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Angelica pachycarpa

Angelica pachycarpa - 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 UUID64400968374e9237932525
Scientific name Angelica pachycarpa
Authority Lange
First published in Descr. Icon. Pl. Nov. : 7 (1864)

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Galician brizo mariño

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

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.

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-0000536323
Tropicos 1700305
INPN 610711
KEW urn:lsid:ipni.org:names:837722-1
The Plant List kew-2639199
Open Tree Of Life 3890367
Observations.org 137143
NCBI Taxonomy 2831626
NBN Atlas NHMSYS0100000506
IPNI 837722-1
iNaturalist 337790
GBIF 5537578
Freebase /m/04zzy18
EPPO ANKPC
Elurikkus 540266
USDA GRIN 462788
Wikipedia Angelica_pachycarpa

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
Environmental filtering drives the shape and breadth of the seed germination niche in coastal plant communities Fernández-Pascual E, Pérez-Arcoiza A, Prieto JA, Díaz TE Ann Bot 27-Feb-2017
PMCID:PMC5604583
doi:10.1093/aob/mcx005
PMID:28334139
Simultaneous determination and pharmacokinetics of sixteen Angelicae dahurica coumarins in vivo by LC-ESI-MS/MS following oral delivery in rats. Zhao AH, Zhang YB, Yang XW Phytomedicine 15-Sep-2016
doi:10.1016/J.PHYMED.2016.06.015
PMID:27444348
Coumarins of Angelica pachycarpa Fruits J. Méndez, J. Rubido Georg Thieme Verlag KG 15-Jan-2009
doi:10.1055/S-0028-1097274
Irritant and cytotoxic coumarins from Angelica glauca Edgew roots. Saeed MA, Sabir AW J Asian Nat Prod Res 01-Jan-2008
doi:10.1080/10286020701273759
PMID:18058380
Furocoumarins from Angelica pachycarpa J. Méndez, J. Castro-Poceiro Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(83)80174-5
Coumarins of Angelica pachycarpa. Méndez J, Rubido J, Mato MC Experientia 15-Mar-1973
doi:10.1007/BF01926538
PMID:4708735

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 / Phenols / Methoxyphenols
Vanillin 1183 Click to see COC1=C(C=CC(=C1)C=O)O 152.15 unknown https://doi.org/10.1055/S-0028-1097274
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
7-Farnesyloxy-coumarin 181996 Click to see CC(=CCCC(=CCCC(=CCOC1=CC2=C(C=C1)C=CC(=O)O2)C)C)C 366.50 unknown https://doi.org/10.1016/0031-9422(83)80174-5
Umbelliprenin 1781413 Click to see CC(=CCCC(=CCCC(=CCOC1=CC2=C(C=C1)C=CC(=O)O2)C)C)C 366.50 unknown https://doi.org/10.1016/0031-9422(83)80174-5
> Phenylpropanoids and polyketides / Coumarins and derivatives
Ulopterol 176475 Click to see CC(C)(C(CC1=C(C=C2C(=C1)C=CC(=O)O2)OC)O)O 278.30 unknown https://doi.org/10.1055/S-0028-1097274
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Angular furanocoumarins
(-)-Columbianetin 442104 Click to see CC(C)(C1CC2=C(O1)C=CC3=C2OC(=O)C=C3)O 246.26 unknown https://doi.org/10.1055/S-0028-1097274
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
(R)-Pabulenol 511358 Click to see CC(=C)C(COC1=C2C=CC(=O)OC2=CC3=C1C=CO3)O 286.28 unknown https://doi.org/10.1016/0031-9422(83)80174-5
https://doi.org/10.1055/S-0028-1097274
2-(2-Hydroxypropan-2-yl)-2,3-dihydrofuro[3,2-g]chromen-7-one 604512 Click to see CC(C)(C1CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)O 246.26 unknown https://doi.org/10.1016/J.PHYMED.2016.06.015
4-(2-Methoxy-3-methylbutoxy)furo[3,2-g]chromen-7-one 162940738 Click to see CC(C)C(COC1=C2C=CC(=O)OC2=CC3=C1C=CO3)OC 302.32 unknown https://doi.org/10.1016/0031-9422(83)80174-5
4-[(2S)-2-methoxy-3-methylbutoxy]furo[3,2-g]chromen-7-one 162940739 Click to see CC(C)C(COC1=C2C=CC(=O)OC2=CC3=C1C=CO3)OC 302.32 unknown https://doi.org/10.1016/0031-9422(83)80174-5
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/10.1016/0031-9422(83)80174-5
Isoimperatorin 68081 Click to see CC(=CCOC1=C2C=CC(=O)OC2=CC3=C1C=CO3)C 270.28 unknown https://doi.org/10.1055/S-0028-1097274
https://doi.org/10.1016/0031-9422(83)80174-5
Marmesin 334704 Click to see CC(C)(C1CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)O 246.26 unknown https://doi.org/10.1016/J.PHYMED.2016.06.015
https://doi.org/10.1080/10286020701273759
Oxypeucedanin 928465 Click to see CC1(C(O1)COC2=C3C=CC(=O)OC3=CC4=C2C=CO4)C 286.28 unknown https://doi.org/10.1016/0031-9422(83)80174-5
https://doi.org/10.1055/S-0028-1097274
Pangelin 44144315 Click to see CC(=C)C(COC1=C2C=CC(=O)OC2=CC3=C1C=CO3)O 286.28 unknown https://doi.org/10.1016/0031-9422(83)80174-5
https://doi.org/10.1055/S-0028-1097274
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-methoxypsoralens
[(1S)-3-hydroxy-1-(4-methoxy-7-oxofuro[3,2-g]chromen-9-yl)oxy-3-methylbutyl] acetate 163187597 Click to see CC(=O)OC(CC(C)(C)O)OC1=C2C(=C(C3=C1OC(=O)C=C3)OC)C=CO2 376.40 unknown https://doi.org/10.1016/0031-9422(83)80174-5
[3-Hydroxy-1-(4-methoxy-7-oxofuro[3,2-g]chromen-9-yl)oxy-3-methylbutyl] acetate 162863032 Click to see CC(=O)OC(CC(C)(C)O)OC1=C2C(=C(C3=C1OC(=O)C=C3)OC)C=CO2 376.40 unknown https://doi.org/10.1016/0031-9422(83)80174-5
4-Methoxy-9-(2-methoxy-3-methylbutoxy)furo[3,2-g]chromen-7-one 163061711 Click to see CC(C)C(COC1=C2C(=C(C3=C1OC(=O)C=C3)OC)C=CO2)OC 332.30 unknown https://doi.org/10.1016/0031-9422(83)80174-5
4-methoxy-9-[(2S)-2-methoxy-3-methylbutoxy]furo[3,2-g]chromen-7-one 163061712 Click to see CC(C)C(COC1=C2C(=C(C3=C1OC(=O)C=C3)OC)C=CO2)OC 332.30 unknown https://doi.org/10.1016/0031-9422(83)80174-5
9-[(2S)-2-hydroxy-3-methoxy-3-methylbutoxy]-4-methoxyfuro[3,2-g]chromen-7-one 163040630 Click to see CC(C)(C(COC1=C2C(=C(C3=C1OC(=O)C=C3)OC)C=CO2)O)OC 348.30 unknown https://doi.org/10.1016/0031-9422(83)80174-5
9-[(2S)-2-hydroxy-3-methylbut-3-enoxy]-4-methoxyfuro[3,2-g]chromen-7-one 92468407 Click to see CC(=C)C(COC1=C2C(=C(C3=C1OC(=O)C=C3)OC)C=CO2)O 316.30 unknown https://doi.org/10.1016/0031-9422(83)80174-5
Byakangelicin 10211 Click to see CC(C)(C(COC1=C2C(=C(C3=C1OC(=O)C=C3)OC)C=CO2)O)O 334.30 unknown https://doi.org/10.1055/S-0028-1097274
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/10.1016/0031-9422(83)80174-5
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/10.1016/0031-9422(83)80174-5
Neobyakangelicol 616064 Click to see CC(=C)C(COC1=C2C(=C(C3=C1OC(=O)C=C3)OC)C=CO2)O 316.30 unknown https://doi.org/10.1016/0031-9422(83)80174-5
Phellopterin 98608 Click to see CC(=CCOC1=C2C(=C(C3=C1OC(=O)C=C3)OC)C=CO2)C 300.30 unknown https://doi.org/10.1055/S-0028-1097274
https://doi.org/10.1016/0031-9422(83)80174-5
tert-OMe-byakangelicin 5319537 Click to see CC(C)(C(COC1=C2C(=C(C3=C1OC(=O)C=C3)OC)C=CO2)O)OC 348.30 unknown https://doi.org/10.1016/0031-9422(83)80174-5
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown https://doi.org/10.1007/BF01926538

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