Brosimum rubescens - Unknown
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Internal ID UUID64400dda1e34f882229670
Scientific name Brosimum rubescens
Authority Taub.
First published in Bot. Jahrb. Syst. 12(1-2, Beibl. 27): 3. 1890 [24 Jun 1890]

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Synonyms Top

Scientific name Authority First published in
Piratinera rubescens Pittier Contr. U.S. Natl. Herb. 20: 100 (1918)
Piratinera angustifolia Ducke Arch. Jard. Bot. Rio de Janeiro 3: 24, footnote (1922)
Alicastrum rubescens Taub. Beibl. Bot. Jahrb. Syst. 34: 16 (1892)
Brosimum angustifolium Ducke Arch. Jard. Bot. Rio de Janeiro 3: 25 (1922)
Brosimum brevipedunculatum Ducke Trop. Woods 90: 8 (1947)
Brosimum caloxylon Standl. Trop. Woods 17: 11 (1929)
Brosimum lanciferum Ducke Arch. Jard. Bot. Rio de Janeiro 3: 24 (1922)
Brosimum longistipulatum Ducke Trop. Woods 90: 7 (1947)
Brosimum paraense Huber Bol. Mus. Goeldi Hist. Nat. Ethnogr. 6: 67 (1910)
Brosimum platyneurum Ducke Arq. Serv. Florest. 1(1): 4 (1939)
Ferolia variegata Lam. Encycl. [J. Lamarck & al.] 2(2): 452. 1788 [14 Apr 1788]
Ferolia guianensis Aubl. Hist. Pl. Guiane , Suppl.: 7 (1775)
Piratinera paraensis (Huber) Ducke Arch. Jard. Bot. Rio de Janeiro 3: 24, footnote (1922)
Piratinera lancifera Ducke Arch. Jard. Bot. Rio de Janeiro 3: 24, footnote (1922)

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Language Common/alternative name
Portuguese amapá-doce
Portuguese apé
Portuguese conduru
Portuguese conduru-de-sangue
Portuguese muirapiranga
Portuguese pau-rainha

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000572443
Tropicos 21300043
INPN 734298
KEW urn:lsid:ipni.org:names:37310-2
The Plant List kew-2683638
Open Tree Of Life 892924
NCBI Taxonomy 241870
IPNI 850837-1
iNaturalist 874644
GBIF 3762826
EOL 6959128
USDA GRIN 401467

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)!
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Title Authors Publication Released IDs
First evidence of a monodominant (Englerodendron, Amherstieae, Detarioideae, Leguminosae) tropical moist forest from the early Miocene (21.73 Ma) of Ethiopia Pan AD, Jacobs BF, Bush RT, de la Estrella M, Grímsson F, Herendeen PS, van der Burgt XM, Currano ED PLoS One 11-Jan-2023
PMCID:PMC9833558
doi:10.1371/journal.pone.0279491
PMID:36630378
Mulberry Diels–Alder-type adducts: isolation, structure, bioactivity, and synthesis Luo SY, Zhu JY, Zou MF, Yin S, Tang GH Nat Prod Bioprospect 02-Sep-2022
PMCID:PMC9436459
doi:10.1007/s13659-022-00355-y
PMID:36050566
Chemical composition of material extractives influences microbial growth and dynamics on wetted wood materials Zhao D, Cardona C, Gottel N, Winton VJ, Thomas PM, Raba DA, Kelley ST, Henry C, Gilbert JA, Stephens B Sci Rep 02-Sep-2020
PMCID:PMC7467922
doi:10.1038/s41598-020-71560-3
PMID:32879425
Ethnopharmacology of Fruit Plants: A Literature Review on the Toxicological, Phytochemical, Cultural Aspects, and a Mechanistic Approach to the Pharmacological Effects of Four Widely Used Species de Carvalho AT, Paes MM, Cunha MS, Brandão GC, Mapeli AM, Rescia VC, Oesterreich SA, Villas-Boas GR Molecules 26-Aug-2020
PMCID:PMC7504726
doi:10.3390/molecules25173879
PMID:32858815
Pharmacological Modulation of Steroid Activity in Hormone-Dependent Breast and Prostate Cancers: Effect of Some Plant Extract Derivatives Bayala B, Zoure AA, Baron S, de Joussineau C, Simpore J, Lobaccaro JM Int J Mol Sci 23-May-2020
PMCID:PMC7279356
doi:10.3390/ijms21103690
PMID:32456259
Different “metabolomic niches” of the highly diverse tree species of the French Guiana rainforests Gargallo-Garriga A, Sardans J, Granda V, Llusià J, Peguero G, Asensio D, Ogaya R, Urbina I, Van Langenhove L, Verryckt LT, Chave J, Courtois EA, Stahl C, Grau O, Klem K, Urban O, Janssens IA, Peñuelas J Sci Rep 24-Apr-2020
PMCID:PMC7181821
doi:10.1038/s41598-020-63891-y
PMID:32332903
Controlling anthracnose by means of extracts, and their major constituents, from Brosimum rubescens Taub Martinez J, Gomez A, Ramirez C, Gil J, Durango D Biotechnol Rep (Amst) 30-Nov-2019
PMCID:PMC6928314
doi:10.1016/j.btre.2019.e00405
PMID:31890645
Rarity of monodominance in hyperdiverse Amazonian forests ter Steege H, Henkel TW, Helal N, Marimon BS, Marimon-Junior BH, Huth A, Groeneveld J, Sabatier D, Coelho LD, Filho DD, Salomão RP, Amaral IL, Matos FD, Castilho CV, Phillips OL, Guevara JE, Carim MD, Cárdenas López D, Magnusson WE, Wittmann F, Irume MV, Martins MP, Guimarães JR, Molino JF, Bánki OS, Piedade MT, Pitman NC, Mendoza AM, Ramos JF, Luize BG, Moraes de Leão Novo EM, Núñez Vargas P, Silva TS, Venticinque EM, Manzatto AG, Reis NF, Terborgh J, Casula KR, Honorio Coronado EN, Montero JC, Feldpausch TR, Duque A, Costa FR, Arboleda NC, Schöngart J, Killeen TJ, Vasquez R, Mostacedo B, Demarchi LO, Assis RL, Baraloto C, Engel J, Petronelli P, Castellanos H, de Medeiros MB, Quaresma A, Simon MF, Andrade A, Camargo JL, Laurance SG, Laurance WF, Rincón LM, Schietti J, Sousa TR, de Sousa Farias E, Lopes MA, Magalhães JL, Mendonça Nascimento HE, Lima de Queiroz H, Aymard C. GA, Brienen R, Revilla JD, Vieira IC, Cintra BB, Stevenson PR, Feitosa YO, Duivenvoorden JF, Mogollón HF, Araujo-Murakami A, Ferreira LV, Lozada JR, Comiskey JA, de Toledo JJ, Damasco G, Dávila N, Draper F, García-Villacorta R, Lopes A, Vicentini A, Alonso A, Dallmeier F, Gomes VH, Lloyd J, Neill D, de Aguiar DP, Arroyo L, Carvalho FA, de Souza FC, do Amaral DD, Feeley KJ, Gribel R, Pansonato MP, Barlow J, Berenguer E, Ferreira J, Fine PV, Guedes MC, Jimenez EM, Licona JC, Peñuela Mora MC, Villa B, Cerón C, Maas P, Silveira M, Stropp J, Thomas R, Baker TR, Daly D, Dexter KG, Huamantupa-Chuquimaco I, Milliken W, Pennington T, Ríos Paredes M, Fuentes A, Klitgaard B, Pena JL, Peres CA, Silman MR, Tello JS, Chave J, Cornejo Valverde F, Di Fiore A, Hilário RR, Phillips JF, Rivas-Torres G, van Andel TR, von Hildebrand P, Noronha JC, Barbosa EM, Barbosa FR, de Matos Bonates LC, Carpanedo RD, Dávila Doza HP, Fonty É, GómeZárate z R, Gonzales T, Gallardo Gonzales GP, Hoffman B, Junqueira AB, Malhi Y, Miranda IP, Pinto LF, Prieto A, Rodrigues DD, Rudas A, Ruschel AR, Silva N, Vela CI, Vos VA, Zent EL, Zent S, Weiss Albuquerque B, Cano A, Carrero Márquez YA, Correa DF, Costa JB, Flores BM, Galbraith D, Holmgren M, Kalamandeen M, Nascimento MT, Oliveira AA, Ramirez-Angulo H, Rocha M, Scudeller VV, Sierra R, Tirado M, Umaña Medina MN, van der Heijden G, Vilanova Torre E, Vriesendorp C, Wang O, Young KR, Ahuite Reategui MA, Baider C, Balslev H, Cárdenas S, Casas LF, Farfan-Rios W, Ferreira C, Linares-Palomino R, Mendoza C, Mesones I, Torres-Lezama A, Giraldo LE, Villarroel D, Zagt R, Alexiades MN, de Oliveira EA, Garcia-Cabrera K, Hernandez L, Palacios Cuenca W, Pansini S, Pauletto D, Ramirez Arevalo F, Sampaio AF, Sandoval EH, Valenzuela Gamarra L, Levesley A, Pickavance G, Melgaço K Sci Rep 25-Sep-2019
PMCID:PMC6761143
doi:10.1038/s41598-019-50323-9
PMID:31554920
Coumarins from the peel of citrus grown in Colombia: composition, elicitation and antifungal activity Ramírez-Pelayo C, Martínez-Quiñones J, Gil J, Durango D Heliyon 15-Jun-2019
PMCID:PMC6582165
doi:10.1016/j.heliyon.2019.e01937
PMID:31245648
Fishermen do more than fish: local ecological knowledge of raftsmen about the arboreal species used to construct rafts (Bahia, Brazil) Andrade IL, Mielke MS, Peroni N, Schiavetti A J Ethnobiol Ethnomed 27-Dec-2018
PMCID:PMC6307309
doi:10.1186/s13002-018-0279-7
PMID:30587245
Palikur traditional roundwood construction in eastern French Guiana: ethnobotanical and cultural perspectives Ogeron C, Odonne G, Cristinoi A, Engel J, Grenand P, Beauchêne J, Clair B, Davy D J Ethnobiol Ethnomed 24-Apr-2018
PMCID:PMC5916587
doi:10.1186/s13002-018-0226-7
PMID:29690891
Species Distribution Modelling: Contrasting presence-only models with plot abundance data Gomes VH, IJff SD, Raes N, Amaral IL, Salomão RP, de Souza Coelho L, de Almeida Matos FD, Castilho CV, de Andrade Lima Filho D, López DC, Guevara JE, Magnusson WE, Phillips OL, Wittmann F, de Jesus Veiga Carim M, Martins MP, Irume MV, Sabatier D, Molino JF, Bánki OS, da Silva Guimarães JR, Pitman NC, Piedade MT, Mendoza AM, Luize BG, Venticinque EM, de Leão Novo EM, Vargas PN, Silva TS, Manzatto AG, Terborgh J, Reis NF, Montero JC, Casula KR, Marimon BS, Marimon BH, Coronado EN, Feldpausch TR, Duque A, Zartman CE, Arboleda NC, Killeen TJ, Mostacedo B, Vasquez R, Schöngart J, Assis RL, Medeiros MB, Simon MF, Andrade A, Laurance WF, Camargo JL, Demarchi LO, Laurance SG, de Sousa Farias E, Nascimento HE, Revilla JD, Quaresma A, Costa FR, Vieira IC, Cintra BB, Castellanos H, Brienen R, Stevenson PR, Feitosa Y, Duivenvoorden JF, Aymard C. GA, Mogollón HF, Targhetta N, Comiskey JA, Vicentini A, Lopes A, Damasco G, Dávila N, García-Villacorta R, Levis C, Schietti J, Souza P, Emilio T, Alonso A, Neill D, Dallmeier F, Ferreira LV, Araujo-Murakami A, Praia D, do Amaral DD, Carvalho FA, de Souza FC, Feeley K, Arroyo L, Pansonato MP, Gribel R, Villa B, Licona JC, Fine PV, Cerón C, Baraloto C, Jimenez EM, Stropp J, Engel J, Silveira M, Mora MC, Petronelli P, Maas P, Thomas-Caesar R, Henkel TW, Daly D, Paredes MR, Baker TR, Fuentes A, Peres CA, Chave J, Pena JL, Dexter KG, Silman MR, Jørgensen PM, Pennington T, Di Fiore A, Valverde FC, Phillips JF, Rivas-Torres G, von Hildebrand P, van Andel TR, Ruschel AR, Prieto A, Rudas A, Hoffman B, Vela CI, Barbosa EM, Zent EL, Gonzales GP, Doza HP, de Andrade Miranda IP, Guillaumet JL, Pinto LF, de Matos Bonates LC, Silva N, Gómez RZ, Zent S, Gonzales T, Vos VA, Malhi Y, Oliveira AA, Cano A, Albuquerque BW, Vriesendorp C, Correa DF, Torre EV, van der Heijden G, Ramirez-Angulo H, Ramos JF, Young KR, Rocha M, Nascimento MT, Medina MN, Tirado M, Wang O, Sierra R, Torres-Lezama A, Mendoza C, Ferreira C, Baider C, Villarroel D, Balslev H, Mesones I, Giraldo LE, Casas LF, Reategui MA, Linares-Palomino R, Zagt R, Cárdenas S, Farfan-Rios W, Sampaio AF, Pauletto D, Sandoval EH, Arevalo FR, Huamantupa-Chuquimaco I, Garcia-Cabrera K, Hernandez L, Gamarra LV, Alexiades MN, Pansini S, Cuenca WP, Milliken W, Ricardo J, Lopez-Gonzalez G, Pos E, ter Steege H Sci Rep 17-Jan-2018
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doi:10.1038/s41598-017-18927-1
PMID:29343741
Isolation of Monoterpene Dihydrochalcones from Piper montealegreanum Yuncker (Piperaceae) Alves HD, da Rocha WR, Braz-Filho R, Chaves MC Molecules 09-Jun-2017
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Molecular Targeted Approaches to Cancer Therapy and Prevention Using Chalcones Jandial DD, Blair CA, Zhang S, Krill LS, Zhang YB, Zi X Curr Cancer Drug Targets 01-Feb-2014
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PMID:24467530
Antimicrobial activity of amazonian medicinal plants Oliveira AA, Segovia JF, Sousa VY, Mata EC, Gonçalves MC, Bezerra RM, Junior PO, Kanzaki LI Springerplus 05-Aug-2013
PMCID:PMC3738913
doi:10.1186/2193-1801-2-371
PMID:23961431

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
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
8-Hydroxy-7-methoxy-5,6-bis(3-methylbut-2-enyl)chromen-2-one 162905505 Click to see CC(=CCC1=C2C=CC(=O)OC2=C(C(=C1CC=C(C)C)OC)O)C 328.40 unknown https://doi.org/10.1016/S0031-9422(00)86395-5
8-Hydroxy-7-methoxy-6-(3-methylbut-2-enyl)chromen-2-one 129710913 Click to see CC(=CCC1=C(C(=C2C(=C1)C=CC(=O)O2)O)OC)C 260.28 unknown https://doi.org/10.1016/S0031-9422(00)86395-5
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Demethylsuberosin 5316525 Click to see CC(=CCC1=C(C=C2C(=C1)C=CC(=O)O2)O)C 230.26 unknown https://doi.org/10.1016/S0031-9422(00)86395-5
https://doi.org/10.1021/NP9607215
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Linear pyranocoumarins
Luvangetin 343582 Click to see CC1(C=CC2=C(O1)C(=C3C(=C2)C=CC(=O)O3)OC)C 258.27 unknown https://doi.org/10.1016/S0031-9422(00)86395-5
Xanthyletin 65188 Click to see CC1(C=CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)C 228.24 unknown https://doi.org/10.1021/NP9607215
https://doi.org/10.1016/S0031-9422(00)86395-5
https://doi.org/10.1002/(SICI)1099-1573(200005)14:3<187::AID-PTR572>3.0.CO;2-I
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
(6bS,10R,10aS,11R)-10-(3,4-dihydroxyphenyl)-5-hydroxy-11-(4-hydroxy-2-methoxyphenyl)-6-methoxy-8-methyl-9,10,10a,11-tetrahydro-6bH-indeno[2,1-f]chromen-3-one 102317067 Click to see CC1=CC2C(C(C1)C3=CC(=C(C=C3)O)O)C(C4=C5C=CC(=O)OC5=C(C(=C24)OC)O)C6=C(C=C(C=C6)O)OC 528.50 unknown https://doi.org/10.1016/S0031-9422(97)00761-9
(6bS,10R,10aS,11S)-10-(3,4-dihydroxyphenyl)-5-hydroxy-11-(4-hydroxy-2-methoxyphenyl)-6-methoxy-8-methyl-9,10,10a,11-tetrahydro-6bH-indeno[2,1-f]chromen-3-one 15834944 Click to see CC1=CC2C(C(C1)C3=CC(=C(C=C3)O)O)C(C4=C5C=CC(=O)OC5=C(C(=C24)OC)O)C6=C(C=C(C=C6)O)OC 528.50 unknown https://doi.org/10.1016/S0031-9422(97)00761-9
(6bS,10R,10aS,11S)-11-(3,4-dihydroxyphenyl)-5-hydroxy-10-(4-hydroxy-2-methoxyphenyl)-6-methoxy-8-methyl-9,10,10a,11-tetrahydro-6bH-indeno[2,1-f]chromen-3-one 102317068 Click to see CC1=CC2C(C(C1)C3=C(C=C(C=C3)O)OC)C(C4=C5C=CC(=O)OC5=C(C(=C24)OC)O)C6=CC(=C(C=C6)O)O 528.50 unknown https://doi.org/10.1016/S0031-9422(97)00761-9
(6bS,10S,10aS,11R)-10-(3,4-dihydroxyphenyl)-5-hydroxy-11-(4-hydroxy-2-methoxyphenyl)-6-methoxy-8-methyl-9,10,10a,11-tetrahydro-6bH-indeno[2,1-f]chromen-3-one 162897641 Click to see CC1=CC2C(C(C1)C3=CC(=C(C=C3)O)O)C(C4=C5C=CC(=O)OC5=C(C(=C24)OC)O)C6=C(C=C(C=C6)O)OC 528.50 unknown https://doi.org/10.1016/S0031-9422(97)00761-9
10-(3,4-dihydroxyphenyl)-5-hydroxy-11-(4-hydroxy-2-methoxyphenyl)-6-methoxy-8-methyl-9,10,10a,11-tetrahydro-6bH-indeno[2,1-f]chromen-3-one 162897640 Click to see CC1=CC2C(C(C1)C3=CC(=C(C=C3)O)O)C(C4=C5C=CC(=O)OC5=C(C(=C24)OC)O)C6=C(C=C(C=C6)O)OC 528.50 unknown https://doi.org/10.1016/S0031-9422(97)00761-9
11-(3,4-dihydroxyphenyl)-5-hydroxy-10-(4-hydroxy-2-methoxyphenyl)-6-methoxy-8-methyl-9,10,10a,11-tetrahydro-6bH-indeno[2,1-f]chromen-3-one 162985792 Click to see CC1=CC2C(C(C1)C3=C(C=C(C=C3)O)OC)C(C4=C5C=CC(=O)OC5=C(C(=C24)OC)O)C6=CC(=C(C=C6)O)O 528.50 unknown https://doi.org/10.1016/S0031-9422(97)00761-9
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 3-prenylated flavans
(4R,4aS,5S,12bS)-4-(3,4-dihydroxyphenyl)-5-(4-hydroxy-2-methoxyphenyl)-2-methyl-4,4a,5,12b-tetrahydro-3H-isochromeno[4,3-g]chromen-9-one 162866426 Click to see CC1=CC2C(C(C1)C3=CC(=C(C=C3)O)O)C(OC4=C2C=C5C=CC(=O)OC5=C4)C6=C(C=C(C=C6)O)OC 498.50 unknown https://doi.org/10.1021/NP9607215
(4R,4aS,5S,12bS)-4-(4-hydroxy-2-methoxyphenyl)-5-(4-hydroxyphenyl)-2-methyl-4,4a,5,12b-tetrahydro-3H-isochromeno[4,3-g]chromen-9-one 162917895 Click to see CC1=CC2C(C(C1)C3=C(C=C(C=C3)O)OC)C(OC4=C2C=C5C=CC(=O)OC5=C4)C6=CC=C(C=C6)O 482.50 unknown https://doi.org/10.1021/NP9607215
(4R,4aS,5S,12bS)-4,5-bis(4-hydroxy-2-methoxyphenyl)-2-methyl-4,4a,5,12b-tetrahydro-3H-isochromeno[4,3-g]chromen-9-one 163018747 Click to see CC1=CC2C(C(C1)C3=C(C=C(C=C3)O)OC)C(OC4=C2C=C5C=CC(=O)OC5=C4)C6=C(C=C(C=C6)O)OC 512.50 unknown https://doi.org/10.1021/NP9607215
(4R,4aS,5S,12bS)-5-(3,4-dihydroxyphenyl)-4-(4-hydroxy-2-methoxyphenyl)-2-methyl-4,4a,5,12b-tetrahydro-3H-isochromeno[4,3-g]chromen-9-one 163045243 Click to see CC1=CC2C(C(C1)C3=C(C=C(C=C3)O)OC)C(OC4=C2C=C5C=CC(=O)OC5=C4)C6=CC(=C(C=C6)O)O 498.50 unknown https://doi.org/10.1021/NP9607215
(4R,4aS,5S,12bS)-5-(4-hydroxy-2-methoxyphenyl)-4-(4-hydroxyphenyl)-2-methyl-4,4a,5,12b-tetrahydro-3H-isochromeno[4,3-g]chromen-9-one 162926157 Click to see CC1=CC2C(C(C1)C3=CC=C(C=C3)O)C(OC4=C2C=C5C=CC(=O)OC5=C4)C6=C(C=C(C=C6)O)OC 482.50 unknown https://doi.org/10.1021/NP9607215
(4S,4aR,5R,12bS)-4-(4-hydroxy-2-methoxyphenyl)-5-(4-hydroxyphenyl)-2-methyl-4,4a,5,12b-tetrahydro-3H-isochromeno[4,3-g]chromen-9-one 162917896 Click to see CC1=CC2C(C(C1)C3=C(C=C(C=C3)O)OC)C(OC4=C2C=C5C=CC(=O)OC5=C4)C6=CC=C(C=C6)O 482.50 unknown https://doi.org/10.1021/NP9607215
4-(3,4-dihydroxyphenyl)-5-(4-hydroxy-2-methoxyphenyl)-2-methyl-4,4a,5,12b-tetrahydro-3H-isochromeno[4,3-g]chromen-9-one 85236111 Click to see CC1=CC2C(C(C1)C3=CC(=C(C=C3)O)O)C(OC4=C2C=C5C=CC(=O)OC5=C4)C6=C(C=C(C=C6)O)OC 498.50 unknown https://doi.org/10.1021/NP9607215
4-(4-hydroxy-2-methoxyphenyl)-5-(4-hydroxyphenyl)-2-methyl-4,4a,5,12b-tetrahydro-3H-isochromeno[4,3-g]chromen-9-one 85089655 Click to see CC1=CC2C(C(C1)C3=C(C=C(C=C3)O)OC)C(OC4=C2C=C5C=CC(=O)OC5=C4)C6=CC=C(C=C6)O 482.50 unknown https://doi.org/10.1021/NP9607215
4,5-bis(4-hydroxy-2-methoxyphenyl)-2-methyl-4,4a,5,12b-tetrahydro-3H-isochromeno[4,3-g]chromen-9-one 163018746 Click to see CC1=CC2C(C(C1)C3=C(C=C(C=C3)O)OC)C(OC4=C2C=C5C=CC(=O)OC5=C4)C6=C(C=C(C=C6)O)OC 512.50 unknown https://doi.org/10.1021/NP9607215
5-(3,4-dihydroxyphenyl)-4-(4-hydroxy-2-methoxyphenyl)-2-methyl-4,4a,5,12b-tetrahydro-3H-isochromeno[4,3-g]chromen-9-one 85218938 Click to see CC1=CC2C(C(C1)C3=C(C=C(C=C3)O)OC)C(OC4=C2C=C5C=CC(=O)OC5=C4)C6=CC(=C(C=C6)O)O 498.50 unknown https://doi.org/10.1021/NP9607215
5-(4-hydroxy-2-methoxyphenyl)-4-(4-hydroxyphenyl)-2-methyl-4,4a,5,12b-tetrahydro-3H-isochromeno[4,3-g]chromen-9-one 85235894 Click to see CC1=CC2C(C(C1)C3=CC=C(C=C3)O)C(OC4=C2C=C5C=CC(=O)OC5=C4)C6=C(C=C(C=C6)O)OC 482.50 unknown https://doi.org/10.1021/NP9607215
Palodesangren A 10696654 Click to see CC1=CC2C(C(C1)C3=CC(=C(C=C3)O)O)C(OC4=C2C=C5C=CC(=O)OC5=C4)C6=C(C=C(C=C6)O)OC 498.50 unknown https://doi.org/10.1021/NP9607215
Palodesangren B 10648988 Click to see CC1=CC2C(C(C1)C3=C(C=C(C=C3)O)OC)C(OC4=C2C=C5C=CC(=O)OC5=C4)C6=CC(=C(C=C6)O)O 498.50 unknown https://doi.org/10.1021/NP9607215
Palodesangren C 10696160 Click to see CC1=CC2C(C(C1)C3=CC=C(C=C3)O)C(OC4=C2C=C5C=CC(=O)OC5=C4)C6=C(C=C(C=C6)O)OC 482.50 unknown https://doi.org/10.1021/NP9607215
Palodesangren D 10005461 Click to see CC1=CC2C(C(C1)C3=C(C=C(C=C3)O)OC)C(OC4=C2C=C5C=CC(=O)OC5=C4)C6=CC=C(C=C6)O 482.50 unknown https://doi.org/10.1021/NP9607215
Palodesangren E 10255841 Click to see CC1=CC2C(C(C1)C3=C(C=C(C=C3)O)OC)C(OC4=C2C=C5C=CC(=O)OC5=C4)C6=C(C=C(C=C6)O)OC 512.50 unknown https://doi.org/10.1021/NP9607215

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