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Forsythia giraldiana

Forsythia giraldiana - Unknown
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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 UUID64402cc95a76f832208055
Scientific name Forsythia giraldiana
Authority Lingelsh.
First published in Jahresber. Schles. Ges. Vaterl. Cult. 86(2b): 1 (1908 publ. 1909)

Description Top

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Synonyms Top

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Common names Top

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Language Common/alternative name
German giralds forsythie
Japanese ギラルディアナ
Chinese 秦连翘
Chinese 蚂蚁

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000832184
Tropicos 23000687
KEW urn:lsid:ipni.org:names:608890-1
The Plant List kew-369410
Open Tree Of Life 628749
NCBI Taxonomy 205689
NBN Atlas NBNSYS0200002199
IPNI 608890-1
iNaturalist 774195
GBIF 7325954
EPPO FOSGI
EOL 2892342
USDA GRIN 403681
CMAUP NPO19064

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
Ancient Herbal Formula Mahuang Lianqiao Chixiaodou Decoction Protects Acute and Acute-on-Chronic Liver Failure via Inhibiting von Willebrand Factor Signaling Lin J, Ling Q, Yan L, Chen B, Wang F, Qian Y, Gao Y, Wang Q, Wu H, Sun X, Shi Y, Kong X Cells 25-Oct-2022
PMCID:PMC9656135
doi:10.3390/cells11213368
PMID:36359765
The complete chloroplast genome of a new candidate cultivar, Sang Jae, of Abeliophyllum distichum Nakai (Oleaceae): initial step of A. distichum intraspecies variations atlas Min J, Kim Y, Xi H, Jang T, Kim G, Park J, Park JH Mitochondrial DNA B Resour 23-Oct-2019
PMCID:PMC7707604
doi:10.1080/23802359.2019.1679678
PMID:33366157
The complete chloroplast genome of a new candidate cultivar, Dae Ryun, of Abeliophyllum distichum Nakai (Oleaceae) Park J, Min J, Kim Y, Xi H, Kwon W, Jang T, Kim G, Park JH Mitochondrial DNA B Resour 23-Oct-2019
PMCID:PMC7707539
doi:10.1080/23802359.2019.1679676
PMID:33366156
Phenolic compounds from Forsythia leaves. II. SHIZUKA KITAGAWA, SANSEI NISHIBE, RENATE BENECKE, HEINZ THIEME Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.36.3667

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 / Benzenesulfonic acids and derivatives
Sulfanilic acid 8479 Click to see C1=CC(=CC=C1N)S(=O)(=O)O 173.19 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Phenethylamines
Tyramine 5610 Click to see C1=CC(=CC=C1CCN)O 137.18 unknown via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Nonacosane 12409 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCC 408.80 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
4-[(3S,3aR,6S,6aR)-6-(3,4-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxyphenol 21722915 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/10.1248/CPB.36.3667
4-[6-(4-Hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxyphenol 234817 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 358.40 unknown https://doi.org/10.1248/CPB.36.3667
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/10.1248/CPB.36.3667
> Lignans, neolignans and related compounds / Lignan glycosides
Forsythin 12314162 Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC5C(C(C(C(O5)CO)O)O)O)OC)OC 534.60 unknown https://doi.org/10.1248/CPB.36.3667
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
(E)-but-2-enedioate;hydron 21883788 Click to see [H+].[H+].C(=CC(=O)[O-])C(=O)[O-] 116.07 unknown via CMAUP database
> Organic acids and derivatives / Keto acids and derivatives / Alpha-keto acids and derivatives
Pyruvic Acid 1060 Click to see CC(=O)C(=O)O 88.06 unknown via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / Quaternary ammonium salts / Cholines
Choline 305 Click to see C[N+](C)(C)CCO 104.17 unknown via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / Quaternary ammonium salts / Cholines / Acyl cholines
Acetylcholine 187 Click to see CC(=O)OCC[N+](C)(C)C 146.21 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glucosinolates / Alkylglucosinolates
Sinigrin 6911854 Click to see C=CCC(=NOS(=O)(=O)O)SC1C(C(C(C(O1)CO)O)O)O 359.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
Galactitol 11850 Click to see C(C(C(C(C(CO)O)O)O)O)O 182.17 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
(-)-Fustin 12310641 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(O2)C=C(C=C3)O)O)O)O 288.25 unknown via CMAUP database
Fustin 5317435 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(O2)C=C(C=C3)O)O)O)O 288.25 unknown via CMAUP database
Garbanzol 442410 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(O2)C=C(C=C3)O)O)O 272.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferide 5281666 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown via CMAUP database
Robinetin 5281692 Click to see C1=CC2=C(C=C1O)OC(=C(C2=O)O)C3=CC(=C(C(=C3)O)O)O 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 44559826 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown via CMAUP database
Diosmin 5281613 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C=C5)OC)O)O)O)O)O)O)O)O 608.50 unknown via CMAUP database
Hesperidin 10621 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC(=C(C=C5)OC)O)O)O)O)O)O)O)O 610.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
Gossypetin hexamethyl ether 146093 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(O2)C(=C(C=C3OC)OC)OC)OC)OC 402.40 unknown via CMAUP database

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