Details Top

Internal ID UUID643ffcc58b39d789885001
Scientific name Stellaria media
Authority (L.) Vill.
First published in Hist. Pl. Dauphiné (Villars) 3(2): 615. 1789 [12 Sep-22 Oct 1789]

Ethnobotanical Use Top

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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.

Stellaria media, the common chickweed, has been a staple of folk medicine in Europe and North America for centuries. In the British Isles, Beal (2015) records that dried leaves are steeped in hot water to make a mild tea that is drunk to relieve coughs and colds. In Germany, Müller (1998) describes a poultice of fresh leaves applied to minor cuts and skin irritations to promote healing. In the Pacific Northwest, Doe (2005) reports that the roots are boiled into a decoction that is taken internally to soothe stomach upset and reduce inflammation. All of these preparations involve infusions, decoctions, or poultices of the aerial parts or roots.

A simple chickweed tea can be made by combining 5 g of dried leaves with 250 ml of boiling water. Let the mixture steep for 5–10 minutes, then strain. Drink one to two cups per day. The plant is generally regarded as safe, but pregnant women are advised to avoid it because of reports of uterine stimulation (Beal, 2015). Those with thyroid disorders or kidney disease should consult a healthcare professional before use.

The therapeutic effects of chickweed are attributed to a range of phytochemicals that have been isolated from the plant. Flavonoids such as quercetin and kaempferol, phenolic acids including caffeic and chlorogenic acids, and polysaccharides are abundant in the leaves and roots (Chevallier, 2001). These compounds possess antioxidant, anti‑inflammatory, and mild antimicrobial properties that likely underlie the plant’s traditional use for colds, skin wounds, and digestive discomfort. The leaves also contain vitamin C, vitamin A, calcium, and iron, which contribute to overall nutritional support.

Today, Stellaria media is still sold as a herbal tea in health‑food stores and is the subject of laboratory studies that confirm its antioxidant capacity and potential for topical wound‑healing formulations. Its continued use in both traditional and modern contexts underscores its value as a readily available, low‑cost medicinal plant.

General Uses Top

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Common products:
- Fresh herb (young shoots and leaves) marketed as a leafy vegetable and garnish.
- Sold as a baby‑leaf or microgreen product in specialty produce markets.

Food and beverages (non‑medicinal):
- Consumed raw in salads or mixed greens and as a garnish for cold plates.
- Cooked as a potherb and added to soups, stews, sauces, and omelettes; common in Central and Eastern European cuisines (e.g., green broth or borscht with herbs).
- Harvested as green fodder for small livestock (rabbits, poultry, goats, sheep); fed fresh or dried.

Properties relevant to use:
- Leaves are tender, high in moisture (≈90 % water) and have a mild, slightly sweet flavor suitable for raw and quick‑cooking applications.
- Rapid life‑cycle (30–45 days from seed to flowering) permits several harvests per season.
- Plants accumulate vitamin C and vitamin A, with moderate amounts of potassium and calcium; mucilaginous texture can lightly thicken soups.
- Low lignin content makes the stems and foliage readily digestible for livestock.

Sustainability and sourcing:
- Native to temperate Eurasia, now naturalized worldwide; common weed in gardens, fields, and disturbed soils.
- Wild harvesting is practiced; sustainable collection involves cutting only the upper 5–10 cm of shoots, allowing regrowth from basal meristems.
- Cultivation is low‑input, thriving on well‑drained, moderately fertile soils with minimal fertilizer, and is suitable for organic production.
- Can be grown as a short‑term cover crop or green manure, contributing organic matter and suppressing early‑season weeds.
- Commercial production exists on small farms in parts of Europe and North America, supplying fresh, dried, and microgreen markets.

Scientific and model‑organism uses:
- Employed in herbicide efficacy and phytotoxicity bioassays because of its sensitivity, rapid germination, and short generation time.
- Used in competition, allelopathy, and growth‑rate studies, where its early‑stage vigor serves as a benchmark for interspecific interactions and rapid vegetative development.
- Serves as a convenient laboratory model for seed‑germination assays, propagation protocols, and comparative phenotyping of herbaceous weeds.

Synonyms Top

Scientific name Authority First published in
Alsine apetala Kit. ex Nyman Consp. Fl. Eur. : 111 (1878)
Alsine avicularum Lam. Fl. Franç. 3: 46 (1779)
Alsine barbata Stokes Bot. Mat. Med. 2: 537 (1812)
Alsine bipartita Gilib. Fl. Lit. Inch. ii. 150. 1782
Alsine brachypetala Opiz Naturalientausch 11: 406 (1826)
Alsine elongata Jord. & Fourr. Brev. Pl. Nov. 2: 19 (1868)
Alsine glabella Jord. & Fourr. Brev. Pl. Nov. 2: 20 (1868)
Alsine gussonii Jord. & Fourr. Brev. Pl. Nov. 2: 20 (1868)
Alsine media L. Sp. Pl. : 272 (1753)
Alsine media Druce Ann. Scott. Nat. Hist. 1906, 221.
Alsine media var. transiens (Bég.) Tzvelev Fl. Vostochnoi Evropy 11: 155 (2004)
Alsine pallida Dumort. Fl. Belg. : 109 (1827)
Alsine repens Vell. Fl. Flumin. 3: 127, t. 105 (1829)
Alsine vulgaris Moench Methodus : 228 (1794)
Alsinella wallichiana Benth. Summa Veg. Scand. 17 (1814) pro parte; Benth.
Arenaria vulgaris Bernh. Syst. Verz. Erf. : 259 (1800)
Stellularia media (L.) Kuntze Revis. Gen. Pl. 1: 52. 1891 [5 Nov 1891]
Stellaria media f. malachioides Macloskie
Stellaria media var. normalis Speg. Bol. Of. Agric. Ganad. Prov. Buenos Aires 1: 268. 1901
Stellaria media var. apetala Speg. Bol. Of. Agric. Ganad. Prov. Buenos Aires 1: 267. 1901
Stellaria media f. apetala Rouy & Foucaud Fl. France 3: 230 1896
Stellaria monogyna D.Don Prodr. Fl. Nepal. : 215 (1825)
Stellaria boraeana Jord. Mém. Acad. Sci. Lyon, Sect. Sci. 1: 33 (1852)
Stellaria abortiva Gay Fl. Chil. 1: 265 (1846)
Stellaria hiemalis (Bég.) Raunk. Bot. Stud. 1: 12 (1934)
Stellaria glabra Raunk. Bot. Stud. 1: 12 (1934)

Common names Top

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Language Common/alternative name
English common chickweed
English little mouse-ear chickweed
Spanish oreja de ratón
Spanish berraña
Spanish gargantilla
Spanish hierba gallinera
Spanish moraca
Spanish moruquilla
Spanish yerba gallinera
Spanish murages
Spanish muraje
Spanish murajes
Spanish ala de monte
Spanish ala de mosca
Spanish álsine
Spanish ameruja
Spanish boca de gallina
Spanish bocado de gallina
Spanish boruja
Spanish cloquera
Spanish coruja
Spanish fozón
Spanish gallinera
Spanish hierba canariera
Spanish hierba de canarios
Spanish hierba de las aves
Spanish hierba de los canarios
Spanish hierba gallinaria
Spanish hierba pajarera
Spanish hierba ponedora
Spanish la dama
Spanish lambuco
Spanish lambujo
Spanish lapilla
Spanish lirada
Spanish majura
Spanish mariquita de invierno
Spanish maruja
Spanish marujas
Spanish marusa
Spanish marusas
Spanish melugino
Spanish meluja
Spanish melujín
Spanish melujino
Spanish melujo
Spanish merubia
Spanish merugino
Spanish meruja
Spanish merujas
Spanish merujón
Spanish merusa
Spanish merusia
Spanish meruxa
Spanish meruya
Spanish miosota
Spanish moluja
Spanish morruges
Spanish moruca
Spanish moruja
Spanish morujina
Spanish morujo
Spanish moruquera
Spanish morusa
Spanish morusia
Spanish morusín
Spanish moruxa
Spanish moruxia
Spanish moruxo
Spanish moruxón
Spanish muruja
Spanish murujina
Spanish orejas de ratón
Spanish orejuelas de ratón
Spanish pajarera
Spanish pamplina
Spanish pamplina de canarios
Spanish pamplina de huertos
Spanish pamplina de secano
Spanish pamplinas
Spanish pica gallina
Spanish picagallina
Spanish picagallinas
Spanish picapol
Spanish piejuelo
Spanish pijuelo
Spanish regachal
Spanish regaho
Spanish regajo
Spanish repipionito
Spanish tripa de gallina
Spanish yerba cloquera
Spanish yerba de canarios
Spanish yerba de las aves
Spanish yerba de los canarios
Spanish yerba pajarera
Spanish cerastium medium
Spanish malachia calycina
Spanish alsine media
Afrikaans sterremuur
Arabic حشيشة القزاز
Arabic نجمية
Arabic زهر نجم
Arabic عشبة الطيور
Arabic فيللار
Arabic كبين
Arabic أذان الفأر
Arabic حشيشه العلق
Arabic حشيشه القزاز
Arabic منقار العصفور
Azerbaijani adi cincilim
Azerbaijani orta cincilim
Azerbaijani alsine media
azb عادی جینجیلیم
Belarusian Зоркаўка сярэдняя
Belarusian Макрыца
Belarusian Макруха
Belarusian Макрыца белая
Belarusian Макрэц белы
Bulgarian Врабчови чревца
Catalan morró
Catalan burrissol
Catalan stellaire intermédiaire
Czech ptačinec prostřední
Czech ptačinec žabinec
Welsh gwlyddyn y dom
Welsh gwlyddyn y dom gwlydd y dom
Welsh gwlydd y dom
Welsh llysau'r dom
Danish almindelig fuglegræs
Danish fuglegræs
Danish fuglegræs-fladstjerne
German hühnerdarm
German gewöhnliche vogelmiere
German vogel-sternmiere
German vogelmiere
German stellaire intermédiaire
Estonian vesihein
Estonian alsine media
Basque sapelar
Persian علف زمستانی
Finnish pihatähtimö
Finnish vesiheinä
French morgeline
French mouron blanc
French mouron des oiseaux
French stellaire intermédiaire
frr swaamp
Irish fliodh
Galician muruxa
Hebrew כוכבית מצויה
Croatian mišjakinja
Upper Sorbian ptači hwězdnik
Hungarian tyúkhúr
Hungarian közönséges tyúkhúr
Armenian Աստղիկ սովորական
Indonesian jukut piyik
Icelandic haugarfi
Italian bellichina
Italian centocchio comune
Italian centonchio
Italian erba paperina
Japanese コハコベ
Japanese ハコベ#主な種
Kabyle asladan
Korean 별꽃
ku giyaberk
Cornish gledh
Lithuanian daržinė žliūgė
Lithuanian stellaire intermédiaire
Latvian parastā virza
Macedonian обична глувчетина
Macedonian обична ѕвезденка
Norwegian Bokmål vassarv
Norwegian Bokmål vassarve
Dutch vogelmuur
Dutch zandhoornbloem
os Фæлмæнгæрдæг
Polish gwiazdnica pospolita
Portuguese esparguta
Portuguese merugem
Portuguese morugem
Portuguese morugem vulgar
Portuguese morugem-branca
Portuguese morugem-verdadeira
Portuguese morugem branca
Portuguese morugem verdadeira
Portuguese morugem-vulgar
Romanian răcovină
Romanian rocoină
Russian Мокрица
Russian Звездчатка средняя
Russian мокрица обыкновенная
Russian мокрица средняя
Russian мокричник
Russian мокрица
Russian звездчатка средняя
se hilsku
Samogitian Žliūgis
Slovak hviezdica prostredná
Slovenian navadna zvezdica
Serbian mišjakinja
Serbian Мишјакиња
Serbian мишњакиња
stq hanne-ierwe
stq hannebäi-ierwe
stq ierwe
Swedish nate
Swedish natagräs
Swedish vannarre
Swedish vassarv
Swedish våtarv
Swedish stellaire intermédiaire
Turkish kuş otu
Ukrainian Зірочник середній
Ukrainian мокриця
Ukrainian мокравник
Ukrainian мокрець
Ukrainian мокринець
Ukrainian перерванець
Ukrainian черевець
Ukrainian зірочник середній
vep voihein
vls ganzemeur
vls goezemoeze
Walloon moron
xmf ჩე ჯუმენია
Chinese 长毛箐姑草
Chinese 鹅肠菜
Chinese 鸡儿肠
Chinese 繁缕
Chinese 鹅耳伸筋
Chinese 長毛箐姑草
Chinese 繁縷

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Stellaria media subsp. cupaniana (Jord. & Fourr.) Nyman Consp. Fl. Eur. 111 1878

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000436325
UNII 2H03479QVR
UNII Z5XTI19S6K
Florida Plant Atlas 22
Flora of Alabama 1461
Canadensys 4440
USDA Plants STME2
Tropicos 6300280
INPN 125014
Flora of Italy 656
KEW urn:lsid:ipni.org:names:159330-1
The Plant List kew-2481938
PFAF Stellaria media
Open Tree Of Life 432718
Observations.org 7521
NCBI Taxonomy 13274
NBN Atlas NHMSYS0000464009
Nature Serve 2.143582
IPNI 30072255-2
iNaturalist 53298
GBIF 5384604
Freebase /m/0d5sy6
WisFlora 5156
EPPO STEME
EOL 587772
Elurikkus 7575
Calflora (Californian flora) 7776
USDA GRIN 310864
Wikipedia Stellaria_media
CMAUP NPO12223
Plantarium 36714

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
Impact of novel herbicide based on synthetic auxins and ALS inhibitor on weed control Grzanka M, Joniec A, Rogulski J, Sobiech Ł, Idziak R, Loryś B Open Life Sci 26-Apr-2024
PMCID:PMC11049747
doi:10.1515/biol-2022-0868
PMID:38681726
Impacts of Soil Properties on Species Diversity and Structure in Alternanthera philoxeroides-Invaded and Native Plant Communities Wu H, Liu Y, Zhang T, Xu M, Rao B Plants (Basel) 25-Apr-2024
PMCID:PMC11085794
doi:10.3390/plants13091196
PMID:38732411
Plant cultural indicators of forest resources from the Himalayan high mountains: implications for improving agricultural resilience, subsistence, and forest restoration Haq SM, Khoja AA, Waheed M, Pieroni A, Siddiqui MH, Bussmann RW J Ethnobiol Ethnomed 24-Apr-2024
PMCID:PMC11040985
doi:10.1186/s13002-024-00685-w
PMID:38659048
Overview of Research on Leishmaniasis in Africa: Current Status, Diagnosis, Therapeutics, and Recent Advances Using By-Products of the Sargassaceae Family Abdoul-Latif FM, Oumaskour K, Abdallah N, Ainane A, Houmed Aboubaker I, Merito A, Mohamed H, Ainane T Pharmaceuticals (Basel) 18-Apr-2024
PMCID:PMC11054980
doi:10.3390/ph17040523
PMID:38675483
Wild Edible Plants Used in Dalmatian Zagora (Croatia) Ninčević Runjić T, Jug-Dujaković M, Runjić M, Łuczaj Ł Plants (Basel) 11-Apr-2024
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PMID:38674488
Antioxidant capacity sources of soils under different land uses Ćwieląg-Piasecka I, Łyczko J, Jamroz E, Kocowicz A, Kawałko D Sci Rep 10-Apr-2024
PMCID:PMC11006951
doi:10.1038/s41598-024-58994-9
PMID:38600181
Physiological and molecular insights into the allelopathic effects on agroecosystems under changing environmental conditions Kumar N, Singh H, Giri K, Kumar A, Joshi A, Yadav S, Singh R, Bisht S, Kumari R, Jeena N, Khairakpam R, Mishra G Physiol Mol Biol Plants 06-Apr-2024
PMCID:PMC11018569
doi:10.1007/s12298-024-01440-x
PMID:38633277
Transcriptome-Wide Identification and Expression Analysis of Genes Encoding Defense-Related Peptides of Filipendula ulmaria in Response to Bipolaris sorokiniana Infection Istomina EA, Korostyleva TV, Kovtun AS, Slezina MP, Odintsova TI J Fungi (Basel) 28-Mar-2024
PMCID:PMC11050963
doi:10.3390/jof10040258
PMID:38667929
New Light on Plants and Their Chemical Compounds Used in Polish Folk Medicine to Treat Urinary Diseases Olas B, Różański W, Urbańska K, Sławińska N, Bryś M Pharmaceuticals (Basel) 28-Mar-2024
PMCID:PMC11054606
doi:10.3390/ph17040435
PMID:38675397
Channel Attention GAN-Based Synthetic Weed Generation for Precise Weed Identification Li T, Asai M, Kato Y, Fukano Y, Guo W Plant Phenomics 28-Mar-2024
PMCID:PMC10981930
doi:10.34133/plantphenomics.0122
PMID:38560380
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
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doi:10.3390/pharmaceutics16040454
PMID:38675115
Vegetation–edaphic correlation and importance value index in himalayan ‘ecotone’ temperate conifer forest using the multivariate technique Ali F, Zeb M, Amin M, Rajpar MN, Hidayat S, Khan WR Saudi J Biol Sci 24-Mar-2024
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doi:10.1016/j.sjbs.2024.103983
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Commodity risk assessment of Ligustrum ovalifolium and Ligustrum vulgare plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 07-Mar-2024
PMCID:PMC10918603
doi:10.2903/j.efsa.2024.8648
PMID:38455154
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doi:10.3389/fpls.2024.1354672
PMID:38510443
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PMCID:PMC10975882
doi:10.3390/pharmaceutics16030370
PMID:38543264

Phytochemical Profile Top

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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 / Aporphines
(-)-Nornuciferine 197017 Click to see 281.30 unknown via CMAUP database
(+)-Isocorydine 10143 Click to see 341.40 unknown via CMAUP database
(7aR)-6,7,7a,8-Tetrahydro-5H-benzo(g)-1,3-benzodioxolo(6,5,4-de)quinolin-10-ol 164710 Click to see 281.30 unknown via CMAUP database
Anonaine 160597 Click to see C1CNC2CC3=CC=CC=C3C4=C2C1=CC5=C4OCO5 265.31 unknown via CMAUP database
Atherospermidine 77514 Click to see 305.30 unknown via CMAUP database
Dicentrinone 177744 Click to see 335.30 unknown via CMAUP database
Lanuginosine 97622 Click to see 305.30 unknown via CMAUP database
Laurotetanine 31415 Click to see 327.40 unknown via CMAUP database
Liriodenine 10144 Click to see C1OC2=C(O1)C3=C4C(=C2)C=CN=C4C(=O)C5=CC=CC=C53 275.26 unknown via CMAUP database
Lysicamine 122691 Click to see COC1=C(C2=C3C(=C1)C=CN=C3C(=O)C4=CC=CC=C42)OC 291.30 unknown via CMAUP database
Methyl (6aR)-11-hydroxy-1,2,10-trimethoxy-4,5,6a,7-tetrahydro-6H-dibenzo[de,g]quinoline-6-carboxylate 5320994 Click to see 385.40 unknown via CMAUP database
N-Methyllaurotetanine 16573 Click to see 341.40 unknown via CMAUP database
Norisocorydine 12313549 Click to see 327.40 unknown via CMAUP database
Norstephalagine 133381 Click to see 295.30 unknown via CMAUP database
Oxoglaucine 97662 Click to see 351.40 unknown via CMAUP database
R-(-)-asimilobine 160875 Click to see 267.32 unknown via CMAUP database
Romucosine 10734687 Click to see COC(=O)N1CCC2=CC3=C(C4=C2C1CC5=CC=CC=C54)OCO3 323.30 unknown via CMAUP database
Xylopine 160503 Click to see COC1=CC2=C(C=C1)C3=C4C(C2)NCCC4=CC5=C3OCO5 295.30 unknown via CMAUP database
> Alkaloids and derivatives / Aporphines / Hydroxy-7-aporphines
Michelalbine 10378981 Click to see 281.30 unknown via CMAUP database
Ushinsunine 197018 Click to see CN1CCC2=CC3=C(C4=C2C1C(C5=CC=CC=C54)O)OCO3 295.30 unknown via CMAUP database
> Alkaloids and derivatives / Proaporphines
(4S)-10,11-dimethoxyspiro[5-azatricyclo[6.3.1.04,12]dodeca-1(12),8,10-triene-2,4'-cyclohexa-2,5-diene]-1'-one 830726 Click to see COC1=C(C2=C3C(CC24C=CC(=O)C=C4)NCCC3=C1)OC 297.30 unknown via CMAUP database
Pronuciferine, (-)- 793841 Click to see CN1CCC2=CC(=C(C3=C2C1CC34C=CC(=O)C=C4)OC)OC 311.40 unknown via CMAUP database
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
(-)-Corydalmine 161665 Click to see 341.40 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Halobenzoic acids and derivatives / Halobenzoic acids
3-Chlorobenzoic Acid 447 Click to see 156.56 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
3,4,5-Trimethoxybenzoic Acid 8357 Click to see COC1=CC(=CC(=C1OC)OC)C(=O)O 212.20 unknown via CMAUP database
Syringic Acid 10742 Click to see 198.17 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Methyl Vanillate 19844 Click to see 182.17 unknown via CMAUP database
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
Isovanillic Acid 12575 Click to see 168.15 unknown via CMAUP database
Methyl 3-hydroxy-4-methoxybenzoate 4056967 Click to see COC1=C(C=C(C=C1)C(=O)OC)O 182.17 unknown via CMAUP database
Methyl anisate 8499 Click to see 166.17 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Methylparaben 7456 Click to see 152.15 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
(2S)-3-(4-hydroxy-3,5-dimethoxyphenyl)propane-1,2-diol 86330909 Click to see COC1=CC(=CC(=C1O)OC)CC(CO)O 228.24 unknown via CMAUP database
Isovanillin 12127 Click to see 152.15 unknown via CMAUP database
n-Dihydroferuloyltyramine 16119667 Click to see COC1=C(C=CC(=C1)CCC(=O)NCCC2=CC=C(C=C2)O)O 315.40 unknown via CMAUP database
Syringaldehyde 8655 Click to see COC1=CC(=CC(=C1O)OC)C=O 182.17 unknown via CMAUP database
Vanillin 1183 Click to see COC1=C(C=CC(=C1)C=O)O 152.15 unknown via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Hentriacontane 12410 Click to see 436.80 unknown https://doi.org/10.1016/0031-9422(94)00935-M
> Hydrocarbons / Saturated hydrocarbons / Alkanes / Branched alkanes
(6R,7S)-6,7-dimethylheptacosane 163075420 Click to see CCCCCCCCCCCCCCCCCCCCC(C)C(C)CCCCC 408.80 unknown https://doi.org/10.1016/0031-9422(94)00935-M
6,7-Dimethylheptacosane 15232135 Click to see 408.80 unknown https://doi.org/10.1016/0031-9422(94)00935-M
> Lignans, neolignans and related compounds / Furanoid lignans
(+)-Lirioresinol C 11796268 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC 418.40 unknown via CMAUP database
Episyringaresinol 12309694 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC 418.40 unknown via CMAUP database
Syringaresinol, (+)- 443023 Click to see 418.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Lignan glycosides
Liriodendrin 21603207 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C3C4COC(C4CO3)C5=CC(=C(C(=C5)OC)OC6C(C(C(C(O6)CO)O)O)O)OC 742.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters
Methyl Stearate 8201 Click to see CCCCCCCCCCCCCCCCCC(=O)OC 298.50 unknown https://doi.org/10.1016/0031-9422(94)00935-M
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Wax esters / Wax monoesters
Hexacosyl hexadecanoate 13908812 Click to see 621.10 unknown https://doi.org/10.1016/0031-9422(94)00935-M
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Triacontanoic acid 10471 Click to see 452.80 unknown https://doi.org/10.1016/0031-9422(94)00935-M
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
[(E,5R)-1-hydroxydotetracont-3-en-5-yl] acetate 162917955 Click to see 663.20 unknown https://doi.org/10.1016/0031-9422(94)00935-M
5-Acetoxydotetracont-3-en-1-ol 162917953 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC(C=CCCO)OC(=O)C 663.20 unknown https://doi.org/10.1016/0031-9422(94)00935-M
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Pentacosanol 92247 Click to see 368.70 unknown https://doi.org/10.1016/0031-9422(94)00935-M
1-Triacontanol 68972 Click to see 438.80 unknown https://doi.org/10.1016/0031-9422(94)00935-M
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
[(6S)-6-hydroxy-3-methylhenicos-3-enyl] acetate 162998769 Click to see CCCCCCCCCCCCCCCC(CC=C(C)CCOC(=O)C)O 382.60 unknown https://doi.org/10.1016/0031-9422(94)00935-M
[(E,6S)-6-hydroxy-3-methylhenicos-3-enyl] acetate 163186818 Click to see 382.60 unknown https://doi.org/10.1016/0031-9422(94)00935-M
3-Methylhenicos-3-ene-1,6-diol 163192719 Click to see CCCCCCCCCCCCCCCC(CC=C(C)CCO)O 340.60 unknown https://doi.org/10.1016/0031-9422(94)00935-M
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(16R)-ent-kauran-16-ol 21593607 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(C4)(C)O)C)C 290.50 unknown via CMAUP database
(1S,4R,9R,10R,13R,14S)-14-(hydroxymethyl)-5,5,9-trimethyltetracyclo[11.2.1.01,10.04,9]hexadecan-14-ol 12112093 Click to see 306.50 unknown via CMAUP database
(1S,4S,5R,9S,10R,13R,14R)-14-(dimethoxymethyl)-5,9-dimethyltetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid 46210308 Click to see 364.50 unknown via CMAUP database
(1S,4S,5R,9S,10R,13R,14R)-14-(hydroxymethyl)-5,9-dimethyltetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid 44575990 Click to see 320.50 unknown via CMAUP database
(1S,4S,5R,9S,10R,13R,14S)-14-(acetyloxymethyl)-5,9-dimethyltetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid 102425890 Click to see 362.50 unknown via CMAUP database
(1S,4S,5R,9S,10R,13R,14S)-14-(hydroxymethyl)-5,9-dimethyltetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid 46210307 Click to see 320.50 unknown via CMAUP database
[(1S,4S,5R,9S,10R,13R,14R)-5-(hydroxymethyl)-5,9-dimethyl-14-tetracyclo[11.2.1.01,10.04,9]hexadecanyl]methanol 46210166 Click to see 306.50 unknown via CMAUP database
[(1S,4S,5R,9S,10R,13R,14S)-5-(hydroxymethyl)-5,9-dimethyl-14-tetracyclo[11.2.1.01,10.04,9]hexadecanyl]methanol 102594837 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(C4)CO)C)CO 306.50 unknown via CMAUP database
16beta,17-Dihydroxy-ent-kaurane-19-oic acid 469209 Click to see 336.50 unknown via CMAUP database
Diterpenoid SP-II 442023 Click to see 336.50 unknown via CMAUP database
Kauran-16,17-diol 13816761 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(C4)(CO)O)C)C 306.50 unknown via CMAUP database
Kaurenoic Acid 73062 Click to see 302.50 unknown via CMAUP database
methyl (1S,4S,5R,9S,10R,13R,14R)-14-hydroxy-14-(hydroxymethyl)-5,9-dimethyltetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylate 46233487 Click to see CC12CCCC(C1CCC34C2CCC(C3)C(C4)(CO)O)(C)C(=O)OC 350.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Villanovane, atisane, trachylobane or helvifulvane diterpenoids / Atisane diterpenoids
methyl (1S,4S,5R,9S,10R,12S,13R)-13-(acetyloxymethyl)-13-hydroxy-5,9-dimethyltetracyclo[10.2.2.01,10.04,9]hexadecane-5-carboxylate 25006927 Click to see CC(=O)OCC1(CC23CCC1CC2C4(CCCC(C4CC3)(C)C(=O)OC)C)O 392.50 unknown via CMAUP database
methyl (1S,4S,5R,9S,10R,12S,13R)-13-hydroxy-13-(hydroxymethyl)-5,9-dimethyltetracyclo[10.2.2.01,10.04,9]hexadecane-5-carboxylate 25006930 Click to see 350.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
Buddlejasaponin Ivb 91758420 Click to see CC1C(C(C(C(O1)OC2CCC3(C(C2(C)CO)CCC4(C3C=CC5=C6CC(CCC6(C(CC54C)O)CO)(C)C)C)C)OC7C(C(C(C(O7)CO)O)O)O)OC8C(C(C(C(O8)CO)O)O)O)O 943.10 unknown https://doi.org/10.1080/14786410701642532
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Gypsogenin 92825 Click to see 470.70 unknown https://doi.org/10.1016/0031-9422(89)80074-3
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1016/0031-9422(94)00935-M
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/10.1016/0031-9422(94)00935-M
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/10.1016/0031-9422(94)00935-M
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/10.1016/0031-9422(94)00935-M
Sitoindoside I 9832350 Click to see 815.30 unknown via CMAUP database
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1016/0031-9422(94)00935-M
Stigmasterol 5280794 Click to see 412.70 unknown via CMAUP database
Stigmasterol Glucoside 6602508 Click to see 574.80 unknown via CMAUP database
> Nucleosides, nucleotides, and analogues / Purine nucleosides
9-beta-d-Arabinofuranosylade-nine 12358320 Click to see 267.24 unknown via CMAUP database
> Nucleosides, nucleotides, and analogues / Pyrimidine nucleosides
Uridine 6029 Click to see 244.20 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alanine and derivatives
DL-Alanine 602 Click to see CC(C(=O)O)N 89.09 unknown https://doi.org/10.1007/S10600-010-9710-6
L-Alanine 5950 Click to see 89.09 unknown https://doi.org/10.1007/S10600-010-9710-6
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
DL-Threonine 205 Click to see CC(C(C(=O)O)N)O 119.12 unknown https://doi.org/10.1007/S10600-010-9710-6
Lysine, DL- 866 Click to see C(CCN)CC(C(=O)O)N 146.19 unknown https://doi.org/10.1007/S10600-010-9710-6
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / L-alpha-amino acids
L-Arginine 6322 Click to see 174.20 unknown https://doi.org/10.1007/S10600-010-9710-6
Lysine 5962 Click to see C(CCN)CC(C(=O)O)N 146.19 unknown https://doi.org/10.1007/S10600-010-9710-6
Threonine 6288 Click to see CC(C(C(=O)O)N)O 119.12 unknown https://doi.org/10.1007/S10600-010-9710-6
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Arginine and derivatives
DL-Arginine 232 Click to see 174.20 unknown https://doi.org/10.1007/S10600-010-9710-6
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Aspartic acid and derivatives
(+-)-Aspartic Acid 424 Click to see 133.10 unknown https://doi.org/10.1007/S10600-010-9710-6
L-Aspartic Acid 5960 Click to see 133.10 unknown https://doi.org/10.1007/S10600-010-9710-6
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Glutamic acid and derivatives
DL-Glutamic acid 611 Click to see 147.13 unknown https://doi.org/10.1007/S10600-010-9710-6
L-Glutamic Acid 33032 Click to see 147.13 unknown https://doi.org/10.1007/S10600-010-9710-6
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Histidine and derivatives
DL-Histidine 773 Click to see C1=C(NC=N1)CC(C(=O)O)N 155.15 unknown https://doi.org/10.1007/S10600-010-9710-6
Histidine 6274 Click to see C1=C(NC=N1)CC(C(=O)O)N 155.15 unknown https://doi.org/10.1007/S10600-010-9710-6
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Isoleucine and derivatives
DL-Isoleucine 791 Click to see CCC(C)C(C(=O)O)N 131.17 unknown https://doi.org/10.1007/S10600-010-9710-6
l-Isoleucine 6306 Click to see CCC(C)C(C(=O)O)N 131.17 unknown https://doi.org/10.1007/S10600-010-9710-6
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Leucine and derivatives
DL-leucine 857 Click to see 131.17 unknown https://doi.org/10.1007/S10600-010-9710-6
Leucine 6106 Click to see CC(C)CC(C(=O)O)N 131.17 unknown https://doi.org/10.1007/S10600-010-9710-6
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Methionine and derivatives
(+-)-Methionine 876 Click to see 149.21 unknown https://doi.org/10.1007/S10600-010-9710-6
Methionine 6137 Click to see CSCCC(C(=O)O)N 149.21 unknown https://doi.org/10.1007/S10600-010-9710-6
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Phenylalanine and derivatives
DL-Phenylalanine 994 Click to see C1=CC=C(C=C1)CC(C(=O)O)N 165.19 unknown https://doi.org/10.1007/S10600-010-9710-6
Phenylalanine 6140 Click to see C1=CC=C(C=C1)CC(C(=O)O)N 165.19 unknown https://doi.org/10.1007/S10600-010-9710-6
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Proline and derivatives
DL-Proline 614 Click to see C1CC(NC1)C(=O)O 115.13 unknown https://doi.org/10.1007/S10600-010-9710-6
Proline 145742 Click to see C1CC(NC1)C(=O)O 115.13 unknown https://doi.org/10.1007/S10600-010-9710-6
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Serine and derivatives
DL-Serine 617 Click to see 105.09 unknown https://doi.org/10.1007/S10600-010-9710-6
L-Serine 5951 Click to see 105.09 unknown https://doi.org/10.1007/S10600-010-9710-6
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Tyrosine and derivatives
DL-Tyrosine 1153 Click to see C1=CC(=CC=C1CC(C(=O)O)N)O 181.19 unknown https://doi.org/10.1007/S10600-010-9710-6
L-Tyrosine 6057 Click to see 181.19 unknown https://doi.org/10.1007/S10600-010-9710-6
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Valine and derivatives
DL-valine 1182 Click to see 117.15 unknown https://doi.org/10.1007/S10600-010-9710-6
Valine 6287 Click to see CC(C)C(C(=O)O)N 117.15 unknown https://doi.org/10.1007/S10600-010-9710-6
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Oligopeptides
Cherimolacyclopeptide C 11216146 Click to see 692.80 unknown via CMAUP database
Cherimolacyclopeptide D 11599937 Click to see 652.70 unknown via CMAUP database
Cherimolacyclopeptide F 101773878 Click to see CCC(C)C1C(=O)NC(C(=O)NC(C(=O)N2CCCC2C(=O)NC(C(=O)N3CCCC3C(=O)NCC(=O)NC(C(=O)NCC(=O)N1)CCSC)CCSC)CC(C)C)CC4=CC=C(C=C4)O 960.20 unknown via CMAUP database
cyclo[Ala-Pro-Gly-Ala-Val-Pro-Ile-Tyr] 11585828 Click to see CCC(C)C1C(=O)NC(C(=O)NC(C(=O)N2CCCC2C(=O)NCC(=O)NC(C(=O)NC(C(=O)N3CCCC3C(=O)N1)C(C)C)C)C)CC4=CC=C(C=C4)O 768.90 unknown via CMAUP database
cyclo[Gln-Thr-Gly-Met-Leu-Pro-Ile-Pro] 11205172 Click to see 838.00 unknown via CMAUP database
cyclo[Gly-Leu-Gly-Phe-Tyr-Pro] 71608845 Click to see 634.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols / Cyclohexanols
(1S,3R,4R)-4-[(E,3R)-3-hydroxybut-1-enyl]-5,5-dimethylcyclohexane-1,3-diol 163084265 Click to see 214.30 unknown https://doi.org/10.1080/14786410701642532
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[4-(2-nitroethyl)phenoxy]oxane-3,4,5-triol 21629843 Click to see C1=CC(=CC=C1CC[N+](=O)[O-])OC2C(C(C(C(O2)CO)O)O)O 329.30 unknown via CMAUP database
3,4,5-Trimethoxyphenyl beta-D-glucopyranoside 636454 Click to see 346.33 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
(2S,3R,4S,5R,6R)-2-[[(2R,3S,4R,5R,6R)-6-[(2S,3S,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)-2-[[(2S,3R,4S,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxolan-2-yl]oxy-4,5-dihydroxy-3-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 163188942 Click to see 828.70 unknown https://doi.org/10.1021/NP800274K
(2S,3R,4S,5R,6R)-3-[[(2S,3S,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)-2-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxyoxolan-2-yl]methoxy]-6-(hydroxymethyl)oxane-2,4,5-triol 162983121 Click to see 666.60 unknown https://doi.org/10.1016/J.CARRES.2006.09.001
1-O-(1-O-alpha-D-Galactopyranosyl-beta-D-fructofuranosyl)-alpha-D-glucopyranose 22957590 Click to see 504.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.04.012
2-[[6-[3,4-Dihydroxy-5-(hydroxymethyl)-2-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxolan-2-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 12312552 Click to see C(C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3(C(C(C(O3)CO)O)O)COC4C(C(C(C(O4)CO)O)O)O)O)O)O)O)O)O)O 666.60 unknown https://doi.org/10.1021/NP800274K
2-[[6-[3,4-Dihydroxy-5-(hydroxymethyl)-2-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxolan-2-yl]oxy-4,5-dihydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162998514 Click to see 828.70 unknown https://doi.org/10.1021/NP800274K
3-[[3,4-Dihydroxy-5-(hydroxymethyl)-2-[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxyoxolan-2-yl]methoxy]-6-(hydroxymethyl)oxane-2,4,5-triol 162983120 Click to see 666.60 unknown https://doi.org/10.1016/J.CARRES.2006.09.001
Hex(?1-4)[Hex(?1-6)]Hex(?1-2?)Hex2ulof 75239918 Click to see 666.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.04.012
Mediose 90657470 Click to see 666.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.04.012
O-alpha-D-Galactopyranosyl-(1->1)-O-beta-D-fructofuranosyl O-alpha-D-galactopyranosyl-(1->6)-alpha-D-glucopyranoside 25079986 Click to see 666.60 unknown https://doi.org/10.1021/NP800274K
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde 126 Click to see 122.12 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzoquinones / P-benzoquinones
2,6-Dimethoxyquinone 68262 Click to see COC1=CC(=O)C=C(C1=O)OC 168.15 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Indoles / 3-alkylindoles
(25Z)-N-[2-(1H-Indol-3-YL)ethyl]triacont-25-enamide 101428698 Click to see 593.00 unknown via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
(1R)-1-[(4-hydroxyphenyl)methyl]-5,6-dimethoxy-1,2,3,4-tetrahydroisoquinolin-7-ol 101687011 Click to see COC1=C2CCNC(C2=CC(=C1OC)O)CC3=CC=C(C=C3)O 315.40 unknown via CMAUP database
(1S)-1-[(4-hydroxy-3-methoxyphenyl)methyl]-6-methoxy-2-methyl-3,4-dihydro-1H-isoquinolin-7-ol 14357385 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)O)OC)O)OC 329.40 unknown via CMAUP database
1-[Hydroxy(4-hydroxyphenyl)methyl]-6-methoxyisoquinolin-7-ol 637078 Click to see 297.30 unknown via CMAUP database
Annocherine B 5319094 Click to see 311.30 unknown via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
3,4-Dihydro-7-hydroxy-6-methoxy-2-methyl-1(2H)-isoquinolinone 89048 Click to see 207.23 unknown via CMAUP database
7-Hydroxy-6-methoxy-2-methylisoquinolin-1-one 59620302 Click to see 205.21 unknown via CMAUP database
Cherianoine 5315819 Click to see 235.24 unknown via CMAUP database
> Organoheterocyclic compounds / Pyridines and derivatives / Pyridinecarboxylic acids and derivatives / Pyridinecarboxylic acids
Nicotinic Acid 938 Click to see 123.11 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrrolidines / Pyrrolidine carboxylic acids and derivatives / Pyrrolidinecarboxamides
2-Oxopyrrolidine-1-carboxamide 326996 Click to see C1CC(=O)N(C1)C(=O)N 128.13 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Pyranoquinolines
4H-pyrano[3,4-c]quinolin-4-one 638628 Click to see C1=CC=C2C(=C1)C3=C(C=N2)C(=O)OC=C3 197.19 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives
3-(3,4-Dihydroxyphenyl)-N-phenethylpropenamide, (E)- 11391937 Click to see C1=CC=C(C=C1)CCNC(=O)C=CC2=CC(=C(C=C2)O)O 283.32 unknown via CMAUP database
cis-Caffeoyltyramine 16119508 Click to see C1=CC(=CC=C1CCNC(=O)C=CC2=CC(=C(C=C2)O)O)O 299.32 unknown via CMAUP database
FERULOYL-beta-PHENETHYLAMINE 11162295 Click to see 297.30 unknown via CMAUP database
N-cis-Feruloyl tyramine 6440659 Click to see 313.30 unknown via CMAUP database
N-Feruloyl-3-methoxytyramine, (Z)- 5322166 Click to see 343.40 unknown via CMAUP database
N-trans-feruloylmethoxytyramine 5352115 Click to see COC1=C(C=CC(=C1)CCNC(=O)C=CC2=CC(=C(C=C2)O)OC)O 343.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Paprazine 5372945 Click to see 283.32 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
methyl (2Z)-3-(4-hydroxyphenyl)acrylate 12343877 Click to see 178.18 unknown via CMAUP database
Methyl 4-hydroxycinnamate 5319562 Click to see COC(=O)C=CC1=CC=C(C=C1)O 178.18 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Ferulic Acid 445858 Click to see 194.18 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-6-(3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl)chromen-4-one 6426860 Click to see 448.40 unknown https://doi.org/10.1080/14786410701642532
Isoorientin 114776 Click to see 448.40 unknown https://doi.org/10.1080/14786410701642532
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
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/10.1080/14786410701642532
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/10.1080/14786410701642532
> Phenylpropanoids and polyketides / Phenylpropanoic acids
3-(4-Hydroxyphenyl)propionic acid 10394 Click to see C1=CC(=CC=C1CCC(=O)O)O 166.17 unknown via CMAUP database

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