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Cinnamomum burmanni

Cinnamomum burmanni - 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 UUID6440112bc28b3746226846
Scientific name Cinnamomum burmanni
Authority (Nees & T.Nees) Blume
First published in Bijdr. Fl. Ned. Ind. : 569 (1826)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Laurus nitida Roxb. Hort. Bengal. : 30 (1814)
Laurus burmanni Nees & T.Nees Cinnam. Disp. : 57 (1823)
Laurus dulcis Roxb. Fl. Ind. ed. 1832 , 2: 303 (1832)
Persea nitida (Roxb.) Spreng. Syst. Veg. 4(2): 156 (1827)
Persea dulcis (Roxb.) Spreng. Syst. Veg. 2: 268 (1825)
Cinnamomum burmanni var. angustifolium Meisn. Prodr. 15(1): 17 1864
Cinnamomum burmanni var. chinense (Blume) Meisn. Prodr. 15(1): 17 1864
Cinnamomum burmanni var. kiamis (Nees) Meisn. Prodr. 15(1): 17 1864
Cinnamomum ammannii Lukman. Nomencl. Icon. Cannel. : 7 (1878)
Cinnamomum chinense Blume Bijdr. Fl. Ned. Ind. : 569 (1826)
Cinnamomum dulce (Roxb.) Nees Pl. Asiat. Rar. 2: 75 (1831)
Cinnamomum hainanense Nakai Fl. Sylv. Kor. 22: 24 (1939)
Cinnamomum macrostemon Hayata Icon. Pl. Formosan. 3: 160 (1913)
Cinnamomum miaoshanense S.Lee & F.N.Wei Guihaia 8: 302 (1988)
Cinnamomum mindanaense Elmer Leafl. Philipp. Bot. 2: 705 (1910)
Cinnamomum mutabile Blume ex Lukman. Nomencl. Icon. Cannel. 12 (1889).
Cinnamomum nitidum (Roxb.) Hook. Exot. Fl. 3: t. 176 (1825)
Cinnamomum suaveolens Lukman. Nomencl. Icon. Cannel. : 9 (1878)
Cinnamomum thunbergii Lukman. Nomencl. Icon. Cannel. : 7 (1878)
Cinnamomum dulce var. ammannii Lukman. Nomencl. Icon. Cannel. 7 1889
Cinnamomum dulce var. sieboldii Lukman. Nomencl. Icon. Cannel. 7 1889
Cinnamomum dulce var. thunbergii Lukman. Nomencl. Icon. Cannel. 7 1889
Cinnamomum mutabile Blume ex Miq. Ann. Mus. Bot. Lugduno-Batavi 1: 264 (1864)

Common names Top

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Language Common/alternative name
English batavia cinnamon
English padang cassia
English java cinnamon
ace kulét manèh
Arabic قرفة بورمة
Arabic قرفة إندونيسية
Arabic قرفة أندونيسية
Arabic قرفه أندونيسيه
Arabic قرفة اندونيسية
Arabic القرفة الأندونيسية
Japanese インドグス
Korean 인도네시아계피나무
Polish cynamonowiec burmana
Thai อบเชยชวา
Chinese 桂子
Chinese 梅片树
Chinese 阴香叶
Chinese 桂皮
Chinese 阴香
Chinese 阴香（梅片树）
Chinese 陰香
Chinese 土肉桂
Chinese 顺江木
Chinese 阴香皮
Chinese 阴香根

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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No forms added yet.

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-central Tropical Africa
      • Gulf Of Guinea Islands
    • Western Indian Ocean
      • Mauritius
  • Asia-temperate
    • China
      • China South-central
      • China Southeast
      • Hainan
    • Eastern Asia
      • Taiwan
  • Asia-tropical
    • Indian Subcontinent
      • Bangladesh
    • Indo-China
      • Myanmar
      • Vietnam
    • Malesia
      • Borneo
      • Jawa
      • Lesser Sunda Islands
      • Philippines
      • Sulawesi
      • Sumatera

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000604944
UNII F9A26B8997
Florida Plant Atlas 4381
USDA Plants CIBU2
Tropicos 17804456
INPN 706050
KEW urn:lsid:ipni.org:names:463328-1
The Plant List kew-2721172
Missouri Botanical Garden 281678
PaleoBotany 97267
Open Tree Of Life 130603
Open Tree Of Life 7589168
NCBI Taxonomy 119261
Nature Serve 2.140965
IUCN Red List 145302576
IPNI 463328-1
iNaturalist 160583
GBIF 3033985
Freebase /m/027b4pd
EPPO CINBU
USDA GRIN 10577
Wikipedia Cinnamomum_burmanni

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
Feeding adaptation of François' langurs (Trachypithecus francoisi) to the fragmented limestone habitats in Southwest China Yao W, Huang C, Zhao J, Huang R, Li W, Fan P, Zhou Q Ecol Evol 22-Apr-2024
PMCID:PMC11035973
doi:10.1002/ece3.11269
PMID:38654711
Unpredictable Chemical Diversity of Essential Oils in Cinnamomum burmanni (Lauraceae) Living Collections: Beyond Maternally Inherited Phylogenetic Relationships Xie P, Yang Q, Chen J, Tu T, Lian H, He B, Cai Y Molecules 08-Mar-2024
PMCID:PMC10975451
doi:10.3390/molecules29061206
PMID:38542843
Mixing with native broadleaf trees modified soil microbial communities of Cunninghamia lanceolata monocultures in South China Zheng F, Gu J, Lu D, Yang J, Shuai X, Li C, Chen H Front Microbiol 05-Mar-2024
PMCID:PMC10949948
doi:10.3389/fmicb.2024.1372128
PMID:38505544
Three-tiered authentication of herbal traditional Chinese medicine ingredients used in women’s health provides progressive qualitative and quantitative insight Mück F, Scotti F, Mauvisseau Q, Thorbek BL, Wangensteen H, de Boer HJ Front Pharmacol 05-Feb-2024
PMCID:PMC10875096
doi:10.3389/fphar.2024.1353434
PMID:38375033
Statistics and Analysis of Digital Information on Vascular Plant Specimens and the History of Plant Collecting in Guangzhou, China Liang M, Qin X Plants (Basel) 20-Sep-2023
PMCID:PMC10535665
doi:10.3390/plants12183325
PMID:37765488
Changes in homegardens in relocation villages, a case study in the Baiku Yao area in Southern China Hu R, Xu C, Nong Y, Luo B J Ethnobiol Ethnomed 27-Feb-2023
PMCID:PMC9972620
doi:10.1186/s13002-023-00578-4
PMID:36849896
The standardized Jamu pahitan, an Indonesian antidiabetic formulation, stimulating the glucose uptake and insulin secretion in the in-vitro models Hartanti D, Chatsumpun N, Kitphati W, Peungvicha P, Supharattanasitthi W Heliyon 23-Feb-2023
PMCID:PMC9982627
doi:10.1016/j.heliyon.2023.e14018
PMID:36873515
Cinnamon: an aromatic condiment applicable to chronic kidney disease Moreira LD, Brum ID, de Vargas Reis DC, Trugilho L, Chermut TR, Esgalhado M, Cardozo LF, Stenvinkel P, Shiels PG, Mafra D Kidney Res Clin Pract 31-Jan-2023
PMCID:PMC9902738
doi:10.23876/j.krcp.22.111
PMID:36747357
Antioxidant and Anti-Inflammatory Effect of Cinnamon (Cinnamomum verum J. Presl) Bark Extract after In Vitro Digestion Simulation Pagliari S, Forcella M, Lonati E, Sacco G, Romaniello F, Rovellini P, Fusi P, Palestini P, Campone L, Labra M, Bulbarelli A, Bruni I Foods 18-Jan-2023
PMCID:PMC9914695
doi:10.3390/foods12030452
PMID:36765979
The Cytotoxic and Inhibitory Effects of Plant Derivatives on Candida albicans Biofilms: A Scoping Review Loaiza-Oliva M, Arias-Durango L, Martínez-Pabón MC Molecules 23-Dec-2022
PMCID:PMC9822484
doi:10.3390/molecules28010130
PMID:36615324
Strategies for Controlling the Sporulation in Fusarium spp. Ajmal M, Hussain A, Ali A, Chen H, Lin H J Fungi (Basel) 21-Dec-2022
PMCID:PMC9861637
doi:10.3390/jof9010010
PMID:36675831
How Do Landscape Heterogeneity, Community Structure, and Topographical Factors Contribute to the Plant Diversity of Urban Remnant Vegetation at Different Scales? Liu X, Yang G, Que Q, Wang Q, Zhang Z, Huang L Int J Environ Res Public Health 01-Nov-2022
PMCID:PMC9658405
doi:10.3390/ijerph192114302
PMID:36361180
Phylogeny and taxonomy of Cinnamomum (Lauraceae) Yang Z, Liu B, Yang Y, Ferguson DK Ecol Evol 01-Oct-2022
PMCID:PMC9526118
doi:10.1002/ece3.9378
PMID:36203627
Diversity of Useful Plants in Cabo Verde Islands: A Biogeographic and Conservation Perspective Duarte MC, Gomes I, Catarino S, Brilhante M, Gomes S, Rendall A, Moreno Â, Fortes AR, Ferreira VS, Baptista I, Dinis H, Romeiras MM Plants (Basel) 15-May-2022
PMCID:PMC9144021
doi:10.3390/plants11101313
PMID:35631738
Natural Products as a Novel Therapeutic Strategy for NLRP3 Inflammasome-Mediated Gout Lee JH, Kim HS, Lee JH, Yang G, Kim HJ Front Pharmacol 16-Mar-2022
PMCID:PMC8967252
doi:10.3389/fphar.2022.861399
PMID:35370689

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
3-Phenylpropanal 7707 Click to see C1=CC=C(C=C1)CCC=O 134.17 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
4-Vinylbenzaldehyde 39389 Click to see C=CC1=CC=C(C=C1)C=O 132.16 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
Benzaldehyde 240 Click to see C1=CC=C(C=C1)C=O 106.12 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
> Benzenoids / Benzene and substituted derivatives / Phenylpropanes
2-(4-Methylphenyl)propan-2-ol 14529 Click to see CC1=CC=C(C=C1)C(C)(C)O 150.22 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
> Benzenoids / Benzene and substituted derivatives / Styrenes
3-Phenylprop-2-enyl acetate 7660 Click to see CC(=O)OCC=CC1=CC=CC=C1 176.21 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
4-Allylphenol 68148 Click to see C=CCC1=CC=C(C=C1)O 134.17 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
> Benzenoids / Phenols / Methoxyphenols
Eugenol 3314 Click to see COC1=C(C=CC(=C1)CC=C)O 164.20 unknown https://doi.org/10.1007/S10600-012-0139-Y
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
gamma-Terpinene 7461 Click to see CC1=CCC(=CC1)C(C)C 136.23 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
> Lignans, neolignans and related compounds / Furanoid lignans
Syringaresinol 100067 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC 418.40 unknown https://doi.org/10.1007/S10600-012-0139-Y
Syringaresinol, (+)- 443023 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC 418.40 unknown https://doi.org/10.1007/S10600-012-0139-Y
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Palmitic Acid 985 Click to see CCCCCCCCCCCCCCCC(=O)O 256.42 unknown https://doi.org/10.1007/S10600-012-0139-Y
Stearic Acid 5281 Click to see CCCCCCCCCCCCCCCCCC(=O)O 284.50 unknown https://doi.org/10.1007/S10600-012-0139-Y
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Geranyl acetate 1549026 Click to see CC(=CCCC(=CCOC(=O)C)C)C 196.29 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
Isopimara-7,15-diene 13969536 Click to see CC1(CCCC2(C1CC=C3C2CCC(C3)(C)C=C)C)C 272.50 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
Phytol 5280435 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Geraniol 637566 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
Linalool, (+/-)- 6549 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
Nerol 643820 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
p-CYMENE 7463 Click to see CC1=CC=C(C=C1)C(C)C 134.22 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
alpha-Bergamotene, (E)-(-)- 6429302 Click to see CC1=CCC2CC1C2(C)CCC=C(C)C 204.35 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
alpha-Fenchene 28930 Click to see CC1(C2CCC1C(=C)C2)C 136.23 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
Bornyl acetate 6448 Click to see CC(=O)OC1CC2CCC1(C2(C)C)C 196.29 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
Camphene 6616 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
alpha-PHELLANDRENE 7460 Click to see CC1=CCC(C=C1)C(C)C 136.23 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
Terpinolene 11463 Click to see CC1=CCC(=C(C)C)CC1 136.23 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
> Lipids and lipid-like molecules / Prenol lipids / Polyprenols
Ficaprenol 11 11411688 Click to see CC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCO)C)C)C)C)C)C)C)C)C)C)C 767.30 unknown https://doi.org/10.1007/S10600-012-0139-Y
Moraprenol 11 375 Click to see CC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCO)C)C)C)C)C)C)C)C)C)C)C 767.30 unknown https://doi.org/10.1007/S10600-012-0139-Y
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-delta-Cadinene 441005 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
(1R,2S,7S,8S)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene 92042749 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
(1R,4S,4aR)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol 5315592 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
(E,Z)-farnesol 1549109 Click to see CC(=CCCC(=CCCC(=CCO)C)C)C 222.37 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
(R)-beta-bisabolene 68128 Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C 204.35 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
5-(1,5-Dimethyl-4-hexenyl)-2-methyl-1,3-cyclohexadiene 57386731 Click to see CC1=CCC(C=C1)C(C)CCC=C(C)C 204.35 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
alpha-Cadinene, (+)- 12306048 Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C 204.35 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
alpha-Cadinol 10398656 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
Beta-Bisabolene 10104370 Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C 204.35 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
beta-CARYOPHYLLENE OXIDE 1742210 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
gamma-Cadinene 15094 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
gamma-Muurolene 12313020 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
T-Muurolol 3084331 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aS,4aS,7S,7aR,7bS)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 97032059 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
(7aR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 5321422 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Himachalane and lippifoliane sesquiterpenoids
(-)-alpha-Himachalene 11830551 Click to see CC1=CC2C(CC1)C(=C)CCCC2(C)C 204.35 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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/10.1007/S10600-012-0139-Y
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/10.1007/S10600-012-0139-Y
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters
Ethyl Acetate 8857 Click to see CCOC(=O)C 88.11 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
Salicylaldehyde 6998 Click to see C1=CC=C(C(=C1)C=O)O 122.12 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
> Phenylpropanoids and polyketides / Cinnamyl alcohols
Cinnamyl alcohol 5315892 Click to see C1=CC=C(C=C1)C=CCO 134.17 unknown https://doi.org/10.1007/S10600-012-0139-Y
Phenylallyl alcohol 308 Click to see C1=CC=C(C=C1)C=CCO 134.17 unknown https://doi.org/10.1007/S10600-012-0139-Y
> Phenylpropanoids and polyketides / Coumarins and derivatives
Coumarin 323 Click to see C1=CC=C2C(=C1)C=CC(=O)O2 146.14 unknown https://doi.org/10.1007/S10600-012-0139-Y
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(1R,5R,6R,7S,13R,21R)-5,13-bis(3,4-dihydroxyphenyl)-16-[(2R,3R,4R)-2-(3,4-dihydroxyphenyl)-8-[(2R,3R,4R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-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 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/10.1248/CPB.33.4338
(1R,5R,6R,7S,13R,21R)-5,13-bis(3,4-dihydroxyphenyl)-16-[(2R,3R,4R)-2-(3,4-dihydroxyphenyl)-8-[(2R,3R,4R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-7-[(2R,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 162931528 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/10.1248/CPB.33.4338
(1R,5R,6R,7S,13S,21R)-5,13-bis(3,4-dihydroxyphenyl)-7-[(2R,3S)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-18-[(2R,3R,4S)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15(20),16,18-hexaene-6,9,17,19,21-pentol 163064110 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/10.1248/CPB.33.4338
2-(3,4-dihydroxyphenyl)-8-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 130556 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown https://doi.org/10.1248/CPB.33.4338
Arecatannin A1 13752000 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C(C(=CC(=C34)O)O)C5C(C(OC6=CC(=CC(=C56)O)O)C7=CC(=C(C=C7)O)O)O)C8=CC(=C(C=C8)O)O)O)O)O)C9=CC(=C(C=C9)O)O)O 866.80 unknown https://doi.org/10.1248/CPB.33.4338
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/10.1248/CPB.33.4338
Cinnamtannin D1 46173958 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/10.1248/CPB.33.4338
Cinnamtannin D2 46173959 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/10.1248/CPB.33.4338
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/10.1248/CPB.33.4338
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/10.1248/CPB.33.4338
Procyanidin B1 11250133 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown https://doi.org/10.1248/CPB.33.4338
Procyanidin B2, (+)- 122738 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown https://doi.org/10.1248/CPB.33.4338
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/10.1248/CPB.33.4338
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
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/10.1248/CPB.33.4338
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/10.1248/CPB.33.4338
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Kaempferol 3-alpha-L-arabinofuranoside-7-rhamnoside 5491390 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(O4)CO)O)O)C5=CC=C(C=C5)O)O)O)O)O 564.50 unknown https://doi.org/10.1016/S0031-9422(00)97707-0
Kaempferol 3-apiosyl-(1->2)-alpha-L-arabinofuranoside-7-rhamnoside 44258945 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(O4)CO)O)OC5C(C(CO5)(CO)O)O)C6=CC=C(C=C6)O)O)O)O)O 696.60 unknown https://doi.org/10.1016/S0031-9422(00)97707-0
Lespedin 5486199 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)C)O)O)O)C5=CC=C(C=C5)O)O)O)O)O 578.50 unknown https://doi.org/10.1016/S0031-9422(00)97707-0

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