(C)C 252.35 unknown https://doi.org/10.1248/CPB.35.2860
1,5-Dimethyl-8-propan-2-yl-11,12-dioxatricyclo[5.3.2.02,6]dodec-9-en-8-ol 13855705 Click to see CC1CCC2C1C3C(C=CC2(OO3)C)(C(C)C)O 252.35 unknown https://doi.org/10.1248/CPB.35.2860
10-Hydroperoxy-1,5-dimethyl-8-propan-2-yl-11,12-dioxatricyclo[5.3.2.02,6]dodec-8-ene 13855707 Click to see CC1CCC2C1C3C(=CC(C2(OO3)C)OO)C(C)C 268.35 unknown https://doi.org/10.1248/CPB.35.2860
3,7-Dimethyl-10-propan-2-yl-11,12-dioxatricyclo[5.3.2.02,6]dodec-9-en-8-ol 13855678 Click to see CC1CCC2C1C3C(=CC(C2(OO3)C)O)C(C)C 252.35 unknown https://doi.org/10.1248/CPB.35.2860
3,7-Dimethyl-10-propan-2-yl-11,12-dioxatricyclo[5.3.2.02,6]dodec-9-en-8-one 13855682 Click to see CC1CCC2C1C3C(=CC(=O)C2(OO3)C)C(C)C 250.33 unknown https://doi.org/10.1248/CPB.35.2860
Alpinenone 13855690 Click to see CC1CCC2C1C3(C(=CC(=O)C2(O3)C)C(C)C)O 250.33 unknown https://doi.org/10.1248/CPB.35.2860
Veizsugaeokhoh-ionokrpisa- 13855679 Click to see CC1CCC2C1C3C(=CC(C2(OO3)C)O)C(C)C 252.35 unknown https://doi.org/10.1248/CPB.35.2860
Vuwotuvajxtkiv-udyjriamsa- 13855708 Click to see CC1CCC2C1C3C(=CC(C2(OO3)C)OO)C(C)C 268.35 unknown https://doi.org/10.1248/CPB.35.2860
Zqoleeahzkxyol-altyaodhsa- 13855684 Click to see CC1CCC2C1C3C(=CC(=O)C2(OO3)C)C(C)C 250.33 unknown https://doi.org/10.1248/CPB.35.2860
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
(1S,4aS,7R,8aR)-1,8a-dimethyl-7-prop-1-en-2-yl-1,2,3,4,5,6,7,8-octahydronaphthalen-4a-ol 13855710 Click to see CC1CCCC2(C1(CC(CC2)C(=C)C)C)O 222.37 unknown https://doi.org/10.1248/CPB.35.2860
1,8a-Dimethyl-7-prop-1-en-2-yl-1,2,3,4,5,6,7,8-octahydronaphthalen-4a-ol 13855709 Click to see CC1CCCC2(C1(CC(CC2)C(=C)C)C)O 222.37 unknown https://doi.org/10.1248/CPB.35.2860
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
7-Isopropenyl-4a-methyl-1-methylenedecahydronaphthalene 519361 Click to see CC(=C)C1CCC2(CCCC(=C)C2C1)C 204.35 unknown https://doi.org/10.1248/CPB.35.2860
beta-Selinene 442393 Click to see CC(=C)C1CCC2(CCCC(=C)C2C1)C 204.35 unknown https://doi.org/10.1248/CPB.35.2860
Intermedeol 15560333 Click to see CC(=C)C1CCC2(CCCC(C2C1)(C)O)C 222.37 unknown https://doi.org/10.1248/CPB.35.2860
Isointermedeol 527217 Click to see CC(=C)C1CCC2(CCCC(C2C1)(C)O)C 222.37 unknown https://doi.org/10.1248/CPB.35.2860
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
(2R)-2-[(1R,2S,5R)-2-acetyl-5-methylcyclopentyl]-3-propan-2-yl-2H-furan-5-one 13855688 Click to see CC1CCC(C1C2C(=CC(=O)O2)C(C)C)C(=O)C 250.33 unknown https://doi.org/10.1248/CPB.35.2860
2-(2-acetyl-5-methylcyclopentyl)-3-propan-2-yl-2H-furan-5-one 13855686 Click to see CC1CCC(C1C2C(=CC(=O)O2)C(C)C)C(=O)C 250.33 unknown https://doi.org/10.1248/CPB.35.2860
> Organoheterocyclic compounds / Heteroaromatic compounds
1-((1R,2R,3R)-2-(3-Isopropylfuran-2-yl)-3-methylcyclopentyl)ethanone 12309974 Click to see CC1CCC(C1C2=C(C=CO2)C(C)C)C(=O)C 234.33 unknown https://doi.org/10.1248/CPB.35.2860
1-((1S,2R,3R)-2-(3-Isopropylfuran-2-yl)-3-methylcyclopentyl)ethanone 527226 Click to see CC1CCC(C1C2=C(C=CO2)C(C)C)C(=O)C 234.33 unknown https://doi.org/10.1248/CPB.35.2860
Furopelargone A 6451194 Click to see CC1CCC(C1C2=C(C=CO2)C(C)C)C(=O)C 234.33 unknown https://doi.org/10.1248/CPB.35.2860
Furopelargone B 12309975 Click to see CC1CCC(C1C2=C(C=CO2)C(C)C)C(=O)C 234.33 unknown https://doi.org/10.1248/CPB.35.2860
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Pinocembrin 7-O-neohesperidoside 4'''-O-acetate 42607859 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC=CC=C5)O)CO)O)O)O)O)OC(=O)C 606.60 unknown https://doi.org/10.1248/CPB.35.2860

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Collections Top

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