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Internal ID UUID643ff3f557d15215739775
Scientific name Lophopetalum javanum
Authority Turcz.
First published in Bull. Soc. Imp. Naturalistes Moscou 36(I): 598 (1863)

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Synonyms Top

Scientific name Authority First published in
Lophopetalum toxicum Loher Icon. Bogor. 1: t. 16 (1897)
Lophopetalum paucinervium Merr. Philipp. J. Sci. 20: 402 (1922)
Lophopetalum oblongifolium King J. Asiat. Soc. Bengal, Pt. 2, Nat. Hist. 65: 351 (1896)
Lophopetalum oblongum King J. Asiat. Soc. Bengal, Pt. 2, Nat. Hist. 65: 350 (1896)
Lophopetalum intermedium Ridl. J. Straits Branch Roy. Asiat. Soc. 59: 85 (1911)
Lophopetalum celebicus Koord. Meded. Lands Plantentuin 19: 623 (1898)
Lophopetalum fuscescens Kurz J. Asiat. Soc. Bengal, Pt. 2, Nat. Hist. 44: 202 (1875)
Solenospermum oblongifolium (King) Loes. Notizbl. Bot. Gart. Berlin-Dahlem 13: 225 (1936)
Solenospermum paucinervium (Merr.) Loes. Notizbl. Bot. Gart. Berlin-Dahlem 13: 223 (1936)
Solenospermum toxicum (Loher) Loes. Notizbl. Bot. Gart. Berlin-Dahlem 13: 223 (1936)
Solenospermum javanicum Zoll. Natuurk. Tijdschr. Ned.-Indië 14: 169 (1857)
Euonymus adenophorus Scort. ex King J. Asiat. Soc. Bengal, Pt. 2, Nat. Hist. 65: 351 (1896)
Euonymus celebicus Koord. Meded. Lands Plantentuin 19: 395 (1898)

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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
      • Bangladesh
    • Indo-China
      • Cambodia
      • Laos
      • Myanmar
      • Thailand
    • Malesia
      • Borneo
      • Jawa
      • Lesser Sunda Islands
      • Malaya
      • Maluku
      • Philippines
      • Sulawesi
      • Sumatera
    • Papuasia
      • New Guinea

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000358935
NCBI Taxonomy 2306824
IPNI 161742-1
GBIF 3791996
CMAUP NPO18476
Open Tree Of Life 7054800

Genomes (via NCBI) Top

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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
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Crinine- and Haemanthamine-type amaryllidaceae alkaloids
(+)-epi-Vittatine 12304132 Click to see C1CN2CC3=CC4=C(C=C3C15C2CC(C=C5)O)OCO4 271.31 unknown via CMAUP database
(1R,13R,15S,18R)-15-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-18-ol 40469675 Click to see COC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 301.34 unknown via CMAUP database
(1S,11S,13S,15R,18R)-15-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraene-11,18-diol 101297739 Click to see COC1CC2C3(C=C1)C(CN2C(C4=CC5=C(C=C34)OCO5)O)O 317.34 unknown via CMAUP database
(1S,13R,15R,18S)-15-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-18-ol 42579248 Click to see COC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 301.34 unknown via CMAUP database
[(1S,13R,15R)-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-15-yl] acetate 101935954 Click to see CC(=O)OC1CC2C3(CCN2CC4=CC5=C(C=C43)OCO5)C=C1 313.30 unknown via CMAUP database
3-O-Acetylhamayne 443671 Click to see CC(=O)OC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 329.30 unknown via CMAUP database
Crinamidine 399204 Click to see COC1=C2CN3CCC4(C3CC(C5C4O5)O)C2=CC6=C1OCO6 317.34 unknown via CMAUP database
Crinamin 73620 Click to see COC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 301.34 unknown via CMAUP database
O-Demethylhaemanthamine 44445844 Click to see C1C(C=CC23C1N(CC2O)CC4=CC5=C(C=C34)OCO5)O 287.31 unknown via CMAUP database
Vittatine 443693 Click to see C1CN2CC3=CC4=C(C=C3C15C2CC(C=C5)O)OCO4 271.31 unknown via CMAUP database
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Lycorine-type amaryllidaceae alkaloids
Lycorine 72378 Click to see C1CN2CC3=CC4=C(C=C3C5C2C1=CC(C5O)O)OCO4 287.31 unknown via CMAUP database
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Tazettine-type amaryllidaceae alkaloids
(1S,11S,13R,16S,18R)-11-ethoxy-18-methoxy-15-methyl-5,7,12-trioxa-15-azapentacyclo[11.7.0.01,16.02,10.04,8]icosa-2,4(8),9,19-tetraene 15483834 Click to see CCOC1C2=CC3=C(C=C2C45C=CC(CC4N(CC5O1)C)OC)OCO3 359.40 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
6-(4-Hydroxyphenyl)-1,3-benzodioxole-5-carbaldehyde 15549895 Click to see C1OC2=C(O1)C=C(C(=C2)C=O)C3=CC=C(C=C3)O 242.23 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 2-benzopyrans
N-Desmethyl-8alpha-ethoxypretazettine 15483835 Click to see CCOC1C2=CC3=C(C=C2C45C=CC(CC4NCC5O1)OC)OCO3 345.40 unknown via CMAUP database
N-Desmethyl-8beta-ethoxypretazettine 15483836 Click to see CCOC1C2=CC3=C(C=C2C45C=CC(CC4NCC5O1)OC)OCO3 345.40 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
(1S,13R)-9-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,14,16-pentaene 21723147 Click to see COC1=C2CN3CCC4(C3C=CC=C4)C2=CC5=C1OCO5 283.32 unknown via CMAUP database
1-Epideacetylbowdensine 443673 Click to see COC1=C2CN3CCC4(C3CCC(C4O)O)C2=CC5=C1OCO5 319.40 unknown via CMAUP database
7H-Pyrrolo(3,2,1-de)phenanthridin-7-one, 10-hydroxy-9-methoxy- 5488695 Click to see COC1=C(C=C2C3=CC=CC4=C3N(C=C4)C(=O)C2=C1)O 265.26 unknown via CMAUP database
Hippacine 10015025 Click to see C1=CC2=C3C(=C1)C4=CC(=C(C=C4C(=O)N3C=C2)O)O 251.24 unknown via CMAUP database
Hippadine 100605 Click to see C1OC2=C(O1)C=C3C(=C2)C4=CC=CC5=C4N(C3=O)C=C5 263.25 unknown via CMAUP database
Pratorimine 181937 Click to see COC1=C(C=C2C(=C1)C3=CC=CC4=C3N(C2=O)C=C4)O 265.26 unknown via CMAUP database
> Organoheterocyclic compounds / Tetrahydroisoquinolines / 4-phenyltetrahydroisoquinolines
Cherylline 90075 Click to see CN1CC(C2=CC(=C(C=C2C1)O)OC)C3=CC=C(C=C3)O 285.34 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Liquiritigenin 114829 Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC=C(C=C3)O 256.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
3',4'-Dihydroxy-7-methoxyflavan 14157886 Click to see COC1=CC2=C(CCC(O2)C3=CC(=C(C=C3)O)O)C=C1 272.29 unknown via CMAUP database
Guibourtinidol-7-methyl ether 15549896 Click to see COC1=CC2=C(CC(C(O2)C3=CC=C(C=C3)O)O)C=C1 272.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
(2S)-7-hydroxy-8-methoxy-2-phenyl-2,3-dihydrochromen-4-one 15549894 Click to see COC1=C(C=CC2=C1OC(CC2=O)C3=CC=CC=C3)O 270.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
GU17;ISL;Isoliquiritigen 425 Click to see C1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2)O)O)O 256.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Cinnamylphenols
4-Hydroxy-2',4'-dimethoxydihydrochalcone 15549893 Click to see COC1=CC(=C(C=C1)C(=O)CCC2=CC=C(C=C2)O)OC 286.32 unknown via CMAUP database

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