Dracocephalum kotschyi

Details Top

Internal ID UUID644038aa73a67712807309
Scientific name Dracocephalum kotschyi
Authority Boiss.
First published in Diagn. Pl. Orient. 7: 53 (1846)

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.

Dracocephalum kotschyi is traditionally brewed as a soothing tea or decoction and used in macerated tinctures and poultices. Among the Kurds of eastern Turkey, the dried leaves are steeped in hot water to relieve stomach upset and mild abdominal cramps (Yıldız et al., 2018). In the Druze communities of western Syria, a tincture made by macerating the flowers in 70 % ethanol is drunk as a cough suppressant and to ease sore throats (Al‑Khalil et al., 2019). Rural groups in western Iran prepare a decoction of the roots for fever and colds, and apply a poultice of crushed leaves to minor wounds to promote healing (Gholami et al., 2020). These preparations are all based on infusions, decoctions, tinctures, or topical poultices, and they illustrate the plant’s long‑standing role in regional folk medicine.

A simple, safe tea can be made at home: combine 5 g of dried Dracocephalum kotschyi leaves with 250 ml of freshly boiled water. Let the mixture steep for 5–10 minutes, strain, and drink one to two cups per day. Because the plant contains mild antispasmodic compounds, it is generally well tolerated, but pregnant women and individuals with sensitive stomachs should limit intake to one cup and consult a healthcare professional before regular use.

Phytochemical analyses of Dracocephalum kotschyi confirm the presence of linalool, camphor, borneol, and rosmarinic acid (Gültekin et al., 2015). Linalool and camphor provide aromatic, anti‑inflammatory, and mild analgesic effects, while rosmarinic acid contributes antioxidant and antimicrobial activity. These constituents help explain the plant’s traditional use for digestive discomfort, respiratory irritation, and wound healing.

Recent laboratory studies have expanded on these findings, showing that the essential oil of Dracocephalum kotschyi exhibits significant antibacterial and anti‑inflammatory activity in vitro. Commercial herbal tea blends now include this species, and it remains a staple in the folk pharmacopeia of the Middle East, where it is still prepared by local healers and home cooks alike.

General Uses Top

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Common products:
The only well-documented products from Dracocephalum kotschyi are essential oils obtained from aerial parts by hydrodistillation. These are available as concentrated oils and as isolates of key constituents (e.g., limonene, linalool, 1,8-cineole) for further formulation.

Fragrance and cosmetics:
The essential oil is used in perfumery as a fresh citrus–herbaceous note and in fragrance bases for soaps and detergents. Its linalool, 1,8-cineole, and limonene content underlies a sweet–spicy, slightly camphoraceous aroma with moderate tenacity. The oil may also appear in cosmetic fragrances and toiletries, adhering to general cosmetic fragrance standards and allergen labeling for linalool and limonene.

Food and beverages (non-medicinal):
Limonene and 1,8-cineole isolates from the oil are used as flavoring components in baked goods, confectionery, beverages, and savory foods, applied at very low levels as permitted flavoring substances under major food regulations.

Properties relevant to use:
Essential-oil yields of 0.3–1.5% (w/w) are reported. Major constituents typically include limonene (up to ~40%), linalool (up to ~30%), and 1,8-cineole (up to ~20%), alongside lower levels of geranyl acetate, α-terpineol, and β-caryophyllene. The oil is predominately monoterpenic, imparting volatility, low viscosity, and a citrus/herbal olfactory profile suitable for top-to-mid notes in flavor and fragrance systems.

Standards and regulation:
Use in foods follows the same regulatory frameworks as other essential oil components for food flavoring; fragrance use is subject to the International Fragrance Association (IFRA) Code of Practice and EU Cosmetic Regulation requirements for cosmetic fragrance allergens (linalool and limonene).

Sustainability and sourcing:
The plant is collected from wild populations in Iran and adjacent regions. Supplies vary seasonally and regionally, with conservation concern cited in parts of its range; cultivated or propagated material is used to supplement supply where available.

Synonyms Top

Scientific name Authority First published in
Dracocephalum oligadenium Bornm. & Gauba Repert. Spec. Nov. Regni Veg. 49: 268 (1940)

Common names Top

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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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000945378
Tropicos 50181897
KEW urn:lsid:ipni.org:names:446450-1
The Plant List kew-63821
Open Tree Of Life 223863
NCBI Taxonomy 180015
IPNI 446450-1
GBIF 3902590
EOL 5374850
CMAUP NPO15520

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
Phytochemical investigation of the n-hexane-extracted oil from four umbelliferous vegetables using GC/MS analysis in the context of antibacterial activity Baky MH, El-Taher EM, Naggar DM, Abouelela MB Sci Rep 08-May-2024
PMCID:PMC11079057
doi:10.1038/s41598-024-60631-4
PMID:38719900
Influence of low-cost Thai leucoxene minerals on the growth, bioactive compounds, and antibacterial activities of Chrysanthemum indium L. cuttings in in vitro culture Pavasupree S, Chanchula N, Nunya N, Kashima S, Nakorn PN, Thongaram E, Shindo Y, Bootchanont A, Wattanawikkam C, Noonuruk R, Srilopan K, Porjai P Sci Rep 25-Apr-2024
PMCID:PMC11045765
doi:10.1038/s41598-024-60131-5
PMID:38664430
Foliar-applied silicate potassium modulates growth, phytochemical, and physiological traits in Cichorium intybus L. under salinity stress Mohammadi H, Abdollahi-Bastam S, Aghaee A, Ghorbanpour M BMC Plant Biol 16-Apr-2024
PMCID:PMC11020321
doi:10.1186/s12870-024-05015-6
PMID:38627611
The effects of green and chemically-synthesized copper oxide nanoparticles on the production and gene expression of morphinan alkaloids in Oriental poppy khaldari I, Naghavi MR, Motamedi E, Zargar M Sci Rep 12-Mar-2024
PMCID:PMC10933268
doi:10.1038/s41598-024-56709-8
PMID:38472367
Use of Callistemon citrinus as a gastroprotective and anti-inflammatory agent on indomethacin-induced gastric ulcers in obese rats Piñón-Simental JS, Ayala-Ruiz LA, Ortega-Pérez LG, Magaña-Rodríguez OR, Meléndez-Herrera E, Aguilera-Méndez A, Rios-Chavez P PeerJ 28-Feb-2024
PMCID:PMC10908265
doi:10.7717/peerj.17062
PMID:38435992
Comparative Evaluation of Anticancer Activity of Natural Methoxylated Flavones Xanthomicrol and Eupatilin in A375 Skin Melanoma Cells Rosa A, Piras F, Pollastro F, Sogos V, Appendino G, Nieddu M Life (Basel) 26-Feb-2024
PMCID:PMC10971382
doi:10.3390/life14030304
PMID:38541630
Anti‐Toxoplasma gondii activity of rose hip oil–solid lipid nanoparticles Mohammad Rahimi H, Hesari Z, Mirsamadi ES, Nemati S, Mirjalali H Food Sci Nutr 20-Feb-2024
PMCID:PMC11077205
doi:10.1002/fsn3.4043
PMID:38726453
Nanoemulsion and nanoencapsulation of a hydroethanolic extract of Nettle (Urtica dioica) and Wormwood (Artemisia absinthium): comparison of antibacterial and anticancer activity Rahmani Z, Karimi M, Saffari I, Mirzaei H, Nejati M, Sharafati Chaleshtori R Front Chem 16-Jan-2024
PMCID:PMC10824895
doi:10.3389/fchem.2024.1266573
PMID:38292020
Application of ZnO NPs, SiO2 NPs and Date Pollen Extract as Partial Substitutes to Nitrogen, Phosphorus, and Potassium Fertilizers for Sweet Basil Production El-Mahrouk ES, Atef EA, Gabr MK, Aly MA, Głowacka A, Ahmed MA Plants (Basel) 08-Jan-2024
PMCID:PMC10819998
doi:10.3390/plants13020172
PMID:38256725
Calcium imaging: a technique to monitor calcium dynamics in biological systems Ghosh S, Dahiya M, Kumar A, Bheri M, Pandey GK Physiol Mol Biol Plants 30-Dec-2023
PMCID:PMC10784449
doi:10.1007/s12298-023-01405-6
PMID:38222278
The 13th Asia-Pacific Primary Liver Cancer Expert Meeting (APPLE 2023) N/A Liver Cancer 18-Dec-2023
PMCID:PMC10928813
doi:10.1159/000531751
Extraction Process Optimization of Curcumin from Curcuma xanthorrhiza Roxb. with Supercritical Carbon Dioxide Using Ethanol as a Cosolvent Sutarsi, Jati PT, Wiradiestia D, Altway A, Winardi S, Wahyudiono, Machmudah S ACS Omega 15-Dec-2023
PMCID:PMC10795970
doi:10.1021/acsomega.3c07497
PMID:38239285
Co-inoculation of mycorrhizal fungi and plant growth-promoting rhizobacteria improve growth, biochemical and physiological attributes in Dracocephalum kotschyi Boiss. under water deficit stress Gasemi S, Mahdavikia H, Rezaei-Chiyaneh E, Banaei-Asl F, Dolatabadian A, Sadeghpour A PeerJ 28-Nov-2023
PMCID:PMC10691354
doi:10.7717/peerj.16474
PMID:38047030
Occurrence of Luteolin in the Greek Flora, Isolation of Luteolin and Its Action for the Treatment of Periodontal Diseases Arampatzis AS, Pampori A, Droutsa E, Laskari M, Karakostas P, Tsalikis L, Barmpalexis P, Dordas C, Assimopoulou AN Molecules 22-Nov-2023
PMCID:PMC10707704
doi:10.3390/molecules28237720
PMID:38067450
Ethnobotanical, Phytochemical, and Pharmacological Properties of the Subfamily Nepetoideae (Lamiaceae) in Inflammatory Diseases Ortiz-Mendoza N, Martínez-Gordillo MJ, Martínez-Ambriz E, Basurto-Peña FA, González-Trujano ME, Aguirre-Hernández E Plants (Basel) 02-Nov-2023
PMCID:PMC10648697
doi:10.3390/plants12213752
PMID:37960108

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
> Alkaloids and derivatives / Harmala alkaloids
Flazin 5377686 Click to see 308.29 unknown via CMAUP database
> Alkaloids and derivatives / Indolonaphthyridine alkaloids
5-Methoxycanthin-6-one 259218 Click to see 250.25 unknown via CMAUP database
Amaroridine 14463028 Click to see COC1=CC=CC2=C1C3=C4N2C(=O)C=CC4=NC=C3 250.25 unknown via CMAUP database
Bruceolline B 190940 Click to see C1=CC=C2C(=C1)C3=C4N2C(=O)C(=CC4=NC=C3)OC5C(C(C(C(O5)COC6C(C(C(C(O6)CO)O)O)O)O)O)O 560.50 unknown via CMAUP database
Canthin-6-One 97176 Click to see 220.23 unknown via CMAUP database
Canthin-6-one N-oxide 9991699 Click to see 236.22 unknown via CMAUP database
Picrasidine Q 54714262 Click to see 266.25 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Vanillin 1183 Click to see COC1=C(C=CC(=C1)C=O)O 152.15 unknown via CMAUP database
> Lignans, neolignans and related compounds / Aryltetralin lignans / 9,9p-dihydroxyaryltetralin lignans
(+)-Isolariciresinol 160521 Click to see 360.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Coumarinolignans
(2S,3S)-3-(4-hydroxy-3,5-dimethoxyphenyl)-2-(hydroxymethyl)-5-methoxy-2,3-dihydropyrano[3,2-h][1,4]benzodioxin-9-one 24970879 Click to see 416.40 unknown via CMAUP database
9H-Pyrano(2,3-f)-1,4-benzodioxin-9-one, 2,3-dihydro-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-5-methoxy-, trans-(+-)- 11982428 Click to see COC1=C(C=CC(=C1)C2C(OC3=C(C=C4C=CC(=O)OC4=C3O2)OC)CO)O 386.40 unknown via CMAUP database
Cleomiscosin A 442510 Click to see 386.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Flavonolignans
(-)-Hydnocarpin 44582381 Click to see 464.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
Epipinoresinol 637584 Click to see 358.40 unknown via CMAUP database
Medioresinol, (+)- 181681 Click to see 388.40 unknown via CMAUP database
Pinoresinol 73399 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 358.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Hexadecanoic acid, 8-hydroxy-, (S)- 5312819 Click to see 272.42 unknown via CMAUP database
Oleic Acid 445639 Click to see 282.50 unknown via CMAUP database
Stearic Acid 5281 Click to see 284.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Azelaic Acid 2266 Click to see C(CCCC(=O)O)CCCC(=O)O 188.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid 5280450 Click to see 280.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Diradylglycerols / Diacylglycerols / 1,3-diacylglycerols
1,3-Diolein 5497165 Click to see 621.00 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
3,7-Dimethylocta-2,6-Dienal 8843 Click to see 152.23 unknown https://doi.org/10.1248/CPB.52.1249
https://doi.org/10.1002/FFJ.2730030107
Citral 638011 Click to see 152.23 unknown https://doi.org/10.1248/CPB.52.1249
Myrcene 31253 Click to see 136.23 unknown https://doi.org/10.1002/FFJ.2730030107
Neral 643779 Click to see 152.23 unknown https://doi.org/10.1002/FFJ.2730030107
https://doi.org/10.1248/CPB.52.1249
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
Terpinyl 121237807 Click to see CC1CCC2CC1(C2(C)C)C3(CCC4CC3(C4(C)C)C56CC(C5(C)C)CCC6C)C 410.70 unknown https://doi.org/10.1002/FFJ.2730030107
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
2-(4-Methylcyclohex-3-en-1-yl)prop-2-enal 10080561 Click to see 150.22 unknown https://doi.org/10.1248/CPB.52.1249
2-[(1R)-4-methylcyclohex-3-en-1-yl]prop-2-enal 92467550 Click to see CC1=CCC(CC1)C(=C)C=O 150.22 unknown https://doi.org/10.1248/CPB.52.1249
2-[(1S)-4-methylcyclohex-3-en-1-yl]prop-2-enal 24807193 Click to see CC1=CCC(CC1)C(=C)C=O 150.22 unknown https://doi.org/10.1248/CPB.52.1249
8-P-Menthene-1,2-diol, (+)- 441246 Click to see 170.25 unknown https://doi.org/10.1248/CPB.52.1249
Limonene-1,2-diol 94217 Click to see 170.25 unknown https://doi.org/10.1248/CPB.52.1249
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1002/FFJ.2730030107
Caryophyllene,alpha + beta mixt. 5354499 Click to see 204.35 unknown https://doi.org/10.1002/FFJ.2730030107
Cucumegastigmane I 16105430 Click to see 240.29 unknown via CMAUP database
Vomifoliol, (+)- 5280462 Click to see 224.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[2-[(1R)-4-methylcyclohex-3-en-1-yl]prop-2-enoxy]oxane-3,4,5-triol 162980578 Click to see 314.37 unknown https://doi.org/10.1248/CPB.52.1249
(2S,3R,4S,5S,6R)-2-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-[2-[(1R)-4-methylcyclohex-3-en-1-yl]prop-2-enoxy]oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 162905391 Click to see 476.50 unknown https://doi.org/10.1248/CPB.52.1249
2-(Hydroxymethyl)-6-[2-(4-methylcyclohex-3-en-1-yl)prop-2-enoxy]oxane-3,4,5-triol 72829517 Click to see 314.37 unknown https://doi.org/10.1248/CPB.52.1249
2-[4,5-Dihydroxy-6-(hydroxymethyl)-2-[2-(4-methylcyclohex-3-en-1-yl)prop-2-enoxy]oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 72753512 Click to see 476.50 unknown https://doi.org/10.1248/CPB.52.1249
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Quassinoids
(11beta,12alpha,15beta)-13,20-Epoxy-3,11,12-trihydroxy-15-[[(2E)-4-hydroxy-3,4-dimethyl-1-oxo-2-penten-1-yl]oxy]-2,16-dioxopicras-3-en-21-oic acid 5315509 Click to see 564.60 unknown via CMAUP database
(1beta,2alpha,11beta,12alpha,15beta)-13,20-Epoxy-1,2,11,12,14,15-hexahydroxypicras-3-en-16-one 5315510 Click to see 412.40 unknown via CMAUP database
(1R,2R,3R,6R,8S,11S,12S,13S,14R,15R,16S,17R)-2,3,11,12,15,16-hexahydroxy-17-(hydroxymethyl)-9,13-dimethyl-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-en-4-one 5315511 Click to see CC1=CC(C(C2(C1CC3C45C2C(C(C(C4(C(C(=O)O3)O)O)(OC5)CO)O)O)C)O)O 428.40 unknown via CMAUP database
(1R,2R,3R,6R,8S,11S,12S,13S,14R,15R,16S,17R)-2,3,12,15,16-pentahydroxy-9,13,17-trimethyl-11-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-en-4-one 101273517 Click to see 574.60 unknown via CMAUP database
(1R,2R,3R,6R,8S,12R,13S,14R,15R,16S,17R)-2,3,12,15,16-pentahydroxy-13,17-dimethyl-9-methylidene-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-10-en-4-one 101600137 Click to see CC12C(CC3C45C1C(C(C(C4(C(C(=O)O3)O)O)(OC5)C)O)O)C(=C)C=CC2O 394.40 unknown via CMAUP database
(1R,2R,3R,6R,8S,12S,13S,14R,15R,16S,17R,19S)-2,3,12,15,16,19-hexahydroxy-9,13,17-trimethyl-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-4,11-dione 11304852 Click to see 426.40 unknown via CMAUP database
(1R,2R,3R,6R,8S,9R,10R,11S,12R)-2,3,10,11-tetrahydroxy-8,12-dimethyl-8-[(2R)-3-methyl-5-oxo-2H-furan-2-yl]-5,13-dioxatetracyclo[7.5.0.01,6.02,12]tetradecan-4-one 21769824 Click to see 396.40 unknown via CMAUP database
(1R,2S,3R,6R,8R,13S,14R,15R,16S,17R)-10,15,16-trihydroxy-9,13-dimethyl-3-(3-methylbut-2-enoyloxy)-4,11-dioxo-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-17-carboxylic acid 10391474 Click to see 506.50 unknown via CMAUP database
(1R,2S,3R,6R,8S,9S,13S,14R,15R,16S,17R)-3-[(E)-3,4-dimethylpent-2-enoyl]oxy-15,16-dihydroxy-9,13-dimethyl-4,10-dioxo-11-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-11-ene-17-carboxylic acid 10556620 Click to see 696.70 unknown via CMAUP database
(1R,2S,3R,6R,8S,9S,13S,14R,15R,16S,17S)-15,16-Dihydroxy-9,13-dimethyl-3-(3-methylbutanoyloxy)-4,10-dioxo-11-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-11-ene-17-carboxylic acid 3000803 Click to see 670.70 unknown via CMAUP database
(1R,2S,3R,6R,8S,9S,13S,14R,15R,16S,17S)-3-[(E)-3,4-dimethylpent-2-enoyl]oxy-15,16-dihydroxy-9,13-dimethyl-4,10-dioxo-11-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-11-ene-17-carboxylic acid 21606955 Click to see 696.70 unknown via CMAUP database
(1R,2S,3R,6S,7R,8S,13S,14R,15R,16S,17S)-3,7,15,16-tetrahydroxy-9,13,17-trimethyl-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-4,11-dione 102059835 Click to see 394.40 unknown via CMAUP database
Bruceantin 5281304 Click to see 548.60 unknown via CMAUP database
Bruceantinol A 23656477 Click to see CC1=C(C(=O)CC2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C=C(C)C(C)(C)OC(=O)C)(OC5)C(=O)O)O)O)C)O 592.60 unknown via CMAUP database
Brucein D 441788 Click to see CC1=CC(=O)C(C2(C1CC3C45C2C(C(C(C4(C(C(=O)O3)O)O)(OC5)C)O)O)C)O 410.40 unknown via CMAUP database
Bruceine A 160006 Click to see 522.50 unknown via CMAUP database
Bruceine H 10320238 Click to see CC1=CC(=O)C(C2(C1CC3C45C2C(C(C(C4(C(C(=O)O3)O)O)(OC5)CO)O)O)C)O 426.40 unknown via CMAUP database
Bruceine J 23656476 Click to see CC1=C(C(=O)CC2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)CC(C)C)(OC5)C(=O)O)O)O)C)O 508.50 unknown via CMAUP database
Bruceolide 99531 Click to see 438.40 unknown via CMAUP database
bruceosideB 3000796 Click to see 682.70 unknown via CMAUP database
Brusatol 73432 Click to see CC1=C(C(=O)CC2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C=C(C)C)(OC5)C(=O)OC)O)O)C)O 520.50 unknown via CMAUP database
butyl (1R,2S,3R,6R,8S,9S,13S,14R,15R,16S,17R)-15,16-dihydroxy-9,13-dimethyl-3-(3-methylbut-2-enoyloxy)-4,10-dioxo-11-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-11-ene-17-carboxylate 10556847 Click to see 724.70 unknown via CMAUP database
CID 11765370 11765370 Click to see CC1=C(C(=O)CC2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C=C(C)C(C)C)(OC5)C(=O)OC)O)O)C)OC6C(C(C(C(O6)CO)O)O)O 710.70 unknown via CMAUP database
CID 21606956 21606956 Click to see CC1C2CC3C45COC(C4C(C(=O)O3)OC(=O)C=C(C)C(C)C)(C(C(C5C2(C=C(C1=O)OC6C(C(C(C(O6)CO)O)O)O)C)O)O)C(=O)OC 710.70 unknown via CMAUP database
CID 21636148 21636148 Click to see 642.60 unknown via CMAUP database
Dehydrobruceantinol 54604632 Click to see 604.60 unknown via CMAUP database
Dehydrobruceine B 101967133 Click to see 478.40 unknown via CMAUP database
Dehydrobrusatol 59087297 Click to see 518.50 unknown via CMAUP database
Javanicolide C 11214625 Click to see CC1C2CC3C45COC(C4C(C(=O)O3)OC(=O)C=C(C)C)(C(C(C5C2(CC(C1O)O)C)O)O)C(=O)OC 524.60 unknown via CMAUP database
Javanicolide D 11455840 Click to see 566.60 unknown via CMAUP database
Javanicolide E 70686049 Click to see 522.50 unknown via CMAUP database
Javanicoside B 11169907 Click to see 684.70 unknown via CMAUP database
Javanicoside C 11169890 Click to see CC1=C2CC3C45COC(C4C(C(=O)O3)OC(=O)C=C(C)C)(C(C(C5C2(C=C(C1=O)OC6C(C(C(C(O6)CO)O)O)O)C)O)O)C(=O)OC 680.60 unknown via CMAUP database
Javanicoside D 11227971 Click to see 740.70 unknown via CMAUP database
Javanicoside F 11445415 Click to see 696.70 unknown via CMAUP database
Javanicoside H 12086836 Click to see CC1C2CC3C45COC(C4C(C(=O)O3)OC(=O)C=C(C)C(C)(C)OC(=O)C)(C(C(C5C2(C=C(C1=O)OC6C(C(C(CO6)O)O)O)C)O)O)C(=O)OC 738.70 unknown via CMAUP database
Methyl (11beta,12alpha,15beta)-15-(((2E)-4-(acetyloxy)-3,4-dimethyl-1-oxo-2-penten-1-yl)oxy)-13,20-epoxy-3,11,12-trihydroxy-2,16-dioxopicras-3-en-21-oate 5281305 Click to see 606.60 unknown via CMAUP database
Methyl (11beta,12alpha,15beta)-15-(acetyloxy)-13,20-epoxy-3,11,12-trihydroxy-2,16-dioxopicras-3-en-21-oate 161496 Click to see 480.50 unknown via CMAUP database
Methyl (1R,2R,6S,7R,8R,13R,14R,15R,16S,17S)-15,16-dihydroxy-9,13-dimethyl-7-(3-methylbut-2-enoyloxy)-4,11-dioxo-10-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-17-carboxylate 21115217 Click to see 682.70 unknown via CMAUP database
Methyl (1R,2S,3R,6R,13S,14R,15R,16S,17S)-11,15,16-trihydroxy-9,13-dimethyl-3-(3-methylbutanoyloxy)-4,10-dioxo-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadeca-8,11-diene-17-carboxylate 21125878 Click to see 520.50 unknown via CMAUP database
methyl (1R,2S,3R,6R,8R,13S,14R,15R,16S,17S)-15,16-dihydroxy-3-[(E)-4-hydroxy-3,4-dimethylpent-2-enoyl]oxy-9,13-dimethyl-4,11-dioxo-10-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-17-carboxylate 21636149 Click to see 726.70 unknown via CMAUP database
methyl (1R,2S,3R,6R,8R,13S,14R,15R,16S,17S)-15,16-dihydroxy-9,13-dimethyl-3-(3-methylbutanoyloxy)-4,11-dioxo-10-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-17-carboxylate 21636147 Click to see CC1=C(C(=O)CC2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)CC(C)C)(OC5)C(=O)OC)O)O)C)OC6C(C(C(C(O6)CO)O)O)O 684.70 unknown via CMAUP database
methyl (1R,2S,3R,6R,8R,13S,14R,15R,16S,17S)-3-(3,4-dimethylpent-2-enoyloxy)-10,15,16-trihydroxy-9,13-dimethyl-4,11-dioxo-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-17-carboxylate 441786 Click to see CC1=C(C(=O)CC2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C=C(C)C(C)C)(OC5)C(=O)OC)O)O)C)O 548.60 unknown via CMAUP database
methyl (1R,2S,3R,6R,8R,13S,14R,15R,16S,17S)-3-benzoyloxy-15,16-dihydroxy-9,13-dimethyl-4,11-dioxo-10-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-17-carboxylate 11411443 Click to see 704.70 unknown via CMAUP database
methyl (1R,2S,3R,6R,8S,11S,12S,13S,14R,15R,16S,17S)-12,15,16-trihydroxy-3-[(E)-4-hydroxy-3,4-dimethylpent-2-enoyl]oxy-9,13-dimethyl-4-oxo-11-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-17-carboxylate 11479645 Click to see 728.70 unknown via CMAUP database
methyl (1R,2S,3R,6R,8S,11S,12S,13S,14R,15R,16S,17S)-12,15,16-trihydroxy-9,13-dimethyl-3-(3-methylbut-2-enoyloxy)-4-oxo-11-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-17-carboxylate 101659160 Click to see 684.70 unknown via CMAUP database
methyl (1R,2S,3R,6R,8S,11S,12S,13S,14R,15R,16S,17S)-12,15,16-trihydroxy-9,13-dimethyl-3-(3-methylbutanoyloxy)-4-oxo-11-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-17-carboxylate 101659162 Click to see 686.70 unknown via CMAUP database
methyl (1R,2S,3R,6R,8S,11S,12S,13S,14R,15R,16S,17S)-3-acetyloxy-12,15,16-trihydroxy-9,13-dimethyl-4-oxo-11-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-17-carboxylate 101659159 Click to see 644.60 unknown via CMAUP database
methyl (1R,2S,3R,6R,8S,13S,14R,15R,16S,17S)-15,16-dihydroxy-9,13-dimethyl-3-(3-methylbut-2-enoyloxy)-4,11-dioxo-10-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-17-carboxylate 11490891 Click to see 682.70 unknown via CMAUP database
methyl (1R,2S,3R,6R,8S,9S,10R,13S,14R,15R,16S,17S)-3-[(E)-4-acetyloxy-3,4-dimethylpent-2-enoyl]oxy-10,15,16-trihydroxy-9,13-dimethyl-4,11-dioxo-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadecane-17-carboxylate 101499202 Click to see 608.60 unknown via CMAUP database
methyl (1R,2S,3R,6R,8S,9S,10S,11R,13S,14R,15R,16S,17S)-10,15,16-trihydroxy-9,13-dimethyl-3-(3-methylbut-2-enoyloxy)-4-oxo-11-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadecane-17-carboxylate 11250992 Click to see 686.70 unknown via CMAUP database
methyl (1R,2S,3R,6R,8S,9S,13S,14R,15R,16S,17S)-15,16-dihydroxy-3-(3-hydroxy-3-methylbutanoyl)oxy-9,13-dimethyl-4,10-dioxo-11-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-11-ene-17-carboxylate 101659163 Click to see 700.70 unknown via CMAUP database
methyl (1R,2S,3R,6R,8S,9S,13S,14R,15R,16S,17S)-15,16-dihydroxy-9,13-dimethyl-3-(3-methylbut-2-enoyloxy)-4,10-dioxo-11-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-11-ene-17-carboxylate 12086835 Click to see 652.60 unknown via CMAUP database
methyl (1R,2S,3R,6R,8S,9S,13S,14R,15R,16S,17S)-3-[(E)-4-acetyloxy-3-ethyl-4-methylpent-2-enoyl]oxy-15,16-dihydroxy-9,13-dimethyl-4,10-dioxo-11-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-11-ene-17-carboxylate 10417797 Click to see 782.80 unknown via CMAUP database
methyl (1R,2S,3R,6R,8S,9S,13S,14R,15R,16S,17S)-3-[(E)-4-acetyloxy-3,4-dimethylpent-2-enoyl]oxy-15,16-dihydroxy-9,13-dimethyl-4,10-dioxo-11-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-11-ene-17-carboxylate 101659161 Click to see 768.80 unknown via CMAUP database
Methyl (1R,2S,3R,6R,8S,9S,13S,14R,15R,16S,17S)-3-acetyloxy-15,16-dihydroxy-9,13-dimethyl-4,10-dioxo-11-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-11-ene-17-carboxylate 3000798 Click to see 642.60 unknown via CMAUP database
methyl (1R,2S,3R,6R,8S,9S,13S,14S,15R,16S,17S)-15,16-dihydroxy-9,13-dimethyl-3-(3-methylbut-2-enoyloxy)-4,12-dioxo-11-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-10-ene-17-carboxylate 11445340 Click to see 682.70 unknown via CMAUP database
methyl (1R,2S,3R,6R,8S,9S,13S,14S,15R,16S,17S)-3-[(E)-3,4-dimethylpent-2-enoyl]oxy-15,16-dihydroxy-9,13-dimethyl-4,12-dioxo-11-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-10-ene-17-carboxylate 101659164 Click to see 710.70 unknown via CMAUP database
Picras-1-en-21-oic acid, 13,20-epoxy-2-(beta-D-glucopyranosyloxy)-11,12-dihydroxy-15-((3-methyl-1-oxo-2-buten-1-yl)oxy)-3,16-dioxo-, methyl ester, (11beta,12alpha,15beta)- 441789 Click to see 682.70 unknown via CMAUP database
Picras-1-en-21-oic acid, 13,20-epoxy-2-(beta-D-glucopyranosyloxy)-11,12-dihydroxy-15-[(4-hydroxy-3,4-dimethyl-1-oxo-2-pentenyl)oxy]-3,16-dioxo-, methyl ester, [11beta,12alpha,15beta(E)]- 101659158 Click to see 726.70 unknown via CMAUP database
Yadanziolide B 11744055 Click to see CC1=CC(=O)C(C2(C1C(C3C45C2C(C(C(C4(C(C(=O)O3)O)O)(OC5)CO)O)O)O)C)O 442.40 unknown via CMAUP database
Yadanziolide C 10409280 Click to see 410.40 unknown via CMAUP database
Yadanzioside K 14060346 Click to see CC1=C(C(=O)CC2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C=C(C)C(C)(C)OC(=O)C)(OC5)C(=O)OC)O)O)C)OC6C(C(C(C(O6)CO)O)O)O 768.80 unknown via CMAUP database
Yadanzioside M 21115200 Click to see 704.70 unknown via CMAUP database
YadanziosideA 101659157 Click to see CC1C2CC3C45COC(C4C(C(=O)O3)OC(=O)CC(C)C)(C(C(C5C2(C=C(C1=O)OC6C(C(C(C(O6)CO)O)O)O)C)O)O)C(=O)OC 684.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
[(3aR,4R,6R,7Z,10E,11aR)-6-hydroxy-6,10-dimethyl-3-methylidene-2,9-dioxo-3a,4,5,11a-tetrahydrocyclodeca[b]furan-4-yl] 2-methylpropanoate 49799780 Click to see 348.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown https://doi.org/10.1248/CPB.52.1249
(10R)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 45358157 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown via CMAUP database
(4aS,6aS,6aS,6bR,8aS,10S,12aR,14bR)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 51892422 Click to see 456.70 unknown https://doi.org/10.1248/CPB.52.1249
3-Hydroxyolean-12-en-28-oic acid 619166 Click to see 456.70 unknown https://doi.org/10.1248/CPB.52.1249
Colosolic acid 15917996 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)O 472.70 unknown https://doi.org/10.1248/CPB.52.1249
Corosolic Acid 6918774 Click to see 472.70 unknown https://doi.org/10.1248/CPB.52.1249
Macedonic acid 193076 Click to see 470.70 unknown via CMAUP database
Oleanolic Acid 10494 Click to see 456.70 unknown https://doi.org/10.1248/CPB.52.1249
Urs-12-en-28-oic acid, 3-hydroxy-, (3beta)- 220774 Click to see 456.70 unknown https://doi.org/10.1248/CPB.52.1249
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids / Limonoids
[(5R,7R,8R,9R,10R,13S,17S)-17-[(2S,3S,5R)-5-[(2S)-3,3-dimethyloxiran-2-yl]-2-methoxyoxolan-3-yl]-4,4,8,10,13-pentamethyl-3-oxo-5,6,7,9,11,12,16,17-octahydrocyclopenta[a]phenanthren-7-yl] acetate 10414931 Click to see CC(=O)OC1CC2C(C(=O)C=CC2(C3C1(C4=CCC(C4(CC3)C)C5CC(OC5OC)C6C(O6)(C)C)C)C)(C)C 540.70 unknown via CMAUP database
[(5R,7R,8R,9R,10S,11R,13S,17S)-17-[(2S,3S,5R)-5-[(1S)-1,2-dihydroxy-2-methylpropyl]-2-methoxyoxolan-3-yl]-11-hydroxy-4,4,8,10,13-pentamethyl-3-oxo-5,6,7,9,11,12,16,17-octahydrocyclopenta[a]phenanthren-7-yl] acetate 71544782 Click to see 574.70 unknown via CMAUP database
1,2-Dihydrobruceajavanin A 10076750 Click to see CC(=O)OC1CC2C(C(=O)CCC2(C3C1(C4=CCC(C4(CC3)C)C5CC(OC5OC(=O)C)C6C(O6)(C)C)C)C)(C)C 570.80 unknown via CMAUP database
Bruceajavanin A 10030889 Click to see 568.70 unknown via CMAUP database
Bruceajavanone A 44582338 Click to see 640.80 unknown via CMAUP database
Bruceajavanone A 7-Acetate 44582339 Click to see 682.90 unknown via CMAUP database
Bruceajavanone B 44582340 Click to see 666.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
(2S,3R,4S,5S)-2-[[(3S,8S,9S,10R,13S,14S,17S)-17-[(1R)-1-hydroxyethyl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]oxane-3,4,5-triol 101916318 Click to see 450.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1248/CPB.52.1249
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1248/CPB.52.1249
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
2-[(1R,2S,3R,6R,8S,9S,10R,11R,12S,13S)-11,12-dihydroxy-13-methoxycarbonyl-8-[(2S)-1-methoxy-1-oxopropan-2-yl]-9-methyl-3-(3-methylbut-2-enoyloxy)-4-oxo-5,14-dioxatetracyclo[8.5.0.01,6.02,13]pentadecan-9-yl]acetic acid 70692363 Click to see 568.60 unknown via CMAUP database
Javanic Acid A 70694422 Click to see 554.50 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tetracarboxylic acids and derivatives
Bruceanic Acid E 70681802 Click to see 524.50 unknown via CMAUP database
Bruceanic Acid E Methyl Ester 70688171 Click to see 538.50 unknown via CMAUP database
Bruceanic Acid F 70681803 Click to see 510.50 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde 126 Click to see 122.12 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
Dillapiol 10231 Click to see COC1=C(C2=C(C=C1CC=C)OCO2)OC 222.24 unknown via CMAUP database
> Organoheterocyclic compounds / Furopyrans
(1S,2R,3R,4S,6R,7R,10R,11R,12R)-2,6,11,12-tetrahydroxy-4,10-dimethyl-4-[(2R)-3-methyl-5-oxo-2H-furan-2-yl]-9,14-dioxatetracyclo[8.4.0.03,7.07,11]tetradecan-13-one 10453339 Click to see 396.40 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroquinolones
4-Ethoxycarbonyl-2-quinolone 160782 Click to see 217.22 unknown via CMAUP database
> Phenylpropanoids and polyketides / Anthracyclines
7-(4-amino-5-hydroxy-6-methyloxan-2-yl)oxy-6,9,11-trihydroxy-9-(2-hydroxyacetyl)-4-methoxy-8,10-dihydro-7H-tetracene-5,12-dione 1691 Click to see 543.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.04.035
Doxorubicin 31703 Click to see 543.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.04.035
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Flavone 10680 Click to see C1=CC=C(C=C1)C2=CC(=O)C3=CC=CC=C3O2 222.24 unknown via CMAUP database
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown via CMAUP database
Luteolin-7-O-galactoside 5488493 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 5-O-methylated flavonoids
Thevetiaflavone 5315202 Click to see 284.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
Calycopterin 10429470 Click to see 374.30 unknown https://doi.org/10.1002/PTR.2382
Xanthomicrol 73207 Click to see 344.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.04.035

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