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Pavetta owariensis

Pavetta owariensis - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID643fe66c4cea8959982660
Scientific name Pavetta owariensis
Authority P.Beauv.
First published in Fl. Oware 1: 87 (1806)

Description Top

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Synonyms Top

Scientific name Authority First published in
Ixora owariensis Poir. Encycl. , Suppl. 3: 207 (1813)

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
Pavetta owariensis var. glaucescens (Hiern) S.D.Manning Ann. Missouri Bot. Gard. 83: 136 (1996)
Pavetta owariensis var. opaca S.D.Manning Ann. Missouri Bot. Gard. 83: 134 (1996)
Pavetta owariensis var. owariensis Unknown
Pavetta owariensis var. satabiei S.D.Manning Ann. Missouri Bot. Gard. 83: 137 (1996)

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
  • Africa
    • West Tropical Africa
      • Ghana
      • Guinea
      • Ivory Coast
      • Liberia
      • Nigeria
      • Sierra Leone
    • West-central Tropical Africa
      • Cabinda
      • Cameroon
      • Congo
      • Equatorial Guinea
      • Gabon
      • Gulf Of Guinea Islands
      • Zaïre

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000265725
Tropicos 27910057
KEW urn:lsid:ipni.org:names:759933-1
The Plant List kew-148796
Open Tree Of Life 7626926
NCBI Taxonomy 2708928
IUCN Red List 110043100
IPNI 759933-1
GBIF 2924870
EOL 1095389

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
Polyphenols and their potential role to fight viral diseases: An overview Montenegro-Landívar MF, Tapia-Quirós P, Vecino X, Reig M, Valderrama C, Granados M, Cortina JL, Saurina J Sci Total Environ 19-Aug-2021
PMCID:PMC8373592
doi:10.1016/j.scitotenv.2021.149719
PMID:34438146
Isolation of five proanthocyanidins from pear (Pyrus pyrifolia Nakai) fruit peels Jeong DE, Cho JY, Lee YG, Jeong HY, Lee HJ, Moon JH Food Sci Biotechnol 22-Sep-2017
PMCID:PMC6049796
doi:10.1007/s10068-017-0157-4
PMID:30263654
Secondary Metabolites from Rubiaceae Species Martins D, Nunez CV Molecules 22-Jul-2015
PMCID:PMC6331836
doi:10.3390/molecules200713422
PMID:26205062
Composition, Standardization and Chemical Profiling of Banisteriopsis caapi, a Plant for the Treatment of Neurodegenerative Disorders Relevant to Parkinson’s Disease Wang YH, Samoylenko V, Tekwani BL, Khan IA, Miller LS, Chaurasiya ND, Rahman MM, Tripathi LM, Khan SI, Joshi VC, Wigger FT, Muhammad I J Ethnopharmacol 26-Feb-2010
PMCID:PMC2878139
doi:10.1016/j.jep.2010.02.013
PMID:20219660
Banisteriopsis caapi, a unique combination of MAO inhibitory and antioxidative constituents for the activities relevant to neurodegenerative disorders and Parkinson’s disease Samoylenko V, Rahman MM, Tekwani BL, Tripathi LM, Wang YH, Khan SI, Khan IA, Miller LS, Joshi VC, Muhammad I J Ethnopharmacol 30-Oct-2009
PMCID:PMC2828149
doi:10.1016/j.jep.2009.10.030
PMID:19879939
Imaging schistosomes in vivo Krautz-Peterson G, Ndegwa D, Vasquez K, Korideck H, Zhang J, Peterson JD, Skelly PJ FASEB J 01-Aug-2009
PMCID:PMC2717771
doi:10.1096/fj.08-127738
PMID:19346298
Effects of Varying Concentrations of the Crude Aqueous and Ethanolic Extracts of Dalbergia Sissoo Plant Parts on Biomphalaria Pfeifferi Egg Masses Adenusi AA, Odaibo AB Afr J Tradit Complement Altern Med 07-Mar-2009
PMCID:PMC2816571
PMID:20209005
Molluscicidal Activities of Doubly-Linked Proanthocyanidins from<i>Pavetta owariensis</i> A. Baldé, S. Geerts, F. Ceulemans, T. Bruyne, L. Pieters, M. Claeys, A. Vlietinck Georg Thieme Verlag KG 07-Nov-2008
doi:10.1055/S-2006-961642
Plant antiviral agents. VII. Antiviral and antibacterial proanthocyanidins from the bark of <i>Pavetta owariensis</i> A. M. Baldé, L. van Hoof, L. A. Pieters, D. A. Vanden Berghe, A. J. Vlietinck Wiley 18-Oct-2006
doi:10.1002/PTR.2650040505
Antimicrobial activity of flavonoids Cushnie TP, Lamb AJ Int J Antimicrob Agents 19-Oct-2005
PMCID:PMC7127073
doi:10.1016/j.ijantimicag.2005.09.002
PMID:16323269
Proanthocyanidins from Stem Bark of Pavetta owariensis, 3. Nmr Study of Acetylated Trimeric Proanthocyanidins Possessing a Doubly-Linked Structure Aliou M. Baldé, Tess De Bruyne, Luc Pieters, Magda Claeys, Dirk Vanden Berghe, Arnold Vlietinck, Victor Wray, Herbert Kolodziej American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50097A011
Tetrameric proanthocyanidins containing a double interflavanoid (A-type) linkage from Pavetta owariensis Aliou Balde, Tess De Bruyne, Luc Pieters, Herbert Kolodziej, Dirk Vanden Berghe, Magda Claeys, Arnold Vlietinck Elsevier BV 01-May-2003
doi:10.1016/0031-9422(95)00331-Z
Oligomeric proanthocyanidins possessing a doubly linked structure from Pavetta owariensis Aliou M. Balde, Tess de Bruyne, Luc Pieters, Herbert Kolodziej, Dirk Vanden Berghe, Magda Claeys, Arnold Vlietinck Elsevier BV 23-Apr-2003
doi:10.1016/0031-9422(94)00660-L
Dimeric and trimeric proanthocyanidins possessing a doubly linked structure from Pavetta owariensis A.M. Baldé, L.A. Pieters, V. Wray, H. Kolodziej, D.A.Vanden Berghe, M. Claeys, A.J. Vlietinck Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(91)83480-9
A-type Proanthocyanidins from stem-bark of Pavetta owariensis A.M. Baldé, L.A. Pieters, A. Gergely, H Kolodziej, M. Claeys, A.J. Vlietinck Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(91)84150-Q

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 / Benzyl alcohols
Benzyl Alcohol 244 Click to see C1=CC=C(C=C1)CO 108.14 unknown https://doi.org/10.1016/0031-9422(91)85302-G
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
Chlorogenic Acid 1794427 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown https://doi.org/10.1002/PTR.2650040505
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
2-Propenoic acid, 3-(4-hydroxy-3-methoxyphenyl)-, octadecyl ester 149044 Click to see CCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC 446.70 unknown https://doi.org/10.1016/0031-9422(91)85302-G
docosyl (Z)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 101677461 Click to see CCCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC 502.80 unknown https://doi.org/10.1016/0031-9422(91)85302-G
Docosyl ferulate 14238616 Click to see CCCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC 502.80 unknown https://doi.org/10.1016/0031-9422(91)85302-G
Docosylferulate 54370069 Click to see CCCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC 502.80 unknown https://doi.org/10.1016/0031-9422(91)85302-G
Eicosyl ferulate 6440080 Click to see CCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC 474.70 unknown https://doi.org/10.1016/0031-9422(91)85302-G
henicosyl (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 101634607 Click to see CCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC 488.70 unknown https://doi.org/10.1016/0031-9422(91)85302-G
Henicosyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 162893394 Click to see CCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC 488.70 unknown https://doi.org/10.1016/0031-9422(91)85302-G
Hexacosyl (E)-ferulate 5318033 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC 558.90 unknown https://doi.org/10.1016/0031-9422(91)85302-G
icosyl (Z)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 5317019 Click to see CCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC 474.70 unknown https://doi.org/10.1016/0031-9422(91)85302-G
Icosyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 149045 Click to see CCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC 474.70 unknown https://doi.org/10.1016/0031-9422(91)85302-G
nonadecyl (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 101186931 Click to see CCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC 460.70 unknown https://doi.org/10.1016/0031-9422(91)85302-G
Nonadecyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 85606197 Click to see CCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC 460.70 unknown https://doi.org/10.1016/0031-9422(91)85302-G
Octacosyl (E)-ferulate 5743442 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC 586.90 unknown https://doi.org/10.1016/0031-9422(91)85302-G
octadecyl (Z)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 14522985 Click to see CCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC 446.70 unknown https://doi.org/10.1016/0031-9422(91)85302-G
Octadecyl ferulate 5320256 Click to see CCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC 446.70 unknown https://doi.org/10.1016/0031-9422(91)85302-G
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
cis-Ferulic acid 1548883 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O 194.18 unknown https://doi.org/10.1016/0031-9422(91)85302-G
Ferulic acid 445858 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O 194.18 unknown https://doi.org/10.1016/0031-9422(91)85302-G
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(1R,5R,6R,7R,13S,21R)-5,13-bis(3,4-dihydroxyphenyl)-7-[(2S,3S)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaene-6,9,17,19,21-pentol 13990887 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C(=CC5=C4C6C(C(O5)(OC7=CC(=CC(=C67)O)O)C8=CC(=C(C=C8)O)O)O)O)C9=CC(=C(C=C9)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 864.80 unknown https://doi.org/10.1016/0031-9422(91)83480-9
(1R,5R,6R,7R,13S,21R)-7,13-bis(3,4-dihydroxyphenyl)-5-[(2R,3R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-8,12,14-trioxapentacyclo[11.7.1.02,11.04,9.015,20]henicosa-2(11),3,9,15,17,19-hexaene-3,6,17,19,21-pentol 163039628 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC5=C(C6C(C(O5)(OC7=CC(=CC(=C67)O)O)C8=CC(=C(C=C8)O)O)O)C(=C34)O)C9=CC(=C(C=C9)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 864.80 unknown https://doi.org/10.1021/NP50097A011
https://doi.org/10.1016/0031-9422(91)83480-9
(1R,5R,6R,7S,13S,21R)-5,13-bis(3,4-dihydroxyphenyl)-7-[(2R,3R,4S)-2-(3,4-dihydroxyphenyl)-4-[(2R,3R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaene-6,9,17,19,21-pentol 162930948 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C(=CC(=C4C5C(C(OC6=C5C(=CC7=C6C8C(C(O7)(OC9=CC(=CC(=C89)O)O)C1=CC(=C(C=C1)O)O)O)O)C1=CC(=C(C=C1)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 1153.00 unknown https://doi.org/10.1016/0031-9422(95)00331-Z
(1R,5R,6S,13R,21R)-5,13-bis(3,4-dihydroxyphenyl)-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaene-6,9,17,19,21-pentol 101165393 Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC(=C(C=C6)O)O)O)O)C7=CC(=C(C=C7)O)O)O 576.50 unknown https://doi.org/10.1016/0031-9422(91)84150-Q
(1R,5R,6S,7R,13S,21R)-7,13-bis(3,4-dihydroxyphenyl)-5-[(2R,3R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-8,12,14-trioxapentacyclo[11.7.1.02,11.04,9.015,20]henicosa-2(11),3,9,15,17,19-hexaene-3,6,17,19,21-pentol 163039627 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC5=C(C6C(C(O5)(OC7=CC(=CC(=C67)O)O)C8=CC(=C(C=C8)O)O)O)C(=C34)O)C9=CC(=C(C=C9)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 864.80 unknown https://doi.org/10.1016/0031-9422(91)83480-9
(1R,5S,6R,7S,13S,21R)-5,13-bis(3,4-dihydroxyphenyl)-7-[(2R,3R,4S)-2-(3,4-dihydroxyphenyl)-4-[(2S,3R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaene-6,9,17,19,21-pentol 163195012 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C(=CC(=C4C5C(C(OC6=C5C(=CC7=C6C8C(C(O7)(OC9=CC(=CC(=C89)O)O)C1=CC(=C(C=C1)O)O)O)O)C1=CC(=C(C=C1)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 1153.00 unknown https://doi.org/10.1016/0031-9422(95)00331-Z
(1R,5S,6S,7R,13S,21R)-5,13-bis(3,4-dihydroxyphenyl)-7-[(2R,3S,4R)-2-(3,4-dihydroxyphenyl)-4-[(2R,3R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaene-6,9,17,19,21-pentol 163195011 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C(=CC(=C4C5C(C(OC6=C5C(=CC7=C6C8C(C(O7)(OC9=CC(=CC(=C89)O)O)C1=CC(=C(C=C1)O)O)O)O)C1=CC(=C(C=C1)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 1153.00 unknown https://doi.org/10.1016/0031-9422(95)00331-Z
(1S,5R,6R,7R,13R,21R)-5,13-bis(3,4-dihydroxyphenyl)-7-[(2R,3R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaene-6,9,17,19,21-pentol 99649069 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C(=CC5=C4C6C(C(O5)(OC7=CC(=CC(=C67)O)O)C8=CC(=C(C=C8)O)O)O)O)C9=CC(=C(C=C9)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 864.80 unknown https://doi.org/10.1016/0031-9422(91)83480-9
(1S,5R,6R,7R,13R,21R)-5,13-bis(3,4-dihydroxyphenyl)-7-[(2S,3S)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaene-6,9,17,19,21-pentol 99649072 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C(=CC5=C4C6C(C(O5)(OC7=CC(=CC(=C67)O)O)C8=CC(=C(C=C8)O)O)O)O)C9=CC(=C(C=C9)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 864.80 unknown https://doi.org/10.1016/0031-9422(91)83480-9
(1S,5R,6R,7R,13R,21R)-7,13-bis(3,4-dihydroxyphenyl)-5-[(2R,3R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-8,12,14-trioxapentacyclo[11.7.1.02,11.04,9.015,20]henicosa-2(11),3,9,15,17,19-hexaene-3,6,17,19,21-pentol 101619555 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC5=C(C6C(C(O5)(OC7=CC(=CC(=C67)O)O)C8=CC(=C(C=C8)O)O)O)C(=C34)O)C9=CC(=C(C=C9)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 864.80 unknown https://doi.org/10.1016/0031-9422(91)83480-9
(1S,5R,6S,7R,13R,21R)-7,13-bis(3,4-dihydroxyphenyl)-5-[(2R,3R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-8,12,14-trioxapentacyclo[11.7.1.02,11.04,9.015,20]henicosa-2(11),3,9,15,17,19-hexaene-3,6,17,19,21-pentol 101619556 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC5=C(C6C(C(O5)(OC7=CC(=CC(=C67)O)O)C8=CC(=C(C=C8)O)O)O)C(=C34)O)C9=CC(=C(C=C9)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 864.80 unknown https://doi.org/10.1016/0031-9422(91)83480-9
(1S,5R,6S,7R,13R,21S)-7,13-bis(3,4-dihydroxyphenyl)-5-[(2R,3R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-8,12,14-trioxapentacyclo[11.7.1.02,11.04,9.015,20]henicosa-2(11),3,9,15,17,19-hexaene-3,6,17,19,21-pentol 163039629 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC5=C(C6C(C(O5)(OC7=CC(=CC(=C67)O)O)C8=CC(=C(C=C8)O)O)O)C(=C34)O)C9=CC(=C(C=C9)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 864.80 unknown https://doi.org/10.1021/NP50097A011
(1S,5S,6R,13R,21S)-5,13-bis(3,4-dihydroxyphenyl)-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaene-6,9,17,19,21-pentol 13556388 Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC(=C(C=C6)O)O)O)O)C7=CC(=C(C=C7)O)O)O 576.50 unknown https://doi.org/10.1016/0031-9422(91)84150-Q
(1S,5S,6R,7S,13R,21R)-5,13-bis(3,4-dihydroxyphenyl)-7-[(2R,3R,4S)-2-(3,4-dihydroxyphenyl)-4-[(2R,3R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaene-6,9,17,19,21-pentol 101683296 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C(=CC(=C4C5C(C(OC6=C5C(=CC7=C6C8C(C(O7)(OC9=CC(=CC(=C89)O)O)C1=CC(=C(C=C1)O)O)O)O)C1=CC(=C(C=C1)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 1153.00 unknown https://doi.org/10.1016/0031-9422(95)00331-Z
5,13-bis(3,4-dihydroxyphenyl)-16-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-7-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaene-6,9,17,19,21-pentol 16165527 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C(=CC5=C4C6C(C(O5)(OC7=C(C(=CC(=C67)O)O)C8C(C(OC9=CC(=CC(=C89)O)O)C1=CC(=C(C=C1)O)O)O)C1=CC(=C(C=C1)O)O)O)O)C1=CC(=C(C=C1)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 1153.00 unknown https://doi.org/10.1016/0031-9422(94)00660-L
5,13-bis(3,4-dihydroxyphenyl)-7-[2-(3,4-dihydroxyphenyl)-4-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaene-6,9,17,19,21-pentol 16165520 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C(=CC(=C4C5C(C(OC6=C5C(=CC7=C6C8C(C(O7)(OC9=CC(=CC(=C89)O)O)C1=CC(=C(C=C1)O)O)O)O)C1=CC(=C(C=C1)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 1153.00 unknown https://doi.org/10.1016/0031-9422(95)00331-Z
7,13-bis(3,4-dihydroxyphenyl)-5-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-8,12,14-trioxapentacyclo[11.7.1.02,11.04,9.015,20]henicosa-2(11),3,9,15,17,19-hexaene-3,6,17,19,21-pentol 163039626 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC5=C(C6C(C(O5)(OC7=CC(=CC(=C67)O)O)C8=CC(=C(C=C8)O)O)O)C(=C34)O)C9=CC(=C(C=C9)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 864.80 unknown https://doi.org/10.1016/0031-9422(91)83480-9
CID 16165471 16165471 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C(=CC5=C4C6C(C(O5)(OC7=C(C(=CC(=C67)O)O)C8C(C(OC9=C(C(=CC(=C89)O)O)C1C(C(OC2=CC(=CC(=C12)O)O)C1=CC(=C(C=C1)O)O)O)C1=CC(=C(C=C1)O)O)O)C1=CC(=C(C=C1)O)O)O)O)C1=CC(=C(C=C1)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 1441.30 unknown https://doi.org/10.1016/0031-9422(94)00660-L
Cinnamtannin B1 475277 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C(=CC5=C4C6C(C(O5)(OC7=CC(=CC(=C67)O)O)C8=CC(=C(C=C8)O)O)O)O)C9=CC(=C(C=C9)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 864.80 unknown https://doi.org/10.1016/0031-9422(91)83480-9
https://doi.org/10.1002/PTR.2650040505
Cinnamtannin B2 16130973 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C(=CC5=C4C6C(C(O5)(OC7=C(C(=CC(=C67)O)O)C8C(C(OC9=CC(=CC(=C89)O)O)C1=CC(=C(C=C1)O)O)O)C1=CC(=C(C=C1)O)O)O)O)C1=CC(=C(C=C1)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 1153.00 unknown https://doi.org/10.1016/0031-9422(94)00660-L
Pavetannin A2 10415767 Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC(=C(C=C6)O)O)O)O)C7=CC(=C(C=C7)O)O)O 576.50 unknown https://doi.org/10.1016/0031-9422(91)83480-9
Pavetannin B2 13990886 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C(=CC5=C4C6C(C(O5)(OC7=CC(=CC(=C67)O)O)C8=CC(=C(C=C8)O)O)O)O)C9=CC(=C(C=C9)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 864.80 unknown https://doi.org/10.1016/0031-9422(91)83480-9
Pavetannin B6 13990885 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C(=CC5=C4C6C(C(O5)(OC7=CC(=CC(=C67)O)O)C8=CC(=C(C=C8)O)O)O)O)C9=CC(=C(C=C9)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 864.80 unknown https://doi.org/10.1016/0031-9422(91)83480-9
Pavetannin C1 16165472 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C(=CC5=C4C6C(C(O5)(OC7=C6C(=C(C(=C7)O)C8C(C(OC9=CC(=CC(=C89)O)O)C1=CC(=C(C=C1)O)O)O)O)C1=CC(=C(C=C1)O)O)O)O)C1=CC(=C(C=C1)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 1153.00 unknown https://doi.org/10.1016/0031-9422(94)00660-L
Pavetannin D1 16165469 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C(=CC5=C4C6C(C(O5)(OC7=C(C(=CC(=C67)O)O)C8C(C(OC9=C(C(=CC(=C89)O)O)C1C(C(OC2=CC(=CC(=C12)O)O)C1=CC(=C(C=C1)O)O)O)C1=CC(=C(C=C1)O)O)O)C1=CC(=C(C=C1)O)O)O)O)C1=CC(=C(C=C1)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 1441.30 unknown https://doi.org/10.1016/0031-9422(94)00660-L
Proanthocyanidin A1 9872976 Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC(=C(C=C6)O)O)O)O)C7=CC(=C(C=C7)O)O)O 576.50 unknown https://doi.org/10.1016/0031-9422(91)83480-9
Proanthocyanidin A4 13556387 Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC(=C(C=C6)O)O)O)O)C7=CC(=C(C=C7)O)O)O 576.50 unknown https://doi.org/10.1016/0031-9422(91)84150-Q
Procyanidin A1 5089889 Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC(=C(C=C6)O)O)O)O)C7=CC(=C(C=C7)O)O)O 576.50 unknown https://doi.org/10.1016/0031-9422(91)84150-Q
https://doi.org/10.1016/0031-9422(91)83480-9
Procyanidin A2 124025 Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC(=C(C=C6)O)O)O)O)C7=CC(=C(C=C7)O)O)O 576.50 unknown https://doi.org/10.1055/S-2006-961642
https://doi.org/10.1016/0031-9422(91)84150-Q
Tannin B 16165473 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C(=CC5=C4C6C(C(O5)(OC7=C6C(=C(C(=C7)O)C8C(C(OC9=CC(=CC(=C89)O)O)C1=CC(=C(C=C1)O)O)O)O)C1=CC(=C(C=C1)O)O)O)O)C1=CC(=C(C=C1)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 1153.00 unknown https://doi.org/10.1016/0031-9422(94)00660-L
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
(+)-Epicatechin 182232 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1016/0031-9422(91)84150-Q
2-(3,4-Dihydroxyphenyl)chroman-3,5,7-triol 1203 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1016/0031-9422(91)84150-Q
Cianidanol 9064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1016/0031-9422(91)84150-Q
https://doi.org/10.1055/S-2006-961642
https://doi.org/10.1002/PTR.2650040505
Epicatechin 72276 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1016/0031-9422(91)84150-Q

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