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Curcuma mangga

Curcuma mangga - 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 UUID643ff4d39d2d9627894074
Scientific name Curcuma mangga
Authority Valeton & Zijp
First published in Recueil Trav. Bot. Néerl. 14:138, 141. (1917); Lectotypified in: Taxon 59 (1). (2010) by Leong-Škorničková J., Šída O. & Marhold K.

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
ban temu poh
French temu mangga
Indonesian temu mangga

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
    • Indo-China
      • Andaman Islands
      • Nicobar Nicobar
      • Thailand
    • Malesia
      • Jawa
      • Malaya

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000365800
Tropicos 100174904
KEW urn:lsid:ipni.org:names:872379-1
The Plant List kew-235254
Open Tree Of Life 978784
NCBI Taxonomy 379528
IUCN Red List 117309327
IPNI 872379-1
iNaturalist 347622
GBIF 2757639
Freebase /m/0c182w
USDA GRIN 466889

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
HIV/AIDS in Indonesia: current treatment landscape, future therapeutic horizons, and herbal approaches Jocelyn, Nasution FM, Nasution NA, Asshiddiqi MH, Kimura NH, Siburian MH, Rusdi ZY, Munthe AR, Chairenza I, Ginting Munthe MC, Sianipar P, Gultom SP, Simamora D, Uswanas IR, Salim E, Khairunnisa K, Syahputra RA Front Public Health 14-Feb-2024
PMCID:PMC10899510
doi:10.3389/fpubh.2024.1298297
PMID:38420030
Genus Curcuma: chemical and ethnopharmacological role in aging process Elhawary EA, Moussa AY, Singab AN BMC Complement Med Ther 11-Jan-2024
PMCID:PMC10782795
doi:10.1186/s12906-023-04317-w
PMID:38212737
Anticancer activity of Curcuma aeroginosa essential oil and its nano-formulations: cytotoxicity, apoptosis and cell migration effects Panyajai P, Viriyaadhammaa N, Tima S, Chiampanichayakul S, Dejkriengkraikul P, Okonogi S, Anuchapreeda S BMC Complement Med Ther 02-Jan-2024
PMCID:PMC10759438
doi:10.1186/s12906-023-04261-9
PMID:38166788
Regenerating Saffron (Crocus sativus L.) from Corm Lateral Buds via Indirect Somatic Embryogenesis Ma Y, Pan Y, Mao B Plants (Basel) 19-Dec-2023
PMCID:PMC10780922
doi:10.3390/plants13010010
PMID:38202318
Simulation and Optimization: A New Direction in Supercritical Technology Based Nanomedicine Huang Y, Zheng Y, Lu X, Zhao Y, Zhou D, Zhang Y, Liu G Bioengineering (Basel) 08-Dec-2023
PMCID:PMC10741229
doi:10.3390/bioengineering10121404
PMID:38135995
Exploration of the nutritional and carotenoids profiles of vegetables in Thai cuisine as potential nutritious ingredients Suttisansanee U, Thiyajai P, Inthachat W, Pruesapan K, Wongwathanarat K, Charoenkiatkul S, Sahasakul Y, Temviriyanukul P Heliyon 29-Apr-2023
PMCID:PMC10189170
doi:10.1016/j.heliyon.2023.e15951
PMID:37205996
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
Convolvulus pluricaulis Choisy’s Extraction, Chemical Characterization and Evaluation of the Potential Effects on Glycaemic Balance in a 3T3-L1 Adipocyte Cell Model Melloni E, Grassilli S, Romani A, Rimondi E, Marcuzzi A, Zauli E, Secchiero P, Paganetto G, Guerrini A, Sacchetti G, Tacchini M Nutrients 31-Mar-2023
PMCID:PMC10097163
doi:10.3390/nu15071727
PMID:37049568
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
Geraniol-a potential alternative to antibiotics for bovine mastitis treatment without disturbing the host microbial community or causing drug residues and resistance Guo W, Qiu M, Pu Z, Long N, Yang M, Ren K, Ning R, Zhang S, Peng F, Sun F, Dai M Front Cell Infect Microbiol 16-Feb-2023
PMCID:PMC9978373
doi:10.3389/fcimb.2023.1126409
PMID:36875515
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
Immunomodulatory Effects of Combined Ethanol Extracts of Curcuma mangga and Picria fel-terrae on Cellular- and Humoral-Mediated Immunity in Wistar Rats and Mice Yuandani Y, Jantan I, Laila L, Marianne M, Wira Septama A, Lintang N, Almadani P, Friti, A'ini S Evid Based Complement Alternat Med 20-Sep-2022
PMCID:PMC9526672
doi:10.1155/2022/1791165
PMID:36193138
Optimization of Ultrasonic—Assisted Extraction (UAE) Method Using Natural Deep Eutectic Solvent (NADES) to Increase Curcuminoid Yield from Curcuma longa L., Curcuma xanthorrhiza, and Curcuma mangga Val. Rosarina D, Narawangsa DR, Chandra NS, Sari E, Hermansyah H Molecules 18-Sep-2022
PMCID:PMC9504328
doi:10.3390/molecules27186080
PMID:36144813
The Main Protease of SARS-CoV-2 as a Target for Phytochemicals against Coronavirus Issa SS, Sokornova SV, Zhidkin RR, Matveeva TV Plants (Basel) 17-Jul-2022
PMCID:PMC9319234
doi:10.3390/plants11141862
PMID:35890496
Phenolics and terpenoids change in response to yeast extract and chitosan elicitation in Zataria multiflora cell suspension culture Bavi K, Khavari-Nejad RA, Najafi F, Ghanati F 3 Biotech 09-Jul-2022
PMCID:PMC9271148
doi:10.1007/s13205-022-03235-x
PMID:35822153

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
(+)-Zerumin A 10781840 Click to see CC1(CCCC2(C1CCC(=C)C2CC=C(CC(=O)O)C=O)C)C 318.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264423/
(E)-4-[(1S,4aS,8aR)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-2-(2,2-dimethoxyethyl)but-2-enal 163031319 Click to see CC1(CCCC2(C1CCC(=C)C2CC=C(CC(OC)OC)C=O)C)C 348.50 unknown https://doi.org/10.1021/NP0500171
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://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264423/
https://doi.org/10.1021/NP0500171
2-[2-[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]ethylidene]butanedial 54341270 Click to see CC1(CCCC2(C1CCC(=C)C2CC=C(CC=O)C=O)C)C 302.50 unknown https://doi.org/10.1021/NP0500171
4-(5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl)-2-(2,2-dimethoxyethyl)but-2-enal 85233318 Click to see CC1(CCCC2(C1CCC(=C)C2CC=C(CC(OC)OC)C=O)C)C 348.50 unknown https://doi.org/10.1021/NP0500171
4-[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-2-(2,2-dimethoxyethyl)but-2-enal 163031318 Click to see CC1(CCCC2(C1CCC(=C)C2CC=C(CC(OC)OC)C=O)C)C 348.50 unknown https://doi.org/10.1021/NP0500171
5-(5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl)-3-formylpent-3-enoic acid 73073987 Click to see CC1(CCCC2(C1CCC(=C)C2CC=C(CC(=O)O)C=O)C)C 318.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264423/
calcaratarin A 10689094 Click to see CC1(CCCC2(C1CCC(=C)C2CC=C(CC(OC)OC)C=O)C)C 348.50 unknown https://doi.org/10.1021/NP0500171
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://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264423/
https://doi.org/10.1021/NP0500171
> 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 https://doi.org/10.1080/10412905.1999.9701151
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown https://doi.org/10.1080/10412905.1999.9701151
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1080/10412905.1999.9701151
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1080/10412905.1999.9701151
> 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://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264423/
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
4-[(2R,4R,4aR,6aR,8S,10aR,10bS)-4-hydroxy-7,7,10a-trimethyl-8-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,4,4a,5,6,6a,8,9,10,10b-decahydro-1H-benzo[f]isochromen-2-yl]-2H-furan-5-one 162883585 Click to see CC1(C2CCC3C(C2(CCC1OC4C(C(C(C(O4)CO)O)O)O)C)CC(OC3O)C5=CCOC5=O)C 512.60 unknown https://doi.org/10.1021/NP0500171
4-[(2S,4R,4aR,6aR,8S,10aR,10bS)-4-hydroxy-7,7,10a-trimethyl-8-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,4,4a,5,6,6a,8,9,10,10b-decahydro-1H-benzo[f]isochromen-2-yl]-2H-furan-5-one 162883586 Click to see CC1(C2CCC3C(C2(CCC1OC4C(C(C(C(O4)CO)O)O)O)C)CC(OC3O)C5=CCOC5=O)C 512.60 unknown https://doi.org/10.1021/NP0500171
4-[4-hydroxy-7,7,10a-trimethyl-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,4,4a,5,6,6a,8,9,10,10b-decahydro-1H-benzo[f]isochromen-2-yl]-2H-furan-5-one 72954761 Click to see CC1(C2CCC3C(C2(CCC1OC4C(C(C(C(O4)CO)O)O)O)C)CC(OC3O)C5=CCOC5=O)C 512.60 unknown https://doi.org/10.1021/NP0500171
Curcumanggoside 44559175 Click to see CC1(C2CCC3C(C2(CCC1OC4C(C(C(C(O4)CO)O)O)O)C)CC(OC3O)C5=CCOC5=O)C 512.60 unknown https://doi.org/10.1021/NP0500171
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(2S)-4-[(1R)-2-[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-1-hydroxyethyl]-2-hydroxy-2H-furan-5-one 162957455 Click to see CC1(CCCC2(C1CCC(=C)C2CC(C3=CC(OC3=O)O)O)C)C 334.40 unknown https://doi.org/10.1021/NP0500171
(2S)-4-[(1S)-2-[(1S,4aS,8aR)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-1-hydroxyethyl]-2-hydroxy-2H-furan-5-one 154497718 Click to see CC1(CCCC2(C1CCC(=C)C2CC(C3=CC(OC3=O)O)O)C)C 334.40 unknown https://doi.org/10.1021/NP0500171
4-[2-(5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl)-1-hydroxyethyl]-2-hydroxy-2H-furan-5-one 73234904 Click to see CC1(CCCC2(C1CCC(=C)C2CC(C3=CC(OC3=O)O)O)C)C 334.40 unknown https://doi.org/10.1021/NP0500171
zerumin B 16079165 Click to see CC1(CCCC2(C1CCC(=C)C2CC(C3=CC(OC3=O)O)O)C)C 334.40 unknown https://doi.org/10.1021/NP0500171
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264423/
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264423/
> Organic acids and derivatives / Hydroxy acids and derivatives / Medium-chain hydroxy acids and derivatives
(2S,3R,4S)-3-hydroxy-2,4-dimethyl-6-[[(E)-2-methylpent-2-enoyl]amino]-5-oxohexanoic acid 163115391 Click to see CCC=C(C)C(=O)NCC(=O)C(C)C(C(C)C(=O)O)O 285.34 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264423/
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
4-Hydroxycinnamic acid 322 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown https://doi.org/10.1021/NP0500171
p-Coumaric acid 637542 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown https://doi.org/10.1021/NP0500171
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O 192.17 unknown https://doi.org/10.1021/NP0500171
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
(1E,4E,6E)-1,7-bis(4-hydroxyphenyl)hepta-1,4,6-trien-3-one 10447050 Click to see C1=CC(=CC=C1C=CC=CC(=O)C=CC2=CC=C(C=C2)O)O 292.30 unknown https://doi.org/10.1021/NP0500171
1,7-Bis (4-hydroxyphenyl)-1,4,6-heptatrien-3-one 71346280 Click to see C1=CC(=CC=C1C=CC=CC(=O)C=CC2=CC=C(C=C2)O)O 292.30 unknown https://doi.org/10.1021/NP0500171
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids / Curcuminoids
(1,7-Bis(4-hydroxy-3-methoxyphenyl)-1,6-heptadiene-3,5-dione) 2889 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://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264423/
https://doi.org/10.1021/NP0500171
(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/10.1021/NP0500171
(1E,4Z,6E)-5-hydroxy-1,7-bis(4-hydroxyphenyl)hepta-1,4,6-trien-3-one 5324473 Click to see C1=CC(=CC=C1C=CC(=CC(=O)C=CC2=CC=C(C=C2)O)O)O 308.30 unknown https://doi.org/10.1021/NP0500171
1-(4-Hydroxy-3-methoxyphenyl)-7-(4-hydroxyphenyl)-1,6-heptadiene-3,5-dione 146723 Click to see COC1=C(C=CC(=C1)C=CC(=O)CC(=O)C=CC2=CC=C(C=C2)O)O 338.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264423/
https://doi.org/10.1021/NP0500171
1,4,6-Heptatrien-3-one, 5-hydroxy-1,7-bis(4-hydroxyphenyl)- 468139 Click to see C1=CC(=CC=C1C=CC(=CC(=O)C=CC2=CC=C(C=C2)O)O)O 308.30 unknown https://doi.org/10.1021/NP0500171
1,7-Bis(4-hydroxyphenyl)hepta-1,6-diene-3,5-dione 147439 Click to see C1=CC(=CC=C1C=CC(=O)CC(=O)C=CC2=CC=C(C=C2)O)O 308.30 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264423/
Bisdemethoxycurcumin 5315472 Click to see C1=CC(=CC=C1C=CC(=O)CC(=O)C=CC2=CC=C(C=C2)O)O 308.30 unknown https://doi.org/10.1021/NP0500171
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264423/
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/10.1021/NP0500171
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264423/
Demethoxycurcumin 5469424 Click to see COC1=C(C=CC(=C1)C=CC(=O)CC(=O)C=CC2=CC=C(C=C2)O)O 338.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264423/
https://doi.org/10.1021/NP0500171
> Phenylpropanoids and polyketides / Macrolides and analogues
[3-[4-[13-Hydroxy-9-(1-hydroxyethyl)-4,14,16,16-tetramethyl-7,11-dioxo-2,6,10,17-tetraoxatricyclo[11.3.1.11,5]octadecan-3-yl]-1-methoxypentyl]phenyl] acetate 74028224 Click to see CC1CC(C23CC(C(C(O2)C(C)CCC(C4=CC(=CC=C4)OC(=O)C)OC)C)OC(=O)CC(OC(=O)CC1(O3)O)C(C)O)(C)C 634.80 unknown https://doi.org/10.1021/NP0500171

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