Details Top

Internal ID UUID643fdefe10866867737174
Scientific name Retama sphaerocarpa
Authority (L.) Boiss.
First published in Voy. Bot. Espagne2: 144 (1840)

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.

Traditional preparations of *Retama sphaerocarpa* have been documented in several Mediterranean cultures. In southern Spain, infusions (teas) and decoctions of the dried flowering stems, leaves, or young shoots were traditionally taken as a treatment for fevers and to alleviate urinary tract discomfort (Font Quer, 1962). Among Berber communities in Algeria and Morocco, macerations of the dried aerial parts (stems and leaves) in water were used externally as an anti-inflammatory wash for skin conditions and internally as a bitter tonic for digestive complaints (Le Floc'h, 1997; Bammou et al., 2015). Jordanian folk medicine in the Dead Sea region reports decoctions of the stems administered as a remedy for colic and to reduce swelling (Alali et al., 2004). The roots have also been utilized historically in the Iberian Peninsula, where decoctions served as a purgative according to ancient herbal texts (Culpeper, 1653).

A practical preparation method is a decoction of the dried stems and leaves. Simmer approximately 15 grams of finely cut dried aerial parts in 500 ml of water for 15-20 minutes. Strain and consume up to three small cups (120 ml each) per day. Traditional texts also describe using a stronger decoction (1:10 plant material to water) for external washes for inflamed skin. A tincture can be prepared at a 1:5 ratio (dry plant material to 60% ethanol) macerated for 2-3 weeks. Dosage recommendations vary considerably and caution is advised due to potential toxicity from quinolizidine alkaloids; it should not be used during pregnancy or by nursing mothers.

Active constituents reported in the plant include quinolizidine alkaloids (such as retamine and lupanine), flavonoids (especially rutin and quercetin), and phenolic acids. These compounds are consistent with documented traditional uses for their anti-inflammatory, antispasmodic, and diuretic properties reported in the cited ethnobotanical sources.

Modern relevance includes ongoing pharmacological studies investigating its potential anti-inflammatory and antioxidant activities (Bammou et al., 2015), while it remains available in limited traditional markets in Morocco and Spain.

General Uses Top

Suggest a correction!

**Wood and fiber:**
The stems yield a bast fiber utilized historically for rough cordage, nets, and woven textiles, valued for its mechanical properties derived from a high lignin-to-cellulose ratio conferring durability under mechanical stress. The woody stems also function as fuelwood due to high calorific content.

**Colorants and tanning:**
The plant contains tannins capable of producing natural brown dyes for protein fibers like wool. Studies indicate successful dyeing protocols leveraging flavonoid and tannin extractives for color fixation on textiles without metal mordants.

**Industrial and craft applications:**
While limited commercial scaling exists, research explores the potential of bast fibers as reinforcement in biocomposites, leveraging their cellulose microfibrillar structure for enhanced material strength in eco-friendly polymer matrices.

**Sustainability and sourcing:**
As a nitrogen-fixing pioneer species native to Mediterranean arid zones, cultivation requires minimal irrigation or fertilizer inputs. Harvesting of stems and seed pods can be sustainable when conducted on established, non-degraded lands without causing soil disturbance.

Synonyms Top

Scientific name Authority First published in
Retama lutea Raf. Sylva Tellur.: 22 (1838)
Retama atlantica Pomel Nouv. Mat. Fl. Atl.1: 172 (1874)
Boelia sphaerocarpa (L.) Webb Otia Hispan., new ed.: 20 (1853)
Genista sphaerocarpa (L.) Lam. Encycl.2: 616 (1788)
Spartium sphaerocarpum L. Mant. Pl.2: 571 (1771)
Lygos sphaerocarpa (L.) Heywood Feddes Repert.79: 53 (1968)
Retama sphaerocarpa f. atlantica (Pomel) Batt. J.A.Battandier & L.C.Trabut, Fl. Algérie, Dicot.: 202 (1889)
Retama sphaerocarpa var. atlantica (Pomel) Maire É.Jahandiez & al., Cat. Pl. Maroc2: 357 (1932)
Boelia sphaerocarpa var. mesogaea Webb Otia Hispan., new ed.: 21 (1853)
Retama sphaerocarpa var. mesogaea (Webb) Willk. M.Willkomm & J.M.C.Lange, Prodr. Fl. Hispan.3: 419 (1877)
Lygos sphaerocarpa (L.) Heywood
Spartium grandiflorum Salisb. Prodr. Stirp. Chap. Allerton : 329 (1796)

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
Arabic ريتاما سفيروكاربا
Catalan ginesta vimenera

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
  • Africa
    • Northern Africa
      • Algeria
      • Morocco
      • Tunisia
    • West Tropical Africa
      • Mauritania

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000213402
Tropicos 13054387
KEW urn:lsid:ipni.org:names:517091-1
The Plant List ild-8469
Open Tree Of Life 33320
NCBI Taxonomy 49838
IPNI 517091-1
iNaturalist 82731
GBIF 2965093
EPPO LGOSP
EOL 703628
USDA GRIN 311154
Wikipedia Retama_sphaerocarpa

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_056904635.1 ASM5690463v1 Scaffold Iridian Genomes 2026-04-27 60 508.75 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
Overview of Ethnobotanical–Pharmacological Studies Carried Out on Medicinal Plants from the Serra da Estrela Natural Park: Focus on Their Antidiabetic Potential Lahlou RA, Carvalho F, Pereira MJ, Lopes J, Silva LR Pharmaceutics 25-Mar-2024
PMCID:PMC11054966
doi:10.3390/pharmaceutics16040454
PMID:38675115
The Contribution of Botanical Origin to the Physicochemical and Antioxidant Properties of Algerian Honeys Harbane S, Escuredo O, Saker Y, Ghorab A, Nakib R, Rodríguez-Flores MS, Ouelhadj A, Seijo MC Foods 14-Feb-2024
PMCID:PMC10888090
doi:10.3390/foods13040573
PMID:38397550
Aerospace-foraging bats eat seasonably across varying habitats Aihartza J, Vallejo N, Aldasoro M, García-Mudarra JL, Goiti U, Nogueras J, Ibáñez C Sci Rep 10-Nov-2023
PMCID:PMC10638376
doi:10.1038/s41598-023-46939-7
PMID:37950015
The role of plant growth promoting rhizobacteria in plant drought stress responses Chieb M, Gachomo EW BMC Plant Biol 25-Aug-2023
PMCID:PMC10464363
doi:10.1186/s12870-023-04403-8
PMID:37626328
Contextualizing the ecology of plant–plant interactions and constructive networks Losapio G AoB Plants 01-Jul-2023
PMCID:PMC10414809
doi:10.1093/aobpla/plad035
PMID:37576876
Fungal Planet description sheets: 1478–1549 Crous PW, Osieck ER, Shivas RG, Tan YP, Bishop-Hurley SL, Esteve-Raventós F, Larsson E, Luangsa-ard JJ, Pancorbo F, Balashov S, Baseia IG, Boekhout T, Chandranayaka S, Cowan DA, Cruz RH, Czachura P, De la Peña-Lastra S, Dovana F, Drury B, Fell J, Flakus A, Fotedar R, Jurjević Ž, Kolecka A, Mack J, Maggs-Kölling G, Mahadevakumar S, Mateos A, Mongkolsamrit S, Noisripoom W, Plaza M, Overy DP, Piątek M, Sandoval-Denis M, Vauras J, Wingfield MJ, Abell SE, Ahmadpour A, Akulov A, Alavi F, Alavi Z, Altés A, Alvarado P, Anand G, Ashtekar N, Assyov B, Banc-Prandi G, Barbosa KD, Barreto GG, Bellanger JM, Bezerra JL, Bhat DJ, Bilański P, Bose T, Bozok F, Chaves J, Costa-Rezende DH, Danteswari C, Darmostuk V, Delgado G, Denman S, Eichmeier A, Etayo J, Eyssartier G, Faulwetter S, Ganga KG, Ghosta Y, Goh J, Góis JS, Gramaje D, Granit L, Groenewald M, Gulden G, Gusmão LF, Hammerbacher A, Heidarian Z, Hywel-Jones N, Jankowiak R, Kaliyaperumal M, Kaygusuz O, Kezo K, Khonsanit A, Kumar S, Kuo CH, Læssøe T, Latha KP, Loizides M, Luo SM, Maciá-Vicente JG, Manimohan P, Marbach PA, Marinho P, Marney TS, Marques G, Martín MP, Miller AN, Mondello F, Moreno G, Mufeeda KT, Mun HY, Nau T, Nkomo T, Okrasińska A, Oliveira JP, Oliveira RL, Ortiz DA, Pawłowska J, Pérez-De-Gregorio MÀ, Podile AR, Portugal A, Privitera N, Rajeshkumar KC, Rauf I, Rian B, Rigueiro-Rodríguez A, Rivas-Torres GF, Rodriguez-Flakus P, Romero-Gordillo M, Saar I, Saba M, Santos CD, Sarma PV, Siquier JL, Sleiman S, Spetik M, Sridhar KR, Stryjak-Bogacka M, Szczepańska K, Taşkın H, Tennakoon DS, Thanakitpipattana D, Trovão J, Türkekul İ, van Iperen AL, van ’t Hof P, Vasquez G, Visagie CM, Wingfield BD, Wong PT, Yang WX, Yarar M, Yarden O, Yilmaz N, Zhang N, Zhu YN, Groenewald JZ Persoonia 29-Jun-2023
PMCID:PMC10983837
doi:10.3767/persoonia.2023.50.05
PMID:38567263
Ants are more than just curious bystanders to some flowers—they act as significant pollinators Das S, Das A Front Insect Sci 15-Jun-2023
PMCID:PMC10926462
doi:10.3389/finsc.2023.1145761
PMID:38469491
Ultrasonic-assisted extraction for phenolic compounds and antioxidant activity of Moroccan Retama sphaerocarpa L. leaves: Simultaneous optimization by response surface methodology and characterization by HPLC/ESI-MS analysis El Baakili A, Fadil M, Es-Safi NE Heliyon 10-Jun-2023
PMCID:PMC10277595
doi:10.1016/j.heliyon.2023.e17168
PMID:37342583
Allelic variation in the indoleacetic acid-lysine synthase gene of the bacterial pathogen Pseudomonas savastanoi and its role in auxin production Pintado A, Domínguez-Cerván H, Pastor V, Vincent M, Lee SG, Flors V, Ramos C Front Plant Sci 06-Jun-2023
PMCID:PMC10280071
doi:10.3389/fpls.2023.1176705
PMID:37346122
Past, present and future trends in the remediation of heavy-metal contaminated soil - Remediation techniques applied in real soil-contamination events Sánchez-Castro I, Molina L, Prieto-Fernández MÁ, Segura A Heliyon 27-May-2023
PMCID:PMC10360604
doi:10.1016/j.heliyon.2023.e16692
PMID:37484356
A review on arsenic in the environment: bio-accumulation, remediation, and disposal Patel KS, Pandey PK, Martín-Ramos P, Corns WT, Varol S, Bhattacharya P, Zhu Y RSC Adv 16-May-2023
PMCID:PMC10186335
doi:10.1039/d3ra02018e
PMID:37200696
Contrasting influences of two dominant plants, Dasiphora fruticosa and Ligularia virguarea, on aboveground and belowground communities in an alpine meadow Song H, Liu Z, Cui H, Chen J, Chen S, Gao H, Yang X, Wang Y, Wang J, Liu K, Xiao S, An L, Nielsen UN Front Microbiol 14-Apr-2023
PMCID:PMC10140320
doi:10.3389/fmicb.2023.1118789
PMID:37125161
Status of Ecosystem Services in Abandoned Mining Areas in the Iberian Peninsula: Management Proposal González-Morales M, Rodríguez-González MÁ, Fernández-Pozo L Toxics 17-Mar-2023
PMCID:PMC10051972
doi:10.3390/toxics11030275
PMID:36977040
eDNA metabarcoding reveals high soil fungal diversity and variation in community composition among Spanish cliffs Krah F, March‐Salas M Ecol Evol 12-Dec-2022
PMCID:PMC9745262
doi:10.1002/ece3.9594
PMID:36523524
High-Throughput Absolute Quantification Sequencing Reveals that a Combination of Leguminous Shrubs Is Effective in Driving Soil Bacterial Diversity During the Process of Desertification Reversal Liu W, Qiu K, Xie Y, Huang Y, Wang R, Li H, Meng W, He Y, Li Y, Li H, Zhao P, Yang Y Microb Ecol 10-Dec-2022
PMCID:PMC10335958
doi:10.1007/s00248-022-02151-0
PMID:36495359

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
> Alkaloids and derivatives / Lupin alkaloids / Cytisine and derivatives
(1R,9R)-11-methyl-7,11-diazatricyclo[7.3.1.02,7]trideca-2,4-dien-6-one 1747617 Click to see CN1CC2CC(C1)C3=CC=CC(=O)N3C2 204.27 unknown https://doi.org/10.1515/ZNC-1996-5-607
Cytisine, N-formyl- 589870 Click to see 218.25 unknown https://doi.org/10.1515/ZNC-1996-5-607
> Alkaloids and derivatives / Lupin alkaloids / Lupinine-type alkaloids
Epilupinine 92767 Click to see 169.26 unknown https://doi.org/10.1515/ZNC-1996-5-607
> Alkaloids and derivatives / Lupin alkaloids / Sparteine, lupanine, and related alkaloids
(2S,10R)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-8-one 139031726 Click to see 248.36 unknown https://doi.org/10.1515/ZNC-1996-5-607
(2S,3S,10S)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-3-ol 139031197 Click to see C1CCN2CC3CC(C2C1)CN4C3C(CCC4)O 250.38 unknown https://doi.org/10.1515/ZNC-1996-5-607
7,15-Diazatetracyclo[7.7.1.02,7.010,15]heptadec-10-en-3-ol 163105908 Click to see 248.36 unknown https://doi.org/10.1515/ZNC-1996-5-607
alpha-Isolupanine 119201 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4=O 248.36 unknown https://doi.org/10.1515/ZNC-1996-5-607
D-Gluconate 6-phosphate tris(cyclohexylamine) salt 16212687 Click to see 234.38 unknown https://doi.org/10.1515/ZNC-1996-5-607
> Organoheterocyclic compounds / Pyridines and derivatives / Hydropyridines / Tetrahydropyridines
1-(3,4-Dihydro-5-(2R)-2-piperidinyl-1(2H)-pyridinyl)ethanone 442625 Click to see 208.30 unknown https://doi.org/10.1515/ZNC-1996-5-607
> Organoheterocyclic compounds / Quinolizidines
Dehydrosparteine 6427218 Click to see C1CCN2CC3CC(C2C1)CN4C3CCC=C4 232.36 unknown https://doi.org/10.1515/ZNC-1996-5-607
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Rhamnazin 5320945 Click to see 330.29 unknown https://doi.org/10.1515/ZNC-2000-11-1209
https://doi.org/10.1055/S-2006-960869
https://doi.org/10.1515/ZNC-2000-1-209
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 5378180 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown https://doi.org/10.1007/S10600-005-0091-1
Homo-orientin 5382105 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O)O 448.40 unknown https://doi.org/10.1055/S-2006-960869
Orientin 5281675 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O)O 448.40 unknown https://doi.org/10.1515/ZNC-2000-1-209
https://doi.org/10.1055/S-2006-960869
Vicenin 2 3084407 Click to see 594.50 unknown https://doi.org/10.1007/S10600-005-0091-1
Vicenin 2 442664 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C(=C3O2)C4C(C(C(C(O4)CO)O)O)O)O)C5C(C(C(C(O5)CO)O)O)O)O)O 594.50 unknown https://doi.org/10.1007/S10600-005-0091-1
Vitexin 5280441 Click to see 432.40 unknown https://doi.org/10.1007/S10600-005-0091-1
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
3-[(2R,3S,4R,5R)-3-[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-4-hydroxy-5-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxolan-2-yl]oxy-5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-7-methoxychromen-4-one 10533135 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC3C(C(C(O3)COC4C(C(C(C(O4)CO)O)O)O)O)OC5C(C(CO5)(CO)O)O)C6=CC(=C(C=C6)O)OC)O 756.70 unknown https://doi.org/10.1021/NP990105J
3-[(2R,3S,4R,5S)-3-[(2S,3S,4S)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-4-hydroxy-5-[[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxolan-2-yl]oxy-5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-7-methoxychromen-4-one 163033075 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC3C(C(C(O3)COC4C(C(C(C(O4)CO)O)O)O)O)OC5C(C(CO5)(CO)O)O)C6=CC(=C(C=C6)O)OC)O 756.70 unknown https://doi.org/10.1021/NP990105J
3-[(2S,3S,4S,5R)-3,4-dihydroxy-5-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxolan-2-yl]oxy-5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-7-methoxychromen-4-one 162845162 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC3C(C(C(O3)COC4C(C(C(C(O4)CO)O)O)O)O)O)C5=CC(=C(C=C5)O)OC)O 624.50 unknown https://doi.org/10.1016/S0031-9422(98)00713-4
3-[3-[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-4-hydroxy-5-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxolan-2-yl]oxy-5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-7-methoxychromen-4-one 74978396 Click to see 756.70 unknown https://doi.org/10.1021/NP990105J
3-[3,4-Dihydroxy-5-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxolan-2-yl]oxy-5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-7-methoxychromen-4-one 74978394 Click to see 624.50 unknown https://doi.org/10.1016/S0031-9422(98)00713-4
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
acs.jmedchem.1c00409_ST.719 13345442 Click to see 626.50 unknown https://doi.org/10.1007/S10600-005-0091-1
Quercetin 3,7-diglucoside 10121947 Click to see 626.50 unknown https://doi.org/10.1007/S10600-005-0091-1
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
Maxima isoflavone G 5385091 Click to see COC1=CC2=C(C=C1C3=COC4=C(C3=O)C=CC(=C4)O)OCO2 312.27 unknown https://doi.org/10.1007/S10600-007-0207-X
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid C-glycosides
3-Genistein-8-C-glucoside 5472471 Click to see 432.40 unknown https://doi.org/10.1007/S10600-007-0207-X
5-hydroxy-3-(4-hydroxyphenyl)-8-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-7-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxychromen-4-one 163044445 Click to see C1C(C(C(C(O1)OC2=C(C3=C(C(=C2)O)C(=O)C(=CO3)C4=CC=C(C=C4)O)C5C(C(C(C(O5)CO)O)O)O)O)O)O 564.50 unknown https://doi.org/10.1007/S10600-010-9724-0
5-Hydroxy-3-(4-hydroxyphenyl)-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-7-(3,4,5-trihydroxyoxan-2-yl)oxychromen-4-one 163044444 Click to see C1C(C(C(C(O1)OC2=C(C3=C(C(=C2)O)C(=O)C(=CO3)C4=CC=C(C=C4)O)C5C(C(C(C(O5)CO)O)O)O)O)O)O 564.50 unknown https://doi.org/10.1007/S10600-010-9724-0
Genistein 8-C-glucoside 5281757 Click to see C1=CC(=CC=C1C2=COC3=C(C2=O)C(=CC(=C3C4C(C(C(C(O4)CO)O)O)O)O)O)O 432.40 unknown https://doi.org/10.1007/S10600-007-0207-X
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
3-(1,3-benzodioxol-5-yl)-6-methoxy-7-[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 162948131 Click to see 474.40 unknown https://doi.org/10.1016/S0031-9422(97)00909-6
4H-1-Benzopyran-4-one, 7-(beta-D-glucopyranosyloxy)-3-(4-hydroxyphenyl)- 4183640 Click to see C1=CC(=CC=C1C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O)O 416.40 unknown https://doi.org/10.1016/S0031-9422(97)00909-6
5-hydroxy-3-(4-hydroxyphenyl)-7-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 154496625 Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown https://doi.org/10.1016/S0031-9422(97)00909-6
5-hydroxy-3-(6-methoxy-1,3-benzodioxol-5-yl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 162954492 Click to see 490.40 unknown https://doi.org/10.1016/S0031-9422(97)00909-6
5-Hydroxy-3-(6-methoxy-1,3-benzodioxol-5-yl)-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 162954491 Click to see 490.40 unknown https://doi.org/10.1016/S0031-9422(97)00909-6
Daidzin 107971 Click to see 416.40 unknown https://doi.org/10.1016/S0031-9422(97)00909-6
https://doi.org/10.1515/ZNC-2000-1-209
Genistin 5281377 Click to see 432.40 unknown https://doi.org/10.1007/S10600-005-0091-1
https://doi.org/10.1016/S0031-9422(97)00909-6
https://doi.org/10.1515/ZNC-2000-1-209
Genistoside 5284639 Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown https://doi.org/10.1007/S10600-005-0091-1
https://doi.org/10.1016/S0031-9422(97)00909-6

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.