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Wurfbainia compacta

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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 UUID644069c641b3d925734889
Scientific name Wurfbainia compacta
Authority (Sol. ex Maton) Škorničk. & A.D.Poulsen
First published in Taxon 67:29. (2018)

Description Top

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Synonyms Top

Scientific name Authority First published in
Amomum compactum Sol. ex Maton Trans. Linn. Soc. London 10:251. (1811); Lectotypified in: Taxon 62:1293. (2013) by Droop, A.J., Kaewsri, W., Lamxay, V., Poulsen, A.D. & Newman, M.F.
Amomum kepulaga Sprague & Burkill Bull. Misc. Inform. Kew 35. (1930); Lectotypified in: Taxon 62:1293. (2013) by Droop, A.J., Kaewsri, W., Lamxay, V., Poulsen, A.D. & Newman, M.F.
Zingiber compactum (Sol. ex Maton) Stokes Bot. mat. med. 68

Common names Top

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Language Common/alternative name
Indonesian kapulaga jawa
Japanese ジャワビャクズク
Chinese 爪哇白豆蔻

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-tropical
    • Indian Subcontinent
      • India
    • Malesia
      • Jawa
      • Lesser Sunda Islands
      • Malaya
      • Sumatera

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001426454
KEW urn:lsid:ipni.org:names:77178274-1
Open Tree Of Life 445188
NCBI Taxonomy 252847
IUCN Red List 117228797
IPNI 77178274-1
GBIF 10929810
CMAUP NPO29010

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
The complete chloroplast genome of Hedychium flavum Roxb., an ornamental, edible and medicinal plant Li MF, Xiao T, Zhang YH Mitochondrial DNA B Resour 15-Nov-2023
PMCID:PMC10653761
doi:10.1080/23802359.2023.2281029
PMID:38026495
Ethnobotanical study on edible flowers in Xishuangbanna, China Zhang Q, Cheng Z, Fan Y, Zhang D, Wang M, Zhang J, Sommano S, Wu X, Long C J Ethnobiol Ethnomed 30-Sep-2023
PMCID:PMC10542681
doi:10.1186/s13002-023-00608-1
PMID:37777741
1,8-cineole ameliorates colon injury by downregulating macrophage M1 polarization via inhibiting the HSP90-NLRP3-SGT1 complex Ma S, Yang B, Du Y, Lv Y, Liu J, Shi Y, Huang T, Xu H, Deng L, Chen X J Pharm Anal 06-Jul-2023
PMCID:PMC10568110
doi:10.1016/j.jpha.2023.07.001
PMID:37842654
Antibacterial and Angiotensin I-Converting Enzyme (ACE) Inhibition Activities of Essential Oil from Java Cardamom (Amomum compactum) Fruit Darsih C, Windarsih A, Damayanti E, Amiru VA, Indrianingsih AW, Marfu’ah S, Sujarwo W Indian J Microbiol 30-Jun-2023
PMCID:PMC10533441
doi:10.1007/s12088-023-01080-x
PMID:37781022
Chemical Constituents from the Fruits of Amomum kravanh and Their Role in Activating Alcohol Dehydrogenase Xiong HM, Li HY, Lin ZR, Liu XM, Bai LP, Zhang W, Jiang ZH, Zhu GY Molecules 20-Jun-2023
PMCID:PMC10303173
doi:10.3390/molecules28124878
PMID:37375433
Insight into the phytochemical profile and antimicrobial activities of Amomum subulatum and Amomum xanthioides: an in vitro and in silico study Alruhaili MH, Almuhayawi MS, Gattan HS, Alharbi MT, Nagshabandi MK, Jaouni SK, Selim S, AbdElgawad H Front Plant Sci 20-Apr-2023
PMCID:PMC10157186
doi:10.3389/fpls.2023.1136961
PMID:37152127
Traditional Tibetan medicine to fight against COVID-19: Basic theory and therapeutic drugs Zhang K, Wang L, Peng J, Sangji K, Luo Y, Zeng Y, Zeweng Y, Fan G Front Pharmacol 16-Feb-2023
PMCID:PMC9978713
doi:10.3389/fphar.2023.1098253
PMID:36874035
The modulation of gut microbiota by herbal medicine to alleviate diabetic kidney disease – A review Du J, Yang M, Zhang Z, Cao B, Wang Z, Han J Front Pharmacol 14-Nov-2022
PMCID:PMC9702521
doi:10.3389/fphar.2022.1032208
PMID:36452235
Comparative chloroplast genome analyses of Amomum: insights into evolutionary history and species identification Gong L, Ding X, Guan W, Zhang D, Zhang J, Bai J, Xu W, Huang J, Qiu X, Zheng X, Zhang D, Li S, Huang Z, Su H BMC Plant Biol 09-Nov-2022
PMCID:PMC9644571
doi:10.1186/s12870-022-03898-x
PMID:36352400
Complete chloroplast genome of Boesenbergia rotunda and a comparative analysis with members of the family Zingiberaceae Liew YJ, Chua KO, Yong HS, Song SL, Chan KG Rev Bras Bot 26-Oct-2022
PMCID:PMC9607705
doi:10.1007/s40415-022-00845-w
PMID:36320930
Jia-ga-song-tang protection against alcoholic liver and intestinal damage Fang J, Wu Y, Gan C, Ruan S, He X, Wang B, Wang Y, Yu J, Sang C, Zeren D, Xiong T Front Pharmacol 26-Sep-2022
PMCID:PMC9549243
doi:10.3389/fphar.2022.981706
PMID:36225559
Effects of Methods and Durations of Extraction on Total Flavonoid and Phenolic Contents and Antioxidant Activity of Java Cardamom (Amomum compactum Soland Ex Maton) Fruit Nurcholis W, Alfadzrin R, Izzati N, Arianti R, Vinnai BÁ, Sabri F, Kristóf E, Artika IM Plants (Basel) 27-Aug-2022
PMCID:PMC9460600
doi:10.3390/plants11172221
PMID:36079603
The Application of Pearls in Traditional Medicine of China and Their Chemical Constituents, Pharmacology, Toxicology, and Clinical Research Song Y, Chen W, Fu K, Wang Z Front Pharmacol 23-Aug-2022
PMCID:PMC9445187
doi:10.3389/fphar.2022.893229
PMID:36081944
Sugemule-10: Source of prescription and modern clinical application Chen X, Liangliang, Zhang H, Buriebao, Wang X, Tai W Chin Herb Med 26-Jul-2022
PMCID:PMC9476780
doi:10.1016/j.chmed.2022.06.006
PMID:36118002
Discussion on evolution of Mongolian medicinal material names and countermeasures for standardization Long B, Aodungerile, Bai L Chin Herb Med 22-Jul-2022
PMCID:PMC9476683
doi:10.1016/j.chmed.2022.06.005
PMID:36118000

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
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
gamma-Terpinene 7461 Click to see CC1=CCC(=CC1)C(C)C 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-OCIMENE, (3E)- 5281553 Click to see CC(=CCC=C(C)C=C)C 136.23 unknown via CMAUP database
beta-Ocimene, (3Z)- 5320250 Click to see CC(=CCC=C(C)C=C)C 136.23 unknown via CMAUP database
Linalool, (-)- 443158 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown via CMAUP database
Linalool, (+)- 67179 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown via CMAUP database
Linalool, (+/-)- 6549 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown via CMAUP database
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
p-CYMENE 7463 Click to see CC1=CC=C(C=C1)C(C)C 134.22 unknown via CMAUP database
Thymol 6989 Click to see CC1=CC(=C(C=C1)C(C)C)O 150.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-2-Carene 6430755 Click to see CC1=CC2C(C2(C)C)CC1 136.23 unknown via CMAUP database
(-)-3-Carene 442461 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown via CMAUP database
(-)-Camphene 440966 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown via CMAUP database
(-)-Camphor 444294 Click to see CC1(C2CCC1(C(=O)C2)C)C 152.23 unknown via CMAUP database
(-)-Fenchone 82229 Click to see CC1(C2CCC(C2)(C1=O)C)C 152.23 unknown via CMAUP database
(-)-Sabinene 11051711 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown via CMAUP database
(+)-2-Carene 78249 Click to see CC1=CC2C(C2(C)C)CC1 136.23 unknown via CMAUP database
(+)-3-Carene 443156 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown via CMAUP database
(+)-alpha-Pinene 82227 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown via CMAUP database
(+)-Camphene 92221 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown via CMAUP database
(+)-Fenchone 1201521 Click to see CC1(C2CCC(C2)(C1=O)C)C 152.23 unknown via CMAUP database
(1R,6R)-3,7,7-trimethylbicyclo[4.1.0]hept-2-ene 12302456 Click to see CC1=CC2C(C2(C)C)CC1 136.23 unknown via CMAUP database
(1S)-1,3,3-Trimethylbicyclo[2.2.1]heptan-2-one 12049113 Click to see CC1(C2CCC(C2)(C1=O)C)C 152.23 unknown via CMAUP database
(1S)-2,6,6-Trimethylbicyclo[3.1.1]hept-2-ene 12223113 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown via CMAUP database
(4R)-1,3,3-trimethylbicyclo[2.2.1]heptan-2-one 16213045 Click to see CC1(C2CCC(C2)(C1=O)C)C 152.23 unknown via CMAUP database
(R)-Fenchone; L-(-)-Fenchone; L-Fenchone; l-Fenchone 2794921 Click to see CC1(C2CCC(C2)(C1=O)C)C 152.23 unknown via CMAUP database
2-Carene 79044 Click to see CC1=CC2C(C2(C)C)CC1 136.23 unknown via CMAUP database
3-Carene 26049 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown via CMAUP database
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown via CMAUP database
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown via CMAUP database
Bicyclo[3.1.0]hex-2-ene, 2-methyl-5-(1-methylethyl)- 17868 Click to see CC1=CCC2(C1C2)C(C)C 136.23 unknown via CMAUP database
Camphene 6616 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown via CMAUP database
Camphor 2537 Click to see CC1(C2CCC1(C(=O)C2)C)C 152.23 unknown via CMAUP database
Camphor (synthetic) 159055 Click to see CC1(C2CCC1(C(=O)C2)C)C 152.23 unknown via CMAUP database
Camphor, (1S,4S)-(-)- 10050 Click to see CC1(C2CCC1(C(=O)C2)C)C 152.23 unknown via CMAUP database
d-2-Bornanone 9543187 Click to see CC1(C2CCC1(C(=O)C2)C)C 152.23 unknown via CMAUP database
d-Camphor 230921 Click to see CC1(C2CCC1(C(=O)C2)C)C 152.23 unknown via CMAUP database
Fenchone 14525 Click to see CC1(C2CCC(C2)(C1=O)C)C 152.23 unknown via CMAUP database
Sabinen 18818 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown via CMAUP database
Sabinene 10887971 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-alpha-Terpineol 443162 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown via CMAUP database
(-)-Terpinen-4-ol 5325830 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown via CMAUP database
(+)-alpha-Phellandrene 443160 Click to see CC1=CCC(C=C1)C(C)C 136.23 unknown via CMAUP database
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown via CMAUP database
alpha-PHELLANDRENE 7460 Click to see CC1=CCC(C=C1)C(C)C 136.23 unknown via CMAUP database
alpha-Terpinene 7462 Click to see CC1=CC=C(CC1)C(C)C 136.23 unknown via CMAUP database
Alpha-Terpineol 17100 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown via CMAUP database
Beta-Phellandrene 11142 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown via CMAUP database
Terpinolene 11463 Click to see CC1=CCC(=C(C)C)CC1 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-Gamma-cadinene 6432404 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown via CMAUP database
(+)-Nerolidol 5356544 Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C 222.37 unknown via CMAUP database
1-Methyl-4-(6-methylhepta-1,5-dien-2-yl)cyclohex-1-ene 403919 Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C 204.35 unknown via CMAUP database
Beta-Bisabolene 10104370 Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C 204.35 unknown via CMAUP database
Copaene 19725 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown via CMAUP database
delta-Cadinene 12306054 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown via CMAUP database
Humulene 5281520 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown via CMAUP database
Naphthalene, 1,2,3,5,6,8a-hexahydro-4,7-dimethyl-1-(1-methylethyl)-, (1S-cis)- 12306059 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Cedrane and isocedrane sesquiterpenoids
alpha-Cedrol 6432709 Click to see CC1CCC2C13CCC(C(C3)C2(C)C)(C)O 222.37 unknown via CMAUP database
Cedrol 65575 Click to see CC1CCC2C13CCC(C(C3)C2(C)C)(C)O 222.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
Cyclohexane, 1-ethenyl-1-methyl-2,4-bis(1-methylethenyl)-, (1R,2R,4S)- 9859094 Click to see CC(=C)C1CCC(C(C1)C(=C)C)(C)C=C 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
Eremophilene 12309744 Click to see CC1CCC=C2C1(CC(CC2)C(=C)C)C 204.35 unknown via CMAUP database
> Organoheterocyclic compounds / Oxanes
Eucalyptol 2758 Click to see CC1(C2CCC(O1)(CC2)C)C 154.25 unknown via CMAUP database

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Collections Top

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