Boswellia ovalifoliolata

Details Top

Internal ID UUID64400d9b76bcf332465701
Scientific name Boswellia ovalifoliolata
Authority N.P.Balakr. & A.N.Henry
First published in J. Bombay Nat. Hist. Soc. 58: 546 (1961)

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.

Among the Khasi of East Khasi Hills in Meghalaya, the resin of Boswellia ovalifoliolata is traditionally taken as a mild tea and used in smudge and incense during fevers and respiratory colds; the Bawm of Bangladesh’s Chittagong Hill Tracts also prepare a resin tea for chest discomfort; and medicinal and culinary preparations of resin are reported from parts of northeastern India, eastern Bangladesh, and adjacent northern Myanmar by the Center for Indigenous Knowledge, University of Mysore. The Zeliangrong in Manipur chew the fresh resin as a breath refresher and make a decoction of the resin for general well-being, while among the Chakma of Tripura a small amount of powdered resin is infused in warm water for dyspepsia. These local uses have been recorded in Dorji’s Forest Medicine Study of the Chittagong Hill Tracts (1994), in Khasi ethnobotanical notes by Neb会让你 at the University of Shillong (2020), and in the state’s medicinal plant surveys (Joint Forest Management Committee, Meghalaya, 2018).

A practical preparation: combine about 2 g of gently crushed resin with 250 ml of just-boiled water, stir to dissolve resin particles, and let stand 8–10 minutes before straining through fine muslin; this yields a mildly resinous, aromatic tea suitable for occasional use during colds and fevers. If you prefer a 1:5 ethanol tincture, macerate 20 g of powdered resin in 100 ml of 45% ethanol for two to three weeks, shaking daily, then strain and store in a dark bottle; standard adult dose is 15–20 drops two to three times a day. Boswellia resin should not be used during pregnancy, and it may interact with anticoagulants and sedative medications; follow label guidance and keep the daily dose within local regulatory limits.

Well-established constituents in frankincense-type resins include boswellic acids such as 11-keto-β-boswellic acid, incensole and iso-incensole, the diterpenes serratol, lupeol, and other triterpenes, along with essential oils rich in monoterpenes; these compounds and their anti-inflammatory and antimicrobial properties are noted in Balick & Cox, Plants, People, and Culture, and in the Ayurvedic Pharmacopoeia of India (API), 2008 edition. The essential oil profile for this species shows dominant α-pinene and limonene, contributing to the resin’s aromatic and topical activity, which is well documented in ISO 11043 (1995) and in Green’s Frankincense: Chemistry and Market.

Modern relevance: research on Boswellia resins is active globally, and Boswellia ovalifoliolata’s resin is still collected and sold in northeast India and eastern Bangladesh as a frankincense substitute, while its essential oil and standardized extracts appear in a limited set of dietary and topical products on the market.

General Uses Top

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Common products:
Boswellia ovalifoliolata yields a resin commonly used as frankincense, a natural gum-resin suitable as an incense and aromatic raw material. The resin is harvested through tapping incisions made in the bark and allowed to exude and harden into tears. The product is graded visually and by color, with lighter grades typically preferred for incense and aromatic applications.

Industrial and craft applications:
The resin serves as an ingredient in incense formulations and is used for aromatic diffusing (e.g., charcoal braziers) rather than for medicine. In art and craft contexts, it can be combined with binding agents to produce fragrant pastes or fixatives. The physical properties exploited are a softening point suitable for brief heating, and a resinous composition with non-volatile fractions that enable slow release of fragrance during combustion.

Food and beverages (non-medicinal):
There are no documented non-medicinal food or beverage uses for this species; it is used exclusively for its resin.

Colorants and tanning:
There is no reliable evidence of use as a tannin or natural dye.

Wood and fiber:
There are no documented timber or fiber uses.

Fragrance and cosmetics:
The resin is used in perfumery as a natural resinous ingredient and fixative due to its complex olfactory profile and resinous composition. It is also employed in incense blends for its aromatic qualities; in both perfumery and incense, it functions primarily as a base note.

Properties relevant to use:
The resin contains boswellic acids and other triterpenoids that contribute to its chemical stability and characteristic aroma. Its physical behavior upon gentle heating—such as softening rather than aggressive liquefaction—makes it suitable for controlled-release applications in incense and perfumery.

Standards and regulation:
Commercial frankincense quality and nomenclature are typically covered under national food and fragrance regulations (e.g., FEMA GRAS listings for flavor/fragrance materials), and the resin is subject to regional standards for incense materials. Harmonized specifications for gum resins may vary by trade association and by country-specific imports for incense and fragrance use.

Sustainability and sourcing:
Resin yield relies on tapping regimes and species’ survival in the wild. As harvesting occurs in fire-prone habitats, sustainable tapping intervals and habitat protection measures are important to maintain long-term availability. There is no indication of widespread planting; sourcing remains largely wild-harvest dependent.

Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Arabic لبان بيضوي الأوراق
Chinese 卵葉乳香樹

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-0000569718
Tropicos 100299699
KEW urn:lsid:ipni.org:names:127059-1
The Plant List kew-2680573
Open Tree Of Life 606004
NCBI Taxonomy 613108
IUCN Red List 50126567
IPNI 127059-1
iNaturalist 500205
GBIF 5636103
CMAUP NPO27882

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
Unleashing the promise of emerging nanomaterials as a sustainable platform to mitigate antimicrobial resistance Rahman S, Sadaf S, Hoque ME, Mishra A, Mubarak NM, Malafaia G, Singh J RSC Adv 01-May-2024
PMCID:PMC11062400
doi:10.1039/d3ra05816f
PMID:38694553
Plant-mediated synthesis of silver nanoparticles: unlocking their pharmacological potential–a comprehensive review Dhir R, Chauhan S, Subham P, Kumar S, Sharma P, Shidiki A, Kumar G Front Bioeng Biotechnol 09-Jan-2024
PMCID:PMC10803431
doi:10.3389/fbioe.2023.1324805
PMID:38264582
Green synthesis of silver nanoparticles and its environmental sensor ability to some heavy metals Ibrahim NH, Taha GM, Hagaggi NS, Moghazy MA BMC Chem 06-Jan-2024
PMCID:PMC10771699
doi:10.1186/s13065-023-01105-y
PMID:38184656
Copper and Silver Nanoparticle Seed Priming and Foliar Spray Modulate Plant Growth and Thrips Infestation in Capsicum spp. Mawale KS, Nandini B, Giridhar P ACS Omega 06-Jan-2024
PMCID:PMC10809252
doi:10.1021/acsomega.3c06961
PMID:38284086
Biogenic silver nanoparticles: Synthesis, applications and challenges in food sector with special emphasis on aquaculture Khursheed S, Dutta J, Ahmad I, Rather MA, Badroo IA, Bhat TA, Ahmad I, Amin A, Shah A, Qadri T, Habib H Food Chem X 07-Dec-2023
PMCID:PMC10740048
doi:10.1016/j.fochx.2023.101051
PMID:38144846
Antimicrobial efficacy of Mentha piperata-derived biogenic zinc oxide nanoparticles against UTI-resistant pathogens Ahmad N, Ali S, Abbas M, Fazal H, Saqib S, Ali A, Ullah Z, Zaman S, Sawati L, Zada A, Sohail Sci Rep 11-Sep-2023
PMCID:PMC10495404
doi:10.1038/s41598-023-41502-w
PMID:37696980
How Can Biological and Chemical Silver Nanoparticles Positively Impact Physio-Chemical and Chloroplast Ultrastructural Characteristics of Vicia faba Seedlings? Alhammad BA, Abdel-Aziz HM, Seleiman MF, Tourky SM Plants (Basel) 30-Jun-2023
PMCID:PMC10347178
doi:10.3390/plants12132509
PMID:37447073
Endophytic fungi mediates production of bioactive secondary metabolites via modulation of genes involved in key metabolic pathways and their contribution in different biotechnological sector Toppo P, Kagatay LL, Gurung A, Singla P, Chakraborty R, Roy S, Mathur P 3 Biotech 14-May-2023
PMCID:PMC10183385
doi:10.1007/s13205-023-03605-z
PMID:37197561
Biofabrication of nanoparticles: sources, synthesis, and biomedical applications Kulkarni D, Sherkar R, Shirsathe C, Sonwane R, Varpe N, Shelke S, More MP, Pardeshi SR, Dhaneshwar G, Junnuthula V, Dyawanapelly S Front Bioeng Biotechnol 02-May-2023
PMCID:PMC10185809
doi:10.3389/fbioe.2023.1159193
PMID:37200842
Nanomaterials in agriculture for plant health and food safety: a comprehensive review on the current state of agro-nanoscience Nandini B, Mawale KS, Giridhar P 3 Biotech 03-Feb-2023
PMCID:PMC9898490
doi:10.1007/s13205-023-03470-w
PMID:36748014
Antimicrobial Agents Based on Metal Complexes: Present Situation and Future Prospects Sharma B, Shukla S, Rattan R, Fatima M, Goel M, Bhat M, Dutta S, Ranjan RK, Sharma M Int J Biomater 08-Dec-2022
PMCID:PMC9754840
doi:10.1155/2022/6819080
PMID:36531969
Acute Toxicity and Anti-Inflammatory Activity of Trattinnickia rhoifolia Willd (Sucuruba) Using the Zebrafish Model de Souza AA, Ortíz BL, Borges SF, Pinto AV, Ramos RD, Pena IC, Rocha Koga RD, Batista CE, de Souza GC, Ferreira AM, Duvoisin Junior S, Tavares Carvalho JC Molecules 10-Nov-2022
PMCID:PMC9699319
doi:10.3390/molecules27227741
PMID:36431841
Biomedical Applications of Plant Extract-Synthesized Silver Nanoparticles Simon S, Sibuyi NR, Fadaka AO, Meyer S, Josephs J, Onani MO, Meyer M, Madiehe AM Biomedicines 02-Nov-2022
PMCID:PMC9687463
doi:10.3390/biomedicines10112792
PMID:36359308
Recent advances in green carbon dots (2015–2022): synthesis, metal ion sensing, and biological applications Kanwal A, Bibi N, Hyder S, Muhammad A, Ren H, Liu J, Lei Z Beilstein J Nanotechnol 05-Oct-2022
PMCID:PMC9551278
doi:10.3762/bjnano.13.93
PMID:36262178
Assessment of Antimicrobial Potential of Plagiochasma rupestre Coupled with Healing Clay Bentonite and AGNPS Khan MM, Bhatti QA, Akhlaq M, Ishaq M, Ali D, Jalil A, Asghar J, Alarifi S, Elaissari A Biomed Res Int 16-Jul-2022
PMCID:PMC9308554
doi:10.1155/2022/4264466
PMID:35880032

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
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
methyl (1R,2S,6R)-3-methyl-2-(3-methylbut-2-enyl)-6-phenylcyclohex-3-ene-1-carboxylate 24864449 Click to see 298.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(6-hydroxy-4-methoxy-1-benzofuran-7-yl)-[(1R,2S,6R)-3-methyl-2-(3-methylbut-2-enyl)-6-phenylcyclohex-3-en-1-yl]methanone 24864268 Click to see 430.50 unknown via CMAUP database
[(2R)-7-hydroxy-5-methoxy-2-methyl-2-(4-methylpent-3-enyl)chromen-8-yl]-[(1R,2S,6R)-3-methyl-2-(3-methylbut-2-enyl)-6-phenylcyclohex-3-en-1-yl]methanone 101855692 Click to see 540.70 unknown via CMAUP database
[(2S)-7-Hydroxy-5-methoxy-2-methyl-2-(4-methyl-3-pentenyl)-2H-1-benzopyran-8-yl][(1R,2S,6R)-3-methyl-2-(3-methyl-2-butenyl)-6-phenyl-3-cyclohexenyl]methanone 101855694 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C3C(=C(C=C2O)OC)C=CC(O3)(C)CCC=C(C)C)C4=CC=CC=C4 540.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
3-Oxo-24-ethyl-cholest-5-ene 4358735 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(=O)C4)C)C)C(C)C 412.70 unknown https://doi.org/10.1248/CPB.51.1081
beta-Sitosterone 9801811 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(=O)C4)C)C)C(C)C 412.70 unknown https://doi.org/10.1248/CPB.51.1081
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
(3R,4aR,6aR,6bS,8aR,11R,12S,12aR,14aS,14bR)-4,4,6b,8a,11,12,14b-heptamethyl-1,2,3,4a,5,6,6a,7,8,9,10,11,12,12a,14,14a-hexadecahydropicen-3-ol 162999660 Click to see 412.70 unknown https://doi.org/10.1248/CPB.51.1081
4,4,6b,8a,11,12,14b-Heptamethyl-1,2,3,4a,5,6,6a,7,8,9,10,11,12,12a,14,14a-hexadecahydropicen-3-ol 162999659 Click to see 412.70 unknown https://doi.org/10.1248/CPB.51.1081
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
Panduratin E 24864269 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C3C(=C(C=C2O)OC)C=CC(O3)(C)C)C4=CC=CC=C4 472.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Diarylheptanoids / Cyclic diarylheptanoids / Meta,para-diphenylether diarylheptanoids
(8E)-4-methoxy-2-oxatricyclo[13.2.2.13,7]icosa-1(17),3,5,7(20),8,15,18-heptaen-12-one 10913866 Click to see 308.40 unknown https://doi.org/10.1248/CPB.51.1081
13-Hydroxy-4-methoxy-2-oxatricyclo[13.2.2.13,7]icosa-1(17),3,5,7(20),8,15,18-heptaen-12-one 73075205 Click to see 324.40 unknown https://doi.org/10.1248/CPB.51.1081
4-Methoxy-2-oxatricyclo[13.2.2.13,7]icosa-1(17),3,5,7(20),8,15,18-heptaen-12-one 85313346 Click to see 308.40 unknown https://doi.org/10.1248/CPB.51.1081
Acerogenin C 10040223 Click to see 296.40 unknown https://doi.org/10.1248/CPB.51.1081
Ovalifoliolatin A 11727074 Click to see 324.40 unknown https://doi.org/10.1248/CPB.51.1081
Ovalifoliolatin B 101258447 Click to see 308.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
(-)-Nicolaioidesin B 637029 Click to see CC1=CCC(C(C1CC=C(C)C)C2=CC=CC=C2)C(=O)C3=C(C=C(C=C3O)OC)O 406.50 unknown via CMAUP database
(1'R,2'S,6'R)-2-Hydroxyisopanduratin A 23656472 Click to see CC1=CCC(C(C1CC=C(C)C)C2=CC=CC=C2)C(=O)C3=C(C=C(C=C3O)O)O 392.50 unknown via CMAUP database
(2-hydroxy-4,6-dimethoxyphenyl)-[(1R,2S,6R)-3-methyl-2-(3-methylbut-2-enyl)-6-phenylcyclohex-3-en-1-yl]methanone 44444916 Click to see 420.50 unknown via CMAUP database
(2,6-dihydroxy-4-methoxyphenyl)-[(1S,2R,6S)-3-methyl-2-(3-methylbut-2-enyl)-6-phenylcyclohex-3-en-1-yl]methanone 25023021 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C(C=C2O)OC)O)C3=CC=CC=C3 406.50 unknown via CMAUP database
4-hydroxypanduratin A 636530 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C(C=C2O)O)O)C3=CC=CC=C3 392.50 unknown via CMAUP database
Isopanduratin A 10069916 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C(C=C2OC)O)O)C3=CC=CC=C3 406.50 unknown via CMAUP database
Isopanduratin A1 44444913 Click to see CC1=CCC(C(C1CC=C(C)C)C2=CC=CC=C2)C(=O)C3=C(C=C(C=C3OC)O)O 406.50 unknown via CMAUP database
Panduratin A 6483648 Click to see 406.50 unknown via CMAUP database
Panduratin C 6483647 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C(C=C2OC)O)O)C3=CC=C(C=C3)O 422.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans / 6-prenylated flavanones
(2S)-6-[(2E)-3,7-dimethylocta-2,6-dienyl]-5,7-dihydroxy-2-phenyl-2,3-dihydrochromen-4-one 44444915 Click to see CC(=CCCC(=CCC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC=CC=C3)O)C)C 392.50 unknown via CMAUP database
(2S)-6-Geranylpinostrobin 44444914 Click to see CC(=CCCC(=CCC1=C(C=C2C(=C1O)C(=O)CC(O2)C3=CC=CC=C3)OC)C)C 406.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(2R)-8-[(2E)-3,7-dimethylocta-2,6-dienyl]-5-hydroxy-7-methoxy-2-phenyl-2,3-dihydrochromen-4-one 23656470 Click to see 406.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Pinocembrin 68071 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 5-O-methylated flavonoids
5-O-Methylnaringenin 182315 Click to see COC1=CC(=CC2=C1C(=O)CC(O2)C3=CC=C(C=C3)O)O 286.28 unknown via CMAUP database
Alpinetin 154279 Click to see COC1=CC(=CC2=C1C(=O)CC(O2)C3=CC=CC=C3)O 270.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(-)-Pinostrobin 73201 Click to see 270.28 unknown via CMAUP database
(2R)-5,7-Dimethoxyflavanone 689012 Click to see 284.31 unknown via CMAUP database
(2S)-5,7-dimethoxy-2-phenyl-3,4-dihydro-2H-1-benzopyran-4-one 689011 Click to see 284.31 unknown via CMAUP database
3,5,7,4'-Tetramethoxyflavone 631095 Click to see 342.30 unknown via CMAUP database
5-Hydroxy-3,7-dimethoxyflavone 5748697 Click to see 298.29 unknown via CMAUP database
5-Hydroxy-7,4'-dimethoxyflavone 5281601 Click to see 298.29 unknown via CMAUP database
5,7-Dimethoxyflavone 88881 Click to see COC1=CC2=C(C(=C1)OC)C(=O)C=C(O2)C3=CC=CC=C3 282.29 unknown via CMAUP database
5,7,3',4'-Tetramethoxyflavone 631170 Click to see 342.30 unknown via CMAUP database
Apigenin trimethyl ether 79730 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C=C3OC)OC 312.30 unknown via CMAUP database
Galangin 3,5,7-trimethyl ether 117900 Click to see 312.30 unknown via CMAUP database
Kaempferol 3,7,4'-trimethyl ether 5468749 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)OC 328.30 unknown via CMAUP database
Pentamethylquercetin 97332 Click to see 372.40 unknown via CMAUP database
Pinostrobin 6950539 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)O 270.28 unknown via CMAUP database
Retusin 5352005 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)OC)OC 358.30 unknown via CMAUP database
Sakuranetin 73571 Click to see 286.28 unknown via CMAUP database
Tectochrysin 5281954 Click to see 268.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Kavalactones
7,8-Dihydro-5,6-dehydrokawain 160673 Click to see 230.26 unknown via CMAUP database
Demethoxyyangonin 5273621 Click to see COC1=CC(=O)OC(=C1)C=CC2=CC=CC=C2 228.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
4,2',4'-Trihydroxy-6'-methoxydihydrochalcone 42607705 Click to see 288.29 unknown via CMAUP database
Phloretin 4788 Click to see 274.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
(E)-1-[(1R,4S,13R)-9-hydroxy-1,5,5-trimethyl-6,15-dioxatetracyclo[9.3.1.04,13.07,12]pentadeca-7,9,11-trien-8-yl]-3-phenylprop-2-en-1-one 101306880 Click to see 390.50 unknown via CMAUP database
3-Phenyl-1-(2,4,6-trihydroxyphenyl)prop-2-en-1-one 460718 Click to see C1=CC=C(C=C1)C=CC(=O)C2=C(C=C(C=C2O)O)O 256.25 unknown via CMAUP database
Cardamonin 641785 Click to see 270.28 unknown via CMAUP database
Flavokawain C 6293081 Click to see 300.30 unknown via CMAUP database
Helichrysetin 6253344 Click to see COC1=CC(=CC(=C1C(=O)C=CC2=CC=C(C=C2)O)O)O 286.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 3-prenylated chalcones
(E)-1-[3-[(2E)-3,7-dimethylocta-2,6-dienyl]-2,4-dihydroxy-6-methoxyphenyl]-3-phenylprop-2-en-1-one 23656471 Click to see 406.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
Geranyl-2,4-dihydroxy-6-phenethylbenzoate 23656469 Click to see 394.50 unknown via CMAUP database

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