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Ferula feruloides

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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 UUID64401c3199466720765559
Scientific name Ferula feruloides
Authority (Steud.) Korovin
First published in Monogr. Ferula : 77 (1947)

Description Top

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Synonyms Top

Scientific name Authority First published in
Peucedanum soongaricum G.Don Gen. Hist. 3: 332 (1834)
Peucedanum pyramidatum Kar. & Kir. Bull. Soc. Imp. Naturalistes Moscou 15: 366 (1842)
Peucedanum ferulaeoides Steud. Nomencl. Bot. , ed. 2, 2: 311 (1841)
Ferula paniculata Ledeb. Fl. Ross. 2: 805 (1846)
Ferula resinosa Siev. Neueste Nord. Beytr. Phys. Geogr. Erd- Völkerbeschreib. 7: 260 (1796)
Peucedanum feruloides Steud. Nomencl. Bot. , ed. 2, 2: 311 (1841)

Common names Top

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Language Common/alternative name
Chinese 砂茴香
Chinese 多伞阿魏
Chinese 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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000686553
Tropicos 1701465
KEW urn:lsid:ipni.org:names:842271-1
The Plant List kew-2808414
Open Tree Of Life 485312
Observations.org 125160
NCBI Taxonomy 200487
IPNI 842271-1
iNaturalist 1062518
GBIF 4928241
GBIF 3638685
USDA GRIN 406704

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
Endoplasmic Reticulum Stress in Gliomas: Exploiting a Dual-Effect Dysfunction through Chemical Pharmaceutical Compounds and Natural Derivatives for Therapeutical Uses García-López D, Zaragoza-Ojeda M, Eguía-Aguilar P, Arenas-Huertero F Int J Mol Sci 06-Apr-2024
PMCID:PMC11012637
doi:10.3390/ijms25074078
PMID:38612890
Structure-dependent activity of plant natural products against methicillin-resistant Staphylococcus aureus Moreno Cardenas C, Çiçek SS Front Microbiol 15-Aug-2023
PMCID:PMC10463185
doi:10.3389/fmicb.2023.1234115
PMID:37649631
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
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
Design, synthesis and anticancer activity studies of 3-(coumarin-3-yl)-acrolein derivatives: Evidenced by integrating network pharmacology and vitro assay Chen L, Lv Q, Cai J, Liang J, Liang Z, Lin J, Xiao Y, Chen R, Zhang Z, Hong Y, Ji H Front Pharmacol 23-Mar-2023
PMCID:PMC10076643
doi:10.3389/fphar.2023.1141121
PMID:37033621
The Impact of Oxidative Stress and AKT Pathway on Cancer Cell Functions and Its Application to Natural Products Shiau JP, Chuang YT, Tang JY, Yang KH, Chang FR, Hou MF, Yen CY, Chang HW Antioxidants (Basel) 19-Sep-2022
PMCID:PMC9495789
doi:10.3390/antiox11091845
PMID:36139919
Integrating Network Pharmacology, Molecular Docking, and Experimental Validation to Investigate the Mechanism of (−)-Guaiol Against Lung Adenocarcinoma Zeng Y, Pan Y, Zhang B, Luo Y, Tian J, Wang Y, Ju X, Wu J, Li Y Med Sci Monit 25-Jul-2022
PMCID:PMC9336205
doi:10.12659/MSM.937131
PMID:35871777
Hedycaryol – Central Intermediates in Sesquiterpene Biosynthesis, Part II Xu H, Dickschat JS Chemistry 21-Mar-2022
PMCID:PMC9310801
doi:10.1002/chem.202200405
PMID:35239190
Toxic Mechanism and Biological Detoxification of Fumonisins Qu L, Wang L, Ji H, Fang Y, Lei P, Zhang X, Jin L, Sun D, Dong H Toxins (Basel) 01-Mar-2022
PMCID:PMC8954241
doi:10.3390/toxins14030182
PMID:35324679
Coumarins and Gastrointestinal Cancer: A New Therapeutic Option? Banikazemi Z, Mirazimi SM, Dashti F, Mazandaranian MR, Akbari M, Morshedi K, Aslanbeigi F, Rashidian A, Chamanara M, Hamblin MR, Taghizadeh M, Mirzaei H Front Oncol 11-Oct-2021
PMCID:PMC8542999
doi:10.3389/fonc.2021.752784
PMID:34707995
Neurofibromatosis: Molecular Pathogenesis and Natural Compounds as Potential Treatments Amaravathi A, Oblinger JL, Welling DB, Kinghorn AD, Chang LS Front Oncol 17-Sep-2021
PMCID:PMC8485038
doi:10.3389/fonc.2021.698192
PMID:34604034
Metabolic Profile, Bioactivities, and Variations in the Chemical Constituents of Essential Oils of the Ferula Genus (Apiaceae) Sonigra P, Meena M Front Pharmacol 12-Mar-2021
PMCID:PMC7994278
doi:10.3389/fphar.2020.608649
PMID:33776754
Nanotechnologies: An Innovative Tool to Release Natural Extracts with Antimicrobial Properties Spizzirri UG, Aiello F, Carullo G, Facente A, Restuccia D Pharmaceutics 06-Feb-2021
PMCID:PMC7915176
doi:10.3390/pharmaceutics13020230
PMID:33562128
Natural Products Targeting the Mitochondria in Cancers Yang Y, He PY, Zhang Y, Li N Molecules 28-Dec-2020
PMCID:PMC7795732
doi:10.3390/molecules26010092
PMID:33379233
A Review on Anti-Tumor Mechanisms of Coumarins Wu Y, Xu J, Liu Y, Zeng Y, Wu G Front Oncol 04-Dec-2020
PMCID:PMC7746827
doi:10.3389/fonc.2020.592853
PMID:33344242

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 / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
2,4-Dihydroxybenzoic acid 1491 Click to see C1=CC(=C(C=C1O)O)C(=O)O 154.12 unknown https://doi.org/10.1007/BF00565209
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
[(6R)-4,4,6-trimethylcyclohexen-1-yl]methyl (2R)-2-methylbutanoate 163105671 Click to see CCC(C)C(=O)OCC1=CCC(CC1C)(C)C 238.37 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.07.001
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(2'R,3S,3'S)-2'-[(Z,7S)-7,8-dihydroxy-4,8-dimethylnon-3-enyl]-3',8-dihydroxy-2'-methylspiro[1,4-benzodioxepine-3,5'-oxolane]-2,5-dione 163190338 Click to see CC(=CCCC1(C(CC2(O1)C(=O)OC3=C(C=CC(=C3)O)C(=O)O2)O)C)CCC(C(C)(C)O)O 464.50 unknown https://doi.org/10.1002/HLCA.200900350
1-Decanol 8174 Click to see CCCCCCCCCCO 158.28 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.07.001
2'-(7,8-Dihydroxy-4,8-dimethylnon-3-enyl)-3',8-dihydroxy-2'-methylspiro[1,4-benzodioxepine-3,5'-oxolane]-2,5-dione 162937929 Click to see CC(=CCCC1(C(CC2(O1)C(=O)OC3=C(C=CC(=C3)O)C(=O)O2)O)C)CCC(C(C)(C)O)O 464.50 unknown https://doi.org/10.1002/HLCA.200900350
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
1-Tetradecanol 8209 Click to see CCCCCCCCCCCCCCO 214.39 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.07.001
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(4E,8E)-1-(2,4-dihydroxyphenyl)-5,9,13-trimethyltetradeca-4,8,12-trien-1-one 10428364 Click to see CC(=CCCC(=CCCC(=CCCC(=O)C1=C(C=C(C=C1)O)O)C)C)C 356.50 unknown https://doi.org/10.1248/CPB.46.1781
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
[(2R)-5-methyl-2-prop-1-en-2-ylhex-4-enyl] 2-methylpropanoate 92004023 Click to see CC(C)C(=O)OCC(CC=C(C)C)C(=C)C 224.34 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.07.001
5-Methyl-2-(1-methylethenyl)-4-hexen-1-ol acetate 14268092 Click to see CC(=CCC(COC(=O)C)C(=C)C)C 196.29 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.07.001
beta-OCIMENE, (3E)- 5281553 Click to see CC(=CCC=C(C)C=C)C 136.23 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.07.001
beta-Ocimene, (3Z)- 5320250 Click to see CC(=CCC=C(C)C=C)C 136.23 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.07.001
Lavandulol 5464156 Click to see CC(=CCC(CO)C(=C)C)C 154.25 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.07.001
Lavandulol, (+/-)- 94060 Click to see CC(=CCC(CO)C(=C)C)C 154.25 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.07.001
Lavandulyl isobutyrate 527270 Click to see CC(C)C(=O)OCC(CC=C(C)C)C(=C)C 224.34 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.07.001
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.07.001
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
Sabinene 10887971 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.07.001
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-Terpinen-4-ol 2724161 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.07.001
Limonene, (+)- 440917 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.07.001
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.07.001
Terpinolene 11463 Click to see CC1=CCC(=C(C)C)CC1 136.23 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.07.001
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-delta-Cadinene 441005 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.07.001
(+)-Epicubenol 11831045 Click to see CC1CCC(C2C1(CCC(=C2)C)O)C(C)C 222.37 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.07.001
(+)-gamma-Bulgarene 12313023 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.07.001
(1R,2S,6S,7S,8R)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene 50919054 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.07.001
(1R,4S,4aS,8aR)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol 12302226 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.07.001
(1S,4S,4aS,8aS)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol 12302228 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.07.001
(3R,6E)-nerolidol 11241545 Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C 222.37 unknown https://doi.org/10.1248/CPB.46.1781
2-(3,8-Dimethyl-1,2,3,4,5,6,7,8-octahydroazulen-5-yl)propan-2-ol 521245 Click to see CC1CCC(CC2=C1CCC2C)C(C)(C)O 222.37 unknown https://doi.org/10.1007/BF00565209
beta-Bourbonene 62566 Click to see CC(C)C1CCC2(C1C3C2CCC3=C)C 204.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.07.001
Cadina-1(10),4-diene 10223 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.07.001
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.07.001
Guaiol 227829 Click to see CC1CCC(CC2=C1CCC2C)C(C)(C)O 222.37 unknown https://doi.org/10.1007/BF00565209
https://doi.org/10.1248/CPB.46.1781
Humulene 5281520 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.07.001
Nerolidol 8888 Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C 222.37 unknown https://doi.org/10.1248/CPB.46.1781
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aR,4aR,7S,7aS,7bR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 13854258 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.07.001
(1aR,4R,4aR,7R,7aR,7bS)-1,1,4,7-tetramethyl-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulen-4-ol 124305339 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.07.001
(7aR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 5321422 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.07.001
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Bicyclogermacrane and isolepidozane sesquiterpenoids
Bicyclogermacrene 13894537 Click to see CC1=CCCC(=CC2C(C2(C)C)CC1)C 204.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.07.001
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
Beta-Elemene 6918391 Click to see CC(=C)C1CCC(C(C1)C(=C)C)(C)C=C 204.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.07.001
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
(4aR,8aR)-4a,5-dimethyl-3-propan-2-ylidene-1,2,4,7,8,8a-hexahydronaphthalene 160195168 Click to see CC1=CCCC2C1(CC(=C(C)C)CC2)C 204.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.07.001
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
alpha-Selinene 10856614 Click to see CC1=CCCC2(C1CC(CC2)C(=C)C)C 204.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.07.001
beta-Selinene 442393 Click to see CC(=C)C1CCC2(CCCC(=C)C2C1)C 204.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.07.001
Neointermedeol 11877394 Click to see CC(=C)C1CCC2(CCCC(C2C1)(C)O)C 222.37 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.07.001
Pterodondiol 10879263 Click to see CC12CCCC(C1CC(CC2)C(C)(C)O)(C)O 240.38 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.07.001
Selin-11-en-4alpha-ol 15560330 Click to see CC(=C)C1CCC2(CCCC(C2C1)(C)O)C 222.37 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.07.001
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
Germacrene D 5317570 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.07.001
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(2'R,3S,3'S)-2'-[(3Z)-4,8-dimethylnona-3,7-dienyl]-3',8-dihydroxy-2'-methylspiro[1,4-benzodioxepine-3,5'-oxolane]-2,5-dione 163185160 Click to see CC(=CCCC(=CCCC1(C(CC2(O1)C(=O)OC3=C(C=CC(=C3)O)C(=O)O2)O)C)C)C 430.50 unknown https://doi.org/10.1002/HLCA.200900350
(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 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/10.1248/CPB.49.1072
(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/10.1248/CPB.49.1072
2'-(4,8-Dimethylnona-3,7-dienyl)-3',8-dihydroxy-2'-methylspiro[1,4-benzodioxepine-3,5'-oxolane]-2,5-dione 163039299 Click to see CC(=CCCC(=CCCC1(C(CC2(O1)C(=O)OC3=C(C=CC(=C3)O)C(=O)O2)O)C)C)C 430.50 unknown https://doi.org/10.1002/HLCA.200900350
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters
[(6S)-4,4,6-trimethylcyclohexen-1-yl]methyl 2-methylpropanoate 163105741 Click to see CC1CC(CC=C1COC(=O)C(C)C)(C)C 224.34 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.07.001
beta-Isocyclolavandulyl acetate 91750007 Click to see CC1CC(CC=C1COC(=O)C)(C)C 196.29 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.07.001
beta-Isocyclolavandulyl propionate 91750010 Click to see CCC(=O)OCC1=CCC(CC1C)(C)C 210.31 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.07.001
> Organic oxygen compounds / Organic oxides
beta-Cyclolavandulal 11105552 Click to see CC1=C(CCC(C1)(C)C)C=O 152.23 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.07.001
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Primary alcohols
[(6S)-4,4,6-trimethylcyclohexen-1-yl]methanol 163049349 Click to see CC1CC(CC=C1CO)(C)C 154.25 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.07.001
> Organoheterocyclic compounds / Benzodioxoles
Myristicin 4276 Click to see COC1=CC(=CC2=C1OCO2)CC=C 192.21 unknown https://doi.org/10.1248/CPB.46.1781
> Phenylpropanoids and polyketides / Coumarins and derivatives
(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/10.1248/CPB.50.675
(2S,3R)-7-hydroxy-2,3-dimethyl-2-[(E)-4-methyl-5-(4-methylfuran-2-yl)pent-3-enyl]-3H-furo[2,3-b]chromen-4-one 11132997 Click to see CC1C2=C(OC3=C(C2=O)C=CC(=C3)O)OC1(C)CCC=C(C)CC4=CC(=CO4)C 394.50 unknown https://doi.org/10.1248/CPB.50.675
(2S,3S)-7-hydroxy-2,3-dimethyl-2-[(E)-4-methyl-5-(4-methylfuran-2-yl)pent-3-enyl]-3H-furo[2,3-b]chromen-4-one 101165121 Click to see CC1C2=C(OC3=C(C2=O)C=CC(=C3)O)OC1(C)CCC=C(C)CC4=CC(=CO4)C 394.50 unknown https://doi.org/10.1248/CPB.50.675
2-(4,8-dimethylnona-3,7-dienyl)-7-hydroxy-2,3-dimethyl-3H-furo[2,3-b]chromen-4-one 162959943 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/10.1248/CPB.50.675
7-hydroxy-2,3-dimethyl-2-[4-methyl-5-(4-methylfuran-2-yl)pent-3-enyl]-3H-furo[2,3-b]chromen-4-one 162891161 Click to see CC1C2=C(OC3=C(C2=O)C=CC(=C3)O)OC1(C)CCC=C(C)CC4=CC(=CO4)C 394.50 unknown https://doi.org/10.1248/CPB.50.675

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