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Angelica cincta

Angelica cincta - 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 UUID6440096288cea008318328
Scientific name Angelica cincta
Authority H.Boissieu
First published in Bull. Soc. Bot. France 53: 436 (1906)

Description Top

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Synonyms Top

Scientific name Authority First published in
Angelica amurensis Schischk. Fl. URSS 17: 352 (1951)

Common names Top

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Language Common/alternative name
Japanese エゾノヨロイグサ
Chinese 湖北当归

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

Area

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

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000536142
Tropicos 1702356
KEW urn:lsid:ipni.org:names:837582-1
The Plant List kew-2639032
Open Tree Of Life 956994
Observations.org 114504
NCBI Taxonomy 62991
IPNI 837582-1
iNaturalist 864430
GBIF 5537827
Elurikkus 540313
USDA GRIN 406654

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
Phylogeny and Taxonomic Revision of the Genus Melanosciadium (Apiaceae), Based on Plastid Genomes and Morphological Evidence Jiang QP, Guo XL, Zhao AQ, Fan X, Li Q, Zhou SD, He XJ Plants (Basel) 21-Mar-2024
PMCID:PMC10974901
doi:10.3390/plants13060907
PMID:38592923
Phytochemicals for the Prevention and Treatment of Renal Cell Carcinoma: Preclinical and Clinical Evidence and Molecular Mechanisms Bajalia EM, Azzouz FB, Chism DA, Giansiracusa DM, Wong CG, Plaskett KN, Bishayee A Cancers (Basel) 04-Jul-2022
PMCID:PMC9265746
doi:10.3390/cancers14133278
PMID:35805049
A Review of the Composition of the Essential Oils and Biological Activities of Angelica Species Sowndhararajan K, Deepa P, Kim M, Park SJ, Kim S Sci Pharm 20-Sep-2017
PMCID:PMC5620520
doi:10.3390/scipharm85030033
PMID:28930168
Coumarins of the fruit ofAngelica cincta E. B. Zorin, V. V. Vandyshev, M. G. Pimenov Springer Science and Business Media LLC 21-Nov-2004
doi:10.1007/BF00574344

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
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Angular furanocoumarins
Oroselol 160600 Click to see CC(C)(C1=CC2=C(O1)C=CC3=C2OC(=O)C=C3)O 244.24 unknown https://doi.org/10.1007/BF00574344
Oroselone 74477 Click to see CC(=C)C1=CC2=C(O1)C=CC3=C2OC(=O)C=C3 226.23 unknown https://doi.org/10.1007/BF00574344
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
(-)-Praeruptorin B 10251869 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 https://doi.org/10.1007/BF00574344
[8,8-Dimethyl-9-(2-methylbut-2-enoyloxy)-2-oxo-9,10-dihydropyrano[2,3-f]chromen-10-yl] 2-methylbut-2-enoate 163334 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 https://doi.org/10.1007/BF00574344
Praeruptorin B 5319259 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 https://doi.org/10.1007/BF00574344
Praeruptorin D 25717254 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 https://doi.org/10.1007/BF00574344

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Contributors Top

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Collections Top

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