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Lindera neesiana

Lindera neesiana - 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 UUID64404748238d9992480008
Scientific name Lindera neesiana
Authority (Wall. ex Nees) Kurz
First published in Prelim. Rep. Forest Pegu App. A. p. ciii.; App. B. 74, in clavi. 1875

Description Top

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Synonyms Top

Scientific name Authority First published in
Litsea fruticosa Gamble Pl. Wilson. 2: 77 (1914)
Tetranthera prunifolia Wall. ex Meisn. Prodr. 15(1): 241 (1864)
Aperula neesiana (Wall. ex Nees) Blume Mus. Bot. 1: 366 (1851)
Benzoin fruticosum (Hemsl.) Rehder J. Arnold Arbor. 1: 145. 1919
Benzoin neesianum Wall. ex Nees Pl. Asiat. Rar. (Wallich). ii. 63.
Calosmon neesianum (Wall. ex Nees) Kostel. Allg. Med.-Pharm. Fl. 2: 478 (1833)
Lindera fruticosa Hemsl. J. Linn. Soc., Bot. 26: 388 (1891)
Lindera fruticosa var. pomiensis H.P.Tsui Acta Phytotax. Sin. 16(4): 65 (1978)
Malapoenna neesiana (Wall. ex Nees) Kuntze Revis. Gen. Pl. 2: 571 (1891)
Lindera pomiensis (H.P.Tsui) H.P.Tsui Acta Bot. Yunnan. 10: 124 (1988)

Common names Top

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Language Common/alternative name
Spanish lindera fruticosa
German lindera fruticosa
Chinese 香叶子
Chinese 绿叶甘橿
Chinese 波密钓樟

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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Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001070756
Tropicos 17802298
KEW urn:lsid:ipni.org:names:465410-1
The Plant List tro-17802298
NCBI Taxonomy 2654225
IUCN Red List 147651751
IPNI 465411-1
GBIF 5685602
USDA GRIN 413264

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
Diversity, distribution, and sustainability of traditional medicinal plants in Kaski district, western Nepal Khakurel D, Uprety Y, Ahn G, Cha JY, Kim WY, Lee SH, Rajbhandary S Front Pharmacol 20-Dec-2022
PMCID:PMC9807671
doi:10.3389/fphar.2022.1076351
PMID:36605393
Ethnoveterinary use of plants and its implication for sustainable livestock management in Nepal Uprety Y, Karki S, Poudel RC, Kunwar RM Front Vet Sci 09-Sep-2022
PMCID:PMC9500146
doi:10.3389/fvets.2022.930533
PMID:36157185
Foods from the wild: Local knowledge, use pattern and distribution in Western Nepal Khakurel D, Uprety Y, Łuczaj Ł, Rajbhandary S PLoS One 21-Oct-2021
PMCID:PMC8530312
doi:10.1371/journal.pone.0258905
PMID:34673823
Nitric Oxide as a Target for Phytochemicals in Anti-Neuroinflammatory Prevention Therapy Subedi L, Gaire BP, Kim SY, Parveen A Int J Mol Sci 30-Apr-2021
PMCID:PMC8124914
doi:10.3390/ijms22094771
PMID:33946349
Therapeutic Potential of Lindera obtusiloba: Focus on Antioxidative and Pharmacological Properties Haque ME, Azam S, Balakrishnan R, Akther M, Kim IS Plants (Basel) 13-Dec-2020
PMCID:PMC7763160
doi:10.3390/plants9121765
PMID:33322185
Reducing Sugar, Total Phenolic Content, and Antioxidant Potential of Nepalese Plants Khatri D, Chhetri SB Biomed Res Int 15-Nov-2020
PMCID:PMC7683130
doi:10.1155/2020/7296859
PMID:33274222
Dataset of non-timber forest products use and impacts of recent climate change in the Upper Madi Watershed, Nepal Gurung LJ, Miller KK, Venn S, Bryan BA Data Brief 10-Oct-2020
PMCID:PMC7569287
doi:10.1016/j.dib.2020.106404
PMID:33102663
Phytochemicals against TNFα-Mediated Neuroinflammatory Diseases Subedi L, Lee SE, Madiha S, Gaire BP, Jin M, Yumnam S, Kim SY Int J Mol Sci 24-Jan-2020
PMCID:PMC7037901
doi:10.3390/ijms21030764
PMID:31991572
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
Traditional use and management of NTFPs in Kangchenjunga Landscape: implications for conservation and livelihoods Uprety Y, Poudel RC, Gurung J, Chettri N, Chaudhary RP J Ethnobiol Ethnomed 03-May-2016
PMCID:PMC4855762
doi:10.1186/s13002-016-0089-8
PMID:27142597
Scientific validation of medicinal plants used by Yakkha community of Chanuwa VDC, Dhankuta, Nepal Subba B, Srivastav C, Kandel RC Springerplus 24-Feb-2016
PMCID:PMC4766171
doi:10.1186/s40064-016-1821-5
PMID:27026852
Himalayan Aromatic Medicinal Plants: A Review of their Ethnopharmacology, Volatile Phytochemistry, and Biological Activities Joshi RK, Satyal P, Setzer WN Medicines (Basel) 19-Feb-2016
PMCID:PMC5456235
doi:10.3390/medicines3010006
PMID:28930116
Medicinal plants used by the Tamang community in the Makawanpur district of central Nepal Luitel DR, Rokaya MB, Timsina B, Münzbergová Z J Ethnobiol Ethnomed 10-Jan-2014
PMCID:PMC3904474
doi:10.1186/1746-4269-10-5
PMID:24410808
Volatiles of<i>Lindera neesiana</i>Benth. Leaf and Branch R. S. Singh, P. B. Kanjilal, M. G. Pathak, A. C. Ghosh Informa UK Limited 24-Apr-2012
doi:10.1080/10412905.1995.9700534
Quantitative 1H NMR: Development and Potential of an Analytical Method – an Update Pauli GF, Gödecke T, Jaki BU, Lankin DC J Nat Prod 06-Apr-2012
PMCID:PMC3384681
doi:10.1021/np200993k
PMID:22482996

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / O-methoxybenzoic acids and derivatives
Benzyl 2-hydroxy-6-methoxybenzoate 6430728 Click to see COC1=CC=CC(=C1C(=O)OCC2=CC=CC=C2)O 258.27 unknown https://doi.org/10.1021/NP060048B
> Benzenoids / Benzene and substituted derivatives / Benzophenones
(4-Methoxybenzo[d][1,3]dioxol-5-yl)(phenyl)methanone 11999967 Click to see COC1=C(C=CC2=C1OCO2)C(=O)C3=CC=CC=C3 256.25 unknown https://doi.org/10.1021/NP060048B
> Benzenoids / Benzene and substituted derivatives / Biphenyls and derivatives
3-Hydroxy-5-methoxybiphenyl 12000323 Click to see COC1=CC(=CC(=C1)O)C2=CC=CC=C2 200.23 unknown https://doi.org/10.1021/NP060048B
3,5-Dimethoxybiphenyl 11469945 Click to see COC1=CC(=CC(=C1)C2=CC=CC=C2)OC 214.26 unknown https://doi.org/10.1021/NP060048B
> Benzenoids / Phenol ethers / Anisoles
Elemicin 10248 Click to see COC1=CC(=CC(=C1OC)OC)CC=C 208.25 unknown https://doi.org/10.1080/10412905.1995.9700534
Estragole 8815 Click to see COC1=CC=C(C=C1)CC=C 148.20 unknown https://doi.org/10.1080/10412905.1995.9700534
> Benzenoids / Phenols / Methoxyphenols
Eugenol 3314 Click to see COC1=C(C=CC(=C1)CC=C)O 164.20 unknown https://doi.org/10.1080/10412905.1995.9700534
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Myristic Acid 11005 Click to see CCCCCCCCCCCCCC(=O)O 228.37 unknown https://doi.org/10.1023/B:CONC.0000018118.52743.A8
Oleic Acid 445639 Click to see CCCCCCCCC=CCCCCCCCC(=O)O 282.50 unknown https://doi.org/10.1023/B:CONC.0000018118.52743.A8
Palmitic Acid 985 Click to see CCCCCCCCCCCCCCCC(=O)O 256.42 unknown https://doi.org/10.1023/B:CONC.0000018118.52743.A8
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Capric Acid 2969 Click to see CCCCCCCCCC(=O)O 172.26 unknown https://doi.org/10.1023/B:CONC.0000018118.52743.A8
Lauric Acid 3893 Click to see CCCCCCCCCCCC(=O)O 200.32 unknown https://doi.org/10.1023/B:CONC.0000018118.52743.A8
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Linalool, (+/-)- 6549 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown https://doi.org/10.1080/10412905.1995.9700534
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1080/10412905.1995.9700534
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1080/10412905.1995.9700534
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1080/10412905.1995.9700534
Beta-Phellandrene 11142 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown https://doi.org/10.1080/10412905.1995.9700534
Terpinolene 11463 Click to see CC1=CCC(=C(C)C)CC1 136.23 unknown https://doi.org/10.1080/10412905.1995.9700534
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
beta-CARYOPHYLLENE OXIDE 1742210 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1080/10412905.1995.9700534
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1080/10412905.1995.9700534
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Disaccharides
(3S,6R,7R,8R,10S,13S,22R)-6,7,13,18,22-pentahydroxy-2,4,9,11,15-pentaoxatetracyclo[15.3.1.110,13.03,8]docosa-1(21),17,19-trien-16-one 163002771 Click to see C1C(C(C2C(O1)OC3=CC(=C(C=C3)O)C(=O)OCC4(COC(C4O)O2)O)O)O 400.30 unknown https://doi.org/10.1248/CPB.56.707
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
methyl 5-[(2R,3R,4R,5R)-4-[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-3,5-dihydroxyoxan-2-yl]oxy-2-hydroxybenzoate 163029887 Click to see COC(=O)C1=C(C=CC(=C1)OC2C(C(C(CO2)O)OC3C(C(CO3)(CO)O)O)O)O 432.40 unknown https://doi.org/10.1248/CPB.56.707
> Organoheterocyclic compounds / Benzodioxoles
(S)-(4-methoxy-1,3-benzodioxol-5-yl)-phenylmethanol 11565120 Click to see COC1=C(C=CC2=C1OCO2)C(C3=CC=CC=C3)O 258.27 unknown https://doi.org/10.1021/NP060048B
Myristicin 4276 Click to see COC1=CC(=CC2=C1OCO2)CC=C 192.21 unknown https://doi.org/10.1080/10412905.1995.9700534
Safrole 5144 Click to see C=CCC1=CC2=C(C=C1)OCO2 162.18 unknown https://doi.org/10.1080/10412905.1995.9700534
Zzautbbjbdohms-uhfffaoysa- 44631605 Click to see COC1=C(C=CC2=C1OCO2)C(C3=CC=CC=C3)O 258.27 unknown https://doi.org/10.1021/NP060048B
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
2,5,7-Trihydroxy-1-methoxy-4a,9a-dihydroxanthen-9-one 44583783 Click to see COC1=C(C=CC2C1C(=O)C3=C(O2)C(=CC(=C3)O)O)O 276.24 unknown https://doi.org/10.1021/NP060048B
2,5,7-Trihydroxy-1-methoxyxanthen-9-one 11579945 Click to see COC1=C(C=CC2=C1C(=O)C3=C(O2)C(=CC(=C3)O)O)O 274.22 unknown https://doi.org/10.1021/NP060048B
Euxanthone 5281631 Click to see C1=CC(=C2C(=C1)OC3=C(C2=O)C=C(C=C3)O)O 228.20 unknown https://doi.org/10.1021/NP060048B

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