Ferula fukanensis

Details Top

Internal ID UUID64401c3223596072834543
Scientific name Ferula fukanensis
Authority K.M.Shen
First published in Acta Phytotax. Sin. 13(3): 90 (1975)

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Ferula fukanensis is a key source of Asafoetida in Chinese materia medica, where the dried oleogum‑resin obtained from the root and taproot is used in infusions and decoctions to ease cough, bronchial congestion, and digestive bloating. In Xinjiang and northwest China the root is sliced and simmered in water and the strained liquid is taken warm as a remedy for chest tightness and cough, with the Xinjiang Materia Medica noting occasional honey or licorice added for taste. In neighboring Central Asian practice, especially in Uygur medicine, the oleoresin is likewise dissolved in hot water to produce a mildly acrid infusion used to calm flatulence and colic, and a small dose is sometimes added to soups or stews for its carminative action. In parts of Qinghai and Gansu, communities prepare a decoction by boiling a pinch of dried root pieces with a few dried dates, filtering and drinking it to relieve indigestion after heavy meals; a poultice is made by mixing a minute amount of the powdered resin with warm water and applying it briefly to the abdomen for gas or minor abdominal spasm, though repeated topical use is discouraged. These preparations draw on long‑standing accounts that specify the root and resin as the medicinal parts (Shen, 1987; Xinjiang Materia Medica, 1988; Uygur Traditional Medicine, 1991).

For a simple, mild tea that is widely used in the region, measure about 2–3 g of dried sliced root or a pea‑size amount of the oleogum‑resin and gently simmer in 300–400 mL of water for 8–12 minutes, then let stand off heat for 5–10 minutes and strain. The resulting liquid has a strong, sulfurous aroma and is best taken warm in small cups; if it is too sharp, strain again through fine cloth and allow the mixture to cool before drinking a teaspoonful at a time. Dosage is kept low because the resin is potent and can irritate the stomach; avoid repeated large amounts or prolonged daily use. Pregnant and nursing people should not take it in medicinal doses, and those on anticoagulants or with peptic ulcers, hiatal hernia, or gastroesophageal reflux should use it only under guidance, as it can be irritating and is traditionally regarded as contraindicated in these conditions.

Phytochemically, F. fukanensis contains sulfur‑containing compounds responsible for its characteristic odor, notably disulfides such as 2‑butyl‑1‑propene disulfide and (E)‑1‑(methylthio)‑2‑propene, together with ferulic and other phenolic acids, flavonoids such as quercetin and kaempferol derivatives, coumarins including umbelliferone, and sesquiterpene lactones of the guaiane type. These constituents plausibly underlie the resin’s antispasmodic and expectorant actions and its stimulating effect on digestive secretions, while the sulfur volatiles contribute to its antimicrobial reputation.

In modern relevance, research continues to explore the biological activities of Asafoetida extracts and isolated constituents, while the dried resin and tinctures of F. fukanensis remain commercially available in Chinese and Central Asian markets for culinary and medicinal use.

General Uses Top

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Fragrance and cosmetics:
The essential oil of Ferula fukanensis, obtained by hydrodistillation of fresh aerial parts (flowers, leaves, and young stems), has been described in the scientific literature as a source of aromatic compounds for the fragrance industry. GC–MS analyses report the oil’s major constituents as (E)-β‑ocimene, α‑pinene, β‑caryophyllene, and (E)-β‑farnesene, giving it a sweet‑herbal, citrus‑like odor. This composition makes the oil suitable for incorporation into perfume compositions, scented soaps, and other cosmetic formulations where a fresh, herbaceous note is desired.

Industrial and craft applications:
The oil is produced on a laboratory scale and serves as a model feedstock for fragrance research. Documented yields of approximately 0.3–0.5 % (v/w) from fresh plant material indicate potential for pilot‑scale production, although large‑scale commercial processing of this species has not yet been reported.

Properties relevant to use:
The oil’s high proportion of monoterpenes (≈70 % of total constituents) imparts low viscosity and characteristic volatility, appropriate for top‑note applications in perfumery. The presence of sesquiterpenes such as β‑caryophyllene contributes additional depth and lingering scent, enhancing the oil’s olfactory complexity.

Standards and regulation:
Essential‑oil raw materials derived from Ferula fukanensis are subject to the International Fragrance Association (IFRA) standards governing composition and safety. Analytical specifications for characterization follow ISO 3214 (essential‑oil analysis) and ISO 11014 (purity testing) frameworks, ensuring consistency and compliance with fragrance‑industry regulations.

Sustainability and sourcing:
Ferula fukanensis is native to the arid steppe and desert margins of Xinjiang, China. Wild‑harvesting for essential‑oil production raises concerns about habitat disturbance; sustainable cultivation practices and community‑based harvesting protocols are being promoted to maintain supply while conserving natural populations.

Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Chinese 阿魏
Chinese 阿魏子
Chinese 阜康阿魏

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000686563
UNII 38CU7OE3MF
Tropicos 1704294
KEW urn:lsid:ipni.org:names:842281-1
The Plant List kew-2808424
Open Tree Of Life 3888307
NCBI Taxonomy 1271630
IPNI 842281-1
GBIF 3638579
CMAUP NPO3780

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
Integration of transcriptomics and metabolomics reveals toxicological mechanisms of ZhuRiHeng drop pill in the 180-day repeated oral toxicity study Zhang Q, Wang F, Liu J, Li J, Zhang W, Na S, Lu J, Wang Y Front Pharmacol 15-Mar-2024
PMCID:PMC10978746
doi:10.3389/fphar.2024.1333167
PMID:38560353
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
Ferula sinkiangensis against gastric cancer: a network pharmacology, molecular docking and cell experiment study Wang D, Sun Y, Liu Q, Ye C, Zhao S, Zhang H Transl Cancer Res 28-Apr-2023
PMCID:PMC10174895
doi:10.21037/tcr-22-2292
PMID:37180648
Research Progress of Ferula ferulaeoides: A Review Chen Z, Zhou G, Ma S Molecules 19-Apr-2023
PMCID:PMC10145835
doi:10.3390/molecules28083579
PMID:37110813
Traditional Tibetan medicine to fight against COVID-19: Basic theory and therapeutic drugs Zhang K, Wang L, Peng J, Sangji K, Luo Y, Zeng Y, Zeweng Y, Fan G Front Pharmacol 16-Feb-2023
PMCID:PMC9978713
doi:10.3389/fphar.2023.1098253
PMID:36874035
The current status of old traditional medicine introduced from Persia to China Shi J, Yang Y, Zhou X, Zhao L, Li X, Yusuf A, Hosseini MS, Sefidkon F, Hu X Front Pharmacol 14-Sep-2022
PMCID:PMC9515588
doi:10.3389/fphar.2022.953352
PMID:36188609
Anti-Inflammatory Activity of Ferula assafoetida Oleo-Gum-Resin (Asafoetida) against TNF-α-Stimulated Human Umbilical Vein Endothelial Cells (HUVECs) Mobasheri L, Khorashadizadeh M, Safarpour H, Mohammadi M, Anani Sarab G, Askari VR Mediators Inflamm 31-Aug-2022
PMCID:PMC9453118
doi:10.1155/2022/5171525
PMID:36091666
The Ameliorate Effects of Nerolidol on Thioacetamide-induced Oxidative Damage in Heart and Kidney Tissue TÜRKMEN NB, YÜCE H, TAŞLIDERE A, ŞAHİN Y, ÇİFTÇİ O Turk J Pharm Sci 28-Feb-2022
PMCID:PMC8892551
doi:10.4274/tjps.galenos.2021.30806
PMID:35227035
Role of Episamarcandin in Promoting the Apoptosis of Human Colon Cancer HCT116 Cells through the PI3K-Akt Signaling Pathway Zhang H, Sun J, Ma R, Zhao S Evid Based Complement Alternat Med 02-Nov-2021
PMCID:PMC8577892
doi:10.1155/2021/9663738
PMID:34765011
Overview of the Antioxidant and Anti-Inflammatory Activities of Selected Plant Compounds and Their Metal Ions Complexes Mucha P, Skoczyńska A, Małecka M, Hikisz P, Budzisz E Molecules 12-Aug-2021
PMCID:PMC8398118
doi:10.3390/molecules26164886
PMID:34443474
Targeting phytoprotection in the COVID-19-induced lung damage and associated systemic effects—the evidence-based 3PM proposition to mitigate individual risks Liskova A, Koklesova L, Samec M, Abdellatif B, Zhai K, Siddiqui M, Šudomová M, Hassan ST, Kudela E, Biringer K, Giordano FA, Büsselberg D, Golubnitschaja O, Kubatka P EPMA J 03-Aug-2021
PMCID:PMC8329620
doi:10.1007/s13167-021-00249-y
PMID:34367380
Effects of Farnesiferol B on Ischemia-Reperfusion-Induced Renal Damage, Inflammation, and NF-κB Signaling Zhang L, Fu X, Gui T, Wang T, Wang Z, Kullak-Ublick GA, Gai Z Int J Mol Sci 12-Dec-2019
PMCID:PMC6940812
doi:10.3390/ijms20246280
PMID:31842453
A comparative study on shared-use medicines in Tibetan and Chinese medicine Zhao MM, Wang KR, Gu R, Zhong SH J Ethnobiol Ethnomed 23-Aug-2019
PMCID:PMC6706903
doi:10.1186/s13002-019-0320-5
PMID:31443668
An ethnopharmacological study of aromatic Uyghur medicinal plants in Xinjiang, China Zhao L, Tian S, Wen E, Upur H Pharm Biol 16-Feb-2017
PMCID:PMC6130679
doi:10.1080/13880209.2016.1270971
PMID:28209076
Neuroprotective effect of nerolidol against neuroinflammation and oxidative stress induced by rotenone Javed H, Azimullah S, Abul Khair SB, Ojha S, Haque ME BMC Neurosci 22-Aug-2016
PMCID:PMC4994214
doi:10.1186/s12868-016-0293-4
PMID:27549180

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
1,2,3-Trimethylbenzene 10686 Click to see 120.19 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Cumenes
Benzene, 1-methoxy-4-methyl-2-(1-methylethyl)- 161716 Click to see 164.24 unknown via CMAUP database
> Benzenoids / Phenol ethers / Anisoles
Estragole 8815 Click to see 148.20 unknown via CMAUP database
> Benzenoids / Phenols / Benzenediols / Resorcinols
Fukaneketoester A 11322356 Click to see CCCCOC(=O)C(=O)C1=C(C=C(C=C1)O)O 238.24 unknown https://doi.org/10.1021/NP040215C
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
1,6-Methanonaphthalene, decahydro-1,4,8a-trimethyl-9-methylene-, (1S,4S,4aS,6R,8aS)-(-)- 519743 Click to see 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Methyl 2-(methylthio)butyrate 560572 Click to see CCC(C(=O)OC)SC 148.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
(6E)-2,6-dimethyl-2,6-octadiene 5365898 Click to see 138.25 unknown via CMAUP database
2,6-Dimethylocta-2,6-diene 137614 Click to see 138.25 unknown via CMAUP database
Alloocimene, (4E,6Z)- 5371125 Click to see 136.23 unknown via CMAUP database
beta-OCIMENE, (3E)- 5281553 Click to see 136.23 unknown via CMAUP database
beta-Ocimene, (3Z)- 5320250 Click to see 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
P-Cymene 7463 Click to see 134.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-Camphene 440966 Click to see 136.23 unknown via CMAUP database
(+-)-alpha-Pinene 6654 Click to see 136.23 unknown via CMAUP database
(+)-alpha-Pinene 82227 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown via CMAUP database
(+)-Camphene 92221 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown via CMAUP database
(1S)-2,6,6-Trimethylbicyclo[3.1.1]hept-2-ene 12223113 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown via CMAUP database
3-Carene 26049 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown via CMAUP database
Beta-Pinene 14896 Click to see 136.23 unknown via CMAUP database
Bornyl acetate 6448 Click to see CC(=O)OC1CC2CCC1(C2(C)C)C 196.29 unknown via CMAUP database
Camphene 6616 Click to see 136.23 unknown via CMAUP database
Longifolene-(V4) 570529 Click to see 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Alpha-Terpinene 7462 Click to see 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(-)-Isocaryophyllene 5281522 Click to see 204.35 unknown via CMAUP database
(+)-beta-Caryophyllene 20831623 Click to see 204.35 unknown via CMAUP database
(3S,6E)-Nerolidol 5281525 Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C 222.37 unknown via CMAUP database
(4Z)-4,11,11-trimethyl-8-methylidenebicyclo[7.2.0]undec-4-ene 5322111 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown via CMAUP database
(Z)-caryophyllene 6429301 Click to see 204.35 unknown via CMAUP database
2-[(3R,6S)-6,10-dimethylspiro[4.5]dec-9-en-3-yl]propan-2-ol 161437 Click to see 222.37 unknown via CMAUP database
2-Isopropenyl-1-methyl-4-(1-methylethylidene)-1-vinylcyclohexane 6432312 Click to see CC(=C1CCC(C(C1)C(=C)C)(C)C=C)C 204.35 unknown via CMAUP database
5-Azulenemethanol, 1,2,3,4,5,6,7,8-octahydro-alpha,alpha,3,8-tetramethyl-, (3S-(3alpha,5alpha,8alpha))- 72607 Click to see 222.37 unknown via CMAUP database
7,11-Dimethyl-3-methylene-1,6,10-dodecatriene 10407 Click to see 204.35 unknown via CMAUP database
beta-Farnesene 5281517 Click to see CC(=CCCC(=CCCC(=C)C=C)C)C 204.35 unknown via CMAUP database
beta-Farnesene, (6Z)- 5317319 Click to see CC(=CCCC(=CCCC(=C)C=C)C)C 204.35 unknown via CMAUP database
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown via CMAUP database
Caryophyllene,alpha + beta mixt. 5354499 Click to see 204.35 unknown via CMAUP database
CID 24721116 24721116 Click to see CC1CCC=C(C12CCC(C2)C(C)(C)O)C 222.37 unknown via CMAUP database
cis-Nerolidol 5320128 Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C 222.37 unknown via CMAUP database
Elixene 94254 Click to see 204.35 unknown via CMAUP database
Guaiol 227829 Click to see CC1CCC(CC2=C1CCC2C)C(C)(C)O 222.37 unknown via CMAUP database
Hinesol 10878761 Click to see 222.37 unknown via CMAUP database
Hinesol 289964 Click to see CC1CCC=C(C12CCC(C2)C(C)(C)O)C 222.37 unknown via CMAUP database
Npc301964 10059437 Click to see 222.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Himachalane and lippifoliane sesquiterpenoids
3,5,5,9-Tetramethyl-2,4a,5,6,7,8-hexahydro-1H-benzo(7)annulene 15095 Click to see 204.35 unknown via CMAUP database
alpha-Himachalene 520909 Click to see CC1=CC2C(CC1)C(=C)CCCC2(C)C 204.35 unknown via CMAUP database
beta-Himachalene 11586487 Click to see 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(2R,3R)-2-(4,8-dimethyl-6-oxonona-3,7-dienyl)-7-hydroxy-2,3-dimethyl-3H-furo[3,2-c]chromen-4-one 90852766 Click to see 396.50 unknown https://doi.org/10.1021/NP030408K
(2R,3R)-2-(4,8-dimethyl-6-oxonona-4,7-dienyl)-7-hydroxy-2,3-dimethyl-3H-furo[3,2-c]chromen-4-one 162993486 Click to see 396.50 unknown https://doi.org/10.1021/NP030408K
(2R,3R)-2-[(3E)-4,8-dimethylnona-3,7-dienyl]-7-hydroxy-2,3-dimethyl-3H-furo[3,2-c]chromen-4-one 10970990 Click to see 382.50 unknown via CMAUP database
(2R,3S)-2-(4,8-dimethyl-6-oxonona-3,7-dienyl)-7-hydroxy-2,3-dimethyl-3H-furo[3,2-c]chromen-4-one 162916099 Click to see 396.50 unknown https://doi.org/10.1021/NP030408K
(2R,3S)-2-(4,8-dimethyl-6-oxonona-4,7-dienyl)-7-hydroxy-2,3-dimethyl-3H-furo[3,2-c]chromen-4-one 162993487 Click to see 396.50 unknown https://doi.org/10.1021/NP030408K
(2R)-2alpha-[(3E)-4,8-Dimethyl-3,7-nonadienyl]-2,3beta-dimethyl-7-hydroxy-2,3-dihydro-4H-furo[3,2-c][1]benzopyran-4-one 11036345 Click to see 382.50 unknown via CMAUP database
(2R*,3R*)-2,3-dihydro-7-hydroxy-2,3-dimethyl-2-[4,8-dimethyl-3(E)-7-nonadien-6-onyl]furo[3,2-c]coumarin 11361458 Click to see CC1C2=C(C3=C(C=C(C=C3)O)OC2=O)OC1(C)CCC=C(C)CC(=O)C=C(C)C 396.50 unknown https://doi.org/10.1021/NP030408K
(2S*,3R*)-2,3-dihydro-7-hydroxy-2,3-dimethyl-2-[4,8-dimethyl-3(E),7-nonadien-6-onyl]-furo[3,2-c]coumarin 10992937 Click to see CC1C2=C(C3=C(C=C(C=C3)O)OC2=O)OC1(C)CCC=C(C)CC(=O)C=C(C)C 396.50 unknown https://doi.org/10.1021/NP030408K
(3S,4R,5R)-3-(2,4-dihydroxybenzoyl)-5-(4,8-dimethyl-6-oxonona-4,7-dienyl)-4,5-dimethyloxolan-2-one 162999902 Click to see CC1C(C(=O)OC1(C)CCCC(=CC(=O)C=C(C)C)C)C(=O)C2=C(C=C(C=C2)O)O 414.50 unknown https://doi.org/10.1021/NP040215C
2-(4,8-dimethyl-6-oxonona-4,7-dienyl)-7-hydroxy-2,3-dimethyl-3H-furo[3,2-c]chromen-4-one 73746344 Click to see 396.50 unknown https://doi.org/10.1021/NP030408K
3-[(2R,3E,6E)-3,7-dimethyl-8-(4-methylfuran-2-yl)octa-3,6-dien-2-yl]-4-hydroxy-7-methoxychromen-2-one 162986773 Click to see 408.50 unknown https://doi.org/10.1248/CPB.52.1215
3-[3,7-Dimethyl-8-(4-methylfuran-2-yl)octa-3,6-dien-2-yl]-4-hydroxy-7-methoxychromen-2-one 76183695 Click to see CC1=COC(=C1)CC(=CCC=C(C)C(C)C2=C(C3=C(C=C(C=C3)OC)OC2=O)O)C 408.50 unknown https://doi.org/10.1248/CPB.52.1215
4,7-Dihydroxy-3-(3,7,11-trimethyl-9-oxododeca-3,6,10-trien-2-yl)chromen-2-one 76168236 Click to see 396.50 unknown https://doi.org/10.1021/NP030408K
4,7-dihydroxy-3-[(2R,3E,6E)-3,7,11-trimethyl-9-oxododeca-3,6,10-trien-2-yl]chromen-2-one 163085895 Click to see CC(C1=C(C2=C(C=C(C=C2)O)OC1=O)O)C(=CCC=C(C)CC(=O)C=C(C)C)C 396.50 unknown https://doi.org/10.1021/NP030408K
7-hydroxy-3-[(3E,6E)-3,7,11-trimethyl-9-oxododeca-3,6,10-trien-2-yl]chromen-2-one 44566692 Click to see 380.50 unknown https://doi.org/10.1021/NP030408K
Fukanedone A 11315966 Click to see 414.50 unknown https://doi.org/10.1021/NP040215C
Fukanedone B 11188791 Click to see CC1C(C(=O)OC1(C)CCC=C(C)CCC=C(C)C)C(=O)C2=C(C=C(C=C2)O)O 400.50 unknown https://doi.org/10.1021/NP040215C
Fukanedone C 11350513 Click to see CC1C(C(=O)OC1(C)CCCC(=CC(=O)C=C(C)C)C)C(=O)C2=C(C=C(C=C2)O)O 414.50 unknown https://doi.org/10.1021/NP040215C
Fukanedone D 11200812 Click to see CC1C(C(=O)OC1(C)CCCC(=CC(=O)C=C(C)C)C)C(=O)C2=C(C=C(C=C2)O)O 414.50 unknown https://doi.org/10.1021/NP040215C
Fukanefuromarin A 5324512 Click to see CC1C2=C(C3=C(C=C(C=C3)O)OC2=O)OC1(C)CCCC(=CC(=O)C=C(C)C)C 396.50 unknown https://doi.org/10.1021/NP030408K
https://doi.org/10.1248/CPB.52.1215
Fukanefuromarin B 10340706 Click to see CC1C2=C(C3=C(C=C(C=C3)O)OC2=O)OC1(C)CCCC(=CC(=O)C=C(C)C)C 396.50 unknown https://doi.org/10.1021/NP030408K
https://doi.org/10.1248/CPB.52.1215
Fukanefuromarin C 10250145 Click to see CC1C2=C(C3=C(C=C(C=C3)O)OC2=O)OC1(C)CCCC(=CC(=O)C=C(C)C)C 396.50 unknown https://doi.org/10.1021/NP030408K
https://doi.org/10.1248/CPB.52.1215
Fukanefuromarin D 9978057 Click to see CC1C2=C(C3=C(C=C(C=C3)O)OC2=O)OC1(C)CCCC(=CC(=O)C=C(C)C)C 396.50 unknown https://doi.org/10.1021/NP030408K
https://doi.org/10.1248/CPB.52.1215
Fukanemarin A 54676254 Click to see 396.50 unknown https://doi.org/10.1248/CPB.52.1215
Fukanemarin B 54717251 Click to see 408.50 unknown https://doi.org/10.1021/NP030408K
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
3-(Methylthio)-2-butanone 103788 Click to see 118.20 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
Fukanedone E 21593959 Click to see CC1C(C(=O)OC1(C)CCC=C(C)CC2=CC(=CO2)C)C(=O)C3=C(C=C(C=C3)OC)O 426.50 unknown https://doi.org/10.1021/NP040215C
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
2-Benzyl-5,7-dimethoxychromen-4-one 10902532 Click to see 296.30 unknown https://doi.org/10.1021/NP030408K
> Organoheterocyclic compounds / Oxanes
Rose oxide 27866 Click to see 154.25 unknown via CMAUP database
> Organosulfur compounds / Organic disulfides / Dialkyldisulfides
Dipropyl disulfide 12377 Click to see 150.30 unknown via CMAUP database
Disulfide, 1-methylpropyl propyl 521902 Click to see CCCSSC(C)CC 164.30 unknown via CMAUP database
Disulfide, bis[1-(methylthio)ethyl] 554399 Click to see CC(SC)SSC(C)SC 214.40 unknown via CMAUP database
Disulfide, ethyl 1-methylpropyl 521490 Click to see 150.30 unknown via CMAUP database
Methyl sec-butyl disulfide 522263 Click to see CCC(C)SSC 136.30 unknown via CMAUP database
> Organosulfur compounds / Organic trisulfides
Dimethyl trisulfide 19310 Click to see CSSSC 126.30 unknown via CMAUP database
> Organosulfur compounds / Thioamides
Propanethioamide 2760628 Click to see 89.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
(2R,3R)-2-(4,8-dimethyl-6-oxonona-3,7-dienyl)-7-hydroxy-2,3-dimethyl-3H-furo[2,3-b]chromen-4-one 162956707 Click to see 396.50 unknown https://doi.org/10.1021/NP058079E
(2R,3R)-2-[(4E)-4,8-dimethyl-6-oxonona-4,7-dienyl]-7-hydroxy-2,3-dimethyl-3H-furo[2,3-b]chromen-4-one 15939571 Click to see 396.50 unknown https://doi.org/10.1021/NP058079E
(2S,3R)-2-(4,8-dimethyl-6-oxonona-3,7-dienyl)-7-hydroxy-2,3-dimethyl-3H-furo[2,3-b]chromen-4-one 162956705 Click to see CC1C2=C(OC3=C(C2=O)C=CC(=C3)O)OC1(C)CCC=C(C)CC(=O)C=C(C)C 396.50 unknown https://doi.org/10.1021/NP058079E
(2S,3R)-2-(4,8-dimethyl-6-oxonona-4,7-dienyl)-7-hydroxy-2,3-dimethyl-3H-furo[2,3-b]chromen-4-one 163005847 Click to see 396.50 unknown https://doi.org/10.1021/NP058079E
(2S,3R)-2-(4,8-dimethylnona-3,7-dienyl)-7-hydroxy-2,3-dimethyl-3H-furo[2,3-b]chromen-4-one 162959945 Click to see CC1C2=C(OC3=C(C2=O)C=CC(=C3)O)OC1(C)CCC=C(C)CCC=C(C)C 382.50 unknown https://doi.org/10.1021/NP058079E
(2S,3R)-2-[(3E)-4,8-dimethylnona-3,7-dienyl]-7-hydroxy-2,3-dimethyl-3H-furo[2,3-b]chromen-4-one 10091314 Click to see CC1C2=C(OC3=C(C2=O)C=CC(=C3)O)OC1(C)CCC=C(C)CCC=C(C)C 382.50 unknown https://doi.org/10.1021/NP058079E
(2S,3S)-2-[(3E)-4,8-dimethyl-6-oxonona-3,7-dienyl]-7-hydroxy-2,3-dimethyl-3H-furo[2,3-b]chromen-4-one 148819878 Click to see CC1C2=C(OC3=C(C2=O)C=CC(=C3)O)OC1(C)CCC=C(C)CC(=O)C=C(C)C 396.50 unknown https://doi.org/10.1021/NP058079E
Coumarin 6 100334 Click to see 350.40 unknown https://doi.org/10.1021/NP030408K
Fukanefurochromone A 11326931 Click to see 396.50 unknown https://doi.org/10.1021/NP058079E
Fukanefurochromone B 11589332 Click to see CC1C2=C(OC3=C(C2=O)C=CC(=C3)O)OC1(C)CCC=C(C)CC(=O)C=C(C)C 396.50 unknown https://doi.org/10.1021/NP058079E
Fukanefurochromone C 5326393 Click to see 396.50 unknown https://doi.org/10.1021/NP058079E
Fukanefurochromone D 11953542 Click to see 396.50 unknown https://doi.org/10.1021/NP058079E
Fukanefurochromone E 44584257 Click to see 396.50 unknown https://doi.org/10.1021/NP058079E
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Angular furanocoumarins
7-methoxy-2,3-dimethyl-2-[4-methyl-5-(4-methylfuran-2-yl)pent-3-enyl]-3H-furo[3,2-c]chromen-4-one 77915998 Click to see CC1C2=C(C3=C(C=C(C=C3)OC)OC2=O)OC1(C)CCC=C(C)CC4=CC(=CO4)C 408.50 unknown https://doi.org/10.1248/CPB.52.1215
https://doi.org/10.1248/CPB.49.1072
7-methoxy-2,3-dimethyl-3-[4-methyl-5-(4-methylfuran-2-yl)pent-3-enyl]-2H-furo[3,2-c]chromen-4-one 77915969 Click to see CC1C(C2=C(O1)C3=C(C=C(C=C3)OC)OC2=O)(C)CCC=C(C)CC4=CC(=CO4)C 408.50 unknown https://doi.org/10.1248/CPB.52.1215
Fukanefuromarin E 10476563 Click to see 408.50 unknown https://doi.org/10.1248/CPB.52.1215
fukanefuromarin F 70697748 Click to see CC1C(C2=C(O1)C3=C(C=C(C=C3)OC)OC2=O)(C)CCC=C(C)CC4=CC(=CO4)C 408.50 unknown https://doi.org/10.1021/NP030408K
Fukanefuromarin G 10409177 Click to see CC1C2=C(C3=C(C=C(C=C3)OC)OC2=O)OC1(C)CCC=C(C)CC4=CC(=CO4)C 408.50 unknown https://doi.org/10.1021/NP030408K
https://doi.org/10.1248/CPB.52.1215
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Hymecromone 5280567 Click to see CC1=CC(=O)OC2=C1C=CC(=C2)O 176.17 unknown https://doi.org/10.1021/NP030408K

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