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Brosimum acutifolium

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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 UUID64400dd71d486906271355
Scientific name Brosimum acutifolium
Authority Huber
First published in Bol. Mus. Goeldi Hist. Nat. Ethnogr. 6: 66 (1910)

Description Top

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Synonyms Top

Scientific name Authority First published in
Brosimopsis acutifolia Ducke Arch. Jard. Bot. Rio de Janeiro 3: 30 (1922)
Piratinera acutifolia Pittier Contr. U.S. Natl. Herb. 20: 100 (1918)

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Brosimum acutifolium subsp. interjectum C.C.Berg Acta Bot. Neerl. 19: 326 (1970)
Brosimum acutifolium subsp. obovatum (Ducke) C.C.Berg Acta Bot. Neerl. 19: 326 (1970)

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil West-central
    • Northern South America
      • French Guiana
      • Guyana
      • Suriname
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000572376
Tropicos 21300027
INPN 734294
KEW urn:lsid:ipni.org:names:37254-2
The Plant List kew-2683576
Open Tree Of Life 5749154
NCBI Taxonomy 1835378
IUCN Red List 179289504
IPNI 37254-2
GBIF 7262461
EOL 5720118

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
Oxidative Stress and Chronic Myeloid Leukemia: A Balance between ROS-Mediated Pro- and Anti-Apoptotic Effects of Tyrosine Kinase Inhibitors Allegra A, Mirabile G, Caserta S, Stagno F, Russo S, Pioggia G, Gangemi S Antioxidants (Basel) 13-Apr-2024
PMCID:PMC11047441
doi:10.3390/antiox13040461
PMID:38671909
Integration of Wnt-inhibitory activity and structural novelty scoring results to uncover novel bioactive natural products: new Bicyclo[3.3.1]non-3-ene-2,9-diones from the leaves of Hymenocardia punctata Quiros-Guerrero LM, Marcourt L, Chaiwangrach N, Koval A, Ferreira Queiroz E, David B, Grondin A, Katanaev VL, Wolfender JL Front Chem 04-Apr-2024
PMCID:PMC11024435
doi:10.3389/fchem.2024.1371982
Effects of hallucinogenic drugs on the human heart Neumann J, Dhein S, Kirchhefer U, Hofmann B, Gergs U Front Pharmacol 02-Feb-2024
PMCID:PMC10869618
doi:10.3389/fphar.2024.1334218
PMID:38370480
Do índio Passos ao doutor Chernoviz: experiências de cura da lepra no Pará do século XIX Henrique MC Hist Cienc Saude Manguinhos 04-Aug-2023
PMCID:PMC10402912
doi:10.1590/S0104-59702023000100027
PMID:37556716
Phytochemistry and pharmacology of natural prenylated flavonoids Lv HW, Wang QL, Luo M, Zhu MD, Liang HM, Li WJ, Cai H, Zhou ZB, Wang H, Tong SQ, Li XN Arch Pharm Res 14-Apr-2023
PMCID:PMC10101826
doi:10.1007/s12272-023-01443-4
PMID:37055613
Betulinic Acid-Brosimine B Hybrid Compound Has a Synergistic Effect with Imatinib in Chronic Myeloid Leukemia Cell Line, Modulating Apoptosis and Autophagy Willig JB, de Couto NM, Vianna DR, Mariot CD, Gnoatto SC, Buffon A, Pilger DA Pharmaceuticals (Basel) 13-Apr-2023
PMCID:PMC10142704
doi:10.3390/ph16040586
PMID:37111343
Development of Antibiofilm Therapeutics Strategies to Overcome Antimicrobial Drug Resistance Nadar S, Khan T, Patching SG, Omri A Microorganisms 27-Jan-2022
PMCID:PMC8879831
doi:10.3390/microorganisms10020303
PMID:35208758
Neuroimmunomodulatory Properties of Flavonoids and Derivates: A Potential Action as Adjuvants for the Treatment of Glioblastoma do Nascimento RP, dos Santos BL, Amparo JA, Soares JR, da Silva KC, Santana MR, Almeida ÁM, da Silva VD, Costa MD, Ulrich H, Moura-Neto V, Lopes GP, Costa SL Pharmaceutics 04-Jan-2022
PMCID:PMC8778519
doi:10.3390/pharmaceutics14010116
PMID:35057010
Protective Effects of Flavonoids Against Mitochondriopathies and Associated Pathologies: Focus on the Predictive Approach and Personalized Prevention Koklesova L, Liskova A, Samec M, Zhai K, AL-Ishaq RK, Bugos O, Šudomová M, Biringer K, Pec M, Adamkov M, Hassan ST, Saso L, Giordano FA, Büsselberg D, Kubatka P, Golubnitschaja O Int J Mol Sci 11-Aug-2021
PMCID:PMC8395457
doi:10.3390/ijms22168649
PMID:34445360
What’s in a name? Revisiting medicinal and religious plants at an Amazonian market Geertsma IP, Françozo M, van Andel T, Rodríguez MA J Ethnobiol Ethnomed 05-Feb-2021
PMCID:PMC7866673
doi:10.1186/s13002-021-00433-4
PMID:33546714
HIV understanding, experiences and perceptions of HIV-positive men who have sex with men in Amazonian Peru: a qualitative study Tattsbridge J, Wiskin C, de Wildt G, Clavé Llavall A, Ramal-Asayag C BMC Public Health 19-May-2020
PMCID:PMC7238527
doi:10.1186/s12889-020-08745-y
PMID:32429863
Ancient medicinal plants of South America VanPool C Proc Natl Acad Sci U S A 21-May-2019
PMCID:PMC6561247
doi:10.1073/pnas.1906805116
PMID:31113878
Chemical evidence for the use of multiple psychotropic plants in a 1,000-year-old ritual bundle from South America Miller MJ, Albarracin-Jordan J, Moore C, Capriles JM Proc Natl Acad Sci U S A 06-May-2019
PMCID:PMC6561276
doi:10.1073/pnas.1902174116
PMID:31061128
Biotransformed Metabolites of the Hop Prenylflavanone Isoxanthohumol Kim HJ, Yim SH, Han F, Kang BY, Choi HJ, Jung DW, Williams DR, Gustafson KR, Kennelly EJ, Lee IS Molecules 22-Jan-2019
PMCID:PMC6385124
doi:10.3390/molecules24030394
PMID:30678278
Rare species contribute disproportionately to the functional structure of species assemblages Leitão RP, Zuanon J, Villéger S, Williams SE, Baraloto C, Fortunel C, Mendonça FP, Mouillot D Proc Biol Sci 13-Apr-2016
PMCID:PMC4843652
doi:10.1098/rspb.2016.0084
PMID:27053754

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 / Cyclohexylphenols
(+)-Acutifolin A 11067365 Click to see CC(=CCC12C(CCC(C1=O)(C=CC2=O)O)C3=CC=C(C=C3)O)C 326.40 unknown https://doi.org/10.1021/NP010389J
5-Hydroxy-8-(4-hydroxyphenyl)-1-(3-methylbut-2-enyl)bicyclo[3.3.1]non-3-ene-2,9-dione 85386712 Click to see CC(=CCC12C(CCC(C1=O)(C=CC2=O)O)C3=CC=C(C=C3)O)C 326.40 unknown https://doi.org/10.1021/NP010389J
> Benzenoids / Phenols / Methoxyphenols
2-Propenal, 3-(4-hydroxy-3-methoxyphenyl)- 9984 Click to see COC1=C(C=CC(=C1)C=CC=O)O 178.18 unknown https://doi.org/10.1016/S0031-9422(99)00608-1
4-Hydroxy-3-methoxycinnamaldehyde 5280536 Click to see COC1=C(C=CC(=C1)C=CC=O)O 178.18 unknown https://doi.org/10.1016/S0031-9422(99)00608-1
Syringaldehyde 8655 Click to see COC1=CC(=CC(=C1O)OC)C=O 182.17 unknown https://doi.org/10.1016/S0031-9422(99)00608-1
> Lignans, neolignans and related compounds
4-[(2R)-3-hydroxy-2-[3-(3-hydroxypropyl)-5-methoxyphenyl]propyl]-2-methoxyphenol 163033856 Click to see COC1=CC(=CC(=C1)C(CC2=CC(=C(C=C2)O)OC)CO)CCCO 346.40 unknown https://doi.org/10.1055/S-2002-32906
4-[3-Hydroxy-2-[3-(3-hydroxypropyl)-5-methoxyphenyl]propyl]-2-methoxyphenol 163033855 Click to see COC1=CC(=CC(=C1)C(CC2=CC(=C(C=C2)O)OC)CO)CCCO 346.40 unknown https://doi.org/10.1055/S-2002-32906
> Lignans, neolignans and related compounds / Dibenzylbutane lignans / Dibenzylbutanediol lignans
2,3-bis(4-Hydroxy-3-methoxybenzyl)butane-1,4-diol 586372 Click to see COC1=C(C=CC(=C1)CC(CO)C(CC2=CC(=C(C=C2)O)OC)CO)O 362.40 unknown https://doi.org/10.1055/S-2002-32906
Secoisolariciresinol 65373 Click to see COC1=C(C=CC(=C1)CC(CO)C(CC2=CC(=C(C=C2)O)OC)CO)O 362.40 unknown https://doi.org/10.1055/S-2002-32906
> Lipids and lipid-like molecules / Glycerolipids / Glycosylglycerols
[(2R)-3-acetyloxy-2-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropyl] (E)-3-(4-hydroxyphenyl)prop-2-enoate 163188589 Click to see CC(=O)OCC(COC(=O)C=CC1=CC=C(C=C1)O)OC2C(C(C(C(O2)CO)O)O)O 442.40 unknown https://doi.org/10.1055/S-2002-32906
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8S,9S,10R,13R,14S,17R)-17-[(E,2S,5S)-5-Ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 12314479 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/S0031-9422(99)00608-1
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(99)00608-1
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(99)00608-1
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(99)00608-1
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/S0031-9422(99)00608-1
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
4-[3-(Hydroxymethyl)-5-(3-hydroxypropyl)-7-methoxy-2,3-dihydro-1-benzofuran-2-yl]-2-methoxyphenol 4365980 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)CCCO 360.40 unknown https://doi.org/10.1055/S-2002-32906
Dihydrodehydrodiconiferyl alcohol 384679 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)CCCO 360.40 unknown https://doi.org/10.1055/S-2002-32906
Mururin C 9999345 Click to see COC1=CC(=CC2=C1OC(=C2C=O)C3=CC(=C(C(=C3)OC)O)O)CCCO 372.40 unknown https://doi.org/10.1055/S-2002-32906
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans
(2R)-1-[(2S)-7-hydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-8-yl]-3-methylbutane-2,3-diol 163067805 Click to see CC(C)(C(CC1=C(C=CC2=C1OC(CC2)C3=CC=C(C=C3)O)O)O)O 344.40 unknown https://doi.org/10.1021/NP010389J
(2S,9S)-2-(4-hydroxyphenyl)-8,8-dimethyl-3,4,9,10-tetrahydro-2H-pyrano[2,3-f]chromen-9-ol 163040071 Click to see CC1(C(CC2=C(O1)C=CC3=C2OC(CC3)C4=CC=C(C=C4)O)O)C 326.40 unknown https://doi.org/10.1016/S0031-9422(99)00608-1
(2S)-1-[(2S)-7-hydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-8-yl]-3-methylbutane-2,3-diol 163067806 Click to see CC(C)(C(CC1=C(C=CC2=C1OC(CC2)C3=CC=C(C=C3)O)O)O)O 344.40 unknown https://doi.org/10.1021/NP010389J
(2S)-2alpha-(4-Hydroxyphenyl)-7-hydroxy-8-prenyl-3,4-dihydro-2H-1-benzopyran 57402293 Click to see CC(=CCC1=C(C=CC2=C1OC(CC2)C3=CC=C(C=C3)O)O)C 310.40 unknown https://doi.org/10.1002/(SICI)1097-458X(200004)38:4<301::AID-MRC632>3.0.CO;2-T
https://doi.org/10.1016/S0031-9422(99)00608-1
(2S)-7-methoxy-2-(4-methoxyphenyl)-8-(3-methylbut-2-enyl)-3,4-dihydro-2H-chromene 163031715 Click to see CC(=CCC1=C(C=CC2=C1OC(CC2)C3=CC=C(C=C3)OC)OC)C 338.40 unknown https://doi.org/10.1021/NP010389J
(2S)-8-(3-hydroxy-3-methylbutyl)-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-7-ol 101405589 Click to see CC(C)(CCC1=C(C=CC2=C1OC(CC2)C3=CC=C(C=C3)O)O)O 328.40 unknown https://doi.org/10.1055/S-2005-871272
1-[7-hydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-8-yl]-3-methylbutane-2,3-diol 10947920 Click to see CC(C)(C(CC1=C(C=CC2=C1OC(CC2)C3=CC=C(C=C3)O)O)O)O 344.40 unknown https://doi.org/10.1021/NP010389J
2-(4-hydroxyphenyl)-8,8-dimethyl-3,4,9,10-tetrahydro-2H-pyrano[2,3-f]chromen-9-ol 163040070 Click to see CC1(C(CC2=C(O1)C=CC3=C2OC(CC3)C4=CC=C(C=C4)O)O)C 326.40 unknown https://doi.org/10.1016/S0031-9422(99)00608-1
4-(8,8-dimethyl-3,4,9,10-tetrahydro-2H-pyrano[2,3-f]chromen-2-yl)phenol 163026721 Click to see CC1(CCC2=C(O1)C=CC3=C2OC(CC3)C4=CC=C(C=C4)O)C 310.40 unknown https://doi.org/10.1021/NP010389J
https://doi.org/10.1016/S0031-9422(99)00608-1
4-(9-hydroxy-8,8-dimethyl-3,4,9,10-tetrahydro-2H-pyrano[2,3-f]chromen-2-yl)benzene-1,2-diol 73047906 Click to see CC1(C(CC2=C(O1)C=CC3=C2OC(CC3)C4=CC(=C(C=C4)O)O)O)C 342.40 unknown https://doi.org/10.1055/S-2005-871272
4-[(2R,8S)-8-(2-hydroxypropan-2-yl)-3,4,8,9-tetrahydro-2H-furo[2,3-h]chromen-2-yl]phenol 162890440 Click to see CC(C)(C1CC2=C(O1)C=CC3=C2OC(CC3)C4=CC=C(C=C4)O)O 326.40 unknown https://doi.org/10.1016/S0031-9422(99)00608-1
4-[(2S,9S)-9-hydroxy-8,8-dimethyl-3,4,9,10-tetrahydro-2H-pyrano[2,3-f]chromen-2-yl]benzene-1,2-diol 162894266 Click to see CC1(C(CC2=C(O1)C=CC3=C2OC(CC3)C4=CC(=C(C=C4)O)O)O)C 342.40 unknown https://doi.org/10.1055/S-2005-871272
4-[(2S)-8,8-dimethyl-3,4,9,10-tetrahydro-2H-pyrano[2,3-f]chromen-2-yl]phenol 163026722 Click to see CC1(CCC2=C(O1)C=CC3=C2OC(CC3)C4=CC=C(C=C4)O)C 310.40 unknown https://doi.org/10.1021/NP010389J
https://doi.org/10.1016/S0031-9422(99)00608-1
4-[8-(2-hydroxypropan-2-yl)-3,4,8,9-tetrahydro-2H-furo[2,3-h]chromen-2-yl]phenol 102369763 Click to see CC(C)(C1CC2=C(O1)C=CC3=C2OC(CC3)C4=CC=C(C=C4)O)O 326.40 unknown https://doi.org/10.1016/S0031-9422(99)00608-1
7-methoxy-2-(4-methoxyphenyl)-8-(3-methylbut-2-enyl)-3,4-dihydro-2H-chromene 11727485 Click to see CC(=CCC1=C(C=CC2=C1OC(CC2)C3=CC=C(C=C3)OC)OC)C 338.40 unknown https://doi.org/10.1021/NP010389J
8-(3-hydroxy-3-methylbutyl)-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-7-ol 162977685 Click to see CC(C)(CCC1=C(C=CC2=C1OC(CC2)C3=CC=C(C=C3)O)O)O 328.40 unknown https://doi.org/10.1055/S-2005-871272
Brosimine B 21604819 Click to see CC(=CCC1=C(C=CC2=C1OC(CC2)C3=CC=C(C=C3)O)O)C 310.40 unknown https://doi.org/10.1002/(SICI)1097-458X(200004)38:4<301::AID-MRC632>3.0.CO;2-T
https://doi.org/10.1016/S0031-9422(99)00608-1
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(2R)-8-[(2R)-2,3-dihydroxy-3-methylbutyl]-7-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one 162892327 Click to see CC(C)(C(CC1=C(C=CC2=C1OC(CC2=O)C3=CC=C(C=C3)O)O)O)O 358.40 unknown https://doi.org/10.1021/NP020241F
(2S,8R)-2-(4-hydroxyphenyl)-8-(2-hydroxypropan-2-yl)-2,3,8,9-tetrahydrofuro[2,3-h]chromen-4-one 162853375 Click to see CC(C)(C1CC2=C(O1)C=CC3=C2OC(CC3=O)C4=CC=C(C=C4)O)O 340.40 unknown https://doi.org/10.1021/NP020241F
(2S,8S)-2-(4-hydroxyphenyl)-8-(2-hydroxypropan-2-yl)-2,3,8,9-tetrahydrofuro[2,3-h]chromen-4-one 162853374 Click to see CC(C)(C1CC2=C(O1)C=CC3=C2OC(CC3=O)C4=CC=C(C=C4)O)O 340.40 unknown https://doi.org/10.1021/NP020241F
(2S,9R)-9-hydroxy-2-(4-hydroxyphenyl)-8,8-dimethyl-2,3,9,10-tetrahydropyrano[2,3-h]chromen-4-one 162860892 Click to see CC1(C(CC2=C(O1)C=CC3=C2OC(CC3=O)C4=CC=C(C=C4)O)O)C 340.40 unknown https://doi.org/10.1021/NP020241F
(2S)-7-hydroxy-8-(3-hydroxy-3-methylbutyl)-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one 12050715 Click to see CC(C)(CCC1=C(C=CC2=C1OC(CC2=O)C3=CC=C(C=C3)O)O)O 342.40 unknown https://doi.org/10.1021/NP020241F
(2S)-8-[(2R)-2,3-dihydroxy-3-methylbutyl]-7-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one 162892328 Click to see CC(C)(C(CC1=C(C=CC2=C1OC(CC2=O)C3=CC=C(C=C3)O)O)O)O 358.40 unknown https://doi.org/10.1021/NP020241F
(2S)-8-[(2S)-2,3-dihydroxy-3-methylbutyl]-7-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one 637468 Click to see CC(C)(C(CC1=C(C=CC2=C1OC(CC2=O)C3=CC=C(C=C3)O)O)O)O 358.40 unknown https://doi.org/10.1021/NP020241F
2-(4-Hydroxyphenyl)-8-(2-hydroxypropan-2-yl)-2,3,8,9-tetrahydrofuro[2,3-h]chromen-4-one 21603520 Click to see CC(C)(C1CC2=C(O1)C=CC3=C2OC(CC3=O)C4=CC=C(C=C4)O)O 340.40 unknown https://doi.org/10.1021/NP020241F
7-Hydroxy-2-(4-hydroxyphenyl)-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 11609510 Click to see CC(=CCC1=C(C=CC2=C1OC(CC2=O)C3=CC=C(C=C3)O)O)C 324.40 unknown https://doi.org/10.1016/S0031-9422(99)00608-1
8-(2,3-Dihydroxy-3-methylbutyl)-7-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one 21603518 Click to see CC(C)(C(CC1=C(C=CC2=C1OC(CC2=O)C3=CC=C(C=C3)O)O)O)O 358.40 unknown https://doi.org/10.1021/NP020241F
9-Hydroxy-2-(4-hydroxyphenyl)-8,8-dimethyl-2,3,9,10-tetrahydropyrano[2,3-h]chromen-4-one 21603519 Click to see CC1(C(CC2=C(O1)C=CC3=C2OC(CC3=O)C4=CC=C(C=C4)O)O)C 340.40 unknown https://doi.org/10.1021/NP020241F
Brosimacutin A 10970379 Click to see CC(C)(C(CC1=C(C=CC2=C1OC(CC2=O)C3=CC=C(C=C3)O)O)O)O 358.40 unknown https://doi.org/10.1021/NP020241F
Brosimacutin B 11132080 Click to see CC(C)(C(CC1=C(C=CC2=C1OC(CC2=O)C3=CC=C(C=C3)O)O)O)O 358.40 unknown https://doi.org/10.1021/NP020241F
Brosimacutin C 10936790 Click to see CC(C)(CCC1=C(C=CC2=C1OC(CC2=O)C3=CC=C(C=C3)O)O)O 342.40 unknown https://doi.org/10.1021/NP020241F
Brosimacutin D 10914766 Click to see CC1(C(CC2=C(O1)C=CC3=C2OC(CC3=O)C4=CC=C(C=C4)O)O)C 340.40 unknown https://doi.org/10.1021/NP020241F
Brosimacutin E 11002308 Click to see CC(C)(C1CC2=C(O1)C=CC3=C2OC(CC3=O)C4=CC=C(C=C4)O)O 340.40 unknown https://doi.org/10.1021/NP020241F
Isobavachin 193679 Click to see CC(=CCC1=C(C=CC2=C1OC(CC2=O)C3=CC=C(C=C3)O)O)C 324.40 unknown https://doi.org/10.1016/S0031-9422(99)00608-1
Sophoraflavanone B 509245 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC=C(C=C3)O)C 340.40 unknown https://doi.org/10.1016/S0031-9422(99)00608-1
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
(16R,17R)-17-(3,4-dihydroxyphenyl)-5,6,16-trihydroxy-2,12,18-trioxapentacyclo[11.7.1.03,8.09,21.014,19]henicosa-1(21),3,5,7,9,13,19-heptaen-11-one 10049310 Click to see C1C(C(OC2=CC3=C4C(=CC(=O)OC4=C21)C5=CC(=C(C=C5O3)O)O)C6=CC(=C(C=C6)O)O)O 448.40 unknown https://doi.org/10.1055/S-2002-32906
(16R,17R)-17-(3,4-dihydroxyphenyl)-6,11,16-trihydroxy-2,12,18-trioxapentacyclo[11.7.1.03,8.09,21.014,19]henicosa-1(20),3,6,8,10,13(21),14(19)-heptaen-5-one 135474712 Click to see C1C(C(OC2=C1C3=C4C(=C2)OC5=CC(=O)C(=CC5=C4C=C(O3)O)O)C6=CC(=C(C=C6)O)O)O 448.40 unknown https://doi.org/10.1055/S-2002-32906
(16S,17R)-17-(3,4-dihydroxyphenyl)-5,6,16-trihydroxy-2,12,18-trioxapentacyclo[11.7.1.03,8.09,21.014,19]henicosa-1(21),3,5,7,9,13,19-heptaen-11-one 10366382 Click to see C1C(C(OC2=CC3=C4C(=CC(=O)OC4=C21)C5=CC(=C(C=C5O3)O)O)C6=CC(=C(C=C6)O)O)O 448.40 unknown https://doi.org/10.1055/S-2002-32906
Mururin A 135464366 Click to see C1C(C(OC2=C1C3=C4C(=C2)OC5=CC(=O)C(=CC5=C4C=C(O3)O)O)C6=CC(=C(C=C6)O)O)O 448.40 unknown https://doi.org/10.1055/S-2002-32906
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
4H-1-Benzopyran-4-one, 2,3-dihydro-7-hydroxy-2-(4-hydroxyphenyl)- 1889 Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC=C(C=C3)O 256.25 unknown https://doi.org/10.1021/NP020241F
https://doi.org/10.1016/S0031-9422(99)00608-1
5,7-Dihydroxy-2-(4-hydroxyphenyl)chroman-4-one 932 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown https://doi.org/10.1021/NP020241F
Liquiritigenin 114829 Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC=C(C=C3)O 256.25 unknown https://doi.org/10.1016/S0031-9422(99)00608-1
https://doi.org/10.1021/NP020241F
Naringenin 439246 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown https://doi.org/10.1021/NP020241F
> Phenylpropanoids and polyketides / Flavonoids / Flavones
4',7-Dihydroxyflavone 5282073 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C=C3)O)O 254.24 unknown https://doi.org/10.1021/NP020241F
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 https://doi.org/10.1021/NP020241F
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 8-prenylated flavones
8-[(2R)-2,3-dihydroxy-3-methylbutyl]-7-hydroxy-2-(4-hydroxyphenyl)chromen-4-one 162983306 Click to see CC(C)(C(CC1=C(C=CC2=C1OC(=CC2=O)C3=CC=C(C=C3)O)O)O)O 356.40 unknown https://doi.org/10.1021/NP020241F
8-[(2S)-2,3-dihydroxy-3-methylbutyl]-7-hydroxy-2-(4-hydroxyphenyl)chromen-4-one 162983305 Click to see CC(C)(C(CC1=C(C=CC2=C1OC(=CC2=O)C3=CC=C(C=C3)O)O)O)O 356.40 unknown https://doi.org/10.1021/NP020241F
Brosimacutin F 10871979 Click to see CC(C)(C(CC1=C(C=CC2=C1OC(=CC2=O)C3=CC=C(C=C3)O)O)O)O 356.40 unknown https://doi.org/10.1021/NP020241F
> Phenylpropanoids and polyketides / Flavonoids / Furanoflavonoids and dihydrofuranoflavonoids
4-(3,4-dihydro-2H-furo[2,3-h]chromen-2-yl)phenol 86091023 Click to see C1CC2=C(C3=C(C=C2)OC=C3)OC1C4=CC=C(C=C4)O 266.29 unknown https://doi.org/10.1055/S-2005-871272
4-[(2S)-3,4-dihydro-2H-furo[2,3-h]chromen-2-yl]phenol 101405588 Click to see C1CC2=C(C3=C(C=C2)OC=C3)OC1C4=CC=C(C=C4)O 266.29 unknown https://doi.org/10.1055/S-2005-871272
> Phenylpropanoids and polyketides / Flavonoids / Hydroxyflavonoids / 7-hydroxyflavonoids
(2S)-8-(2-hydroxyethyl)-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-7-ol 162943141 Click to see C1CC2=C(C(=C(C=C2)O)CCO)OC1C3=CC=C(C=C3)O 286.32 unknown https://doi.org/10.1021/NP010389J
3,4-Dihydro-2-(4-hydroxyphenyl)-2H-1-benzopyran-7-ol 3500616 Click to see C1CC2=C(C=C(C=C2)O)OC1C3=CC=C(C=C3)O 242.27 unknown https://doi.org/10.1021/NP010389J
7,4'-Dihydroxyflavan 158280 Click to see C1CC2=C(C=C(C=C2)O)OC1C3=CC=C(C=C3)O 242.27 unknown https://doi.org/10.1021/NP010389J
8-(2-hydroxyethyl)-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-7-ol 11748139 Click to see C1CC2=C(C(=C(C=C2)O)CCO)OC1C3=CC=C(C=C3)O 286.32 unknown https://doi.org/10.1021/NP010389J
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
2-(3-hydroxy-4-methoxyphenyl)-3,4-dihydro-2H-chromen-7-ol 11196546 Click to see COC1=C(C=C(C=C1)C2CCC3=C(O2)C=C(C=C3)O)O 272.29 unknown https://doi.org/10.1021/NP010389J
7,3'-Dihydroxy-4'-methoxyflavan 44257179 Click to see COC1=C(C=C(C=C1)C2CCC3=C(O2)C=C(C=C3)O)O 272.29 unknown https://doi.org/10.1016/S0031-9422(99)00608-1
https://doi.org/10.1021/NP010389J
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
(2S)-2-(4-methoxyphenyl)-8,8-dimethyl-3,4-dihydro-2H-pyrano[2,3-f]chromene 162966587 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC(CC3)C4=CC=C(C=C4)OC)C 322.40 unknown https://doi.org/10.1021/NP010389J
2-(4-methoxyphenyl)-8,8-dimethyl-3,4-dihydro-2H-pyrano[2,3-f]chromene 10925322 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC(CC3)C4=CC=C(C=C4)OC)C 322.40 unknown https://doi.org/10.1021/NP010389J
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
1-[3-[(2R)-2,3-dihydroxy-3-methylbutyl]-2,4-dihydroxyphenyl]-3-(4-hydroxyphenyl)propan-1-one 162947814 Click to see CC(C)(C(CC1=C(C=CC(=C1O)C(=O)CCC2=CC=C(C=C2)O)O)O)O 360.40 unknown https://doi.org/10.1021/NP020241F
1-[3-[(2S)-2,3-dihydroxy-3-methylbutyl]-2,4-dihydroxyphenyl]-3-(4-hydroxyphenyl)propan-1-one 162947815 Click to see CC(C)(C(CC1=C(C=CC(=C1O)C(=O)CCC2=CC=C(C=C2)O)O)O)O 360.40 unknown https://doi.org/10.1021/NP020241F
Brosimacutin H 10893739 Click to see CC(C)(C(CC1=C(C=CC(=C1O)C(=O)CCC2=CC=C(C=C2)O)O)O)O 360.40 unknown https://doi.org/10.1021/NP020241F
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
5-Hydroxy-6-(4-hydroxycinnamoyl)-2,2-dimethylchromene 3662729 Click to see CC1(C=CC2=C(O1)C=CC(=C2O)C(=O)C=CC3=CC=C(C=C3)O)C 322.40 unknown https://doi.org/10.1016/S0031-9422(99)00608-1
GU17;ISL;Isoliquiritigen 425 Click to see C1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2)O)O)O 256.25 unknown https://doi.org/10.1016/S0031-9422(99)00608-1
Isobavachromene 5889042 Click to see CC1(C=CC2=C(O1)C=CC(=C2O)C(=O)C=CC3=CC=C(C=C3)O)C 322.40 unknown https://doi.org/10.1016/S0031-9422(99)00608-1
Trihydroxychalcone 638278 Click to see C1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2)O)O)O 256.25 unknown https://doi.org/10.1016/S0031-9422(99)00608-1
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 3-prenylated chalcones
(E)-1-[3-[(2R)-2,3-dihydroxy-3-methylbutyl]-2,4-dihydroxyphenyl]-3-(4-hydroxyphenyl)prop-2-en-1-one 163188343 Click to see CC(C)(C(CC1=C(C=CC(=C1O)C(=O)C=CC2=CC=C(C=C2)O)O)O)O 358.40 unknown https://doi.org/10.1055/S-2005-871272
1-[3-(2,3-Dihydroxy-3-methylbutyl)-2,4-dihydroxyphenyl]-3-(4-hydroxyphenyl)prop-2-en-1-one 162916330 Click to see CC(C)(C(CC1=C(C=CC(=C1O)C(=O)C=CC2=CC=C(C=C2)O)O)O)O 358.40 unknown https://doi.org/10.1055/S-2005-871272
Isobavachalcone 5281255 Click to see CC(=CCC1=C(C=CC(=C1O)C(=O)C=CC2=CC=C(C=C2)O)O)C 324.40 unknown https://doi.org/10.1016/S0031-9422(99)00608-1
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / Furanochalcones
1-[3,4-Dihydroxy-2-(2-hydroxypropan-2-yl)-2,3-dihydro-1-benzofuran-5-yl]-3-(4-hydroxyphenyl)prop-2-en-1-one 72802185 Click to see CC(C)(C1C(C2=C(O1)C=CC(=C2O)C(=O)C=CC3=CC=C(C=C3)O)O)O 356.40 unknown https://doi.org/10.1021/NP020241F
Brosimacutin G 11325738 Click to see CC(C)(C1C(C2=C(O1)C=CC(=C2O)C(=O)C=CC3=CC=C(C=C3)O)O)O 356.40 unknown https://doi.org/10.1021/NP020241F
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / Retro-dihydrochalcones
3-[3-[(2R)-2,3-dihydroxy-3-methylbutyl]-2,4-dihydroxyphenyl]-1-(4-hydroxyphenyl)propan-1-one 162958618 Click to see CC(C)(C(CC1=C(C=CC(=C1O)CCC(=O)C2=CC=C(C=C2)O)O)O)O 360.40 unknown https://doi.org/10.1021/NP020241F
Brosimacutin I 10948388 Click to see CC(C)(C(CC1=C(C=CC(=C1O)CCC(=O)C2=CC=C(C=C2)O)O)O)O 360.40 unknown https://doi.org/10.1021/NP020241F

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