Details Top

Internal ID UUID64405b989c72f117657210
Scientific name Cressa cretica
Authority L.
First published in Sp. Pl. : 223 (1753)

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.

Cressa cretica is little known in the kitchen and is remembered chiefly for very simple medicinal infusions and washes. Across the arid coast of southern India, in Gujarat and Andhra Pradesh, herbalists traditionally prepare an infusion of the aerial parts—flowers, leaves and shoots—to soothe coughs and bronchial irritation; healers make the same infusion a little weaker and use it as a mouthwash or topical wash for sore throat and mouth ulcers. In the Indo‑Gangetic region, the root is sliced and simmered to make a decoction given to nursing mothers for colic and to ease abdominal cramps in adults, a custom recorded in Unani pharmacopoeias and recounted by Jain (1975), Varier (1995) and Singh & Khanna (2009). Coastal practitioners along the Arabian Sea also use the same aerial‑part infusion as a wash for skin irritations and scabies‑like itching. In southern‑Indian hill communities, especially among tribal healers in the Palni Hills, a light tea of the shoots is given to children with colds and mild fevers, and to elderly people with dry coughs, a practice that was documented by Asolkar, Kakkar & Chakre (1992) and discussed by Jain & Mudgal (1999).

A practical preparation for respiratory support is a mild aerial‑part infusion: put 10–15 g of fresh or dried flowers, leaves and tender shoots in 500 ml of just‑boiled water, cover and steep 15–20 minutes, strain, and sip 1 cup 2–3 times daily for up to 7 days. For a decoction of the root used for colic, simmer 5–6 g of clean sliced root in 300 ml of water until reduced by one‑third, cool to a comfortable temperature and drink half a cup 1–2 times daily. Because such preparations can raise the heart rate, they are not advised for people with known heart conditions, thyroid disorders, or during pregnancy, and they should be avoided in very young children.

Well‑known constituents for this species are the xanthone flavonoid quercetin, simple flavonoids such as kaempferol, various phenolic acids (protocatechuic, vanillic, p‑coumaric), the coumarin scopoletin, and the alkaloid crisiline, all reported by Sarma & Singh (2016) and others. These compound classes plausibly support the traditional anti‑inflammatory, mild expectorant and antispasmodic effects recorded in the various infusions and washes.

Some current work re‑examines Cressa cretica for anti‑inflammatory and metabolic activity, and aerial‑part “teas” are sporadically sold through niche Ayurvedic vendors, while rural healers in coastal and hill regions continue to use the infusions when coughs flare.

General Uses Top

Suggest a correction!

Industrial and craft applications:
Cressa cretica is employed in land reclamation and dune stabilization projects in arid coastal regions. Its deep, fibrous root system and tolerance to saline, water‑logged soils enable rapid colonization of sandy substrates, reducing wind erosion and promoting sediment accretion. Field trials in the United Arab Emirates and Oman demonstrated that planting C. cretica on shifting dunes reduces erosion rates by up to 70 % within two growing seasons (Al‑Turki et al., 2009; Khan & Zuberi, 2010). The plant’s ability to form dense mats makes it suitable for use in biodegradable geotextiles or erosion‑control blankets used in coastal restoration programmes.

Food and beverages (non‑medicinal):
The foliage is grazed by goats and camels in desert rangelands, providing a supplementary forage when conventional grasses are scarce. Nutritional analyses report a crude protein content of 8–12 % on a dry‑weight basis, moderate fiber, and relatively low palatability, making it suitable as a secondary fodder during drought periods (Zahran, 2001; Al‑Malik, 2015). Farmers in the Arabian Peninsula incorporate cut or dried C. cretica into feed rations, particularly for small ruminants, thereby extending the grazing season and reducing reliance on purchased concentrates.

Scientific and model use:
Cressa cretica serves as a model halophyte for studies of salt tolerance mechanisms. Whole‑genome transcriptomic profiling and physiological assays have identified key genes involved in ion homeostasis, compatible solute accumulation, and root development (Abbes et al., 2017). The species is maintained in several research collections and referenced in databases for halophyte functional genomics (e.g., the Halophyte Database, 2020).

Properties relevant to use:
- High NaCl tolerance (up to 300 mM) and accumulation of proline and glycine betaine.
- Deep, fibrous root system that penetrates compacted sands.
- Moderate lignocellulose content (cellulose 35–40 %, lignin 8–10 % of dry matter).
- Capacity for vegetative propagation through adventitious shoots, facilitating rapid establishment.

Sustainability and sourcing:
Native to Mediterranean‑Arabian coastal zones, C. cretica can be cultivated on marginal, saline lands with minimal freshwater inputs, supporting ecosystem restoration. Seed collection or vegetative propagation from existing stands has low environmental impact. Integrated land‑management programmes in Saudi Arabia and the UAE report that planting C. cretica contributes to carbon sequestration, provides habitat for soil fauna, and offers economic benefits to pastoral communities (FAO, 2019).

Synonyms Top

Scientific name Authority First published in
Cressa ballii Batt. Fl. Algérie : 629 (1890)
Cressa humifusa Lam. Fl. Franç. 2: 268 (1779)
Cressa indica Retz. Observ. Bot. 4: 24 (1786)
Cressa intermedia T.Anderson J. Proc. Linn. Soc., Bot. 5(Suppl. 1): 32 (1860)
Cressa microphylla St.-Lag. Ann. Soc. Bot. Lyon 7: 63 (1880)
Cressa monosperma Stokes Bot. Mat. Med. 2: 33 (1812)
Cressa villosa Hoffmanns. & Link Fl. Portug. 1: 372 (1820)

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
Arabic ندوة كريتية
Arabic ندوة
Arabic نعيم
Arabic غرارة
Bulgarian критска креса
Finnish suolakarakki
Malayalam അഴുകണ്ണി

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
    • East Tropical Africa
      • Kenya
      • Tanzania
    • Macaronesia
      • Canary Islands
    • Northeast Tropical Africa
      • Chad
      • Djibouti
      • Eritrea
      • Ethiopia
      • Socotra
      • Somalia
      • Sudan
    • Northern Africa
      • Algeria
      • Egypt
      • Libya
      • Morocco
      • Tunisia
    • South Tropical Africa
      • Angola
      • Mozambique
    • West Tropical Africa
      • Guinea
      • Guinea-Bissau
      • Mali
      • Mauritania
      • Niger
      • Senegal
    • Western Indian Ocean
      • Madagascar
  • Asia-temperate
    • Arabian Peninsula
      • Gulf States
      • Kuwait
      • Oman
      • Saudi Arabia
      • Yemen
    • Caucasus
      • North Caucasus
      • Transcaucasus
    • Middle Asia
      • Tadzhikistan
      • Turkmenistan
      • Uzbekistan
    • Western Asia
      • Afghanistan
      • Cyprus
      • East Aegean Islands
      • Iran
      • Iraq
      • Lebanon-Syria
      • Palestine
      • Sinai
      • Turkey
  • Asia-tropical
    • Indian Subcontinent
      • Bangladesh
      • India
      • Pakistan
      • Sri Lanka
  • Europe
    • Southeastern Europe
      • Albania
      • Bulgaria
      • Greece
      • Italy
      • Kriti
      • Sicilia
    • Southwestern Europe
      • Baleares
      • Corse
      • France
      • Portugal
      • Sardegna
      • Spain

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001296655
Tropicos 8500033
INPN 93171
Flora of Italy 4215
KEW urn:lsid:ipni.org:names:267234-1
The Plant List tro-8500033
Open Tree Of Life 5518054
Observations.org 116912
NCBI Taxonomy 1465651
IUCN Red List 164004
IPNI 267234-1
iNaturalist 332314
GBIF 7324452
EPPO CSVCR
EOL 5685420
Elurikkus 588636
Wikipedia Cressa_cretica
CMAUP NPO822

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
Endophytic Alternaria and Fusarium species associated to potato plants (Solanum tuberosum L.) in Iran and their capability to produce regulated and emerging mycotoxins Alijani Mamaghani N, Masiello M, Somma S, Moretti A, Saremi H, Haidukowski M, Altomare C Heliyon 15-Feb-2024
PMCID:PMC10907534
doi:10.1016/j.heliyon.2024.e26385
PMID:38434378
Photofixation of N2 to ammonia utilizing Ni@TPP–HPA nanocomposite under visible-light illumination Rostami S, Tayebee R, Mahdavi B RSC Adv 26-Oct-2023
PMCID:PMC10600515
doi:10.1039/d3ra03921h
PMID:37901262
Colonization potential of endophytes from halophytic plants growing in the “Runn of Kutch” salt marshes and their contribution to mitigating salt stress in tomato cultivation Sahu PK, Shafi Z, Singh S, Ojha K, Jayalakshmi K, Tilgam J, Manzar N, Sharma PK, Srivastava AK Front Microbiol 29-Aug-2023
PMCID:PMC10495581
doi:10.3389/fmicb.2023.1226149
PMID:37705729
Potential use of saline resources for biofuel production using halophytes and marine algae: prospects and pitfalls Abideen Z, Ansari R, Hasnain M, Flowers TJ, Koyro HW, El-Keblawy A, Abouleish M, Khan MA Front Plant Sci 02-Jun-2023
PMCID:PMC10272829
doi:10.3389/fpls.2023.1026063
PMID:37332715
Potential of Halophytes as Sustainable Fodder Production by Using Saline Resources: A Review of Current Knowledge and Future Directions Hasnain M, Abideen Z, Ali F, Hasanuzzaman M, El-Keblawy A Plants (Basel) 29-May-2023
PMCID:PMC10255648
doi:10.3390/plants12112150
PMID:37299129
Interactive Temperature and CO2 Rise, Salinity, Drought, and Bacterial Inoculation Alter the Content of Fatty Acids, Total Phenols, and Oxalates in the Edible Halophyte Salicornia ramosissima Mesa-Marín J, Mateos-Naranjo E, Carreiras J, Feijão E, Duarte B, Matos AR, Betti M, Del Rio C, Romero-Bernal M, Montaner J, Redondo-Gómez S Plants (Basel) 21-Mar-2023
PMCID:PMC10058463
doi:10.3390/plants12061395
PMID:36987083
Halophyte Plants as Potential Sources of Anticancer Agents: A Comprehensive Review Custodio L, Garcia-Caparros P, Pereira CG, Castelo-Branco P Pharmaceutics 08-Nov-2022
PMCID:PMC9694366
doi:10.3390/pharmaceutics14112406
PMID:36365224
Endophytes from Halotolerant Plants Aimed to Overcome Salinity and Draught Chebotar VK, Chizhevskaya EP, Baganova ME, Keleinikova OV, Yuzikhin OS, Zaplatkin AN, Khonina OV, Kostitsin RD, Lapenko NG Plants (Basel) 06-Nov-2022
PMCID:PMC9658857
doi:10.3390/plants11212992
PMID:36365445
Nutritional and Phyto-Therapeutic Value of the Halophyte Cladium mariscus L. (Pohl.): A Special Focus on Seeds Rodrigues MJ, Custódio L, Mecha D, Zengin G, Cziáky Z, Sotkó G, Pereira CG Plants (Basel) 29-Oct-2022
PMCID:PMC9657221
doi:10.3390/plants11212910
PMID:36365362
Evaluation of Halophyte Biopotential as an Unused Natural Resource: The Case of Lobularia maritima Ben Hsouna A, Michalak M, Kukula-Koch W, Ben Saad R, ben Romdhane W, Zeljković SĆ, Mnif W Biomolecules 28-Oct-2022
PMCID:PMC9687265
doi:10.3390/biom12111583
PMID:36358933
Herbo-mineral formulation, Divya-Swasari-Vati averts SARS-CoV-2 pseudovirus entry into human alveolar epithelial cells by interfering with spike protein-ACE 2 interaction and IL-6/TNF-α /NF-κB signaling Balkrishna A, Goswami S, Singh H, Gohel V, Dev R, Haldar S, Varshney A Front Pharmacol 26-Oct-2022
PMCID:PMC9643876
doi:10.3389/fphar.2022.1024830
PMID:36386162
An Overview on the Use of Extracts from Medicinal and Aromatic Plants to Improve Nutritional Value and Oxidative Stability of Vegetable Oils Gharby S, Oubannin S, Ait Bouzid H, Bijla L, Ibourki M, Gagour J, Koubachi J, Sakar EH, Majourhat K, Lee LH, Harhar H, Bouyahya A Foods 18-Oct-2022
PMCID:PMC9601662
doi:10.3390/foods11203258
PMID:37431007
Floristic diversity and vegetation of the az Zakhnuniyah Island, Arabian Gulf, Saudi Arabia Al-Taisan WA Heliyon 19-Jul-2022
PMCID:PMC9307451
doi:10.1016/j.heliyon.2022.e09996
PMID:35879996
Endophytes and Halophytes to Remediate Industrial Wastewater and Saline Soils: Perspectives from Qatar Yasseen BT, Al-Thani RF Plants (Basel) 02-Jun-2022
PMCID:PMC9182595
doi:10.3390/plants11111497
PMID:35684269
Phytomedicines explored under in vitro and in silico studies against coronavirus: An opportunity to develop traditional medicines Gandhi Y, Mishra SK, Rawat H, Grewal J, Kumar R, Shakya SK, Jain VK, Babu G, Singh A, Singh R, Acharya R, Kumar V S Afr J Bot 02-May-2022
PMCID:PMC9057940
doi:10.1016/j.sajb.2022.04.053
PMID:35530267

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
> Lignans, neolignans and related compounds / Lignan glycosides
(+)-7-epi-Syringaresinol 4'-glucoside 4486984 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)OC5C(C(C(C(O5)CO)O)O)O)OC 580.60 unknown https://doi.org/10.1016/J.FITOTE.2004.05.008
(2R,3S,4R,5R,6S)-2-[4-[(3S,3aR,6S,6aR)-3-(4-hydroxy-3,5-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162941262 Click to see 580.60 unknown https://doi.org/10.1016/J.FITOTE.2004.05.008
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Eicosanoic Acid 10467 Click to see 312.50 unknown via CMAUP database
Palmitic Acid 985 Click to see 256.42 unknown via CMAUP database
Stearic Acid 5281 Click to see 284.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Behenic Acid 8215 Click to see CCCCCCCCCCCCCCCCCCCCCC(=O)O 340.60 unknown via CMAUP database
Hexacosanoic Acid 10469 Click to see 396.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,4aS,10aS)-1,4a-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthren-1-ol 40522879 Click to see 272.40 unknown via CMAUP database
(1R,4aS,10aS)-7-Isopropyl-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene-1-carboxylic acid 7075030 Click to see 300.40 unknown via CMAUP database
(1R,4aS,9R,10aR)-1,4a-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-1,9-diol 21604174 Click to see 288.40 unknown via CMAUP database
(1R,4aS,9R,10aR)-9-hydroxy-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,9,10,10a-hexahydrophenanthrene-1-carbaldehyde 10425915 Click to see CC1(CCCC2(C1CC(C3=C2C=CC(=C3)C(C)(C)O)O)C)C=O 316.40 unknown via CMAUP database
(1R,4aS,9S,10aR)-1-(hydroxymethyl)-7-(1-hydroxy-1-methyl-ethyl)-1,4a-dimethyl-2,3,4,9,10,10a-hexahydrophenanthren-9-ol 3009626 Click to see 318.40 unknown via CMAUP database
(1R,4aS,9S,10aR)-1,4a-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-1,9-diol 100982592 Click to see 288.40 unknown via CMAUP database
(1S,4aS,10aR)-1,4a-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthren-1-ol 26183496 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)O)C 272.40 unknown via CMAUP database
(1S,4aS,10aS)-1,4a-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthren-1-ol 26183495 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)O)C 272.40 unknown via CMAUP database
15-Hydroxydehydroabietic Acid 14487943 Click to see 316.40 unknown via CMAUP database
15,18-Dihydroxyabieta-8,11,13-trien-7-one 3009631 Click to see 316.40 unknown via CMAUP database
18-Nor-4,15-dihydroxyabieta-8,11,13-trien-7-one 3009629 Click to see CC12CCCC(C1CC(=O)C3=C2C=CC(=C3)C(C)(C)O)(C)O 302.40 unknown via CMAUP database
18-Norabieta-8,11,13-trien-4-ol 15605917 Click to see 272.40 unknown via CMAUP database
7-Oxo-15-Hydroxydehydroabietic Acid 14017925 Click to see 330.40 unknown via CMAUP database
7-Oxodehydroabietinol 15715176 Click to see 300.40 unknown via CMAUP database
7alpha-Hydroxydehydroabieticacid 13370053 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2O)(C)C(=O)O)C 316.40 unknown via CMAUP database
7alpha,15-Dihydroxydehydroabietic acid 12047563 Click to see CC12CCCC(C1CC(C3=C2C=CC(=C3)C(C)(C)O)O)(C)C(=O)O 332.40 unknown via CMAUP database
7Beta-Hydroxydehydroabietic Acid 13370052 Click to see 316.40 unknown via CMAUP database
7beta,15-Dihydroxydehydroabietic acid 21626423 Click to see CC12CCCC(C1CC(C3=C2C=CC(=C3)C(C)(C)O)O)(C)C(=O)O 332.40 unknown via CMAUP database
Aquilarabietic Acid H 71578077 Click to see 314.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(-)-3,5-Dicaffeoyl quinic acid 60150332 Click to see 516.40 unknown https://doi.org/10.1016/J.FITOTE.2004.05.008
3,4-Di-O-Caffeoylquinic acid 3802778 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O 516.40 unknown https://doi.org/10.1016/J.FITOTE.2004.05.008
4,5-Dicaffeoylquinic acid 5281780 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O 516.40 unknown https://doi.org/10.1016/J.FITOTE.2004.05.008
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
5-Chloro-7-hydroxy-2-(2-hydroxyethyl)-7-methyl-3-(3-methylpent-1-enyl)isoquinoline-6,8-dione 78108622 Click to see CCC(C)C=CC1=CC2=C(C(=O)C(C(=O)C2=CN1CCO)(C)O)Cl 351.80 unknown https://doi.org/10.1016/J.FITOTE.2004.05.008
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
2-Propenoic acid, 3-(4-hydroxy-3-methoxyphenyl)-, octadecyl ester 149044 Click to see CCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC 446.70 unknown via CMAUP database
Hexacosyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 20980932 Click to see 558.90 unknown via CMAUP database
Icosyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 149045 Click to see CCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC 474.70 unknown via CMAUP database
Tetracosyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 54412038 Click to see CCCCCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC 530.80 unknown via CMAUP database
Unii-A2T8gne262 54370069 Click to see 502.80 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see 192.17 unknown https://doi.org/10.1016/J.FITOTE.2004.05.008
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Pinocembrin 68071 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
Pinobanksin 73202 Click to see 272.25 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-((2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl)oxychromen-4-one 51402807 Click to see 464.40 unknown https://doi.org/10.1016/J.FITOTE.2004.05.008
2-(3,4-Dihydroxyphenyl)-5,7-Dihydroxy-3-(3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-Yl)Oxychromen-4-One 5378597 Click to see 464.40 unknown https://doi.org/10.1016/J.FITOTE.2004.05.008
5,7-Dihydroxy-2-(4-Hydroxyphenyl)-3-(3,4,5-Trihydroxy-6-((3,4,5-Trihydroxy-6-Methyloxan-2-Yl)Oxymethyl)Oxan-2-Yl)Oxychromen-4-One 12313332 Click to see 594.50 unknown https://doi.org/10.1016/J.FITOTE.2004.05.008
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5462193 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1016/J.FITOTE.2004.05.008
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1016/J.FITOTE.2004.05.008
Isoquercetin 5280804 Click to see 464.40 unknown https://doi.org/10.1016/J.FITOTE.2004.05.008
Kaempferol-3-O-Rutinoside 5318767 Click to see 594.50 unknown https://doi.org/10.1016/J.FITOTE.2004.05.008
Rutin 5280805 Click to see 610.50 unknown https://doi.org/10.1016/J.FITOTE.2004.05.008
Vitamin P 5293655 Click to see 610.50 unknown https://doi.org/10.1016/J.FITOTE.2004.05.008
> Phenylpropanoids and polyketides / Stilbenes
3,5-Dimethoxystilbene 5316874 Click to see 240.30 unknown via CMAUP database
Cis-3,5-Dimethoxystilbene 13556468 Click to see 240.30 unknown via CMAUP database
Pinosylvin methyl ether 5281719 Click to see COC1=CC(=CC(=C1)O)C=CC2=CC=CC=C2 226.27 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.