Scolopia chinensis - Unknown
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Internal ID UUID644046395c265786204053
Scientific name Scolopia chinensis
Authority (Lour.) Clos
First published in Ann. Sci. Nat., Bot. , sér. 4, 8: 249 (1857)

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Synonyms Top

Scientific name Authority First published in
Rumea chinensis (Lour.) Wall. ex Steud. Nomencl. Bot. , ed. 2, 2: 475 (1841)
Scolopia cochinchinensis (Lour.) Clos Ann. Sci. Nat., Bot. , sér. 4, 8: 253 (1857)
Scolopia elliptica Regel Index Seminum (LE, Petropolitanus) 1866: 35 (1867)
Rumea cochinchinensis (Lour.) Wall. Numer. List : n.º 6680 (1832)
Phoberos chinensis Lour. Fl. Cochinch. : 318 (1790)
Phoberos cochinchinensis Lour. Fl. Cochinch. : 318 (1790)
Phoberos arnottiana Thwaites Enum. Pl. Zeyl. : 16 (1858)
Scolopia siamensis Warb. Repert. Spec. Nov. Regni Veg. 16: 255 (1919)

Common names Top

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Language Common/alternative name
Chinese 箣柊
Chinese 莿柊
Chinese 蜈蚣
Chinese 土烏藥

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) 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
      • Laos
      • Thailand
      • Vietnam
    • Malesia
      • Jawa
      • Malaya

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001063087
Tropicos 13201142
KEW urn:lsid:ipni.org:names:112061-1
The Plant List tro-13201142
Open Tree Of Life 5763668
NCBI Taxonomy 1603833
IPNI 112061-1
iNaturalist 181945
GBIF 3879433
EPPO SKOCH
EOL 2889954
USDA GRIN 33397
CMAUP NPO15875

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
Does local soil factor drive functional leaf trait variation? A test on Neilingding Island, South China Tong S, Zhang J, Qiao X, Li B, Yang Q, Hu P, Yu S BMC Ecol Evol 10-Apr-2024
PMCID:PMC11005248
doi:10.1186/s12862-024-02227-0
PMID:38600505
Molecular Phylogeny and Morphology Reveal Four Novel Species of Corynespora and Kirschsteiniothelia (Dothideomycetes, Ascomycota) from China: A Checklist for Corynespora Reported Worldwide Liu J, Hu Y, Luo X, Castañeda-Ruíz RF, Xia J, Xu Z, Cui R, Shi X, Zhang L, Ma J J Fungi (Basel) 12-Jan-2023
PMCID:PMC9863821
doi:10.3390/jof9010107
PMID:36675928
Plant-Derived Toxin Inhibitors as Potential Candidates to Complement Antivenom Treatment in Snakebite Envenomations Adrião AA, dos Santos AO, de Lima EJ, Maciel JB, Paz WH, da Silva FM, Pucca MB, Moura-da-Silva AM, Monteiro WM, Sartim MA, Koolen HH Front Immunol 09-May-2022
PMCID:PMC9126284
doi:10.3389/fimmu.2022.842576
PMID:35615352
Frequent ploidy changes in Salicaceae indicates widespread sharing of the salicoid whole genome duplication by the relatives of Populus L. and Salix L. Zhang ZS, Zeng QY, Liu YJ BMC Plant Biol 13-Nov-2021
PMCID:PMC8590345
doi:10.1186/s12870-021-03313-x
PMID:34773988
Intergeneric Relationships within the Family Salicaceae s.l. Based on Plastid Phylogenomics Li MM, Wang DY, Zhang L, Kang MH, Lu ZQ, Zhu RB, Mao XX, Xi ZX, Ma T Int J Mol Sci 02-Aug-2019
PMCID:PMC6696080
doi:10.3390/ijms20153788
PMID:31382526
Constituents from Leaves of <i>Scolopia chinensis</i> Ya‐Nan Lu, Guang‐Bo Xie, Dan Bi, Hai‐Ming Shi, Peng‐Fei Tu Wiley 20-May-2008
doi:10.1002/HLCA.200890084

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 / Aporphines
(+/-)-Dicentrine 630859 Click to see CN1CCC2=CC3=C(C4=C2C1CC5=CC(=C(C=C54)OC)OC)OCO3 339.40 unknown https://doi.org/10.1002/HLCA.200890084
Dicentrine 101300 Click to see CN1CCC2=CC3=C(C4=C2C1CC5=CC(=C(C=C54)OC)OC)OCO3 339.40 unknown https://doi.org/10.1002/HLCA.200890084
> Alkaloids and derivatives / Lupin alkaloids / Cytisine and derivatives
(1R)-1,2,3,4,5,6-Hexahydro-1,5-methano-8H-pyrido[1,2-a][1,5]diazocin-8-one 1278189 Click to see CN1CC2CC(C1)C3=CC=CC(=O)N3C2 204.27 unknown via CMAUP database
Cytisinicline 10235 Click to see C1C2CNCC1C3=CC=CC(=O)N3C2 190.24 unknown via CMAUP database
N-Formylcytisine, (-)- 6604689 Click to see C1C2CN(CC1C3=CC=CC(=O)N3C2)C=O 218.25 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)O 170.12 unknown https://doi.org/10.1002/HLCA.200890084
> Lignans, neolignans and related compounds / Furanoid lignans
(-)-Syringaresinol 11604108 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC 418.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Hexacosanoic acid 10469 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCC(=O)O 396.70 unknown https://doi.org/10.1002/HLCA.200890084
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Selina-4(15),7(11)-dien-8-one 13986100 Click to see CC(=C1CC2C(=C)CCCC2(CC1=O)C)C 218.33 unknown https://doi.org/10.1002/HLCA.200890084
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1002/HLCA.200890084
Lupenone 92158 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C 424.70 unknown via CMAUP database
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
Olean-12-en-3beta-ol 225689 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1002/HLCA.200890084
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
[(2R,3S,4S,5R,6S)-6-(4-acetylphenoxy)-3,4,5-trihydroxyoxan-2-yl]methyl 4-hydroxybenzoate 101861836 Click to see CC(=O)C1=CC=C(C=C1)OC2C(C(C(C(O2)COC(=O)C3=CC=C(C=C3)O)O)O)O 418.40 unknown https://doi.org/10.1002/HLCA.200890084
[(2S,3S,4S,5R,6S)-3,4,5-Trihydroxy-6-(4-hydroxyphenoxy)tetrahydropyran-2-yl]methyl 4-hydroxybenzoate 11176815 Click to see C1=CC(=CC=C1C(=O)OCC2C(C(C(C(O2)OC3=CC=C(C=C3)O)O)O)O)O 392.40 unknown https://doi.org/10.1002/HLCA.200890084
[2-[(2S,3R,4S,5S,6R)-3-benzoyloxy-6-(benzoyloxymethyl)-4,5-dihydroxyoxan-2-yl]oxy-5-hydroxyphenyl]methyl (1R,2R,6R)-1,2-dihydroxy-6-(4-hydroxybenzoyl)oxy-5-oxocyclohex-3-ene-1-carboxylate 101861835 Click to see C1=CC=C(C=C1)C(=O)OCC2C(C(C(C(O2)OC3=C(C=C(C=C3)O)COC(=O)C4(C(C=CC(=O)C4OC(=O)C5=CC=C(C=C5)O)O)O)OC(=O)C6=CC=CC=C6)O)O 800.70 unknown https://doi.org/10.1002/HLCA.200890084
[2-[3-Benzoyloxy-6-(benzoyloxymethyl)-4,5-dihydroxyoxan-2-yl]oxy-5-hydroxyphenyl]methyl 1,2-dihydroxy-6-(4-hydroxybenzoyl)oxy-5-oxocyclohex-3-ene-1-carboxylate 163049368 Click to see C1=CC=C(C=C1)C(=O)OCC2C(C(C(C(O2)OC3=C(C=C(C=C3)O)COC(=O)C4(C(C=CC(=O)C4OC(=O)C5=CC=C(C=C5)O)O)O)OC(=O)C6=CC=CC=C6)O)O 800.70 unknown https://doi.org/10.1002/HLCA.200890084
[3,4,5-Trihydroxy-6-[2-(hydroxymethyl)phenoxy]oxan-2-yl]methyl benzoate 278591 Click to see C1=CC=C(C=C1)C(=O)OCC2C(C(C(C(O2)OC3=CC=CC=C3CO)O)O)O 390.40 unknown https://doi.org/10.1002/HLCA.200890084
[6-(4-Acetylphenoxy)-3,4,5-trihydroxyoxan-2-yl]methyl 4-hydroxybenzoate 163036616 Click to see CC(=O)C1=CC=C(C=C1)OC2C(C(C(C(O2)COC(=O)C3=CC=C(C=C3)O)O)O)O 418.40 unknown https://doi.org/10.1002/HLCA.200890084
Populin 92735 Click to see C1=CC=C(C=C1)C(=O)OCC2C(C(C(C(O2)OC3=CC=CC=C3CO)O)O)O 390.40 unknown https://doi.org/10.1002/HLCA.200890084
> Organoheterocyclic compounds / Oxepanes
Xylarenal B 139588412 Click to see CCCCCCCCCC(=O)OC1CCC(C2(C13C(O3)C(=O)C(C2)C(=C)C=O)C)C 418.60 unknown https://doi.org/10.1002/HLCA.200890084
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
2-Propenoic acid, 3-(3,4-dihydroxyphenyl)-, octadecyl ester, (E)-; trans-Caffeic acid stearyl ester 71374400 Click to see CCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)O 432.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Naringenin 439246 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
Aromadendrin 122850 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 288.25 unknown via CMAUP database
> 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
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
[(2R,3R,4S,5R,6S)-4-acetyloxy-3,5-dihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxyoxan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate 101999899 Click to see CC(=O)OC1C(C(OC(C1O)OC2=CC(=C3C(=C2)OC(=CC3=O)C4=CC=C(C=C4)O)O)COC(=O)C=CC5=CC=C(C=C5)O)O 620.60 unknown https://doi.org/10.1002/HLCA.200890084
[(2R,3S,4R,5R,6S)-3-acetyloxy-4,5-dihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxyoxan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate 101861837 Click to see CC(=O)OC1C(OC(C(C1O)O)OC2=CC(=C3C(=C2)OC(=CC3=O)C4=CC=C(C=C4)O)O)COC(=O)C=CC5=CC=C(C=C5)O 620.60 unknown https://doi.org/10.1002/HLCA.200890084
[3,4,5-Trihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxyoxan-2-yl]methyl 3-(4-hydroxyphenyl)prop-2-enoate 162916367 Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)O)O)O)O)O)O 578.50 unknown https://doi.org/10.1002/HLCA.200890084
[4-Acetyloxy-3,5-dihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxyoxan-2-yl]methyl 3-(4-hydroxyphenyl)prop-2-enoate 74977536 Click to see CC(=O)OC1C(C(OC(C1O)OC2=CC(=C3C(=C2)OC(=CC3=O)C4=CC=C(C=C4)O)O)COC(=O)C=CC5=CC=C(C=C5)O)O 620.60 unknown https://doi.org/10.1002/HLCA.200890084
Echinacin 6439941 Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)O)O)O)O)O)O 578.50 unknown https://doi.org/10.1002/HLCA.200890084
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
5-O-Methylgenistein 5748551 Click to see COC1=CC(=CC2=C1C(=O)C(=CO2)C3=CC=C(C=C3)O)O 284.26 unknown via CMAUP database
Daidzein 5281708 Click to see C1=CC(=CC=C1C2=COC3=C(C2=O)C=CC(=C3)O)O 254.24 unknown via CMAUP database
Genistein 5280961 Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)O)O 270.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
3-(4-hydroxyphenyl)-5-methoxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 189922 Click to see COC1=CC(=CC2=C1C(=O)C(=CO2)C3=CC=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O 446.40 unknown via CMAUP database
Kakkanin 44257291 Click to see COC1=CC=C(C=C1)C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O 578.50 unknown via CMAUP database
Sophoricoside 5321398 Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)O)OC4C(C(C(C(O4)CO)O)O)O 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
Biochanin A 5280373 Click to see COC1=CC=C(C=C1)C2=COC3=CC(=CC(=C3C2=O)O)O 284.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 7-O-methylated isoflavonoids / 7-O-methylisoflavones
4',7-Dimethoxyisoflavone 136419 Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)OC 282.29 unknown via CMAUP database
7,4'-Dimethoxy-5-hydroxyisoflavone 5386259 Click to see COC1=CC=C(C=C1)C2=COC3=CC(=CC(=C3C2=O)O)OC 298.29 unknown via CMAUP database
Isoformononetin 3764 Click to see COC1=CC2=C(C=C1)C(=O)C(=CO2)C3=CC=C(C=C3)O 268.26 unknown via CMAUP database

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