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Haplophyllum patavinum

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID64401fb9baa66010401111
Scientific name Haplophyllum patavinum
Authority G.Don
First published in Gen. Hist. 1: 780 (1831)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Ruta patavina L. Sp. Pl. : 384 (1753)
Haplophyllum boissierianum Beck Glasn. Zem. Mus. Bosn. i Hercegov. (Fl. Bosn. Hercegov. &c.) xxxii. 117(1920)

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
  • Europe
    • Southeastern Europe
      • Albania
      • Greece
      • Italy
      • Romania
      • Yugoslavia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000715576
Flora of Italy 2992
KEW urn:lsid:ipni.org:names:771308-1
Open Tree Of Life 1081345
Observations.org 137798
NCBI Taxonomy 452780
IPNI 771308-1
iNaturalist 1225673
GBIF 8078240
Freebase /m/025_gtv
Elurikkus 643034
Wikipedia Haplophyllum_patavinum

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
Bioactivities and Mechanisms of Action of Diphyllin and Its Derivatives: A Comprehensive Systematic Review Hou W, Huang LJ, Huang H, Liu SL, Dai W, Li ZM, Zhang ZY, Xin SY, Wang JY, Zhang ZY, Ouyang X, Lan JX Molecules 30-Nov-2023
PMCID:PMC10707837
doi:10.3390/molecules28237874
PMID:38067601
Therapeutic Potential of Phenolic Compounds in Medicinal Plants—Natural Health Products for Human Health Sun W, Shahrajabian MH Molecules 15-Feb-2023
PMCID:PMC9960276
doi:10.3390/molecules28041845
PMID:36838831
Plant Pyranocoumarins: Description, Biosynthesis, Application Khandy MT, Sofronova AK, Gorpenchenko TY, Chirikova NK Plants (Basel) 16-Nov-2022
PMCID:PMC9693251
doi:10.3390/plants11223135
PMID:36432864
7-Isopentenyloxycoumarin: What Is New across the Last Decade Preziuso F, Genovese S, Marchetti L, Sharifi-Rad M, Palumbo L, Epifano F, Fiorito S Molecules 14-Dec-2020
PMCID:PMC7765079
doi:10.3390/molecules25245923
PMID:33327602
Justicidin B: A Promising Bioactive Lignan Hemmati S, Seradj H Molecules 23-Jun-2016
PMCID:PMC6272961
doi:10.3390/molecules21070820
PMID:27347906
Lignans and other constituents from aerial parts of Haplophyllum villosum. Parhoodeh P, Rahmani M, Hashim NM, Sukari MA, Lian GE Molecules 07-Mar-2011
PMCID:PMC6259757
doi:10.3390/MOLECULES16032268
PMID:21383663
Lignans and Other Constituents from Aerial Parts of Haplophyllum Villosum Parhoodeh P, Rahmani M, Hashim NM, Sukari MA, Cheng Lian GE Molecules 07-Mar-2011
PMCID:PMC6259757
doi:10.3390/molecules16032268
PMID:21383663
Production of Lignans by Haplophyllum patavinum in vivo and in vitro Rosy Caniato, Lucia Puricelli, Gabbriella Innocenti, Sonia Piacente, Raffaella Filippini, Elsa M. Cappelletti The Japan Institute of Heterocyclic Chemistry 09-Mar-2009
doi:10.3987/COM-01-S(K)71
Production of coumarin compounds by Haplophyllum patavinum in vivo and in vitro Raffaella Filippini, Anna Piovan, Gabbriella Innocenti, Rosy Caniato, Elsa M. Cappelletti Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(98)00356-2
Patavine, a new arylnaphthalene lignan glycoside from shoot cultures of Haplophyllum patavinum. Innocenti G, Puricelli L, Piacente S, Caniato R, Filippini R, Cappelletti EM Chem Pharm Bull (Tokyo) 01-Jun-2002
doi:10.1248/CPB.50.844
PMID:12045345
In vivo and in vitro production of alkaloids by Haplophyllum patavinum. Puricelli L, Innocenti G, Delle Monache G, Caniato R, Filippini R, Cappelletti EM Nat Prod Lett 01-Apr-2002
doi:10.1080/10575630290019985
PMID:11990434

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Lignans, neolignans and related compounds / Arylnaphthalene lignans
9-(1,3-Benzodioxol-5-yl)-4-hydroxy-6,7-dimethoxynaphtho(2,3-c)furan-1(3H)-one 100492 Click to see 380.30 unknown https://doi.org/10.1248/CPB.50.844
https://doi.org/10.3987/COM-01-S(K)71
9-(3,4-Dimethoxy-phenyl)-8-H-furo(3',4':6,7)naphtho(2,3-d)(1,3)dioxol-6-one 122805 Click to see 364.30 unknown https://doi.org/10.1248/CPB.50.844
https://doi.org/10.3987/COM-01-S(K)71
Justicidin B 442882 Click to see COC1=CC2=CC3=C(C(=C2C=C1OC)C4=CC5=C(C=C4)OCO5)C(=O)OC3 364.30 unknown https://doi.org/10.3987/COM-01-S(K)71
https://doi.org/10.1248/CPB.50.844
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
Arctigenin 64981 Click to see COC1=C(C=C(C=C1)CC2COC(=O)C2CC3=CC(=C(C=C3)O)OC)OC 372.40 unknown https://doi.org/10.3987/COM-01-S(K)71
> Lignans, neolignans and related compounds / Lignan glycosides
9-(1,3-benzodioxol-5-yl)-4-[(2R,3R,4R)-3-[(2S,3R,4R,5S)-5-[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-3,4-dihydroxyoxan-2-yl]oxy-4-hydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-6,7-dimethoxy-3H-benzo[f][2]benzofuran-1-one 162965945 Click to see COC1=C(C=C2C(=C1)C(=C3C(=C2OC4C(C(CO4)(CO)O)OC5C(C(C(CO5)OC6C(C(CO6)(CO)O)O)O)O)COC3=O)C7=CC8=C(C=C7)OCO8)OC 776.70 unknown https://doi.org/10.1248/CPB.50.844
9-(1,3-benzodioxol-5-yl)-4-[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-6,7-dimethoxy-1H-benzo[f][2]benzofuran-3-one 101293623 Click to see 512.50 unknown https://doi.org/10.1248/CPB.50.844
9-(1,3-benzodioxol-5-yl)-4-[(2S,3R,4R)-4-hydroxy-4-(hydroxymethyl)-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxolan-2-yl]oxy-6,7-dimethoxy-3H-benzo[f][2]benzofuran-1-one 14731302 Click to see COC1=C(C=C2C(=C1)C(=C3C(=C2OC4C(C(CO4)(CO)O)OC5C(C(C(CO5)O)O)O)COC3=O)C6=CC7=C(C=C6)OCO7)OC 644.60 unknown https://doi.org/10.1248/CPB.50.844
9-(1,3-benzodioxol-5-yl)-4-[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-6,7-dimethoxy-1H-benzo[f][2]benzofuran-3-one 162821327 Click to see 512.50 unknown https://doi.org/10.1248/CPB.50.844
https://doi.org/10.3987/COM-01-S(K)71
9-(1,3-benzodioxol-5-yl)-6,7-dimethoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxy-3H-benzo[f][2]benzofuran-1-one 163012042 Click to see 674.60 unknown https://doi.org/10.1248/CPB.50.844
Arabelline 14731306 Click to see 674.60 unknown https://doi.org/10.1248/CPB.50.844
Patavine 10101750 Click to see 776.70 unknown https://doi.org/10.1248/CPB.50.844
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
Umbelliprenin 1781413 Click to see CC(=CCCC(=CCCC(=CCOC1=CC2=C(C=C1)C=CC(=O)O2)C)C)C 366.50 unknown https://doi.org/10.1016/S0031-9422(98)00356-2
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives / Xanthines
(R)-dyphylline 688353 Click to see 254.24 unknown https://doi.org/10.1248/CPB.50.844
> Organoheterocyclic compounds / Quinolines and derivatives / Dihydrofuranoquinolines
Isoplatydesmine 11219133 Click to see CC(C)(C1CC2=C(O1)N(C3=CC=CC=C3C2=O)C)O 259.30 unknown https://doi.org/10.1080/10575630290019985
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
4,8-dimethoxy-9H-furo[2,3-b]quinolin-7-one 165368 Click to see COC1=C2C=CC(=O)C(=C2NC3=C1C=CO3)OC 245.23 unknown https://doi.org/10.1080/10575630290019985
Haplopine 5281846 Click to see COC1=C2C=COC2=NC3=C1C=CC(=C3OC)O 245.23 unknown https://doi.org/10.1080/10575630290019985
Skimmianine 6760 Click to see COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC 259.26 unknown https://doi.org/10.1080/10575630290019985
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroquinolones
(S)-Edulinine 356087 Click to see 291.34 unknown https://doi.org/10.1080/10575630290019985
3-[(2S)-2,3-dihydroxy-3-methylbutyl]-4-methoxy-1-methylquinolin-2-one 10902387 Click to see CC(C)(C(CC1=C(C2=CC=CC=C2N(C1=O)C)OC)O)O 291.34 unknown https://doi.org/10.1080/10575630290019985
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Pyranoquinolines
(3S)-3-hydroxy-2,2,10-trimethyl-3,4-dihydropyrano[2,3-b]quinolin-5-one 932818 Click to see 259.30 unknown https://doi.org/10.1080/10575630290019985
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Angular furanocoumarins
Columbianetin 92201 Click to see CC(C)(C1CC2=C(O1)C=CC3=C2OC(=O)C=C3)O 246.26 unknown https://doi.org/10.1016/S0031-9422(98)00356-2
Isopsoralen 10658 Click to see 186.16 unknown https://doi.org/10.1016/S0031-9422(98)00356-2
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
Psoralen 6199 Click to see 186.16 unknown https://doi.org/10.1016/S0031-9422(98)00356-2
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Osthenol 5320318 Click to see 230.26 unknown https://doi.org/10.1016/S0031-9422(98)00356-2
Scopoletin 5280460 Click to see 192.17 unknown https://doi.org/10.1016/S0031-9422(98)00356-2
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259757/
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown https://doi.org/10.1016/S0031-9422(98)00356-2

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