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Lindera praecox

Lindera praecox - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID6440473add0fb200305798
Scientific name Lindera praecox
Authority (Siebold & Zucc.) Blume
First published in Mus. Bot. 1: 324 (1851)

Description Top

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Synonyms Top

Scientific name Authority First published in
Benzoin praecox Siebold & Zucc. Abh. Math.-Phys. Cl. Königl. Bayer. Akad. Wiss. 4(3): 205. 1846
Parabenzoin praecox (Siebold & Zucc.) Nakai Bull. Soc. Bot. France 71: 1181 (1924 publ. 1925)
Lindera praecox f. pubescens (Honda) H.Ohba Fl. Jap. (Iwatsuki et al., eds.) 2a: 246. 2006 [24 Feb 2006]
Parabenzoin praecox var. pubescens Honda Bot. Mag. (Tokyo) 43(510): 293. 1929 [Jun 1929]
Parabenzoin praecox var. stipitatum Nakai Bull. Natl. Sci. Mus. Tokyo 33: 8 (1953)
Parabenzoin praecox var. oleopubescens Nakai Bull. Natl. Sci. Mus. Tokyo 33: 8 (1953)
Parabenzoin praecox var. stipititoides Nakai Bull. Natl. Sci. Mus. Tokyo 33: 8 (1953)
Parabenzoin praecox f. angustifolium Sugim. New Keys Jap. Trees: 464 (1961)

Common names Top

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Language Common/alternative name
Japanese アブラチャン
Malayalam ലിൻഡേര പ്രെകോക്സ്
Chinese 大果山胡椒

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China South-central
      • China Southeast
    • Eastern Asia
      • Japan

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001070368
Tropicos 17800798
KEW urn:lsid:ipni.org:names:465429-1
The Plant List tro-17800798
Open Tree Of Life 5699258
NCBI Taxonomy 1715696
IPNI 465429-1
iNaturalist 452215
GBIF 7304475
EPPO LIEPR
EOL 5394475
USDA GRIN 403145
Wikipedia Lindera_praecox

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
Pyrenopeziza orientalipetiolaris sp. nov. in Japan and morphological and genetic comparison with its relevant species P. petiolaris in Europe Itagaki H, Hosoya T Mycoscience 11-Aug-2022
PMCID:PMC10012338
doi:10.47371/mycosci.2022.07.003
PMID:37090199
The complete chloroplast genome sequence of China Lindera praecox (Lauraceae) and intra-species diversity Yu J, Li Z, Dong H Mitochondrial DNA B Resour 01-Jul-2021
PMCID:PMC8253210
doi:10.1080/23802359.2021.1944829
PMID:34263040
Taxonomy and phylogeny of the Erysiphe lonicerae complex (Helotiales, Erysiphaceae) on Lonicera spp. Bradshaw M, Braun U, Götz M, Takamatsu S Fungal Syst Evol 26-Nov-2020
PMCID:PMC8165964
doi:10.3114/fuse.2021.07.03
PMID:34124617
Characterization of 20 complete plastomes from the tribe Laureae (Lauraceae) and distribution of small inversions Jo S, Kim YK, Cheon SH, Fan Q, Kim KJ PLoS One 01-Nov-2019
PMCID:PMC6824564
doi:10.1371/journal.pone.0224622
PMID:31675370
Insect Antifeeding Substances in<i>Parabenzoin praecox</i>and<i>Piper futokadzura</i> Kuniaki Matsui, Kojiro Wada, Katsura Munakata Oxford University Press (OUP) 13-Apr-2016
doi:10.1080/00021369.1976.10862166
Aporphine alkaloids from Parabenzoin praecox (Sieb. et Zucc.) Nakai. MUTSUO KOZUKA, AKIRA INADA, TAKAO KONOSHIMA, TOKUNOSUKE SAWADA Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.32.5055
Sesquiterpenoids of Pardbenzoin praecox Keiko Ohara, Yoshimoto Ohta, Yoshio Hirose Oxford University Press (OUP) 20-Jul-2006
doi:10.1246/BCSJ.46.641
A chalcone derivative from the bark of Lindera umbellata Hiroko Shimomura, Yutaka Sashida, Yoshihiro Mimaki, Motomu Oohara, Yasuomi Fukai Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(88)83049-8
A lignan from Lindera praecox Kazuhiko Ichino, Hitoshi Tanaka, Kazuo Ito Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(88)80479-5
Phenolic glucosides from Parabenzoin praecox Hiroko Shimomura, Yutaka Sashida, Motomu Oohara, Hiroko Tenma Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(88)83166-2

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
(S)-Nandigerine 422682 Click to see COC1=C(C=CC2=C1C3=C4C(C2)NCCC4=CC5=C3OCO5)O 311.30 unknown https://doi.org/10.1248/CPB.32.5055
1,2,11-trimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-10-ol 12314672 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)O)OC)OC)OC 341.40 unknown https://doi.org/10.1248/CPB.32.5055
Hernangerine 497804 Click to see COC1=C(C=CC2=C1C3=C4C(C2)NCCC4=CC5=C3OCO5)O 311.30 unknown https://doi.org/10.1248/CPB.32.5055
N-Methylhernagine 26212851 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)O)OC)OC)OC 341.40 unknown https://doi.org/10.1248/CPB.32.5055
> Lignans, neolignans and related compounds / Furanoid lignans
(-)-Epieudesmin 7299790 Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC)OC)OC 386.40 unknown https://doi.org/10.1016/0031-9422(88)80479-5
(+)-Epieudesmine 7000209 Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC)OC)OC 386.40 unknown https://doi.org/10.1016/0031-9422(88)80479-5
https://doi.org/10.1080/00021369.1976.10862166
(+)-Eudesmin 73117 Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC)OC)OC 386.40 unknown https://doi.org/10.1016/0031-9422(88)80479-5
https://doi.org/10.1080/00021369.1976.10862166
(3aS,6aS)-3,6-bis(3,4-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan 137795855 Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC)OC)OC 386.40 unknown https://doi.org/10.1016/0031-9422(88)80479-5
2-Methoxy-4-[6-(3,4,5-trimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]phenol 14134108 Click to see COC1=CC(=CC(=C1OC)OC)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC 402.40 unknown https://doi.org/10.1016/0031-9422(88)80479-5
4-[(3S,3aR,6R,6aR)-6-(3,4,5-trimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxyphenol 14134109 Click to see COC1=CC(=CC(=C1OC)OC)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC 402.40 unknown https://doi.org/10.1016/0031-9422(88)80479-5
5-[(3aR,6R,6aR)-3-(1,3-benzodioxol-5-yl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-1,3-benzodioxole 102004873 Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 354.40 unknown https://doi.org/10.1016/0031-9422(88)80479-5
Asarinin 101612 Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 354.40 unknown https://doi.org/10.1016/0031-9422(88)80479-5
CID 233333 233333 Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 354.40 unknown https://doi.org/10.1016/0031-9422(88)80479-5
Episesamin 5204 Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 354.40 unknown https://doi.org/10.1016/0031-9422(88)80479-5
Eudesmin 234823 Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC)OC)OC 386.40 unknown https://doi.org/10.1016/0031-9422(88)80479-5
Phillygenol; Epipinoresinol methyl ether; (+)-Phillygenin 4166098 Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)OC 372.40 unknown https://doi.org/10.1016/0031-9422(88)80479-5
Sylvatesmin 3083590 Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)OC 372.40 unknown https://doi.org/10.1016/0031-9422(88)80479-5
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
2-[(1S,2S,3R,6R,7S)-6,8-dimethyl-3-tricyclo[4.4.0.02,7]dec-8-enyl]propan-2-ol 163088948 Click to see CC1=CCC2C3C1C2(CCC3C(C)(C)O)C 220.35 unknown https://doi.org/10.1246/BCSJ.46.641
alpha-Copaen-11-ol 521030 Click to see CC1=CCC2C3C1C2(CCC3C(C)(C)O)C 220.35 unknown https://doi.org/10.1246/BCSJ.46.641
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
[5-Ethenyl-2-(2-hydroxypropan-2-yl)-5-methyl-4-prop-1-en-2-ylcyclohexyl] acetate 14138885 Click to see CC(=C)C1CC(C(CC1(C)C=C)OC(=O)C)C(C)(C)O 280.40 unknown https://doi.org/10.1246/BCSJ.46.641
8-Acetoxyelemol 14138886 Click to see CC(=C)C1CC(C(CC1(C)C=C)OC(=O)C)C(C)(C)O 280.40 unknown https://doi.org/10.1246/BCSJ.46.641
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
2-(Hydroxymethyl)-6-(3,4,5-trimethoxyphenoxy)oxane-3,4,5-triol 13922637 Click to see COC1=CC(=CC(=C1OC)OC)OC2C(C(C(C(O2)CO)O)O)O 346.33 unknown https://doi.org/10.1016/0031-9422(88)83049-8
https://doi.org/10.1016/0031-9422(88)83166-2
Koaburaside monomethyl ether 636454 Click to see COC1=CC(=CC(=C1OC)OC)OC2C(C(C(C(O2)CO)O)O)O 346.33 unknown https://doi.org/10.1016/0031-9422(88)83049-8
https://doi.org/10.1016/0031-9422(88)83166-2
Thalictoside 21629843 Click to see C1=CC(=CC=C1CC[N+](=O)[O-])OC2C(C(C(C(O2)CO)O)O)O 329.30 unknown https://doi.org/10.1016/0031-9422(88)83166-2

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