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Morina chinensis

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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 UUID64405422d0ed0563496999
Scientific name Morina chinensis
Authority Y.Y.Pai
First published in Repert. Spec. Nov. Regni Veg. 44: 122 (1938)

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Chinese 圆萼刺参
Chinese 蘑苓草

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 North-central
      • China South-central
      • Inner Mongolia
      • Qinghai
      • Tibet

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001225482
Tropicos 50044187
KEW urn:lsid:ipni.org:names:319559-1
The Plant List tro-50044187
Open Tree Of Life 68249
NCBI Taxonomy 180071
IPNI 319559-1

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
Prediction of potential distributions of Morina kokonorica and Morina chinensis in China Yuan Q, Zhang J, Yao Z, Zhou Q, Liu P, Liu W, Liu H Ecol Evol 10-Mar-2024
PMCID:PMC10925826
doi:10.1002/ece3.11121
PMID:38469051
Physiological, biochemical and phytohormone responses of Elymus nutans to α-pinene-induced allelopathy Chen M, Qiao Y, Quan X, Shi H, Duan Z PeerJ 29-Sep-2022
PMCID:PMC9527024
doi:10.7717/peerj.14100
PMID:36196396
Long-term warming results in species-specific shifts in seed mass in alpine communities Zhang C, Ma Z, Zhou H, Zhao X PeerJ 31-Jul-2019
PMCID:PMC6679644
doi:10.7717/peerj.7416
PMID:31396451
Trait‐abundance relation in response to nutrient addition in a Tibetan alpine meadow: The importance of species trade‐off in resource conservation and acquisition Liu H, Li Y, Ren F, Lin L, Zhu W, He J, Niu K Ecol Evol 03-Nov-2017
PMCID:PMC5743641
doi:10.1002/ece3.3439
PMID:29299239
Control of Floret Symmetry by RAY3, SvDIV1B, and SvRAD in the Capitulum of Senecio vulgaris Garcês HM, Spencer VM, Kim M Plant Physiol 12-May-2016
PMCID:PMC4936572
doi:10.1104/pp.16.00395
PMID:27208229
Molecular Phylogeny and Biogeographic Diversification of Linnaeoideae (Caprifoliaceae s. l.) Disjunctly Distributed in Eurasia, North America and Mexico Wang HF, Landrein S, Dong WP, Nie ZL, Kondo K, Funamoto T, Wen J, Zhou SL PLoS One 10-Mar-2015
PMCID:PMC4355296
doi:10.1371/journal.pone.0116485
PMID:25756215
Transmissive Olefination Route to Putative “Morinol I” Lignans Yao L, Pitta B, Ravikumar PC, Purzycki M, Fleming FF J Org Chem 20-Mar-2012
PMCID:PMC3331789
doi:10.1021/jo3001723
PMID:22432777
Morinins L-P, Five New Phenylpropanol Derivatives from Morina chinensis. Bao-Ning SU, Yoshihisa TAKAISHI Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.47.1569
Alkenenitrile Transmissive Olefination: Synthesis of the Putative Lignan "Morinol I" Fleming FF, Liu W, Yao L, Pitta B, Purzycki M, Ravikumar PC European J Org Chem 28-Oct-2011
PMCID:PMC3336159
doi:10.1002/ejoc.201101235
PMID:22545004
Morinols A and B, Two Novel Tetrahydropyran Sesquineolignans with a New Carbon Skeleton from <i>Morina chinensis</i> Bao-Ning Su, Yoshihisa Takaishi Oxford University Press (OUP) 01-Dec-2003
doi:10.1246/CL.1999.1315
Morinols A-L, twelve novel sesquineolignans and neolignans with a new carbon skeleton from morina chinensis Bao-Ning Su, Yoshihisa Takaishi, Takenori Kusumi Elsevier BV 04-Mar-2003
doi:10.1016/S0040-4020(99)00933-3
Phenylpropanol derivatives from morina chinensis. Su BN, Takaishi Y, Duan HQ, Chen B J Nat Prod 01-Oct-1999
doi:10.1021/NP990091H
PMID:10543893
Morinins H-K, four novel phenylpropanol ester lipid metabolites from morina chinensis. Su BN, Takaishi Y J Nat Prod 01-Sep-1999
doi:10.1021/NP990145N
PMID:10514326

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
(E,2Z)-5-(3,4-dimethoxyphenyl)-2-[(3,4-dimethoxyphenyl)methylidene]pent-4-en-1-ol 57380335 Click to see COC1=C(C=C(C=C1)C=CCC(=CC2=CC(=C(C=C2)OC)OC)CO)OC 370.40 unknown https://doi.org/10.1016/S0040-4020(99)00933-3
[(E)-3-(3,4-dimethoxyphenyl)prop-2-enyl] (Z)-2-(3-methylbutanoyloxymethyl)but-2-enoate 10595689 Click to see CC=C(COC(=O)CC(C)C)C(=O)OCC=CC1=CC(=C(C=C1)OC)OC 376.40 unknown https://doi.org/10.1248/CPB.47.1569
[(E)-3-(3,4-dimethoxyphenyl)prop-2-enyl] (Z)-2-(hydroxymethyl)but-2-enoate 10708762 Click to see CC=C(CO)C(=O)OCC=CC1=CC(=C(C=C1)OC)OC 292.33 unknown https://doi.org/10.1021/NP990145N
[(E)-3-(3,4-dimethoxyphenyl)prop-2-enyl] (Z)-2-[[(Z)-2-methylbut-2-enoyl]oxymethyl]but-2-enoate 10339381 Click to see CC=C(C)C(=O)OCC(=CC)C(=O)OCC=CC1=CC(=C(C=C1)OC)OC 374.40 unknown https://doi.org/10.1248/CPB.47.1569
[(E)-3-(3,4-dimethoxyphenyl)prop-2-enyl] (Z)-2-methyl-4-[(Z)-2-methylbut-2-enoyl]oxybut-2-enoate 10619399 Click to see CC=C(C)C(=O)OCC=C(C)C(=O)OCC=CC1=CC(=C(C=C1)OC)OC 374.40 unknown https://doi.org/10.1248/CPB.47.1569
[(E)-3-(3,4-dimethoxyphenyl)prop-2-enyl] (Z)-2-methylbut-2-enoate 10850064 Click to see CC=C(C)C(=O)OCC=CC1=CC(=C(C=C1)OC)OC 276.33 unknown https://doi.org/10.1021/NP990145N
1,2-dimethoxy-4-[(1R)-1-methoxyprop-2-enyl]benzene 162908621 Click to see COC1=C(C=C(C=C1)C(C=C)OC)OC 208.25 unknown https://doi.org/10.1021/NP990091H
> Benzenoids / Phenol ethers / Anisoles
(2E)-3-(4-methoxyphenyl)prop-2-en-1-yl (2Z)-2-methylbut-2-enoate 643822 Click to see CC=C(C)C(=O)OCC=CC1=CC=C(C=C1)OC 246.30 unknown https://doi.org/10.1021/NP990145N
[(E)-2-[(E)-3-(4-methoxyphenyl)prop-2-enoxy]carbonylbut-2-enyl] (Z)-octadec-9-enoate 100948408 Click to see CCCCCCCCC=CCCCCCCCC(=O)OCC(=CC)C(=O)OCC=CC1=CC=C(C=C1)OC 526.70 unknown https://doi.org/10.1021/NP990145N
[(E)-2-[(E)-3-(4-methoxyphenyl)prop-2-enoxy]carbonylbut-2-enyl] hexadecanoate 100948409 Click to see CCCCCCCCCCCCCCCC(=O)OCC(=CC)C(=O)OCC=CC1=CC=C(C=C1)OC 500.70 unknown https://doi.org/10.1021/NP990145N
[(E)-3-(4-methoxyphenyl)prop-2-enyl] (Z)-2-(3-methylbut-2-enoyloxymethyl)but-2-enoate 10807400 Click to see CC=C(COC(=O)C=C(C)C)C(=O)OCC=CC1=CC=C(C=C1)OC 344.40 unknown https://doi.org/10.1021/NP990145N
[(E)-3-(4-methoxyphenyl)prop-2-enyl] (Z)-2-[[(Z)-2-methylbut-2-enoyl]oxymethyl]but-2-enoate 10066093 Click to see CC=C(C)C(=O)OCC(=CC)C(=O)OCC=CC1=CC=C(C=C1)OC 344.40 unknown https://doi.org/10.1021/NP990145N
[(E)-3-(4-methoxyphenyl)prop-2-enyl] (Z)-2-methyl-4-(3-methylbutanoyloxy)but-2-enoate 10712594 Click to see CC(C)CC(=O)OCC=C(C)C(=O)OCC=CC1=CC=C(C=C1)OC 346.40 unknown https://doi.org/10.1248/CPB.47.1569
[(E)-3-(4-methoxyphenyl)prop-2-enyl] (Z)-2-methyl-4-[(Z)-2-methylbut-2-enoyl]oxybut-2-enoate 10617424 Click to see CC=C(C)C(=O)OCC=C(C)C(=O)OCC=CC1=CC=C(C=C1)OC 344.40 unknown https://doi.org/10.1021/NP990145N
[(Z)-2-[(E)-3-(4-methoxyphenyl)prop-2-enoxy]carbonylbut-2-enyl] (Z)-octadec-9-enoate 10506307 Click to see CCCCCCCCC=CCCCCCCCC(=O)OCC(=CC)C(=O)OCC=CC1=CC=C(C=C1)OC 526.70 unknown https://doi.org/10.1021/NP990145N
[(Z)-2-[(E)-3-(4-methoxyphenyl)prop-2-enoxy]carbonylbut-2-enyl] hexadecanoate 11799567 Click to see CCCCCCCCCCCCCCCC(=O)OCC(=CC)C(=O)OCC=CC1=CC=C(C=C1)OC 500.70 unknown https://doi.org/10.1021/NP990145N
> Lignans, neolignans and related compounds / Furanoid lignans
4-[(3aS,6aR)-6-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxyphenol 137705081 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 358.40 unknown https://doi.org/10.1016/S0040-4020(99)00933-3
Pinoresinol 73399 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 358.40 unknown https://doi.org/10.1016/S0040-4020(99)00933-3
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
Lariciresinol 332427 Click to see COC1=C(C=CC(=C1)CC2COC(C2CO)C3=CC(=C(C=C3)O)OC)O 360.40 unknown https://doi.org/10.1016/S0040-4020(99)00933-3
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
[(E)-2-[(E)-3-(4-methoxyphenyl)prop-2-enoxy]carbonylbut-2-enyl] (9Z,12Z,15Z)-octadeca-9,12,15-trienoate 100948406 Click to see CCC=CCC=CCC=CCCCCCCCC(=O)OCC(=CC)C(=O)OCC=CC1=CC=C(C=C1)OC 522.70 unknown https://doi.org/10.1021/NP990145N
[(E)-2-[(E)-3-(4-methoxyphenyl)prop-2-enoxy]carbonylbut-2-enyl] (9Z,12Z)-octadeca-9,12-dienoate 100948407 Click to see CCCCCC=CCC=CCCCCCCCC(=O)OCC(=CC)C(=O)OCC=CC1=CC=C(C=C1)OC 524.70 unknown https://doi.org/10.1021/NP990145N
[(Z)-2-[(E)-3-(4-methoxyphenyl)prop-2-enoxy]carbonylbut-2-enyl] (9Z,12Z)-octadeca-9,12-dienoate 10554079 Click to see CCCCCC=CCC=CCCCCCCCC(=O)OCC(=CC)C(=O)OCC=CC1=CC=C(C=C1)OC 524.70 unknown https://doi.org/10.1021/NP990145N
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
[(Z)-2-[(E)-3-(4-methoxyphenyl)prop-2-enoxy]carbonylbut-2-enyl] (Z)-2-[[(Z)-2-methylbut-2-enoyl]oxymethyl]but-2-enoate 10694491 Click to see CC=C(C)C(=O)OCC(=CC)C(=O)OCC(=CC)C(=O)OCC=CC1=CC=C(C=C1)OC 442.50 unknown https://doi.org/10.1248/CPB.47.1569
> Phenylpropanoids and polyketides / Cinnamaldehydes
2-Propenal, 3-(4-methoxyphenyl)- 230995 Click to see COC1=CC=C(C=C1)C=CC=O 162.18 unknown https://doi.org/10.1248/CPB.47.1569
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
Morinol A 10099435 Click to see COC1=C(C=C(C=C1)C=CCC2CC(COC2C3=CC(=C(C=C3)OC)OC)C(C4=CC(=C(C=C4)OC)OC)O)OC 564.70 unknown https://doi.org/10.1016/S0040-4020(99)00933-3
https://doi.org/10.1246/CL.1999.1315
Morinol B 10008077 Click to see COC1=C(C=C(C=C1)C=CCC2CC(COC2C3=CC(=C(C=C3)OC)OC)C(C4=CC(=C(C=C4)OC)OC)O)OC 564.70 unknown https://doi.org/10.1016/S0040-4020(99)00933-3
https://doi.org/10.1246/CL.1999.1315

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