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Syneilesis aconitifolia

Syneilesis aconitifolia - 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 UUID643fc6ffb361d245208751
Scientific name Syneilesis aconitifolia
Authority (Bunge) Maxim.
First published in Mém. Acad. Imp. Sci. St.-Pétersbourg Divers Savans 9: 165 (1859)

Description Top

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Synonyms Top

Scientific name Authority First published in
Cacalia aconitifolia Bunge Enum. Pl. China Bor. : 37 (1833)
Senecio aconitifolius Turcz. Bull. Soc. Imp. Naturalistes Moscou 7: 155 (1837)

Common names Top

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Language Common/alternative name
Chinese 兔儿伞
Chinese 菟儿伞
Chinese 兔兒傘

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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No forms added yet.

Germination/Propagation Top

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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.
sets very little viable seed (good seed is fat and substantial and does not yield pressure)

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • China Southeast
      • Inner Mongolia
      • Manchuria
    • Eastern Asia
      • Japan
      • Korea
    • Russian Far East
      • Amur
      • Khabarovsk
      • Primorye

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000010912
Tropicos 2732458
KEW urn:lsid:ipni.org:names:252028-1
The Plant List gcc-110573
Missouri Botanical Garden 277676
Open Tree Of Life 567894
NCBI Taxonomy 186972
IPNI 252028-1
iNaturalist 709804
GBIF 3092759
EOL 6276212
USDA GRIN 460192

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
Research progress of Chinese herbal medicine compounds and their bioactivities: Fruitful 2020 Gu X, Hao D, Xiao P Chin Herb Med 17-Mar-2022
PMCID:PMC9476823
doi:10.1016/j.chmed.2022.03.004
PMID:36117669
Strengthening Structures in the Petiole–Lamina Junction of Peltate Leaves Wunnenberg J, Rjosk A, Neinhuis C, Lautenschläger T Biomimetics (Basel) 02-Apr-2021
PMCID:PMC8167582
doi:10.3390/biomimetics6020025
PMID:33918405
Wing loading, not terminal velocity, is the best parameter to predict capacity of diaspores for secondary wind dispersal Liang W, Liu Z, Liu M, Qin X, Baskin CC, Baskin JM, Xin Z, Wang Z, Su Z, Zhou Q J Exp Bot 03-Apr-2020
PMCID:PMC7475251
doi:10.1093/jxb/eraa170
PMID:32242240
Pyrrolizidine Alkaloids: Chemistry, Pharmacology, Toxicology and Food Safety Moreira R, Pereira DM, Valentão P, Andrade PB Int J Mol Sci 05-Jun-2018
PMCID:PMC6032134
doi:10.3390/ijms19061668
PMID:29874826
An integrated assessment of wild vegetable resources in Inner Mongolian Autonomous Region, China Wujisguleng W, Khasbagen K J Ethnobiol Ethnomed 06-Dec-2010
PMCID:PMC3009950
doi:10.1186/1746-4269-6-34
PMID:21134268
Terpenglucoside aus Syneilesis aconitifolia Ferdinand Bohlmann, Michael Grenz Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)86728-X
Search for naturally occurring substances to prevent the complications of diabetes. II. Inhibitory effect of coumarin and flavonoid derivatives on bovine lens aldose reductase and rabbit platelet aggregation. Okada Y, Miyauchi N, Suzuki K, Kobayashi T, Tsutsui C, Mayuzumi K, Nishibe S, Okuyama T Chem Pharm Bull (Tokyo) 01-Aug-1995
doi:10.1248/CPB.43.1385
PMID:7553983
Pyrrolizidine alkaloids from Syneilesis aconitifolia. Roeder E, Wiedenfeld H, Liu K, Kröger R Planta Med 01-Feb-1995
doi:10.1055/S-2006-958021
PMID:7701010

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
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
1,6-Cyclodecadiene, 1-methyl-5-methylene-8-(1-methylethyl)- 91104 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)86728-X
Germacrene D 5317570 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)86728-X
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
(4-Ethyl-7-hydroxy-6,7,14-trimethyl-3,8,17-trioxo-2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-en-5-yl) acetate 162872240 Click to see CCC1C(C(C(C(=O)OCC2=CCN(CCC(C2=O)OC1=O)C)(C)O)C)OC(=O)C 425.50 unknown https://doi.org/10.1055/S-2006-958021
[(1R,4S,5R,6R,7R,11Z)-4-ethyl-7-hydroxy-6,7,14-trimethyl-3,8,17-trioxo-2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-en-5-yl] acetate 162872241 Click to see CCC1C(C(C(C(=O)OCC2=CCN(CCC(C2=O)OC1=O)C)(C)O)C)OC(=O)C 425.50 unknown https://doi.org/10.1055/S-2006-958021
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown https://doi.org/10.1248/CPB.43.1385
https://doi.org/10.1016/S0031-9422(00)86728-X
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 51402807 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/S0031-9422(00)86728-X
Afzelin 5316673 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O 432.40 unknown https://doi.org/10.1016/S0031-9422(00)86728-X
Quercitrin 5280459 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown https://doi.org/10.1248/CPB.43.1385
https://doi.org/10.1016/S0031-9422(00)86728-X
> Phenylpropanoids and polyketides / Macrolides and analogues
(1R,4S,5R,6R,7R,11Z)-4-ethyl-5,7-dihydroxy-6,7,14-trimethyl-2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-ene-3,8,17-trione 162880731 Click to see CCC1C(C(C(C(=O)OCC2=CCN(CCC(C2=O)OC1=O)C)(C)O)C)O 383.40 unknown https://doi.org/10.1055/S-2006-958021
4-Ethyl-5,7-dihydroxy-6,7,14-trimethyl-2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-ene-3,8,17-trione 78410037 Click to see CCC1C(C(C(C(=O)OCC2=CCN(CCC(C2=O)OC1=O)C)(C)O)C)O 383.40 unknown https://doi.org/10.1055/S-2006-958021

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