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Cinnamomum osmophloeum

Cinnamomum osmophloeum - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID644011399c804489931338
Scientific name Cinnamomum osmophloeum
Authority Kaneh.
First published in Formos. Trees : 428 (1917)

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Arabic دارصوص
Arabic دارصيني الدون
Arabic الدارصوص
Arabic الدارصيني الدون
Arabic دارصيني دون
Chinese 土肉桂
Chinese 大叶山桂

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-0000605291
Tropicos 17801972
KEW urn:lsid:ipni.org:names:463589-1
The Plant List kew-2721492
Open Tree Of Life 582938
NCBI Taxonomy 258907
IUCN Red List 31334
IPNI 463589-1
iNaturalist 190593
GBIF 4181555
Freebase /m/047t_4r
EPPO CINOS
EOL 5395728
USDA GRIN 468413
Wikipedia Cinnamomum_osmophloeum

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
Pest categorisation of Pyrrhoderma noxium Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Golic D, Gobbi A, Maiorano A, Pautasso M, Reignault PL EFSA J 19-Mar-2024
PMCID:PMC10949325
doi:10.2903/j.efsa.2024.8667
PMID:38505477
Integrated transcriptomics and metabolomics analysis provides insights into aromatic volatiles formation in Cinnamomum cassia bark at different harvesting times Yao S, Tan X, Huang D, Li L, Chen J, Ming R, Huang R, Yao C BMC Plant Biol 02-Feb-2024
PMCID:PMC10835945
doi:10.1186/s12870-024-04754-w
PMID:38308239
Exploring the Therapeutic Potential of Ampelopsis grossedentata Leaf Extract as an Anti-Inflammatory and Antioxidant Agent in Human Immune Cells Chervet A, Nehme R, Decombat C, Longechamp L, Habanjar O, Rousset A, Fraisse D, Blavignac C, Filaire E, Berthon JY, Delort L, Caldefie-Chezet F Int J Mol Sci 28-Dec-2023
PMCID:PMC10779184
doi:10.3390/ijms25010416
PMID:38203587
WRKY Transcription Factors in Jasminum sambac: An Insight into the Regulation of Aroma Synthesis Lu Z, Wang X, Mostafa S, Noor I, Lin X, Ren S, Cui J, Jin B Biomolecules 21-Nov-2023
PMCID:PMC10742223
doi:10.3390/biom13121679
PMID:38136552
A study on the effect of natural products against the transmission of B.1.1.529 Omicron Alkafaas SS, Abdallah AM, Hussien AM, Bedair H, Abdo M, Ghosh S, Elkafas SS, Apollon W, Saki M, Loutfy SA, Onyeaka H, Hessien M Virol J 25-Aug-2023
PMCID:PMC10464336
doi:10.1186/s12985-023-02160-6
PMID:37626376
Analysis of bioactive compounds in cinnamon leaves and preparation of nanoemulsion and byproducts for improving Parkinson’s disease in rats Wang YC, Wang V, Chen BH Front Nutr 02-Aug-2023
PMCID:PMC10433916
doi:10.3389/fnut.2023.1229192
PMID:37599679
Essential Oils: Chemistry and Pharmacological Activities de Sousa DP, Damasceno RO, Amorati R, Elshabrawy HA, de Castro RD, Bezerra DP, Nunes VR, Gomes RC, Lima TC Biomolecules 18-Jul-2023
PMCID:PMC10377445
doi:10.3390/biom13071144
PMID:37509180
Chemical Composition, Analgesic and Anti-Inflammatory Activity of Pelargonium peltatum Essential Oils from Eastern Cape, South Africa Rungqu P, Oyedeji O, Gondwe M, Oyedeji A Molecules 08-Jul-2023
PMCID:PMC10385469
doi:10.3390/molecules28145294
PMID:37513168
The Use of Natural Bioactive Nutraceuticals in the Management of Tick-Borne Illnesses Shor SM, Schweig SK Microorganisms 05-Jul-2023
PMCID:PMC10384908
doi:10.3390/microorganisms11071759
PMID:37512931
Antidepressant Effects of Essential Oils: A Review of the Past Decade (2012–2022) and Molecular Docking Study of Their Major Chemical Components Fonseca EC, Ferreira LR, Figueiredo PL, Maia CD, Setzer WN, Da Silva JK Int J Mol Sci 25-May-2023
PMCID:PMC10252423
doi:10.3390/ijms24119244
PMID:37298210
Oligomeric Proanthocyanidins: An Updated Review of Their Natural Sources, Synthesis, and Potentials Nie F, Liu L, Cui J, Zhao Y, Zhang D, Zhou D, Wu J, Li B, Wang T, Li M, Yan M Antioxidants (Basel) 26-Apr-2023
PMCID:PMC10215713
doi:10.3390/antiox12051004
PMID:37237870
Trans-cinnamaldehyde-related overproduction of benzoic acid and oxidative stress on Arabidopsis thaliana López-González D, Ferradás Y, Araniti F, Graña E, Hermida-Ramón JM, González MV, Teijeira M, Rey M, Reigosa MJ, Sánchez-Moreiras AM Front Plant Sci 21-Apr-2023
PMCID:PMC10160683
doi:10.3389/fpls.2023.1157309
PMID:37152151
Multi-Dimensional Antioxidant Screening of Selected Australian Native Plants and Putative Annotation of Active Compounds Ghani MA, Barril C, Bedgood DR Jr, Burrows GE, Ryan D, Prenzler PD Molecules 30-Mar-2023
PMCID:PMC10095623
doi:10.3390/molecules28073106
PMID:37049870
GC-MS Profiling and Biomedical Applications of Essential Oil of Euphorbia larica Boiss.: A New Report Shah M, Khan F, Ullah S, Mohanta TK, Khan A, Zainab R, Rafiq N, Ara H, Alam T, Rehman NU, Al-Harrasi A Antioxidants (Basel) 07-Mar-2023
PMCID:PMC10045896
doi:10.3390/antiox12030662
PMID:36978910
Effects of Vegetal Extracts and Metabolites against Oxidative Stress and Associated Diseases: Studies in Caenorhabditis elegans Hernández-Cruz EY, Eugenio-Pérez D, Ramírez-Magaña KJ, Pedraza-Chaverri J ACS Omega 27-Feb-2023
PMCID:PMC10018526
doi:10.1021/acsomega.2c07025
PMID:36936291

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
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
Benzaldehyde 240 Click to see C1=CC=C(C=C1)C=O 106.12 unknown https://doi.org/10.1016/S0378-8741(01)00273-2
> Benzenoids / Benzene and substituted derivatives / Styrenes
3-Phenylprop-2-enyl acetate 7660 Click to see CC(=O)OCC=CC1=CC=CC=C1 176.21 unknown https://doi.org/10.1016/S0378-8741(01)00273-2
Cinnamyl acetate 5282110 Click to see CC(=O)OCC=CC1=CC=CC=C1 176.21 unknown https://doi.org/10.1016/S0378-8741(01)00273-2
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Geranyl acetate 1549026 Click to see CC(=CCCC(=CCOC(=O)C)C)C 196.29 unknown https://doi.org/10.1016/S0378-8741(01)00273-2
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Geraniol 637566 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1016/S0378-8741(01)00273-2
Linalool, (+/-)- 6549 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown https://doi.org/10.1016/S0378-8741(01)00273-2
Neral 643779 Click to see CC(=CCCC(=CC=O)C)C 152.23 unknown https://doi.org/10.1016/S0378-8741(01)00273-2
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol 64685 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1016/S0378-8741(01)00273-2
trans-Borneol 44630107 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1016/S0378-8741(01)00273-2
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Alpha-Terpineol 17100 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown https://doi.org/10.1016/S0378-8741(01)00273-2
> Phenylpropanoids and polyketides / Cinnamaldehydes
3-Phenyl-propenal 307 Click to see C1=CC=C(C=C1)C=CC=O 132.16 unknown https://doi.org/10.1016/S0378-8741(01)00273-2
Cinnamaldehyde 637511 Click to see C1=CC=C(C=C1)C=CC=O 132.16 unknown https://doi.org/10.1016/S0378-8741(01)00273-2
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
3-[(2S,3R,4S,5R,6S)-3,4-dihydroxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-7-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 102312101 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)C)OC5C(C(C(C(O5)CO)O)O)O)O)O)C6=CC=C(C=C6)O)O)O)O)O 740.70 unknown https://doi.org/10.1016/J.BMC.2005.01.050
3-[(2S,3R,4S,5R,6S)-5-[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-3,4-dihydroxy-6-methyloxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-7-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 101021023 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)C)OC5C(C(CO5)(CO)O)O)O)O)C6=CC=C(C=C6)O)O)O)O)O 710.60 unknown https://doi.org/10.1016/J.BMC.2005.01.050
3-[(2S,3R,4S,5S)-3-[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-7-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 102076696 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(O4)CO)O)OC5C(C(CO5)(CO)O)O)C6=CC=C(C=C6)O)O)O)O)O 696.60 unknown https://doi.org/10.1016/J.BMC.2005.01.050
3-[3,4-Dihydroxy-6-methyl-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-7-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxychromen-4-one 74325934 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)C)OC5C(C(C(C(O5)CO)O)O)O)O)O)C6=CC=C(C=C6)O)O)O)O)O 740.70 unknown https://doi.org/10.1016/J.BMC.2005.01.050
3-[5-[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-3,4-dihydroxy-6-methyloxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-7-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxychromen-4-one 74978104 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)C)OC5C(C(CO5)(CO)O)O)O)O)C6=CC=C(C=C6)O)O)O)O)O 710.60 unknown https://doi.org/10.1016/J.BMC.2005.01.050
Kaempferol 3-apiosyl-(1->2)-alpha-L-arabinofuranoside-7-rhamnoside 44258945 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(O4)CO)O)OC5C(C(CO5)(CO)O)O)C6=CC=C(C=C6)O)O)O)O)O 696.60 unknown https://doi.org/10.1016/J.BMC.2005.01.050
Lespedin 5486199 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)C)O)O)O)C5=CC=C(C=C5)O)O)O)O)O 578.50 unknown https://doi.org/10.1016/J.BMC.2005.01.050
Lespedin;Lespenephryl 12305415 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)C)O)O)O)C5=CC=C(C=C5)O)O)O)O)O 578.50 unknown https://doi.org/10.1016/J.BMC.2005.01.050

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