Curcuma heyneana

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Description

Synonyms

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Germination/Propagation

Distribution

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Genome

Scientific Literature

Phytochemical Profile

Biological Material

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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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Filter by language:

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

Asia-tropical click to expand
- Malesia
  - Jawa
  - Lesser Sunda Islands

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

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

Characterization, Classification and Authentication of Turmeric and Curry Samples by Targeted LC-HRMS Polyphenolic and Curcuminoid Profiling and Chemometrics

Núñez N, Vidal-Casanella O, Sentellas S, Saurina J, Núñez O

Molecules

26-Jun-2020

PMCID:	PMC7355898
doi:	10.3390/molecules25122942
PMID:	32604759

Revisiting Inflammatory Bowel Disease: Pathology, Treatments, Challenges and Emerging Therapeutics Including Drug Leads from Natural Products

Yeshi K, Ruscher R, Hunter L, Daly NL, Loukas A, Wangchuk P

J Clin Med

28-Apr-2020

PMCID:	PMC7288008
doi:	10.3390/jcm9051273
PMID:	32354192

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 / 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
(+)-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
(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/10.1021/NP300694A https://doi.org/10.1016/0031-9422(88)83038-3
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
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/10.1016/0031-9422(88)83038-3 https://doi.org/10.1021/NP300694A
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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Curcuma heyneana

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top