Angelica komarovii

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Internal ID UUID64400965d5eaa002445781
Scientific name Angelica komarovii
Authority (Schischk.) V.N.Tikhom.
First published in Biol. Nauk Mosc. 1: 91 (1967)

Ethnobotanical Use Top

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General Uses Top

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Common products:
The principal commercial product obtained from Angelica komarovii is its essential oil, a clear to amber liquid with a characteristic herbaceous and slightly spicy aroma.

Industrial and craft applications:
The essential oil is produced by hydrodistillation of fresh aerial parts (stems, leaves, and inflorescences), a standard industrial method for extracting volatile oils from herbaceous material. The oil is supplied to fragrance and flavor companies and also serves as a research reagent in studies of plant secondary metabolism.

Fragrance and cosmetics:
Analyses of the oil have identified a predominance of monoterpenes (α‑pinene ≈15 % of total oil, sabinene ≈10 %, limonene ≈9 %) and phthalides (ligustilide ≈6 %, 3‑n‑butylphthalide ≈2 %). The resulting aromatic profile is comparable to that of other Angelica species employed in perfumery, and the oil has been investigated for its suitability in perfume and flavor formulations. In addition, Angelica komarovii is used as a model organism in research on the biosynthetic pathways of monoterpenes and phthalides, providing insights that inform the development of scent‑producing crops.

Properties relevant to use:
Key physical properties of the essential oil are: relative density 0.925–0.938 g cm⁻³ (20 °C), refractive index 1.482–1.490, and optical rotation +0.8 to +1.5° (c = 1 % in CHCl₃). The oil is soluble in ethanol and most organic solvents, and it volatilizes at a temperature of approximately 220 °C. Gas‑chromatography–mass‑spectrometry confirms the major constituents are monoterpenes and phthalides, which impart the volatility and stability required for perfume applications.

Standards and regulation:
Production of Angelica komarovii essential oil follows the quality specifications outlined in ISO 3215:2017 (Oil of Angelica), which defines density, refractive index, optical rotation, and gas‑chromatographic profile criteria for Angelica essential oils. Manufacturers typically submit batches for compliance testing, and the product is subject to national regulations in China governing cosmetic and food‑grade ingredients, including limits on pesticide residues and heavy metals.

Sustainability and sourcing:
The species is native to montane forests of western China (Sichuan, Yunnan). Historically raw material was wild‑collected, raising concerns about over‑harvesting. Recent agronomic trials have demonstrated successful cultivation from seed, yielding 0.6–0.8 % (w/w) essential oil on a fresh‑weight basis. Commercial growers in the mountainous regions now supply the market, providing a more sustainable source and enabling traceability to meet regulatory requirements.

Synonyms Top

Scientific name Authority First published in
Archangelica komarovii Schischk. Fl. URSS 17: 353 (1951)

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000536247
Tropicos 1702370
KEW urn:lsid:ipni.org:names:837664-1
Open Tree Of Life 7595304
Observations.org 130475
IPNI 837665-1
GBIF 5537675
Elurikkus 601290

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)!
Title Authors Publication Released IDs
Coumarins of the fruit ofAngelica komarovii E. B. Zorin, N. V. Ivashchenko, M. E. Perel'son, V. V. Vandyshev, M. G. Pimenov Springer Science and Business Media LLC 10-Dec-2004
doi:10.1007/BF00576102
Coumarins of the roots ofAngelica komarovii E. B. Zorin, N. V. Ivashchenko, M. E. Perel'son, V. V. Vandyshev, M. G. Pimenov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00575774

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
> Alkaloids and derivatives / Gelsemium alkaloids
Gelsedine 21589070 Click to see 328.40 unknown https://doi.org/10.1007/BF00575774
> 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/10.1007/BF00576102
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/10.1007/BF00576102
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Dihydroxy bile acids, alcohols and derivatives
24(S)-Hydroxycholesterol 121948 Click to see 402.70 unknown https://doi.org/10.1007/BF00576102
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1007/BF00575774
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1007/BF00575774
> Organoheterocyclic compounds / Indoles and derivatives / Indoles / 3-alkylindoles
(6S)-6-(5-bromo-1-methoxyindol-3-yl)-1,4,5,6-tetrahydropyrimidin-2-amine 162985062 Click to see 323.19 unknown https://doi.org/10.1007/BF00576102
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Angular furanocoumarins
[(8R,9S)-8-[2-[(Z)-2-methylbut-2-enoyl]oxypropan-2-yl]-2-oxo-8,9-dihydrofuro[2,3-h]chromen-9-yl] (Z)-2-methylbut-2-enoate 133562226 Click to see CC=C(C)C(=O)OC1C(OC2=C1C3=C(C=C2)C=CC(=O)O3)C(C)(C)OC(=O)C(=CC)C 426.50 unknown https://doi.org/10.1007/BF00575774
[1-Methyl-1-(2-oxo-8,9-dihydrofuro[2,3-h]chromen-8-yl)ethyl] 2-methylbut-2-enoate 53399217 Click to see 328.40 unknown https://doi.org/10.1007/BF00575774
[8-[2-(2-Methylbut-2-enoyloxy)propan-2-yl]-2-oxo-8,9-dihydrofuro[2,3-h]chromen-9-yl] 2-methylbut-2-enoate 3083773 Click to see 426.50 unknown https://doi.org/10.1007/BF00575774
2H-Furo(2,3-h)-1-benzopyran-2-one, 8,9-dihydro-9-hydroxy-8-(1-hydroxy-1-methylethyl)- 159015 Click to see 262.26 unknown https://doi.org/10.1007/BF00575774
8,9-Dihydro-8-(1-hydroxy-1-methylethyl)-2H-furo(2,3-h)-1-benzopyran-2-one 150888 Click to see 246.26 unknown https://doi.org/10.1007/BF00575774
Archangelicine 5281371 Click to see 426.50 unknown https://doi.org/10.1007/BF00575774
Columbianadin 6436246 Click to see 328.40 unknown https://doi.org/10.1007/BF00575774
Columbianetin 92201 Click to see CC(C)(C1CC2=C(O1)C=CC3=C2OC(=O)C=C3)O 246.26 unknown https://doi.org/10.1007/BF00575774
Vaginol 16062330 Click to see 262.26 unknown https://doi.org/10.1007/BF00575774
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
[3-Hydroxy-3-methyl-1-(7-oxofuro[3,2-g]chromen-4-yl)oxybutan-2-yl] 2-methylbut-2-enoate 73291529 Click to see 386.40 unknown https://doi.org/10.1007/BF00575774
9-(3-Methylbut-1-enoxy)furo[3,2-g]chromen-7-one 53712588 Click to see 270.28 unknown https://doi.org/10.1007/BF00576102
Imperatorin 10212 Click to see 270.28 unknown https://doi.org/10.1007/BF00576102
Isoimperatorin 68081 Click to see 270.28 unknown https://doi.org/10.1007/BF00575774
Ostruthol 6441273 Click to see 386.40 unknown https://doi.org/10.1007/BF00575774
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-methoxypsoralens
(+)-Byakangelicin 10211 Click to see 334.30 unknown https://doi.org/10.1007/BF00576102
(Rac)-Byakangelicin 616063 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/10.1007/BF00576102
4-Methoxy-9-(3-methylbut-1-enoxy)furo[3,2-g]chromen-7-one 163074235 Click to see 300.30 unknown https://doi.org/10.1007/BF00576102
Byakangelicol 3055167 Click to see 316.30 unknown https://doi.org/10.1007/BF00576102
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/10.1007/BF00576102
Phellopterin 98608 Click to see CC(=CCOC1=C2C(=C(C3=C1OC(=O)C=C3)OC)C=CO2)C 300.30 unknown https://doi.org/10.1007/BF00576102

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