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Ferula moschata

Ferula moschata - 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 UUID64401c3ab9330631577525
Scientific name Ferula moschata
Authority (Reinsch) Koso-Pol.
First published in Byull. Obshch. Estestvoisp. Voronezhsk. Gosud. Univ. 1: 94 (1926)

Description Top

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Ferula moschata, also known as musk root or sumbul, is a flowering plant found in Central Asia and western Xinjiang. Its roots are used as a substitute for animal musk in medicinal and perfumery purposes. This plant belongs to the Apiaceae family and is also known as Ferula sumbul.

Synonyms Top

Scientific name Authority First published in
Peucedanum sumbul Baill. Hist. Pl. 7: 186 (1879)
Euryangium sumbul Kauffm. Nouv. Mém. Soc. Imp. Naturalistes Moscou 13: 258 (1871)
Ferula sumbul (Kauffm.) Hook.f. Bot. Mag. 101: t. 6196 (1875)
Ferula urceolata Korovin Novosti Sist. Vyssh. Rast. 1: 249 (1964)
Sumbulus moschatus H.Reinsch Jahrb. Pract. Pharm. Verwandte Fächer 13: 69 (1846)

Common names Top

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Language Common/alternative name
Arabic سامبول
Russian Мускусный корень
Russian Сумбул
Russian Ферула мускусная
Chinese 麝香阿魏

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • Xinjiang
    • Middle Asia
      • Kirgizstan
      • Tadzhikistan
      • Uzbekistan

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000686695
Tropicos 1702764
KEW urn:lsid:ipni.org:names:842394-1
The Plant List kew-2808547
PFAF Ferula moschata
Open Tree Of Life 1085929
NCBI Taxonomy 555413
IPNI 842394-1
iNaturalist 777057
GBIF 3637382
EOL 2906755
Wikipedia Ferula_moschata

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
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
Bioactive Compounds as Potential Agents for Sexually Transmitted Diseases Management: A Review to Explore Molecular Mechanisms of Action Sharifi-Rad J, Quispe C, Rahavian A, Pereira Carneiro JN, Rocha JE, Alves Borges Leal AL, Bezerra Morais Braga MF, Melo Coutinho HD, Ansari Djafari A, Alarcón-Zapata P, Martorell M, Antika G, Tumer TB, Cruz-Martins N, Helon P, Paprocka P, Koch W, Docea AO, Calina D Front Pharmacol 24-Aug-2021
PMCID:PMC8421529
doi:10.3389/fphar.2021.674682
PMID:34504422
Medicinal Plants Used in the Treatment of Human Immunodeficiency Virus Salehi B, Kumar NV, Şener B, Sharifi-Rad M, Kılıç M, Mahady GB, Vlaisavljevic S, Iriti M, Kobarfard F, Setzer WN, Ayatollahi SA, Ata A, Sharifi-Rad J Int J Mol Sci 14-May-2018
PMCID:PMC5983620
doi:10.3390/ijms19051459
PMID:29757986
Terpenoid coumarins ofFerula sumbul É. Kh. Khalilova, A. I. Saidkhodzhaev Springer Science and Business Media LLC 14-Mar-2006
doi:10.1007/BF02329608
Coumarins of Ferula syreitschikowii K. Bizhanova, G. K. Nikonov Springer Science and Business Media LLC 10-Dec-2004
doi:10.1007/BF00563960
Components of the resin of the roots ofFerula kirialovii T. V. Bukreeva Springer Science and Business Media LLC 24-Nov-2004
doi:10.1007/BF00598697
Structure of the coumarin reoselin Kh. M. Kamilov, G. K. Nikonov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00568234
Coumarins and bicoumarin from Ferula sumbul: anti-HIV activity and inhibition of cytokine release. Zhou P, Takaishi Y, Duan H, Chen B, Honda G, Itoh M, Takeda Y, Kodzhimatov OK, Lee KH Phytochemistry 01-Mar-2000
doi:10.1016/S0031-9422(99)00554-3
PMID:10746882

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
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
Reoselin A 6445962 Click to see CC(=CCCC(=CCOC1=CC2=C(C=C1)C=CC(=O)O2)C)CCC(C(C)(C)O)OC3C(C(C(C(O3)CO)O)O)OC4C(C(C(C(O4)CO)O)O)O 724.80 unknown https://doi.org/10.1007/BF00568234
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Beta-Sitosterol 222284 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/BF00598697
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
(3R,4R,5R)-3-(2-hydroxy-4-methoxybenzoyl)-4,5-dimethyl-5-(4-oxopentyl)oxolan-2-one 163044640 Click to see CC1C(C(=O)OC1(C)CCCC(=O)C)C(=O)C2=C(C=C(C=C2)OC)O 348.40 unknown https://doi.org/10.1007/BF00563960
(3R,4R,5S)-3-(2-hydroxy-4-methoxybenzoyl)-4,5-dimethyl-5-(4-oxopentyl)oxolan-2-one 163044642 Click to see CC1C(C(=O)OC1(C)CCCC(=O)C)C(=O)C2=C(C=C(C=C2)OC)O 348.40 unknown https://doi.org/10.1007/BF00563960
3-(2-Hydroxy-4-methoxybenzoyl)-4,5-dimethyl-5-(4-oxopentyl)oxolan-2-one 74039133 Click to see CC1C(C(=O)OC1(C)CCCC(=O)C)C(=O)C2=C(C=C(C=C2)OC)O 348.40 unknown https://doi.org/10.1007/BF00563960
> Phenylpropanoids and polyketides / Coumarins and derivatives
2H-1-Benzopyran-2-one, 7-[[(1R,2S,4aS,6S,8aR)-decahydro-2,6-dihydroxy-2,5,5,8a-tetramethyl-1-naphthalenyl]methoxy]- 11873225 Click to see CC1(C2CCC(C(C2(CCC1O)C)COC3=CC4=C(C=C3)C=CC(=O)O4)(C)O)C 400.50 unknown https://doi.org/10.1007/BF00598697
8-(2,3-Dihydroxy-3-methylbutyl)-7-methoxychromen-2-one 5070783 Click to see CC(C)(C(CC1=C(C=CC2=C1OC(=O)C=C2)OC)O)O 278.30 unknown https://doi.org/10.1016/S0031-9422(99)00554-3
CID 13343541 13343541 Click to see CC(=C)C(CC1=C(C=CC2=C1OC(=O)C=C2)OC)O 260.28 unknown https://doi.org/10.1016/S0031-9422(99)00554-3
Conferol 11892267 Click to see CC1=CCC2C(C(CCC2(C1COC3=CC4=C(C=C3)C=CC(=O)O4)C)O)(C)C 382.50 unknown https://doi.org/10.1007/BF02329608
https://doi.org/10.1016/S0031-9422(99)00554-3
Conferone 3108117 Click to see CC1=CCC2C(C(=O)CCC2(C1COC3=CC4=C(C=C3)C=CC(=O)O4)C)(C)C 380.50 unknown https://doi.org/10.1016/S0031-9422(99)00554-3
https://doi.org/10.1007/BF02329608
Feselol 179577 Click to see CC1=CCC2C(C(CCC2(C1COC3=CC4=C(C=C3)C=CC(=O)O4)C)O)(C)C 382.50 unknown https://doi.org/10.1007/BF02329608
https://doi.org/10.1016/S0031-9422(99)00554-3
Nevskin 495442 Click to see CC1(C2CCC(C(C2(CCC1O)C)COC3=CC4=C(C=C3)C=CC(=O)O4)(C)O)C 400.50 unknown https://doi.org/10.1007/BF00598697
Osthol 10228 Click to see CC(=CCC1=C(C=CC2=C1OC(=O)C=C2)OC)C 244.28 unknown https://doi.org/10.1016/S0031-9422(99)00554-3
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
(-)-Heraclenol 40429858 Click to see CC(C)(C(COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)O)O 304.29 unknown https://doi.org/10.1016/S0031-9422(99)00554-3
(+)-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/S0031-9422(99)00554-3
(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/S0031-9422(99)00554-3
[3-Hydroxy-3-methyl-1-(7-oxofuro[3,2-g]chromen-4-yl)oxybutan-2-yl] 2-hydroxypropanoate 10643224 Click to see CC(C(=O)OC(COC1=C2C=CC(=O)OC2=CC3=C1C=CO3)C(C)(C)O)O 376.40 unknown https://doi.org/10.1016/S0031-9422(99)00554-3
[3-Hydroxy-3-methyl-1-(7-oxofuro[3,2-g]chromen-9-yl)oxybutan-2-yl] 2-hydroxypropanoate 10643225 Click to see CC(C(=O)OC(COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)C(C)(C)O)O 376.40 unknown https://doi.org/10.1016/S0031-9422(99)00554-3
9-[[(2S,4R)-4'-(2,3-dihydroxy-3-methylbutoxy)-5,5-dimethylspiro[1,3-dioxolane-2,7'-furo[3,2-g]chromene]-4-yl]methoxy]furo[3,2-g]chromen-7-one 101062476 Click to see CC1(C(OC2(O1)C=CC3=C(O2)C=C4C(=C3OCC(C(C)(C)O)O)C=CO4)COC5=C6C(=CC7=C5OC=C7)C=CC(=O)O6)C 590.60 unknown https://doi.org/10.1016/S0031-9422(99)00554-3
9-[[(2S,4R)-4'-[(3,3-dimethyloxiran-2-yl)methoxy]-5,5-dimethylspiro[1,3-dioxolane-2,7'-furo[3,2-g]chromene]-4-yl]methoxy]furo[3,2-g]chromen-7-one 101062477 Click to see CC1(C(O1)COC2=C3C=COC3=CC4=C2C=CC5(O4)OC(C(O5)(C)C)COC6=C7C(=CC8=C6OC=C8)C=CC(=O)O7)C 572.60 unknown https://doi.org/10.1016/S0031-9422(99)00554-3
9-[[(2S,4R)-9'-[(2R)-2,3-dihydroxy-3-methylbutoxy]-5,5-dimethylspiro[1,3-dioxolane-2,7'-furo[3,2-g]chromene]-4-yl]methoxy]furo[3,2-g]chromen-7-one 10769724 Click to see CC1(C(OC2(O1)C=CC3=C(O2)C(=C4C(=C3)C=CO4)OCC(C(C)(C)O)O)COC5=C6C(=CC7=C5OC=C7)C=CC(=O)O6)C 590.60 unknown https://doi.org/10.1016/S0031-9422(99)00554-3
9-[[(2S,4R)-9'-[(3,3-dimethyloxiran-2-yl)methoxy]-5,5-dimethylspiro[1,3-dioxolane-2,7'-furo[3,2-g]chromene]-4-yl]methoxy]furo[3,2-g]chromen-7-one 10578982 Click to see CC1(C(O1)COC2=C3C(=CC4=C2OC5(C=C4)OC(C(O5)(C)C)COC6=C7C(=CC8=C6OC=C8)C=CC(=O)O7)C=CO3)C 572.60 unknown https://doi.org/10.1016/S0031-9422(99)00554-3
9-[[(2S,4S)-9'-(2,3-dihydroxy-3-methylbutoxy)-5,5-dimethylspiro[1,3-dioxolane-2,7'-furo[3,2-g]chromene]-4-yl]methoxy]furo[3,2-g]chromen-7-one 101062475 Click to see CC1(C(OC2(O1)C=CC3=C(O2)C(=C4C(=C3)C=CO4)OCC(C(C)(C)O)O)COC5=C6C(=CC7=C5OC=C7)C=CC(=O)O6)C 590.60 unknown https://doi.org/10.1016/S0031-9422(99)00554-3
9-[[(2S,4S)-9'-[(3,3-dimethyloxiran-2-yl)methoxy]-5,5-dimethylspiro[1,3-dioxolane-2,7'-furo[3,2-g]chromene]-4-yl]methoxy]furo[3,2-g]chromen-7-one 483512 Click to see CC1(C(O1)COC2=C3C(=CC4=C2OC5(C=C4)OC(C(O5)(C)C)COC6=C7C(=CC8=C6OC=C8)C=CC(=O)O7)C=CO3)C 572.60 unknown https://doi.org/10.1016/S0031-9422(99)00554-3
9-[[(2S)-3,3-dimethyloxiran-2-yl]methoxy]furo[3,2-g]chromen-7-one 17897 Click to see CC1(C(O1)COC2=C3C(=CC4=C2OC=C4)C=CC(=O)O3)C 286.28 unknown https://doi.org/10.1016/S0031-9422(99)00554-3
9-[3-Hydroxy-2-[3-hydroxy-2-methyl-4-(7-oxofuro[3,2-g]chromen-4-yl)oxybutan-2-yl]oxy-3-methylbutoxy]furo[3,2-g]chromen-7-one 10674925 Click to see CC(C)(C(COC1=C2C=CC(=O)OC2=CC3=C1C=CO3)O)OC(COC4=C5C(=CC6=C4OC=C6)C=CC(=O)O5)C(C)(C)O 590.60 unknown https://doi.org/10.1016/S0031-9422(99)00554-3
Heraclenin 458010 Click to see CC1(C(O1)COC2=C3C(=CC4=C2OC=C4)C=CC(=O)O3)C 286.28 unknown https://doi.org/10.1016/S0031-9422(99)00554-3
Heraclenol 73253 Click to see CC(C)(C(COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)O)O 304.29 unknown https://doi.org/10.1016/S0031-9422(99)00554-3
Pabulenol 3009225 Click to see CC(=C)C(COC1=C2C=CC(=O)OC2=CC3=C1C=CO3)O 286.28 unknown https://doi.org/10.1016/S0031-9422(99)00554-3
Pentosalen 10212 Click to see CC(=CCOC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)C 270.28 unknown https://doi.org/10.1016/S0031-9422(99)00554-3
Pranferol 159751 Click to see CC(C)C(COC1=C2C=CC(=O)OC2=CC3=C1C=CO3)O 288.29 unknown https://doi.org/10.1016/S0031-9422(99)00554-3
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-hydroxypsoralens
Xanthotoxol 65090 Click to see C1=CC(=O)OC2=C(C3=C(C=CO3)C=C21)O 202.16 unknown https://doi.org/10.1016/S0031-9422(99)00554-3
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-methoxypsoralens
Methoxsalen 4114 Click to see COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2 216.19 unknown https://doi.org/10.1016/S0031-9422(99)00554-3
> 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/BF00598697

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