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Internal ID UUID644001ebce5f7885101923
Scientific name Piper aequale
Authority Vahl
First published in Eclog. Amer. 1: 4 (1797)

Description Top

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Synonyms Top

Scientific name Authority First published in
Piper crispans Trel. in Publ. Field Mus. Nat. Hist. Chicago, Bot. Ser. xviii. 339 (1937).
Piper colemanense Trel. Publ. Field Mus. Nat. Hist., Bot. Ser. 18: 337. 1937
Piper caripense Kunth Nov. Gen. Sp. 1: 48 (1816)
Piper cheyennense Trel. & Standl. Fieldiana, Bot. 24(3): 292 (1952)
Piper epilosipes Trel. Publ. Field Columb. Mus., Bot. Ser. 17: 344 (1938)
Piper donnell-smithii C.DC. Bot. Gaz. 19: 239 (1891)
Piper dominicanum C.DC. Symb. Antill. 3: 205 (1902)
Piper funckii C.DC. Prodr. 16(1): 310 (1869)
Piper frioense Standl. & Steyerm. Fieldiana, Bot. 24(3): 299 (1952)
Piper cabagranum C.DC. in Pittier Prim. Fl. Costaric. 2: 273. 1899
Piper rivulare C.DC. Linnaea 37: 360 (1872)
Piper seductum Trel. Contr. U.S. Natl. Herb. 23: 135. 1929
Piper santa-martanum C.DC. Annuaire Conserv. Jard. Bot. Genève 21: 231 (1920)
Piper johnstonii C.DC. Proc. Amer. Acad. Arts 40: 685 (1905)
Piper oppressum Trel. Contr. U.S. Natl. Herb. 26: 161 (1929)
Piper paso-anchoense Trel. Ann. Missouri Bot. Gard. 27: 295 (1940)
Piper mombachanum C.DC. Bot. Gaz. 70: 180 (1920)
Piper micranthera C.DC. Linnaea 37: 354 (1872)
Piper epilosipes var. heterophyllum Trel. Publ. Field Columb. Mus., Bot. Ser. 17: 345 (1938)
Piper aequale var. santa-martanum (C.DC.) Trel. & Yunck. Piperac. N. South Amer. : 219 (1950)
Artanthe aequalis Miq. Syst. Piperac. : 511 (1844)
Artanthe caripensis Miq. Syst. Piperac. : 522 (1844)
Piper aequale var. laurifolium (Trel.) Yunck. Ann. Missouri Bot. Gard. 37: 48 (1950)
Piper aequale var. substenocarpum C.DC. Annuaire Conserv. Jard. Bot. Genève 21: 253 (1920)
Piper amphioxys var. laurifolium Trel. Contr. U.S. Natl. Herb. 26: 31 (1927)
Piper caledonianum C.DC. Repert. Spec. Nov. Regni Veg. 15: 1 (1917)
Piper concinnum var. trinitense C.DC. Symb. Antill. 3: 204 (1902)
Piper dunlapii Trel. Contr. U.S. Natl. Herb. 26: 23. 1927
Piper substenocarpum C.DC. Bull. Herb. Boissier 6: 492 (1898)
Schilleria aequalis Kunth Linnaea 13: 687 (1840)
Piper playa-blancanum Trel. in Publ. Field Mus. Nat. Hist. Chicago, Bot. Ser. xviii. 355 (1937).
Piper atrichopus Trel. J. Washington Acad. Sci. 19: 330 (1929)
Piper jericoense Trel. & Yunck. Piperac. N. South Amer. 1: 397, fig. 359. 1950
Piper aequale var. dussii C.DC. Symb. Antill. 3: 204 (1902)
Piper aequale var. fimbribracteatum Trel. & Yunck. Piperac. N. South Amer. : 220 (1950)
Piper aequale var. hirtinervulum Yunck. Piperac. N. South Amer. : 220 (1950)
Piper aequale var. lasiocarpum C.DC. Symb. Antill. 3: 204 (1902)
Piper aequale var. latum Trel. ex Stehlé Bull. Agric. Martinique 9: 158 (1941)
Piper aequale var. ovalifolium C.DC. Prodr. 16(1): 311 (1869)
Piper donnell-smithii var. longipetiolatum C.DC. Notizbl. Königl. Bot. Gart. Berlin 6: 440 (1917)

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Piper aequale var. schackii (Miq.) Yunck. Lilloa 26: 251 (1953)

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
  • Northern America
    • Mexico
      • Mexico Central
      • Mexico Gulf
      • Mexico Northeast
      • Mexico Southwest
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil South
      • Brazil Southeast
      • Brazil West-central
    • Caribbean
      • Leeward Islands
      • Trinidad-Tobago
      • Venezuelan Antilles
      • Windward Islands
    • Northern South America
      • French Guiana
      • Guyana
      • Suriname
      • Venezuela
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador
      • Peru

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000479663
USDA Plants PIAE3
Tropicos 25001129
INPN 630424
KEW urn:lsid:ipni.org:names:680300-1
The Plant List kew-2559293
Open Tree Of Life 993725
NCBI Taxonomy 405316
IUCN Red List 146775821
IPNI 680300-1
iNaturalist 278324
GBIF 3086344
EOL 596625
CMAUP NPO22188

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
Ethnobotanical inventory of medicinal plants used by Cashinahua (Huni Kuin) herbalists in Purus Province, Peruvian Amazon Horackova J, Chuspe Zans ME, Kokoska L, Sulaiman N, Clavo Peralta ZM, Bortl L, Polesny Z J Ethnobiol Ethnomed 12-May-2023
PMCID:PMC10176740
doi:10.1186/s13002-023-00586-4
PMID:37170108
Pathways to healing: Plants with therapeutic potential for neurodegenerative diseases Tyler SE, Tyler LD IBRO Neurosci Rep 10-Feb-2023
PMCID:PMC9984566
doi:10.1016/j.ibneur.2023.01.006
PMID:36880056
Natural essential oils as a new therapeutic tool in colorectal cancer Garzoli S, Alarcón-Zapata P, Seitimova G, Alarcón-Zapata B, Martorell M, Sharopov F, Fokou PV, Dize D, Yamthe LR, Les F, Cásedas G, López V, Iriti M, Rad JS, Gürer ES, Calina D, Pezzani R, Vitalini S Cancer Cell Int 13-Dec-2022
PMCID:PMC9749237
doi:10.1186/s12935-022-02806-5
PMID:36514100
Essential Oil of the Plants Growing in the Brazilian Amazon: Chemical Composition, Antioxidants, and Biological Applications Ferreira OO, Cruz JN, de Moraes ÂA, de Jesus Pereira Franco C, Lima RR, dos Anjos TO, Siqueira GM, do Nascimento LD, Cascaes MM, de Oliveira MS, Andrade EH Molecules 08-Jul-2022
PMCID:PMC9318482
doi:10.3390/molecules27144373
PMID:35889245
Piper Species: A Comprehensive Review on Their Phytochemistry, Biological Activities and Applications Salehi B, Zakaria ZA, Gyawali R, Ibrahim SA, Rajkovic J, Shinwari ZK, Khan T, Sharifi-Rad J, Ozleyen A, Turkdonmez E, Valussi M, Tumer TB, Monzote Fidalgo L, Martorell M, Setzer WN Molecules 07-Apr-2019
PMCID:PMC6479398
doi:10.3390/molecules24071364
PMID:30959974
The Emergence of Earliest Angiosperms may be Earlier than Fossil Evidence Indicates Salomo K, Smith JF, Feild TS, Samain MS, Bond L, Davidson C, Zimmers J, Neinhuis C, Wanke S Syst Bot 18-Dec-2017
PMCID:PMC5792071
doi:10.1600/036364417X696438
PMID:29398773
In Vitro Testing of Crude Natural Plant Extracts from Costa Rica for Their Ability to Boost Innate Immune Cells against Staphylococcus aureus Yaseen R, Branitzki-Heinemann K, Moubasher H, Setzer WN, Naim HY, von Köckritz-Blickwede M Biomedicines 05-Jul-2017
PMCID:PMC5618298
doi:10.3390/biomedicines5030040
PMID:28678207
Photosynthetic induction and its diffusional, carboxylation and electron transport processes as affected by CO2 partial pressure, temperature, air humidity and blue irradiance Kaiser E, Kromdijk J, Harbinson J, Heuvelink E, Marcelis LF Ann Bot 26-Dec-2016
PMCID:PMC5218377
doi:10.1093/aob/mcw226
PMID:28025286
Composition and cytotoxic and antioxidant activities of the oil of Piper aequale Vahl da Silva JK, Pinto LC, Burbano RM, Montenegro RC, Andrade EH, Maia JG Lipids Health Dis 07-Oct-2016
PMCID:PMC5054595
doi:10.1186/s12944-016-0347-8
PMID:27717404
Antileishmanial Potential of Tropical Rainforest Plant Extracts Monzote L, Piñón A, Setzer WN Medicines (Basel) 19-Nov-2014
PMCID:PMC5532977
doi:10.3390/medicines1010032
PMID:28933376
Photocatalytic Synthesis of Dihydrobenzofurans by Oxidative [3+2] Cycloaddition of Phenols Blum TR, Zhu Y, Nordeen SA, Yoon TP Angew Chem Int Ed Engl 25-Aug-2014
PMCID:PMC4220618
doi:10.1002/anie.201406393
PMID:25155300
Tropical Secondary Forest Management Influences Frugivorous Bat Composition, Abundance and Fruit Consumption in Chiapas, Mexico Vleut I, Levy-Tacher SI, de Boer WF, Galindo-González J, Vazquez LB PLoS One 11-Oct-2013
PMCID:PMC3795674
doi:10.1371/journal.pone.0077584
PMID:24147029
Herbivore pressure increases toward the equator Salazar D, Marquis RJ Proc Natl Acad Sci U S A 16-Jul-2012
PMCID:PMC3411992
doi:10.1073/pnas.1202907109
PMID:22802664
Strong spatial genetic structure in five tropical Piper species: should the Baker–Fedorov hypothesis be revived for tropical shrubs? Lasso E, Dalling JW, Bermingham E Ecol Evol 01-Dec-2011
PMCID:PMC3287332
doi:10.1002/ece3.40
PMID:22393518
A Key to New World Distatrix Mason (Hymenoptera: Braconidae), with Descriptions of Six New Reared Neotropical Species Grinter CC, Whitfield JB, Connahs H, Dyer LA, Hallwachs W, Janzen DH J Insect Sci 02-Jun-2009
PMCID:PMC3383309
doi:10.1673/031.009.2901
PMID:19619026

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
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
2-Hydroxy-3-methoxybenzoic acid 70140 Click to see COC1=CC=CC(=C1O)C(=O)O 168.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
p-Anisic acid 7478 Click to see COC1=CC=C(C=C1)C(=O)O 152.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Salicylic acid and derivatives / Salicylic acids
2,3-Dihydroxybenzoic acid 19 Click to see C1=CC(=C(C(=C1)O)O)C(=O)O 154.12 unknown via CMAUP database
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
(1S,6R,7R)-7-[(1S)-1,2-dihydroxyethyl]-6-hydroxy-1-(4-hydroxyphenyl)-4,8-dioxaspiro[4.4]nonane-3,9-dione 193664 Click to see C1C(C2(C(C(OC2=O)C(CO)O)O)OC1=O)C3=CC=C(C=C3)O 324.28 unknown https://doi.org/10.1016/S0031-9422(98)00545-7
> Benzenoids / Phenols / 1-hydroxy-4-unsubstituted benzenoids
Hydron;phenoxide 20488062 Click to see [H+].C1=CC=C(C=C1)[O-] 94.11 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Vanillin 1183 Click to see COC1=C(C=CC(=C1)C=O)O 152.15 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Myristic Acid 11005 Click to see CCCCCCCCCCCCCC(=O)O 228.37 unknown via CMAUP database
Oleic Acid 445639 Click to see CCCCCCCCC=CCCCCCCCC(=O)O 282.50 unknown via CMAUP database
Palmitoleic Acid 445638 Click to see CCCCCCC=CCCCCCCCC(=O)O 254.41 unknown via CMAUP database
Stearic Acid 5281 Click to see CCCCCCCCCCCCCCCCCC(=O)O 284.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Behenic Acid 8215 Click to see CCCCCCCCCCCCCCCCCCCCCC(=O)O 340.60 unknown via CMAUP database
Hexacosanoic acid 10469 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCC(=O)O 396.70 unknown via CMAUP database
Tetracosanoic acid 11197 Click to see CCCCCCCCCCCCCCCCCCCCCCCC(=O)O 368.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
8,11,13-Abietatriene-3beta-ol 13996029 Click to see CC(C)C1=CC2=C(C=C1)C3(CCC(C(C3CC2)(C)C)O)C 286.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
Dihydrosolidagenone 101717490 Click to see CC1CC(=O)C2C(CCCC2(C1(CCC3=COC=C3)O)C)(C)C 318.40 unknown via CMAUP database
Rotundifuran 9841926 Click to see CC1CC(C2C(CCCC2(C1(CCC3=COC=C3)O)C)(C)C)OC(=O)C 362.50 unknown via CMAUP database
Vitetrifolin B 15543011 Click to see CC1CC(C2C(CCCC2(C1(CCC3=COC=C3)O)C)(C)C)OC(=O)C 362.50 unknown via CMAUP database
Vitetrifolin C 15543012 Click to see CC1C(C=C2C(CCCC2(C1(CCC3=COC=C3)O)C)(C)C)OC(=O)C 360.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-alpha-Terpineol 442501 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown via CMAUP database
2-[(1S)-4-methylcyclohex-3-en-1-yl]propan-2-yl acetate 93317 Click to see CC1=CCC(CC1)C(C)(C)OC(=O)C 196.29 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds / Tocopherols
gamma-Tocopherol 92729 Click to see CC1=C(C=C2CCC(OC2=C1C)(C)CCCC(C)CCCC(C)CCCC(C)C)O 416.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Illudanes and illudins / Melleolides and analogues
Armillyl orsellinate 14707323 Click to see CC1=CC(=CC(=C1C(=O)OC2CC3(C2=C(C(C4C3CC(C4)(C)C)O)CO)C)O)O 402.50 unknown https://doi.org/10.1016/S0031-9422(98)00545-7
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
Taraxerone 92785 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(=O)CCC5(C4CCC3(C2C1)C)C)(C)C)C)C)C 424.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
[(1R,4aS,5R,7aR)-5-hydroxy-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-7-yl]methyl 4-hydroxybenzoate 51346123 Click to see C1=COC(C2C1C(C=C2COC(=O)C3=CC=C(C=C3)O)O)OC4C(C(C(C(O4)CO)O)O)O 466.40 unknown via CMAUP database
6'-O-p-Hydroxybenzoylmussaenosidic acid 23955877 Click to see CC1(CCC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)COC(=O)C4=CC=C(C=C4)O)O)O)O)O 496.50 unknown via CMAUP database
Mussaenosidic acid 21633105 Click to see CC1(CCC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)O)O 376.36 unknown via CMAUP database
Negundoside 9935561 Click to see CC1(CCC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)OC(=O)C4=CC=C(C=C4)O)O 496.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(5S,6R,8R,9R,10S)-6-Acetoxy-9,15-dihydroxylabda-13-ene-16-oic acid 16,15-lactone 10022565 Click to see CC1CC(C2C(CCCC2(C1(CCC3=CCOC3=O)O)C)(C)C)OC(=O)C 378.50 unknown via CMAUP database
(8alpha)-9,16-Dihydroxylabda-13-ene-15-oic acid gamma-lactone 102105798 Click to see CC1CCC2C(CCCC2(C1(CCC3=CC(=O)OC3)O)C)(C)C 320.50 unknown via CMAUP database
Previtexilactone 21636179 Click to see CC1CC(C2C(CCCC2(C13CCC4(O3)CC(=O)OC4)C)(C)C)OC(=O)C 378.50 unknown via CMAUP database
Vitexilactone 21636178 Click to see CC1CC(C2C(CCCC2(C1(CCC3=CC(=O)OC3)O)C)(C)C)OC(=O)C 378.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
3-Epiursolic acid 7163177 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown via CMAUP database
alpha-Amyrin 73170 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown via CMAUP database
Betulinic Acid 64971 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown via CMAUP database
Corosolic acid 6918774 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)O 472.70 unknown via CMAUP database
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
[(1R,2R,4aalpha,5'E)-2alpha,5,5,8abeta-Tetramethyl-4beta-acetoxy-4',5'-dihydrospiro[decalin-1,2'(3'H)-furan]-5'-ylidene]acetic acid 101357917 Click to see CC1CC(C2C(CCCC2(C13CCC(=CC(=O)O)O3)C)(C)C)OC(=O)C 364.50 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
Isoambreinolide 15559824 Click to see CC1CCC2C(CCCC2(C13CCC(=O)O3)C)(C)C 264.40 unknown via CMAUP database
> Organoheterocyclic compounds / Tetrahydrofurans
Vitex norditerpenoid 1 11208535 Click to see CC1CCC2C(CCCC2(C13CCC(=CC=O)O3)C)(C)C 290.40 unknown via CMAUP database
Vitex norditerpenoid 2 11462191 Click to see CC1CC(C2C(CCCC2(C13CCC(=CC=O)O3)C)(C)C)OC(=O)C 348.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(+)-Conocarpan 6474521 Click to see CC=CC1=CC2=C(C=C1)OC(C2C)C3=CC=C(C=C3)O 266.30 unknown https://doi.org/10.1016/S0031-9422(98)00545-7
(2S,3R)-3-[2-(1,3-benzodioxol-5-yl)-3-methyl-1-benzofuran-5-yl]butan-2-ol 162898642 Click to see CC1=C(OC2=C1C=C(C=C2)C(C)C(C)O)C3=CC4=C(C=C3)OCO4 324.40 unknown https://doi.org/10.1016/S0031-9422(98)00545-7
2-(1,3-Benzodioxole-5-yl)-3-methyl-5-(2-oxopropyl)benzofuran 5319626 Click to see CC1=C(OC2=C1C=C(C=C2)CC(=O)C)C3=CC4=C(C=C3)OCO4 308.30 unknown https://doi.org/10.1016/S0031-9422(98)00545-7
2-(4-Hydroxyphenyl)-3-methyl-2,3-dihydro-1-benzofuran-5-carbaldehyde 85231246 Click to see CC1C(OC2=C1C=C(C=C2)C=O)C3=CC=C(C=C3)O 254.28 unknown https://doi.org/10.1016/S0031-9422(98)00545-7
2-methoxy-4-[(2R,3R)-3-methyl-5-[(E)-prop-1-enyl]-2,3-dihydro-1-benzofuran-2-yl]phenol 14213227 Click to see CC=CC1=CC2=C(C=C1)OC(C2C)C3=CC(=C(C=C3)O)OC 296.40 unknown https://doi.org/10.1016/S0031-9422(98)00545-7
2-Methoxy-4-[3-methyl-5-(1-propenyl)-2-benzofuranyl]-phenol 193821 Click to see CC=CC1=CC2=C(C=C1)OC(=C2C)C3=CC(=C(C=C3)O)OC 294.30 unknown https://doi.org/10.1016/S0031-9422(98)00545-7
3-[2-(1,3-Benzodioxol-5-yl)-3-methyl-1-benzofuran-5-yl]butan-2-ol 162898641 Click to see CC1=C(OC2=C1C=C(C=C2)C(C)C(C)O)C3=CC4=C(C=C3)OCO4 324.40 unknown https://doi.org/10.1016/S0031-9422(98)00545-7
4-(3-Methyl-5-prop-1-enyl-1-benzofuran-2-yl)-2-[3-(3-methyl-5-prop-1-enyl-1-benzofuran-2-yl)phenoxy]phenol 78384852 Click to see CC=CC1=CC2=C(C=C1)OC(=C2C)C3=CC(=CC=C3)OC4=C(C=CC(=C4)C5=C(C6=C(O5)C=CC(=C6)C=CC)C)O 526.60 unknown https://doi.org/10.1016/S0031-9422(98)00545-7
4-(3-Methyl-5-prop-1-enyl-1-benzofuran-2-yl)-2-[4-(3-methyl-5-prop-1-enyl-1-benzofuran-2-yl)phenoxy]phenol 162976997 Click to see CC=CC1=CC2=C(C=C1)OC(=C2C)C3=CC=C(C=C3)OC4=C(C=CC(=C4)C5=C(C6=C(O5)C=CC(=C6)C=CC)C)O 526.60 unknown https://doi.org/10.1016/S0031-9422(98)00545-7
4-(3-Methyl-5-prop-1-enyl-1-benzofuran-2-yl)phenol 3001232 Click to see CC=CC1=CC2=C(C=C1)OC(=C2C)C3=CC=C(C=C3)O 264.30 unknown https://doi.org/10.1016/S0031-9422(98)00545-7
4-(3-Methyl-5-prop-1-enyl-2,3-dihydro-1-benzofuran-2-yl)phenol 70414118 Click to see CC=CC1=CC2=C(C=C1)OC(C2C)C3=CC=C(C=C3)O 266.30 unknown https://doi.org/10.1016/S0031-9422(98)00545-7
4-(5-Methoxy-3-methyl-7-prop-2-enyl-2,3-dihydro-1-benzofuran-2-yl)phenol 78384825 Click to see CC1C(OC2=C(C=C(C=C12)OC)CC=C)C3=CC=C(C=C3)O 296.40 unknown https://doi.org/10.1016/S0031-9422(98)00545-7
4-[(2R,3R)-5-methoxy-3-methyl-7-prop-2-enyl-2,3-dihydro-1-benzofuran-2-yl]phenol 100959307 Click to see CC1C(OC2=C(C=C(C=C12)OC)CC=C)C3=CC=C(C=C3)O 296.40 unknown https://doi.org/10.1016/S0031-9422(98)00545-7
4-[(3R)-5-methoxy-3-methyl-7-prop-2-enyl-2,3-dihydro-1-benzofuran-2-yl]phenol 5316721 Click to see CC1C(OC2=C(C=C(C=C12)OC)CC=C)C3=CC=C(C=C3)O 296.40 unknown via CMAUP database
4-[3-methyl-5-[(E)-prop-1-enyl]-1-benzofuran-2-yl]-2-[3-[3-methyl-5-[(E)-prop-1-enyl]-1-benzofuran-2-yl]phenoxy]phenol 5316907 Click to see CC=CC1=CC2=C(C=C1)OC(=C2C)C3=CC(=CC=C3)OC4=C(C=CC(=C4)C5=C(C6=C(O5)C=CC(=C6)C=CC)C)O 526.60 unknown https://doi.org/10.1016/S0031-9422(98)00545-7
4-[3-methyl-5-[(E)-prop-1-enyl]-1-benzofuran-2-yl]-2-[4-[3-methyl-5-[(E)-prop-1-enyl]-1-benzofuran-2-yl]phenoxy]phenol 100959308 Click to see CC=CC1=CC2=C(C=C1)OC(=C2C)C3=CC=C(C=C3)OC4=C(C=CC(=C4)C5=C(C6=C(O5)C=CC(=C6)C=CC)C)O 526.60 unknown https://doi.org/10.1016/S0031-9422(98)00545-7
5-(3-Methyl-5-prop-1-enyl-1-benzofuran-2-yl)-1,3-benzodioxole 261729 Click to see CC=CC1=CC2=C(C=C1)OC(=C2C)C3=CC4=C(C=C3)OCO4 292.30 unknown https://doi.org/10.1016/S0031-9422(98)00545-7
5-[3-methyl-5-[(E)-prop-1-enyl]-1-benzofuran-2-yl]-1,3-benzodioxole 6051545 Click to see CC=CC1=CC2=C(C=C1)OC(=C2C)C3=CC4=C(C=C3)OCO4 292.30 unknown https://doi.org/10.1016/S0031-9422(98)00545-7
Conocarpan 10999992 Click to see CC=CC1=CC2=C(C=C1)OC(C2C)C3=CC=C(C=C3)O 266.30 unknown https://doi.org/10.1016/S0031-9422(98)00545-7
Eupomatenoid 5 6443783 Click to see CC=CC1=CC2=C(C=C1)OC(=C2C)C3=CC(=C(C=C3)O)OC 294.30 unknown https://doi.org/10.1016/S0031-9422(98)00545-7
Eupomatenoid 6 6261723 Click to see CC=CC1=CC2=C(C=C1)OC(=C2C)C3=CC=C(C=C3)O 264.30 unknown https://doi.org/10.1016/S0031-9422(98)00545-7
rel-(2R,3R)-2,3-Dihydro-2-(4-hydroxyphenyl)-3-methyl-5-benzofurancarboxaldehyde 101712154 Click to see CC1C(OC2=C1C=C(C=C2)C=O)C3=CC=C(C=C3)O 254.28 unknown https://doi.org/10.1016/S0031-9422(98)00545-7
> Phenylpropanoids and polyketides / Flavonoids / Flavones
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 / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
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 / O-methylated flavonoids / 6-O-methylated flavonoids
5,7-Dihydroxy-3,6,3',4'-tetramethoxyflavone 5379563 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC)OC 374.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Artemetin 5320351 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)OC 388.40 unknown via CMAUP database
Casticin 5315263 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)O 374.30 unknown via CMAUP database
chrysoplenol D 5280699 Click to see COC1=C(C(=C2C(=C1)OC(=C(C2=O)OC)C3=CC(=C(C=C3)O)O)O)OC 360.30 unknown via CMAUP database

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