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Angelica furcijuga

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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 UUID64400963e0e92199299386
Scientific name Angelica furcijuga
Authority Kitag.
First published in J. Jap. Bot. 46: 286 (1971)

Description Top

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Synonyms Top

Scientific name Authority First published in
Angelica tenuisecta var. furcijuga (Kitag.) H.Ohba Fl. Japan 2c: 295 (1999)

Common names Top

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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-0000536194
UNII 612ATU497Q
Tropicos 100289158
KEW urn:lsid:ipni.org:names:837626-1
The Plant List kew-2639080
Open Tree Of Life 248568
NCBI Taxonomy 358456
IPNI 837626-1
GBIF 5537754
EOL 5038777
USDA GRIN 460163
CMAUP NPO3509

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
Phytochemicals with Chemopreventive Activity Obtained from the Thai Medicinal Plant Mammea siamensis (Miq.) T. Anders.: Isolation and Structure Determination of New Prenylcoumarins with Inhibitory Activity against Aromatase Luo F, Manse Y, Chaipech S, Pongpiriyadacha Y, Muraoka O, Morikawa T Int J Mol Sci 23-Sep-2022
PMCID:PMC9570088
doi:10.3390/ijms231911233
PMID:36232534
Natural Enantiomers: Occurrence, Biogenesis and Biological Properties Yu JH, Yu ZP, Capon RJ, Zhang H Molecules 14-Feb-2022
PMCID:PMC8880303
doi:10.3390/molecules27041279
PMID:35209066
Extraction of Functional Components from Freeze-Dried Angelica furcijuga Leaves Using Supercritical Carbon Dioxide Hoshino Y, Wahyudiono, Machmudah S, Hirayama S, Kanda H, Hoshino M, Goto M ACS Omega 03-Feb-2022
PMCID:PMC8851661
doi:10.1021/acsomega.1c06105
PMID:35187326
Oxypeucedanin: Chemotaxonomy, Isolation, and Bioactivities Mottaghipisheh J Plants (Basel) 30-Jul-2021
PMCID:PMC8401860
doi:10.3390/plants10081577
PMID:34451622
Bioactive C17 and C18 Acetylenic Oxylipins from Terrestrial Plants as Potential Lead Compounds for Anticancer Drug Development Christensen LP Molecules 31-May-2020
PMCID:PMC7321150
doi:10.3390/molecules25112568
PMID:32486470
Novel Approach to Classify Plants Based on Metabolite-Content Similarity Liu K, Abdullah AA, Huang M, Nishioka T, Altaf-Ul-Amin M, Kanaya S Biomed Res Int 09-Jan-2017
PMCID:PMC5253511
doi:10.1155/2017/5296729
PMID:28164123
Hepatoprotective Limonoids from Andiroba (Carapa guianensis) Ninomiya K, Miyazawa S, Ozeki K, Matsuo N, Muraoka O, Kikuchi T, Yamada T, Tanaka R, Morikawa T Int J Mol Sci 19-Apr-2016
PMCID:PMC4849045
doi:10.3390/ijms17040591
PMID:27104518
Plant-based Paste Fermented by Lactic Acid Bacteria and Yeast: Functional Analysis and Possibility of Application to Functional Foods Kuwaki S, Nakajima N, Tanaka H, Ishihara K Biochem Insights 31-Oct-2012
PMCID:PMC4122547
doi:10.4137/BCI.S10529
PMID:25114554
Antinociceptive Activity of Ethanol Extract from Duguetia chrysocarpa Maas (Annonaceae) Almeida JR, Araújo EC, Ribeiro LA, de Lima JT, Nunes XP, Lúcio AS, Agra MD, Barbosa Filho JM ScientificWorldJournal 03-May-2012
PMCID:PMC3356742
doi:10.1100/2012/859210
PMID:22645460
Falcarindiol impairs the expression of inducible nitric oxide synthase by abrogating the activation of IKK and JAK in rat primary astrocytes Shiao YJ, Lin YL, Sun YH, Chi CW, Chen CF, Wang CN Br J Pharmacol 29-Nov-2004
PMCID:PMC1575975
doi:10.1038/sj.bjp.0706022
PMID:15644867

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 / P-methoxybenzoic acids and derivatives
3-Ethoxy-4-methoxybenzoic acid 2822957 Click to see CCOC1=C(C=CC(=C1)C(=O)O)OC 196.20 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzyl cyanides
4-Hydroxybenzyl cyanide 26548 Click to see C1=CC(=CC=C1CC#N)O 133.15 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
Falcarindiol 5281148 Click to see CCCCCCCC=CC(C#CC#CC(C=C)O)O 260.40 unknown via CMAUP database
Falcarinol 5281149 Click to see CCCCCCCC=CCC#CC#CC(C=C)O 244.37 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / L-alpha-amino acids
3-(3-Carboxyfuran-4-yl)alanine 102328187 Click to see C1=C(C(=CO1)C(=O)O)CC(C(=O)O)N 199.16 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
3-[(2R)-2-(2-hydroxypropan-2-yl)-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydro-1-benzofuran-5-yl]propanoic acid 102207341 Click to see CC(C)(C1CC2=CC(=C(C=C2O1)OC3C(C(C(C(O3)CO)O)O)O)CCC(=O)O)O 428.40 unknown via CMAUP database
Cnidioside B methyl ester 45359747 Click to see COC1=C2C(=CC(=C1OC3C(C(C(C(O3)CO)O)O)O)CCC(=O)OC)C=CO2 412.40 unknown via CMAUP database
Hyuganoside II 11293284 Click to see CC(C)(C1CC2=C(O1)C=CC(=C2OC3C(C(C(C(O3)CO)O)O)O)CCC(=O)O)O 428.40 unknown via CMAUP database
Hyuganoside IV 11351264 Click to see CC(C)(C1C(C2=C(O1)C=CC(=C2OC3C(C(C(C(O3)CO)O)O)O)CCC(=O)O)O)O 444.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
Apiosylskimmin 14236613 Click to see C1C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C=C3)C=CC(=O)O4)O)O)O)O)(CO)O 456.40 unknown via CMAUP database
Peucedanol 7-O-glucoside 44144279 Click to see CC(C)(C(CC1=C(C=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O)O)O 426.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Angular furanocoumarins
(8S,9R)-9-hydroxy-8-[2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropan-2-yl]-8,9-dihydrofuro[2,3-h]chromen-2-one 15945058 Click to see CC(C)(C1C(C2=C(O1)C=CC3=C2OC(=O)C=C3)O)OC4C(C(C(C(O4)CO)O)O)O 424.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Linear furanocoumarins
9-Hydroxy-5,6-dihydrofuro[3,2-g]chromen-7-one 29920867 Click to see C1CC(=O)OC2=C1C=C3C=COC3=C2O 204.18 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
Isoimperatorin 68081 Click to see CC(=CCOC1=C2C=CC(=O)OC2=CC3=C1C=CO3)C 270.28 unknown via CMAUP database
Oxypeucedanin hydrate 17536 Click to see CC(C)(C(COC1=C2C=CC(=O)OC2=CC3=C1C=CO3)O)O 304.29 unknown via CMAUP database
Pentosalen 10212 Click to see CC(=CCOC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)C 270.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-methoxypsoralens
Bergapten 2355 Click to see COC1=C2C=CC(=O)OC2=CC3=C1C=CO3 216.19 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
3,4,5,6,8-Pentadeuterio-7-hydroxychromen-2-one 45358955 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 167.17 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
(-)-trans-Khellactone 9992853 Click to see CC1(C(C(C2=C(O1)C=CC3=C2OC(=O)C=C3)O)O)C 262.26 unknown via CMAUP database
(3'R,4'R)-3'-Epoxyangeloyloxy-4'-acetoxy-3',4'-dihydroseselin 442130 Click to see CC1C(O1)(C)C(=O)OC2C(C3=C(C=CC4=C3OC(=O)C=C4)OC2(C)C)OC(=O)C 402.40 unknown via CMAUP database
(9S,10R)-9,10-Dihydro-9-hydroxy-10-tigloyloxy-8,8-dimethyl-2H,8H-benzo[1,2-b:3,4-b']dipyran-2-one 10807381 Click to see CC=C(C)C(=O)OC1C(C(OC2=C1C3=C(C=C2)C=CC(=O)O3)(C)C)O 344.40 unknown via CMAUP database
[(9R,10R)-8,8-dimethyl-10-(2-methylpropanoyloxy)-2-oxo-9,10-dihydropyrano[2,3-f]chromen-9-yl] (E)-2-methylbut-2-enoate 44310195 Click to see CC=C(C)C(=O)OC1C(C2=C(C=CC3=C2OC(=O)C=C3)OC1(C)C)OC(=O)C(C)C 414.40 unknown via CMAUP database
[(9R,10R)-8,8-dimethyl-9-[(E)-2-methylbut-2-enoyl]oxy-2-oxo-9,10-dihydropyrano[2,3-f]chromen-10-yl] (E)-2-methylbut-2-enoate 5319252 Click to see CC=C(C)C(=O)OC1C(C(OC2=C1C3=C(C=C2)C=CC(=O)O3)(C)C)OC(=O)C(=CC)C 426.50 unknown via CMAUP database
[(9R,10R)-8,8-dimethyl-9-[(E)-2-methylbut-2-enoyl]oxy-2-oxo-9,10-dihydropyrano[2,3-f]chromen-10-yl] 2-methylbutanoate 44309848 Click to see CCC(C)C(=O)OC1C(C(OC2=C1C3=C(C=C2)C=CC(=O)O3)(C)C)OC(=O)C(=CC)C 428.50 unknown via CMAUP database
[(9R,10R)-9-acetyloxy-8,8-dimethyl-2-oxo-9,10-dihydropyrano[2,3-f]chromen-10-yl] (E)-2-methylbut-2-enoate 5320509 Click to see CC=C(C)C(=O)OC1C(C(OC2=C1C3=C(C=C2)C=CC(=O)O3)(C)C)OC(=O)C 386.40 unknown via CMAUP database
[(9R,10R)-9-acetyloxy-8,8-dimethyl-2-oxo-9,10-dihydropyrano[2,3-f]chromen-10-yl] 2-methylbutanoate 10068841 Click to see CCC(C)C(=O)OC1C(C(OC2=C1C3=C(C=C2)C=CC(=O)O3)(C)C)OC(=O)C 388.40 unknown via CMAUP database
DL-Praeruptorin A 10023029 Click to see CC=C(C)C(=O)OC1C(C2=C(C=CC3=C2OC(=O)C=C3)OC1(C)C)OC(=O)C 386.40 unknown via CMAUP database
Hyuganin C 100946026 Click to see CC(COC1C(C(OC2=C1C3=C(C=C2)C=CC(=O)O3)(C)C)OC(=O)C)C(=O)C 388.40 unknown via CMAUP database
Hyuganin D 10317265 Click to see CC(C)C(=O)OC1C(C(OC2=C1C3=C(C=C2)C=CC(=O)O3)(C)C)OC(=O)C 374.40 unknown via CMAUP database
Khellactone, cis-(+)- 455821 Click to see CC1(C(C(C2=C(O1)C=CC3=C2OC(=O)C=C3)O)O)C 262.26 unknown via CMAUP database
Praeroside II 24066895 Click to see CC1(C(C(C2=C(O1)C=CC3=C2OC(=O)C=C3)O)OC4C(C(C(C(O4)CO)O)O)O)C 424.40 unknown via CMAUP database
praeroside IV 44144278 Click to see CC1(C(CC2=C(O1)C=CC3=C2OC(=O)C=C3)OC4C(C(C(C(O4)CO)O)O)O)C 408.40 unknown via CMAUP database
Suksdorfin 72414 Click to see CC(C)CC(=O)OC1C(C(OC2=C1C3=C(C=C2)C=CC(=O)O3)(C)C)OC(=O)C 388.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Kaempferol oxoanion 25202062 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)[O-])O 285.23 unknown via CMAUP database

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