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Internal ID UUID6440476f8af3b564648459
Scientific name Neolitsea konishii
Authority (Hayata) Kaneh. & Sasaki
First published in Trans. Nat. Hist. Soc. Formosa 20: 381 (1930)

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Synonyms Top

Scientific name Authority First published in
Litsea konishii Hayata J. Coll. Sci. Imp. Univ. Tokyo 30(1): 248 (1911)
Tetradenia konishii (Hayata) Hayata Icon. Pl. Formosan. 3: 167. 1913 [25 Dec 1913]

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Language Common/alternative name
Chinese 五掌楠

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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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001071973
Tropicos 17805896
KEW urn:lsid:ipni.org:names:466982-1
The Plant List tro-17805896
Open Tree Of Life 5699237
NCBI Taxonomy 1609886
IUCN Red List 175604896
IPNI 466982-1
iNaturalist 577627
GBIF 4179736
EOL 5397448
CMAUP NPO20064

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
Isoquinoline Alkaloids from Neolitsea Konishii Shoei‐Sheng Lee, Hsih‐Chin Yang Wiley 04-Jun-2015
doi:10.1002/JCCS.199200031
Chemical Constituents of <i>Neolitsea parvigemma</i> and <i>Neolitsea konishii</i> Keh‐Shaw Chen, Fang‐Rong Chang, Yi‐Chen Chia, Tian‐Shung Wu, Yang‐Chang Wu Wiley 01-May-2015
doi:10.1002/JCCS.199800018
Antioxidant Activities and Phytochemical Study of Leaf Extracts from 18 Indigenous Tree Species in Taiwan Ho ST, Tung YT, Chen YL, Zhao YY, Chung MJ, Wu JH Evid Based Complement Alternat Med 02-Feb-2012
PMCID:PMC3291425
doi:10.1155/2012/215959
PMID:22454657
Flavonoid Composition in the Leaves of Twelve <i>Litsea</i> and <i>Neolitsea</i> Plants Sheng‐Fa Tsai, Shoei‐Sheng Lee Wiley 27-Sep-2011
doi:10.1002/JCCS.201190040
Thaliporphine selectively inhibits expression of the inducible, but not the constitutive, nitric oxide synthase. Yu SM Biochem J 01-Oct-1994
PMCID:PMC1137589
doi:10.1042/bj3030289
PMID:7524482

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
(+/-)-Corydine 111119 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)OC)O)OC 341.40 unknown https://doi.org/10.1002/JCCS.199800018
1,10-Dimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline-2,9-diol 248507 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)OC)O 327.40 unknown https://doi.org/10.1002/JCCS.199800018
Actinodaphnine 160502 Click to see COC1=C(C=C2CC3C4=C(C2=C1)C5=C(C=C4CCN3)OCO5)O 311.30 unknown https://doi.org/10.1002/JCCS.199200031
Boldine 10154 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)OC)O 327.40 unknown https://doi.org/10.1002/JCCS.199800018
https://doi.org/10.1002/JCCS.199200031
Boldine 2-methyl ether 16573 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)OC)OC 341.40 unknown https://doi.org/10.1002/JCCS.199200031
Corydine 10153 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)OC)O)OC 341.40 unknown https://doi.org/10.1002/JCCS.199800018
Corytuberine 160500 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)O)OC 327.40 unknown https://doi.org/10.1002/JCCS.199200031
Corytuberine, pentahydrate 347379 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)O)OC 327.40 unknown https://doi.org/10.1002/JCCS.199200031
Isoboldine 133323 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)O)OC 327.40 unknown https://doi.org/10.1002/JCCS.199200031
Laurolitsine 22179 Click to see COC1=C(C=C2CC3C4=C(C2=C1)C(=C(C=C4CCN3)O)OC)O 313.30 unknown https://doi.org/10.1002/JCCS.199200031
Laurotetanine 31415 Click to see COC1=C(C2=C3C(CC4=CC(=C(C=C42)OC)O)NCCC3=C1)OC 327.40 unknown https://doi.org/10.1002/JCCS.199200031
N-Nornuciferine 12313579 Click to see COC1=C(C2=C3C(CC4=CC=CC=C42)NCCC3=C1)OC 281.30 unknown https://doi.org/10.1002/JCCS.199200031
Nornuciferine 41169 Click to see COC1=C(C2=C3C(CC4=CC=CC=C42)NCCC3=C1)OC 281.30 unknown https://doi.org/10.1002/JCCS.199200031
> Alkaloids and derivatives / Harmala alkaloids
4-(6-methoxy-9H-pyrido[3,4-b]indol-1-yl)pyrimidin-2-amine 5257255 Click to see COC1=CC2=C(C=C1)NC3=C2C=CN=C3C4=NC(=NC=C4)N 291.31 unknown https://doi.org/10.1002/JCCS.199800018
> Alkaloids and derivatives / Proaporphines
(+)-Stepharine 193686 Click to see COC1=C(C2=C3C(CC24C=CC(=O)C=C4)NCCC3=C1)OC 297.30 unknown https://doi.org/10.1002/JCCS.199200031
Glaziovine 65631 Click to see CN1CCC2=CC(=C(C3=C2C1CC34C=CC(=O)C=C4)O)OC 297.30 unknown https://doi.org/10.1002/JCCS.199200031
Stepharine 98455 Click to see COC1=C(C2=C3C(CC24C=CC(=O)C=C4)NCCC3=C1)OC 297.30 unknown https://doi.org/10.1002/JCCS.199200031
Suavedol 442245 Click to see CN1CCC2=CC(=C(C3=C2C1CC34C=CC(=O)C=C4)O)OC 297.30 unknown https://doi.org/10.1002/JCCS.199200031
> Benzenoids / Anthracenes / Anthraquinones
1-Hydroxy-2-methoxyanthraquinone 80103 Click to see COC1=C(C2=C(C=C1)C(=O)C3=CC=CC=C3C2=O)O 254.24 unknown via CMAUP database
1-Methoxy-2-methylanthracene-9,10-dione 3534338 Click to see CC1=C(C2=C(C=C1)C(=O)C3=CC=CC=C3C2=O)OC 252.26 unknown via CMAUP database
1,3-Dimethoxyanthraquinone 361511 Click to see COC1=CC2=C(C(=C1)OC)C(=O)C3=CC=CC=C3C2=O 268.26 unknown via CMAUP database
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
1,3-Dihydroxyanthraquinone 196978 Click to see C1=CC=C2C(=C1)C(=O)C3=C(C2=O)C(=CC(=C3)O)O 240.21 unknown via CMAUP database
2-Hydroxyanthraquinone 11796 Click to see C1=CC=C2C(=C1)C(=O)C3=C(C2=O)C=C(C=C3)O 224.21 unknown via CMAUP database
Alizarin 6293 Click to see C1=CC=C2C(=C1)C(=O)C3=C(C2=O)C(=C(C=C3)O)O 240.21 unknown via CMAUP database
Alizarin 1-methyl ether 80309 Click to see COC1=C(C=CC2=C1C(=O)C3=CC=CC=C3C2=O)O 254.24 unknown via CMAUP database
Lucidin 10163 Click to see C1=CC=C2C(=C1)C(=O)C3=CC(=C(C(=C3C2=O)O)CO)O 270.24 unknown via CMAUP database
Purpurin 6683 Click to see C1=CC=C2C(=C1)C(=O)C3=C(C2=O)C(=C(C=C3O)O)O 256.21 unknown via CMAUP database
Rubiadin 124062 Click to see CC1=C(C=C2C(=C1O)C(=O)C3=CC=CC=C3C2=O)O 254.24 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 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 via CMAUP database
> Benzenoids / Naphthalenes / Naphthols and derivatives
4-Methoxy-1-naphthol 66542 Click to see COC1=CC=C(C2=CC=CC=C21)O 174.20 unknown via CMAUP database
> Benzenoids / Phenanthrenes and derivatives
5-Hydroxy-4,13-dimethoxy-17-methyl-17-azatetracyclo[7.5.3.01,10.02,7]heptadeca-2,4,6,10,13-pentaen-12-one 5320383 Click to see CN1CCC23C=C(C(=O)C=C2C1CC4=CC(=C(C=C34)OC)O)OC 327.40 unknown https://doi.org/10.1002/JCCS.199200031
Pallidine 12313923 Click to see CN1CCC23C=C(C(=O)C=C2C1CC4=CC(=C(C=C34)OC)O)OC 327.40 unknown https://doi.org/10.1002/JCCS.199200031
> Benzenoids / Phenols / Methoxyphenols
Vanillin 1183 Click to see COC1=C(C=CC(=C1)C=O)O 152.15 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Annonaceous acetogenins
(2R)-4-[(13R)-13-[(2R,5R)-5-[(2R,5R)-5-[(1S,5S)-1,5-dihydroxyundecyl]oxolan-2-yl]oxolan-2-yl]-13-hydroxytridecyl]-2-methyl-2H-furan-5-one 101222383 Click to see CCCCCCC(CCCC(C1CCC(O1)C2CCC(O2)C(CCCCCCCCCCCCC3=CC(OC3=O)C)O)O)O 622.90 unknown https://doi.org/10.1002/JCCS.201190040
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
4,4,6a,8a,11,11,12b,14b-Octamethyl-1,4,4a,5,6,6a,8,8a,9,10,11,12,12a,12b,13,14,14a,14b-octadecahydro-3(2H)-picenone 500344 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(=O)CCC5(C4CCC3(C2C1)C)C)(C)C)C)C)C 424.70 unknown https://doi.org/10.1002/JCCS.199800018
CID 12443227 12443227 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C 426.70 unknown https://doi.org/10.1002/JCCS.199800018
Epitaraxerol 344467 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C 426.70 unknown https://doi.org/10.1002/JCCS.199800018
Taraxerone 92785 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(=O)CCC5(C4CCC3(C2C1)C)C)(C)C)C)C)C 424.70 unknown https://doi.org/10.1002/JCCS.199800018
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
Monotropein 73466 Click to see C1=CC(C2C1C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)O)(CO)O 390.34 unknown via CMAUP database
> 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://doi.org/10.1002/JCCS.199800018
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/10.1002/JCCS.199800018
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Asperuloside 84298 Click to see CC(=O)OCC1=CC2C3C1C(OC=C3C(=O)O2)OC4C(C(C(C(O4)CO)O)O)O 414.40 unknown via CMAUP database
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
Zeylanicin 604345 Click to see CC1=COC2=C1C3C=C(CCC4C(C2OC(=O)C)(O4)C)C(=O)O3 318.32 unknown https://doi.org/10.1002/JCCS.199800018
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
Reticulin 10233 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)O)O)OC 329.40 unknown https://doi.org/10.1002/JCCS.199200031
Reticuline 439653 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)O)O)OC 329.40 unknown https://doi.org/10.1002/JCCS.199200031
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives
n-Feruloyl-3-methoxytyramine 134313 Click to see COC1=C(C=CC(=C1)CCNC(=O)C=CC2=CC(=C(C=C2)O)OC)O 343.40 unknown https://doi.org/10.1002/JCCS.199800018
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
(E)-3-(3,4-dihydroxyphenyl)prop-2-enoic acid 2518 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown via CMAUP database
4-Hydroxycinnamic acid 322 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
Coumarin 323 Click to see C1=CC=C2C(=C1)C=CC(=O)O2 146.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Quercetin 3-apiosyl-(1->2)-alpha-L-arabinopyranoside 21676283 Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)OC5C(C(CO5)(CO)O)O)O)O 566.50 unknown https://doi.org/10.1002/JCCS.201190040

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