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Curcuma heyneana

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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 UUID643ff4c9bfadf821686529
Scientific name Curcuma heyneana
Authority Valeton & Zijp
First published in Recueil Trav. Bot. Néerl. 14:132, 136. (1917)

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
ban temu giring
French temu giring
Indonesian kuning gajah
Indonesian temu giring
mad temmo laṭè

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000365660
UNII OZV188KD62
Tropicos 100174882
KEW urn:lsid:ipni.org:names:872371-1
The Plant List kew-235231
Open Tree Of Life 615606
NCBI Taxonomy 378295
IUCN Red List 117309148
IPNI 872371-1
iNaturalist 347645
GBIF 2757572
EOL 1122318
CMAUP NPO17780

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
Disclosing the Functional Potency of Three Oxygenated Monoterpenes in Combating Microbial Pathogenesis: From Targeting Virulence Factors to Chicken Meat Preservation Akermi S, Chaari M, Elhadef K, Fourati M, Chakchouk Mtibaa A, Agriopoulou S, Smaoui S, Mellouli L Foods 21-Mar-2024
PMCID:PMC10970324
doi:10.3390/foods13060965
PMID:38540955
Designed Fabrication of Phloretin-Loaded Propylene Glycol Binary Ethosomes: Stability, Skin Permeability and Antioxidant Activity Zhang M, Zhuang X, Li S, Wang Y, Zhang X, Li J, Wu D Molecules 21-Dec-2023
PMCID:PMC10780158
doi:10.3390/molecules29010066
PMID:38202649
The pattern of herbal medicines use for breastfeeding mother in Jogonalan, Klaten, Indonesia: a mini survey Sayuti NA, Atikah N BMC Complement Med Ther 07-Nov-2023
PMCID:PMC10629069
doi:10.1186/s12906-023-04235-x
PMID:37936188
Anti-Aging Potential of Plants of the Anak Dalam Tribe, Jambi, Indonesia Lestari U, Muhaimin M, Chaerunisaa AY, Sujarwo W Pharmaceuticals (Basel) 14-Sep-2023
PMCID:PMC10534538
doi:10.3390/ph16091300
PMID:37765107
Antibacterial and Antifungal Terpenes from the Medicinal Angiosperms of Asia and the Pacific: Haystacks and Gold Needles Wiart C, Kathirvalu G, Raju CS, Nissapatorn V, Rahmatullah M, Paul AK, Rajagopal M, Sathiya Seelan JS, Rusdi NA, Lanting S, Sulaiman M Molecules 04-May-2023
PMCID:PMC10180233
doi:10.3390/molecules28093873
PMID:37175283
Immunomodulatory effect from ethanol extract and ethyl acetate fraction of Curcuma heyneana Valeton and Zijp: Transient receptor vanilloid protein approach Fajrin FA, Sulistyowaty MI, Ghiffary ML, Zuhra SA, Panggalih WR, Pratoko DK, Christianty FM, Matsunami K, Indrianingsih AW Heliyon 20-Apr-2023
PMCID:PMC10160745
doi:10.1016/j.heliyon.2023.e15582
PMID:37153401
Current Naturopathy to Combat Alzheimer’s Disease Chakrovorty A, Bhattacharjee B, Saxena A, Samadder A, Nandi S Curr Neuropharmacol 30-Mar-2023
PMCID:PMC10227918
doi:10.2174/1570159X20666220927121022
PMID:36173068
Recent Advances in Herbal-Derived Products with Skin Anti-Aging Properties and Cosmetic Applications Costa EF, Magalhães WV, Di Stasi LC Molecules 03-Nov-2022
PMCID:PMC9658815
doi:10.3390/molecules27217518
PMID:36364354
Isoquercitrin isolated from newly bred Green ball apple peel in lipopolysaccharide-stimulated macrophage regulates NF-κB inflammatory pathways and cytokines Lee EH, Park HJ, Jung HY, Kang IK, Kim BO, Cho YJ 3 Biotech 22-Mar-2022
PMCID:PMC8938568
doi:10.1007/s13205-022-03118-1
PMID:35463046
Antioxidant and antidiabetic compounds identification in several Indonesian underutilized Zingiberaceae spices using SPME-GC/MS-based volatilomics and in silico methods Tunnisa F, Nur Faridah D, Afriyanti A, Rosalina D, Ana Syabana M, Darmawan N, Dewi Yuliana N Food Chem X 16-Mar-2022
PMCID:PMC8943257
doi:10.1016/j.fochx.2022.100285
PMID:35342880
Metabolite Fingerprinting Based on 1H-NMR Spectroscopy and Liquid Chromatography for the Authentication of Herbal Products Riswanto FD, Windarsih A, Lukitaningsih E, Rafi M, Fadzilah NA, Rohman A Molecules 10-Feb-2022
PMCID:PMC8874729
doi:10.3390/molecules27041198
PMID:35208988
Antiviral Therapeutic Potential of Curcumin: An Update Ardebili A, Pouriayevali MH, Aleshikh S, Zahani M, Ajorloo M, Izanloo A, Siyadatpanah A, Razavi Nikoo H, Wilairatana P, Coutinho HD Molecules 19-Nov-2021
PMCID:PMC8617637
doi:10.3390/molecules26226994
PMID:34834089
Plant-Based Natural Products and Extracts: Potential Source to Develop New Antiviral Drug Candidates Thomas E, Stewart LE, Darley BA, Pham AM, Esteban I, Panda SS Molecules 14-Oct-2021
PMCID:PMC8537559
doi:10.3390/molecules26206197
PMID:34684782
Variable Secondary Metabolite Profiles Across Cultivars of Curcuma longa L. and C. aromatica Salisb. Kulyal P, Acharya S, Ankari AB, Kokkiripati PK, Tetali SD, Raghavendra AS Front Pharmacol 30-Jun-2021
PMCID:PMC8278146
doi:10.3389/fphar.2021.659546
PMID:34276362
The Application of NMR Spectroscopy and Chemometrics in Authentication of Spices Pacholczyk-Sienicka B, Ciepielowski G, Albrecht Ł Molecules 13-Jan-2021
PMCID:PMC7828335
doi:10.3390/molecules26020382
PMID:33450910

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
(2E)-2-[2-[(1S,4aS,8aR)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]ethylidene]butanedial 163068846 Click to see CC1(CCCC2(C1CCC(=C)C2CC=C(CC=O)C=O)C)C 302.50 unknown https://doi.org/10.1016/0031-9422(88)83038-3
2-[2-(5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl)ethylidene]butanedial 75094027 Click to see CC1(CCCC2(C1CCC(=C)C2CC=C(CC=O)C=O)C)C 302.50 unknown https://doi.org/10.1016/0031-9422(88)83038-3
5-[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-formylpent-3-enoic acid 163026565 Click to see CC1(CCCC2(C1CCC(=C)C2CC=C(CC(=O)O)C=O)C)C 318.40 unknown https://doi.org/10.1021/NP300694A
Labda-8(17),12-diene-15,16-dial 11077520 Click to see CC1(CCCC2(C1CCC(=C)C2CC=C(CC=O)C=O)C)C 302.50 unknown https://doi.org/10.1016/0031-9422(88)83038-3
Zerumin A 11723433 Click to see CC1(CCCC2(C1CCC(=C)C2CC=C(CC(=O)O)C=O)C)C 318.40 unknown https://doi.org/10.1021/NP300694A
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
2-[(1R,4aR,5R,6S,7R,8aS)-6,7-dihydroxy-5-(hydroxymethyl)-8a-methyl-2-methylidene-1,3,4,4a,5,6,7,8-octahydronaphthalen-1-yl]-1-(furan-3-yl)ethanone 163070528 Click to see CC12CC(C(C(C1CCC(=C)C2CC(=O)C3=COC=C3)CO)O)O 334.40 unknown https://doi.org/10.1021/NP300694A
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
15,16-Dinor-8(17),11-labdadien-13-one 13994560 Click to see CC(=O)C=CC1C(=C)CCC2C1(CCCC2(C)C)C 260.40 unknown https://doi.org/10.1021/NP300694A
CID 5725 5725 Click to see CC1=CCC(C=CC(=O)C(=CCC1)C)(C)C 218.33 unknown https://doi.org/10.1016/0031-9422(88)83038-3
Zerumbone 5470187 Click to see CC1=CCC(C=CC(=O)C(=CCC1)C)(C)C 218.33 unknown https://doi.org/10.1016/0031-9422(88)83038-3
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
Cyperusol C 11230158 Click to see CC(=C)C1CCC2(C(CCC(C2C1)(C)O)O)C 238.37 unknown https://doi.org/10.1021/NP300694A
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(6E,10S)-6,10-dimethyl-3-propan-2-ylidenecyclodec-6-ene-1,4-dione 10421549 Click to see CC1CCC=C(CC(=O)C(=C(C)C)CC1=O)C 234.33 unknown https://doi.org/10.1016/0031-9422(88)83038-3
3,7-Cyclodecadien-1-one, 3,7-dimethyl-10-(1-methylethylidene)-, (Z,E)- 81323 Click to see CC1=CCC(=C(C)C)C(=O)CC(=CCC1)C 218.33 unknown https://doi.org/10.1016/0031-9422(88)83038-3
6,10-Dimethyl-3-propan-2-ylidenecyclodec-6-ene-1,4-dione 78173043 Click to see CC1CCC=C(CC(=O)C(=C(C)C)CC1=O)C 234.33 unknown https://doi.org/10.1016/0031-9422(88)83038-3
Dehydrocurdione 14191392 Click to see CC1CCC=C(CC(=O)C(=C(C)C)CC1=O)C 234.33 unknown https://doi.org/10.1016/0031-9422(88)83038-3
Germacrone 6436348 Click to see CC1=CCC(=C(C)C)C(=O)CC(=CCC1)C 218.33 unknown https://doi.org/10.1016/0031-9422(88)83038-3
Heyneanone A 71578079 Click to see CC1=CC(=O)C(=C(C)C)CC(C(CCC1O)(C)O)O 268.35 unknown https://doi.org/10.1021/NP300694A
Heyneanone B 71578637 Click to see CC1=CC(=O)C(=C(C)C)CC(C(CCC1O)(C)O)O 268.35 unknown https://doi.org/10.1021/NP300694A
Heyneanone D 71578716 Click to see CC1=CC(=O)C(=CC=C(C(=O)CC1)C)C(C)(C)O 248.32 unknown https://doi.org/10.1021/NP300694A
Heyneanones C 71578080 Click to see CC1=CC(=O)C(=C(C)C)CC(C(CCC1O)(C)O)O 268.35 unknown https://doi.org/10.1021/NP300694A
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Guaianes
(1S,2S,5S,8R,9R)-2,3',3',6-tetramethylspiro[11-oxatricyclo[6.2.1.01,5]undec-6-ene-9,2'-oxirane]-8-ol 14191396 Click to see CC1CCC2C13CC4(C(O4)(C)C)C(O3)(C=C2C)O 250.33 unknown https://doi.org/10.1016/0031-9422(88)83038-3
(1S,2S,5S,8S)-2-methyl-6-methylidene-9-propan-2-ylidene-11-oxatricyclo[6.2.1.01,5]undecan-8-ol 12310886 Click to see CC1CCC2C13CC(=C(C)C)C(O3)(CC2=C)O 234.33 unknown https://doi.org/10.1021/NP300694A
(1S,3abeta,8abeta)-Octahydro-1beta,4beta-dihydroxy-7-isopropylidene-1,4-dimethylazulen-6(5H)-one 14632999 Click to see CC(=C1CC2C(CCC2(C)O)C(CC1=O)(C)O)C 252.35 unknown https://doi.org/10.1021/NP300694A
12-Hydroxycurcumenol 71578718 Click to see CC1CCC2C13CC(=C(C)CO)C(O3)(C=C2C)O 250.33 unknown https://doi.org/10.1021/NP300694A
15-Hydroxyprocurcurmenol 71578717 Click to see CC(=C1CC2C(CCC2(C)O)C(=CC1=O)CO)C 250.33 unknown https://doi.org/10.1021/NP300694A
2-Methyl-6-methylidene-9-(propan-2-ylidene)-11-oxatricyclo[6.2.1.0^{1,5}]undecan-8-ol 5255901 Click to see CC1CCC2C13CC(=C(C)C)C(O3)(CC2=C)O 234.33 unknown https://doi.org/10.1080/14786410903052951
https://doi.org/10.1016/0031-9422(88)83038-3
https://doi.org/10.1021/NP300694A
2,3',3',6-Tetramethylspiro[11-oxatricyclo[6.2.1.01,5]undec-6-ene-9,2'-oxirane]-8-ol 14191395 Click to see CC1CCC2C13CC4(C(O4)(C)C)C(O3)(C=C2C)O 250.33 unknown https://doi.org/10.1016/0031-9422(88)83038-3
3-Hydroxy-3,8-dimethyl-5-(propan-2-ylidene)-1,2,3,3a,4,5,6,8a-octahydroazulen-6-one 5320710 Click to see CC1=CC(=O)C(=C(C)C)CC2C1CCC2(C)O 234.33 unknown https://doi.org/10.1021/NP300694A
4,10-Epizedoarondiol 24834047 Click to see CC(=C1CC2C(CCC2(C)O)C(CC1=O)(C)O)C 252.35 unknown https://doi.org/10.1021/NP300694A
8a-hydroxy-1,3',3',4-tetramethylspiro[2,3,3a,8-tetrahydro-1H-azulene-7,2'-oxirane]-6-one 14191400 Click to see CC1CCC2C1(CC3(C(=O)C=C2C)C(O3)(C)C)O 250.33 unknown https://doi.org/10.1080/14786410903052951
Aerugidiol 11776892 Click to see CC1=CC(=O)C(=C(C)C)CC2C1(CCC2(C)O)O 250.33 unknown https://doi.org/10.1021/NP300694A
Curcumenol 387977 Click to see CC1CCC2C13CC(=C(C)C)C(O3)(C=C2C)O 234.33 unknown https://doi.org/10.1080/14786410903052951
https://doi.org/10.1016/0031-9422(88)83038-3
Curcumenol 167812 Click to see CC1CCC2C13CC(=C(C)C)C(O3)(C=C2C)O 234.33 unknown https://doi.org/10.1016/0031-9422(88)83038-3
https://doi.org/10.1080/14786410903052951
Epiguaidiol A 71719409 Click to see CC(=C)C1CCC(C2CCC(C2C1)(C)O)(C)O 238.37 unknown https://doi.org/10.1021/NP300694A
Guaidiol 10633702 Click to see CC(=C)C1CCC(C2CCC(C2C1)(C)O)(C)O 238.37 unknown https://doi.org/10.1021/NP300694A
Isocurcumenol 10399139 Click to see CC1CCC2C13CC(=C(C)C)C(O3)(CC2=C)O 234.33 unknown https://doi.org/10.1080/14786410903052951
https://doi.org/10.1016/0031-9422(88)83038-3
Isozedoarondiol 14632998 Click to see CC(=C1CC2C(CCC2(C)O)C(CC1=O)(C)O)C 252.35 unknown https://doi.org/10.1021/NP300694A
Oxycurcumenol Epoxide 10264129 Click to see CC1CCC2C1(CC3(C(=O)C=C2C)C(O3)(C)C)O 250.33 unknown https://doi.org/10.1021/NP300694A
https://doi.org/10.1080/14786410903052951
Procurcumenol 189061 Click to see CC1=CC(=O)C(=C(C)C)CC2C1CCC2(C)O 234.33 unknown https://doi.org/10.1021/NP300694A
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
Caulolactone B 71720006 Click to see CC(=C1CC2C(CCC2(OC1=O)C)C(=C)C)C 234.33 unknown https://doi.org/10.1021/NP300694A
Curcumanolide A 14191393 Click to see CC1CCC(C12CC(=C(C)C)C(=O)O2)C(=C)C 234.33 unknown https://doi.org/10.1016/0031-9422(88)83038-3
Curcumanolide B 14191394 Click to see CC1CCC(C12CC(=C(C)C)C(=O)O2)C(=C)C 234.33 unknown https://doi.org/10.1021/NP300694A
https://doi.org/10.1016/0031-9422(88)83038-3
Curcumanolides A 10014272 Click to see CC1CCC(C12CC(=C(C)C)C(=O)O2)C(=C)C 234.33 unknown https://doi.org/10.1021/NP300694A
https://doi.org/10.1016/0031-9422(88)83038-3
Gajutsulactone A 10263441 Click to see CC(=C1CC2C(CCC2(OC1=O)C)C(=C)C)C 234.33 unknown https://doi.org/10.1021/NP300694A
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Carotenes
Beta-Carotene 5280489 Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2=C(CCCC2(C)C)C)C)C 536.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids / Limonoids
[(5R,7R,8S,9S,10S,13R,17S)-17-acetyloxy-17-[(2R)-2-hydroxy-5-oxo-2H-furan-3-yl]-4,4,8,10,13-pentamethyl-3,16-dioxo-5,6,7,9,11,12-hexahydrocyclopenta[a]phenanthren-7-yl] acetate 163042119 Click to see CC(=O)OC1CC2C(C(=O)C=CC2(C3C1(C4=CC(=O)C(C4(CC3)C)(C5=CC(=O)OC5O)OC(=O)C)C)C)(C)C 540.60 unknown https://doi.org/10.1016/0031-9422(88)83038-3
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
Curcumanolide C 71578719 Click to see CC1CCC(C12C=C(C(=O)O2)C(C)(C)O)C(=C)C 250.33 unknown https://doi.org/10.1021/NP300694A
Curcumanolide D 71578720 Click to see CC1CCC(C12C=C(C(=O)O2)C(C)(C)O)C(=C)C 250.33 unknown https://doi.org/10.1021/NP300694A
> Organoheterocyclic compounds / Pyrrolidines / Phenylpyrrolidines
(2R,3R,4R,5R)-2-(4-Methoxyphenyl)-1,5-dimethylpyrrolidine-3,4-diol 10889945 Click to see CC1C(C(C(N1C)C2=CC=C(C=C2)OC)O)O 237.29 unknown via CMAUP database
Codonopsine 442631 Click to see CC1C(C(C(N1C)C2=CC(=C(C=C2)OC)OC)O)O 267.32 unknown via CMAUP database

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