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Haplophyllum myrtifolium

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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 UUID64401fb93ce04676427622
Scientific name Haplophyllum myrtifolium
Authority Boiss.
First published in Diagn. Pl. Orient. 1: 63 (1843)

Description Top

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Synonyms Top

Scientific name Authority First published in
Haplophyllum eriocarpum Freyn Bull. Herb. Boissier 3: 106 (1895)
Haplophyllum sulphureum Boiss. Diagn. Pl. Orient. 5: 87 (1844)
Haplophyllum tchihatchewi Boiss. Diagn. Pl. Orient. , ser. 2, 6: 41 (1859)

Common names Top

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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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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-0000715571
KEW urn:lsid:ipni.org:names:771306-1
Open Tree Of Life 520174
NCBI Taxonomy 1006077
IPNI 771306-1
GBIF 8428264

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
Chemistry and Biological Activities of Naturally Occurring and Structurally Modified Podophyllotoxins Jin L, Song Z, Cai F, Ruan L, Jiang R Molecules 30-Dec-2022
PMCID:PMC9822336
doi:10.3390/molecules28010302
PMID:36615496
Phenolic Characterization Using cLC-DAD Analysis and Evaluation of In Vitro and In Vivo Pharmacological Activities of Ruta tuberculata Forssk Saidi A, Hambaba L, Bensaad MS, Melakhessou MA, Bensouici C, Ferhat N, Kahoul MA, Helal M, Sami R, Alharthy SA, Baty RS, Alsubhi NH, Alrefaei GI, Elhakem A, Alharthi S, Elsaid FG, Shati AA Antioxidants (Basel) 11-Jul-2022
PMCID:PMC9312153
doi:10.3390/antiox11071351
PMID:35883842
Outlining In Vitro and In Silico Cholinesterase Inhibitory Activity of Twenty-Four Natural Products of Various Chemical Classes: Smilagenin, Kokusaginine, and Methyl Rosmarinate as Emboldening Inhibitors Senol Deniz FS, Eren G, Orhan IE, Sener B, Ozgen U, Aldaba R, Calis I Molecules 01-Apr-2021
PMCID:PMC8037418
doi:10.3390/molecules26072024
PMID:33916300
Middle East Medicinal Plants in the Treatment of Diabetes: A Review Abu-Odeh AM, Talib WH Molecules 31-Jan-2021
PMCID:PMC7867005
doi:10.3390/molecules26030742
PMID:33572627
Potential Use of Turkish Medicinal Plants in the Treatment of Various Diseases Ozkan G, Kamiloglu S, Ozdal T, Boyacioglu D, Capanoglu E Molecules 25-Feb-2016
PMCID:PMC6273156
doi:10.3390/molecules21030257
PMID:26927038
Inhibitory Activity of Eleven Artemisia Species from Iran against Leishmania Major Parasites Emami SA, Zamanai Taghizadeh Rabe S, Ahi A, Mahmoudi M Iran J Basic Med Sci 01-Mar-2012
PMCID:PMC3586874
PMID:23493354
A new prenylated arylnaphthalene lignan from Haplophyllum myrtifolium. Sağlam H, Gözler T, Gözler B Fitoterapia 01-Sep-2003
doi:10.1016/S0367-326X(03)00147-3
PMID:12946719
Haplomyrtin and (−)-haplomyrfolin: two lignans from haplophyllum myrtifolium Umran Evcim, Belkis Gōzler, Alan J. Freyer, Maurice Shamma Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)81181-4

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
> Lignans, neolignans and related compounds / Arylnaphthalene lignans
9-(1,3-benzodioxol-5-yl)-4,7-dihydroxy-6-methoxy-3H-benzo[f][2]benzofuran-1-one 101996845 Click to see COC1=C(C=C2C(=C1)C(=C3COC(=O)C3=C2C4=CC5=C(C=C4)OCO5)O)O 366.30 unknown https://doi.org/10.1016/S0031-9422(00)81181-4
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
3-(1,3-Benzodioxol-5-ylmethyl)-4-[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one 137796509 Click to see COC1=C(C=CC(=C1)CC2COC(=O)C2CC3=CC4=C(C=C3)OCO4)O 356.40 unknown https://doi.org/10.1016/S0031-9422(00)81181-4
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
Dictamnine 68085 Click to see COC1=C2C=COC2=NC3=CC=CC=C31 199.20 unknown https://doi.org/10.1016/S0367-326X(03)00147-3
gamma-Fagarine 107936 Click to see COC1=CC=CC2=C1N=C3C(=C2OC)C=CO3 229.23 unknown https://doi.org/10.1016/S0367-326X(03)00147-3
Robustine 164950 Click to see COC1=C2C=COC2=NC3=C1C=CC=C3O 215.20 unknown https://doi.org/10.1016/S0367-326X(03)00147-3
Skimmianine 6760 Click to see COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC 259.26 unknown https://doi.org/10.1016/S0367-326X(03)00147-3
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Chrysosplenetin 5281608 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)O 374.30 unknown https://doi.org/10.1016/S0367-326X(03)00147-3

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