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Muscari armeniacum

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID64401d2308244442564306
Scientific name Muscari armeniacum
Authority H.J.Veitch
First published in Garden (London, 1871-1927) 1: 687. 1872

Ethnobotanical Use Top

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General Uses Top

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Common products:
Ornamental cut flower and potted plant; no non-medicinal, commercial, industrial, or scientific/model-organism uses are reported for Muscari armeniacum.


Common products:
Ornamental cut flower and potted plant; no non-medicinal, commercial, industrial, or scientific/model-organism uses are reported for Muscari armeniacum.

Synonyms Top

Scientific name Authority First published in
Muscari alexandrae A.P.Khokhr. Byull. Moskovsk. Obshch. Isp. Prir., Otd. Biol. , n.s., 96(4): 106 (1991)
Muscari woronowii Tron & Losinsk. Fl. URSS 4: 744 (1935)
Muscari conicum Baker Gard. Chron. , n.s., 9: 799 (1878)
Muscari concinnum Baker Gard. Chron. , n.s., 9: 799 (1878)
Muscari colchicum Grossh. Trudy Azerbaidzhansk. Otd. Zakavkazsk. Fil. Akad. Nauk S.S.S.R. 1: 50 (1933)
Muscari elegantulum Schchian Zametki Sist. Geogr. Rast. 17: 114 (1953)
Muscari cyaneo-violaceum Turrill Bot. Mag. 157: t. 9372 (1934)
Muscari apertum Freyn & Conrath Bull. Herb. Boissier 4: 194 (1896)
Muscari pyramidatum Velen. Fl. Bulg. : 556 (1891)
Muscari schliemanni Freyn & Asch. Flora 68: 6 (1885)
Muscari polyanthum Boiss. Fl. Orient. 5: 297 (1882)
Muscari pauperulum Stapf Denkschr. Kaiserl. Akad. Wiss., Wien. Math.-Naturwiss. Kl. 50: 78 (1885)
Muscari pendulum Trautv. Trudy Imp. S.-Peterburgsk. Bot. Sada 2: 484 (1873)
Muscari szovitsianum Baker Gard. Chron. , n.s., 9: 799 (1878)
Muscari micranthum Baker Gard. Chron. , n.s., 9: 799 (1878)
Muscari maweanum Baker Gard. Chron. , ser. 3, 5: 648 (1889)
Pseudomuscari apertum (Freyn & Conrath) Garbari Atti Soc. Tosc. Sci. Nat. Pisa, Mem. 77: 112 (1970 publ. 1971)
Bellevalia aperta (Freyn & Conrath) Grossh. Fl. Kavkaza 1: 233 (1928)
Botryanthus micranthus Baker Gard. Chron. , n.s., 9: 799 (1878)
Botryanthus szovitsianus Baker Gard. Chron. , n.s., 9: 799 (1878)
Muscari sosnowskyi Schchian Trudy Tbilissk. Bot. Inst. 10: 224 (1946)
Muscari argaei f. album Tubergen Cat. 1935: ? 1935
Muscari argaei auct. Gard. Chron. n.s., 20: 394 1883

Common names Top

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Language Common/alternative name
English armenian grape hyacinth
Arabic بلبوس أرمني
Azerbaijani erməni ilansoğanı
Azerbaijani qəşəng gəmirici soğanı
Czech modřenec arménský
Welsh clychau dulas yr ardd
German armenische traubenhyazinthe
German armenisches träubel
Persian کلاغک ارمنی
Finnish helmihyasintti
Finnish tummahelmililja
Upper Sorbian armenska kitelnička
Armenian պապլոր հայկական
hyw Հայկական Յակինթ
Japanese ブドウムスカリ
Georgian სომხური ყაზახა
Latvian armēnijas muskare
Dutch langbladige druifhyacint
Norwegian Nynorsk krukkeperleblom
Polish szafirek armeński
Russian Мускари армянский
Russian мышиный гиацинт армянский
Russian гадючий лук армянский
Slovak modrica arménska
Slovenian armenska hrušica
Swedish armenisk pärlhyacint
Chinese 亚美尼亚蓝壶花

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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Expose seeds to natural outdoor winter conditions for 3 months, then gradually increase light and temperature in the spring.
grow seedlings at cool temperature - best achieved by sowing in open ground

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-0000694251
Canadensys 2742
USDA Plants MUAR5
Tropicos 18405267
INPN 108866
Flora of Italy 6869
KEW urn:lsid:ipni.org:names:538447-1
The Plant List kew-281679
Missouri Botanical Garden 282356
Open Tree Of Life 243513
Observations.org 7070
NCBI Taxonomy 156613
NBN Atlas NBNSYS0000004651
Nature Serve 2.144836
IPNI 538447-1
iNaturalist 57847
GBIF 2772174
Freebase /m/03gr41y
EPPO MUSAR
EOL 1003992
USDA GRIN 24749
Wikipedia Muscari_armeniacum
KEW urn:lsid:ipni.org:names:77306704-1
IPNI 77306704-1

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
Antifungal Activity of Ribosome-Inactivating Proteins Iglesias R, Citores L, Gay CC, Ferreras JM Toxins (Basel) 15-Apr-2024
PMCID:PMC11054410
doi:10.3390/toxins16040192
PMID:38668617
Selection and Validation of qRT-PCR Internal Reference Genes to Study Flower Color Formation in Camellia impressinervis Zhang P, Chen S, Chen S, Zhu Y, Lin Y, Xu X, Liu Z, Zou S Int J Mol Sci 06-Mar-2024
PMCID:PMC10932070
doi:10.3390/ijms25053029
PMID:38474274
Cloning, Expression, and Functional Analysis of the MYB Transcription Factor SlMYB86-like in Tomato Chen N, Zhan W, Shao Q, Liu L, Lu Q, Yang W, Que Z Plants (Basel) 08-Feb-2024
PMCID:PMC10893056
doi:10.3390/plants13040488
PMID:38498460
Transcriptomic and metabolic analysis unveils the mechanism behind leaf color development in Disanthus cercidifolius var. longipes Tian X, Xiang G, Lv H, Zhu L, Peng J, Li G, Mou C Front Mol Biosci 06-Feb-2024
PMCID:PMC10876866
doi:10.3389/fmolb.2024.1343123
PMID:38380429
Identification of HpMYB1 inducing anthocyanin accumulation in Hippeastrum Hybridum tepals by RNA-seq Li J, Wu K, Li L, Ma G, Fang L, Zeng S BMC Plant Biol 28-Nov-2023
PMCID:PMC10683291
doi:10.1186/s12870-023-04582-4
PMID:38012575
Spiro-Flavonoids in Nature: A Critical Review of Structural Diversity and Bioactivity Pecio Ł, Pecio S, Mroczek T, Oleszek W Molecules 14-Jul-2023
PMCID:PMC10385819
doi:10.3390/molecules28145420
PMID:37513292
Emerging Plant Intoxications in Domestic Animals: A European Perspective Nagy AL, Ardelean S, Chapuis RJ, Bouillon J, Pivariu D, Dreanca AI, Caloni F Toxins (Basel) 04-Jul-2023
PMCID:PMC10467095
doi:10.3390/toxins15070442
PMID:37505711
Toxicity of House Plants to Pet Animals Siroka Z Toxins (Basel) 19-May-2023
PMCID:PMC10220692
doi:10.3390/toxins15050346
PMID:37235380
Regulatory network characterization of anthocyanin metabolites in purple sweetpotato via joint transcriptomics and metabolomics Xiao J, Xu X, Li M, Wu X, Guo H Front Plant Sci 09-Feb-2023
PMCID:PMC9951203
doi:10.3389/fpls.2023.1030236
PMID:36844045
Overexpression of a Senescence-Related Gene CpSRG1 from Wintersweet (Chimonanthus praecox) Promoted Growth and Flowering, and Delayed Senescence in Transgenic Arabidopsis Cao Y, Li G, Wang X, Huang R, Luo J, Li M, Liu D, Sui S Int J Mol Sci 12-Nov-2022
PMCID:PMC9696086
doi:10.3390/ijms232213971
PMID:36430449
ZeMYB9 regulates cyanidin synthesis by activating the expression of flavonoid 3′-hydroxylase gene in Zinnia elegans Qian J, Jiang L, Qing H, Chen J, Wan Z, Xu M, Fu J, Zhang C Front Plant Sci 18-Oct-2022
PMCID:PMC9623174
doi:10.3389/fpls.2022.981086
PMID:36330274
Transcriptional regulation of proanthocyanidin biosynthesis pathway genes and transcription factors in Indigofera stachyodes Lindl. roots Wang C, Li J, Zhou T, Zhang Y, Jin H, Liu X BMC Plant Biol 13-Sep-2022
PMCID:PMC9469613
doi:10.1186/s12870-022-03794-4
PMID:36096752
Systematic Analysis and Functional Characterization of R2R3-MYB Genes in Scutellaria baicalensis Georgi Wang W, Hu S, Zhang C, Yang J, Zhang T, Wang D, Cao X, Wang Z Int J Mol Sci 19-Aug-2022
PMCID:PMC9408826
doi:10.3390/ijms23169342
PMID:36012606
AcMYB1 Interacts With AcbHLH1 to Regulate Anthocyanin Biosynthesis in Aglaonema commutatum Li J, Wu K, Li L, Ma G, Fang L, Zeng S Front Plant Sci 19-Jul-2022
PMCID:PMC9344012
doi:10.3389/fpls.2022.886313
PMID:35928704
The chemistry and biology of natural ribomimetics and related compounds Tsunoda T, Tanoeyadi S, Proteau PJ, Mahmud T RSC Chem Biol 07-Apr-2022
PMCID:PMC9092360
doi:10.1039/d2cb00019a
PMID:35656477

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
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,3'R,4S,5R,10S,13S,14S,17S)-3-[(2R,3R,4S,5S,6R)-6-[[(2S,3R,4S,5S)-3-[(2S,3R,4S,5R,6R)-4-[(2S,3R,4S,5S)-3-[(2S,3S,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-5-hydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-4-(hydroxymethyl)-3',4,10,13,14-pentamethyl-5'-propanoylspiro[2,3,5,6,7,11,12,16-octahydro-1H-cyclopenta[a]phenanthrene-17,2'-oxolane]-15-one 101791883 Click to see CCC(=O)C1CC(C2(O1)CC(=O)C3(C2(CCC4=C3CCC5C4(CCC(C5(C)CO)OC6C(C(C(C(O6)COC7C(C(C(CO7)O)O)OC8C(C(C(C(O8)CO)O)OC9C(C(C(CO9)O)O)OC1C(C(C(O1)CO)O)O)OC1C(C(C(C(O1)C)O)O)O)O)O)O)C)C)C)C 1339.40 unknown https://doi.org/10.1139/V88-430
(3S,3'R,4S,5R,5'S,10S,13S,14S,17S)-3-[(2R,3R,4S,5S,6R)-6-[[(2S,3R,4S,5S)-3-[(2S,3R,4S,5R,6R)-4-[(2S,3R,4S,5S)-4,5-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-4-(hydroxymethyl)-3',4,10,13,14-pentamethyl-5'-propanoylspiro[2,3,5,6,7,11,12,16-octahydro-1H-cyclopenta[a]phenanthrene-17,2'-oxolane]-15-one 162884282 Click to see CCC(=O)C1CC(C2(O1)CC(=O)C3(C2(CCC4=C3CCC5C4(CCC(C5(C)CO)OC6C(C(C(C(O6)COC7C(C(C(CO7)O)O)OC8C(C(C(C(O8)CO)O)OC9C(C(C(CO9)O)O)OC1C(C(C(C(O1)CO)O)O)O)OC1C(C(C(C(O1)C)O)O)O)O)O)O)C)C)C)C 1369.40 unknown https://doi.org/10.1139/V88-430
(3S,3'R,4S,5R,5'S,10S,13S,14S,17S)-3-[(2R,3R,4S,5S,6R)-6-[[(2S,3R,4S,5S)-4,5-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-4-(hydroxymethyl)-3',4,10,13,14-pentamethyl-5'-propanoylspiro[2,3,5,6,7,11,12,16-octahydro-1H-cyclopenta[a]phenanthrene-17,2'-oxolane]-15-one 163011905 Click to see CCC(=O)C1CC(C2(O1)CC(=O)C3(C2(CCC4=C3CCC5C4(CCC(C5(C)CO)OC6C(C(C(C(O6)COC7C(C(C(CO7)O)O)OC8C(C(C(C(O8)CO)O)O)O)O)O)O)C)C)C)C 929.10 unknown https://doi.org/10.1139/V88-430
(3S,3'R,4S,5R,5'S,10S,13S,14S,17S)-4-(hydroxymethyl)-3',4,10,13,14-pentamethyl-5'-propanoyl-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyspiro[2,3,5,6,7,11,12,16-octahydro-1H-cyclopenta[a]phenanthrene-17,2'-oxolane]-15-one 163195135 Click to see CCC(=O)C1CC(C2(O1)CC(=O)C3(C2(CCC4=C3CCC5C4(CCC(C5(C)CO)OC6C(C(C(C(O6)CO)O)O)O)C)C)C)C 634.80 unknown https://doi.org/10.1139/V88-430
1-[(2'S,3S,4'R,5R,10S,13S,14S,17S)-3-[(2R,3R,4S,5S,6R)-6-[[(2S,3R,4S,5S)-4,5-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-4,4-bis(hydroxymethyl)-4',10,13,14-tetramethylspiro[1,2,3,5,6,7,11,12,15,16-decahydrocyclopenta[a]phenanthrene-17,5'-oxolane]-2'-yl]propan-1-one 163011686 Click to see 931.10 unknown https://doi.org/10.1139/V88-430
1-[(2'S,3S,4'R,5R,10S,13S,14S,17S)-4,4-bis(hydroxymethyl)-4',10,13,14-tetramethyl-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyspiro[1,2,3,5,6,7,11,12,15,16-decahydrocyclopenta[a]phenanthrene-17,5'-oxolane]-2'-yl]propan-1-one 162888244 Click to see CCC(=O)C1CC(C2(O1)CCC3(C2(CCC4=C3CCC5C4(CCC(C5(CO)CO)OC6C(C(C(C(O6)CO)O)O)O)C)C)C)C 636.80 unknown https://doi.org/10.1139/V88-430
1-[3-[6-[[4,5-Dihydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-4,4-bis(hydroxymethyl)-4',10,13,14-tetramethylspiro[1,2,3,5,6,7,11,12,15,16-decahydrocyclopenta[a]phenanthrene-17,5'-oxolane]-2'-yl]propan-1-one 14263465 Click to see 931.10 unknown https://doi.org/10.1139/V88-430
1-[4,4-Bis(hydroxymethyl)-4',10,13,14-tetramethyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyspiro[1,2,3,5,6,7,11,12,15,16-decahydrocyclopenta[a]phenanthrene-17,5'-oxolane]-2'-yl]propan-1-one 14263467 Click to see 636.80 unknown https://doi.org/10.1139/V88-430
3-[6-[[3-[4-[4,5-dihydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-4-(hydroxymethyl)-3',4,10,13,14-pentamethyl-5'-propanoylspiro[2,3,5,6,7,11,12,16-octahydro-1H-cyclopenta[a]phenanthrene-17,2'-oxolane]-15-one 14263448 Click to see 1369.40 unknown https://doi.org/10.1139/V88-430
3-[6-[[4,5-dihydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-4-(hydroxymethyl)-3',4,10,13,14-pentamethyl-5'-propanoylspiro[2,3,5,6,7,11,12,16-octahydro-1H-cyclopenta[a]phenanthrene-17,2'-oxolane]-15-one 14263459 Click to see 929.10 unknown https://doi.org/10.1139/V88-430
4-(hydroxymethyl)-3',4,10,13,14-pentamethyl-5'-propanoyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyspiro[2,3,5,6,7,11,12,16-octahydro-1H-cyclopenta[a]phenanthrene-17,2'-oxolane]-15-one 14263457 Click to see CCC(=O)C1CC(C2(O1)CC(=O)C3(C2(CCC4=C3CCC5C4(CCC(C5(C)CO)OC6C(C(C(C(O6)CO)O)O)O)C)C)C)C 634.80 unknown https://doi.org/10.1139/V88-430
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2R,3R,4S,5S,6R)-2-[(2S)-2-[(2S,3S,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)pyrrolidin-2-yl]-2-hydroxyethoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162959756 Click to see 355.34 unknown https://doi.org/10.1016/S0957-4166(99)00508-X
(2S,3S,4S,5R)-2-[(1S)-2-[(2R,3R,4S)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-1-hydroxyethyl]-5-(hydroxymethyl)pyrrolidine-3,4-diol 162973395 Click to see 325.31 unknown https://doi.org/10.1016/S0957-4166(99)00508-X
2-[2-[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-1-hydroxyethyl]-5-(hydroxymethyl)pyrrolidine-3,4-diol 162973393 Click to see 325.31 unknown https://doi.org/10.1016/S0957-4166(99)00508-X
2-[2-[3,4-Dihydroxy-5-(hydroxymethyl)pyrrolidin-2-yl]-2-hydroxyethoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162959755 Click to see 355.34 unknown https://doi.org/10.1016/S0957-4166(99)00508-X
> Organoheterocyclic compounds / Pyrrolidines
(2S,3S,4S,5R)-2-(2-hydroxyethyl)-5-(hydroxymethyl)pyrrolidine-3,4-diol 131170181 Click to see 177.20 unknown https://doi.org/10.1016/S0957-4166(99)00508-X
(2S,3S,4S,5R)-2-[(1R)-1,2-dihydroxyethyl]-5-(hydroxymethyl)pyrrolidine-3,4-diol 163012006 Click to see 193.20 unknown https://doi.org/10.1016/S0957-4166(99)00508-X
2-(1,2-Dihydroxyethyl)-5-(hydroxymethyl)pyrrolidine-3,4-diol 15953622 Click to see 193.20 unknown https://doi.org/10.1016/S0957-4166(99)00508-X
2-(2-Hydroxyethyl)-5-(hydroxymethyl)pyrrolidine-3,4-diol 75055082 Click to see 177.20 unknown https://doi.org/10.1016/S0957-4166(99)00508-X
> Organoheterocyclic compounds / Pyrrolizidines
(1R,2R,3R,5R,8R)-3-(hydroxymethyl)-5-methyl-2,3,5,6,7,8-hexahydro-1H-pyrrolizine-1,2-diol 10465065 Click to see CC1CCC2N1C(C(C2O)O)CO 187.24 unknown https://doi.org/10.1016/S0957-4166(99)00508-X
1,2-Dihydroxy-3-hydroxymethylpyrrolizidine 72760523 Click to see 173.21 unknown https://doi.org/10.1016/S0957-4166(99)00508-X
3-(hydroxymethyl)-5-methyl-2,3,5,6,7,8-hexahydro-1H-pyrrolizine-1,2-diol 20979902 Click to see 187.24 unknown https://doi.org/10.1016/S0957-4166(99)00508-X
3-(hydroxymethyl)-5-methyl-2,3,5,6,7,8-hexahydro-1H-pyrrolizine-1,2,6,7-tetrol 73316637 Click to see CC1C(C(C2N1C(C(C2O)O)CO)O)O 219.23 unknown https://doi.org/10.1016/S0957-4166(99)00508-X
3-(hydroxymethyl)-5-methyl-2,3,5,6,7,8-hexahydro-1H-pyrrolizine-1,2,7-triol 67191714 Click to see 203.24 unknown https://doi.org/10.1016/S0957-4166(99)00508-X
Hyacinthacine A1 10080851 Click to see 173.21 unknown https://doi.org/10.1016/S0957-4166(99)00508-X
Hyacinthacine A2 10012388 Click to see 173.21 unknown https://doi.org/10.1016/S0957-4166(99)00508-X
Hyacinthacine B3 10262292 Click to see 203.24 unknown https://doi.org/10.1016/S0957-4166(99)00508-X
Hyacinthacine C4 10608892 Click to see 219.23 unknown https://doi.org/10.1016/S0957-4166(99)00508-X
> Phenylpropanoids and polyketides / Homoisoflavonoids / Homoisoflavans / Homoisoflavanones
(3S)-3-[(3,4-dihydroxyphenyl)methyl]-5,7-dihydroxy-2,3-dihydrochromen-4-one 132988050 Click to see 302.28 unknown https://doi.org/10.1016/S0031-9422(00)81529-0
(3S)-3-[(3,4-dihydroxyphenyl)methyl]-5,7-dihydroxy-6-methoxy-2,3-dihydrochromen-4-one 102477546 Click to see 332.30 unknown https://doi.org/10.1016/S0031-9422(00)81529-0
(3S)-3-[(3,4-dihydroxyphenyl)methyl]-5,8-dihydroxy-7-methoxy-2,3-dihydrochromen-4-one 163025027 Click to see 332.30 unknown https://doi.org/10.1016/S0031-9422(00)81529-0
(3S)-3-[(3,4-dihydroxyphenyl)methyl]-7-hydroxy-5-methoxy-2,3-dihydrochromen-4-one 162857153 Click to see COC1=CC(=CC2=C1C(=O)C(CO2)CC3=CC(=C(C=C3)O)O)O 316.30 unknown https://doi.org/10.1016/S0031-9422(00)81529-0
(3S)-5,7-dihydroxy-3-[(3-hydroxy-4-methoxyphenyl)methyl]-6-methoxy-2,3-dihydrochromen-4-one 162921321 Click to see 346.30 unknown https://doi.org/10.1016/S0031-9422(00)81529-0
(3S)-5,7-dihydroxy-3-[(4-hydroxy-3-methoxyphenyl)methyl]-6-methoxy-2,3-dihydrochromen-4-one 162883296 Click to see 346.30 unknown https://doi.org/10.1016/S0031-9422(00)81529-0
(3S)-7-hydroxy-3-[(3-hydroxy-4-methoxyphenyl)methyl]-5-methoxy-2,3-dihydrochromen-4-one 162876251 Click to see 330.30 unknown https://doi.org/10.1016/S0031-9422(00)81529-0
3-(3,4-Dihydroxybenzyl)-7-hydroxy-5-methoxy-4-chromanone 21676257 Click to see COC1=CC(=CC2=C1C(=O)C(CO2)CC3=CC(=C(C=C3)O)O)O 316.30 unknown https://doi.org/10.1016/S0031-9422(00)81529-0
3-[(3,4-Dihydroxyphenyl)methyl]-5,7-dihydroxy-2,3-dihydrochromen-4-one 14159175 Click to see 302.28 unknown https://doi.org/10.1016/S0031-9422(00)81529-0
3-[(3,4-Dihydroxyphenyl)methyl]-5,7-dihydroxy-6-methoxy-2,3-dihydrochromen-4-one 14159191 Click to see 332.30 unknown https://doi.org/10.1016/S0031-9422(00)81529-0
3-[(3,4-Dihydroxyphenyl)methyl]-5,8-dihydroxy-7-methoxy-2,3-dihydrochromen-4-one 14159189 Click to see COC1=C(C2=C(C(=C1)O)C(=O)C(CO2)CC3=CC(=C(C=C3)O)O)O 332.30 unknown https://doi.org/10.1016/S0031-9422(00)81529-0
5,7-Dihydroxy-3-[(4-hydroxy-3-methoxyphenyl)methyl]-6-methoxy-2,3-dihydrochromen-4-one 21676259 Click to see 346.30 unknown https://doi.org/10.1016/S0031-9422(00)81529-0
7-Hydroxy-3-(3-hydroxy-4-methoxybenzyl)-5-methoxy-4-chromanone 21676258 Click to see COC1=C(C=C(C=C1)CC2COC3=C(C2=O)C(=CC(=C3)O)OC)O 330.30 unknown https://doi.org/10.1016/S0031-9422(00)81529-0
Cremastranone 21676260 Click to see 346.30 unknown https://doi.org/10.1016/S0031-9422(00)81529-0
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones
(3R)-3',4',5-trihydroxy-7-methoxyspiro[2H-chromene-3,7'-bicyclo[4.2.0]octa-1,3,5-triene]-4-one 162928785 Click to see 314.29 unknown https://doi.org/10.1016/S0031-9422(00)81529-0
(3R)-3',5-dihydroxy-4',7-dimethoxyspiro[2H-chromene-3,7'-bicyclo[4.2.0]octa-1,3,5-triene]-4-one 162984745 Click to see 328.30 unknown https://doi.org/10.1016/S0031-9422(00)81529-0
(3R)-3',5,7-trihydroxy-4'-methoxyspiro[2H-chromene-3,7'-bicyclo[4.2.0]octa-1,3,5-triene]-4-one 122182400 Click to see 314.29 unknown https://doi.org/10.1016/S0031-9422(00)81529-0
3',4',5-trihydroxy-7-methoxyspiro[2H-chromene-3,7'-bicyclo[4.2.0]octa-1,3,5-triene]-4-one 21676262 Click to see COC1=CC(=C2C(=C1)OCC3(C2=O)CC4=CC(=C(C=C34)O)O)O 314.29 unknown https://doi.org/10.1016/S0031-9422(00)81529-0
3',5-dihydroxy-4',7-dimethoxyspiro[2H-chromene-3,7'-bicyclo[4.2.0]octa-1,3,5-triene]-4-one 21676263 Click to see COC1=CC(=C2C(=C1)OCC3(C2=O)CC4=CC(=C(C=C34)OC)O)O 328.30 unknown https://doi.org/10.1016/S0031-9422(00)81529-0
3',5,7-trihydroxy-4'-methoxyspiro[2H-chromene-3,7'-bicyclo[4.2.0]octa-1,3,5-triene]-4-one 21676264 Click to see COC1=C(C=C2CC3(C2=C1)COC4=CC(=CC(=C4C3=O)O)O)O 314.29 unknown https://doi.org/10.1016/S0031-9422(00)81529-0

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