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Sorocea guilleminiana

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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 UUID6440496bb17e1607117694
Scientific name Sorocea guilleminiana
Authority Gaudich.
First published in Voy. Bonite, Bot. 3: t. 74 (1843)

Description Top

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Synonyms Top

Scientific name Authority First published in
Trophis hilariana Casar. Nov. Stirp. Bras. 9: 80 (1845)
Sorocea hilariana Bureau Prodr. 17: 254 (1873)
Sorocea castaneifolia Huber Bol. Mus. Goeldi Hist. Nat. Ethnogr. 5: 333 (1909)
Sorocea grandifolia S.Moore Trans. Linn. Soc. London, Bot. 4: 476 (1895)
Sorocea houllettiana Gaudich. Voy. Bonite, Bot. 3: t. 74 (1843)
Sorocea macrogyne Lanj. & Wess.Boer Acta Bot. Neerl. 11: 459 (1962)
Balanostreblus ilicifolius Kurz J. Asiat. Soc. Bengal, Pt. 2, Nat. Hist. 42: 247 1873

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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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 Northeast
      • Brazil Southeast
      • Brazil West-central
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001084959
Tropicos 21301845
KEW urn:lsid:ipni.org:names:856566-1
The Plant List tro-21301845
Open Tree Of Life 6108832
NCBI Taxonomy 2321349
IUCN Red List 36210
IPNI 856566-1
iNaturalist 443867
GBIF 3762938
Freebase /m/02y_lpz
EOL 5720682
Wikipedia Sorocea_guilleminiana

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
Wound Healing Properties of Natural Products: Mechanisms of Action Criollo-Mendoza MS, Contreras-Angulo LA, Leyva-López N, Gutiérrez-Grijalva EP, Jiménez-Ortega LA, Heredia JB Molecules 06-Jan-2023
PMCID:PMC9867334
doi:10.3390/molecules28020598
PMID:36677659
Medicinal Plants from Latin America with Wound Healing Activity: Ethnomedicine, Phytochemistry, Preclinical and Clinical Studies—A Review Salazar-Gómez A, Alonso-Castro AJ Pharmaceuticals (Basel) 31-Aug-2022
PMCID:PMC9505834
doi:10.3390/ph15091095
PMID:36145316
An Overview of the Isoprenoid Emissions From Tropical Plant Species Mu Z, Llusià J, Zeng J, Zhang Y, Asensio D, Yang K, Yi Z, Wang X, Peñuelas J Front Plant Sci 20-May-2022
PMCID:PMC9163954
doi:10.3389/fpls.2022.833030
PMID:35668805
Opposite latitudinal patterns for bird and arthropod predation revealed in experiments with differently colored artificial prey Zvereva EL, Castagneyrol B, Cornelissen T, Forsman A, Hernández‐Agüero JA, Klemola T, Paolucci L, Polo V, Salinas N, Theron KJ, Xu G, Zverev V, Kozlov MV Ecol Evol 25-Nov-2019
PMCID:PMC6953658
doi:10.1002/ece3.5862
PMID:31938518
Traditional knowledge hiding in plain sight – twenty-first century ethnobotany of the Chácobo in Beni, Bolivia Paniagua Zambrana NY, Bussmann RW, Hart RE, Moya Huanca AL, Ortiz Soria G, Ortiz Vaca M, Ortiz Álvarez D, Soria Morán J, Soria Morán M, Chávez S, Chávez Moreno B, Chávez Moreno G, Roca O, Siripi E J Ethnobiol Ethnomed 10-Oct-2017
PMCID:PMC5634836
doi:10.1186/s13002-017-0179-2
PMID:29017576
A new phenolic glycoside from Sorocea ilicifolia stem bark. Ferrari F, Monache FD Fitoterapia 01-Jun-2004
doi:10.1016/J.FITOTE.2003.12.011
PMID:15159011
Prenylated flavanones from Sorocea ilicifolia Franco Ferrari, Irene Messana Elsevier BV 23-Apr-2003
doi:10.1016/0031-9422(94)00529-3
Sorocein L and sorocein M: two Diels-Alder type adducts from Sorocea ilicifolia. Ferrari F, Filho VC, Cabras T, Messana I J Nat Prod 01-Apr-2003
doi:10.1021/NP020515Z
PMID:12713424
Sorocein I, a new Diels-Alder type adduct from Sorocea ilicifolia. Ferrari F, Delle Monache F Fitoterapia 01-Mar-2001
doi:10.1016/S0367-326X(00)00307-5
PMID:11295312

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
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Glycosylamines
2,6-Dichloro-5-hydroxy-8-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromeno[2,3-b]pyrrol-4-one 10072231 Click to see CC1=CC(=C(C2=C1OC3=C(C2=O)C=C(N3C4C(C(C(C(O4)CO)O)O)O)Cl)O)Cl 446.20 unknown https://doi.org/10.1016/S0367-326X(00)00307-5
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
2,4-Dihydroxybenzaldehyde 7213 Click to see C1=CC(=C(C=C1O)O)C=O 138.12 unknown https://doi.org/10.1016/S0367-326X(00)00307-5
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
(5aR,10aR)-1,3,8,10a-tetrahydroxy-2,4,5a-tris(3-methylbut-2-enyl)-[1]benzofuro[3,2-b]chromen-11-one 162860900 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C3(C(O2)(C4=C(O3)C=C(C=C4)O)CC=C(C)C)O)CC=C(C)C)O)C 506.60 unknown https://doi.org/10.1016/0031-9422(94)00529-3
(5aR,10aS)-1,3,8,10a-tetrahydroxy-2,4,5a-tris(3-methylbut-2-enyl)-[1]benzofuro[3,2-b]chromen-11-one 163188052 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C3(C(O2)(C4=C(O3)C=C(C=C4)O)CC=C(C)C)O)CC=C(C)C)O)C 506.60 unknown https://doi.org/10.1016/0031-9422(94)00529-3
(5aS,10aR)-1,3,8,10a-tetrahydroxy-2,5a,9-tris(3-methylbut-2-enyl)-[1]benzofuro[3,2-b]chromen-11-one 162897812 Click to see CC(=CCC1=C(C=CC2=C1OC3(C2(OC4=C(C3=O)C(=C(C(=C4)O)CC=C(C)C)O)CC=C(C)C)O)O)C 506.60 unknown https://doi.org/10.1016/0031-9422(94)00529-3
1,3,8,10a-Tetrahydroxy-2,4,5a-tris(3-methylbut-2-enyl)-[1]benzofuro[3,2-b]chromen-11-one 10368917 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C3(C(O2)(C4=C(O3)C=C(C=C4)O)CC=C(C)C)O)CC=C(C)C)O)C 506.60 unknown https://doi.org/10.1016/0031-9422(94)00529-3
1,3,8,10a-Tetrahydroxy-2,5a,9-tris(3-methylbut-2-enyl)-[1]benzofuro[3,2-b]chromen-11-one 10323932 Click to see CC(=CCC1=C(C=CC2=C1OC3(C2(OC4=C(C3=O)C(=C(C(=C4)O)CC=C(C)C)O)CC=C(C)C)O)O)C 506.60 unknown https://doi.org/10.1016/0031-9422(94)00529-3
sorocein F 44559966 Click to see CC(=CCC1=C(C=CC2=C1OC3(C2(OC4=C(C3=O)C(=C(C(=C4)O)CC=C(C)C)O)CC=C(C)C)O)O)C 506.60 unknown https://doi.org/10.1016/0031-9422(94)00529-3
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Pyranochromenes
(3S,11R)-7,11,14-trihydroxy-18,18-dimethyl-3,8-bis(3-methylbut-2-enyl)-2,10,17-trioxapentacyclo[11.8.0.03,11.04,9.016,21]henicosa-1(13),4(9),5,7,14,16(21),19-heptaen-12-one 162974630 Click to see CC(=CCC1=C(C=CC2=C1OC3(C2(OC4=C(C3=O)C(=CC5=C4C=CC(O5)(C)C)O)CC=C(C)C)O)O)C 504.60 unknown https://doi.org/10.1016/0031-9422(94)00529-3
(3S,11S)-7,11,14-trihydroxy-18,18-dimethyl-3,8-bis(3-methylbut-2-enyl)-2,10,17-trioxapentacyclo[11.8.0.03,11.04,9.016,21]henicosa-1(13),4(9),5,7,14,16(21),19-heptaen-12-one 162974629 Click to see CC(=CCC1=C(C=CC2=C1OC3(C2(OC4=C(C3=O)C(=CC5=C4C=CC(O5)(C)C)O)CC=C(C)C)O)O)C 504.60 unknown https://doi.org/10.1016/0031-9422(94)00529-3
7,11,14-Trihydroxy-18,18-dimethyl-3,8-bis(3-methylbut-2-enyl)-2,10,17-trioxapentacyclo[11.8.0.03,11.04,9.016,21]henicosa-1(13),4(9),5,7,14,16(21),19-heptaen-12-one 9983600 Click to see CC(=CCC1=C(C=CC2=C1OC3(C2(OC4=C(C3=O)C(=CC5=C4C=CC(O5)(C)C)O)CC=C(C)C)O)O)C 504.60 unknown https://doi.org/10.1016/0031-9422(94)00529-3
7,11,14-Trihydroxy-18,18-dimethyl-3,8-bis(3-methylbut-2-enyl)-2,10,19-trioxapentacyclo[11.8.0.03,11.04,9.015,20]henicosa-1(13),4(9),5,7,14,16,20-heptaen-12-one 75069674 Click to see CC(=CCC1=C(C=CC2=C1OC3(C2(OC4=C(C3=O)C(=C5C=CC(OC5=C4)(C)C)O)CC=C(C)C)O)O)C 504.60 unknown https://doi.org/10.1016/0031-9422(94)00529-3
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(1S,9S,13S,21R)-17-(6-hydroxy-1-benzofuran-2-yl)-1-(5-hydroxy-2,2-dimethylchromen-8-yl)-11-methyl-2,20-dioxapentacyclo[11.7.1.03,8.09,21.014,19]henicosa-3(8),4,6,11,14,16,18-heptaene-5,15-diol 163008477 Click to see CC1=CC2C3C(C1)C4=C(C=C(C=C4)O)OC3(OC5=CC(=CC(=C25)O)C6=CC7=C(O6)C=C(C=C7)O)C8=C9C(=C(C=C8)O)C=CC(O9)(C)C 628.70 unknown https://doi.org/10.1016/S0367-326X(00)00307-5
(9R)-1-(2,4-dihydroxyphenyl)-17-(6-hydroxy-1-benzofuran-2-yl)-11-methyl-2,20-dioxapentacyclo[11.7.1.03,8.09,21.014,19]henicosa-3(8),4,6,11,14,16,18-heptaene-5,15-diol 373222 Click to see CC1=CC2C3C(C1)C4=C(C=C(C=C4)O)OC3(OC5=CC(=CC(=C25)O)C6=CC7=C(O6)C=C(C=C7)O)C8=C(C=C(C=C8)O)O 562.60 unknown https://doi.org/10.1016/J.FITOTE.2003.12.011
https://doi.org/10.1016/S0367-326X(00)00307-5
[(1R,2S,5S)-5-[2,6-dihydroxy-4-(6-hydroxy-1-benzofuran-2-yl)phenyl]-2-(2,4-dihydroxyphenyl)-3-methylcyclohex-3-en-1-yl]-[2,4-dihydroxy-3-(3-methylbut-2-enyl)phenyl]methanone 5458824 Click to see CC1=CC(CC(C1C2=C(C=C(C=C2)O)O)C(=O)C3=C(C(=C(C=C3)O)CC=C(C)C)O)C4=C(C=C(C=C4O)C5=CC6=C(O5)C=C(C=C6)O)O 648.70 unknown https://doi.org/10.1016/J.FITOTE.2003.12.011
https://doi.org/10.1016/0031-9422(94)00529-3
[(1R,2S,6S)-2-[2,6-dihydroxy-4-(6-hydroxy-1-benzofuran-2-yl)phenyl]-6-(2,4-dihydroxyphenyl)-4-methylcyclohex-3-en-1-yl]-(5-hydroxy-2,2-dimethylchromen-6-yl)methanone 154497035 Click to see CC1=CC(C(C(C1)C2=C(C=C(C=C2)O)O)C(=O)C3=C(C4=C(C=C3)OC(C=C4)(C)C)O)C5=C(C=C(C=C5O)C6=CC7=C(O6)C=C(C=C7)O)O 646.70 unknown https://doi.org/10.1021/NP020515Z
[(1S,2R,6R)-2-[2,6-dihydroxy-4-(6-hydroxy-1-benzofuran-2-yl)phenyl]-6-(2,4-dihydroxyphenyl)-4-methylcyclohex-3-en-1-yl]-(5-hydroxy-2,2-dimethylchromen-6-yl)methanone 102375661 Click to see CC1=CC(C(C(C1)C2=C(C=C(C=C2)O)O)C(=O)C3=C(C4=C(C=C3)OC(C=C4)(C)C)O)C5=C(C=C(C=C5O)C6=CC7=C(O6)C=C(C=C7)O)O 646.70 unknown https://doi.org/10.1021/NP020515Z
[(1S,2R,6R)-2-[2,6-dihydroxy-4-(6-hydroxy-1-benzofuran-2-yl)phenyl]-6-(2,4-dihydroxyphenyl)-4-methylcyclohex-3-en-1-yl]-(6-hydroxy-2,2-dimethylchromen-7-yl)methanone 162998188 Click to see CC1=CC(C(C(C1)C2=C(C=C(C=C2)O)O)C(=O)C3=C(C=C4C=CC(OC4=C3)(C)C)O)C5=C(C=C(C=C5O)C6=CC7=C(O6)C=C(C=C7)O)O 646.70 unknown https://doi.org/10.1021/NP020515Z
[2-[2,6-Dihydroxy-4-(6-hydroxy-1-benzofuran-2-yl)phenyl]-6-(2,4-dihydroxyphenyl)-4-methylcyclohex-3-en-1-yl]-(5-hydroxy-2,2-dimethylchromen-6-yl)methanone 5319931 Click to see CC1=CC(C(C(C1)C2=C(C=C(C=C2)O)O)C(=O)C3=C(C4=C(C=C3)OC(C=C4)(C)C)O)C5=C(C=C(C=C5O)C6=CC7=C(O6)C=C(C=C7)O)O 646.70 unknown https://doi.org/10.1021/NP020515Z
[2-[2,6-Dihydroxy-4-(6-hydroxy-1-benzofuran-2-yl)phenyl]-6-(2,4-dihydroxyphenyl)-4-methylcyclohex-3-en-1-yl]-(6-hydroxy-2,2-dimethylchromen-7-yl)methanone 162998187 Click to see CC1=CC(C(C(C1)C2=C(C=C(C=C2)O)O)C(=O)C3=C(C=C4C=CC(OC4=C3)(C)C)O)C5=C(C=C(C=C5O)C6=CC7=C(O6)C=C(C=C7)O)O 646.70 unknown https://doi.org/10.1021/NP020515Z
Chalcomoracin 434768 Click to see CC1=CC(C(C(C1)C2=C(C=C(C=C2)O)O)C(=O)C3=C(C(=C(C=C3)O)CC=C(C)C)O)C4=C(C=C(C=C4O)C5=CC6=C(O5)C=C(C=C6)O)O 648.70 unknown https://doi.org/10.1016/J.FITOTE.2003.12.011
https://doi.org/10.1016/0031-9422(94)00529-3
CID 495296 495296 Click to see CC1=CC2C3C(C1)C4=C(C=C(C=C4)O)OC3(OC5=CC(=CC(=C25)O)C6=CC7=C(O6)C=C(C=C7)O)C8=C9C(=C(C=C8)O)C=CC(O9)(C)C 628.70 unknown https://doi.org/10.1016/S0367-326X(00)00307-5
Mulberrofuran F 3086294 Click to see CC1=CC2C3C(C1)C4=C(C=C(C=C4)O)OC3(OC5=CC(=CC(=C25)O)C6=CC7=C(O6)C=C(C=C7)O)C8=C(C(=C(C=C8)O)CC=C(C)C)O 630.70 unknown https://doi.org/10.1016/0031-9422(94)00529-3
Mulberrofuran K 14334316 Click to see CC1=CC2C3C(C1)C4=C(C=C(C=C4)O)OC3(OC5=CC(=CC(=C25)O)C6=CC7=C(O6)C=C(C=C7)O)C8=C9C(=C(C=C8)O)C=CC(O9)(C)C 628.70 unknown https://doi.org/10.1016/J.FITOTE.2003.12.011
https://doi.org/10.1016/S0367-326X(00)00307-5
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
(2E)-1-[3-[(1S,5S,6R)-6-[2,4-Dihydroxy-3-(3-methyl-2-buten-1-yl)benzoyl]-5-(2,4-dihydroxyphenyl)-3-methyl-2-cyclohexen-1-yl]-2,4-dihydroxyphenyl]-3-(2,4-dihydroxyphenyl)-2-propen-1-one 13194890 Click to see CC1=CC(C(C(C1)C2=C(C=C(C=C2)O)O)C(=O)C3=C(C(=C(C=C3)O)CC=C(C)C)O)C4=C(C=CC(=C4O)C(=O)C=CC5=C(C=C(C=C5)O)O)O 678.70 unknown https://doi.org/10.1021/NP020515Z
(E)-1-[3-[(1R,5R,6S)-6-[2,4-dihydroxy-3-(3-methylbut-2-enyl)benzoyl]-5-(2,4-dihydroxyphenyl)-3-methylcyclohex-2-en-1-yl]-2,4-dihydroxyphenyl]-3-(2,4-dihydroxyphenyl)prop-2-en-1-one 13194889 Click to see CC1=CC(C(C(C1)C2=C(C=C(C=C2)O)O)C(=O)C3=C(C(=C(C=C3)O)CC=C(C)C)O)C4=C(C=CC(=C4O)C(=O)C=CC5=C(C=C(C=C5)O)O)O 678.70 unknown https://doi.org/10.1021/NP020515Z
https://doi.org/10.1016/J.FITOTE.2003.12.011
[2,4-dihydroxy-3-(3-hydroxy-3-methylbutyl)phenyl]-[(1R,2S,6S)-6-(2,4-dihydroxyphenyl)-2-[4-[(E)-2-(2,4-dihydroxyphenyl)ethenyl]-2,6-dihydroxyphenyl]-4-methylcyclohex-3-en-1-yl]methanone 10941398 Click to see CC1=CC(C(C(C1)C2=C(C=C(C=C2)O)O)C(=O)C3=C(C(=C(C=C3)O)CCC(C)(C)O)O)C4=C(C=C(C=C4O)C=CC5=C(C=C(C=C5)O)O)O 668.70 unknown https://doi.org/10.1021/NP020515Z
[2,4-Dihydroxy-3-(3-hydroxy-3-methylbutyl)phenyl]-[6-(2,4-dihydroxyphenyl)-2-[4-[2-(2,4-dihydroxyphenyl)ethenyl]-2,6-dihydroxyphenyl]-4-methylcyclohex-3-en-1-yl]methanone 85324514 Click to see CC1=CC(C(C(C1)C2=C(C=C(C=C2)O)O)C(=O)C3=C(C(=C(C=C3)O)CCC(C)(C)O)O)C4=C(C=C(C=C4O)C=CC5=C(C=C(C=C5)O)O)O 668.70 unknown https://doi.org/10.1021/NP020515Z
[2,4-dihydroxy-3-(3-methylbut-2-enyl)phenyl]-[(1S,2R,6R)-6-(2,4-dihydroxyphenyl)-2-[4-[(E)-2-(2,4-dihydroxyphenyl)ethenyl]-2,6-dihydroxyphenyl]-4-methylcyclohex-3-en-1-yl]methanone 101685339 Click to see CC1=CC(C(C(C1)C2=C(C=C(C=C2)O)O)C(=O)C3=C(C(=C(C=C3)O)CC=C(C)C)O)C4=C(C=C(C=C4O)C=CC5=C(C=C(C=C5)O)O)O 650.70 unknown https://doi.org/10.1016/J.FITOTE.2003.12.011
https://doi.org/10.1016/0031-9422(94)00529-3
1-[3-[6-[2,4-Dihydroxy-3-(3-methylbut-2-enyl)benzoyl]-5-(2,4-dihydroxyphenyl)-3-methylcyclohex-2-en-1-yl]-2,4-dihydroxyphenyl]-3-(2,4-dihydroxyphenyl)prop-2-en-1-one 73167443 Click to see CC1=CC(C(C(C1)C2=C(C=C(C=C2)O)O)C(=O)C3=C(C(=C(C=C3)O)CC=C(C)C)O)C4=C(C=CC(=C4O)C(=O)C=CC5=C(C=C(C=C5)O)O)O 678.70 unknown https://doi.org/10.1021/NP020515Z
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 3-prenylated flavans
(1R,9S,13R,21R)-1-[2,4-dihydroxy-3-(3-hydroxy-3-methylbutyl)phenyl]-17-[(E)-2-(2,4-dihydroxyphenyl)ethenyl]-11-methyl-2,20-dioxapentacyclo[11.7.1.03,8.09,21.014,19]henicosa-3(8),4,6,11,14,16,18-heptaene-5,15-diol 162892775 Click to see CC1=CC2C3C(C1)C4=C(C=C(C=C4)O)OC3(OC5=CC(=CC(=C25)O)C=CC6=C(C=C(C=C6)O)O)C7=C(C(=C(C=C7)O)CCC(C)(C)O)O 650.70 unknown https://doi.org/10.1021/NP020515Z
(1S,9R,13R,21S)-1-[2,4-dihydroxy-3-(3-methylbut-2-enyl)phenyl]-17-[(E)-2-(2,4-dihydroxyphenyl)ethenyl]-11-methyl-2,20-dioxapentacyclo[11.7.1.03,8.09,21.014,19]henicosa-3(8),4,6,11,14,16,18-heptaene-5,15-diol 163186798 Click to see CC1=CC2C3C(C1)C4=C(C=C(C=C4)O)OC3(OC5=CC(=CC(=C25)O)C=CC6=C(C=C(C=C6)O)O)C7=C(C(=C(C=C7)O)CC=C(C)C)O 632.70 unknown https://doi.org/10.1016/S0367-326X(00)00307-5
(1S,9R,13R,21S)-7,17-dihydroxy-1-(5-hydroxy-2,2-dimethylchromen-8-yl)-11-methyl-2,20-dioxapentacyclo[11.7.1.03,8.09,21.014,19]henicosa-3,5,7,10,14(19),15,17-heptaene-5-carbaldehyde 162949121 Click to see CC1=CC2C3C(C1)C4=C(C=C(C=C4)O)OC3(OC5=CC(=CC(=C25)O)C=O)C6=C7C(=C(C=C6)O)C=CC(O7)(C)C 524.60 unknown https://doi.org/10.1016/S0367-326X(00)00307-5
(1S,9S,13S,21R)-1-[2,4-dihydroxy-3-(3-hydroxy-3-methylbutyl)phenyl]-17-[(E)-2-(2,4-dihydroxyphenyl)ethenyl]-11-methyl-2,20-dioxapentacyclo[11.7.1.03,8.09,21.014,19]henicosa-3(8),4,6,11,14,16,18-heptaene-5,15-diol 163185739 Click to see CC1=CC2C3C(C1)C4=C(C=C(C=C4)O)OC3(OC5=CC(=CC(=C25)O)C=CC6=C(C=C(C=C6)O)O)C7=C(C(=C(C=C7)O)CCC(C)(C)O)O 650.70 unknown https://doi.org/10.1021/NP020515Z
(E)-1-[7,17-dihydroxy-1-(5-hydroxy-2,2-dimethylchromen-8-yl)-11-methyl-2,20-dioxapentacyclo[11.7.1.03,8.09,21.014,19]henicosa-3(8),4,6,10,14(19),15,17-heptaen-6-yl]-3-(2,4-dihydroxyphenyl)prop-2-en-1-one 72548999 Click to see CC1=CC2C3C(C1)C4=C(C=C(C=C4)O)OC3(OC5=C2C(=C(C=C5)C(=O)C=CC6=C(C=C(C=C6)O)O)O)C7=C8C(=C(C=C7)O)C=CC(O8)(C)C 658.70 unknown https://doi.org/10.1016/J.FITOTE.2003.12.011
https://doi.org/10.1016/0031-9422(94)00529-3
1-[2,4-Dihydroxy-3-(3-hydroxy-3-methylbutyl)phenyl]-17-[2-(2,4-dihydroxyphenyl)ethenyl]-11-methyl-2,20-dioxapentacyclo[11.7.1.03,8.09,21.014,19]henicosa-3(8),4,6,11,14,16,18-heptaene-5,15-diol 73079438 Click to see CC1=CC2C3C(C1)C4=C(C=C(C=C4)O)OC3(OC5=CC(=CC(=C25)O)C=CC6=C(C=C(C=C6)O)O)C7=C(C(=C(C=C7)O)CCC(C)(C)O)O 650.70 unknown https://doi.org/10.1021/NP020515Z
1-[2,4-Dihydroxy-3-(3-methylbut-2-enyl)phenyl]-17-[2-(2,4-dihydroxyphenyl)ethenyl]-11-methyl-2,20-dioxapentacyclo[11.7.1.03,8.09,21.014,19]henicosa-3(8),4,6,11,14,16,18-heptaene-5,15-diol 163037434 Click to see CC1=CC2C3C(C1)C4=C(C=C(C=C4)O)OC3(OC5=CC(=CC(=C25)O)C=CC6=C(C=C(C=C6)O)O)C7=C(C(=C(C=C7)O)CC=C(C)C)O 632.70 unknown https://doi.org/10.1016/S0367-326X(00)00307-5
7,17-Dihydroxy-1-(5-hydroxy-2,2-dimethylchromen-8-yl)-11-methyl-2,20-dioxapentacyclo[11.7.1.03,8.09,21.014,19]henicosa-3,5,7,10,14(19),15,17-heptaene-5-carbaldehyde 73657349 Click to see CC1=CC2C3C(C1)C4=C(C=C(C=C4)O)OC3(OC5=CC(=CC(=C25)O)C=O)C6=C7C(=C(C=C6)O)C=CC(O7)(C)C 524.60 unknown https://doi.org/10.1016/S0367-326X(00)00307-5
Soroceal 102339032 Click to see CC1=CC2C3C(C1)C4=C(C=C(C=C4)O)OC3(OC5=CC(=CC(=C25)O)C=O)C6=C7C(=C(C=C6)O)C=CC(O7)(C)C 524.60 unknown https://doi.org/10.1016/S0367-326X(00)00307-5
Sorocein A 6443653 Click to see CC1=CC2C3C(C1)C4=C(C=C(C=C4)O)OC3(OC5=CC(=CC(=C25)O)C=CC6=C(C=C(C=C6)O)O)C7=C8C(=C(C=C7)O)C=CC(O8)(C)C 630.70 unknown https://doi.org/10.1016/J.FITOTE.2003.12.011
https://doi.org/10.1016/0031-9422(94)00529-3
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans
3,6,10,24-Tetrahydroxy-20-(5-hydroxy-2,2-dimethylchromen-8-yl)-30-methyl-14-(3-methylbut-2-enyl)-7,15,19,21-tetraoxaoctacyclo[18.11.1.02,18.04,16.06,14.08,13.022,27.028,32]dotriaconta-2,4(16),8(13),9,11,17,22(27),23,25,30-decaen-5-one 162890059 Click to see CC1=CC2C3C(C1)C4=C(C=C(C=C4)O)OC3(OC5=CC6=C(C(=C25)O)C(=O)C7(C(O6)(C8=C(O7)C=C(C=C8)O)CC=C(C)C)O)C9=C1C(=C(C=C9)O)C=CC(O1)(C)C 756.80 unknown https://doi.org/10.1016/0031-9422(94)00529-3

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