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Daphne odora

Daphne odora - 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 UUID644015bfd8b45214954463
Scientific name Daphne odora
Authority Thunb.
First published in Syst. Veg., ed. 14 (J. A. Murray). 372. 1784 [May-Jun 1784]

Description Top

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Synonyms Top

Scientific name Authority First published in
Daphne chinensis Spreng. Syst. Veg. 2: 237 (1825)
Daphne indica Loisel. Herb. Amat. ii. t. 105.
Daphne japonica Thunb. Mus. Nat. Acad. Upsal. 13: 106 (1792)
Daphne mazelii Carrière Rev. Hort. (Paris) 44: 392 (1872)
Daphne odora var. leucantha Makino Bot. Mag. (Tokyo) 23: 70 1909
Daphne odora f. leucantha (Makino) Yong J.Li Fl. Coreana 5: 63 (1998).
Daphne odora f. marginata (Miq.) Makino Bot. Mag. (Tokyo) 23: 69 1909
Daphne odora var. rosacea Makino J. Jap. Bot. 5: 46 1928
Daphne sinensis Lam. Encycl. 3: 438 (1792)
Daphne triflora Lour. Fl. Cochinch. : 236 (1790)
Daphne kiusiana var. odora (Thunb.) Makino Bot. Mag. (Tokyo) 6: 52 1892
Daphne odora f. alba (Hemsl.) H.Hara Enum. Sperm. Jap. 3: 232 1954
Daphne odora f. rosacea (Makino) H.Hara Enum. Sperm. Jap. 3: 233 1954
Daphne odora var. alba Hemsl. Garden (London 1871-1927) 14: 442 1878
Daphne odora var. macrantha Franch. ex Lecomte Notul. Syst. (Paris) 3: 216 1916
Daphne odora var. marginata Miq. Ann. Mus. Bot. Lugduno-Batavi 3: 133 1867
Daphne odora var. mazelii (Carrière) Hemsl. Garden (London 1871-1927) 14: 442 1878
Daphne odora var. punctata Hemsl. Garden (London 1871-1927) 14: 442 1878
Daphne odora var. rubra Hemsl. Garden (London 1871-1927) 14: 442 1878
Daphne odora var. variegata Bean Trees Shrubs Brit. Isl. 1: 472 1914
Daphne speciosissima Carrière Rev. Hort. 1867: 300 1867
Daphne jejudoensis M.Kim Korean J. Pl. Taxon. 43: 95 (2013)

Common names Top

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Language Common/alternative name
Arabic دفنة ذات رائحة
Bulgarian ароматно бясно дърво
Persian میخک هندی
gan 金邊瑞香
Italian dahpne odora
Japanese ジンチョウゲ
Japanese チンチョウゲ
Japanese 沈丁花
Japanese 金辺瑞香
Korean 서향
Korean 서향나무
lzh 瑞香
Russian Волчеягодник душистый
Vietnamese thụy hương
Chinese 风流树
Chinese 露甲
Chinese 蓬莱花
Chinese 蓬莱紫
Chinese 睡香
Chinese 瑞兰
Chinese 沈丁花
Chinese 夺皮香
Chinese 千里香
Chinese 铜牛皮
Chinese 铁牛皮
Chinese 瑞香花
Chinese 瑞香根
Chinese 瑞香叶
Chinese 瑞香

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-0000637782
UNII 00OI587YQE
Tropicos 50177137
KEW urn:lsid:ipni.org:names:831309-1
The Plant List kew-2757136
Missouri Botanical Garden 292288
PFAF Daphne odora
Open Tree Of Life 5747002
NCBI Taxonomy 329675
IPNI 927343-1
iNaturalist 126930
GBIF 7311546
Freebase /m/02q292_
EPPO DAPOD
USDA GRIN 13276
Wikipedia Daphne_odora
CMAUP NPO4035

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
A new versatile peroxidase with extremophilic traits over-produced in MicroTom cell cultures Gogliettino M, Cocca E, Apone F, Del Prete S, Balestrieri M, Mirino S, Arciello S, Palmieri G Sci Rep 15-Sep-2023
PMCID:PMC10504257
doi:10.1038/s41598-023-42597-x
PMID:37714949
Advances of the small molecule drugs regulating fibroblast-like synovial proliferation for rheumatoid arthritis Tong Y, Li X, Deng Q, Shi J, Feng Y, Bai L Front Pharmacol 21-Jul-2023
PMCID:PMC10400780
doi:10.3389/fphar.2023.1230293
PMID:37547337
Spiro-Flavonoids in Nature: A Critical Review of Structural Diversity and Bioactivity Pecio Ł, Pecio S, Mroczek T, Oleszek W Molecules 14-Jul-2023
PMCID:PMC10385819
doi:10.3390/molecules28145420
PMID:37513292
Diversity and traditional knowledge of medicinal plants used by Shui people in Southwest China Liu S, Zhang B, Lei Q, Zhou J, Ali M, Long C J Ethnobiol Ethnomed 30-May-2023
PMCID:PMC10230803
doi:10.1186/s13002-023-00594-4
PMID:37254191
Natural Coumarin Derivatives Activating Nrf2 Signaling Pathway as Lead Compounds for the Design and Synthesis of Intestinal Anti-Inflammatory Drugs Di Stasi LC Pharmaceuticals (Basel) 30-Mar-2023
PMCID:PMC10142712
doi:10.3390/ph16040511
PMID:37111267
Methyl vanillate for inhibiting the proliferation, migration, and epithelial-mesenchymal transition of ovarian cancer cells via the ZEB2/Snail signaling pathway Wang L, Miao Y, Wen J, Cheng J, Wen Q, Zhao Z, Wu J Transl Cancer Res 27-Mar-2023
PMCID:PMC10174767
doi:10.21037/tcr-22-2240
PMID:37180664
Antioxidant Potential-Rich Betel Leaves (Piper betle L.) Exert Depigmenting Action by Triggering Autophagy and Downregulating MITF/Tyrosinase In Vitro and In Vivo Alam MB, Park NH, Song BR, Lee SH Antioxidants (Basel) 03-Feb-2023
PMCID:PMC9952209
doi:10.3390/antiox12020374
PMID:36829933
Natural Products as Anticancer Agents: Current Status and Future Perspectives Naeem A, Hu P, Yang M, Zhang J, Liu Y, Zhu W, Zheng Q Molecules 30-Nov-2022
PMCID:PMC9737905
doi:10.3390/molecules27238367
PMID:36500466
Lead/Drug Discovery from Natural Resources Xu Z, Eichler B, Klausner EA, Duffy-Matzner J, Zheng W Molecules 28-Nov-2022
PMCID:PMC9736696
doi:10.3390/molecules27238280
PMID:36500375
Screening of traditional Chinese medicine monomers as ribonucleotide reductase M2 inhibitors for tumor treatment Qin YY, Feng S, Zhang XD, Peng B World J Clin Cases 06-Nov-2022
PMCID:PMC9649558
doi:10.12998/wjcc.v10.i31.11299
PMID:36387821
Plants in vitro propagation with its applications in food, pharmaceuticals and cosmetic industries; current scenario and future approaches Hasnain A, Naqvi SA, Ayesha SI, Khalid F, Ellahi M, Iqbal S, Hassan MZ, Abbas A, Adamski R, Markowska D, Baazeem A, Mustafa G, Moustafa M, Hasan ME, Abdelhamid MM Front Plant Sci 13-Oct-2022
PMCID:PMC9606719
doi:10.3389/fpls.2022.1009395
PMID:36311115
Traditional Chinese Medicine Regulates Th17/Treg Balance in Treating Inflammatory Bowel Disease Xie F, Xiong Q, Li Y, Yao C, Wu R, Wang Q, Luo L, Liu H, Feng P Evid Based Complement Alternat Med 15-Sep-2022
PMCID:PMC9499767
doi:10.1155/2022/6275136
PMID:36159571
Potential Utility of Natural Products against Oxidative Stress in Animal Models of Multiple Sclerosis Zha Z, Liu S, Liu Y, Li C, Wang L Antioxidants (Basel) 29-Jul-2022
PMCID:PMC9404913
doi:10.3390/antiox11081495
PMID:36009214
Daphne odora Exerts Depigmenting Effects via Inhibiting CREB/MITF and Activating AKT/ERK-Signaling Pathways Eom YS, Jeong D, Ryu AR, Song KH, Im DS, Lee MY Curr Issues Mol Biol 22-Jul-2022
PMCID:PMC9332310
doi:10.3390/cimb44080228
PMID:35892714
7,8-Dihydroxycoumarin Alleviates Synaptic Loss by Activated PI3K-Akt-CREB-BDNF Signaling in Alzheimer’s Disease Model Mice Yan L, Jin Y, Pan J, He X, Zhong S, Zhang R, Choi L, Su W, Chen J J Agric Food Chem 03-Jun-2022
PMCID:PMC9204815
doi:10.1021/acs.jafc.2c02140
PMID:35657168

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
Phenylethyl Alcohol 6054 Click to see C1=CC=C(C=C1)CCO 122.16 unknown https://doi.org/10.1271/BBB1961.47.483
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
Benzyl Benzoate 2345 Click to see C1=CC=C(C=C1)COC(=O)C2=CC=CC=C2 212.24 unknown https://doi.org/10.1271/BBB1961.47.483
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters / o-Hydroxybenzoic acid esters
Benzyl salicylate 8363 Click to see C1=CC=C(C=C1)COC(=O)C2=CC=CC=C2O 228.24 unknown https://doi.org/10.1271/BBB1961.47.483
Methyl Salicylate 4133 Click to see COC(=O)C1=CC=CC=C1O 152.15 unknown https://doi.org/10.1271/BBB1961.47.483
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown https://doi.org/10.1007/S10600-009-9389-8
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
Benzaldehyde 240 Click to see C1=CC=C(C=C1)C=O 106.12 unknown https://doi.org/10.1271/BBB1961.47.483
> Benzenoids / Benzene and substituted derivatives / Benzyl alcohols
Benzyl Alcohol 244 Click to see C1=CC=C(C=C1)CO 108.14 unknown https://doi.org/10.1271/BBB1961.47.483
> Benzenoids / Benzene and substituted derivatives / Benzyloxycarbonyls
Benzyl acetate 8785 Click to see CC(=O)OCC1=CC=CC=C1 150.17 unknown https://doi.org/10.1271/BBB1961.47.483
> Benzenoids / Benzene and substituted derivatives / Phenylacetaldehydes
Phenylacetaldehyde 998 Click to see C1=CC=C(C=C1)CC=O 120.15 unknown https://doi.org/10.1271/BBB1961.47.483
> Benzenoids / Benzene and substituted derivatives / Styrenes
4-Vinylphenol 62453 Click to see C=CC1=CC=C(C=C1)O 120.15 unknown https://doi.org/10.1271/BBB1961.47.483
> Benzenoids / Naphthalenes
Naphthalene 931 Click to see C1=CC=C2C=CC=CC2=C1 128.17 unknown https://doi.org/10.1271/BBB1961.47.483
> Benzenoids / Phenols / 1-hydroxy-4-unsubstituted benzenoids
Phenol 996 Click to see C1=CC=C(C=C1)O 94.11 unknown https://doi.org/10.1271/BBB1961.47.483
> Benzenoids / Phenols / Cresols / Meta cresols
m-Cresol 342 Click to see CC1=CC(=CC=C1)O 108.14 unknown https://doi.org/10.1271/BBB1961.47.483
> Benzenoids / Phenols / Cresols / Ortho cresols
o-Cresol 335 Click to see CC1=CC=CC=C1O 108.14 unknown https://doi.org/10.1271/BBB1961.47.483
> Benzenoids / Phenols / Cresols / Para cresols
P-Cresol 2879 Click to see CC1=CC=C(C=C1)O 108.14 unknown https://doi.org/10.1271/BBB1961.47.483
> Benzenoids / Phenols / Methoxyphenols
2-Methoxy-4-methylphenol 7144 Click to see CC1=CC(=C(C=C1)O)OC 138.16 unknown https://doi.org/10.1271/BBB1961.47.483
2-Methoxy-5-methylphenol 14519 Click to see CC1=CC(=C(C=C1)OC)O 138.16 unknown https://doi.org/10.1271/BBB1961.47.483
Guaiacol 460 Click to see COC1=CC=CC=C1O 124.14 unknown https://doi.org/10.1271/BBB1961.47.483
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Docosane 12405 Click to see CCCCCCCCCCCCCCCCCCCCCC 310.60 unknown https://doi.org/10.1271/BBB1961.47.483
Heneicosane 12403 Click to see CCCCCCCCCCCCCCCCCCCCC 296.60 unknown https://doi.org/10.1271/BBB1961.47.483
Heptacosane 11636 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCC 380.70 unknown https://doi.org/10.1271/BBB1961.47.483
Hexacosane 12407 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCC 366.70 unknown https://doi.org/10.1271/BBB1961.47.483
Hexadecane 11006 Click to see CCCCCCCCCCCCCCCC 226.44 unknown https://doi.org/10.1271/BBB1961.47.483
Nonacosane 12409 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCC 408.80 unknown https://doi.org/10.1271/BBB1961.47.483
Nonadecane 12401 Click to see CCCCCCCCCCCCCCCCCCC 268.50 unknown https://doi.org/10.1271/BBB1961.47.483
Octacosane 12408 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCC 394.80 unknown https://doi.org/10.1271/BBB1961.47.483
Octadecane 11635 Click to see CCCCCCCCCCCCCCCCCC 254.50 unknown https://doi.org/10.1271/BBB1961.47.483
Pentacosane 12406 Click to see CCCCCCCCCCCCCCCCCCCCCCCCC 352.70 unknown https://doi.org/10.1271/BBB1961.47.483
Pentadecane 12391 Click to see CCCCCCCCCCCCCCC 212.41 unknown https://doi.org/10.1271/BBB1961.47.483
Tetracosane 12592 Click to see CCCCCCCCCCCCCCCCCCCCCCCC 338.70 unknown https://doi.org/10.1271/BBB1961.47.483
Tetradecane 12389 Click to see CCCCCCCCCCCCCC 198.39 unknown https://doi.org/10.1271/BBB1961.47.483
Tricosane 12534 Click to see CCCCCCCCCCCCCCCCCCCCCCC 324.60 unknown https://doi.org/10.1271/BBB1961.47.483
Undecane 14257 Click to see CCCCCCCCCCC 156.31 unknown https://doi.org/10.1271/BBB1961.47.483
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Octatriene, dimethyl- 6434062 Click to see CC(C)C=CC=C(C)C=C 136.23 unknown https://doi.org/10.1271/BBB1961.47.483
> Hydrocarbons / Unsaturated hydrocarbons / Unsaturated aliphatic hydrocarbons
1-Docosene 74138 Click to see CCCCCCCCCCCCCCCCCCCCC=C 308.60 unknown https://doi.org/10.1271/BBB1961.47.483
1-Eicosene 18936 Click to see CCCCCCCCCCCCCCCCCCC=C 280.50 unknown https://doi.org/10.1271/BBB1961.47.483
1-Hexadecene 12395 Click to see CCCCCCCCCCCCCCC=C 224.42 unknown https://doi.org/10.1271/BBB1961.47.483
1-Octadecene 8217 Click to see CCCCCCCCCCCCCCCCC=C 252.50 unknown https://doi.org/10.1271/BBB1961.47.483
> Lignans, neolignans and related compounds / Coumarinolignans
Daphneticin 158341 Click to see COC1=CC(=CC(=C1O)OC)C2C(OC3=C(O2)C=CC4=C3OC(=O)C=C4)CO 386.40 unknown https://doi.org/10.1248/CPB.34.595
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
(-)-Lariciresinol 23815394 Click to see COC1=C(C=CC(=C1)CC2COC(C2CO)C3=CC(=C(C=C3)O)OC)O 360.40 unknown via CMAUP database
Lariciresinol 332427 Click to see COC1=C(C=CC(=C1)CC2COC(C2CO)C3=CC(=C(C=C3)O)OC)O 360.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Lignan glycosides
3-hydroxy-3-[(4-hydroxy-3-methoxyphenyl)methyl]-4-[[3-methoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methyl]oxolan-2-one 5320221 Click to see COC1=C(C=CC(=C1)CC2COC(=O)C2(CC3=CC(=C(C=C3)O)OC)O)OC4C(C(C(C(O4)CO)O)O)O 536.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Ethyl palmitate 12366 Click to see CCCCCCCCCCCCCCCC(=O)OCC 284.50 unknown https://doi.org/10.1271/BBB1961.47.483
Ethyl tetradecanoate 31283 Click to see CCCCCCCCCCCCCC(=O)OCC 256.42 unknown https://doi.org/10.1271/BBB1961.47.483
Propyl palmitate 75232 Click to see CCCCCCCCCCCCCCCC(=O)OCCC 298.50 unknown https://doi.org/10.1271/BBB1961.47.483
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters
Methyl nonanoate 15606 Click to see CCCCCCCCC(=O)OC 172.26 unknown https://doi.org/10.1271/BBB1961.47.483
Methyl octanoate 8091 Click to see CCCCCCCC(=O)OC 158.24 unknown https://doi.org/10.1271/BBB1961.47.483
Methyl palmitate 8181 Click to see CCCCCCCCCCCCCCCC(=O)OC 270.50 unknown https://doi.org/10.1271/BBB1961.47.483
Methyl Stearate 8201 Click to see CCCCCCCCCCCCCCCCCC(=O)OC 298.50 unknown https://doi.org/10.1271/BBB1961.47.483
Methyl tetradecanoate 31284 Click to see CCCCCCCCCCCCCC(=O)OC 242.40 unknown https://doi.org/10.1271/BBB1961.47.483
Methyl undecanoate 15607 Click to see CCCCCCCCCCC(=O)OC 200.32 unknown https://doi.org/10.1271/BBB1961.47.483
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Wax esters / Wax monoesters
Citronellyl myristate 85793156 Click to see CCCCCCCCCCCCCC(=O)OCCC(C)CCC=C(C)C 366.60 unknown https://doi.org/10.1271/BBB1961.47.483
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Myristic Acid 11005 Click to see CCCCCCCCCCCCCC(=O)O 228.37 unknown https://doi.org/10.1271/BBB1961.47.483
Palmitic Acid 985 Click to see CCCCCCCCCCCCCCCC(=O)O 256.42 unknown https://doi.org/10.1271/BBB1961.47.483
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Capric Acid 2969 Click to see CCCCCCCCCC(=O)O 172.26 unknown https://doi.org/10.1271/BBB1961.47.483
Caproic Acid 8892 Click to see CCCCCC(=O)O 116.16 unknown https://doi.org/10.1271/BBB1961.47.483
Heptanoic Acid 8094 Click to see CCCCCCC(=O)O 130.18 unknown https://doi.org/10.1271/BBB1961.47.483
Nonanoic acid 8158 Click to see CCCCCCCCC(=O)O 158.24 unknown https://doi.org/10.1271/BBB1961.47.483
Octanoic acid 379 Click to see CCCCCCCC(=O)O 144.21 unknown https://doi.org/10.1271/BBB1961.47.483
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Citronellyl acetate 9017 Click to see CC(CCC=C(C)C)CCOC(=O)C 198.30 unknown https://doi.org/10.1271/BBB1961.47.483
Citronellyl formate 7778 Click to see CC(CCC=C(C)C)CCOC=O 184.27 unknown https://doi.org/10.1271/BBB1961.47.483
Geranyl acetate 1549026 Click to see CC(=CCCC(=CCOC(=O)C)C)C 196.29 unknown https://doi.org/10.1271/BBB1961.47.483
Geranyl formate 5282109 Click to see CC(=CCCC(=CCOC=O)C)C 182.26 unknown https://doi.org/10.1271/BBB1961.47.483
Neryl acetate 1549025 Click to see CC(=CCCC(=CCOC(=O)C)C)C 196.29 unknown https://doi.org/10.1271/BBB1961.47.483
Neryl formate 5354882 Click to see CC(=CCCC(=CCOC=O)C)C 182.26 unknown https://doi.org/10.1271/BBB1961.47.483
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Hexanol 8103 Click to see CCCCCCO 102.17 unknown https://doi.org/10.1271/BBB1961.47.483
1-Octanol 957 Click to see CCCCCCCCO 130.23 unknown https://doi.org/10.1271/BBB1961.47.483
1-Octen-3-OL 18827 Click to see CCCCCC(C=C)O 128.21 unknown https://doi.org/10.1271/BBB1961.47.483
2-Octanol 20083 Click to see CCCCCCC(C)O 130.23 unknown https://doi.org/10.1271/BBB1961.47.483
6-Methylhept-5-en-2-ol 20745 Click to see CC(CCC=C(C)C)O 128.21 unknown https://doi.org/10.1271/BBB1961.47.483
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
Stearyl Alcohol 8221 Click to see CCCCCCCCCCCCCCCCCCO 270.50 unknown https://doi.org/10.1271/BBB1961.47.483
> Lipids and lipid-like molecules / Fatty Acyls / Fatty aldehydes
Octadecanal 12533 Click to see CCCCCCCCCCCCCCCCCC=O 268.50 unknown https://doi.org/10.1271/BBB1961.47.483
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Ethyl Linoleate 5282184 Click to see CCCCCC=CCC=CCCCCCCCC(=O)OCC 308.50 unknown https://doi.org/10.1271/BBB1961.47.483
Ethyl linolenate 5367460 Click to see CCC=CCC=CCC=CCCCCCCCC(=O)OCC 306.50 unknown https://doi.org/10.1271/BBB1961.47.483
Methyl elaidolinolenate 5367462 Click to see CCC=CCC=CCC=CCCCCCCCC(=O)OC 292.50 unknown https://doi.org/10.1271/BBB1961.47.483
Methyl linoleate 5284421 Click to see CCCCCC=CCC=CCCCCCCCC(=O)OC 294.50 unknown https://doi.org/10.1271/BBB1961.47.483
Methyl linolenate 5319706 Click to see CCC=CCC=CCC=CCCCCCCCC(=O)OC 292.50 unknown https://doi.org/10.1271/BBB1961.47.483
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
3,7,11,15-Tetramethyl-2-hexadecen-1-OL 5366244 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown https://doi.org/10.1271/BBB1961.47.483
3,7,11,15-Tetramethylhexadec-2-EN-1-YL acetate 6428538 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCOC(=O)C)C 338.60 unknown https://doi.org/10.1271/BBB1961.47.483
6,10,14-Trimethylpentadeca-5,9,13-trien-2-one 61206 Click to see CC(=CCCC(=CCCC(=CCCC(=O)C)C)C)C 262.40 unknown https://doi.org/10.1271/BBB1961.47.483
Farnesylacetone 1711945 Click to see CC(=CCCC(=CCCC(=CCCC(=O)C)C)C)C 262.40 unknown https://doi.org/10.1271/BBB1961.47.483
Phytol 5280435 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown https://doi.org/10.1271/BBB1961.47.483
Phytyl acetate 637195 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCOC(=O)C)C 338.60 unknown https://doi.org/10.1271/BBB1961.47.483
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Rhamnofolane and daphnane diterpenoids
[(1R,2R,6S,7S,8R,10S,11S,12R,14S,16S,17R,18R)-6,7-dihydroxy-8-(hydroxymethyl)-16-isopropenyl-4,18-dimethyl-14-[(1E,3E,5E)-nona-1,3,5-trienyl]-5-oxo-9,13,15,19-tetraoxahexacyclo[12.4.1.01,11.02,6.08,10.012,16]nonadec-3-en-17-yl] benzoate 162650645 Click to see CCCC=CC=CC=CC12OC3C4C5C(O5)(C(C6(C(C4(O1)C(C(C3(O2)C(=C)C)OC(=O)C7=CC=CC=C7)C)C=C(C6=O)C)O)O)CO 646.70 unknown https://doi.org/10.1271/BBB1961.46.2605
[(1R,2R,6S,7S,8R,10S,11S,12R,14S,16S,17R,18R)-6,7-dihydroxy-8-(hydroxymethyl)-16-isopropenyl-4,18-dimethyl-14-[(1E,3E)-nona-1,3-dienyl]-5-oxo-9,13,15,19-tetraoxahexacyclo[12.4.1.01,11.02,6.08,10.012,16]nonadec-3-en-17-yl] (E)-3-phenylprop-2-enoate 162671169 Click to see CCCCCC=CC=CC12OC3C4C5C(O5)(C(C6(C(C4(O1)C(C(C3(O2)C(=C)C)OC(=O)C=CC7=CC=CC=C7)C)C=C(C6=O)C)O)O)CO 674.80 unknown https://doi.org/10.1271/BBB1961.46.2605
[(1R,2R,6S,7S,8R,10S,11S,12R,14S,16S,17R,18R)-6,7-dihydroxy-8-(hydroxymethyl)-4,18-dimethyl-5-oxo-14-phenyl-16-prop-1-en-2-yl-9,13,15,19-tetraoxahexacyclo[12.4.1.01,11.02,6.08,10.012,16]nonadec-3-en-17-yl] (2E,4E,6Z)-deca-2,4,6-trienoate 163195074 Click to see CCCC=CC=CC=CC(=O)OC1C(C23C4C=C(C(=O)C4(C(C5(C(C2C6C1(OC(O6)(O3)C7=CC=CC=C7)C(=C)C)O5)CO)O)O)C)C 646.70 unknown https://doi.org/10.1271/BBB1961.46.2605
[(2R,6S,7S,8R,10S,11S,17R,18R)-6,7-dihydroxy-8-(hydroxymethyl)-4,18-dimethyl-5-oxo-14-phenyl-16-prop-1-en-2-yl-9,13,15,19-tetraoxahexacyclo[12.4.1.01,11.02,6.08,10.012,16]nonadec-3-en-17-yl] (2E,4E,6E)-deca-2,4,6-trienoate 46905268 Click to see CCCC=CC=CC=CC(=O)OC1C(C23C4C=C(C(=O)C4(C(C5(C(C2C6C1(OC(O6)(O3)C7=CC=CC=C7)C(=C)C)O5)CO)O)O)C)C 646.70 unknown via CMAUP database
[15-Deca-2,4-dienoyloxy-5,6,11,14-tetrahydroxy-4-(hydroxymethyl)-8,12-dimethyl-7-oxo-14-prop-1-en-2-yl-3-oxatetracyclo[9.4.0.02,4.06,10]pentadec-8-en-13-yl] benzoate 75216382 Click to see CCCCCC=CC=CC(=O)OC1C2C3C(O3)(C(C4(C(C2(C(C(C1(C(=C)C)O)OC(=O)C5=CC=CC=C5)C)O)C=C(C4=O)C)O)O)CO 666.80 unknown https://doi.org/10.1271/BBB1961.46.2605
[6,7-Dihydroxy-8-(hydroxymethyl)-4,18-dimethyl-14-nona-1,3-dienyl-5-oxo-16-prop-1-en-2-yl-9,13,15,19-tetraoxahexacyclo[12.4.1.01,11.02,6.08,10.012,16]nonadec-3-en-17-yl] 3-phenylprop-2-enoate 162950540 Click to see CCCCCC=CC=CC12OC3C4C5C(O5)(C(C6(C(C4(O1)C(C(C3(O2)C(=C)C)OC(=O)C=CC7=CC=CC=C7)C)C=C(C6=O)C)O)O)CO 674.80 unknown https://doi.org/10.1271/BBB1961.46.2605
[6,7-Dihydroxy-8-(hydroxymethyl)-4,18-dimethyl-14-nona-1,3,5-trienyl-5-oxo-16-prop-1-en-2-yl-9,13,15,19-tetraoxahexacyclo[12.4.1.01,11.02,6.08,10.012,16]nonadec-3-en-17-yl] benzoate 162861794 Click to see CCCC=CC=CC=CC12OC3C4C5C(O5)(C(C6(C(C4(O1)C(C(C3(O2)C(=C)C)OC(=O)C7=CC=CC=C7)C)C=C(C6=O)C)O)O)CO 646.70 unknown https://doi.org/10.1271/BBB1961.46.2605
Gnidilatidin 429656 Click to see CCCCCC=CC=CC12OC3C4C5C(O5)(C(C6(C(C4(O1)C(C(C3(O2)C(=C)C)OC(=O)C7=CC=CC=C7)C)C=C(C6=O)C)O)O)CO 648.70 unknown https://doi.org/10.1271/BBB1961.46.2605
https://doi.org/10.1080/00021369.1976.10862367
Yuanhuacin 6440205 Click to see CCCCCC=CC=CC12OC3C4C5C(O5)(C(C6(C(C4(O1)C(C(C3(O2)C(=C)C)OC(=O)C7=CC=CC=C7)C)C=C(C6=O)C)O)O)CO 648.70 unknown via CMAUP database
Yuanhuacine 5358691 Click to see CCCCCC=CC=CC12OC3C4C5C(O5)(C(C6(C(C4(O1)C(C(C3(O2)C(=C)C)OC(=O)C7=CC=CC=C7)C)C=C(C6=O)C)O)O)CO 648.70 unknown https://doi.org/10.1271/BBB1961.46.2605
https://doi.org/10.1080/00021369.1976.10862367
Yuanhuaoate E 73348817 Click to see CCCCCC=CC=CC(=O)OC1C2C3C(O3)(C(C4(C(C2(C(C(C1(C(=C)C)O)OC(=O)C5=CC=CC=C5)C)O)C=C(C4=O)C)O)O)CO 666.80 unknown https://doi.org/10.1271/BBB1961.46.2605
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
(2E,6E)-3,7-dimethylnona-2,6-dienoic acid 21561550 Click to see CCC(=CCCC(=CC(=O)O)C)C 182.26 unknown https://doi.org/10.1271/BBB1961.47.483
beta-CITRONELLOL, (+/-)- 8842 Click to see CC(CCC=C(C)C)CCO 156.26 unknown https://doi.org/10.1271/BBB1961.47.483
beta-OCIMENE, (3E)- 5281553 Click to see CC(=CCC=C(C)C=C)C 136.23 unknown https://doi.org/10.1271/BBB1961.47.483
Citral 638011 Click to see CC(=CCCC(=CC=O)C)C 152.23 unknown https://doi.org/10.1271/BBB1961.47.483
Citronellal 7794 Click to see CC(CCC=C(C)C)CC=O 154.25 unknown https://doi.org/10.1271/BBB1961.47.483
Citronellic acid 10402 Click to see CC(CCC=C(C)C)CC(=O)O 170.25 unknown https://doi.org/10.1271/BBB1961.47.483
Geranic acid 5275520 Click to see CC(=CCCC(=CC(=O)O)C)C 168.23 unknown https://doi.org/10.1271/BBB1961.47.483
Geraniol 637566 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1271/BBB1961.47.483
Geranylacetone 1549778 Click to see CC(=CCCC(=CCCC(=O)C)C)C 194.31 unknown https://doi.org/10.1271/BBB1961.47.483
Isogeraniol 5362876 Click to see CC(=CCC=C(C)CCO)C 154.25 unknown https://doi.org/10.1271/BBB1961.47.483
Linalool, (+/-)- 6549 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown https://doi.org/10.1271/BBB1961.47.483
Linalyl acetate 8294 Click to see CC(=CCCC(C)(C=C)OC(=O)C)C 196.29 unknown https://doi.org/10.1271/BBB1961.47.483
Methyl citronellate 61290 Click to see CC(CCC=C(C)C)CC(=O)OC 184.27 unknown https://doi.org/10.1271/BBB1961.47.483
Methyl geranate 5365910 Click to see CC(=CCCC(=CC(=O)OC)C)C 182.26 unknown https://doi.org/10.1271/BBB1961.47.483
Neral 643779 Click to see CC(=CCCC(=CC=O)C)C 152.23 unknown https://doi.org/10.1271/BBB1961.47.483
Nerol 643820 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1271/BBB1961.47.483
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
Citronellyl benzoate 112049 Click to see CC(CCC=C(C)C)CCOC(=O)C1=CC=CC=C1 260.40 unknown https://doi.org/10.1271/BBB1961.47.483
Geranyl benzoate 5353011 Click to see CC(=CCCC(=CCOC(=O)C1=CC=CC=C1)C)C 258.35 unknown https://doi.org/10.1271/BBB1961.47.483
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(-)-beta-Bourbonene 324224 Click to see CC(C)C1CCC2(C1C3C2CCC3=C)C 204.35 unknown https://doi.org/10.1271/BBB1961.47.483
(+)-delta-Cadinene 441005 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1271/BBB1961.47.483
(1R,2S,7S,8S)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene 92042749 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1271/BBB1961.47.483
(3R,6E)-nerolidol 11241545 Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C 222.37 unknown https://doi.org/10.1271/BBB1961.47.483
(E,Z)-farnesol 1549109 Click to see CC(=CCCC(=CCCC(=CCO)C)C)C 222.37 unknown https://doi.org/10.1271/BBB1961.47.483
3,7,11-Trimethyldodeca-2,6,10-trienyl acetate 94403 Click to see CC(=CCCC(=CCCC(=CCOC(=O)C)C)C)C 264.40 unknown https://doi.org/10.1271/BBB1961.47.483
3,7,11-Trimethyldodeca-2,6,10-trienyl formate 54010569 Click to see CC(=CCCC(=CCCC(=CCOC=O)C)C)C 250.38 unknown https://doi.org/10.1271/BBB1961.47.483
3,7,11-Trimethyldodeca-2,6,10-trienyl nonanoate 76463753 Click to see CCCCCCCCC(=O)OCC=C(C)CCC=C(C)CCC=C(C)C 362.60 unknown https://doi.org/10.1271/BBB1961.47.483
Alpha-Farnesene 5281516 Click to see CC(=CCCC(=CCC=C(C)C=C)C)C 204.35 unknown https://doi.org/10.1271/BBB1961.47.483
beta Farnesene 15228937 Click to see CCC(=C)CCC=C(C)CCC=C(C)C 206.37 unknown https://doi.org/10.1271/BBB1961.47.483
beta-Bourbonene 62566 Click to see CC(C)C1CCC2(C1C3C2CCC3=C)C 204.35 unknown https://doi.org/10.1271/BBB1961.47.483
beta-Ionone 638014 Click to see CC1=C(C(CCC1)(C)C)C=CC(=O)C 192.30 unknown https://doi.org/10.1271/BBB1961.47.483
Cadina-1(10),4-diene 10223 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1271/BBB1961.47.483
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1271/BBB1961.47.483
Caryophyllene,alpha + beta mixt. 5354499 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1271/BBB1961.47.483
Copaene 19725 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1271/BBB1961.47.483
Farnesal 5280598 Click to see CC(=CCCC(=CCCC(=CC=O)C)C)C 220.35 unknown https://doi.org/10.1271/BBB1961.47.483
Farnesol 3327 Click to see CC(=CCCC(=CCCC(=CCO)C)C)C 222.37 unknown https://doi.org/10.1271/BBB1961.47.483
Farnesol formate 19373487 Click to see CC(=CCCC(=CCCC(=CCOC=O)C)C)C 250.38 unknown https://doi.org/10.1271/BBB1961.47.483
Humulene 5281520 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown https://doi.org/10.1271/BBB1961.47.483
Nerolidol 8888 Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C 222.37 unknown https://doi.org/10.1271/BBB1961.47.483
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(S,1Z,6Z)-8-Isopropyl-1-methyl-5-methylenecyclodeca-1,6-diene 91723653 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1271/BBB1961.47.483
Germacrene D 5317570 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1271/BBB1961.47.483
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
[(25S)-19,21,24-triacetyloxy-20-(acetyloxymethyl)-14,18,25-trihydroxy-3,13,14,25-tetramethyl-6,15-dioxo-2,5,16-trioxa-9-azapentacyclo[15.7.1.01,20.03,23.07,12]pentacosa-7(12),8,10-trien-22-yl] furan-3-carboxylate 5315303 Click to see CC1C2=C(C=NC=C2)C(=O)OCC3(C4C(C(C5(C(C(C(C(C5(C4OC(=O)C)O3)(C)O)OC(=O)C1(C)O)O)OC(=O)C)COC(=O)C)OC(=O)C)OC(=O)C6=COC=C6)C 831.80 unknown via CMAUP database
7-{[(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]oxy}-2H-chromen-2-one 5287282 Click to see CC(=CCCC(=CCCC(=CCOC1=CC2=C(C=C1)C=CC(=O)O2)C)C)C 366.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
6-(Hydroxymethyl)-10-methyl-3-methylidene-3a,4,7,8,11,11a-hexahydrocyclodeca[b]furan-2-one 162902658 Click to see CC1=CCCC(=CCC2C(C1)OC(=O)C2=C)CO 248.32 unknown https://doi.org/10.1271/BBB1961.46.2605
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Squalene 638072 Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C 410.70 unknown https://doi.org/10.1271/BBB1961.47.483
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Primary alcohols
1-Pentanol 6276 Click to see CCCCCO 88.15 unknown https://doi.org/10.1271/BBB1961.47.483
Isoamyl alcohol 31260 Click to see CC(C)CCO 88.15 unknown https://doi.org/10.1271/BBB1961.47.483
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Acyloins
Acetoin 179 Click to see CC(C(=O)C)O 88.11 unknown https://doi.org/10.1271/BBB1961.47.483
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Alpha-hydrogen aldehydes
Isovaleraldehyde 11552 Click to see CC(C)CC=O 86.13 unknown https://doi.org/10.1271/BBB1961.47.483
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
Decanal 8175 Click to see CCCCCCCCCC=O 156.26 unknown https://doi.org/10.1271/BBB1961.47.483
Heptanal 8130 Click to see CCCCCCC=O 114.19 unknown https://doi.org/10.1271/BBB1961.47.483
Hexanal 6184 Click to see CCCCCC=O 100.16 unknown https://doi.org/10.1271/BBB1961.47.483
Nonanal 31289 Click to see CCCCCCCCC=O 142.24 unknown https://doi.org/10.1271/BBB1961.47.483
Octanal 454 Click to see CCCCCCCC=O 128.21 unknown https://doi.org/10.1271/BBB1961.47.483
Undecanal 8186 Click to see CCCCCCCCCCC=O 170.29 unknown https://doi.org/10.1271/BBB1961.47.483
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
6-Methyl-5-hepten-2-one 9862 Click to see CC(=CCCC(=O)C)C 126.20 unknown https://doi.org/10.1271/BBB1961.47.483
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
Acetophenone 7410 Click to see CC(=O)C1=CC=CC=C1 120.15 unknown https://doi.org/10.1271/BBB1961.47.483
Daphneolone 5316300 Click to see C1=CC=C(C=C1)CCC(CC(=O)C2=CC=C(C=C2)O)O 270.32 unknown via CMAUP database
> Organoheterocyclic compounds / Heteroaromatic compounds
2-Pentylfuran 19602 Click to see CCCCCC1=CC=CO1 138.21 unknown https://doi.org/10.1271/BBB1961.47.483
> Organoheterocyclic compounds / Indoles and derivatives / Indoles
Indole 798 Click to see C1=CC=C2C(=C1)C=CN2 117.15 unknown https://doi.org/10.1271/BBB1961.47.483
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
gamma-Decalactone 12813 Click to see CCCCCCC1CCC(=O)O1 170.25 unknown https://doi.org/10.1271/BBB1961.47.483
gamma-Dodecalactone 16821 Click to see CCCCCCCCC1CCC(=O)O1 198.30 unknown https://doi.org/10.1271/BBB1961.47.483
> Organoheterocyclic compounds / Oxanes
Rose oxide 27866 Click to see CC1CCOC(C1)C=C(C)C 154.25 unknown https://doi.org/10.1271/BBB1961.47.483
> Organoheterocyclic compounds / Pyridines and derivatives / Pyridinecarboxylic acids and derivatives / Pyridinecarboxylic acids
Methyl nicotinate 7151 Click to see COC(=O)C1=CN=CC=C1 137.14 unknown https://doi.org/10.1271/BBB1961.47.483
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(2S,2'R,3'S,8'S)-3',4,5',6-tetrahydroxy-2',8'-bis(4-hydroxyphenyl)spiro[1-benzofuran-2,9'-2,3,4,8-tetrahydrofuro[2,3-h]chromene]-3-one 100885566 Click to see C1C(C(OC2=C1C(=CC3=C2C4(C(O3)C5=CC=C(C=C5)O)C(=O)C6=C(C=C(C=C6O4)O)O)O)C7=CC=C(C=C7)O)O 542.50 unknown https://doi.org/10.1016/0031-9422(96)00136-7
(2S,2'R,8'S)-3',4,5',6-tetrahydroxy-2',8'-bis(4-hydroxyphenyl)spiro[1-benzofuran-2,9'-2,3,4,8-tetrahydrofuro[2,3-h]chromene]-3-one 101995336 Click to see C1C(C(OC2=C1C(=CC3=C2C4(C(O3)C5=CC=C(C=C5)O)C(=O)C6=C(C=C(C=C6O4)O)O)O)C7=CC=C(C=C7)O)O 542.50 unknown https://doi.org/10.1016/0031-9422(96)00136-7
[(2R,3S,8S,9R)-3,5-dihydroxy-2,8-bis(4-hydroxyphenyl)-3,4,8,9-tetrahydro-2H-furo[2,3-h]chromen-9-yl]-(3,4,5-trihydroxyphenyl)methanone 101701124 Click to see C1C(C(OC2=C1C(=CC3=C2C(C(O3)C4=CC=C(C=C4)O)C(=O)C5=CC(=C(C(=C5)O)O)O)O)C6=CC=C(C=C6)O)O 544.50 unknown https://doi.org/10.1016/S0031-9422(96)00800-X
[(2R)-5-hydroxy-2,8-bis(4-hydroxyphenyl)-3,4-dihydro-2H-furo[2,3-h]chromen-9-yl]-(2,4,6-trihydroxyphenyl)methanone 162886106 Click to see C1CC2=C(C3=C(C=C2O)OC(=C3C(=O)C4=C(C=C(C=C4O)O)O)C5=CC=C(C=C5)O)OC1C6=CC=C(C=C6)O 526.50 unknown https://doi.org/10.1248/CPB.33.416
https://doi.org/10.1248/CPB.34.595
[(2S,8S,9R)-5-hydroxy-2,8-bis(4-hydroxyphenyl)-3,4,8,9-tetrahydro-2H-furo[2,3-h]chromen-9-yl]-(2,4,6-trihydroxyphenyl)methanone 162979213 Click to see C1CC2=C(C3=C(C=C2O)OC(C3C(=O)C4=C(C=C(C=C4O)O)O)C5=CC=C(C=C5)O)OC1C6=CC=C(C=C6)O 528.50 unknown https://doi.org/10.1016/S0031-9422(96)00800-X
[(2S,8S,9S)-5-hydroxy-2,8-bis(4-hydroxyphenyl)-3,4,8,9-tetrahydro-2H-furo[2,3-h]chromen-9-yl]-(2,4,6-trihydroxyphenyl)methanone 162979214 Click to see C1CC2=C(C3=C(C=C2O)OC(C3C(=O)C4=C(C=C(C=C4O)O)O)C5=CC=C(C=C5)O)OC1C6=CC=C(C=C6)O 528.50 unknown https://doi.org/10.1016/S0031-9422(96)00800-X
[3,5-dihydroxy-2,8-bis(4-hydroxyphenyl)-3,4-dihydro-2H-furo[2,3-h]chromen-9-yl]-(2,4,6-trihydroxyphenyl)methanone 500378 Click to see C1C(C(OC2=C1C(=CC3=C2C(=C(O3)C4=CC=C(C=C4)O)C(=O)C5=C(C=C(C=C5O)O)O)O)C6=CC=C(C=C6)O)O 542.50 unknown https://doi.org/10.1248/CPB.33.416
https://doi.org/10.1248/CPB.34.595
https://doi.org/10.1007/S10600-009-9389-8
[5-hydroxy-2,8-bis(4-hydroxyphenyl)-3,4-dihydro-2H-furo[2,3-h]chromen-9-yl]-(2,4,6-trihydroxyphenyl)methanone 13915094 Click to see C1CC2=C(C3=C(C=C2O)OC(=C3C(=O)C4=C(C=C(C=C4O)O)O)C5=CC=C(C=C5)O)OC1C6=CC=C(C=C6)O 526.50 unknown https://doi.org/10.1248/CPB.33.416
https://doi.org/10.1248/CPB.34.595
[5-hydroxy-2,8-bis(4-hydroxyphenyl)-3,4,8,9-tetrahydro-2H-furo[2,3-h]chromen-9-yl]-(2,4,6-trihydroxyphenyl)methanone 162979212 Click to see C1CC2=C(C3=C(C=C2O)OC(C3C(=O)C4=C(C=C(C=C4O)O)O)C5=CC=C(C=C5)O)OC1C6=CC=C(C=C6)O 528.50 unknown https://doi.org/10.1016/S0031-9422(96)00800-X
3',4,5',6-Tetrahydroxy-2',8'-bis(4-hydroxyphenyl)spiro[1-benzofuran-2,9'-2,3,4,8-tetrahydrofuro[2,3-h]chromene]-3-one 500379 Click to see C1C(C(OC2=C1C(=CC3=C2C4(C(O3)C5=CC=C(C=C5)O)C(=O)C6=C(C=C(C=C6O4)O)O)O)C7=CC=C(C=C7)O)O 542.50 unknown https://doi.org/10.1016/0031-9422(96)00136-7
Daphnodorin A 72426 Click to see C1CC2=C(C3=C(C=C2O)OC(=C3C(=O)C4=C(C=C(C=C4O)O)O)C5=CC=C(C=C5)O)OC1C6=CC=C(C=C6)O 526.50 unknown https://doi.org/10.1248/CPB.35.3931
https://doi.org/10.1248/CPB.33.416
https://doi.org/10.1248/CPB.34.595
https://doi.org/10.1016/S0024-3205(99)00135-6
https://doi.org/10.1248/YAKUSHI1947.107.11_863
Daphnodorin B 72427 Click to see C1C(C(OC2=C1C(=CC3=C2C(=C(O3)C4=CC=C(C=C4)O)C(=O)C5=C(C=C(C=C5O)O)O)O)C6=CC=C(C=C6)O)O 542.50 unknown https://doi.org/10.1248/CPB.34.595
https://doi.org/10.1248/CPB.33.416
https://doi.org/10.1248/CPB.35.3931
https://doi.org/10.1007/S10600-009-9389-8
Daphnodorin C 72428 Click to see C1CC2=C(C3=C(C=C2O)OC(C34C(=O)C5=C(C=C(C=C5O4)O)O)C6=CC=C(C=C6)O)OC1C7=CC=C(C=C7)O 526.50 unknown https://doi.org/10.1248/CPB.35.3931
https://doi.org/10.1248/CPB.33.416
https://doi.org/10.1248/CPB.35.1853
https://doi.org/10.1248/CPB.34.595
https://doi.org/10.1248/CPB.34.2680
https://doi.org/10.1248/YAKUSHI1947.107.11_863
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
8-hydroxy-7-[(3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one 10315179 Click to see C1=CC(=C(C2=C1C=CC(=O)O2)O)OC3C(C(C(C(O3)CO)O)O)O 340.28 unknown via CMAUP database
Daphnetin-8-glucoside 5316301 Click to see C1=CC(=C(C2=C1C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O)O 340.28 unknown via CMAUP database
Daphnin 439499 Click to see C1=CC(=C(C2=C1C=CC(=O)O2)O)OC3C(C(C(C(O3)CO)O)O)O 340.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 4-hydroxycoumarins
4,8-Dihydroxy-2H-chromen-2-one 54719604 Click to see C1=CC2=C(C(=C1)O)OC(=O)C=C2O 178.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7,8-dihydroxycoumarins
Daphnetin 5280569 Click to see C1=CC(=C(C2=C1C=CC(=O)O2)O)O 178.14 unknown https://doi.org/10.1007/S10600-009-9389-8
https://doi.org/10.1248/CPB.34.595
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
3,4,5,6,8-Pentadeuterio-7-hydroxychromen-2-one 45358955 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 167.17 unknown via CMAUP database
Daphnoretin 5281406 Click to see COC1=C(C=C2C(=C1)C=C(C(=O)O2)OC3=CC4=C(C=C3)C=CC(=O)O4)O 352.30 unknown https://doi.org/10.1248/CPB.34.595
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown https://doi.org/10.1248/CPB.34.595
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(1R,5S,13R)-1,9,17,19-tetrahydroxy-5,13-bis(4-hydroxyphenyl)-4,12,14-trioxapentacyclo[11.8.0.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaen-21-one 162938069 Click to see C1CC2=C(C3=C(C=C2O)OC4(C3(C(=O)C5=C(C=C(C=C5O4)O)O)O)C6=CC=C(C=C6)O)OC1C7=CC=C(C=C7)O 542.50 unknown https://doi.org/10.1016/0031-9422(94)00676-K
(1S,5R,13S)-9,17,19-trihydroxy-5,13-bis(4-hydroxyphenyl)-4,12,14-trioxapentacyclo[11.8.0.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaen-21-one 162910872 Click to see C1CC2=C(C3=C(C=C2O)OC4(C3C(=O)C5=C(C=C(C=C5O4)O)O)C6=CC=C(C=C6)O)OC1C7=CC=C(C=C7)O 526.50 unknown https://doi.org/10.1248/CPB.33.416
https://doi.org/10.1248/CPB.34.595
(1S,5S,13R)-1,9,17,19-tetrahydroxy-5,13-bis(4-hydroxyphenyl)-4,12,14-trioxapentacyclo[11.8.0.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaen-21-one 76317993 Click to see C1CC2=C(C3=C(C=C2O)OC4(C3(C(=O)C5=C(C=C(C=C5O4)O)O)O)C6=CC=C(C=C6)O)OC1C7=CC=C(C=C7)O 542.50 unknown https://doi.org/10.1016/0031-9422(94)00676-K
1,6,9,17,19-Pentahydroxy-5,13-bis(4-hydroxyphenyl)-4,12,14-trioxapentacyclo[11.8.0.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaen-21-one 73211601 Click to see C1C(C(OC2=C1C(=CC3=C2C4(C(=O)C5=C(C=C(C=C5OC4(O3)C6=CC=C(C=C6)O)O)O)O)O)C7=CC=C(C=C7)O)O 558.50 unknown https://doi.org/10.1016/0031-9422(96)00136-7
1,9,17,19-Tetrahydroxy-5,13-bis(4-hydroxyphenyl)-4,12,14-trioxapentacyclo[11.8.0.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaen-21-one 74078684 Click to see C1CC2=C(C3=C(C=C2O)OC4(C3(C(=O)C5=C(C=C(C=C5O4)O)O)O)C6=CC=C(C=C6)O)OC1C7=CC=C(C=C7)O 542.50 unknown https://doi.org/10.1016/0031-9422(94)00676-K
3-[5,7-dihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-8-yl]-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 13941112 Click to see C1CC2=C(C(=C(C=C2O)O)C3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)OC1C6=CC=C(C=C6)O 526.50 unknown https://doi.org/10.1007/S10600-009-9389-8
9,17,19-Trihydroxy-5,13-bis(4-hydroxyphenyl)-4,12,14-trioxapentacyclo[11.8.0.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaen-21-one 162910871 Click to see C1CC2=C(C3=C(C=C2O)OC4(C3C(=O)C5=C(C=C(C=C5O4)O)O)C6=CC=C(C=C6)O)OC1C7=CC=C(C=C7)O 526.50 unknown https://doi.org/10.1248/CPB.33.416
https://doi.org/10.1248/CPB.34.595
daphnodorin D2 13941113 Click to see C1CC2=C(C(=C(C=C2O)O)C3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)OC1C6=CC=C(C=C6)O 526.50 unknown https://doi.org/10.1007/S10600-009-9389-8
Daphnodorin F 70688394 Click to see C1CC2=C(C3=C(C=C2O)OC4(C3(C(=O)C5=C(C=C(C=C5O4)O)O)O)C6=CC=C(C=C6)O)OC1C7=CC=C(C=C7)O 542.50 unknown https://doi.org/10.1016/0031-9422(94)00676-K
Daphnodorin G 15984106 Click to see C1C(C(OC2=C1C(=CC3=C2C4(C(=O)C5=C(C=C(C=C5OC4(O3)C6=CC=C(C=C6)O)O)O)O)O)C7=CC=C(C=C7)O)O 558.50 unknown https://doi.org/10.1016/0031-9422(96)00136-7
Daphnodorin H 15984107 Click to see C1C(C(OC2=C1C(=CC3=C2C4(C(=O)C5=C(C=C(C=C5OC4(O3)C6=CC=C(C=C6)O)O)O)O)O)C7=CC=C(C=C7)O)O 558.50 unknown https://doi.org/10.1016/0031-9422(96)00136-7
> Phenylpropanoids and polyketides / Flavonoids / Hydroxyflavonoids / 7-hydroxyflavonoids
1-[(2S)-5,7-dihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-8-yl]-2-(4-hydroxyphenyl)ethane-1,2-dione 163049685 Click to see C1CC2=C(C(=C(C=C2O)O)C(=O)C(=O)C3=CC=C(C=C3)O)OC1C4=CC=C(C=C4)O 406.40 unknown https://doi.org/10.1016/S0031-9422(96)00800-X
1-[5,7-dihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-8-yl]-2-(4-hydroxyphenyl)ethane-1,2-dione 101701427 Click to see C1CC2=C(C(=C(C=C2O)O)C(=O)C(=O)C3=CC=C(C=C3)O)OC1C4=CC=C(C=C4)O 406.40 unknown https://doi.org/10.1016/S0031-9422(96)00800-X
ethyl (2S)-5,7-dihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromene-8-carboxylate 162997075 Click to see CCOC(=O)C1=C(C=C(C2=C1OC(CC2)C3=CC=C(C=C3)O)O)O 330.30 unknown https://doi.org/10.1016/J.FITOTE.2004.09.014
ethyl 5,7-dihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromene-8-carboxylate 76317994 Click to see CCOC(=O)C1=C(C=C(C2=C1OC(CC2)C3=CC=C(C=C3)O)O)O 330.30 unknown https://doi.org/10.1016/J.FITOTE.2004.09.014
> Phenylpropanoids and polyketides / Isoflavonoids / Pyranoisoflavonoids
3-[(2S)-5,7-dihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-6-yl]-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 163026454 Click to see C1CC2=C(C=C(C(=C2O)C3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)OC1C6=CC=C(C=C6)O 526.50 unknown https://doi.org/10.1016/S0031-9422(96)00800-X
3-[5,7-dihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-6-yl]-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 101701125 Click to see C1CC2=C(C=C(C(=C2O)C3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)OC1C6=CC=C(C=C6)O 526.50 unknown https://doi.org/10.1016/S0031-9422(96)00800-X

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