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Cressa cretica

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

Description Top

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No description added yet. Help us by writing one.

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

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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

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Varieties (abbr. var.) Top

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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
  • 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

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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
> 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 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
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Arachidic Acid 10467 Click to see CCCCCCCCCCCCCCCCCCCC(=O)O 312.50 unknown via CMAUP database
Palmitic Acid 985 Click to see CCCCCCCCCCCCCCCC(=O)O 256.42 unknown via CMAUP database
Stearic Acid 5281 Click to see CCCCCCCCCCCCCCCCCC(=O)O 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 CCCCCCCCCCCCCCCCCCCCCCCCCC(=O)O 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 CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)O)C 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 CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C(=O)O)C 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 CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2O)(C)O)C 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 CC1(CCCC2(C1CC(C3=C2C=CC(=C3)C(C)(C)O)O)C)CO 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 CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2O)(C)O)C 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-Hydroxy-7-oxodehydroabietic acid 14017925 Click to see CC12CCCC(C1CC(=O)C3=C2C=CC(=C3)C(C)(C)O)(C)C(=O)O 330.40 unknown via CMAUP database
15-Hydroxydehydroabietic Acid 14487943 Click to see CC12CCCC(C1CCC3=C2C=CC(=C3)C(C)(C)O)(C)C(=O)O 316.40 unknown via CMAUP database
15,18-Dihydroxyabieta-8,11,13-trien-7-one 3009631 Click to see CC1(CCCC2(C1CC(=O)C3=C2C=CC(=C3)C(C)(C)O)C)CO 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 CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)O)C 272.40 unknown via CMAUP database
7-Oxodehydroabietinol 15715176 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2=O)(C)CO)C 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 CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2O)(C)C(=O)O)C 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 CC(=C)C1=CC2=C(C=C1)C3(CCCC(C3CC2O)(C)C(=O)O)C 314.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
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
3,5-Dicaffeoyl-epi-quinic acid 60150332 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)OC(=O)C=CC3=CC(=C(C=C3)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
Docosylferulate 54370069 Click to see CCCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC 502.80 unknown via CMAUP database
Hexacosyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 20980932 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC 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
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O 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 C1=CC=C(C=C1)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O 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 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/J.FITOTE.2004.05.008
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/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
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 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 594.50 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 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/J.FITOTE.2004.05.008
Kaempferol-3-O-rutinoside 5318767 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 594.50 unknown https://doi.org/10.1016/J.FITOTE.2004.05.008
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 https://doi.org/10.1016/J.FITOTE.2004.05.008
Vitamin P 5293655 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 https://doi.org/10.1016/J.FITOTE.2004.05.008
> Phenylpropanoids and polyketides / Stilbenes
3,5-Dimethoxystilbene 5316874 Click to see COC1=CC(=CC(=C1)C=CC2=CC=CC=C2)OC 240.30 unknown via CMAUP database
Cis-3,5-Dimethoxystilbene 13556468 Click to see COC1=CC(=CC(=C1)C=CC2=CC=CC=C2)OC 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

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