Lysidice rhodostegia - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

Lysidice rhodostegia - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

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Internal ID UUID643fd67eb8b1d630607868
Scientific name Lysidice rhodostegia
Authority Hance
First published in J. Bot.5: 299 (1867)

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Synonyms Top

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Common names Top

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Language Common/alternative name
Vietnamese mí (thực vật)
Chinese 仪花
Chinese 铁罗伞
Chinese 单刀根
Chinese 龙眼参
Chinese 儀花

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Varieties (abbr. var.) 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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • East Tropical Africa
      • Tanzania
      • Uganda
    • West Tropical Africa
      • Sierra Leone
  • Asia-tropical
    • Indian Subcontinent
      • Sri Lanka
    • Indo-China
      • Myanmar
      • Vietnam

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000169560
Tropicos 13047683
KEW urn:lsid:ipni.org:names:505290-1
The Plant List ild-1586
Open Tree Of Life 692769
NCBI Taxonomy 162836
IPNI 505290-1
iNaturalist 747002
GBIF 5354459
EOL 416354
USDA GRIN 23005

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
The complete plastid genome sequence of Lysidice brevicalyx (Fabaceae: Detarioideae), an arbor species endemic to China Li JX, Meng Y, Nie ZL, Tu TY Mitochondrial DNA B Resour 21-Sep-2023
PMCID:PMC10515688
doi:10.1080/23802359.2023.2259041
PMID:37746035
Screening for broad-spectrum antimicrobial endophytes from Rosa roxburghii and multi-omic analyses of biosynthetic capacity Zhang H, Yang MF, Zhang Q, Yan B, Jiang YL Front Plant Sci 16-Nov-2022
PMCID:PMC9709285
doi:10.3389/fpls.2022.1060478
PMID:36466255
Sulfur-Containing Compounds from Endophytic Fungi: Sources, Structures and Bioactivities Fan Y, Ma Z, Zhang Y, Wang Y, Ding Y, Wang C, Cao S J Fungi (Basel) 13-Jun-2022
PMCID:PMC9224594
doi:10.3390/jof8060628
PMID:35736111
Flavanols from Nature: A Phytochemistry and Biological Activity Review Luo Y, Jian Y, Liu Y, Jiang S, Muhammad D, Wang W Molecules 22-Jan-2022
PMCID:PMC8838462
doi:10.3390/molecules27030719
PMID:35163984
Spirocyclic derivatives as antioxidants: a review Acosta-Quiroga K, Rojas-Peña C, Nerio LS, Gutiérrez M, Polo-Cuadrado E RSC Adv 21-Jun-2021
PMCID:PMC9034179
doi:10.1039/d1ra01170g
PMID:35480788
Current State and Future Directions of Genetics and Genomics of Endophytic Fungi for Bioprospecting Efforts Sagita R, Quax WJ, Haslinger K Front Bioeng Biotechnol 15-Mar-2021
PMCID:PMC8005728
doi:10.3389/fbioe.2021.649906
PMID:33791289
Genome mining combined metabolic shunting and OSMAC strategy of an endophytic fungus leads to the production of diverse natural products Wei Q, Bai J, Yan D, Bao X, Li W, Liu B, Zhang D, Qi X, Yu D, Hu Y Acta Pharm Sin B 05-Aug-2020
PMCID:PMC7893140
doi:10.1016/j.apsb.2020.07.020
PMID:33643832
Pollution Assessment Based on Element Concentration of Tree Leaves and Topsoil in Ayutthaya Province, Thailand Molnár VÉ, Simon E, Ninsawat S, Tóthmérész B, Szabó S Int J Environ Res Public Health 17-Jul-2020
PMCID:PMC7400151
doi:10.3390/ijerph17145165
PMID:32708947
Nutrient contents predict the bamboo‐leaf‐based diet of Assamese macaques living in limestone forests of southwest Guangxi, China Li Y, Ma G, Zhou Q, Li Y, Huang Z Ecol Evol 28-Apr-2020
PMCID:PMC7319238
doi:10.1002/ece3.6297
PMID:32607175
Structural Diversity and Biological Activities of Novel Secondary Metabolites from Endophytes Gao H, Li G, Lou HX Molecules 13-Mar-2018
PMCID:PMC6017594
doi:10.3390/molecules23030646
PMID:29534010
Structural Diversity and Biological Activities of the Cyclodipeptides from Fungi Wang X, Li Y, Zhang X, Lai D, Zhou L Molecules 23-Nov-2017
PMCID:PMC6149763
doi:10.3390/molecules22122026
PMID:29168781
Phloroglucinols with Antioxidant Activities Isolated from Lysidice rhodostegia Wu XF, Li L, Li Y, Lv HN, Liu YB, Hu YC Molecules 23-May-2017
PMCID:PMC6152794
doi:10.3390/molecules22060855
PMID:28545244
The Floras of Southern and Tropical Southeastern Yunnan Have Been Shaped by Divergent Geological Histories Hua Z PLoS One 28-May-2013
PMCID:PMC3665894
doi:10.1371/journal.pone.0064213
PMID:23724036
Lysidicins F-H, three new phloroglucinols from Lysidice rhodostegia. Wu XF, Hu YC, Yu SS, Jiang N, Ma J, Tan RX, Li Y, Lv HN, Liu J, Ma SG Org Lett 21-May-2010
doi:10.1021/OL100735F
PMID:20420380
Resveratrol/phloroglucinol glycosides from the roots of Lysidice rhodostegia. Gao S, Liu J, Fu GM, Hu YC, Yu SS, Fan LH, Yu DQ, Qu J Planta Med 01-Feb-2007
doi:10.1055/S-2006-951770
PMID:17415877

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 / Butyrophenones
1-[4,6-dihydroxy-2-[[(2R,3'S)-4,4',6,6'-tetrahydroxy-7,7'-bis(3-methylbutanoyl)-2,2'-spirobi[3H-1-benzofuran]-3'-yl]methyl]-1-benzofuran-5-yl]-3-methylbutan-1-one 162901509 Click to see CC(C)CC(=O)C1=C(C2=C(C=C1O)OC(=C2)CC3C4=C(C(=C(C=C4O)O)C(=O)CC(C)C)OC35CC6=C(O5)C(=C(C=C6O)O)C(=O)CC(C)C)O 702.70 unknown https://doi.org/10.1021/OL060514O
1-[4,6-dihydroxy-2-[[4,4',6,6'-tetrahydroxy-7,7'-bis(3-methylbutanoyl)-2,2'-spirobi[3H-1-benzofuran]-3'-yl]methyl]-1-benzofuran-5-yl]-3-methylbutan-1-one 162901508 Click to see CC(C)CC(=O)C1=C(C2=C(C=C1O)OC(=C2)CC3C4=C(C(=C(C=C4O)O)C(=O)CC(C)C)OC35CC6=C(O5)C(=C(C=C6O)O)C(=O)CC(C)C)O 702.70 unknown https://doi.org/10.1021/OL060514O
> Lignans, neolignans and related compounds
1-[3-[[6,8-dihydroxy-5-(3-methylbutanoyl)-1-[2,4,6-trihydroxy-3-(3-methylbutanoyl)phenyl]-2,8b-dihydro-1H-furo[2,3-b][1]benzofuran-3a-yl]methyl]-2,4,6-trihydroxyphenyl]-3-methylbutan-1-one 75220760 Click to see CC(C)CC(=O)C1=C(C=C(C(=C1O)CC23C(C(CO2)C4=C(C(=C(C=C4O)O)C(=O)CC(C)C)O)C5=C(O3)C(=C(C=C5O)O)C(=O)CC(C)C)O)O 708.70 unknown https://doi.org/10.1021/OL100735F
Lysidicin G 46849043 Click to see CC(C)CC(=O)C1=C(C=C(C(=C1O)CC23C(C(CO2)C4=C(C(=C(C=C4O)O)C(=O)CC(C)C)O)C5=C(O3)C(=C(C=C5O)O)C(=O)CC(C)C)O)O 708.70 unknown https://doi.org/10.1021/OL100735F
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
1-[2,4-dihydroxy-3-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-6-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-3-methylbutan-1-one 102033038 Click to see CC(C)CC(=O)C1=C(C=C(C(=C1O)C2C(C(C(C(O2)CO)O)O)O)O)OC3C(C(C(C(O3)CO)O)O)O 534.50 unknown https://doi.org/10.1055/S-2006-951770
1-[2,4-Dihydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-3-methylbutan-1-one 162940815 Click to see CC(C)CC(=O)C1=C(C=C(C(=C1O)C2C(C(C(C(O2)CO)O)O)O)O)OC3C(C(C(C(O3)CO)O)O)O 534.50 unknown https://doi.org/10.1055/S-2006-951770
1-[2,6-dihydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxyphenyl]-3-methylbutan-1-one 129863221 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C(C(=C3)O)C(=O)CC(C)C)O)O)O)O)O)O)O 518.50 unknown https://doi.org/10.1055/S-2006-951770
1-[2,6-Dihydroxy-4-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxyphenyl]-3-methylbutan-1-one 162889994 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C(C(=C3)O)C(=O)CC(C)C)O)O)O)O)O)O)O 518.50 unknown https://doi.org/10.1055/S-2006-951770
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
1-[(2R,3aR,8bR)-4',6,6',8-tetrahydroxy-5-(3-methylbutanoyl)-3a-[[2,4,6-trihydroxy-3-(3-methylbutanoyl)phenyl]methyl]spiro[1,8b-dihydrofuro[2,3-b][1]benzofuran-2,2'-3H-1-benzofuran]-5'-yl]-3-methylbutan-1-one 57325949 Click to see CC(C)CC(=O)C1=C(C2=C(C=C1O)OC3(C2)CC4C5=C(C(=C(C=C5O)O)C(=O)CC(C)C)OC4(O3)CC6=C(C(=C(C=C6O)O)C(=O)CC(C)C)O)O 720.80 unknown https://doi.org/10.1021/OL060514O
1-[3-[[(1R,3aS,8bR)-1,6,8-trihydroxy-5-(3-methylbutanoyl)-2,8b-dihydro-1H-furo[2,3-b][1]benzofuran-3a-yl]methyl]-2,4,6-trihydroxyphenyl]-3-methylbutan-1-one 46849042 Click to see CC(C)CC(=O)C1=C(C=C(C(=C1O)CC23C(C(CO2)O)C4=C(O3)C(=C(C=C4O)O)C(=O)CC(C)C)O)O 516.50 unknown https://doi.org/10.1021/OL100735F
1-[3-[[(1S,2R,3aR,8bR)-1,6,8-trihydroxy-2-(hydroxymethyl)-5-(3-methylbutanoyl)-2,8b-dihydro-1H-furo[2,3-b][1]benzofuran-3a-yl]methyl]-2,4,6-trihydroxyphenyl]-3-methylbutan-1-one 46849044 Click to see CC(C)CC(=O)C1=C(C=C(C(=C1O)CC23C(C(C(O2)CO)O)C4=C(O3)C(=C(C=C4O)O)C(=O)CC(C)C)O)O 546.60 unknown https://doi.org/10.1021/OL100735F
3-methyl-1-[2,4,6-trihydroxy-3-[[1,6,8-trihydroxy-2-(hydroxymethyl)-5-(3-methylbutanoyl)-2,8b-dihydro-1H-furo[2,3-b][1]benzofuran-3a-yl]methyl]phenyl]butan-1-one 75220761 Click to see CC(C)CC(=O)C1=C(C=C(C(=C1O)CC23C(C(C(O2)CO)O)C4=C(O3)C(=C(C=C4O)O)C(=O)CC(C)C)O)O 546.60 unknown https://doi.org/10.1021/OL100735F
3-methyl-1-[2,4,6-trihydroxy-3-[[1,6,8-trihydroxy-5-(3-methylbutanoyl)-2,8b-dihydro-1H-furo[2,3-b][1]benzofuran-3a-yl]methyl]phenyl]butan-1-one 75220759 Click to see CC(C)CC(=O)C1=C(C=C(C(=C1O)CC23C(C(CO2)O)C4=C(O3)C(=C(C=C4O)O)C(=O)CC(C)C)O)O 516.50 unknown https://doi.org/10.1021/OL100735F
3-methyl-1-[4',6,6',8-tetrahydroxy-5-(3-methylbutanoyl)-3a-[[2,4,6-trihydroxy-3-(3-methylbutanoyl)phenyl]methyl]spiro[1,8b-dihydrofuro[2,3-b][1]benzofuran-2,2'-3H-1-benzofuran]-5'-yl]butan-1-one 76510885 Click to see CC(C)CC(=O)C1=C(C2=C(C=C1O)OC3(C2)CC4C5=C(C(=C(C=C5O)O)C(=O)CC(C)C)OC4(O3)CC6=C(C(=C(C=C6O)O)C(=O)CC(C)C)O)O 720.80 unknown https://doi.org/10.1021/OL060514O
Lysidicin C 102513811 Click to see CC(C)CC(=O)C1=C(C2=C(C=C1O)OC(=C2)CC3=C(OC4=C3C(=CC(=C4C(=O)CC(C)C)O)O)CC5=C(C(=C(C=C5O)O)C(=O)CC(C)C)O)O 702.70 unknown https://doi.org/10.1021/OL060514O
> Phenylpropanoids and polyketides / Stilbenes / Stilbene glycosides
2-[4,5-Dihydroxy-2-[3-hydroxy-5-[2-(4-hydroxyphenyl)ethenyl]phenoxy]oxan-3-yl]oxy-6-methyloxane-3,4,5-triol 75115272 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3=CC(=CC(=C3)O)C=CC4=CC=C(C=C4)O)O)O)O)O)O 506.50 unknown https://doi.org/10.1055/S-2006-951770
lysidiside E 45481961 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3=CC(=CC(=C3)O)C=CC4=CC=C(C=C4)O)O)O)O)O)O 506.50 unknown https://doi.org/10.1055/S-2006-951770
Lysidiside F 101846309 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3=CC(=CC(=C3)O)C=CC4=CC=C(C=C4)O)O)O)O)O)O 506.50 unknown https://doi.org/10.1055/S-2006-951770

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