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Drymaria cordata

Drymaria cordata - Unknown
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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 UUID6440187911dbf054722750
Scientific name Drymaria cordata
Authority Willd. ex Schult.
First published in Syst. Veg., ed. 15 bis [Roemer & Schultes] v. 406. 1819 [Dec 1819]

Description Top

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Drymaria cordata, also known as tropical chickweed, West Indian chickweed, or golondrina, is a flowering plant found in the Caryophyllaceae family. It is typically found in moist environments in Latin America and sub-Saharan Africa, but has been introduced to various tropical and subtropical regions such as the southeast US, the Caribbean, and parts of Asia. This plant is considered one of the most invasive weeds in these areas, and has spread to many islands as well.

Synonyms Top

Scientific name Authority First published in
Alsine media Vell. Fl. Flumin. 127. 1829 [1825 publ. 7 Sep-28 Nov 1829] ; see also Fl. Flumin. Icon. 3: t. 106. 1831. [1827 publ. 29 Oct 1831]
Alsine rotundifolia Stokes Bot. Mat. Med. 2: 537 (1812)
Bufonia rotundifolia Buch.-Ham. ex Steud. Nomencl. Bot. , ed. 2, 1: 235 (1840)
Drymaria adenophora Urb. Repert. Spec. Nov. Regni Veg. 21: 213 (1925)
Drymaria cordata var. diandra (Sw.) Griseb. Fl. Brit. W. I. : 56 (1859)
Drymaria cordata var. pacifica M.Mizush. J. Jap. Bot. 32: 78 (1957)
Drymaria cordata var. puberula Triana & Planch. Ann. Sci. Nat., Bot. , sér. 4, 17: 148 (1862)
Drymaria diandra (Sw.) Macfad. Fl. Jamaica 1: 52 1837
Drymaria procumbens Rose Contr. U.S. Natl. Herb. 1: 304 (1895)
Drymaria sessilifolia Fiori Anal. Bot. Fieni Imp. (VIII Congr. Internaz. Agric. Trop. e Subtrop. IV-A, No.(92)) : 20 (1939)
Holosteum cordatum L. Sp. Pl. : 88 (1753)
Holosteum diandrum Sw. Prodr. Veg. Ind. Occ. : 27 (1788)
Stellaria adenophora (Urb.) León Contr. Ocas. Mus. Hist. Nat. Colegio "De La Salle" 9: 4 (1950)

Common names Top

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Language Common/alternative name
English whitesnow
Malayalam പിപ്പിലി
Chinese 二蕊荷莲豆草（荷莲豆）
Chinese 荷莲豆草
Chinese 荷莲豆草（荷莲豆）
Chinese 荷莲豆菜
Chinese 串莲草
Chinese 水荷兰
Chinese 荷莲豆
Chinese 二蕊荷莲豆草
Chinese 荷蓮豆草

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Drymaria cordata subsp. diandra (Blume) J.A.Duke Annals of the Missouri Botanical Garden 48 1961

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

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000657240
Florida Plant Atlas 714
Flora of Alabama 1419
USDA Plants DRCO2
Tropicos 6301172
INPN 447070
KEW urn:lsid:ipni.org:names:30172747-2
The Plant List kew-2778492
Open Tree Of Life 182465
NCBI Taxonomy 191453
Nature Serve 2.137834
IPNI 154112-1
iNaturalist 48556
GBIF 5384509
EPPO DRYCO
EOL 587233
USDA GRIN 14710
Wikipedia Drymaria_cordata
CMAUP NPO27397

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
An ethnobotanical survey on phytomedicines based on traditional knowledge in the Barpeta district, Assam, India Bhattacharjya DK, Akhtar J, Deka P, Bharadwaj A J Ayurveda Integr Med 19-Jul-2023
PMCID:PMC10371788
doi:10.1016/j.jaim.2023.100763
PMID:37478633
Ethnoveterinary practises of medicinal plants used for the treatment of different cattle diseases: A case study in East Khasi Hill district of Meghalaya, North East India Bhat NA, Jeri L, Karmakar D, Mipun P, Bharali P, Sheikh N, Nongkynrih CJ, Kumar Y Heliyon 13-Jul-2023
PMCID:PMC10368863
doi:10.1016/j.heliyon.2023.e18214
PMID:37501975
Important Medicinal and Food Taxa (Orders and Families) in Kenya, Based on Three Quantitative Approaches Mutie FM, Mbuni YM, Rono PC, Mkala EM, Nzei JM, Phumthum M, Hu GW, Wang QF Plants (Basel) 02-Mar-2023
PMCID:PMC10005506
doi:10.3390/plants12051145
PMID:36904005
Diversity, distribution, and sustainability of traditional medicinal plants in Kaski district, western Nepal Khakurel D, Uprety Y, Ahn G, Cha JY, Kim WY, Lee SH, Rajbhandary S Front Pharmacol 20-Dec-2022
PMCID:PMC9807671
doi:10.3389/fphar.2022.1076351
PMID:36605393
A Biocultural Study on Gaoligongshan Pig (Sus scrofa domesticus), an Important Hog Landrace, in Nujiang Prefecture of China Chu Y, Lin C, Cheng Z, Zhao X, Fan Y, Luo B, Long C Biology (Basel) 02-Nov-2022
PMCID:PMC9687789
doi:10.3390/biology11111603
PMID:36358304
Recent Advances on Natural Aryl-C-glycoside Scaffolds: Structure, Bioactivities, and Synthesis—A Comprehensive Review Liu CF Molecules 01-Nov-2022
PMCID:PMC9654268
doi:10.3390/molecules27217439
PMID:36364266
Investigating Potential GLP-1 Receptor Agonists in Cyclopeptides from Pseudostellaria heterophylla, Linum usitatissimum, and Drymaria diandra, and Peptides Derived from Heterophyllin B for the Treatment of Type 2 Diabetes: An In Silico Study Liao HJ, Tzen JT Metabolites 15-Jun-2022
PMCID:PMC9227353
doi:10.3390/metabo12060549
PMID:35736482
The Potential Role of Cyclopeptides from Pseudostellaria heterophylla, Linum usitatissimum and Drymaria diandra, and Peptides Derived from Heterophyllin B as Dipeptidyl Peptidase IV Inhibitors for the Treatment of Type 2 Diabetes: An In Silico Study Liao HJ, Tzen JT Metabolites 24-Apr-2022
PMCID:PMC9146144
doi:10.3390/metabo12050387
PMID:35629891
Biosynthetic pathways of triterpenoids and strategies to improve their Biosynthetic Efficiency Noushahi HA, Khan AH, Noushahi UF, Hussain M, Javed T, Zafar M, Batool M, Ahmed U, Liu K, Harrison MT, Saud S, Fahad S, Shu S Plant Growth Regul 31-Mar-2022
PMCID:PMC8969394
doi:10.1007/s10725-022-00818-9
PMID:35382096
Ethnomedicinal study of medicinal plants used by Mizo tribes in Champhai district of Mizoram, India Laldingliani TB, Thangjam NM, Zomuanawma R, Bawitlung L, Pal A, Kumar A J Ethnobiol Ethnomed 24-Mar-2022
PMCID:PMC8944157
doi:10.1186/s13002-022-00520-0
PMID:35331291
Beneficial insects are associated with botanically rich margins with trees on small farms Arnold SE, Elisante F, Mkenda PA, Tembo YL, Ndakidemi PA, Gurr GM, Darbyshire IA, Belmain SR, Stevenson PC Sci Rep 26-Jul-2021
PMCID:PMC8313545
doi:10.1038/s41598-021-94536-3
PMID:34312457
Ethnopharmacological Survey on Treatment of Hypertension by Traditional Healers in Bukavu City, DR Congo Mushagalusa Kasali F, Ahadi Irenge C, Murhula Hamuli P, Birindwa Mulashe P, Murhula Katabana D, Mangambu Mokoso JD, Mpiana PT, Ntokamunda Kadima J Evid Based Complement Alternat Med 09-Jul-2021
PMCID:PMC8289594
doi:10.1155/2021/6684855
PMID:34335835
Medicinal Plants Used for the Treatment of Erectile Dysfunction in Ethiopia: A Systematic Review Asmerom D, Kalay TH, Araya TY, Desta DM, Wondafrash DZ, Tafere GG Biomed Res Int 07-Jun-2021
PMCID:PMC8205584
doi:10.1155/2021/6656406
PMID:34212038
Natural Enemies of Fall Armyworm Spodoptera frugiperda (Lepidoptera: Noctuidae) in Different Agro-Ecologies Abang AF, Nanga SN, Fotso Kuate A, Kouebou C, Suh C, Masso C, Saethre MG, Fiaboe KK Insects 31-May-2021
PMCID:PMC8227933
doi:10.3390/insects12060509
PMID:34072988
Review of Whole Plant Extracts With Activity Against Herpes Simplex Viruses In Vitro and In Vivo Garber A, Barnard L, Pickrell C J Evid Based Integr Med 16-Feb-2021
PMCID:PMC7894602
doi:10.1177/2515690X20978394
PMID:33593082

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 / Indolonaphthyridine alkaloids
Drimaritin 3012902 Click to see COC1=CN2C3=CC=CC=C3C4=C2C(=NC=C4)C1=O 250.25 unknown https://doi.org/10.1021/NP0400196
> 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 https://doi.org/10.1021/NP0400196
> Lipids and lipid-like molecules / Glycerolipids / Monoradylglycerols / Monoacylglycerols / 1-monoacylglycerols
[(2R)-2,3-dihydroxypropyl] tetracosanoate 163004763 Click to see CCCCCCCCCCCCCCCCCCCCCCCC(=O)OCC(CO)O 442.70 unknown https://doi.org/10.1021/NP0400196
2,3-Dihydroxypropyl tetracosanoate 14542801 Click to see CCCCCCCCCCCCCCCCCCCCCCCC(=O)OCC(CO)O 442.70 unknown https://doi.org/10.1021/NP0400196
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
Panduratin H 24864449 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)OC)C2=CC=CC=C2 298.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
[(2R)-7-Hydroxy-5-methoxy-2-methyl-2-(4-methyl-3-pentenyl)-2H-1-benzopyran-8-yl][(1R,2S,6R)-3-methyl-2-(3-methyl-2-butenyl)-6-phenyl-3-cyclohexenyl]methanone 101855692 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C3C(=C(C=C2O)OC)C=CC(O3)(C)CCC=C(C)C)C4=CC=CC=C4 540.70 unknown via CMAUP database
[(2S)-7-Hydroxy-5-methoxy-2-methyl-2-(4-methyl-3-pentenyl)-2H-1-benzopyran-8-yl][(1R,2S,6R)-3-methyl-2-(3-methyl-2-butenyl)-6-phenyl-3-cyclohexenyl]methanone 101855694 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C3C(=C(C=C2O)OC)C=CC(O3)(C)CCC=C(C)C)C4=CC=CC=C4 540.70 unknown via CMAUP database
Panduratin D 24864268 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C3C(=C(C=C2O)OC)C=CO3)C4=CC=CC=C4 430.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
3beta-[(6-Deoxy-beta-D-glucopyranosyl)oxy]-27-norolean-13-en-28-oic acid beta-D-glucopyranosyl ester 21625902 Click to see CC1C(C(C(C(O1)OC2CCC3(C4CCC5=C(C4(CCC3C2(C)C)C)CCC6(C5CC(CC6)(C)C)C(=O)OC7C(C(C(C(O7)CO)O)O)O)C)O)O)O 751.00 unknown via CMAUP database
Uncariaside A 102480386 Click to see CC1CCC2(CCC3=C(C2C1C)C(=O)CC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)CO)O)O)O)C)C)C(=O)OC7C(C(C(C(O7)CO)O)O)O 780.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
3-Oxo-22alpha-hydroxyurs-12-ene-27,28-dioic acid 102480385 Click to see CC1CC(C2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1C)C(=O)O)C(=O)O)O 500.70 unknown via CMAUP database
3beta,13beta-Dihydroxy-27-noroleana-28-oic acid 28,13-lactone 102480384 Click to see CC1(CCC23CCC4C5(CCC6C(C(CCC6(C5CCC4(C2C1)OC3=O)C)O)(C)C)C)C 442.70 unknown via CMAUP database
Quinovic acid 120678 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C(=O)O)C(=O)O 486.70 unknown via CMAUP database
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
2-[[17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 73157301 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 574.80 unknown https://doi.org/10.1021/NP0400196
alpha-Spinasterol glucoside 12960505 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 574.80 unknown https://doi.org/10.1021/NP0400196
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 via CMAUP database
> Organic acids and derivatives / Keto acids and derivatives / Gamma-keto acids and derivatives
Methyl 5-hydroxy-4-oxopentanoate 10464455 Click to see COC(=O)CCC(=O)CO 146.14 unknown https://doi.org/10.1021/NP0400196
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
3beta-Hydroxy-27-norolean-13-en-28-oic acid ethyl ester 101682287 Click to see CCOC(=O)C12CCC3=C(C1CC(CC2)(C)C)CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C 470.70 unknown via CMAUP database
Pyrocincholic acid 12314810 Click to see CC1(CCC2(CCC3=C(C2C1)CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C(=O)O)C 442.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1S,3R,4R,5S)-3-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy-1,4,5-trihydroxycyclohexane-1-carboxylic acid 7067333 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde 126 Click to see C1=CC(=CC=C1C=O)O 122.12 unknown https://doi.org/10.1021/NP0400196
p-Hydroxybenzaldehyde-d5 10701848 Click to see C1=CC(=CC=C1C=O)O 127.15 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
Panduratin E 24864269 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C3C(=C(C=C2O)OC)C=CC(O3)(C)C)C4=CC=CC=C4 472.60 unknown via CMAUP database
> Organoheterocyclic compounds / Indolizidines
Mitraphylline 94160 Click to see CC1C2CN3CCC4(C3CC2C(=CO1)C(=O)OC)C5=CC=CC=C5NC4=O 368.40 unknown via CMAUP database
Uncarine A 188999 Click to see CC1C2CN3CCC4(C3CC2C(=CO1)C(=O)OC)C5=CC=CC=C5NC4=O 368.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
(-)-nicolaioidesin B 637029 Click to see CC1=CCC(C(C1CC=C(C)C)C2=CC=CC=C2)C(=O)C3=C(C=C(C=C3O)OC)O 406.50 unknown via CMAUP database
(1'R,2'S,6'R)-2-Hydroxyisopanduratin A 23656472 Click to see CC1=CCC(C(C1CC=C(C)C)C2=CC=CC=C2)C(=O)C3=C(C=C(C=C3O)O)O 392.50 unknown via CMAUP database
(2-hydroxy-4,6-dimethoxyphenyl)-[(1R,2S,6R)-3-methyl-2-(3-methylbut-2-enyl)-6-phenylcyclohex-3-en-1-yl]methanone 44444916 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C(C=C2OC)OC)O)C3=CC=CC=C3 420.50 unknown via CMAUP database
2,6-Dihydroxy-4-methoxyphenyl[2beta-(3-methyl-2-butenyl)-3-methyl-6alpha-phenyl-3-cyclohexene-1beta-yl]methanone 25023021 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C(C=C2O)OC)O)C3=CC=CC=C3 406.50 unknown via CMAUP database
4-hydroxypanduratin A 636530 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C(C=C2O)O)O)C3=CC=CC=C3 392.50 unknown via CMAUP database
Isopanduratin A 10069916 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C(C=C2OC)O)O)C3=CC=CC=C3 406.50 unknown via CMAUP database
Isopanduratin A1 44444913 Click to see CC1=CCC(C(C1CC=C(C)C)C2=CC=CC=C2)C(=O)C3=C(C=C(C=C3OC)O)O 406.50 unknown via CMAUP database
Panduratin A 6483648 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C(C=C2O)OC)O)C3=CC=CC=C3 406.50 unknown via CMAUP database
Panduratin C 6483647 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C(C=C2OC)O)O)C3=CC=C(C=C3)O 422.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans / 6-prenylated flavanones
(2S)-6-geranylpinostrobin 44444914 Click to see CC(=CCCC(=CCC1=C(C=C2C(=C1O)C(=O)CC(O2)C3=CC=CC=C3)OC)C)C 406.50 unknown via CMAUP database
2alpha-Phenyl-6-[(E)-3,7-dimethyl-2,6-octadienyl]-2,3-dihydro-5,7-dihydroxy-4H-1-benzopyran-4-one 44444915 Click to see CC(=CCCC(=CCC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC=CC=C3)O)C)C 392.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(2R)-8-geranylpinostrobin 23656470 Click to see CC(=CCCC(=CCC1=C(C=C(C2=C1OC(CC2=O)C3=CC=CC=C3)O)OC)C)C 406.50 unknown via CMAUP database
> 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 / Flavonoid glycosides / Flavonoid C-glycosides
6-(4,5-Dihydroxy-6-methyloxan-2-yl)-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 14445194 Click to see CC1C(C(CC(O1)C2=C(C3=C(C=C2O)OC(=CC3=O)C4=CC=C(C=C4)O)O)O)O 400.40 unknown https://doi.org/10.1021/NP0400196
6-[(2R,4R,5R,6R)-4,5-dihydroxy-6-methyloxan-2-yl]-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 14445195 Click to see CC1C(C(CC(O1)C2=C(C3=C(C=C2O)OC(=CC3=O)C4=CC=C(C=C4)O)O)O)O 400.40 unknown https://doi.org/10.1021/NP0400196
6-beta-D-Glucopyranosyl-4',5,7-trihydroxyflavone 44257794 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown via CMAUP database
Torosaflavone A 44257658 Click to see CC1C(C(CC(O1)C2=C(C3=C(C=C2O)OC(=CC3=O)C4=CC=C(C=C4)O)O)O)O 400.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
6-(4,5-Dihydroxy-6-methyloxan-2-yl)-5-hydroxy-7-methoxy-2-[4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one 73804419 Click to see CC1C(C(CC(O1)C2=C(C=C3C(=C2O)C(=O)C=C(O3)C4=CC=C(C=C4)OC5C(C(C(C(O5)CO)O)O)O)OC)O)O 576.50 unknown https://doi.org/10.1021/NP0400196
6-[(2R,4R,5R,6R)-4,5-dihydroxy-6-methyloxan-2-yl]-5-hydroxy-7-methoxy-2-[4-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one 162937179 Click to see CC1C(C(CC(O1)C2=C(C=C3C(=C2O)C(=O)C=C(O3)C4=CC=C(C=C4)OC5C(C(C(C(O5)CO)O)O)O)OC)O)O 576.50 unknown https://doi.org/10.1021/NP0400196
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyl-tetrahydropyran-2-yl]oxy-chromen-4-one 15939939 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown via CMAUP database
5,7-dihydroxy-2-(4-hydroxyphenyl)-3-((2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yloxy)-4H-chromen-4-one 5318763 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O 432.40 unknown via CMAUP database
Hyperoside 5281643 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 via CMAUP database
Quercetin-3-o-rutinose 46936193 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 via CMAUP database
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 via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
(S)-7-(((2-O-6-Deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranosyl)oxy)-2,3-dihydro-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-4H-1-benzopyran-4-one 442439 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC(=C(C=C5)OC)O)O)CO)O)O)O)O)O 610.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 5-O-methylated flavonoids
5-O-Methylnaringenin 182315 Click to see COC1=CC(=CC2=C1C(=O)CC(O2)C3=CC=C(C=C3)O)O 286.28 unknown via CMAUP database
Alpinetin 154279 Click to see COC1=CC(=CC2=C1C(=O)CC(O2)C3=CC=CC=C3)O 270.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(2R)-5,7-Dimethoxyflavanone 689012 Click to see COC1=CC2=C(C(=O)CC(O2)C3=CC=CC=C3)C(=C1)OC 284.31 unknown via CMAUP database
(2S)-5,7-dimethoxy-2-phenyl-3,4-dihydro-2H-1-benzopyran-4-one 689011 Click to see COC1=CC2=C(C(=O)CC(O2)C3=CC=CC=C3)C(=C1)OC 284.31 unknown via CMAUP database
3,5,7-Trimethoxyflavone 117900 Click to see COC1=CC2=C(C(=C1)OC)C(=O)C(=C(O2)C3=CC=CC=C3)OC 312.30 unknown via CMAUP database
3',4',5,7-Tetramethoxyflavone 631170 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C=C3OC)OC)OC 342.30 unknown via CMAUP database
4H-1-Benzopyran-4-one, 5-hydroxy-3,7-dimethoxy-2-phenyl- 5748697 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC=CC=C3)O 298.29 unknown via CMAUP database
5-Hydroxy-7-methoxy-2-phenylchroman-4-one 73201 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)O 270.28 unknown via CMAUP database
5,7-Dimethoxyflavone 88881 Click to see COC1=CC2=C(C(=C1)OC)C(=O)C=C(O2)C3=CC=CC=C3 282.29 unknown via CMAUP database
Apigenin 7,4'-dimethyl ether 5281601 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC)O 298.29 unknown via CMAUP database
Apigenin trimethyl ether 79730 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C=C3OC)OC 312.30 unknown via CMAUP database
Kaempferol 3,7,4'-trimethyl ether 5468749 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)OC 328.30 unknown via CMAUP database
Pinostrobin 6950539 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)O 270.28 unknown via CMAUP database
Quercetin pentamethyl ether 97332 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(O2)C=C(C=C3OC)OC)OC)OC 372.40 unknown via CMAUP database
Retusin 5352005 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)OC)OC 358.30 unknown via CMAUP database
Sakuranetin 73571 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O 286.28 unknown via CMAUP database
Tectochrysin 5281954 Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC=CC=C3)O 268.26 unknown via CMAUP database
Tetramethylkaempferol 631095 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(O2)C=C(C=C3OC)OC)OC 342.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Kavalactones
2H-Pyran-2-one, 4-methoxy-6-(2-phenylethyl)- 160673 Click to see COC1=CC(=O)OC(=C1)CCC2=CC=CC=C2 230.26 unknown via CMAUP database
Demethoxyyangonin 5273621 Click to see COC1=CC(=O)OC(=C1)C=CC2=CC=CC=C2 228.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
4,2',4'-Trihydroxy-6'-methoxydihydrochalcone 42607705 Click to see COC1=CC(=CC(=C1C(=O)CCC2=CC=C(C=C2)O)O)O 288.29 unknown via CMAUP database
Phloretin 4788 Click to see C1=CC(=CC=C1CCC(=O)C2=C(C=C(C=C2O)O)O)O 274.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
(E)-1-[(1R,4S,13R)-9-hydroxy-1,5,5-trimethyl-6,15-dioxatetracyclo[9.3.1.04,13.07,12]pentadeca-7,9,11-trien-8-yl]-3-phenylprop-2-en-1-one 101306880 Click to see CC1(C2CCC3(CC2C4=C(O3)C=C(C(=C4O1)C(=O)C=CC5=CC=CC=C5)O)C)C 390.50 unknown via CMAUP database
2',4-Dihydroxy-4',6'-dimethoxychalcone 6293081 Click to see COC1=CC(=C(C(=C1)OC)C(=O)C=CC2=CC=C(C=C2)O)O 300.30 unknown via CMAUP database
Cardamonin 641785 Click to see COC1=CC(=CC(=C1C(=O)C=CC2=CC=CC=C2)O)O 270.28 unknown via CMAUP database
CID 460718 460718 Click to see C1=CC=C(C=C1)C=CC(=O)C2=C(C=C(C=C2O)O)O 256.25 unknown via CMAUP database
Helichrysetin 6253344 Click to see COC1=CC(=CC(=C1C(=O)C=CC2=CC=C(C=C2)O)O)O 286.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 3-prenylated chalcones
2',4'-Dihydroxy-3'-[(2E)-3,7-dimethyl-2,6-octadienyl]-6'-methoxychalcone 23656471 Click to see CC(=CCCC(=CCC1=C(C(=C(C=C1O)OC)C(=O)C=CC2=CC=CC=C2)O)C)C 406.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
2,4-Dihydroxy-6-phenethylbenzoic acid (2E)-3,7-dimethyl-2,6-octadienyl ester 23656469 Click to see CC(=CCCC(=CCOC(=O)C1=C(C=C(C=C1O)O)CCC2=CC=CC=C2)C)C 394.50 unknown via CMAUP database

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