Melicope lunu-ankenda - Unknown
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Internal ID UUID6440577d1103f175924734
Scientific name Melicope lunu-ankenda
Authority (Gaertn.) T.G.Hartley
First published in Sandakania 4: 61 (1994)

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Synonyms Top

Scientific name Authority First published in
Zanthoxylum nilagiricum Miq. Nieuwe Verh. Eerste Kl. Kon. Ned. Inst. Wetensch. Amsterdam , ser. 3, 5: 6 (1852)
Zanthoxylum zeylanicum DC. Prodr. 1: 728 (1824)
Ampacus aromatica Kuntze Revis. Gen. Pl. 1: 98 (1891)
Ampacus roxburghiana Kuntze Revis. Gen. Pl. 1: 98 (1891)
Fagara lunu-ankenda Gaertn. Fruct. Sem. Pl. 1: 334 (1788)
Fagara zeylanica J.F.Gmel. Syst. Nat. ed. 13[bis] : 258 (1791)
Euodia roxburghiana Benth. Fl. Hongk. : 59 (1861)
Euodia lunu-ankenda (Gaertn.) Merr. Philipp. J. Sci., C 7: 378 (1912 publ. 1913)
Euodia arborea Elmer Leafl. Philipp. Bot. 8: 2806 (1915)
Euodia arborescens D.D.Tao Acta Bot. Yunnan. 6: 285 (1984)
Euodia aromatica Blume Bijdr. Fl. Ned. Ind. 5: 246. 1825 [20 Sep-7 Dec 1825]
Euodia concinna Ridl. Bull. Misc. Inform. Kew 1930: 78 (1930)
Euodia lucida Miq. Ann. Mus. Bot. Lugduno-Batavi 3: 244 (1867)
Euodia marambong (Miq.) Miq. Ann. Mus. Bot. Lugduno-Batavi 3: 244 (1867)
Euodia punctata Merr. J. Straits Branch Roy. Asiat. Soc. 86: 315 (1922)
Zanthoxylum roxburghianum Cham. Linnaea 5: 58 (1830)
Euodia roxburghiana var. longipes W.G.Craib
Zanthoxylum lucidum Miq. Fl. Ned. Ind., Eerste Bijv. 3: 532. 1861 [Dec 1861] Alternate title: Flora Indiae Batavae,...Supplementum Primum. Prodromus Florae Sumatranae
Zanthoxylum marambong Miq. Fl. Ned. Ind., Eerste Bijv. : 533 (1861)
Euodia lepta var. roxburghiana (Benth.) M.Hiroe Forest Pl. Hist. Jap. Islands 1: 191 (1974)
Euodia lunu-ankenda var. tirunelvelica A.N.Henry & Chandrab. Bull. Bot. Surv. India 15: 144 (1973 publ. 1976)

Common names Top

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Language Common/alternative name
Spanish evodia lunur-ankenda
an evodia lunur-ankenda
Bulgarian evodia lunur-ankenda
Catalan evodia lunur-ankenda
ceb evodia lunur-ankenda
Esperanto evodia lunur-ankenda
Basque evodia lunur-ankenda
ext evodia lunur-ankenda
Finnish evodia lunur-ankenda
French evodia lunur-ankenda
Irish evodia lunur-ankenda
Galician evodia lunur-ankenda
ia evodia lunur-ankenda
ie evodia lunur-ankenda
io evodia lunur-ankenda
Italian evodia lunur-ankenda
Malayalam കമ്പിളിമരം
Dutch evodia lunur-ankenda
oc evodia lunur-ankenda
Polish evodia lunur-ankenda
Portuguese evodia lunur-ankenda
Romanian evodia lunur-ankenda
Russian evodia lunur-ankenda
Albanian evodia lunur-ankenda
Ukrainian evodia lunur-ankenda
Vietnamese evodia lunur-ankenda
vo evodia lunur-ankenda
war evodia lunur-ankenda
Chinese 三刈叶吴萸
Chinese 三刈叶蜜茱萸

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
    • Indian Subcontinent
      • Assam
      • East Himalaya
      • India
      • Nepal
      • Sri Lanka
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Myanmar
      • Thailand
      • Vietnam
    • Malesia
      • Jawa
      • Malaya
      • Philippines
      • Sulawesi

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001261494
Tropicos 50199186
KEW urn:lsid:ipni.org:names:979137-1
The Plant List tro-50199186
Open Tree Of Life 5146055
NCBI Taxonomy 1487112
IUCN Red List 38842
IPNI 979137-1
iNaturalist 427162
GBIF 3832621
Freebase /m/02x90gr
USDA GRIN 403456
Wikipedia Euodia_lunuankenda
CMAUP NPO19509

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
p-O-geranylcoumaric acid from Melicope lunu-ankenda. Ramli I, Kamarulzaman NH, Shaari K, Ee GC Nat Prod Res 01-Aug-2004
doi:10.1080/14786410310001622068
PMID:15214478
Bacteriostatic heterocycles from Euodia lunu-ankenda Mangala D. Manandhar, Falak A. Hussaini, Randhir S. Kapil, Aboo Shoeb Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)80844-4
Two fungicidal phenylethanones from Euodia lunu-ankenda root bark Vijaya Kumar, Veranja Karunaratne, M.R. Sanath, K. Meegalle, John K. MacLeod Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(90)89042-8
HIV inhibitory natural products. 26. Quinoline alkaloids from Euodia roxburghiana. McCormick JL, McKee TC, Cardellina JH 2nd, Boyd MR J Nat Prod 01-May-1996
doi:10.1021/NP960250M
PMID:8778237

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 / Saturated hydrocarbons / Alkanes
Docosane 12405 Click to see CCCCCCCCCCCCCCCCCCCCCC 310.60 unknown https://doi.org/10.1080/14786410310001622068
Eicosane 8222 Click to see CCCCCCCCCCCCCCCCCCCC 282.50 unknown https://doi.org/10.1080/14786410310001622068
Hentriacontane 12410 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC 436.80 unknown https://doi.org/10.1080/14786410310001622068
Octacosane 12408 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCC 394.80 unknown https://doi.org/10.1080/14786410310001622068
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Oleic Acid 445639 Click to see CCCCCCCCC=CCCCCCCCC(=O)O 282.50 unknown https://doi.org/10.1080/14786410310001622068
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(8S,11bS)-7,11-dihydroxy-3,4,8,11b-tetramethyl-1,2,8,9-tetrahydronaphtho[2,1-f][1]benzofuran-6-one 11174780 Click to see CC1COC2=C(C3=C(C(=O)C=C4C3(CCC(=C4C)C)C)C(=C12)O)O 326.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
3-O-Acetyloleanolic acid 151202 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C(=O)O)C)C)C 498.70 unknown via CMAUP database
O-Acetyloleanolic aldehyde 14829106 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C=O)C)C)C 482.70 unknown via CMAUP database
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown via CMAUP database
Squalene 638072 Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C 410.70 unknown https://doi.org/10.1080/14786410310001622068
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8S,9S,10R,13R,14S,17S)-17-[(2R,5R)-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 122411793 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/S0031-9422(00)80844-4
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/S0031-9422(00)80844-4
22-Dehydroclerosterol 15608667 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(=C)C 410.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
4-Hydroxy-4-(2-hydroxyethyl)cyclohexan-1-one 184824 Click to see C1CC(CCC1=O)(CCO)O 158.19 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
1-[2-(3,7-Dimethylocta-2,6-dienoxy)-4,6-dihydroxy-3-(3-methylbut-2-enyl)phenyl]ethanone 129836233 Click to see CC(=CCCC(=CCOC1=C(C(=CC(=C1C(=O)C)O)O)CC=C(C)C)C)C 372.50 unknown https://doi.org/10.1016/0031-9422(90)89042-8
1-[2-[(2E)-3,7-dimethylocta-2,6-dienoxy]-4,6-dihydroxy-3-(3-methylbut-2-enyl)phenyl]ethanone 14466254 Click to see CC(=CCCC(=CCOC1=C(C(=CC(=C1C(=O)C)O)O)CC=C(C)C)C)C 372.50 unknown https://doi.org/10.1016/0031-9422(90)89042-8
1-[4,6-Dihydroxy-2-(3-methylbut-2-enoxy)-3-(3-methylbut-2-enyl)phenyl]ethanone 14466253 Click to see CC(=CCC1=C(C(=C(C=C1O)O)C(=O)C)OCC=C(C)C)C 304.40 unknown https://doi.org/10.1016/0031-9422(90)89042-8
> Organoheterocyclic compounds / Benzofurans
Cleroindicin C 10975728 Click to see C1CC2(CCOC2CC1=O)O 156.18 unknown via CMAUP database
Cleroindicin E 11744892 Click to see C1CC2(CCOC2CC1O)O 158.19 unknown via CMAUP database
epi-Cleroindicin D 10749706 Click to see C1COC2C1(C(CC(=O)C2)O)O 172.18 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
1-(3,4-Dihydroxy-5,7-dimethoxy-2,2-dimethyl-3,4-dihydrochromen-8-yl)ethanone 162959302 Click to see CC(=O)C1=C(C=C(C2=C1OC(C(C2O)O)(C)C)OC)OC 296.31 unknown https://doi.org/10.1016/S0031-9422(00)80844-4
1-(5,7-Dimethoxy-2,2-dimethyl-2H-chromen-6-yl)ethanone 66573258 Click to see CC(=O)C1=C(C=C2C(=C1OC)C=CC(O2)(C)C)OC 262.30 unknown https://doi.org/10.1016/S0031-9422(00)80844-4
1-[(3S,4S)-3,4-dihydroxy-5,7-dimethoxy-2,2-dimethyl-3,4-dihydrochromen-8-yl]ethanone 145962841 Click to see CC(=O)C1=C(C=C(C2=C1OC(C(C2O)O)(C)C)OC)OC 296.31 unknown https://doi.org/10.1016/S0031-9422(00)80844-4
Isoevodionol 11128652 Click to see CC(=O)C1=C(C=C2C(=C1O)C=CC(O2)(C)C)OC 248.27 unknown https://doi.org/10.1016/S0031-9422(00)80844-4
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans / Precocenes
1-(5,7-Dimethoxy-2,2-dimethyl-2H-chromen-8-yl)ethanone 12468042 Click to see CC(=O)C1=C(C=C(C2=C1OC(C=C2)(C)C)OC)OC 262.30 unknown https://doi.org/10.1016/S0031-9422(00)80844-4
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
Evolitrine 196980 Click to see COC1=CC2=C(C=C1)C(=C3C=COC3=N2)OC 229.23 unknown https://doi.org/10.1016/S0031-9422(00)80844-4
Roxiamine A 3000862 Click to see CC(CCOC1=CC2=C(C=C1)C(=C3C=COC3=N2)OC)C(=O)OC 329.30 unknown https://doi.org/10.1021/NP960250M
Roxiamine B 638622 Click to see CC(=CCOC1=CC2=C(C=C1)C(=C3C=COC3=N2)OC)C(=O)OC 327.30 unknown https://doi.org/10.1021/NP960250M
Roxiamine C 3000863 Click to see CC(CCOC1=CC2=C(C=C1)C(=C3C=COC3=N2)OC)O 287.31 unknown https://doi.org/10.1021/NP960250M
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives
2(1H)-Quinolinone, 3-(3-methyl-2-butenyl)-4-[(3-methyl-2-butenyl)oxy]- 4556 Click to see CC(=CCC1=C(C2=CC=CC=C2NC1=O)OCC=C(C)C)C 297.40 unknown https://doi.org/10.1021/NP960250M
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroquinolones
4-Methoxy-1-methylquinolin-2-one 182073 Click to see CN1C2=CC=CC=C2C(=CC1=O)OC 189.21 unknown https://doi.org/10.1016/S0031-9422(00)80844-4
Buchapine 461150 Click to see CC(=CCC1(C(=O)C2=CC=CC=C2NC1=O)C(C)(C)C=C)C 297.40 unknown https://doi.org/10.1021/NP960250M
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown via CMAUP database
Scutellarein 5281697 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)O)O)O 286.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
(2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-6-methoxy-4-oxochromen-7-yl]oxyoxane-2-carboxylic acid 5318059 Click to see COC1=C(C=C2C(=C1O)C(=O)C=C(O2)C3=CC=C(C=C3)O)OC4C(C(C(C(O4)C(=O)O)O)O)O 476.40 unknown via CMAUP database
beta-D-Glucopyranosiduronic acid, 2-(3,4-dihydroxyphenyl)-5-hydroxy-6-methoxy-4-oxo-4H-1-benzopyran-7-yl 158227 Click to see COC1=C(C=C2C(=C1O)C(=O)C=C(O2)C3=CC(=C(C=C3)O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O 492.40 unknown via CMAUP database
Scutellarin 185617 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O)O 462.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Eupafolin 5317284 Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O 316.26 unknown via CMAUP database
Hispidulin 5281628 Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC=C(C=C3)O)O 300.26 unknown via CMAUP database
Pectolinarigenin 5320438 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O 314.29 unknown via CMAUP database

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