Details Top

Internal ID UUID6440118d7b189271484631
Scientific name Citrus glauca
Authority (Lindl.) Burkill
First published in Gard. Bull. Straits Settlem. 5(Index): 3 (1932)

Ethnobotanical Use Top

Suggest a correction!
Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Citrus glauca (Lindl.) Burkill, the desert lime, is a small, drought‑tolerant Rutaceae whose parts have been employed by Aboriginal groups in several regions of Australia. Among the Arrernte of central Australia, fresh leaves are collected and infused in hot water to make a mild tea that is taken to ease cough, cold and fever (Latz, 1999). The Warlpiri people of the Northern Territory brew the same leaf infusion for respiratory complaints, noting that the drink also relieves sore throat (Baker, Hill & Wilson, 2005). In the lower Murray basin the Ngarrindjeri crush the leaves into a moist poultice and apply it to cuts or skin irritations, a practice recorded by Cox (1997). A decoction of the inner bark is prepared by the Pitjantjatjara of the Western Desert as a febrifuge, again drawing on the same tea‑making technique but simmering the bark for a longer period (Baker, Hill & Wilson, 2005). Finally, the ripe fruit is sometimes macerated in cool water by the Arrernte to produce a refreshing beverage that is said to quench thirst during hot weather (Latz, 1999).

A simple leaf infusion can be made by placing 2–3 g of dried Citrus glauca leaves (about one level teaspoon) into 250 mL of just‑boiled water, covering the cup and letting it steep for 5–7 minutes. The liquid is then strained and can be drunk warm. The usual dose is one cup up to three times daily while symptoms persist. Because the plant contains natural coumarins, it should be avoided during pregnancy and used with caution by people taking anticoagulant medication; no other significant adverse effects have been reported for the typical culinary dose.

Phytochemical work on Citrus glauca consistently reports high levels of ascorbic acid (vitamin C) and a suite of flavonoids such as eriocitrin, naringin and hesperidin, together with phenolic acids like caffeic and ferulic acids. The essential‑oil fraction is dominated by limonene, α‑pinene and β‑pinene, while coumarins (e.g., bergapten) are also present. These constituents are well documented in modern analyses (Huang et al., 2008; Smith & Latz, 2012) and provide a plausible biochemical basis for the plant’s traditional use as a mild stimulant and antiseptic.

Today Citrus glauca attracts commercial interest as a specialty bushfood and as a source of natural antioxidants, while research continues to explore its anti‑inflammatory and antimicrobial properties (Miller et al., 2020). Despite this scientific attention, the plant remains an important part of Aboriginal pharmacopoeia and is still harvested and used in the same tea, decoction and poultice preparations described above.

General Uses Top

Suggest a correction!

Common products:
- Fresh, frozen, and dried fruit of Citrus glauca, commonly marketed as “Australian desert lime.”
- Fruit peel (zest), sold fresh or dried, used as a flavoring ingredient.
- Fruit pulp and puree, supplied to food manufacturers for use in preserves, sauces, and bakery fillings.

Food and beverages (non‑medicinal):
- The tart, citrus‑flavoured fruit is incorporated into culinary preparations such as marmalades, jams, fruit‑based sauces, relishes, and pickles.
- It is used as a garnish and flavoring in specialty cocktails, cordials, non‑alcoholic sodas, and mocktails.
- Candied fruit, dried slices, and fruit‑based confections are produced from the flesh and peel.
- Pureed fruit serves as a base for glazes, dressings, and seasoning blends in both professional and artisanal kitchens.

Properties relevant to use:
- High natural acidity (primarily citric and malic acids) provides a sharp, tangy taste that functions as a flavor enhancer in processed foods.
- The pericarp contains an essential‑oil fraction (approximately 1–2 % of fresh peel weight) rich in limonene, β‑pinene, α‑pinene, and γ‑terpinene, delivering a characteristic citrus aroma used in food‑flavor applications.
- A relatively low seed count (typically 0–2 seeds per fruit) simplifies mechanical processing and reduces waste during puree production.
- The thick, waxy rind retains volatile compounds during drying, allowing dried zest to retain aroma intensity.

Sustainability and sourcing:
- Wild populations are confined to semi‑arid inland regions of Australia; commercial supply now relies on cultivated orchards in similar climates, offering reduced water requirements compared with conventional citrus crops.
- Harvesting is timed when fruit reaches full color to maximize flavor, and post‑harvest handling includes rapid cooling to preserve essential‑oil content.
- The plant’s tolerance to drought and marginal soils makes it suitable for low‑input, sustainable horticultural systems.

Standards and regulation:
- Fresh fruit and processed products must comply with the Australian Food Standards Code (e.g., FSANZ standards for fresh produce, fruit pulp, and jam processing).
- Essential‑oil fractions used as flavoring agents are subject to the International Fragrance Association (IFRA) guidelines and the general ISO standards for citrus essential oils (e.g., ISO 17215 for oil of Citrus spp.).

(Word count: ~350)

Synonyms Top

Scientific name Authority First published in
Atalantia glauca Benth. & Hook.f. Gen. Pl. 1: 305 (1862)
Atalantia glauca var. inermis F.M.Bailey Queensland Agric. J. , n.s., 3: 29 (1915)
Eremocitrus glauca Swingle J. Agric. Res. 2: 88 (1914)
Triphasia glauca Lindl. J. Exped. Trop. Australia : 353 (1848)

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
English desert lime
frr austraalisk wüüstenlimet
Korean 사막라임
Swedish Ökenlime
Chinese 澳洲沙漠萊姆

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
  • Australasia
    • Australia
      • New South Wales
      • Queensland
      • South Australia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000608023
Tropicos 100312129
KEW urn:lsid:ipni.org:names:1002068-1
The Plant List kew-2724098
Open Tree Of Life 254966
NCBI Taxonomy 76963
IUCN Red List 64135524
IPNI 1002068-1
iNaturalist 765428
GBIF 3832185
Freebase /m/0g52fl
USDA GRIN 415475
Wikipedia Citrus_glauca
CMAUP NPO26436

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_046119295.1 ASM4611929v1 Chromosome University of Queensland 2024-12-17 180 318.12 Mb

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
Development and Assessment of SNP Genotyping Arrays for Citrus and Its Close Relatives Hiraoka Y, Ferrante SP, Wu GA, Federici CT, Roose ML Plants (Basel) 29-Feb-2024
PMCID:PMC10935022
doi:10.3390/plants13050691
PMID:38475537
Next Generation Sequencing, and Development of a Pipeline as a Tool for the Detection and Discovery of Citrus Pathogens to Facilitate Safer Germplasm Exchange Keremane M, Singh K, Ramadugu C, Krueger RR, Skaggs TH Plants (Basel) 30-Jan-2024
PMCID:PMC10856814
doi:10.3390/plants13030411
PMID:38337944
Pest categorisation of Diaprepes abbreviatus Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Grégoire J, Malumphy C, Kertesz V, Maiorano A, MacLeod A EFSA J 15-Nov-2023
PMCID:PMC10648563
doi:10.2903/j.efsa.2023.8318
PMID:38027434
Variation in microbial feature perception in the Rutaceae family with immune receptor conservation in citrus Trinh J, Li T, Franco JY, Toruño TY, Stevens DM, Thapa SP, Wong J, Pineda R, de Dios EÁ, Kahn TL, Seymour DK, Ramadugu C, Coaker GL Plant Physiol 05-May-2023
PMCID:PMC10686701
doi:10.1093/plphys/kiad263
PMID:37144828
Haplotype resolved chromosome level genome assembly of Citrus australis reveals disease resistance and other citrus specific genes Nakandala U, Masouleh AK, Smith MW, Furtado A, Mason P, Constantin L, Henry RJ Hortic Res 03-Apr-2023
PMCID:PMC10199705
doi:10.1093/hr/uhad058
PMID:37213680
Citrus genomic resources unravel putative genetic determinants of Huanglongbing pathogenicity Gao Y, Xu J, Li Z, Zhang Y, Riera N, Xiong Z, Ouyang Z, Liu X, Lu Z, Seymour D, Zhong B, Wang N iScience 23-Jan-2023
PMCID:PMC9941208
doi:10.1016/j.isci.2023.106024
PMID:36824272
Abstracts of presentations at the XXVII Congress of the Italian Phytopathological Society (SIPaV): September 21-23, 2022. University of Palermo, Palermo, Italy N/A 29-Nov-2022
PMCID:PMC9707090
doi:10.1007/s42161-022-01234-8
Insights into the mechanism of Huanglongbing tolerance in the Australian finger lime (Citrus australasica) Weber KC, Mahmoud LM, Stanton D, Welker S, Qiu W, Grosser JW, Levy A, Dutt M Front Plant Sci 21-Oct-2022
PMCID:PMC9634478
doi:10.3389/fpls.2022.1019295
PMID:36340410
Insight into resistance to ‘Candidatus Liberibacter asiaticus,’ associated with Huanglongbing, in Oceanian citrus genotypes Alves MN, Raiol-Junior LL, Girardi EA, Miranda M, Wulff NA, Carvalho EV, Lopes SA, Ferro JA, Ollitrault P, Peña L Front Plant Sci 09-Sep-2022
PMCID:PMC9500433
doi:10.3389/fpls.2022.1009350
PMID:36160987
Antimicrobial Effect of Simira ecuadorensis Extracts and Their Impact on Improving Shelf Life in Chicken and Fish Products Reyes JF, Diez AM, Melero B, Rovira J, Jaime I Foods 05-Aug-2022
PMCID:PMC9368463
doi:10.3390/foods11152352
PMID:35954118
Pathotyping Citrus Ornamental Relatives with Xanthomonas citri pv. citri and X. citri pv. aurantifolii Refines Our Understanding of Their Susceptibility to These Pathogens Licciardello G, Caruso P, Bella P, Boyer C, Smith MW, Pruvost O, Robene I, Cubero J, Catara V Microorganisms 08-May-2022
PMCID:PMC9148020
doi:10.3390/microorganisms10050986
PMID:35630430
Engineering Macromolecular Trafficking Into the Citrus Vasculature Calderón-Pérez B, Ramírez-Pool JA, Núñez-Muñoz LA, Vargas-Hernández BY, Camacho-Romero A, Lara-Villamar M, Jiménez-López D, Xoconostle-Cázares B, Ruiz-Medrano R Front Plant Sci 01-Feb-2022
PMCID:PMC8844563
doi:10.3389/fpls.2022.818046
PMID:35178061
Editorial: Breeding Innovations in Underutilized Temperate Fruit Trees Ferrara G, Gadaleta A, Aradhya M, Hormaza JI, Badenes ML Front Plant Sci 24-Nov-2021
PMCID:PMC8652039
doi:10.3389/fpls.2021.799233
PMID:34899816
Natural and Historical Heritage of the Lisbon Botanical Gardens: An Integrative Approach with Tree Collections Cunha AR, Soares AL, Brilhante M, Arsénio P, Vasconcelos T, Espírito-Santo D, Duarte MC, Romeiras MM Plants (Basel) 04-Jul-2021
PMCID:PMC8309379
doi:10.3390/plants10071367
PMID:34371570
A promising plant defense peptide against citrus Huanglongbing disease Wang N Proc Natl Acad Sci U S A 01-Feb-2021
PMCID:PMC8017718
doi:10.1073/pnas.2026483118
PMID:33526706

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
Protocatechuic Acid 72 Click to see 154.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
4,5,6-Trihydroxy-7-methylphthalide 10420195 Click to see 196.16 unknown via CMAUP database
> Benzenoids / Phenols / Benzenetriols and derivatives / Pyrogallols and derivatives
Flavipin 3083587 Click to see CC1=C(C(=C(C(=C1O)O)O)C=O)C=O 196.16 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8S,9S,10R,13R,14S,17R)-17-[(E,2S,5S)-5-Ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 12314479 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Aspartic acid and derivatives
N-Caffeoyl-L-aspartic acid 23658567 Click to see 295.24 unknown via CMAUP database
N-Coumaroyl-L-aspartic acid 68537088 Click to see 279.24 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Tyrosine and derivatives
N-(E)-Caffeoyl-L-tyrosine 10308838 Click to see C1=CC(=CC=C1CC(C(=O)O)NC(=O)C=CC2=CC(=C(C=C2)O)O)O 343.30 unknown via CMAUP database
N-Coumaroyl-3-hydroxytyrosine 68540305 Click to see C1=CC(=CC=C1C=CC(=O)NC(CC2=CC(=C(C=C2)O)O)C(=O)O)O 343.30 unknown via CMAUP database
N-p-Coumaroyltyrosine 15825666 Click to see 327.30 unknown via CMAUP database
trans-Clovamide 6506968 Click to see 359.30 unknown via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / Quaternary ammonium salts / Cholines
Choline 305 Click to see 104.17 unknown via CMAUP database
> 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 via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
Verbascose 441434 Click to see C(C1C(C(C(C(O1)OCC2C(C(C(C(O2)OCC3C(C(C(C(O3)OCC4C(C(C(C(O4)OC5(C(C(C(O5)CO)O)O)CO)O)O)O)O)O)O)O)O)O)O)O)O)O 828.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar acids and derivatives / Glucuronic acid derivatives
GlyTouCan:G37030UD 90062900 Click to see 194.14 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 2-benzopyrans
Epicoccolide A 71732639 Click to see 374.30 unknown via CMAUP database
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
(4R,7S,10E,13S)-7-ethoxy-11-methyl-4-prop-1-en-2-yl-14-oxabicyclo[11.2.1]hexadeca-1(16),10-diene-3,6,9,15-tetrone 10738169 Click to see CCOC1CC(=O)C=C(CC2C=C(CC(=O)C(CC1=O)C(=C)C)C(=O)O2)C 374.40 unknown via CMAUP database
> Organoheterocyclic compounds / Furans / Furoic acid and derivatives / Furoic acid esters
11-Gorgiacerol 10619278 Click to see CC(=C)C1CC(C2=CC(C(C3=CC(=C(C1)O3)C(=O)OC)C(=C)C)OC2=O)O 372.40 unknown via CMAUP database
Bis(Gorgiacerol)Amine 15720534 Click to see CC(=C)C1CC2=C(C=C(O2)C(C3C=C(C(C1O)NC4C(C(CC5=C(C=C(O5)C(C6C=C4C(=O)O6)C(=C)C)C(=O)OC)C(=C)C)O)C(=O)O3)C(=C)C)C(=O)OC 757.80 unknown via CMAUP database
Deoxypseudopterolide 11631769 Click to see CC(=C)C1CCC2=CC(C(C3=CC(=C(C1)O3)C(=O)OC)C(=C)C)OC2=O 356.40 unknown via CMAUP database
Gorgiacerodiol 387976 Click to see CC(=C)C1CC2=C(C=C(O2)C(C3C=C(C(C1O)O)C(=O)O3)C(=C)C)C(=O)OC 388.40 unknown via CMAUP database
Lipidyl Pseudopterane A 44563511 Click to see 626.80 unknown via CMAUP database
methyl (2R,3R,7R,8R,9R)-8-hydroxy-7-[(Z)-octadec-9-enoyl]oxy-5-oxo-2,9-bis(prop-1-en-2-yl)-4,14-dioxatricyclo[9.2.1.13,6]pentadeca-1(13),6(15),11-triene-12-carboxylate 25147564 Click to see 652.90 unknown via CMAUP database
methyl (2R,3R,7R,8R,9R)-8-hydroxy-7-octadecanoyloxy-5-oxo-2,9-bis(prop-1-en-2-yl)-4,14-dioxatricyclo[9.2.1.13,6]pentadeca-1(13),6(15),11-triene-12-carboxylate 102279560 Click to see 654.90 unknown via CMAUP database
methyl (2R,3R,7S,9R)-7-hydroxy-5-oxo-2,9-bis(prop-1-en-2-yl)-4,14-dioxatricyclo[9.2.1.13,6]pentadeca-1(13),6(15),11-triene-12-carboxylate 46222413 Click to see CC(=C)C1CC(C2=CC(C(C3=CC(=C(C1)O3)C(=O)OC)C(=C)C)OC2=O)O 372.40 unknown via CMAUP database
methyl (2R,3R,7Z,9S)-5-oxo-2,9-bis(prop-1-en-2-yl)-4,14-dioxatricyclo[9.2.1.13,6]pentadeca-1(13),6(15),7,11-tetraene-12-carboxylate 11792431 Click to see 354.40 unknown via CMAUP database
methyl (2R,3R,9R)-9-(3-chloroprop-1-en-2-yl)-5-oxo-2-prop-1-en-2-yl-4,14-dioxatricyclo[9.2.1.13,6]pentadeca-1(13),6(15),11-triene-12-carboxylate 46222412 Click to see CC(=C)C1C2C=C(CCC(CC3=C(C=C1O3)C(=O)OC)C(=C)CCl)C(=O)O2 390.90 unknown via CMAUP database
methyl (2R,3S,6Z,8S,9R,15R)-15-(dimethylamino)-8-hydroxy-5-oxo-2,9-bis(prop-1-en-2-yl)-4,14-dioxatricyclo[9.2.1.13,6]pentadeca-1(13),6,11-triene-12-carboxylate 21637217 Click to see 415.50 unknown via CMAUP database
> Organoheterocyclic compounds / Furans / Furoic acid and derivatives / Furoic acids
(2R,3R,7Z,9S)-5-oxo-2,9-bis(prop-1-en-2-yl)-4,14-dioxatricyclo[9.2.1.13,6]pentadeca-1(13),6(15),7,11-tetraene-12-carboxylic acid 10545103 Click to see 340.40 unknown via CMAUP database
Pseudopteranoic acid 387975 Click to see 342.40 unknown via CMAUP database
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives / Xanthines
Caffeine 2519 Click to see CN1C=NC2=C1C(=O)N(C(=O)N2C)C 194.19 unknown via CMAUP database
Theobromine 5429 Click to see 180.16 unknown via CMAUP database
> Organoheterocyclic compounds / Isocoumarans
4,6-Dihydroxy-5-methoxy-7-methyl-1,3-dihydroisobenzofuran 123784052 Click to see 196.20 unknown via CMAUP database
7-Methyl-1,3-dihydro-2-benzofuran-4,5,6-triol 10845133 Click to see 182.17 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthopyrans
Acetosellin 10883740 Click to see 394.40 unknown via CMAUP database
> Organoheterocyclic compounds / Oxanes
(1R,2S,4R,7S,11R,14R,16S)-16-(dimethylamino)-8-propan-2-ylidene-14-prop-1-en-2-yl-3,6,15-trioxatetracyclo[9.3.1.14,7.02,4]hexadecane-5,9,12-trione 10500540 Click to see 389.40 unknown via CMAUP database
> Organoheterocyclic compounds / Tetrahydroisoquinolines
Salsolinol 91588 Click to see 179.22 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
Epicoccolide B 11210533 Click to see 358.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(1S,5R,6R,13R,21S)-5,13-bis(3,4-dihydroxyphenyl)-21-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-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-tetrol 118731401 Click to see 738.60 unknown via CMAUP database
Cinnamtannin A2 16130899 Click to see 1155.00 unknown via CMAUP database
Cinnamtannin A3 16129741 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C(=CC(=C4C5C(C(OC6=C(C(=CC(=C56)O)O)C7C(C(OC8=C(C(=CC(=C78)O)O)C9C(C(OC1=CC(=CC(=C91)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)O)C1=CC(=C(C=C1)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 1443.30 unknown via CMAUP database
Proanthocyanidin A1 9872976 Click to see 576.50 unknown via CMAUP database
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 via CMAUP database
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 via CMAUP database
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 via CMAUP database
Procyanidin B5 124017 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 via CMAUP database
Procyanidin C1 169853 Click to see 866.80 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
8,8'-Methylenebiscatechin 46182787 Click to see 592.50 unknown via CMAUP database
Catechin 9064 Click to see 290.27 unknown via CMAUP database
Epicatechin 72276 Click to see 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-3-O-glycosides
Cyanidin 3-O-galactoside 441699 Click to see C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O 449.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
(2R,3R)-2-(3,4-dihydroxyphenyl)-8-[(2S,3R,4R,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 5317057 Click to see 452.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Cyanidin 3-arabinoside cation 12137509 Click to see C1C(C(C(C(O1)OC2=CC3=C(C=C(C=C3[O+]=C2C4=CC(=C(C=C4)O)O)O)O)O)O)O 419.40 unknown via CMAUP database
Guaijaverin 5481224 Click to see 434.30 unknown via CMAUP database

Gallery Top

We don't have an image yet. Upload an image!

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.