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Kielmeyera coriacea

Kielmeyera coriacea - 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 UUID643ff39ccfb51077562998
Scientific name Kielmeyera coriacea
Authority Mart.
First published in Nov. Gen. Sp. Pl. Bras. 1: 112 (1826)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Kielmeyera oblonga Pohl Pl. Bras. Icon. Descr. 2: 47 (1830)
Martinieria arborea Vell. Fl. Flumin. : 232 (1829)
Bonnetia coriacea Spreng. Syst. Veg. 4(2): 207 (1827)
Kielmeyera amplexicaulis S.Moore Trans. Linn. Soc. London, Bot. 4: 311 (1895)
Kielmeyera coriacea Mart. & Zucc. Flora 8: 30 (-31). 1825 [14 Jan 1825]

Common names Top

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Language Common/alternative name
Persian کیلمیرا کوریاسی

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Name Authority First published in
Kielmeyera coriacea var. pseudocoriacea Saddi Publ. Avulsas Herb. Centr. Univ. Fed. Mato Grosso 10: 54 (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
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil South
      • Brazil Southeast
      • Brazil West-central
    • Southern South America
      • Paraguay
    • Western South America
      • Bolivia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000356264
Tropicos 7801213
KEW urn:lsid:ipni.org:names:828950-1
The Plant List kew-2333753
Open Tree Of Life 1047461
NCBI Taxonomy 639202
IPNI 828950-1
iNaturalist 601744
GBIF 7330272
Freebase /m/02rdd_l
Wikipedia Kielmeyera_coriacea
CMAUP NPO777

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
Anemochorous and zoochorous seeds of trees from the Brazilian savannas differ in fatty acid content and composition Franco AC, de Melo RB, Ferreira CS, Williams TC AoB Plants 17-Aug-2023
PMCID:PMC10433789
doi:10.1093/aobpla/plad042
PMID:37600502
Carbon Storage in Different Compartments in Eucalyptus Stands and Native Cerrado Vegetation Ribeiro FP, Gatto A, de Oliveira AD, Pulrolnik K, Valadão MB, Araújo JB, de Carvalho AM, Ferreira EA Plants (Basel) 24-Jul-2023
PMCID:PMC10386474
doi:10.3390/plants12142751
PMID:37514365
The complete chloroplast genome of Calophyllum soulattri Burm. f. (Calophyllaceae) Pahayo DG, Cadorna CA, Quimado MO, Rey JD Mitochondrial DNA B Resour 25-May-2023
PMCID:PMC10215020
doi:10.1080/23802359.2023.2215350
PMID:37250208
Phenolic Compounds in Bacterial Inactivation: A Perspective from Brazil Kauffmann AC, Castro VS Antibiotics (Basel) 24-Mar-2023
PMCID:PMC10135396
doi:10.3390/antibiotics12040645
PMID:37107007
Xanthones: Biosynthesis and Trafficking in Plants, Fungi and Lichens Badiali C, Petruccelli V, Brasili E, Pasqua G Plants (Basel) 04-Feb-2023
PMCID:PMC9967055
doi:10.3390/plants12040694
PMID:36840041
Biphenyls in Clusiaceae: Isolation, structure diversity, synthesis and bioactivity Wang Y, Huang Q, Zhang L, Zheng C, Xu H Front Chem 01-Dec-2022
PMCID:PMC9751493
doi:10.3389/fchem.2022.987009
PMID:36531325
Phytochemical screening and antibacterial activity of Skimmia anquetilia N.P. Taylor and Airy Shaw: A first study from Kashmir Himalaya Nabi M, Tabassum N, Ganai BA Front Plant Sci 12-Aug-2022
PMCID:PMC9412939
doi:10.3389/fpls.2022.937946
PMID:36035710
Toxic Potential of Cerrado Plants on Different Organisms Rocha JD, Carneiro FM, Fernandes AS, Morais JM, Borges LL, Chen-Chen L, de Almeida LM, Bailão EF Int J Mol Sci 22-Mar-2022
PMCID:PMC8998518
doi:10.3390/ijms23073413
PMID:35408775
Chemical Composition of Salix koreensis Anderss Flower Absolute and Its Skin Wound Healing Activities In Vitro Kim NY, Won KJ, Kim HB, Kim DY, Kim MJ, Won YR, Lee HM Plants (Basel) 18-Jan-2022
PMCID:PMC8838726
doi:10.3390/plants11030246
PMID:35161226
Calophyllaceae plastomes, their structure and insights in relationships within the clusioids Trad RJ, Cabral FN, Bittrich V, Silva SR, Amaral MD Sci Rep 20-Oct-2021
PMCID:PMC8528878
doi:10.1038/s41598-021-99178-z
PMID:34671062
Anti-apoptotic effect of Buchholzia coriacea Engl. stem back extracts on AsPC-1 and mechanisms of action Onohuean H, Adisa RA, Alagbonsi AI BMC Complement Med Ther 09-Oct-2021
PMCID:PMC8501612
doi:10.1186/s12906-021-03433-9
PMID:34627212
A Molecular Networking Strategy: High-Throughput Screening and Chemical Analysis of Brazilian Cerrado Plant Extracts against Cancer Cells Cortelo PC, Demarque DP, Dusi RG, Albernaz LC, Braz-Filho R, Goncharova EI, Bokesch HR, Gustafson KR, Beutler JA, Espindola LS Cells 20-Mar-2021
PMCID:PMC8004027
doi:10.3390/cells10030691
PMID:33804755
Fungal Planet description sheets: 1042–1111 Crous PW, Wingfield MJ, Chooi YH, Gilchrist CL, Lacey E, Pitt JI, Roets F, Swart WJ, Cano-Lira JF, Valenzuela-Lopez N, Hubka V, Shivas RG, Stchigel AM, Holdom DG, Jurjević Ž, Kachalkin AV, Lebel T, Lock C, Martín MP, Tan YP, Tomashevskaya MA, Vitelli JS, Baseia IG, Bhatt VK, Brandrud TE, De Souza JT, Dima B, Lacey HJ, Lombard L, Johnston PR, Morte A, Papp V, Rodríguez A, Rodríguez-Andrade E, Semwal KC, Tegart L, Abad ZG, Akulov A, Alvarado P, Alves A, Andrade JP, Arenas F, Asenjo C, Ballarà J, Barrett MD, Berná LM, Berraf-Tebbal A, Bianchinotti MV, Bransgrove K, Burgess TI, Carmo FS, Chávez R, Čmoková A, Dearnaley JD, de A. Santiago AL, Freitas-Neto JF, Denman S, Douglas B, Dovana F, Eichmeier A, Esteve-Raventós F, Farid A, Fedosova AG, Ferisin G, Ferreira RJ, Ferrer A, Figueiredo CN, Figueiredo YF, Reinoso-Fuentealba CG, Garrido-Benavent I, Cañete-Gibas CF, Gil-Durán C, Glushakova AM, Gonçalves MF, González M, Gorczak M, Gorton C, Guard FE, Guarnizo AL, Guarro J, Gutiérrez M, Hamal P, Hien LT, Hocking AD, Houbraken J, Hunter GC, Inácio CA, Jourdan M, Kapitonov VI, Kelly L, Khanh TN, Kisło K, Kiss L, Kiyashko A, Kolařík M, Kruse J, Kubátová A, Kučera V, Kučerová I, Kušan I, Lee HB, Levicán G, Lewis A, Liem NV, Liimatainen K, Lim HJ, Lyons MN, Maciá-Vicente JG, Magaña-Dueñas V, Mahiques R, Malysheva EF, Marbach PA, Marinho P, Matočec N, McTaggart AR, Mešić A, Morin L, Muñoz-Mohedano JM, Navarro-Ródenas A, Nicolli CP, Oliveira RL, Otsing E, Ovrebo CL, Pankratov TA, Paños A, Paz-Conde A, Pérez-Sierra A, Phosri C, Pintos Á, Pošta A, Prencipe S, Rubio E, Saitta A, Sales LS, Sanhueza L, Shuttleworth LA, Smith J, Smith ME, Spadaro D, Spetik M, Sochor M, Sochorová Z, Sousa JO, Suwannasai N, Tedersoo L, Thanh HM, Thao LD, Tkalčec Z, Vaghefi N, Venzhik AS, Verbeken A, Vizzini A, Voyron S, Wainhouse M, Whalley AJ, Wrzosek M, Zapata M, Zeil-Rolfe I, Groenewald JZ Persoonia 29-Jun-2020
PMCID:PMC7567971
doi:10.3767/persoonia.2020.44.11
PMID:33116344
Estimation of the aboveground biomass and carbon stocks in open Brazilian Savannah developed on sandy soils de Oliveira CP, Francelino MR, Daher M, de Araújo EJ, de Souza Sanches L, de Andrade KD, de Campos JS Carbon Balance Manag 04-May-2019
PMCID:PMC7227269
doi:10.1186/s13021-019-0121-0
PMID:31055669
Timing of seed dispersal and seed dormancy in Brazilian savanna: two solutions to face seasonality Escobar DF, Silveira FA, Morellato LP Ann Bot 07-Feb-2018
PMCID:PMC5946880
doi:10.1093/aob/mcy006
PMID:29425261

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
> Alkaloids and derivatives / Aporphines
N-acetylanonaine 6453733 Click to see CC(=O)N1CCC2=CC3=C(C4=C2C1CC5=CC=CC=C54)OCO3 307.30 unknown via CMAUP database
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Secobenzophenanthridine alkaloids
Formamide, N-(6-(2-hydroxy-3,4-dimethoxyphenyl)naphtho(2,3-d)-1,3-dioxol-5-yl)-N-methyl- 3085181 Click to see CN(C=O)C1=C(C=CC2=CC3=C(C=C21)OCO3)C4=C(C(=C(C=C4)OC)OC)O 381.40 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Biphenyls and derivatives
Aucuparin 442508 Click to see COC1=CC(=CC(=C1O)OC)C2=CC=CC=C2 230.26 unknown https://doi.org/10.1016/S0031-9422(97)00731-0
> Benzenoids / Phenol ethers / Anisoles
Estragole 8815 Click to see COC1=CC=C(C=C1)CC=C 148.20 unknown via CMAUP database
> 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 via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty amides / N-acyl amines
(2E,4E,8E,10E,12E)-N-(2-hydroxy-2-methylpropyl)tetradeca-2,4,8,10,12-pentaenamide 14135316 Click to see CC=CC=CC=CCCC=CC=CC(=O)NCC(C)(C)O 289.40 unknown via CMAUP database
(2E,4E,8Z,11E)-N-(2-hydroxy-2-methylpropyl)tetradeca-2,4,8,11-tetraenamide 14135320 Click to see CCC=CCC=CCCC=CC=CC(=O)NCC(C)(C)O 291.40 unknown via CMAUP database
(2E,4E,8Z,11Z)-N-(2-hydroxy-2-methylpropyl)tetradeca-2,4,8,11-tetraenamide 14135319 Click to see CCC=CCC=CCCC=CC=CC(=O)NCC(C)(C)O 291.40 unknown via CMAUP database
(2E,6R,7E,9E)-6-Hydroxy-N-(2-hydroxy-2-methylpropyl)-11-oxo-2,7,9-dodecatrienamide 101357058 Click to see CC(=O)C=CC=CC(CCC=CC(=O)NCC(C)(C)O)O 295.37 unknown via CMAUP database
(2E,6Z,8E,10Z)-N-(2-hydroxy-2-methylpropyl)dodeca-2,6,8,10-tetraenamide 46870578 Click to see CC=CC=CC=CCCC=CC(=O)NCC(C)(C)O 263.37 unknown via CMAUP database
Hydroxy-alpha-sanshool 10084135 Click to see CC=CC=CC=CCCC=CC(=O)NCC(C)(C)O 263.37 unknown via CMAUP database
Hydroxy-Beta-Sanshool 10220912 Click to see CC=CC=CC=CCCC=CC(=O)NCC(C)(C)O 263.37 unknown via CMAUP database
Hydroxy-gamma-Sanshool 14135317 Click to see CC=CC=CC=CCCC=CC=CC(=O)NCC(C)(C)O 289.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
(+)-Linalyl acetate 6999980 Click to see CC(=CCCC(C)(C=C)OC(=O)C)C 196.29 unknown via CMAUP database
Linalool, (+)- 67179 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
4-Isopropylbenzyl alcohol 325 Click to see CC(C)C1=CC=C(C=C1)CO 150.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-Terpinen-4-ol 5325830 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown via CMAUP database
(+)-alpha-Terpineol 442501 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds
(2R)-6-[[(2R)-2,8-dimethyl-2-[(3E,7E)-4,8,12-trimethyltrideca-3,7,11-trienyl]-3,4-dihydrochromen-6-yl]peroxy]-2,8-dimethyl-2-[(3E,7E)-4,8,12-trimethyltrideca-3,7,11-trienyl]-3,4-dihydrochromene 163185406 Click to see CC1=CC(=CC2=C1OC(CC2)(C)CCC=C(C)CCC=C(C)CCC=C(C)C)OOC3=CC4=C(C(=C3)C)OC(CC4)(C)CCC=C(C)CCC=C(C)CCC=C(C)C 791.20 unknown https://doi.org/10.1016/J.BMC.2010.10.044
6-[[2,8-Dimethyl-2-(4,8,12-trimethyltrideca-3,7,11-trienyl)-3,4-dihydrochromen-6-yl]peroxy]-2,8-dimethyl-2-(4,8,12-trimethyltrideca-3,7,11-trienyl)-3,4-dihydrochromene 75597500 Click to see CC1=CC(=CC2=C1OC(CC2)(C)CCC=C(C)CCC=C(C)CCC=C(C)C)OOC3=CC4=C(C(=C3)C)OC(CC4)(C)CCC=C(C)CCC=C(C)CCC=C(C)C 791.20 unknown https://doi.org/10.1016/J.BMC.2010.10.044
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds / Tocotrienols
(c)(1/2)-Tocotrienol pound>>Tocotrienol, delta 53394607 Click to see CC1=CC(=CC2=C1OC(CC2)(C)CCC=C(C)CCC=C(C)CCC=C(C)C)O 396.60 unknown https://doi.org/10.1016/J.BMC.2010.10.044
2,5,8-Trimethyl-2-(4,8,12-trimethyltrideca-3,7,11-trien-1-yl)-3,4-dihydro-2H-1-benzopyran-6-ol 53798831 Click to see CC1=CC(=C(C2=C1OC(CC2)(C)CCC=C(C)CCC=C(C)CCC=C(C)C)C)O 410.60 unknown https://doi.org/10.1016/J.BMC.2010.10.044
delta-Tocotrienol 5282350 Click to see CC1=CC(=CC2=C1OC(CC2)(C)CCC=C(C)CCC=C(C)CCC=C(C)C)O 396.60 unknown https://doi.org/10.1016/J.BMC.2010.10.044
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3aS,5aS,5bR,7aR,9S,11aR,11bR,13aR,13bR)-9-hydroxy-5a-[[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxymethyl]-5b,8,8,11a-tetramethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 15816316 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)COC(=O)C=CC6=CC=C(C=C6)O)C)(C)C)O)C)C(=O)O 618.80 unknown https://doi.org/10.1016/S0031-9422(97)00731-0
9-Hydroxy-5a-[3-(4-hydroxyphenyl)prop-2-enoyloxymethyl]-5b,8,8,11a-tetramethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 162861870 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)COC(=O)C=CC6=CC=C(C=C6)O)C)(C)C)O)C)C(=O)O 618.80 unknown https://doi.org/10.1016/S0031-9422(97)00731-0
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1S,3R,4R,5R)-3-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxy-cyclohexanecarboxylic acid 9476 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 via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
(R-(E))-5-Isopropyl-8-methylnona-6,8-dien-2-one 16058296 Click to see CC(C)C(CCC(=O)C)C=CC(=C)C 194.31 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxanes / Phenylbenzodioxanes / Phenylbenzo-1,4-dioxanes
3-(4-Hydroxy-3-methoxyphenyl)-2-(hydroxymethyl)-5-methoxy-2,3-dihydro-[1,4]dioxino[2,3-c]xanthen-7-one 580166 Click to see COC1=C(C=CC(=C1)C2C(OC3=C4C(=CC(=C3O2)OC)C(=O)C5=CC=CC=C5O4)CO)O 436.40 unknown https://doi.org/10.1016/S0031-9422(97)00731-0
7H-1,4-Dioxino[2,3-c]xanthen-7-one, 2,3-dihydro-3-(4-hydroxy-3-methoxyphenyl)-2-(hydroxymethyl)-5-methoxy-, trans-(+/-)- 23242592 Click to see COC1=C(C=CC(=C1)C2C(OC3=C4C(=CC(=C3O2)OC)C(=O)C5=CC=CC=C5O4)CO)O 436.40 unknown https://doi.org/10.1016/S0031-9422(97)00731-0
Kielcorin 13834128 Click to see COC1=C(C=CC(=C1)C2C(OC3=C4C(=CC(=C3O2)OC)C(=O)C5=CC=CC=C5O4)CO)O 436.40 unknown https://doi.org/10.1016/S0031-9422(97)00731-0
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
2-Hydroxy-1-methoxy-xanthen-9-one 10399460 Click to see COC1=C(C=CC2=C1C(=O)C3=CC=CC=C3O2)O 242.23 unknown https://doi.org/10.1016/S0031-9422(97)00731-0
4-Hydroxy-2,3-dimethoxyxanthone 378690 Click to see COC1=C(C(=C2C(=C1)C(=O)C3=CC=CC=C3O2)O)OC 272.25 unknown https://doi.org/10.1016/S0031-9422(97)00731-0
https://doi.org/10.1016/S0031-9422(00)97240-6
6-Hydroxy-1,3,5-trimethoxyxanthen-9-one 76320914 Click to see COC1=CC2=C(C(=C1)OC)C(=O)C3=C(O2)C(=C(C=C3)O)OC 302.28 unknown https://doi.org/10.1016/S0031-9422(97)00731-0
9H-Xanthen-9-one, 3-hydroxy-2,4-dimethoxy- 12214333 Click to see COC1=C(C(=C2C(=C1)C(=O)C3=CC=CC=C3O2)OC)O 272.25 unknown https://doi.org/10.1016/S0031-9422(97)00731-0
https://doi.org/10.1016/S0031-9422(00)97240-6
Swertinin 5491517 Click to see COC1=C(C2=C(C=C1)OC3=CC(=CC(=C3C2=O)O)O)OC 288.25 unknown https://doi.org/10.1016/S0031-9422(97)00731-0
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 2-prenylated xanthones
1,3,6-Trihydroxy-2-(3-methylbut-2-enyl)xanthen-9-one 26250237 Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C=CC(=C3)O)O)C 312.30 unknown https://doi.org/10.1016/S0031-9422(97)00731-0
1,3,7-Trihydroxy-2-(3-hydroxy-3-methylbutyl)xanthen-9-one 15378072 Click to see CC(C)(CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C=C(C=C3)O)O)O 330.30 unknown https://doi.org/10.1016/S0031-9422(97)00731-0
1,3,7-Trihydroxy-2-prenylxanthone 5495920 Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C=C(C=C3)O)O)C 312.30 unknown https://doi.org/10.1016/J.PHYMED.2009.07.002
https://doi.org/10.1016/S0031-9422(97)00731-0
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / Pyranoxanthones
Jacareubin 5281644 Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C4=C(O3)C(=C(C=C4)O)O)C 326.30 unknown https://doi.org/10.1016/S0031-9422(97)00731-0
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
Nitidine 4501 Click to see C[N+]1=CC2=CC(=C(C=C2C3=C1C4=CC5=C(C=C4C=C3)OCO5)OC)OC 348.40 unknown via CMAUP database
Norchelerythrine 443719 Click to see COC1=C(C2=CN=C3C(=C2C=C1)C=CC4=CC5=C(C=C43)OCO5)OC 333.30 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
Skimmianine 6760 Click to see COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC 259.26 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroquinolones
Schinifoline 133504 Click to see CCCCCCCC1=CC(=O)C2=CC=CC=C2N1C 257.37 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Pyranoquinolines
Zanthobungeanine 5315422 Click to see CC1(C=CC2=C(O1)C3=C(C(=CC=C3)OC)N(C2=O)C)C 271.31 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Epicatechin 72276 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
3,5,6-Trihydroxy-7,4'-dimethoxyflavone 5322058 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)O)O)O 330.29 unknown via CMAUP database
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2R,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxychromen-4-one 5317847 Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 434.30 unknown via CMAUP database
5,7-dihydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 94858662 Click to see COC1=CC(=CC(=C1O)OC)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O 508.40 unknown via CMAUP database
Guaijaverin 5481224 Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 434.30 unknown via CMAUP database
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
isorhamnetin 3-O-glucoside 5318645 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 478.40 unknown via CMAUP database
Quercitrin 5280459 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown via CMAUP database
Rutin 5280805 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
3,7-Bis(beta-D-glucopyranosyloxy)-3',5-dihydroxy-4'-methoxyflavone 102574483 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)OC5C(C(C(C(O5)CO)O)O)O)O 640.50 unknown via CMAUP database
Isorhamnetin 7-glucoside 6455477 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 478.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
4-(beta-D-Glucopyranosyloxy)-3-methoxybenzoic acid 14132337 Click to see COC1=C(C=CC(=C1)C(=O)O)OC2C(C(C(C(O2)CO)O)O)O 330.29 unknown via CMAUP database

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