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Ostericum grossiserratum

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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 UUID644047248e47f337090724
Scientific name Ostericum grossiserratum
Authority (Maxim.) Kitag.
First published in J. Jap. Bot. 12: 233 (1936)

Description Top

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Synonyms Top

Scientific name Authority First published in
Peucedanum mirabile H.Wolff Repert. Spec. Nov. Regni Veg. 21: 248 (1925)
Angelica grosseserrata Maxim. Bull. Acad. Imp. Sci. Saint-Pétersbourg , sér. 3, 19: 275 (1874)
Angelica koreana Maxim. Bull. Acad. Imp. Sci. Saint-Pétersbourg , sér. 3, 31: 51 (1886)
Angelica mongolica Franch. Nouv. Arch. Mus. Hist. Nat. , sér. 2, 6: 21 (1883)
Angelica peucedanoides H.Wolff Acta Horti Gothob. 2: 321 (1926)
Angelica smithii H.Wolff Acta Horti Gothob. 2: 320 (1926)
Ostericum koreanum (Maxim.) Kitag. J. Jap. Bot. 12: 235 (1936)

Common names Top

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Language Common/alternative name
Chinese 隔山香
Chinese 大齿山芹
Chinese 大齿当归
Chinese 山水芹菜
Chinese 大齿独活
Chinese 朝鲜独活
Chinese 朝鲜羌活
Chinese 碎叶山芹
Chinese 大齒山芹

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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No germination or propagation data was added yet.

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

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001069251
Tropicos 1704495
KEW urn:lsid:ipni.org:names:845576-1
Open Tree Of Life 706490
NCBI Taxonomy 182415
iNaturalist 1147783
GBIF 5832015

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
Chemical Relationship among Genetically Authenticated Medicinal Species of Genus Angelica Kim JH, Doh EJ, Kim HY, Lee G Plants (Basel) 30-Apr-2024
PMCID:PMC11085054
doi:10.3390/plants13091252
PMID:38732467
Anti-Obesity and Anti-Diabetic Effects of Ostericum koreanum (Ganghwal) Extract Lee E, Nam JO Int J Mol Sci 30-Apr-2024
PMCID:PMC11084156
doi:10.3390/ijms25094908
PMID:38732125
Fungal Endophytes: Discovering What Lies within Some of Canada’s Oldest and Most Resilient Grapevines Ali S, Wright AH, Tanney JB, Renaud JB, Sumarah MW J Fungi (Basel) 26-Jan-2024
PMCID:PMC10890244
doi:10.3390/jof10020105
PMID:38392777
Insampaedok-San Extract Exerts an Immune-Enhancing Effect through NF-κB p65 Pathway Activation Huh G, Oh Y, Jeon Y, Kang KS, Kim SN, Jung SH, Kim SH, Kim YJ Biomed Res Int 22-Sep-2023
PMCID:PMC10541303
doi:10.1155/2023/5458504
PMID:37780486
Herbal medicine use in Republic of Korea to alleviate side effects of COVID-19 vaccines: A cross-sectional study Yoon HC J Integr Med 08-Jun-2023
PMCID:PMC10249366
doi:10.1016/j.joim.2023.06.002
PMID:37349213
Apiaceae Medicinal Plants in China: A Review of Traditional Uses, Phytochemistry, Bolting and Flowering (BF), and BF Control Methods Li M, Li M, Wang L, Li M, Wei J Molecules 27-May-2023
PMCID:PMC10254214
doi:10.3390/molecules28114384
PMID:37298861
GC-MS/MS Method for Determination of Polycyclic Aromatic Hydrocarbons in Herbal Medicines Park J, Kim K, Ryu D, Whang JH, Mah JH Molecules 02-May-2023
PMCID:PMC10179879
doi:10.3390/molecules28093853
PMID:37175264
Chemical Constituents from the Roots of Angelica reflexa That Improve Glucose-Stimulated Insulin Secretion by Regulating Pancreatic β-Cell Metabolism Kim HS, Lee D, Seo YH, Ryu SM, Lee AY, Moon BC, Kim WJ, Kang KS, Lee J Pharmaceutics 13-Apr-2023
PMCID:PMC10146581
doi:10.3390/pharmaceutics15041239
PMID:37111724
Effects of the administration of Shinbaro 2 in a rat lumbar disk herniation model Kim WK, Shin JS, Lee J, Koh W, Ha IH, Park HJ, Lee SK, Hong JY Front Neurol 10-Mar-2023
PMCID:PMC10036394
doi:10.3389/fneur.2023.1044724
PMID:36970511
Evaluation of Propiophenone, 4-Methylacetophenone and 2′,4′-Dimethylacetophenone as Phytotoxic Compounds of Labdanum Oil from Cistus ladanifer L. Espinosa-Colín M, Hernandez-Caballero I, Infante C, Gago I, García-Muñoz J, Sosa T Plants (Basel) 06-Mar-2023
PMCID:PMC10006901
doi:10.3390/plants12051187
PMID:36904046
Preclinical evidence of polyherbal formulations on wound healing: A systematic review on research trends and perspectives Dubey S, Dixit AK J Ayurveda Integr Med 24-Feb-2023
PMCID:PMC9988554
doi:10.1016/j.jaim.2023.100688
PMID:36841194
Caffeic acid N-[3,5-bis(trifluoromethyl)phenyl] amide as a non-steroidal inhibitor for steroid 5α-reductase type 1 using a human keratinocyte cell-based assay and molecular dynamics Lin AC, Netcharoensirisuk P, Sanachai K, Sukma W, Chansriniyom C, Chaotham C, De-Eknamkul W, Rungrotmongkol T, Chamni S Sci Rep 02-Dec-2022
PMCID:PMC9718795
doi:10.1038/s41598-022-25335-7
PMID:36460729
Exploring Contact Toxicity of Essential Oils against Sitophilus zeamais through a Meta-Analysis Approach Achimón F, Peschiutta ML, Brito VD, Beato M, Pizzolitto RP, Zygadlo JA, Zunino MP Plants (Basel) 13-Nov-2022
PMCID:PMC9696113
doi:10.3390/plants11223070
PMID:36432799
The Impact of Oxidative Stress and AKT Pathway on Cancer Cell Functions and Its Application to Natural Products Shiau JP, Chuang YT, Tang JY, Yang KH, Chang FR, Hou MF, Yen CY, Chang HW Antioxidants (Basel) 19-Sep-2022
PMCID:PMC9495789
doi:10.3390/antiox11091845
PMID:36139919
The Modulation of Melanogenesis in B16 Cells Upon Treatment with Plant Extracts and Isolated Plant Compounds Merecz-Sadowska A, Sitarek P, Kowalczyk T, Zajdel K, Kucharska E, Zajdel R Molecules 07-Jul-2022
PMCID:PMC9324663
doi:10.3390/molecules27144360
PMID:35889231

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 / Hydroxybenzoic acid derivatives
3,4-Dihydroxybenzoic acid 72 Click to see C1=CC(=C(C=C1C(=O)O)O)O 154.12 unknown https://doi.org/10.1248/CPB.55.1065
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(E,2S)-2,6-dihydroxy-2-(2-hydroxy-4-methylphenyl)-6-methylhept-4-en-3-one 26238733 Click to see CC1=CC(=C(C=C1)C(C)(C(=O)C=CC(C)(C)O)O)O 264.32 unknown https://doi.org/10.1248/CPB.55.1065
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
4,5-Dicaffeoylquinic acid 5281780 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O 516.40 unknown https://doi.org/10.1248/CPB.55.1065
Neochlorogenic acid methyl ester 46230348 Click to see COC(=O)C1(CC(C(C(C1)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O)O 368.30 unknown https://doi.org/10.1248/CPB.55.1065
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
4-[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyfuro[3,2-g]chromen-7-one 162903141 Click to see C1=CC(=O)OC2=CC3=C(C=CO3)C(=C21)OC4C(C(C(C(O4)CO)O)O)O 364.30 unknown https://doi.org/10.1248/CPB.55.1065
bergaptol-O-glucopyranoside 125494 Click to see C1=CC(=O)OC2=CC3=C(C=CO3)C(=C21)OC4C(C(C(C(O4)CO)O)O)O 364.30 unknown https://doi.org/10.1248/CPB.55.1065
> Organoheterocyclic compounds / Benzofurans
(+)-Angelikoreanol;Angelikoreanol;Bisabolangelone 85132655 Click to see CC1=CC(=O)C2C(C1)OC(=CC=C(C)C)C2(C)O 248.32 unknown https://doi.org/10.1016/S0040-4039(00)89436-8
Bisabolangelone 12300142 Click to see CC1=CC(=O)C2C(C1)OC(=CC=C(C)C)C2(C)O 248.32 unknown https://doi.org/10.1055/S-2002-20258
https://doi.org/10.1016/S0040-4039(00)89436-8
https://doi.org/10.1007/BF02978248
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones / Furanochromones
2-(2-hydroxypropan-2-yl)-4-methoxy-7-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-2,3-dihydrofuro[3,2-g]chromen-5-one 11968852 Click to see CC(C)(C1CC2=C(O1)C=C3C(=C2OC)C(=O)C=C(O3)COC4C(C(C(C(O4)CO)O)O)O)O 468.40 unknown https://doi.org/10.1248/CPB.55.1065
Cimifugin 441960 Click to see CC(C)(C1CC2=C(O1)C=C3C(=C2OC)C(=O)C=C(O3)CO)O 306.31 unknown https://doi.org/10.1248/CPB.55.1065
https://doi.org/10.3724/SP.J.1009.2010.00264
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Pyranochromenes
sec-O-Glucosylhamaudol 10478277 Click to see CC1=CC(=O)C2=C(C3=C(C=C2O1)OC(C(C3)OC4C(C(C(C(O4)CO)O)O)O)(C)C)O 438.40 unknown https://doi.org/10.1248/CPB.55.1065
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
5-Chloro-7-hydroxy-2-(2-hydroxyethyl)-7-methyl-3-(3-methylpent-1-enyl)isoquinoline-6,8-dione 78108622 Click to see CCC(C)C=CC1=CC2=C(C(=O)C(C(=O)C2=CN1CCO)(C)O)Cl 351.80 unknown https://doi.org/10.1248/CPB.55.1065
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid 689043 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown https://doi.org/10.3724/SP.J.1009.2010.00264
> Phenylpropanoids and polyketides / Coumarins and derivatives
Coumarin 323 Click to see C1=CC=C2C(=C1)C=CC(=O)O2 146.14 unknown https://doi.org/10.3724/SP.J.1009.2010.00264
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
Esculin 5281417 Click to see C1=CC(=O)OC2=CC(=C(C=C21)OC3C(C(C(C(O3)CO)O)O)O)O 340.28 unknown https://doi.org/10.3724/SP.J.1009.2010.00264
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
(+)-Oxypeucedanin 928465 Click to see CC1(C(O1)COC2=C3C=CC(=O)OC3=CC4=C2C=CO4)C 286.28 unknown https://doi.org/10.1055/S-2001-11509
4-(2,3-Dihydroxy-3-Methylbutoxy)Furo(3,2-G)Chromen-7-One 483513 Click to see CC(C)(C(COC1=C2C=CC(=O)OC2=CC3=C1C=CO3)O)O 304.29 unknown https://doi.org/10.1055/S-2001-11509
4-[(3,3-Dimethyloxiran-2-yl)methoxy]furo[3,2-g]chromen-7-one 160544 Click to see CC1(C(O1)COC2=C3C=CC(=O)OC3=CC4=C2C=CO4)C 286.28 unknown https://doi.org/10.1055/S-2001-11509
Ammijin 216283 Click to see CC(C)(C1CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)OC4C(C(C(C(O4)CO)O)O)O 408.40 unknown https://doi.org/10.1248/CPB.55.1065
Cnidicin 10043694 Click to see CC(=CCOC1=C2C=COC2=C(C3=C1C=CC(=O)O3)OCC=C(C)C)C 354.40 unknown https://doi.org/10.1055/S-2001-11509
Isoimperatorin 68081 Click to see CC(=CCOC1=C2C=CC(=O)OC2=CC3=C1C=CO3)C 270.28 unknown https://doi.org/10.1055/S-2002-20258
https://doi.org/10.1055/S-2001-11509
Oxypeucedanin hydrate 17536 Click to see CC(C)(C(COC1=C2C=CC(=O)OC2=CC3=C1C=CO3)O)O 304.29 unknown https://doi.org/10.1055/S-2001-11509
https://doi.org/10.1248/CPB.55.1065
Pentosalen 10212 Click to see CC(=CCOC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)C 270.28 unknown https://doi.org/10.1055/S-2001-11509
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-methoxypsoralens
Byakangelicol 3055167 Click to see CC1(C(O1)COC2=C3C(=C(C4=C2OC(=O)C=C4)OC)C=CO3)C 316.30 unknown https://doi.org/10.1055/S-2001-11509
Byakangelicol (Biacangelicol) 616062 Click to see CC1(C(O1)COC2=C3C(=C(C4=C2OC(=O)C=C4)OC)C=CO3)C 316.30 unknown https://doi.org/10.1055/S-2001-11509
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Osthenol 5320318 Click to see CC(=CCC1=C(C=CC2=C1OC(=O)C=C2)O)C 230.26 unknown https://doi.org/10.1055/S-2002-20258

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