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Cinnamomum reticulatum

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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 UUID6440113d81836755506596
Scientific name Cinnamomum reticulatum
Authority Hayata
First published in J. Coll. Sci. Imp. Univ. Tokyo 30(1): 239 (1911)

Description Top

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Synonyms Top

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Common names Top

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Language Common/alternative name
Chinese 土樟
Chinese 网脉桂

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-0000605381
Tropicos 17801727
KEW urn:lsid:ipni.org:names:463649-1
The Plant List kew-2721573
Open Tree Of Life 644826
NCBI Taxonomy 1222053
IUCN Red List 31249
IPNI 463649-1
iNaturalist 190597
GBIF 4180681
EOL 5395802

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
Chemical characteristics of the sesquiterpenes and diterpenes from Lauraceae family and their multifaceted health benefits: A review Feng H, Jiang Y, Cao H, Shu Y, Yang X, Zhu D, Shao M Heliyon 07-Dec-2022
PMCID:PMC9801090
doi:10.1016/j.heliyon.2022.e12013
PMID:36590503
Phylogeny and taxonomy of Cinnamomum (Lauraceae) Yang Z, Liu B, Yang Y, Ferguson DK Ecol Evol 01-Oct-2022
PMCID:PMC9526118
doi:10.1002/ece3.9378
PMID:36203627
Quantitative ethnopharmacological documentation and molecular confirmation of medicinal plants used by the Manobo tribe of Agusan del Sur, Philippines Dapar ML, Alejandro GJ, Meve U, Liede-Schumann S J Ethnobiol Ethnomed 05-Mar-2020
PMCID:PMC7227330
doi:10.1186/s13002-020-00363-7
PMID:32138749
Chemical constituents from the leaves of Cinnamomum reticulatum Yi-Chen Chia, Hung-Chun Yeh, Yu-Ting Yeh, Chung-Yi Chen Springer Science and Business Media LLC 06-Jun-2011
doi:10.1007/S10600-011-9887-3
Chemical constituents from the roots of Cinnamomum reticulatum Chung-Yi Chen Springer Science and Business Media LLC 06-Jun-2011
doi:10.1007/S10600-011-9915-3
A new butanolide from the leaves of Cinnamomum reticulatum I. J. Lin, H. C. Yeh, T. M. Cham, C. Y. Chen Springer Science and Business Media LLC 05-Apr-2011
doi:10.1007/S10600-011-9826-3
A new amide from the stems of Cinnamomum reticulatum Hay. Chen CY, Yeh HC Nat Prod Res 01-Jan-2011
doi:10.1080/14786411003757929
PMID:21240757

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 / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
3,4-Dihydroxybenzoic acid 72 Click to see C1=CC(=C(C=C1C(=O)O)O)O 154.12 unknown https://doi.org/10.1007/S10600-011-9915-3
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown https://doi.org/10.1007/S10600-011-9887-3
https://doi.org/10.1007/S10600-011-9826-3
https://doi.org/10.1007/S10600-011-9915-3
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
3-[(1S)-4-hydroxy-5-methoxycyclohexa-2,4-dien-1-yl]-N-[2-(4-hydroxyphenyl)ethyl]propanamide 163091001 Click to see COC1=C(C=CC(C1)CCC(=O)NCCC2=CC=C(C=C2)O)O 317.40 unknown https://doi.org/10.1007/S10600-011-9826-3
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde 126 Click to see C1=CC(=CC=C1C=O)O 122.12 unknown https://doi.org/10.1007/S10600-011-9915-3
> Organoheterocyclic compounds / Benzodioxoles
(5-Methoxy-14,16-dioxatetracyclo[9.7.0.02,7.013,17]octadeca-1(18),2(7),3,5,9,11,13(17)-heptaen-10-yl)methanol 44557485 Click to see COC1=CC2=C(C=C1)C3=CC4=C(C=C3C(=CC2)CO)OCO4 296.30 unknown https://doi.org/10.1007/S10600-011-9915-3
https://doi.org/10.1007/S10600-011-9826-3
10-(Hydroxymethyl)-14,16-dioxatetracyclo[9.7.0.02,7.013,17]octadeca-1(18),2(7),3,5,9,11,13(17)-heptaen-5-ol 135024930 Click to see C1C=C(C2=CC3=C(C=C2C4=C1C=C(C=C4)O)OCO3)CO 282.29 unknown https://doi.org/10.1007/S10600-011-9887-3
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives
N-[1-hydroxy-3-(4-hydroxy-3-methoxyphenyl)propan-2-yl]-3-(4-hydroxy-3-methoxyphenyl)prop-2-enamide 163018759 Click to see COC1=C(C=CC(=C1)CC(CO)NC(=O)C=CC2=CC(=C(C=C2)O)OC)O 373.40 unknown https://doi.org/10.1080/14786411003757929
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
2-Propenoic acid, 3-(4-hydroxyphenyl)-, methyl ester 92203 Click to see COC(=O)C=CC1=CC=C(C=C1)O 178.18 unknown https://doi.org/10.1007/S10600-011-9826-3
Methyl 4-hydroxycinnamate 5319562 Click to see COC(=O)C=CC1=CC=C(C=C1)O 178.18 unknown https://doi.org/10.1007/S10600-011-9826-3
https://doi.org/10.1007/S10600-011-9915-3
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Ferulic acid 445858 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O 194.18 unknown https://doi.org/10.1007/S10600-011-9826-3
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2",4"-Di-O-(Z-p-coumaroyl)afzelin 73066482 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)OC(=O)C=CC5=CC=C(C=C5)O)O)OC(=O)C=CC6=CC=C(C=C6)O 724.70 unknown https://doi.org/10.1007/S10600-011-9887-3
> Phenylpropanoids and polyketides / Phenylpropanoic acids
3-(4-Hydroxyphenyl)propionic acid 10394 Click to see C1=CC(=CC=C1CCC(=O)O)O 166.17 unknown https://doi.org/10.1007/S10600-011-9826-3

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