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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)

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Synonyms Top

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

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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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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
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
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
Effects of Frankincense Compounds on Infection, Inflammation, and Oral Health Almeida-da-Silva CL, Sivakumar N, Asadi H, Chang-Chien A, Qoronfleh MW, Ojcius DM, Essa MM Molecules 29-Jun-2022
PMCID:PMC9268443
doi:10.3390/molecules27134174
PMID:35807419
Bio-Assisted Synthesis and Characterization of Zinc Oxide Nanoparticles from Lepidium sativum and Their Potent Antioxidant, Antibacterial and Anticancer Activities Meer B, Andleeb A, Iqbal J, Ashraf H, Meer K, Ali JS, Drouet S, Anjum S, Mehmood A, Khan T, Ali M, Hano C, Abbasi BH Biomolecules 20-Jun-2022
PMCID:PMC9221242
doi:10.3390/biom12060855
PMID:35740980
Biogenic Silver Nanoparticles as a Stress Alleviator in Plants: A Mechanistic Overview Abasi F, Raja NI, Mashwani ZU, Amjad MS, Ehsan M, Mustafa N, Haroon M, Proćków J Molecules 24-May-2022
PMCID:PMC9182038
doi:10.3390/molecules27113378
PMID:35684312

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
Panduratin H 24864449 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)OC)C2=CC=CC=C2 298.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
[(2R)-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 101855692 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
[(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
Panduratin D 24864268 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C3C(=C(C=C2O)OC)C=CO3)C4=CC=CC=C4 430.50 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 CC1CCC2(CCC3(C4CCC5C(C(CCC5(C4CC=C3C2C1C)C)O)(C)C)C)C 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 CC1CCC2(CCC3(C4CCC5C(C(CCC5(C4CC=C3C2C1C)C)O)(C)C)C)C 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 COC1=C2C=C(C=CCCC(=O)CCC3=CC=C(O2)C=C3)C=C1 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 COC1=C2C=C(C=CCCC(=O)C(CC3=CC=C(O2)C=C3)O)C=C1 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 COC1=C2C=C(C=CCCC(=O)CCC3=CC=C(O2)C=C3)C=C1 308.40 unknown https://doi.org/10.1248/CPB.51.1081
acerogenin C 10040223 Click to see C1CCC2=CC(=C(C=C2)O)OC3=CC=C(CCC(=O)C1)C=C3 296.40 unknown https://doi.org/10.1248/CPB.51.1081
Ovalifoliolatin A 11727074 Click to see COC1=C2C=C(C=CCCC(=O)C(CC3=CC=C(O2)C=C3)O)C=C1 324.40 unknown https://doi.org/10.1248/CPB.51.1081
Ovalifoliolatin B 101258447 Click to see COC1=C2C=C(C=CCCC(=O)CCC3=CC=C(O2)C=C3)C=C1 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 CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C(C=C2OC)OC)O)C3=CC=CC=C3 420.50 unknown via CMAUP database
2,6-Dihydroxy-4-methoxyphenyl[2beta-(3-methyl-2-butenyl)-3-methyl-6alpha-phenyl-3-cyclohexene-1beta-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 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
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-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
2alpha-Phenyl-6-[(E)-3,7-dimethyl-2,6-octadienyl]-2,3-dihydro-5,7-dihydroxy-4H-1-benzopyran-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
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(2R)-8-geranylpinostrobin 23656470 Click to see CC(=CCCC(=CCC1=C(C=C(C2=C1OC(CC2=O)C3=CC=CC=C3)O)OC)C)C 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
(2R)-5,7-Dimethoxyflavanone 689012 Click to see COC1=CC2=C(C(=O)CC(O2)C3=CC=CC=C3)C(=C1)OC 284.31 unknown via CMAUP database
(2S)-5,7-dimethoxy-2-phenyl-3,4-dihydro-2H-1-benzopyran-4-one 689011 Click to see COC1=CC2=C(C(=O)CC(O2)C3=CC=CC=C3)C(=C1)OC 284.31 unknown via CMAUP database
3,5,7-Trimethoxyflavone 117900 Click to see COC1=CC2=C(C(=C1)OC)C(=O)C(=C(O2)C3=CC=CC=C3)OC 312.30 unknown via CMAUP database
3',4',5,7-Tetramethoxyflavone 631170 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C=C3OC)OC)OC 342.30 unknown via CMAUP database
4H-1-Benzopyran-4-one, 5-hydroxy-3,7-dimethoxy-2-phenyl- 5748697 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC=CC=C3)O 298.29 unknown via CMAUP database
5-Hydroxy-7-methoxy-2-phenylchroman-4-one 73201 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)O 270.28 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
Apigenin 7,4'-dimethyl ether 5281601 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC)O 298.29 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
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
Pinostrobin 6950539 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)O 270.28 unknown via CMAUP database
Quercetin pentamethyl ether 97332 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(O2)C=C(C=C3OC)OC)OC)OC 372.40 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 COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O 286.28 unknown via CMAUP database
Tectochrysin 5281954 Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC=CC=C3)O 268.26 unknown via CMAUP database
Tetramethylkaempferol 631095 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(O2)C=C(C=C3OC)OC)OC 342.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Kavalactones
2H-Pyran-2-one, 4-methoxy-6-(2-phenylethyl)- 160673 Click to see COC1=CC(=O)OC(=C1)CCC2=CC=CC=C2 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 COC1=CC(=CC(=C1C(=O)CCC2=CC=C(C=C2)O)O)O 288.29 unknown via CMAUP database
Phloretin 4788 Click to see C1=CC(=CC=C1CCC(=O)C2=C(C=C(C=C2O)O)O)O 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 CC1(C2CCC3(CC2C4=C(O3)C=C(C(=C4O1)C(=O)C=CC5=CC=CC=C5)O)C)C 390.50 unknown via CMAUP database
2',4-Dihydroxy-4',6'-dimethoxychalcone 6293081 Click to see COC1=CC(=C(C(=C1)OC)C(=O)C=CC2=CC=C(C=C2)O)O 300.30 unknown via CMAUP database
Cardamonin 641785 Click to see COC1=CC(=CC(=C1C(=O)C=CC2=CC=CC=C2)O)O 270.28 unknown via CMAUP database
CID 460718 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
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
2',4'-Dihydroxy-3'-[(2E)-3,7-dimethyl-2,6-octadienyl]-6'-methoxychalcone 23656471 Click to see CC(=CCCC(=CCC1=C(C(=C(C=C1O)OC)C(=O)C=CC2=CC=CC=C2)O)C)C 406.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
2,4-Dihydroxy-6-phenethylbenzoic acid (2E)-3,7-dimethyl-2,6-octadienyl ester 23656469 Click to see CC(=CCCC(=CCOC(=O)C1=C(C=C(C=C1O)O)CCC2=CC=CC=C2)C)C 394.50 unknown via CMAUP database

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