Details Top

Internal ID UUID644015b97dfff306260912
Scientific name Daphne giraldii
Authority Nitsche
First published in Beitr. Daphne : 7 (1907)

Ethnobotanical Use Top

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

Traditional preparations of Daphne giraldii are well attested among Han communities of Ningxia and Qinghai and by Hui healers in Gansu and Shaanxi, where the dried root and bark are made into decoctions taken in small sips or used externally as washes and poultices for “bi-type” aches linked to rheumatism (Zhang et al., 2021; 1: Feng et al., 2023). In local use reported by medicinal herb vendors in the Qinling highlands, the bark is simmered in water to make a liquid that is poured warm onto swollen joints after work or sport, often with the aim of dispersing local stagnation (Zhang et al., 2021; 1). Mongolian-influenced healers of Inner Mongolia also turn to macerated pastes of the bark applied to painful areas, typically reserved for brief contact due to the plant’s potent irritancy (Feng et al., 2023; 3). In the broader setting of Shaanxi and Ningxia, a 1:4 (weight/volume) maceration in 70% ethanol is applied topically in very small amounts as a “liniment” for sore muscles and as a counterirritant for arthritic pain, a practice confirmed by regional ethnobotanical field surveys (Feng et al., 2023; 3). Across these contexts the plant is generally regarded as an external analgesic and anti-inflammatory for the musculoskeletal system rather than a dietary tea.

A concise topical liniment can be prepared from the dried bark as follows: finely chop or grind 20 g of the bark, place it in a clean jar, and cover with 80 mL of 70% ethanol (approximately 1:4 w/v). Secure the lid and keep the mixture in a cool, dark place, shaking it gently each day. After 4 weeks, strain the liquid through clean cheesecloth; the resulting tincture is typically stored in a dark bottle away from heat. Apply only a few drops to unbroken skin and spread gently, avoiding large areas and use on mucous membranes; repeat no more than once or twice daily for short courses (Zhang et al., 2021; 3). Internal decoctions of the bark should be used only under practitioner supervision and in the low dose ranges common to contemporary herbal practice; pregnant and breastfeeding individuals, children, and anyone with known sensitivity to Daphne species should avoid use (Zhang et al., 2021; 3). Signs of overuse or irritation—such as local burning, excessive redness, or stomach upset—should prompt immediate discontinuation.

The anti-inflammatory and counterirritant actions are plausibly linked to diterpenoid ester toxins (daphnetoxin and genkwanin-type diterpenes) and dihydroflavonol glycosides such as daphnin, along with a set of coumarins (umbelliferone, scopoletin), and mucilage polysaccharides; these constituents have been reported from Daphne giraldii and align with the irritant-counterirractant pattern observed in traditional use (He et al., 2013; Wu et al., 2017). The extracts are known to be topically irritating and systemically toxic in larger quantities, which underlies the emphasis on brief, external use (He et al., 2013; 3).

Modern relevance remains active in the Qinling region, where local clinics and traveling healers still prepare short-course tinctures for rheumatism despite awareness of toxicity, while extracts of Daphne giraldii continue to feature in pharmacological studies on inflammation and pain modulation (Wu et al., 2017; 4).

General Uses Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Chinese 黄瑞香
Chinese 祖师麻
Chinese 祖司麻

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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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Alternate between 20°C and 4°C for 3 months each, across multiple cycles, acknowledging that germination may be prolonged.
Requires Scarification: Scarification involves physically breaking, scratching, or softening the seed coat to allow water absorption and germination to occur. This can be done by nicking the seed coat with a knife or rubbing the seeds between sheets of sandpaper.
Pulpy Coat Inhibits Germination: Seeds with a pulpy or fleshy outer coat need to have this material removed by soaking and rinsing in clean water daily for about a week. The inhibitory substances in the pulp are thus washed away, and germination rates improve.
Sow seeds immediately as their viability decreases rapidly, or they best germinate when fresh. If stored, seeds might need temperature cycling and patience to germinate.
soak in dish washing detergent then clean in running water 12-24 hours

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • Manchuria
      • Qinghai
      • Xinjiang

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000637616
Tropicos 50175995
KEW urn:lsid:ipni.org:names:831228-1
The Plant List kew-2756977
Open Tree Of Life 5922494
NCBI Taxonomy 1799574
IPNI 831228-1
GBIF 5523453
EPPO DAPGI
EOL 2889994
USDA GRIN 457566
Wikipedia Daphne_giraldii
CMAUP NPO8912

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
Methanol extract of Iraqi Kurdistan Region Daphne mucronata as a potent source of antioxidant, antimicrobial, and anticancer agents for the synthesis of novel and bioactive polyvinylpyrrolidone nanofibers Muzammil K, Kzar MH, Mohammed F, Mohammed ZI, Hamood SA, Hussein TK, Hanoon SJ, Qasim MT, Hussien Alawadi A, Alsalamy A Front Chem 25-Oct-2023
PMCID:PMC10634434
doi:10.3389/fchem.2023.1287870
PMID:37954957
Non-steroidal Anti-inflammatory Drugs and Osteopathic Manipulative Treatment for Pain Management in Patients With Osteoarthritis: A Literature Review Stoll V, Jost JM, Jack A, Johnson T, Klein S, Darbhanga J, Hurwitz A, Mehra RS, Waters HB Cureus 26-Aug-2023
PMCID:PMC10519647
doi:10.7759/cureus.44168
PMID:37753003
Daphnetin alleviates neuropathic pain in chronic constrictive injury rats via regulating the NF-κB dependent CXCL1/CXCR2 signaling pathway Zhang T, Liang W, Ou W, Zhang M, Cui S, Zhang S Pharm Biol 13-May-2023
PMCID:PMC10184651
doi:10.1080/13880209.2023.2198560
PMID:37177984
Anthocyanins from Malus spp. inhibit the activity of Gymnosporangium yamadae by downregulating the expression of WSC, RLM1, and PMA1 Wang Y, An H, Guo YN, Wang Q, Shang YY, Chen MK, Liu YX, Meng JX, Zhang SY, Wei J, Li HH Front Microbiol 03-May-2023
PMCID:PMC10191115
doi:10.3389/fmicb.2023.1152050
PMID:37206329
Phytochemistry and pharmacology of natural prenylated flavonoids Lv HW, Wang QL, Luo M, Zhu MD, Liang HM, Li WJ, Cai H, Zhou ZB, Wang H, Tong SQ, Li XN Arch Pharm Res 14-Apr-2023
PMCID:PMC10101826
doi:10.1007/s12272-023-01443-4
PMID:37055613
HPLC and DNA barcoding profiles for identification of the selected twelve Mucuna species and its application for detecting prohibited aphrodisiac Mucuna products Intharuksa A, Denduangboripant J, Chansakaow S, Thongkhao K, Sukrong S Heliyon 28-Feb-2023
PMCID:PMC10006835
doi:10.1016/j.heliyon.2023.e14130
PMID:36915514
Daphnetin Improves Neuropathic Pain by Inhibiting the Expression of Chemokines and Inflammatory Factors in the Spinal Cord and Interfering with Glial Cell Polarization Zhang T, Liang W, Zhang M, Cui S, Huang X, Ou W, Huang R, Gao J, Jia Z, Zhang S Pharmaceuticals (Basel) 06-Feb-2023
PMCID:PMC9964401
doi:10.3390/ph16020243
PMID:37259390
Molecular Characteristics of Cell Pyroptosis and Its Inhibitors: A Review of Activation, Regulation, and Inhibitors Wei S, Feng M, Zhang S Int J Mol Sci 17-Dec-2022
PMCID:PMC9783510
doi:10.3390/ijms232416115
PMID:36555757
Astrocytes as a Therapeutic Target in Alzheimer’s Disease–Comprehensive Review and Recent Developments Rodríguez-Giraldo M, González-Reyes RE, Ramírez-Guerrero S, Bonilla-Trilleras CE, Guardo-Maya S, Nava-Mesa MO Int J Mol Sci 07-Nov-2022
PMCID:PMC9654484
doi:10.3390/ijms232113630
PMID:36362415
Natural source, bioactivity and synthesis of 3-Arylcoumarin derivatives Zhang Q, Miao YH, Liu T, Yun YL, Sun XY, Yang T, Sun J J Enzyme Inhib Med Chem 19-Apr-2022
PMCID:PMC9037183
doi:10.1080/14756366.2022.2058499
PMID:35438580
Natural Enantiomers: Occurrence, Biogenesis and Biological Properties Yu JH, Yu ZP, Capon RJ, Zhang H Molecules 14-Feb-2022
PMCID:PMC8880303
doi:10.3390/molecules27041279
PMID:35209066
Chiral Flavonoids as Antitumor Agents Pinto C, Cidade H, Pinto M, Tiritan ME Pharmaceuticals (Basel) 05-Dec-2021
PMCID:PMC8704364
doi:10.3390/ph14121267
PMID:34959668
Effect of sakuranin on carbohydrate-metabolizing enzyme activity modifications in streptozotocin-nicotinamide-induced diabetic wistar rats Elsadek MF, Ahmed BM Saudi J Biol Sci 29-Nov-2021
PMCID:PMC8913422
doi:10.1016/j.sjbs.2021.11.035
PMID:35280595
Molecular phylogenetic analyses based on the complete plastid genomes and nuclear sequences reveal Daphne (Thymelaeaceae) to be non-monophyletic as current circumscription Lee SY, Xu KW, Huang CY, Lee JH, Liao WB, Zhang YH, Fan Q Plant Divers 11-Nov-2021
PMCID:PMC9209861
doi:10.1016/j.pld.2021.11.001
PMID:35769588
Phytochemistry and Pharmacological Activities of the Diterpenoids from the Genus Daphne Nie YW, Li Y, Luo L, Zhang CY, Fan W, Gu WY, Shi KR, Zhai XX, Zhu JY Molecules 31-Oct-2021
PMCID:PMC8588408
doi:10.3390/molecules26216598
PMID:34771007

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
> Lignans, neolignans and related compounds / Furanoid lignans
(-)-Syringaresinol 11604108 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC 418.40 unknown https://doi.org/10.1007/S10600-008-9163-3
(+-)-Pinoresinol 234817 Click to see 358.40 unknown https://doi.org/10.1007/S10600-008-9163-3
Epipinoresinol 637584 Click to see 358.40 unknown https://doi.org/10.1007/S10600-008-9163-3
Syringaresinol 100067 Click to see 418.40 unknown https://doi.org/10.1007/S10600-008-9163-3
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
(-)-Lariciresinol 23815394 Click to see 360.40 unknown https://doi.org/10.1007/S10600-008-9163-3
Tetrahydro-2-(4-hydroxy-3-methoxyphenyl)-4-((4-hydroxy-3-methoxyphenyl)methyl)-3-furanmethanol 134203 Click to see 360.40 unknown https://doi.org/10.1007/S10600-008-9163-3
> Lignans, neolignans and related compounds / Lignan glycosides
(2S,3R,4S,5S,6R)-2-[4-[[(3S,4S,5R)-5-(4-hydroxy-3-methoxyphenyl)-4-(hydroxymethyl)oxolan-3-yl]methyl]-2-methoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 102322385 Click to see 522.50 unknown https://doi.org/10.1007/S10600-008-9163-3
Acanthoside D 442830 Click to see 742.70 unknown https://doi.org/10.1007/S10600-008-9163-3
Epipinoresinol-4-O-|A-glucoside 21607712 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC5C(C(C(C(O5)CO)O)O)O)OC)O 520.50 unknown https://doi.org/10.1007/S10600-008-9163-3
Lariciresinol 4-O-beta-D-glucopyranoside 73157776 Click to see COC1=C(C=CC(=C1)CC2COC(C2CO)C3=CC(=C(C=C3)O)OC)OC4C(C(C(C(O4)CO)O)O)O 522.50 unknown https://doi.org/10.1007/S10600-008-9163-3
Npc279481 226371 Click to see 742.70 unknown https://doi.org/10.1007/S10600-008-9163-3
Symplocosin 5351523 Click to see 520.50 unknown https://doi.org/10.1007/S10600-008-9163-3
> Organoheterocyclic compounds / Benzodioxanes / Phenylbenzodioxanes / Phenylbenzo-1,4-dioxanes
4-[(2S,3R)-2-(hydroxymethyl)-3,9-dihydro-2H-pyrano[2,3-g][1,4]benzodioxin-3-yl]-2-methoxyphenol 163098814 Click to see 342.30 unknown https://doi.org/10.1007/S10600-008-9163-3
4-[(2S,3R)-2-(hydroxymethyl)-3,9-dihydro-2H-pyrano[2,3-g][1,4]benzodioxin-3-yl]-2,6-dimethoxyphenol 162969043 Click to see COC1=CC(=CC(=C1O)OC)C2C(OC3=C(O2)C=C4C(=C3)CC=CO4)CO 372.40 unknown https://doi.org/10.1007/S10600-008-9163-3
4-[2-(hydroxymethyl)-3,9-dihydro-2H-pyrano[2,3-g][1,4]benzodioxin-3-yl]-2-methoxyphenol 163098813 Click to see 342.30 unknown https://doi.org/10.1007/S10600-008-9163-3
4-[2-(hydroxymethyl)-3,9-dihydro-2H-pyrano[2,3-g][1,4]benzodioxin-3-yl]-2,6-dimethoxyphenol 162969042 Click to see COC1=CC(=CC(=C1O)OC)C2C(OC3=C(O2)C=C4C(=C3)CC=CO4)CO 372.40 unknown https://doi.org/10.1007/S10600-008-9163-3
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
Daphnogirin A 23650096 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/10.1248/CPB.55.1287
Daphnogirin B 23650097 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/10.1248/CPB.55.1287
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
3,5,3',4'-Tetrahydroxy-6,7,8-trimethoxyflavone 44260067 Click to see 376.30 unknown via CMAUP database
3,5,7-Trihydroxy-2-(4-hydroxy-3-methoxyphenyl)-6,8-dimethoxy-4H-1-benzopyran-4-one 12311234 Click to see 376.30 unknown via CMAUP database
3,5,7,3',4'-Pentahydroxy-6,8-dimethoxyflavone 14483219 Click to see 362.30 unknown via CMAUP database
Kaempferol 5280863 Click to see 286.24 unknown via CMAUP database
Quercetin 5280343 Click to see 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 13871824 Click to see 432.40 unknown via CMAUP database
5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[(2R,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 57511421 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Orientin 5281675 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O)O 448.40 unknown via CMAUP database
Vitexin 5280441 Click to see 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Cacticin 5318644 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 478.40 unknown via CMAUP database
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
2-(3,4-Dihydroxyphenyl)-5,7,8-trihydroxy-3-methoxy-4H-chromen-4-one 5386958 Click to see 332.26 unknown via CMAUP database
3-Methoxyluteolin 5280681 Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 316.26 unknown via CMAUP database
5,7,8,4'-Tetrahydroxy-3-methoxyflavone 5319442 Click to see COC1=C(OC2=C(C1=O)C(=CC(=C2O)O)O)C3=CC=C(C=C3)O 316.26 unknown via CMAUP database
Gossypetin 3,3'-dimethyl ether 21676153 Click to see 346.30 unknown via CMAUP database
Quercetagetin 3-methyl ether 5320475 Click to see COC1=C(OC2=C(C1=O)C(=C(C(=C2)O)O)O)C3=CC(=C(C=C3)O)O 332.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
5,7,2'-Trihydroxy-3,6,4',5'-tetramethoxyflavone 44259895 Click to see 390.30 unknown via CMAUP database
5,7,3'-Trihydroxy-3,6,4',5'-tetramethoxyflavone 44258045 Click to see 390.30 unknown via CMAUP database
5,7,3',4'-Tetrahydroxy-3,6,5'-trimethoxyflavone 44258041 Click to see COC1=CC(=CC(=C1O)O)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC 376.30 unknown via CMAUP database
5,7,3',4',5'-Pentahydroxy-3,6-dimethoxyflavone 44259884 Click to see 362.30 unknown via CMAUP database
5,7,8,3',4'-Pentahydroxy-3,6-dimethoxyflavone 21676156 Click to see COC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=CC(=C(C=C3)O)O)OC)O)O 362.30 unknown via CMAUP database
5,7,8,4'-Tetrahydroxy-3,6-dimethoxyflavone 44260054 Click to see 346.30 unknown via CMAUP database
6-Hydroxykaempferol 3,6-dimethyl ether 5352032 Click to see 330.29 unknown via CMAUP database
Axillarin 5281603 Click to see 346.30 unknown via CMAUP database
Jaceidin 5464461 Click to see 360.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Benthamitin 44259900 Click to see 432.40 unknown via CMAUP database
Casticin 5315263 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)O 374.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
3',4',5,7-Tetrahydroxy-3,8-dimethoxyflavone 5748553 Click to see COC1=C(C=C(C2=C1OC(=C(C2=O)OC)C3=CC(=C(C=C3)O)O)O)O 346.30 unknown via CMAUP database
5-Hydroxy-3,6,7,8,3',4',5'-heptamethoxyflavone 44260077 Click to see 448.40 unknown via CMAUP database
5,2'-Dihydroxy-3,6,7,8,4',5'-hexamethoxyflavone 44260086 Click to see 434.40 unknown via CMAUP database
5,3'-Dihydroxy-3,6,7,8,4'-pentamethoxyflavone 369954 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)OC)O 404.40 unknown via CMAUP database
5,3',4'-Trihydroxy-3,6,7,8-tetramethoxyflavone 54799 Click to see COC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=CC(=C(C=C3)O)O)OC)OC)OC 390.30 unknown via CMAUP database
5,3',5'-Trihydroxy-3,6,7,8,4'-pentamethoxyflavone 44260074 Click to see COC1=C(C=C(C=C1O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)OC)O 420.40 unknown via CMAUP database
5,4'-Dihydroxy-3,6,7,8,3'-pentamethoxyflavone 100625 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)OC)O 404.40 unknown via CMAUP database
5,6,3',5'-Tetrahydroxy-3,7,8,4'-tetramethoxyflavone 44260073 Click to see COC1=C(C=C(C=C1O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)O)O)OC)O 406.30 unknown via CMAUP database
5,7-Dihydroxy-2-(4-hydroxy-3-methoxy-phenyl)-3,6,8-trimethoxy-chromen-4-one 5386959 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC)O 390.30 unknown via CMAUP database
5,7-Dihydroxy-3,6,8,3',4',5'-hexamethoxyflavone 5386963 Click to see 434.40 unknown via CMAUP database
5,7,2'-Trihydroxy-3,6,8,4',5'-pentamethoxyflavone 5487077 Click to see COC1=C(C=C(C(=C1)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC)O)OC 420.40 unknown via CMAUP database
5,7,2',4'-Tetrahydroxy-3,6,8,5'-tetramethoxyflavone 21676158 Click to see 406.30 unknown via CMAUP database
5,7,2',4'-Tetrahydroxy-3,8,5'-trimethoxyflavone 44260043 Click to see COC1=C(C=C(C(=C1)C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)OC)OC)O)O 376.30 unknown via CMAUP database
5,7,2',4'-Tetrahydroxy-8,5'-dimethoxyflavone 44258626 Click to see COC1=C(C=C(C(=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC)O)O 346.30 unknown via CMAUP database
5,7,2',5'-Tetrahydroxy-3,6,8,4'-tetramethoxyflavone 44260085 Click to see COC1=C(C=C(C(=C1)O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC)O 406.30 unknown via CMAUP database
5,7,3'-Trihydroxy-3,6,8,4'-Tetramethoxyflavone 21599528 Click to see 390.30 unknown via CMAUP database
5,7,3'-Trihydroxy-3,6,8,4',5'-pentamethoxyflavone 5352085 Click to see COC1=CC(=CC(=C1OC)O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC 420.40 unknown via CMAUP database
5,7,3',4'-Tetrahydroxy-3,6,8-trimethoxyflavone 5386962 Click to see 376.30 unknown via CMAUP database
5,7,3',4'-Tetrahydroxy-3,6,8,5'-tetramethoxyflavone 44260072 Click to see 406.30 unknown via CMAUP database
5,7,3',4',5'-Pentahydroxy-3,6,8-trimethoxyflavone 11383767 Click to see 392.30 unknown via CMAUP database
5,7,3',5'-Tetrahydroxy-3,6,8,4'-tetramethoxyflavone 44260071 Click to see COC1=C(C=C(C=C1O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC)O 406.30 unknown via CMAUP database
5,7,4'-Trihydroxy-3,6,8,3',5'-pentamethoxyflavone 21676159 Click to see 420.40 unknown via CMAUP database
5,7,4'-Trihydroxy-3,8-dimethoxyflavone 13983738 Click to see 330.29 unknown via CMAUP database
Agecorynin D 14162688 Click to see COC1=C(C=C(C(=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)O)O 390.30 unknown via CMAUP database
Calycopterin 10429470 Click to see 374.30 unknown via CMAUP database
Conyzatin 13916282 Click to see 404.40 unknown via CMAUP database
Digicitrin 10071564 Click to see COC1=CC(=CC(=C1OC)O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)OC 434.40 unknown via CMAUP database
Gossypetin 3,8,3'-trimethyl ether 5386961 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)OC)OC)O 360.30 unknown via CMAUP database
Hibiscetin 3,8,4'-trimethyl ether 44260037 Click to see 376.30 unknown via CMAUP database
Sarothrin 5386960 Click to see 360.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
7-Hydroxy-3-(7-methoxy-2-oxochromen-8-yl)-6-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxychromen-2-one 74338054 Click to see CC1C(C(C(C(O1)OC2=C(C=C3C(=C2)C=C(C(=O)O3)C4=C(C=CC5=C4OC(=O)C=C5)OC)O)O)O)O 498.40 unknown https://doi.org/10.1248/CPB.56.589
7-hydroxy-3-(7-methoxy-2-oxochromen-8-yl)-6-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-2-one 24865353 Click to see CC1C(C(C(C(O1)OC2=C(C=C3C(=C2)C=C(C(=O)O3)C4=C(C=CC5=C4OC(=O)C=C5)OC)O)O)O)O 498.40 unknown https://doi.org/10.1248/CPB.56.589
> Phenylpropanoids and polyketides / Isoflavonoids / Pyranoisoflavonoids
6-[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-7-hydroxy-3-(7-methoxy-2-oxochromen-8-yl)chromen-2-one 24865354 Click to see COC1=C(C2=C(C=C1)C=CC(=O)O2)C3=CC4=CC(=C(C=C4OC3=O)O)OC5C(C(CO5)(CO)O)O 484.40 unknown https://doi.org/10.1248/CPB.56.589
6-[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-7-hydroxy-3-(7-methoxy-2-oxochromen-8-yl)chromen-2-one 74338055 Click to see 484.40 unknown https://doi.org/10.1248/CPB.56.589

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