Byrsonima crassifolia - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

Byrsonima crassifolia - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

Upload a new image!

Details Top

Internal ID UUID64400e67ad989972492660
Scientific name Byrsonima crassifolia
Authority Kunth
First published in Nov. Gen. Sp. 5: 149 (1822)

Description Top

Suggest a correction or write a new one!
Byrsonima crassifolia, also known as nance, is a flowering plant native to tropical America. It is a slow-growing shrub or tree that produces small, sweet, and strongly scented yellow fruits. These fruits are commonly used in desserts and drinks, such as pesada de nance and carbonated beverages. Nance is also used to make a variety of alcoholic beverages, including rum and mezcal-based liqueurs. It is a popular ingredient in many Central and South American countries, and is highly valued for its unique flavor and scent.

Synonyms Top

Scientific name Authority First published in
Malpighia montana Spreng. Syst. Veg. 2: 385 (1825)
Malpighia laurifolia Spreng. Syst. Veg. 2: 385 (1825)
Malpighia rufa Poir. Encycl. 4: 332 (1797)
Malpighia pulchra Sessé & Moc. Fl. Mexic. , ed. 2: 115 (1894)
Malpighia rhopalaefolia Spreng. Syst. Veg. 2: 384 (1825)
Malpighia cotinifolia Spreng. Syst. Veg. 2: 384 (1825)
Malpighia crassifolia L. Sp. Pl. : 426 (1753)
Malpighia coriacea Sw. Prodr. Veg. Ind. Occ. : 74 (1788)
Byrsonima coriacea DC. Prodr. 1: 580 (1824)
Byrsonima cotinifolia Kunth Nov. Gen. Sp. 5: 152 (1822)
Byrsonima crassifolia f. cubensis Nied. Arbeiten Bot. Inst. Königl. Lyceums Hosianum Braunsberg 1: 17 (1901)
Byrsonima crassifolia f. ferruginea Nied. Byrsonima pt. 2, 16. 1901
Byrsonima crassifolia subsp. insulata Cuatrec. Webbia 13: 611 (1958)
Byrsonima crassifolia var. jamaicensis Urb. & Nied. Arbeiten Bot. Inst. Königl. Lyceums Hosianum Braunsberg 1: 18 (1901)
Byrsonima crassifolia f. kunthiana Nied. Arbeiten Bot. Inst. Königl. Lyceums Hosianum Braunsberg 1: 16 1901
Byrsonima crassifolia var. lanceolata Cuatrec. Webbia 13: 611 (1958)
Byrsonima crassifolia var. moureila (Aubl.) DC. Prodr. 1: 579 (1824)
Byrsonima crassifolia var. peruviana Nied. Pflanzenr. , IV, 141: 733 (1928)
Byrsonima crassifolia var. spruceana Nied. Arbeiten Bot. Inst. Königl. Lyceums Hosianum Braunsberg 1: 18 (1901)
Byrsonima cubensis A.Juss. Malpigh. Syn. : 58 (1840)
Byrsonima cumingiana A.Juss. Ann. Sci. Nat., Bot. sér. 2, 13: 332. 1840 [May 1840]
Byrsonima fagifolia Nied. Arbeiten Bot. Inst. Königl. Lyceums Hosianum Braunsberg 1: 20 (1901)
Byrsonima fendleri Turcz. Bull. Soc. Imp. Naturalistes Moscou 36(I): 582 (1863)
Byrsonima ferruginea Kunth Nov. Gen. Sp. 5: 151 (1822)
Byrsonima ferruginea var. moureila Benth. London J. Bot. 7: 119 (1848)
Byrsonima jamaicensis Urb. & Nied. Bull. Bot. Dept., Jamaica 5: 68 1898
Byrsonima karwinskiana A.Juss. Malpigh. Syn. : 58 (1840)
Byrsonima lanceolata DC. Prodr. 1: 580 (1824)
Byrsonima laurifolia Kunth Nov. Gen. Sp. 5: 147 (1822)
Byrsonima laurifolia var. guatemalensis Nied. Pflanzenr. , IV, 141: 724 (1928)
Byrsonima montana Kunth Nov. Gen. Sp. 5: 149 (1822)
Byrsonima moritziana Turcz. Bull. Soc. Imp. Naturalistes Moscou 31(I): 891 (1858)
Byrsonima moureila Loudon Hort. Brit. [Loudon] 182. 1830
Byrsonima panamensis Beurl. Kongl. Vetensk. Acad. Handl. 1854: 117 (1854)
Byrsonima pulchra DC. Prodr. 1: 580 (1824)
Byrsonima rhopalaefolia Kunth Nov. Gen. Sp. 5: 148 (1822)
Byrsonima rufescens Bertol. Fl. Guatimal. : 18 (1840)
Byrsonima spruceana Nied. Nat. Pflanzenfam. Nachtr. [Engler & Prantl] I. 207.
Byrsonima cubensis var. brachypoda Turcz. Bull. Soc. Imp. Naturalistes Moscou 31: 392 1858
Malpighia moureila Aubl. Hist. Pl. Guiane : 459 (1775)

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
English chacunga
English maricao cimun
English savanna serrette
English savanna serret
English nanche
English nance
English muruçi
English kraabu
English golden spoon
English craboo
English changunga
Spanish yoco
Spanish nanche
Spanish nance blanco
Spanish maricao cimarrón
Spanish maricao cimarron
Spanish manteco sabanero
Spanish chaparro de chinche
Spanish changugo
Spanish nanchi
Spanish manero
Spanish cimarron
Spanish indano
Persian نانس
French nance
gn murisi
Japanese ナンセ
koi Нансе
kv Нансе
lbe Нансе
mrj Нансе
Dutch nance
Portuguese muruci
Russian Нансе
Russian Бирсонима толстолистная
udm Нансе
Ukrainian Нансе
Chinese 厚葉金匙木
Chinese 厚叶金匙木
Chinese 金湯匙果
Chinese 金汤匙果
Chinese 南茜果

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Northern America
    • Mexico
      • Mexico Central
      • Mexico Gulf
      • Mexico Northeast
      • Mexico Northwest
      • Mexico Southeast
      • Mexico Southwest
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil South
      • Brazil Southeast
      • Brazil West-central
    • Caribbean
      • Cuba
      • Dominican Republic
      • Haiti
      • Netherlands Antilles
      • Puerto Rico
      • Southwest Caribbean
      • Trinidad-Tobago
      • Venezuelan Antilles
      • Windward Islands
    • Central America
      • Belize
      • Costa Rica
      • El Salvador
      • Guatemala
      • Honduras
      • Nicaragua
      • Panamá
    • Northern South America
      • French Guiana
      • Guyana
      • Suriname
      • Venezuela
    • Southern South America
      • Paraguay
    • Western South America
      • Bolivia
      • Colombia
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000576794
USDA Plants BYCR
Tropicos 19500795
INPN 734000
KEW urn:lsid:ipni.org:names:556033-1
The Plant List kew-2688172
Open Tree Of Life 414971
Observations.org 198921
NCBI Taxonomy 4270
IUCN Red List 61780518
IPNI 556033-1
iNaturalist 154528
GBIF 3191361
Freebase /m/0669z5
EPPO BYSCR
EOL 592366
Elurikkus 374596
USDA GRIN 8222
Wikipedia Byrsonima_crassifolia

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
Recent progress in TiO2–biochar-based photocatalysts for water contaminants treatment: strategies to improve photocatalytic performance Liu Y, Dai X, Li J, Cheng S, Zhang J, Ma Y RSC Adv 02-Jan-2024
PMCID:PMC10759041
doi:10.1039/d3ra06910a
PMID:38173568
Candida krusei M4CK Produces a Bioemulsifier That Acts on Melaleuca Essential Oil and Aids in Its Antibacterial and Antibiofilm Activity Araujo JM, Monteiro JM, Silva DH, Veira AK, Silva MR, Ferraz FA, Braga FH, de Siqueira EP, Monteiro AD Antibiotics (Basel) 30-Nov-2023
PMCID:PMC10740703
doi:10.3390/antibiotics12121686
PMID:38136720
Contrasting patterns of foraging behavior in neotropical stingless bees using pollen and honey metabarcoding Martins AC, Proença CE, Vasconcelos TN, Aguiar AJ, Farinasso HC, de Lima AT, Faria JE, Norrana K, Costa MB, Carvalho MM, Dias RL, Bustamante MM, Carvalho FA, Keller A Sci Rep 02-Sep-2023
PMCID:PMC10475120
doi:10.1038/s41598-023-41304-0
PMID:37660141
Snakebite envenomations and access to treatment in communities of two indigenous areas of the Western Brazilian Amazon: A cross-sectional study de Farias AS, Gomes Filho MR, da Costa Arévalo M, Cristino JS, Farias FR, Sachett A, Silva-Neto AV, de Carvalho FG, Ambrosio SA, da Silva Carvalho E, Lacerda M, Murta F, Machado VA, Wen FH, Monteiro W, Sachett J PLoS Negl Trop Dis 13-Jul-2023
PMCID:PMC10368234
doi:10.1371/journal.pntd.0011485
PMID:37440596
Induction role of chitosan nanoparticles to Anethum graveolens extract against food-borne bacteria, oxidant, and diabetic activities in vitro Mashraqi A Front Microbiol 04-Jul-2023
PMCID:PMC10352794
doi:10.3389/fmicb.2023.1209524
PMID:37469433
Prospecting Plant Extracts and Bioactive Molecules with Antimicrobial Activity in Brazilian Biomes: A Review de Queiroz JC, Leite JR, Vasconcelos AG Antibiotics (Basel) 21-Feb-2023
PMCID:PMC10044579
doi:10.3390/antibiotics12030427
PMID:36978294
Mexican traditional medicines for women’s reproductive health Cabada-Aguirre P, López López AM, Mendoza KC, Garay Buenrostro KD, Luna-Vital DA, Mahady GB Sci Rep 16-Feb-2023
PMCID:PMC9935858
doi:10.1038/s41598-023-29921-1
PMID:36797354
Neuroprotective Potentials of Flavonoids: Experimental Studies and Mechanisms of Action Bellavite P Antioxidants (Basel) 27-Jan-2023
PMCID:PMC9951959
doi:10.3390/antiox12020280
PMID:36829840
Neuropharmacological Effects in Animal Models and HPLC-Phytochemical Profiling of Byrsonima crassifolia (L.) Kunth Bark Extracts de la Cabeza Fernández M, Sánchez M, Caceres A, Iglesias I, Gómez-Serranillos MP Molecules 12-Jan-2023
PMCID:PMC9867209
doi:10.3390/molecules28020764
PMID:36677821
Phytochemical Characterization and Efficacy of Artemisia judaica Extract Loaded Chitosan Nanoparticles as Inhibitors of Cancer Proliferation and Microbial Growth Qanash H, Bazaid AS, Aldarhami A, Alharbi B, Almashjary MN, Hazzazi MS, Felemban HR, Abdelghany TM Polymers (Basel) 11-Jan-2023
PMCID:PMC9865519
doi:10.3390/polym15020391
PMID:36679271
Pyrolysis Kinetics of Byrsonima crassifolia Stone as Agro-Industrial Waste through Isoconversional Models Sanchez-Silva JM, Ocampo-Pérez R, Padilla-Ortega E, Sangaré D, Escobedo-Bretado MA, Domínguez-Arvizu JL, Hernández-Majalca BC, Salinas-Gutiérrez JM, López-Ortiz A, Collins-Martínez V Molecules 05-Jan-2023
PMCID:PMC9862415
doi:10.3390/molecules28020544
PMID:36677602
Murici (Byrsonima crassifolia (L.) Kunth and verbascifolia (L.)) and Tapereba (Spondias mombin) Improve Hepatic and Inflammatory Biomarkers in High-Fat-Diet Rats de Souza VR, Lima TP, Bedê TP, Faria SB, Alves R, Louzada A, de Moraes BP, Silva AR, Gonçalves de Albuquerque CF, de Azeredo VB, Teodoro AJ Foods 05-Jan-2023
PMCID:PMC9857676
doi:10.3390/foods12020255
PMID:36673347
Optimization of the Acid Cleavage of Proanthocyanidins and Other Polyphenols Extracted from Plant Matrices Souza JN, Tolosa T, Teixeira B, Moura F, Silva E, Rogez H Molecules 21-Dec-2022
PMCID:PMC9821962
doi:10.3390/molecules28010066
PMID:36615261
Phenotypic and Target-Directed Screening Yields New Acaricidal Alternatives for the Control of Ticks Saporiti T, Cabrera M, Bentancur J, Ferrari ME, Cabrera N, Pérez-Montfort R, Aguirre-Crespo FJ, Gil J, Cuore U, Matiadis D, Sagnou M, Alvarez G Molecules 13-Dec-2022
PMCID:PMC9781803
doi:10.3390/molecules27248863
PMID:36557996
Surveying the elimination of hazardous heavy metal from the multi-component systems using various sorbents: a review Masoumi H, Ghaemi A, Ghanadzadeh Gilani H J Environ Health Sci Eng 01-Sep-2022
PMCID:PMC9672201
doi:10.1007/s40201-022-00832-z
PMID:36406597

Phytochemical Profile Top

Add a new one!
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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)O 170.12 unknown https://doi.org/10.1016/0031-9422(94)00934-L
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
Methyl gallate 7428 Click to see COC(=O)C1=CC(=C(C(=C1)O)O)O 184.15 unknown https://doi.org/10.3109/13880209509088143
> Lipids and lipid-like molecules / Glycerolipids / Glycosylglycerols / Glycosyldiacylglycerols
[(2R)-2-[(Z)-hexadec-8-enoyl]oxy-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropyl] (Z)-hexadec-8-enoate 163188280 Click to see CCCCCCCC=CCCCCCCC(=O)OCC(COC1C(C(C(C(O1)CO)O)O)O)OC(=O)CCCCCCC=CCCCCCCC 727.00 unknown https://doi.org/10.1016/S0031-9422(96)00842-4
[(2R)-2-hexadecanoyloxy-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropyl] hexadecanoate 15608202 Click to see CCCCCCCCCCCCCCCC(=O)OCC(COC1C(C(C(C(O1)CO)O)O)O)OC(=O)CCCCCCCCCCCCCCC 731.10 unknown https://doi.org/10.1016/S0031-9422(96)00842-4
[2-Hexadec-8-enoyloxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropyl] hexadec-8-enoate 163070564 Click to see CCCCCCCC=CCCCCCCC(=O)OCC(COC1C(C(C(C(O1)CO)O)O)O)OC(=O)CCCCCCC=CCCCCCCC 727.00 unknown https://doi.org/10.1016/S0031-9422(96)00842-4
1-O-beta-D-Glucopyranosyl-2,3-di-O-palmitoylglycerol 10462651 Click to see CCCCCCCCCCCCCCCC(=O)OCC(COC1C(C(C(C(O1)CO)O)O)O)OC(=O)CCCCCCCCCCCCCCC 731.10 unknown https://doi.org/10.1016/S0031-9422(96)00842-4
> Lipids and lipid-like molecules / Glycerolipids / Glycosylglycerols / Glycosyldiacylglycerols / Sulfoquinovosyldiacylglycerols
[(2S,3S,4S,5R,6S)-6-[(2R)-2,3-di(hexadecanoyloxy)propoxy]-3,4,5-trihydroxyoxan-2-yl]methanesulfonic acid 102201395 Click to see CCCCCCCCCCCCCCCC(=O)OCC(COC1C(C(C(C(O1)CS(=O)(=O)O)O)O)O)OC(=O)CCCCCCCCCCCCCCC 795.10 unknown https://doi.org/10.1016/S0031-9422(96)00842-4
1,2-Di-O-palmitoyl-3-O-(6-sulfoquinovopyranosyl)glycerol 14463145 Click to see CCCCCCCCCCCCCCCC(=O)OCC(COC1C(C(C(C(O1)CS(=O)(=O)O)O)O)O)OC(=O)CCCCCCCCCCCCCCC 795.10 unknown https://doi.org/10.1016/S0031-9422(96)00842-4
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3aR,5aR,5bR,7aR,9R,10S,11aR,11bR,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-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-9,10-diol 68414054 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(CC(C(C5(C)C)O)O)C)C)C 442.70 unknown https://doi.org/10.1016/S0031-9422(96)00842-4
2,3-Dihydroxyolean-12-en-28-oic acid 3694932 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown https://doi.org/10.1016/S0031-9422(96)00842-4
3-Hydroxyolean-12-en-28-oic acid 619166 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1016/S0031-9422(96)00842-4
3a,5a,5b,8,8,11a-Hexamethyl-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-9,10-diol 72745631 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(CC(C(C5(C)C)O)O)C)C)C 442.70 unknown https://doi.org/10.1016/S0031-9422(96)00842-4
Augustic acid 15560128 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown https://doi.org/10.1016/S0031-9422(96)00842-4
Betulin 72326 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown https://doi.org/10.3109/13880209509088143
Betulinic Acid 64971 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown https://doi.org/10.3109/13880209509088143
Lup-20(29)-en-3-ol, (3beta)- 521518 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(96)00842-4
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.3109/13880209509088143
https://doi.org/10.1016/S0031-9422(96)00842-4
Maslinic Acid 73659 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown https://doi.org/10.1016/S0031-9422(96)00842-4
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1016/S0031-9422(96)00842-4
https://doi.org/10.3109/13880209509088143
> 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/10.3109/13880209509088143
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/10.3109/13880209509088143
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.3109/13880209509088143
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.3109/13880209509088143
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alanine and derivatives
Alanine 5950 Click to see CC(C(=O)O)N 89.09 unknown https://doi.org/10.3109/13880209509088143
D-alanine 71080 Click to see CC(C(=O)O)N 89.09 unknown https://doi.org/10.3109/13880209509088143
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
5-Hydroxypiperidine-2-carboxylic acid 151730 Click to see C1CC(NCC1O)C(=O)O 145.16 unknown https://doi.org/10.3109/13880209509088143
Pipecolic acid 849 Click to see C1CCNC(C1)C(=O)O 129.16 unknown https://doi.org/10.3109/13880209509088143
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Aspartic acid and derivatives
Aspartic Acid 5960 Click to see C(C(C(=O)O)N)C(=O)O 133.10 unknown https://doi.org/10.3109/13880209509088143
D-Aspartic acid 83887 Click to see C(C(C(=O)O)N)C(=O)O 133.10 unknown https://doi.org/10.3109/13880209509088143
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Valine and derivatives
Valine 6287 Click to see CC(C)C(C(=O)O)N 117.15 unknown https://doi.org/10.3109/13880209509088143
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
hyperibone K 44575719 Click to see CC(=CCC12CC3C(C(C1=O)(C(=O)C(C2=O)(C3(C)C)CC=C(C)C)C(=O)C4=CC=CC=C4)C=C(C)C)C 500.70 unknown https://doi.org/10.1016/0031-9422(94)00934-L
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(2S,3S)-2-(3,4-dihydroxyphenyl)-6-[(2S,3S,4R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 101928783 Click to see C1C(C(OC2=C1C(=C(C(=C2)O)C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown https://doi.org/10.1016/0031-9422(94)00934-L
(2S,3S)-2-(3,4-dihydroxyphenyl)-8-[(2S,3S,4S)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 13269084 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/10.1016/0031-9422(94)00934-L
[(2R,3R,4R)-2-(3,4-dihydroxyphenyl)-4-[(2S,3S,4R)-2-(3,4-dihydroxyphenyl)-4-[(2S,3S)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-5,7-dihydroxy-3-(3,4,5-trihydroxybenzoyl)oxy-3,4-dihydro-2H-chromen-8-yl]-5,7-dihydroxy-3,4-dihydro-2H-chromen-3-yl] 3,4,5-trihydroxybenzoate 16139089 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)OC(=O)C8=CC(=C(C(=C8)O)O)O)C9=CC(=C(C=C9)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 1171.00 unknown https://doi.org/10.1016/0031-9422(94)00934-L
[(2S,3S,4S)-2-(3,4-dihydroxyphenyl)-4-[(2S,3S,4R)-2-(3,4-dihydroxyphenyl)-4-[(2S,3S)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-5,7-dihydroxy-3-(3,4,5-trihydroxybenzoyl)oxy-3,4-dihydro-2H-chromen-8-yl]-5,7-dihydroxy-3,4-dihydro-2H-chromen-3-yl] 3,4,5-trihydroxybenzoate 16200970 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)OC(=O)C8=CC(=C(C(=C8)O)O)O)C9=CC(=C(C=C9)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 1171.00 unknown https://doi.org/10.1016/0031-9422(94)00934-L
[(2S,3S,4S)-2-(3,4-dihydroxyphenyl)-4-[(2S,3S)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-5,7-dihydroxy-3,4-dihydro-2H-chromen-3-yl] 3,4,5-trihydroxybenzoate 10327599 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O)O)O)C7=CC(=C(C=C7)O)O)O 730.60 unknown https://doi.org/10.1016/0031-9422(94)00934-L
[(2S,3S)-2-(3,4-dihydroxyphenyl)-8-[(2S,3S,4S)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-5,7-dihydroxy-3,4-dihydro-2H-chromen-3-yl] 3,4,5-trihydroxybenzoate 10101461 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)OC(=O)C7=CC(=C(C(=C7)O)O)O 730.60 unknown https://doi.org/10.1016/0031-9422(94)00934-L
[(2S,3S)-2-(3,4-dihydroxyphenyl)-8-[(2S,3S,4S)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-(3,4,5-trihydroxybenzoyl)oxy-3,4-dihydro-2H-chromen-4-yl]-5,7-dihydroxy-3,4-dihydro-2H-chromen-3-yl] 3,4,5-trihydroxybenzoate 10485861 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O)O)O)C7=CC(=C(C=C7)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O 882.70 unknown https://doi.org/10.1016/0031-9422(94)00934-L
[2-(3,4-dihydroxyphenyl)-4-[2-(3,4-dihydroxyphenyl)-4-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-5,7-dihydroxy-3-(3,4,5-trihydroxybenzoyl)oxy-3,4-dihydro-2H-chromen-8-yl]-5,7-dihydroxy-3,4-dihydro-2H-chromen-3-yl] 3,4,5-trihydroxybenzoate 162996529 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)OC(=O)C8=CC(=C(C(=C8)O)O)O)C9=CC(=C(C=C9)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 1171.00 unknown https://doi.org/10.1016/0031-9422(94)00934-L
Endotelon 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/10.1016/0031-9422(94)00934-L
ent-Epicatechin-(4alpha->6)-ent-epicatechin 13990892 Click to see C1C(C(OC2=C1C(=C(C(=C2)O)C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown https://doi.org/10.1016/0031-9422(94)00934-L
ent-Epicatechin-(4alpha->8)-ent-epicatechin 3-gallate 12795889 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O)O)O)C7=CC(=C(C=C7)O)O)O 730.60 unknown https://doi.org/10.1016/0031-9422(94)00934-L
ent-Epicatechin-(4alpha->8)-ent-epicatechin 3,3'-digallate 12795893 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O)O)O)C7=CC(=C(C=C7)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O 882.70 unknown https://doi.org/10.1016/0031-9422(94)00934-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(94)00934-L
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(94)00934-L
https://doi.org/10.1016/S0031-9422(96)00842-4
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/S0031-9422(96)00842-4
https://doi.org/10.3109/13880209509088143
https://doi.org/10.1016/0031-9422(94)00934-L
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(94)00934-L
https://doi.org/10.1016/S0031-9422(96)00842-4
https://doi.org/10.3109/13880209509088143
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
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 https://doi.org/10.3109/13880209509088143
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 51402807 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 https://doi.org/10.1016/S0031-9422(96)00842-4
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5378597 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 https://doi.org/10.1016/S0031-9422(96)00842-4
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,5S)-3,4,5-trihydroxyoxan-2-yl]oxychromen-4-one 44259215 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 https://doi.org/10.3109/13880209509088143
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 https://doi.org/10.3109/13880209509088143
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 https://doi.org/10.3109/13880209509088143
https://doi.org/10.1016/S0031-9422(96)00842-4
Isoquercetin 5280804 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 https://doi.org/10.1016/S0031-9422(96)00842-4

Biological Material Top ebay Auctions

Please wait .. loading items ..
Loading...

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.