Melicope latifolia - Unknown
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Internal ID UUID6440577cebc23138152721
Scientific name Melicope latifolia
Authority (DC.) T.G.Hartley
First published in Sandakania 4: 72 (1994)

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Synonyms Top

Scientific name Authority First published in
Zanthoxylum rumphianum Cham. Linnaea 5: 58 (1830)
Zanthoxylum lanuginosum Kostel. Allg. Med.-Pharm. Fl. 5: 1783 (1836)
Zanthoxylum latifolium G.Don Gen. Hist. 1: 804 (1831)
Ampacus latifolia Kuntze Revis. Gen. Pl. 1: 98 (1891)
Euodia latifolia DC. Prodr. 1: 724 (1824)

Common names Top

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Language Common/alternative name
ban empag

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-tropical
    • Indo-China
      • Myanmar
    • Malesia
      • Borneo
      • Jawa
      • Lesser Sunda Islands
      • Malaya
      • Maluku
      • Philippines
      • Sulawesi
    • Papuasia
      • Bismarck Archipelago
      • New Guinea
      • Solomon Islands

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001261493
Tropicos 50199185
KEW urn:lsid:ipni.org:names:979143-1
The Plant List tro-50199185
Open Tree Of Life 5233094
NCBI Taxonomy 1336624
IPNI 979143-1
GBIF 3832733
Freebase /m/01317l_y
EOL 5619014
Wikipedia Melicope_latifolia

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
Methoxyfuranocoumarins of Natural Origin–Updating Biological Activity Research and Searching for New Directions—A Review Bartnik M Curr Issues Mol Biol 19-Jan-2024
PMCID:PMC10813879
doi:10.3390/cimb46010055
PMID:38275669
New Insights into the Latest Advancement in α-Amylase Inhibitors of Plant Origin with Anti-Diabetic Effects Kashtoh H, Baek KH Plants (Basel) 14-Aug-2023
PMCID:PMC10458243
doi:10.3390/plants12162944
PMID:37631156
Promising alkaloids and flavonoids compounds as anti-hepatitis c virus agents: a review Rizaldi G, Hafid AF, Wahyuni TS J Public Health Afr 16-Mar-2023
PMCID:PMC10365654
doi:10.4081/jphia.2023.2514
PMID:37492538
Methyl P-Coumarate Ameliorates the Inflammatory Response in Activated-Airway Epithelial Cells and Mice with Allergic Asthma Park JW, Choi J, Lee J, Park JM, Kim SM, Min JH, Seo DY, Goo SH, Kim JH, Kwon OK, Lee K, Ahn KS, Oh SR, Lee JW Int J Mol Sci 28-Nov-2022
PMCID:PMC9736825
doi:10.3390/ijms232314909
PMID:36499236
A review on phytochemical and pharmacological facets of tropical ethnomedicinal plants as reformed DPP-IV inhibitors to regulate incretin activity Chhabria S, Mathur S, Vadakan S, Sahoo DK, Mishra P, Paital B Front Endocrinol (Lausanne) 11-Nov-2022
PMCID:PMC9691845
doi:10.3389/fendo.2022.1027237
PMID:36440220
α-Amylase and dipeptidyl peptidase-4 (DPP-4) inhibitory effects of Melicope latifolia bark extracts and identification of bioactive constituents using in vitro and in silico approaches Quek A, Kassim NK, Lim PC, Tan DC, Mohammad Latif MA, Ismail A, Shaari K, Awang K Pharm Biol 04-Aug-2021
PMCID:PMC8344235
doi:10.1080/13880209.2021.1948065
PMID:34347568
New Acetophenones and Chromenes from the Leaves of Melicope barbigera A. Gray Le KT, Bandolik JJ, Kassack MU, Wood KR, Paetzold C, Appelhans MS, Passreiter CM Molecules 28-Jan-2021
PMCID:PMC7865373
doi:10.3390/molecules26030688
PMID:33525713
Alkaloid and benzopyran compounds of Melicope latifolia fruit exhibit anti-hepatitis C virus activities Widyawaruyanti A, Tanjung M, Permanasari AA, Saputri R, Tumewu L, Adianti M, Aoki-Utsubo C, Hotta H, Hafid AF, Wahyuni TS BMC Complement Med Ther 12-Jan-2021
PMCID:PMC7802229
doi:10.1186/s12906-021-03202-8
PMID:33435968
Rapid Quantification and Validation of Biomarker Scopoletin in Paederia foetida by qNMR and UV–Vis for Herbal Preparation Tan DC, Quek A, Kassim NK, Ismail IS, Lee JJ Molecules 06-Nov-2020
PMCID:PMC7664186
doi:10.3390/molecules25215162
PMID:33171900
Bioactive Natural Antivirals: An Updated Review of the Available Plants and Isolated Molecules Mohan S, Elhassan Taha MM, Makeen HA, Alhazmi HA, Al Bratty M, Sultana S, Ahsan W, Najmi A, Khalid A Molecules 22-Oct-2020
PMCID:PMC7659943
doi:10.3390/molecules25214878
PMID:33105694
Quantitative ethnopharmacological documentation and molecular confirmation of medicinal plants used by the Manobo tribe of Agusan del Sur, Philippines Dapar ML, Alejandro GJ, Meve U, Liede-Schumann S J Ethnobiol Ethnomed 05-Mar-2020
PMCID:PMC7227330
doi:10.1186/s13002-020-00363-7
PMID:32138749
Ethnomedicine of Tetun ethnic people in West Timor Indonesia: philosophy and practice in the treatment of malaria Taek MM, Banilodu L, Neonbasu G, Watu YV, E.W. BP, Agil M Integr Med Res 04-Jun-2019
PMCID:PMC6600717
doi:10.1016/j.imr.2019.05.005
PMID:31304086
Anticancer Activity of Methanol Extract of Ficus carica Leaves and Fruits Against Proliferation, Apoptosis, and Necrosis in Huh7it Cells Purnamasari R, Winarni D, Permanasari AA, Agustina E, Hayaza S, Darmanto W Cancer Inform 19-Apr-2019
PMCID:PMC6475848
doi:10.1177/1176935119842576
PMID:31037025
Medicinal plants against hepatitis C virus Ashfaq UA, Idrees S World J Gastroenterol 21-Mar-2014
PMCID:PMC3961971
doi:10.3748/wjg.v20.i11.2941
PMID:24659884
Antiviral activities of Indonesian medicinal plants in the East Java region against hepatitis C virus Wahyuni TS, Tumewu L, Permanasari AA, Apriani E, Adianti M, Rahman A, Widyawaruyanti A, Lusida MI, Fuad A, Soetjipto, Nasronudin, Fuchino H, Kawahara N, Shoji I, Deng L, Aoki C, Hotta H Virol J 13-Aug-2013
PMCID:PMC3751543
doi:10.1186/1743-422X-10-259
PMID:24089993

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 / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(3S,8S,9S,14S,17R)-17-[(2R,5R)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 134766514 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown https://doi.org/10.1016/0031-9422(90)80154-9
5-Cholestene-3-ol, 24-methyl- 312822 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown https://doi.org/10.1016/0031-9422(90)80154-9
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8S,9S,10R,13R,14S,17R)-17-[(E,2S,5S)-5-Ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 12314479 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/0031-9422(90)80154-9
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 122544 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/0031-9422(90)80154-9
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://doi.org/10.1016/0031-9422(90)80154-9
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/0031-9422(90)80154-9
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/0031-9422(90)80154-9
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/0031-9422(90)80154-9
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
1-(9-Hydroxy-1,5,5-trimethyl-6,15-dioxatetracyclo[9.3.1.04,13.07,12]pentadeca-7,9,11-trien-8-yl)ethanone 321017 Click to see CC(=O)C1=C2C3=C(C=C1O)OC4(CCC(C3C4)C(O2)(C)C)C 302.40 unknown https://doi.org/10.1016/0031-9422(90)80154-9
1-(9-Hydroxy-1,5,5-trimethyl-6,15-dioxatetracyclo[9.3.1.04,13.07,12]pentadeca-7(12),8,10-trien-10-yl)ethanone 14543428 Click to see CC(=O)C1=C2C3=C(C=C1O)OC(C4C3CC(O2)(CC4)C)(C)C 302.40 unknown https://doi.org/10.1016/0031-9422(90)80154-9
1-[(1S,4R,13S)-9-hydroxy-1,5,5-trimethyl-6,15-dioxatetracyclo[9.3.1.04,13.07,12]pentadeca-7,9,11-trien-8-yl]ethanone 92144938 Click to see CC(=O)C1=C2C3=C(C=C1O)OC4(CCC(C3C4)C(O2)(C)C)C 302.40 unknown https://doi.org/10.1016/0031-9422(90)80154-9
1-[(1S,4R,13S)-9-hydroxy-1,5,5-trimethyl-6,15-dioxatetracyclo[9.3.1.04,13.07,12]pentadeca-7(12),8,10-trien-10-yl]ethanone 163188324 Click to see CC(=O)C1=C2C3=C(C=C1O)OC(C4C3CC(O2)(CC4)C)(C)C 302.40 unknown https://doi.org/10.1016/0031-9422(90)80154-9
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-methoxypsoralens
Bergapten 2355 Click to see COC1=C2C=CC(=O)OC2=CC3=C1C=CO3 216.19 unknown https://doi.org/10.1016/0031-9422(90)80154-9

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