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Ferula fukanensis

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

Description Top

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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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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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No forms added yet.

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

Suggest others/fix!
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!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives
Trimethylbenzene 10686 Click to see CC1=C(C(=CC=C1)C)C 120.19 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Cumenes
2-Isopropyl-1-methoxy-4-methylbenzene 161716 Click to see CC1=CC(=C(C=C1)OC)C(C)C 164.24 unknown via CMAUP database
> Benzenoids / Phenol ethers / Anisoles
Estragole 8815 Click to see COC1=CC=C(C=C1)CC=C 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
Seychellene 519743 Click to see CC1CCC2(C(=C)C3CCC2(C1C3)C)C 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
(E,Z)-2,6-Dimethylocta-2,4,6-triene 5371125 Click to see CC=C(C)C=CC=C(C)C 136.23 unknown via CMAUP database
2,6-Dimethylocta-2,6-diene 137614 Click to see CC=C(C)CCC=C(C)C 138.25 unknown via CMAUP database
2,6-Octadiene, 2,6-dimethyl- 5365898 Click to see CC=C(C)CCC=C(C)C 138.25 unknown via CMAUP database
beta-OCIMENE, (3E)- 5281553 Click to see CC(=CCC=C(C)C=C)C 136.23 unknown via CMAUP database
beta-Ocimene, (3Z)- 5320250 Click to see CC(=CCC=C(C)C=C)C 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
p-CYMENE 7463 Click to see CC1=CC=C(C=C1)C(C)C 134.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-Camphene 440966 Click to see CC1(C2CCC(C2)C1=C)C 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
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown via CMAUP database
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 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 CC1(C2CCC(C2)C1=C)C 136.23 unknown via CMAUP database
Longifolene-(V4) 570529 Click to see CC1(CC=CC2(C3C1CC2(CC3)C)C)C 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
alpha-Terpinene 7462 Click to see CC1=CC=C(CC1)C(C)C 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(-)-Hinesol 10878761 Click to see CC1CCC=C(C12CCC(C2)C(C)(C)O)C 222.37 unknown via CMAUP database
(+)-beta-Caryophyllene 20831623 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown via CMAUP database
(2S,5R,10R)-alpha,alpha,6,10-Tetramethylspiro[4.5]dec-6-ene-2-methanol 10059437 Click to see CC1CCC=C(C12CCC(C2)C(C)(C)O)C 222.37 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
(E)-beta-farnesene 10407 Click to see CC(=CCCC(=CCCC(=C)C=C)C)C 204.35 unknown via CMAUP database
(Z)-caryophyllene 6429301 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown via CMAUP database
1-Methyl-4-(1-methylethylidene)-2-(1-methylvinyl)-1-vinylcyclohexane 94254 Click to see CC(=C1CCC(C(C1)C(=C)C)(C)C=C)C 204.35 unknown via CMAUP database
2-[(3r,5s,8r)-3,8-Dimethyl-1,2,3,4,5,6,7,8-octahydroazulen-5-yl]propan-2-ol 72607 Click to see CC1CCC(CC2=C1CCC2C)C(C)(C)O 222.37 unknown via CMAUP database
2-[(3R,6S)-6,10-dimethylspiro[4.5]dec-9-en-3-yl]propan-2-ol 161437 Click to see CC1CCC=C(C12CCC(C2)C(C)(C)O)C 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
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 CC1=CCCC(=C)C2CC(C2CC1)(C)C 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
Guaiol 227829 Click to see CC1CCC(CC2=C1CCC2C)C(C)(C)O 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
Isocaryophyllene 5281522 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 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 CC1=CC2C(=C(CCCC2(C)C)C)CC1 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 CC1=CC2C(=C(CCCC2(C)C)C)CC1 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 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
(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 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
(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/10.1021/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 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
(2R)-2alpha-[(3E)-4,8-Dimethyl-3,7-nonadienyl]-2,3alpha-dimethyl-7-hydroxy-2,3-dihydro-4H-furo[3,2-c][1]benzopyran-4-one 10970990 Click to see CC1C2=C(C3=C(C=C(C=C3)O)OC2=O)OC1(C)CCC=C(C)CCC=C(C)C 382.50 unknown via CMAUP database
(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 CC1C2=C(C3=C(C=C(C=C3)O)OC2=O)OC1(C)CCC=C(C)CCC=C(C)C 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 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
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 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
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 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
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 CC(C1=CC2=C(C=C(C=C2)O)OC1=O)C(=CCC=C(C)CC(=O)C=C(C)C)C 380.50 unknown https://doi.org/10.1021/NP030408K
Fukanedone A 11315966 Click to see CC1C(C(=O)OC1(C)CCC=C(C)CCC=C(C)C)C(=O)C2=C(C=C(C=C2)OC)O 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 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/10.1248/CPB.52.1215
Fukanemarin B 54717251 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/10.1021/NP030408K
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
3-(Methylthio)-2-butanone 103788 Click to see CC(C(=O)C)SC 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 COC1=CC2=C(C(=C1)OC)C(=O)C=C(O2)CC3=CC=CC=C3 296.30 unknown https://doi.org/10.1021/NP030408K
> Organoheterocyclic compounds / Oxanes
Rose oxide 27866 Click to see CC1CCOC(C1)C=C(C)C 154.25 unknown via CMAUP database
> Organosulfur compounds / Organic disulfides / Dialkyldisulfides
Dipropyl disulfide 12377 Click to see CCCSSCCC 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 CCC(C)SSCC 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 CCC(=S)N 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 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
(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 CC1C2=C(OC3=C(C2=O)C=CC(=C3)O)OC1(C)CCCC(=CC(=O)C=C(C)C)C 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 CC1C2=C(OC3=C(C2=O)C=CC(=C3)O)OC1(C)CCCC(=CC(=O)C=C(C)C)C 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 CCN(CC)C1=CC2=C(C=C1)C=C(C(=O)O2)C3=NC4=CC=CC=C4S3 350.40 unknown https://doi.org/10.1021/NP030408K
Fukanefurochromone A 11326931 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 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 CC1C2=C(OC3=C(C2=O)C=CC(=C3)O)OC1(C)CCCC(=CC(=O)C=C(C)C)C 396.50 unknown https://doi.org/10.1021/NP058079E
Fukanefurochromone D 11953542 Click to see CC1C2=C(OC3=C(C2=O)C=CC(=C3)O)OC1(C)CCCC(=CC(=O)C=C(C)C)C 396.50 unknown https://doi.org/10.1021/NP058079E
Fukanefurochromone E 44584257 Click to see CC1C2=C(OC3=C(C2=O)C=CC(=C3)O)OC1(C)CCCC(=CC(=O)C=C(C)C)C 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 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 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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