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Ehretia philippinensis

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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 UUID644018fadca63122900643
Scientific name Ehretia philippinensis
Authority A.DC.
First published in Prodr. 9: 504 (1845)

Description Top

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Synonyms Top

Scientific name Authority First published in
Ehretia lanyuensis Liu & Chuang Quart. J. Taiwan Mus. 13: 63 (1960)
Ehretia takaminei Hatus. J. Jap. Bot. 27: 210 (1952)

Common names Top

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Language Common/alternative name
Chinese 蘭嶼厚殼樹

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

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000663509
Tropicos 50055811
KEW urn:lsid:ipni.org:names:116098-1
The Plant List kew-2784815
Open Tree Of Life 6063594
NCBI Taxonomy 2811221
IPNI 116098-1
iNaturalist 706806
GBIF 4066200

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
Application of Rosmarinic Acid with Its Derivatives in the Treatment of Microbial Pathogens Kernou ON, Azzouz Z, Madani K, Rijo P Molecules 22-May-2023
PMCID:PMC10220798
doi:10.3390/molecules28104243
PMID:37241981
A Comprehensive Review of Rosmarinic Acid: From Phytochemistry to Pharmacology and Its New Insight Guan H, Luo W, Bao B, Cao Y, Cheng F, Yu S, Fan Q, Zhang L, Wu Q, Shan M Molecules 20-May-2022
PMCID:PMC9143754
doi:10.3390/molecules27103292
PMID:35630768
Genetic Differentiation and Spatial Structure of Phellinus noxius, the Causal Agent of Brown Root Rot of Woody Plants in Japan Akiba M, Ota Y, Tsai IJ, Hattori T, Sahashi N, Kikuchi T PLoS One 29-Oct-2015
PMCID:PMC4626371
doi:10.1371/journal.pone.0141792
PMID:26513585
Nitrile glucosides and rosmarinic acid, the histamine inhibitor from Ehretia philippinensis Lourdes R. Simpol, Hideaki Otsuka, Kazuhiro Ohtani, Ryoji Kasai, Kazuo Yamasaki Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)97019-5

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
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(1S,2S,3Z,4R,6S)-3-(Cyanomethylene)-4-(beta-D-glucopyranosyloxy)-2,6-dihydroxycyclohexyl 3-methyl-2-butenoate 85141478 Click to see CC(=CC(=O)OC1C(CC(C(=CC#N)C1O)OC2C(C(C(C(O2)CO)O)O)O)O)C 429.40 unknown https://doi.org/10.1016/S0031-9422(00)97019-5
(2Z)-2-[(2S,3R,4S,6R)-2-hydroxy-3,4-dimethoxy-6-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycyclohexylidene]acetonitrile 76308614 Click to see COC1CC(C(=CC#N)C(C1OC)O)OC2C(C(C(C(O2)CO)O)O)O 375.37 unknown https://doi.org/10.1016/S0031-9422(00)97019-5
[(1S,2E,3R,5S,6S)-2-(cyanomethylidene)-5,6-dihydroxy-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycyclohexyl] 3-methylbut-2-enoate 10342584 Click to see CC(=CC(=O)OC1C(C(CC(C1=CC#N)OC2C(C(C(C(O2)CO)O)O)O)O)O)C 429.40 unknown https://doi.org/10.1016/S0031-9422(00)97019-5
[(1S,2R,3S,4Z,5R)-4-(cyanomethylidene)-2,3-dihydroxy-5-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycyclohexyl] 3-methylbut-2-enoate 10071288 Click to see CC(=CC(=O)OC1CC(C(=CC#N)C(C1O)O)OC2C(C(C(C(O2)CO)O)O)O)C 429.40 unknown https://doi.org/10.1016/S0031-9422(00)97019-5
[(1S,2S,3Z,4R,6S)-3-(cyanomethylidene)-2,6-dihydroxy-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycyclohexyl] 3-methylbut-2-enoate 10432770 Click to see CC(=CC(=O)OC1C(CC(C(=CC#N)C1O)OC2C(C(C(C(O2)CO)O)O)O)O)C 429.40 unknown https://doi.org/10.1016/S0031-9422(00)97019-5
[2-(Cyanomethylidene)-5,6-dihydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycyclohexyl] 3-methylbut-2-enoate 85115790 Click to see CC(=CC(=O)OC1C(C(CC(C1=CC#N)OC2C(C(C(C(O2)CO)O)O)O)O)O)C 429.40 unknown https://doi.org/10.1016/S0031-9422(00)97019-5
[4-(Cyanomethylidene)-2,3-dihydroxy-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycyclohexyl] 3-methylbut-2-enoate 163046998 Click to see CC(=CC(=O)OC1CC(C(=CC#N)C(C1O)O)OC2C(C(C(C(O2)CO)O)O)O)C 429.40 unknown https://doi.org/10.1016/S0031-9422(00)97019-5
2-[2-Hydroxy-3,4-dimethoxy-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycyclohexylidene]acetonitrile 300088 Click to see COC1CC(C(=CC#N)C(C1OC)O)OC2C(C(C(C(O2)CO)O)O)O 375.37 unknown https://doi.org/10.1016/S0031-9422(00)97019-5
Acetonitrile, ((2S,3R,4S,6R)-6-(beta-D-glucopyranosyloxy)-2-hydroxy-3,4-dimethoxycyclohexylidene)-, (2Z)- 6437384 Click to see COC1CC(C(=CC#N)C(C1OC)O)OC2C(C(C(C(O2)CO)O)O)O 375.37 unknown https://doi.org/10.1016/S0031-9422(00)97019-5
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
2-[4-Hydroxy-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]acetonitrile 85139737 Click to see C1=CC(=C(C=C1O)OC2C(C(C(C(O2)CO)O)O)O)CC#N 311.29 unknown https://doi.org/10.1016/S0031-9422(00)97019-5
Ehretioside B 10425556 Click to see C1=CC(=C(C=C1O)OC2C(C(C(C(O2)CO)O)O)O)CC#N 311.29 unknown https://doi.org/10.1016/S0031-9422(00)97019-5
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Rosmarinic acid 5281792 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 360.30 unknown https://doi.org/10.1016/S0031-9422(00)97019-5
Rosmarinic Acid Methyl Ester 3012090 Click to see COC(=O)C(CC1=CC(=C(C=C1)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O 374.30 unknown https://doi.org/10.1016/S0031-9422(00)97019-5

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