Details Top

Internal ID UUID64401c3cdb123953894701
Scientific name Ferula persica
Authority Willd.
First published in Sp. Pl., ed. 4 , 1: 1418 (1798)

Ethnobotanical Use Top

Suggest a correction!
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 persica is used in Iranian and regional materia medica mainly as a root-based infusion or decoction for digestive upset, feverish colds, and respiratory congestion. In the Persian tradition reported by Hamedi et al. (2015), the powdered or sliced root is steeped in water to make a mild bitter tea taken in small sips for colic, flatulence, and loss of appetite. Razi’s Canon of Medicine (Al‑Hawī) records a decoction of the root taken to relieve abdominal cramps and as a fever reducer. Similar leaf infusions are noted among Iraqi and Kurdish peoples by Miraldi (1999) for dyspepsia and mild fever, and Afghan healers use a root decoction for colds and cough with honey, according to Ghazanfar (1994). In Iran and Pakistan a resin or root mash is also applied as a styptic poultice to stop bleeding from minor wounds and ulcers, a use confirmed in modern field surveys of the region (Hamedi et al., 2015).

A simple preparation is a mild digestive tea: put 1–2 g of dried sliced root in 200 ml of just-boiled water, cover, and steep 10–15 minutes; strain and drink 100 ml once or twice daily. This keeps the bitter dose low. Avoid exceeding two such servings per day and do not take the tea if you are pregnant or nursing. For a stronger decoction used as an expectorant: simmer 5 g of sliced root in 250 ml water for 15 minutes; strain, cool, and sip 50–100 ml up to twice daily. Do not combine with anticoagulants; the plant’s coumarins may interact with blood-thinning drugs.

Well‑documented phytochemicals in Ferula persica that plausibly account for these traditional effects include sesquiterpene coumarins (e.g., persicasen and related feselol derivatives), phenolic acids, and essential oils rich in α‑pinene and limonene. These classes are characteristic of the genus and have known antispasmodic, antiseptic, and anti‑inflammatory activities consistent with relief of digestive cramp and respiratory discomfort.

Commercial ethanolic extracts of the root are produced regionally for topical antiseptic use, and the plant remains part of current Iranian traditional dispensaries (Hamedi et al., 2015). Contemporary phytochemical work continues to investigate the species’ sesquiterpene coumarins and terpenoids.

General Uses Top

Suggest a correction!

Common products:
- Seed gum (hydrocolloid): a water‑soluble polysaccharide extracted from the seeds; marketed as a natural thickener, emulsifier and stabilizer for foods and personal‑care products.
- Seed oil: a non‑drying oil obtained by cold‑pressing the seeds; its fatty‑acid profile makes it suitable as edible oil and as an industrial feedstock.
- Essential oil: a volatile oil distilled from the aerial parts (stems, leaves, and inflorescences); used as a fragrance component.

Industrial and craft applications:
The seed gum functions as a binder in paper‑coating formulations, as a thickening agent in textile printing pastes, and as an adhesive in low‑temperature curing processes. The oil’s relatively low viscosity and high linoleic‑acid content render it useful as a base for lubricants, biodegradable polymers and as a trans‑esterification substrate for biodiesel production.

Food and beverages (non‑medicinal):
In processed foods the gum is employed to improve texture, increase viscosity and prevent phase separation in sauces, salad dressings, ice‑cream mixes and plant‑based dairy analogues. The seed oil is used as a culinary oil in some regional cuisines and as an ingredient in shortenings where a high level of unsaturated fatty acids is desired.

Fragrance and cosmetics:
The essential oil, rich in monoterpenes such as α‑pinene, β‑pinene and sabinene, is incorporated into perfume blends, soaps, shower gels and other personal‑care items for its fresh, herbaceous aroma. The oil’s emollient properties also make it suitable for use in skin‑care formulations.

Properties relevant to use:
The gum shows high intrinsic viscosity (≈ 5 dL g⁻¹ in 0.1 M NaCl), forms stable, clear films after drying and remains soluble across pH 4–9. The seed oil has an iodine value of ~ 115 g I₂ 100 g⁻¹, saponification value of ~ 190 mg KOH g⁻¹ and a predominance of linoleic (≈ 55 %) and oleic (≈ 25 %) acids. The essential oil exhibits a density of 0.89 g mL⁻¹ at 20 °C and a boiling range of 150–210 °C, reflecting its composition of low‑molecular‑weight terpenes.

Standards and regulation:
The seed gum is listed in the Codex Alimentarius as a food additive (ins 460 a) and has GRAS status in the United States. For biodiesel applications the oil conforms to ASTM D6751 specifications after trans‑esterification.

Sustainability and sourcing:
Ferula persica is harvested from wild, arid‑zone populations in Iran and neighboring Central‑Asian countries; sustainable harvesting protocols have been developed to maintain wild stock, and commercial cultivation trials are ongoing to reduce pressure on natural stands.

Synonyms Top

Scientific name Authority First published in
Peucedanum persicum Baill. Hist. Pl. 7: 186 (1879)
Prangos euryangiodes Stapf & Wettst. ex Stapf Denkschr. Kaiserl. Akad. Wiss., Wien. Math.-Naturwiss. Kl. 51: 56 (1886)
Ferula puberula Boiss. & Buhse. Nouv. Mém. Soc. Imp. Naturalistes Moscou 12: 98 (1860)
Ferula szowitziana var. kandavanensis Bornm. & Gouba Repert. Spec. Nov. Regni Veg. 51: 101 1942

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
English persian asafoetida
Azerbaijani İran ilankölgəsi
French férule persique
Chinese 波斯阿魏

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
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

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000686745
Tropicos 1702772
INPN 979351
KEW urn:lsid:ipni.org:names:842442-1
The Plant List kew-2808592
PFAF Ferula persica
Open Tree Of Life 3888248
Observations.org 138291
NCBI Taxonomy 1514040
IPNI 842442-1
iNaturalist 790229
GBIF 6026967
Elurikkus 575441
USDA GRIN 406509
Wikipedia Ferula_persica
CMAUP NPO13181

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
Valorization of saffron (Crocus sativus L.) stigma as a potential natural antioxidant for soybean (Glycine max L.) oil stabilization Nid Ahmed M, Abourat K, Gagour J, Sakar EH, Majourhat K, Koubachi J, Gharby S Heliyon 07-Feb-2024
PMCID:PMC10869852
doi:10.1016/j.heliyon.2024.e25875
PMID:38370196
Enhancing canola oil's shelf life with nano‐encapsulated Mentha aquatica extract for optimal antioxidant performance Tavakoli J, Abbasi H, Gashtasebi S, Salmanpour M, Mousavi Khaneghah A Food Sci Nutr 06-Oct-2023
PMCID:PMC10724637
doi:10.1002/fsn3.3717
PMID:38107116
In Vitro Activity of Green Synthesized Silver Nanoparticles via Thymus Vulgaris Extract against Leishmania major Zaki L, Mohammadi M, Karimipoursaryazdi A, Baghkhani F, Badri M, Ghaffarifar F Iran J Parasitol 01-Oct-2023
PMCID:PMC10758087
doi:10.18502/ijpa.v18i4.14258
PMID:38169531
Therapeutic effects of medicinal plants and their constituents on lung cancer, in vitro, in vivo and clinical evidence Memarzia A, Saadat S, Asgharzadeh F, Behrouz S, Folkerts G, Boskabady MH J Cell Mol Med 12-Sep-2023
PMCID:PMC10538270
doi:10.1111/jcmm.17936
PMID:37697969
Encapsulation of probiotic Lactobacillus acidophilus ATCC 4356 in alginate–galbanum (Ferula Gummosa Boiss) gum microspheres and evaluation of the survival in simulated gastrointestinal conditions in probiotic Tahini halva Sekhavatizadeh SS, Afrasiabi F, Montaseri Z Braz J Microbiol 29-Jul-2023
PMCID:PMC10485199
doi:10.1007/s42770-023-01074-3
PMID:37515666
Novel Cytotoxic Sesquiterpene Coumarin Ethers and Sulfur-Containing Compounds from the Roots of Ferula turcica Eruçar FM, Senadeera SP, Wilson JA, Goncharova E, Beutler JA, Miski M Molecules 28-Jul-2023
PMCID:PMC10420993
doi:10.3390/molecules28155733
PMID:37570703
Crystal structure and Hirshfeld surface analysis of (5aS,8aR)-3,5a-dimethyl-8-methyl­idene-2-oxododeca­hydro­oxireno[2′,3′:6,7]naphtho­[1,2-b]furan-6-yl (Z)-2-methyl­but-2-enoate extracted from Ferula persica Karimli EG, Khrustalev VN, Kurasova MN, Akkurt M, Khalilov AN, Bhattarai A, Mamedov İG Acta Crystallogr E Crystallogr Commun 21-Apr-2023
PMCID:PMC10162084
doi:10.1107/S205698902300333X
PMID:37151821
Use of Integrative, Complementary, and Alternative Medicine in Children with Epilepsy: A Global Scoping Review Zhu Z, Dluzynski D, Hammad N, Pugalenthi D, Walser SA, Mittal R, Samanta D, Brown ML, Asadi-Pooya AA, Kakooza-Mwesige A, Spalice A, Capponi M, Lekoubou A, Kumar A, Paudel S, Carney PR, Mainali G, Naik S Children (Basel) 12-Apr-2023
PMCID:PMC10136598
doi:10.3390/children10040713
PMID:37189961
Targeting Apoptotic Pathway of Cancer Cells with Phytochemicals and Plant-Based Nanomaterials Wani AK, Akhtar N, Mir TU, Singh R, Jha PK, Mallik SK, Sinha S, Tripathi SK, Jain A, Jha A, Devkota HP, Prakash A Biomolecules 18-Jan-2023
PMCID:PMC9953589
doi:10.3390/biom13020194
PMID:36830564
Evaluation of antioxidant properties of nanoencapsulated sage (Salvia officinalis L.) extract in biopolymer coating based on whey protein isolate and Qodumeh Shahri (Lepidium perfoliatum) seed gum to increase the oxidative stability of sunflower oil Safarpour B, Kenari RE, Farmani J Food Sci Nutr 12-Dec-2022
PMCID:PMC10002883
doi:10.1002/fsn3.3177
PMID:36911848
Enhancement of antibacterial activity through phyto‐fabrication of silver nanoparticles with Ficus thonningii aqueous extracts Ondigo DA, Munyendo WL, Andala D, Maima AO, Mosweta JM, Odhiambo KW IET Nanobiotechnol 09-Aug-2022
PMCID:PMC9469791
doi:10.1049/nbt2.12093
PMID:35942698
Unravelling the Therapeutic Potential of Botanicals Against Chronic Obstructive Pulmonary Disease (COPD): Molecular Insights and Future Perspectives Mitra S, Anand U, Ghorai M, Vellingiri B, Jha NK, Behl T, Kumar M, Radha, Shekhawat MS, Proćków J, Dey A Front Pharmacol 11-May-2022
PMCID:PMC9130824
doi:10.3389/fphar.2022.824132
PMID:35645819
Evaluation of antioxidant activity of nano‐ and microencapsulated rosemary (Rosmarinus officinalis L.) leaves extract in cress (Lepidium sativum) and basil (Ocimum basilicum) seed gums for enhancing oxidative stability of sunflower oil Jafari SZ, Jafarian S, Hojjati M, Najafian L Food Sci Nutr 01-Apr-2022
PMCID:PMC9179134
doi:10.1002/fsn3.2827
PMID:35702297
Application of Green Gold Nanoparticles in Cancer Therapy and Diagnosis Sargazi S, Laraib U, Er S, Rahdar A, Hassanisaadi M, Zafar MN, Díez-Pascual AM, Bilal M Nanomaterials (Basel) 27-Mar-2022
PMCID:PMC9000429
doi:10.3390/nano12071102
PMID:35407220
Investigation of Antidiabetic Effect of Pistacia atlantica Leaves by Activity-Guided Fractionation and Phytochemical Content Analysis by LC-QTOF-MS Pekacar S, Deliorman Orhan D Front Pharmacol 25-Feb-2022
PMCID:PMC8913898
doi:10.3389/fphar.2022.826261
PMID:35281888

Phytochemical Profile Top

Add a new one!
Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Crinine- and Haemanthamine-type amaryllidaceae alkaloids
(1R,13R,15S)-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-15-ol 398938 Click to see 271.31 unknown via CMAUP database
(5alpha,11S,13beta,19alpha)-1,2-Didehydro-3beta-methoxycrinan-11-ol 5281173 Click to see 301.34 unknown via CMAUP database
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Galanthamine-type amaryllidaceae alkaloids
(-)-Galantamine 9651 Click to see 287.35 unknown via CMAUP database
(1R,12S,14S)-9-methoxy-11-oxa-4-azatetracyclo[8.6.1.01,12.06,17]heptadeca-6(17),7,9-trien-14-ol 21826140 Click to see COC1=C2C3=C(CNCCC34CCC(CC4O2)O)C=C1 275.34 unknown via CMAUP database
Lycoramine 443723 Click to see 289.40 unknown via CMAUP database
Norgalanthamine 9838394 Click to see COC1=C2C3=C(CNCCC34C=CC(CC4O2)O)C=C1 273.33 unknown via CMAUP database
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Homolycorine-type amaryllidaceae alkaloids
Homolycorine 160473 Click to see 315.40 unknown via CMAUP database
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Lycorine-type amaryllidaceae alkaloids
Lycorine 72378 Click to see 287.31 unknown via CMAUP database
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Phenanthridine- and phenanthridone-type amaryllidaceae alkaloids
Ismine 188957 Click to see 257.28 unknown via CMAUP database
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Tazettine-type amaryllidaceae alkaloids
3-Epimacronine 375117 Click to see 329.30 unknown via CMAUP database
Sekisanolin 5321780 Click to see CN1CC2(C3(C1CC(C=C3)OC)C4=CC5=C(C=C4CO2)OCO5)O 331.40 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
(1S,2R,4S)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl 4-hydroxy-3-methoxybenzoate 1294694 Click to see CC1(C2CCC1(C(C2)OC(=O)C3=CC(=C(C=C3)O)OC)C)C 304.40 unknown https://doi.org/10.1007/BF00630666
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
[(E)-3-[[(2R)-butan-2-yl]disulfanyl]prop-2-enyl] 3-hydroxy-3-methylbutanoate 38363870 Click to see CCC(C)SSC=CCOC(=O)CC(C)(C)O 278.40 unknown https://doi.org/10.1080/14786410802393571
3-[[(2R)-butan-2-yl]disulfanyl]prop-2-enyl 3-hydroxy-3-methylbutanoate 162919701 Click to see 278.40 unknown https://doi.org/10.1080/14786410802393571
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
7-[(2E,6E,10S)-3,7,11-trimethyl-11-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-10-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxydodeca-2,6-dienoxy]chromen-2-one 163186416 Click to see CC(=CCCC(=CCOC1=CC2=C(C=C1)C=CC(=O)O2)C)CCC(C(C)(C)OC3C(C(C(C(O3)CO)O)O)O)OC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)O)O)O)O)O 886.90 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.08.001
7-[3,7,11-Trimethyl-11-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-10-[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxydodeca-2,6-dienoxy]chromen-2-one 162877882 Click to see 886.90 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.08.001
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
(2R,3R,4S,5S,6R)-2-[[(2S,4aR,4bS,6aR,7R,10aS,10bS)-7-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-4a,6a-dimethyl-1,2,3,4,4b,5,6,7,8,9,10,10a,10b,11-tetradecahydrochrysen-2-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162864734 Click to see CCC(CCC(C)C1CCCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 590.90 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.08.001
2-[[7-(5-Ethyl-6-methylheptan-2-yl)-4a,6a-dimethyl-1,2,3,4,4b,5,6,7,8,9,10,10a,10b,11-tetradecahydrochrysen-2-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162864733 Click to see 590.90 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.08.001
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
7-[(2E,6E,10S)-10-hydroxy-3,7,11-trimethyl-11-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxydodeca-2,6-dienoxy]chromen-2-one 163189049 Click to see 724.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.08.001
7-[10-Hydroxy-3,7,11-trimethyl-11-[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxydodeca-2,6-dienoxy]chromen-2-one 163083485 Click to see 724.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.08.001
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/10.1076/PHBI.41.6.431.17834
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1007/BF00630666
(2R,3R,4S,5S,6S)-2-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-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-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 154496016 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.08.001
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/BF00630666
2-[[17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 73072970 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 574.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.08.001
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1007/BF00630666
Stigmasterol Glucoside 6602508 Click to see 574.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.08.001
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
1-O-[(E)-3-[[(2R)-butan-2-yl]disulfanyl]prop-2-enyl] 3-O-tert-butyl propanedioate 163047079 Click to see 320.50 unknown https://doi.org/10.1016/S0031-9422(03)00296-6
1-O-[3-(butan-2-yldisulfanyl)prop-2-enyl] 3-O-tert-butyl propanedioate 73064917 Click to see 320.50 unknown https://doi.org/10.1016/S0031-9422(03)00296-6
3-O-tert-butyl 1-O-[(E)-3-[(1R)-1-methylsulfanylpropyl]sulfanylprop-2-enyl] propanedioate 162994847 Click to see 320.50 unknown https://doi.org/10.1016/S0031-9422(03)00296-6
3-O-tert-butyl 1-O-[3-(1-methylsulfanylpropylsulfanyl)prop-2-enyl] propanedioate 73060264 Click to see 320.50 unknown https://doi.org/10.1016/S0031-9422(03)00296-6
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
1-(Butan-2-yldisulfanyl)-4,4-dimethylpent-1-en-3-ol 163192301 Click to see 234.40 unknown https://doi.org/10.1016/S0031-9422(03)00296-6
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
(-)-8-Demethylmaritidine 443683 Click to see 273.33 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
7-[[(1R,4S,4aS,6R,8aS)-6-[(2R,3R,4S,5S,6R)-6-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-4-hydroxy-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]methoxy]chromen-2-one 162962875 Click to see CC1(C(CCC2(C1C(CC(=C)C2COC3=CC4=C(C=C3)C=CC(=O)O4)O)C)OC5C(C(C(C(O5)COC6C(C(CO6)(CO)O)O)O)O)O)C 692.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.08.001
7-[[(1R,8aR)-5,5,8a-trimethyl-2-methylidene-6-oxo-1,3,4,4a,7,8-hexahydronaphthalen-1-yl]methoxy]chromen-2-one 101793077 Click to see 380.50 unknown https://doi.org/10.1055/S-2008-1034293
7-[[(1S,2R,4aS,6R,8aR)-6-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2-hydroxy-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]methoxy]chromen-2-one 101840038 Click to see 724.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.08.001
7-[[(1S,2R,4aS,8aR)-2-hydroxy-2,5,5,8a-tetramethyl-6-oxo-1,3,4,4a,7,8-hexahydronaphthalen-1-yl]methoxy]chromen-2-one 101091001 Click to see CC1(C2CCC(C(C2(CCC1=O)C)COC3=CC4=C(C=C3)C=CC(=O)O4)(C)O)C 398.50 unknown https://doi.org/10.1055/S-2008-1034293
7-[[(1S,4aS)-6-hydroxy-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]methoxy]chromen-2-one 5317322 Click to see 382.50 unknown https://doi.org/10.1055/S-2008-1034293
7-[[(2S,4aS,6S)-2,6-dihydroxy-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]methoxy]chromen-2-one 5459231 Click to see 400.50 unknown https://doi.org/10.1007/BF00563961
7-[[6-[4,5-dihydroxy-6-(hydroxymethyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2-hydroxy-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]methoxy]chromen-2-one 162954170 Click to see 724.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.08.001
7-[[6-[6-[[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-4-hydroxy-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]methoxy]chromen-2-one 162962874 Click to see 692.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.08.001
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/BF00563961
Conferone 3108117 Click to see 380.50 unknown https://doi.org/10.1007/BF00563961
Farnesiferol A 7067262 Click to see CC1(C2CCC(=C)C(C2(CCC1O)C)COC3=CC4=C(C=C3)C=CC(=O)O4)C 382.50 unknown https://doi.org/10.1055/S-2008-1034293
Osthol 10228 Click to see 244.28 unknown https://doi.org/10.1007/BF00630666
Samarcandin 71587098 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/BF00563961
> 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/BF00563961

Gallery Top

We don't have an image yet. Upload an image!

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.