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Pityrogramma ebenea

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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 UUID6440773e06f0f604095756
Scientific name Pityrogramma ebenea
Authority (L.) Proctor
First published in Brit. Fern Gaz. 9: 219 (1965)

Description Top

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Synonyms Top

Scientific name Authority First published in
Ceropteris pallescens Fée
Ceropteris peruviana (Desv.) Link Fil. Spec. 142. 1841 (1841)
Gymnogramma mayi Anon.
Gymnogramma pallescens T.Moore Index Fil. : 231 (1861)
Gymnogramma plicata T.Moore Index Fil. : 231 (1861)
Neurogramma peruviana Hieron. Bot. Jahrb. Syst. 34(4): 482 (1904)
Pityrogramma dualis Domin Rozpr. Ceske Akad. Ved, Tr. 2, Vedy Mat. Prir. 38(4): reprint p. 72. 1929
Pityrogramma tartarea (Cav.) Maxon Contr. U.S. Natl. Herb. 17: 173. 1913
Acrostichum tartareum Cav. Descr. Pl. (Cavanilles) 1: 242. 1801
Gymnogramma peruviana Desv. Ges. Naturf. Freunde Berlin Mag. Neuesten Entdeck. Gesammten Naturk. 5: 329 (1811)
Pityrogramma peruviana Maxon Contr. U.S. Natl. Herb. 17: 173 (1913)
Pityrogramma calomelanos var. peruviana Farw. Amer. Midl. Naturalist 12: 280 (1931)
Gymnogramma tartarea Desv. Ges. Naturf. Freunde Berlin Mag. Neuesten Entdeck. Gesammten Naturk. 5: 305 (1811)
Acrostichum ebeneum L. Sp. Pl. : 1071 (1753)
Pityrogramma tripinnata Domin Spisy Prír. Fak. Karlovy Univ. 1928, pt. 88: 7 (1928)
Ceropteris tartarea (Cav.) Link Fil. Spec. 142. 1841
Ceropteris plicata Fée Mém. Foug. 8: 81 1857
Gymnogramma calomelanos var. peruviana (Desv.) Baker Syn. Fil. : 385 (1868)
Gymnogramma calomelanos f. tartarea (Cav.) J.Bommer & Christ Bull. Soc. Roy. Bot. Belgique 35, pt. 1: 236 (1896)
Gymnogramma calomelanos f. peruviana J.Bommer & Christ Bull. Soc. Roy. Bot. Belgique 35, pt. 1: 236 (1896)
Gymnogramma calomelanos var. tartarea (Cav.) Baker Fl. Bras. (Martius) 1(2): 556. 1870 [1 May 1870] , as 'Gymnogramme'
Gymnogramma tartarea var. aureo-pallida E.Fourn. Mexic. Pl. 1: 72. 1872
Pityrogramma tartarea var. arcuata Domin Věstn. Ceské Společn. Nauk, Tř. Mat.-Přír. 1941(15): 5. 1942
Pityrogramma tartarea var. delicatula Domin Věstn. Ceské Společn. Nauk, Tř. Mat.-Přír. 1941(15): 7. 1942
Pityrogramma tartarea var. fallax Domin Věstn. Ceské Společn. Nauk, Tř. Mat.-Přír. 1941(15): 8. 1942
Pityrogramma tartarea var. kalbreyeri Domin Věstn. Ceské Společn. Nauk, Tř. Mat.-Přír. 1941(15): 6. 1942
Pityrogramma tartarea var. mathewsii Domin Věstn. Ceské Společn. Nauk, Tř. Mat.-Přír. 1941(15): 6. 1942
Pityrogramma tartarea var. pteridioides Domin Věstn. Ceské Společn. Nauk, Tř. Mat.-Přír. 1941(15): 7. 1942

Common names Top

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Language Common/alternative name
English mountain silverback fern

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Pityrogramma ebenea var. aurata (T.Moore) Lellinger Proc. Biol. Soc. Washington 98: 387 (1985)

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
  • Northern America
    • Mexico
      • Mexican Pacific Islands
      • Mexico Central
      • Mexico Gulf
      • Mexico Northeast
      • Mexico Northwest
      • Mexico Southeast
      • Mexico Southwest
  • Southern America
    • Brazil
      • Brazil West-central
    • Caribbean
      • Cuba
      • Dominican Republic
      • Haiti
      • Jamaica
      • Puerto Rico
      • Venezuelan Antilles
    • Central America
      • Costa Rica
      • El Salvador
      • Guatemala
      • Honduras
      • Nicaragua
      • Panamá
    • Northern South America
      • Guyana
      • Venezuela
    • Southern South America
      • Argentina Northeast
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador
      • Galápagos
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001109228
USDA Plants PIEB
Tropicos 26602387
KEW urn:lsid:ipni.org:names:200935-2
The Plant List tro-26602387
Open Tree Of Life 3866544
NCBI Taxonomy 1643356
IPNI 200935-2
iNaturalist 275622
GBIF 2651796
EPPO PIYEB
EOL 597261
CMAUP NPO22602
CMAUP NPO24462

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
Poorly Investigated Ecuadorian Medicinal Plants Armijos C, Ramírez J, Vidari G Plants (Basel) 16-Jun-2022
PMCID:PMC9229133
doi:10.3390/plants11121590
PMID:35736741
Geometry, Allometry and Biomechanics of Fern Leaf Petioles: Their Significance for the Evolution of Functional and Ecological Diversity Within the Pteridaceae Mahley JN, Pittermann J, Rowe N, Baer A, Watkins JE, Schuettpelz E, Wheeler JK, Mehltreter K, Windham M, Testo W, Beck J Front Plant Sci 07-Mar-2018
PMCID:PMC5850050
doi:10.3389/fpls.2018.00197
PMID:29563920
“Horchata” drink in Southern Ecuador: medicinal plants and people’s wellbeing Rios M, Tinitana F, Jarrín-V P, Donoso N, Romero-Benavides JC J Ethnobiol Ethnomed 09-Mar-2017
PMCID:PMC5345160
doi:10.1186/s13002-017-0145-z
PMID:28279218
Dihydrochalcones from the Fronds of Pityrogramma chrysophylla var. marginata, Domin. Martin Nilsson, H. Høeg, Kirsten Michelsen, G. Bech Nielsen, H. Nord, Aage Jart Danish Chemical Society 19-Jun-2008
doi:10.3891/ACTA.CHEM.SCAND.15-0154
Flavonoids in frond exudates of Pityrogramma tartarea Munekazu Iinuma, Toshiyuki Tanaka, Fujio Asai Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)90467-9
Flavonoid frond exudates from two Jamaican ferns, Pityrogramma tartarea and P. calomelanos Aura E. Star, Tom J. Mabry Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)97288-1
Flavonoids from the ferns Blechnum regnellianum and Pityrogramma ebenea Maria Do Carmo M. Miraglia, Adolfo P. De Pádua, Antonio A.L. Mesquita, Otto R. Gottlieb Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)83205-7

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
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Hentriacontane 12410 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC 436.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
(1R,3R,4R,4aS,8S,8aR)-4-[2-(furan-3-yl)ethyl]-8-(hydroxymethyl)-3,4a,8-trimethyl-2,3,5,6,7,8a-hexahydro-1H-naphthalene-1,4-diol 38350347 Click to see CC1CC(C2C(CCCC2(C1(CCC3=COC=C3)O)C)(C)CO)O 336.50 unknown via CMAUP database
Marrubenol 10449689 Click to see CC1CC(C2C(CCCC2(C1(CCC3=COC=C3)O)C)(C)CO)O 336.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
Campesterol 173183 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Clerosterol 5283638 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(=C)C 412.70 unknown via CMAUP database
Clionasterol 457801 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
Fucosterol 5281326 Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
Poriferasterol 5281330 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / L-alpha-amino acids
Dencichin 440259 Click to see C(C(C(=O)O)N)NC(=O)C(=O)O 176.13 unknown via CMAUP database
L-Homoarginine 9085 Click to see C(CCN=C(N)N)CC(C(=O)O)N 188.23 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Proline and derivatives
Betonicine 164642 Click to see C[N+]1(CC(CC1C(=O)[O-])O)C 159.18 unknown via CMAUP database
L-Turicine 1550239 Click to see C[N+]1(CC(CC1C(=O)[O-])O)C 159.18 unknown via CMAUP database
Turicine 6560290 Click to see C[N+]1(CC(CC1C(=O)[O-])O)C 159.18 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / N-acyl-alpha amino acids
(2R)-3-amino-2-(oxaloamino)propanoic acid 121488562 Click to see C(C(C(=O)O)NC(=O)C(=O)O)N 176.13 unknown via CMAUP database
L-gammaGlu-3-(5-Oxo-3-isoxazolin-2-yl)-L-Ala-OH 15167929 Click to see C1=CN(OC1=O)CC(C(=O)O)NC(=O)CCC(C(=O)O)N 301.25 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / N-acyl-alpha amino acids / N-acyl-L-alpha-amino acids
3-Amino-N-(carboxycarbonyl)-L-alanine 6454151 Click to see C(C(C(=O)O)NC(=O)C(=O)O)N 176.13 unknown via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / Amines / Primary amines / Monoalkylamines
1,4-Diaminobutane 1045 Click to see C(CCN)CN 88.15 unknown via CMAUP database
Cadaverine 273 Click to see C(CCN)CCN 102.18 unknown via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / Amines / Secondary amines / Dialkylamines
Spermidine 1102 Click to see C(CCNCCCN)CN 145.25 unknown via CMAUP database
Spermine 1103 Click to see C(CCNCCCN)CNCCCN 202.34 unknown via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / Guanidines
1-(5-Aminopentyl)guanidine 21298950 Click to see C(CCN)CCN=C(N)N 144.22 unknown via CMAUP database
Agmatine 199 Click to see C(CCN=C(N)N)CN 130.19 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
Forsythoside B 23928102 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)COC4C(C(CO4)(CO)O)O)OCCC5=CC(=C(C=C5)O)O)O)O)O)O 756.70 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(1R,4S,8S,9R,10S,12R)-9-[2-(furan-3-yl)ethyl]-9-hydroxy-4,8,10-trimethyl-2-oxatricyclo[6.3.1.04,12]dodecan-3-one 25728881 Click to see CC1CC2C3C(CCCC3(C1(CCC4=COC=C4)O)C)(C(=O)O2)C 332.40 unknown via CMAUP database
Marrubiin 73401 Click to see CC1CC2C3C(CCCC3(C1(CCC4=COC=C4)O)C)(C(=O)O2)C 332.40 unknown via CMAUP database
Premarrubiin 168199 Click to see CC1CC2C3C(CCCC3(C14CCC5(O4)COC=C5)C)(C(=O)O2)C 332.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Acetoside 44429837 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown via CMAUP database
Phaselic acid, (-)- 92299542 Click to see C1=CC(=C(C=C1C=CC(=O)OC(CC(=O)O)C(=O)O)O)O 296.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
(4R)-5,7-dihydroxy-4-phenyl-8-(3-phenylpropanoyl)-3,4-dihydrochromen-2-one 163040754 Click to see C1C(C2=C(C(=C(C=C2O)O)C(=O)CCC3=CC=CC=C3)OC1=O)C4=CC=CC=C4 388.40 unknown https://doi.org/10.1016/S0031-9422(00)90467-9
Calomelanol D-1 14586249 Click to see C1C(C2=C(C(=C(C=C2O)O)C(=O)CCC3=CC=CC=C3)OC1=O)C4=CC=CC=C4 388.40 unknown https://doi.org/10.1016/S0031-9422(00)90467-9
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown via CMAUP database
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown via CMAUP database
Rhamnocitrin 5320946 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)O)C3=CC=C(C=C3)O)O 300.26 unknown https://doi.org/10.1016/S0031-9422(00)97288-1
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Vicenin 2 442664 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C(=C3O2)C4C(C(C(C(O4)CO)O)O)O)O)C5C(C(C(C(O5)CO)O)O)O)O)O 594.50 unknown via CMAUP database
Vitexin 5280441 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
Luteolin 7-glucuronide 5280601 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O)O 462.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Apigetrin 5280704 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown via CMAUP database
Echinacin 6439941 Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)O)O)O)O)O)O 578.50 unknown via CMAUP database
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 5-O-methylated flavonoids
CID 45273057 45273057 Click to see COC1=CC=C(C=C1)C2CC(=O)C3=C(O2)C=C(C=C3OC)O 300.30 unknown https://doi.org/10.1016/S0031-9422(00)90467-9
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
5-Hydroxy-7-methoxy-2-phenylchroman-4-one 73201 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)O 270.28 unknown https://doi.org/10.1016/S0031-9422(00)90467-9
Genkwanin 5281617 Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O 284.26 unknown https://doi.org/10.1016/S0031-9422(00)97288-1
Ladanein 3084066 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)O)O 314.29 unknown via CMAUP database
Pinostrobin 6950539 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)O 270.28 unknown https://doi.org/10.1016/S0031-9422(00)90467-9
Sakuranetin 73571 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O 286.28 unknown https://doi.org/10.1016/S0031-9422(00)90467-9
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
(10S)-3,5-dihydroxy-2-(4-hydroxyphenyl)-10-phenyl-9,10-dihydropyrano[2,3-h]chromene-4,8-dione 162912263 Click to see C1C(C2=C(C=C(C3=C2OC(=C(C3=O)O)C4=CC=C(C=C4)O)O)OC1=O)C5=CC=CC=C5 416.40 unknown https://doi.org/10.1016/S0031-9422(00)90467-9
(10S)-5-hydroxy-2-(4-hydroxyphenyl)-10-phenyl-9,10-dihydropyrano[2,3-h]chromene-4,8-dione 92448130 Click to see C1C(C2=C(C=C(C3=C2OC(=CC3=O)C4=CC=C(C=C4)O)O)OC1=O)C5=CC=CC=C5 400.40 unknown https://doi.org/10.1016/S0031-9422(00)90467-9
(10S)-5-hydroxy-2,10-diphenyl-9,10-dihydropyrano[2,3-h]chromene-4,8-dione 162885043 Click to see C1C(C2=C(C=C(C3=C2OC(=CC3=O)C4=CC=CC=C4)O)OC1=O)C5=CC=CC=C5 384.40 unknown https://doi.org/10.1016/S0031-9422(00)90467-9
(6S)-5-hydroxy-2-(4-hydroxyphenyl)-6-phenyl-6,7-dihydropyrano[3,2-g]chromene-4,8-dione 162950441 Click to see C1C(C2=C(C=C3C(=C2O)C(=O)C=C(O3)C4=CC=C(C=C4)O)OC1=O)C5=CC=CC=C5 400.40 unknown https://doi.org/10.1016/S0031-9422(00)90467-9
5-Hydroxy-2-(4-hydroxyphenyl)-10-phenyl-9,10-dihydropyrano[2,3-f]chromene-4,8-dione 91637138 Click to see C1C(C2=C(C=C(C3=C2OC(=CC3=O)C4=CC=C(C=C4)O)O)OC1=O)C5=CC=CC=C5 400.40 unknown https://doi.org/10.1016/S0031-9422(00)90467-9
5-Hydroxy-2-(4-hydroxyphenyl)-6-phenyl-6,7-dihydropyrano[3,2-g]chromene-4,8-dione 162950440 Click to see C1C(C2=C(C=C3C(=C2O)C(=O)C=C(O3)C4=CC=C(C=C4)O)OC1=O)C5=CC=CC=C5 400.40 unknown https://doi.org/10.1016/S0031-9422(00)90467-9
5-Hydroxy-2,10-diphenyl-9,10-dihydropyrano[2,3-h]chromene-4,8-dione 14586257 Click to see C1C(C2=C(C=C(C3=C2OC(=CC3=O)C4=CC=CC=C4)O)OC1=O)C5=CC=CC=C5 384.40 unknown https://doi.org/10.1016/S0031-9422(00)90467-9
Calomelanol D 44259049 Click to see C1C(C2=C(C=C(C3=C2OC(=C(C3=O)O)C4=CC=C(C=C4)O)O)OC1=O)C5=CC=CC=C5 416.40 unknown https://doi.org/10.1016/S0031-9422(00)90467-9
Calomelanol H 42607934 Click to see C1C(C2=C(C3=C(C=C2OC1=O)OC(CC3=O)C4=CC=C(C=C4)O)O)C5=CC=CC=C5 402.40 unknown https://doi.org/10.1016/S0031-9422(00)90467-9
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
2',6'-Dihydroxy-3,4,4'-trimethoxydihydrochalcone 42607708 Click to see COC1=C(C=C(C=C1)CCC(=O)C2=C(C=C(C=C2O)OC)O)OC 332.30 unknown https://doi.org/10.1016/S0031-9422(00)90467-9
2',6'-Dihydroxy-4,3'-dimethoxy-4',5'-methylenedioxydihydrochalcone 42607718 Click to see COC1=CC=C(C=C1)CCC(=O)C2=C(C3=C(C(=C2O)OC)OCO3)O 346.30 unknown https://doi.org/10.1016/S0031-9422(00)83205-7
2',6'-Dihydroxy-4,4'-dimethoxydihydrochalcone 3084606 Click to see COC1=CC=C(C=C1)CCC(=O)C2=C(C=C(C=C2O)OC)O 302.32 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.15-0154
https://doi.org/10.1016/S0031-9422(00)97288-1
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
2',6'-Dihydroxy-4,4'-dimethoxychalcone 6438580 Click to see COC1=CC=C(C=C1)C=CC(=O)C2=C(C=C(C=C2O)OC)O 300.30 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.15-0154
Pinostrobin chalcone 5316793 Click to see COC1=CC(=C(C(=C1)O)C(=O)C=CC2=CC=CC=C2)O 270.28 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.15-0154

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