Rhododendron simsii - Unknown
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Internal ID UUID64407308204fb877129132
Scientific name Rhododendron simsii
Authority Planch.
First published in Fl. Serres Jard. Eur. 9: 78 (1853)

Description Top

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Synonyms Top

Scientific name Authority First published in
Rhododendron annamense Rehder J. Arnold Arbor. 10: 182 (1929)
Rhododendron vittatum Planch. Rev. Hort. (Paris) , sér. 4, 3: 66 (1854)
Azalea fimbriata Dum.Cours Bot. Cult., ed. 2. 3: 337. 1811
Azalea prolifera Poit. Ann. Inst. Roy. Hort. Fromont 1: 104 (1829)
Azalea simsii (Planch.) H.F.Copel. Amer. Midl. Naturalist 30: 597 (1943)
Azalea vittata (Planch.) Dum.Cours Bot. Cult., ed. 2. 3: 337. 1811
Azalea vittatopunctata Lem. Ill. Hort. 1: t. 20 (1854)
Azalea indica var. simsii (Planch.) L.H.Bailey Cycl. Amer. Hort. 1: 122 1900
Rhododendron indicum var. simsii (Planch.) Maxim. Mém. Acad. Imp. Sci. Saint Pétersbourg, Sér. 7 16(9): 38 1870
Rhododendron viburnifolium W.P.Fang Acta Phytotax. Sin. 21: 469 (1983)
Rhododendron indicum var. formosanum Hayata Icon. Pl. Formosan. 3: 134 1913
Rhododendron indicum var. ignescens Sweet Brit. Fl. Gard. 2: , pl. 128 1833
Rhododendron indicum var. puniceum Sweet Brit. Fl. Gard. 2: , pl. 128 1833
Rhododendron calleryi Planch. Fl. Serres Jard. Eur. 9: 81 (1853)
Rhododendron bicolor P.C.Tam Surv. Genus Rhododendron S. China 101, 46. 1983 [Mar 1983]
Rhododendron petilum P.C.Tam Survey Gen. Rhododendron S. China : 101 (1983)
Rhododendron bellum W.P.Fang & G.Z.Li Bull. Bot. Res., Harbin 4(1): 3 (1984)
Rhododendron breynii Planch. Fl. Serres Jard. Eur. 9: 77 (1853)
Rhododendron simsii var. strigosistylum G.Z.Li Guihaia 15: 298 (1995)
Rhododendron simsii var. bellum (W.P.Fang & G.Z.Li) G.Z.Li Fl. Guangxi 3: 612. 2011 [1 Dec 2011]

Common names Top

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Language Common/alternative name
Hungarian azálea
lzh 杜鵑
Thai กุหลาบแดง
Vietnamese Đỗ quyên
Chinese 唐杜鹃
Chinese 照山红
Chinese 山踯躅
Chinese 山石榴
Chinese 映山红
Chinese 杜鹃(映山红)
Chinese 杜鹃
Chinese 唐杜鵑
Chinese 杜鹃花根
Chinese 杜鹃花果实
Chinese 杜鹃花叶
Chinese 杜鹃花

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Rhododendron simsii var. albiflorum R.L.Liu Acta Bot. Yunnan. 15: 190 (1993)

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China South-central
      • China Southeast
      • Tibet
    • Eastern Asia
      • Korea
      • Nansei-shoto
      • Taiwan

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000405453
Tropicos 50054234
INPN 117693
KEW urn:lsid:ipni.org:names:333359-1
The Plant List kew-2427105
Open Tree Of Life 269864
NCBI Taxonomy 118357
IPNI 333359-1
iNaturalist 410380
GBIF 7327627
Freebase /m/0ncd358
EPPO RHOSI
USDA GRIN 31591
Wikipedia Rhododendron_simsii

Genomes (via NCBI) Top

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Accession Assembly
Name Level Submitter Released Coverage Size
GCA_014282245.1 ASM1428224v1 Chromosome Ori-Gene Co. Ltd. 2020-08-25 100.0x 503.24 Mb

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
Quadrat soil pollen signal reflects plant important values in forests and shrublands from subtropical China Li K, Tan B, Liao M, Ni J Front Plant Sci 20-Mar-2024
PMCID:PMC10987713
doi:10.3389/fpls.2024.1348182
PMID:38571712
Organic Materials Promote Rhododendron simsii Growth and Rhizosphere Soil Properties in a Lead–Zinc Mining Wasteland Chen Y, Li W, Cai X, Li B, Zhan F, Zu Y, He Y Plants (Basel) 20-Mar-2024
PMCID:PMC10975995
doi:10.3390/plants13060891
PMID:38592957
Pest categorisation of Pyrrhoderma noxium Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Golic D, Gobbi A, Maiorano A, Pautasso M, Reignault PL EFSA J 19-Mar-2024
PMCID:PMC10949325
doi:10.2903/j.efsa.2024.8667
PMID:38505477
Mitochondrial genome features and systematic evolution of diospyros kaki thunb 'Taishuu' Yang Y, Duan C BMC Genomics 18-Mar-2024
PMCID:PMC10946091
doi:10.1186/s12864-024-10199-0
PMID:38500026
Local knowledge of homegarden plants in Miao ethnic communities in Laershan region, Xiangxi area, China Luo J, Li Q, He J, Yan J, Zhang S, Chang X, Wu T J Ethnobiol Ethnomed 18-Mar-2024
PMCID:PMC10946099
doi:10.1186/s13002-024-00676-x
PMID:38500123
Genomics insights into flowering and floral pattern formation: regional duplication and seasonal pattern of gene expression in Camellia Hu Z, Fan Z, Li S, Wang M, Huang M, Ma X, Liu W, Wang Y, Yu Y, Li Y, Sun Y, Li X, Li J, Yin H BMC Biol 27-Feb-2024
PMCID:PMC10900828
doi:10.1186/s12915-024-01851-y
PMID:38414012
Integrated Transcriptome and Metabolome Analyses Reveal Bamboo Culm Color Formation Mechanisms Involved in Anthocyanin Biosynthetic in Phyllostachys nigra Cai O, Zhang H, Yang L, Wu H, Qin M, Yao W, Huang F, Li L, Lin S Int J Mol Sci 01-Feb-2024
PMCID:PMC10855043
doi:10.3390/ijms25031738
PMID:38339012
Differential gene expression and potential regulatory network of fatty acid biosynthesis during fruit and leaf development in yellowhorn (Xanthoceras sorbifolium), an oil-producing tree with significant deployment values Shi TL, Ma HY, Wang X, Liu H, Yan XM, Tian XC, Li ZC, Bao YT, Chen ZY, Zhao SW, Xiang Q, Jia KH, Nie S, Guan W, Mao JF Front Plant Sci 19-Jan-2024
PMCID:PMC10834690
doi:10.3389/fpls.2023.1297817
PMID:38312356
Vertical distribution characteristics of soil organic carbon and vegetation types under different elevation gradients in Cangshan, Dali Yang X, Xu J, Wang H, Quan H, Yu H, Luan J, Wang D, Li Y, Lv D PeerJ 04-Jan-2024
PMCID:PMC10771771
doi:10.7717/peerj.16686
PMID:38188153
Nectar cardenolides and floral volatiles mediate a specialized wasp pollination system Burger H, Buttala S, Koch H, Ayasse M, Johnson SD, Stevenson PC J Exp Biol 04-Jan-2024
PMCID:PMC10785657
doi:10.1242/jeb.246156
PMID:38180227
The complete chloroplast genome sequence of Rhododendron farrerae Tate ex Sweet (Ericaceae) Shen J, Huang L Mitochondrial DNA B Resour 04-Jan-2024
PMCID:PMC10769518
doi:10.1080/23802359.2023.2294897
PMID:38187010
Response of grassland ecosystem function to plant functional traits under different vegetation restoration models in areas of karst desertification Song S, Xiong K, Chi Y Front Plant Sci 12-Dec-2023
PMCID:PMC10749941
doi:10.3389/fpls.2023.1239190
PMID:38148857
High-quality assembly and methylome of a Tibetan wild tree peony genome (Paeonia ludlowii) reveal the evolution of giant genome architecture Xiao PX, Li Y, Lu J, Zuo H, Pingcuo G, Ying H, Zhao F, Xu Q, Zeng X, Jiao WB Hortic Res 10-Nov-2023
PMCID:PMC10753165
doi:10.1093/hr/uhad241
PMID:38156287
A chromosome-level genome assembly provides insights into Cornus wilsoniana evolution, oil biosynthesis, and floral bud development He Z, Chao H, Zhou X, Ni Q, Hu Y, Yu R, Wang M, Li C, Chen J, Chen Y, Chen Y, Cui C, Zhang L, Chen M, Chen D Hortic Res 29-Sep-2023
PMCID:PMC10673659
doi:10.1093/hr/uhad196
PMID:38023476
Research Progress on Anthocyanin-Mediated Regulation of ‘Black’ Phenotypes of Plant Organs Wang F, Chen J, Tang R, Wang R, Ahmad S, Liu Z, Peng D Curr Issues Mol Biol 01-Sep-2023
PMCID:PMC10527681
doi:10.3390/cimb45090458
PMID:37754242

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
3,4-Dihydroxybenzoic acid 72 Click to see C1=CC(=C(C=C1C(=O)O)O)O 154.12 unknown https://doi.org/10.1016/S0031-9422(00)00493-3
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Protocatechuic acid, methyl ester 287064 Click to see COC(=O)C1=CC(=C(C=C1)O)O 168.15 unknown https://doi.org/10.1016/S0031-9422(00)00493-3
> Benzenoids / Naphthalenes / Naphthalenecarboxylic acids and derivatives / Naphthalenecarboxylic acids
Fisheacid 139583718 Click to see C1C(C(=CC2=CC=CC=C21)C3=CC4=CC=CC=C4CC3C(=O)O)C(=O)O 346.40 unknown https://doi.org/10.1016/0031-9422(93)85102-W
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
[(1S,6R,7S,8R,10S,11R,13S,14R,15S,16S)-16-benzamido-7-[(1S)-1-(dimethylamino)ethyl]-13-hydroxy-6,10,15-trimethyl-19-oxapentacyclo[13.3.2.01,14.03,11.06,10]icosa-3,17-dien-8-yl] acetate 162857717 Click to see CC(C1C(CC2(C1(CC=C3C2CC(C4C5(COC4(C3)C=CC5NC(=O)C6=CC=CC=C6)C)O)C)C)OC(=O)C)N(C)C 576.80 unknown https://doi.org/10.1016/0031-9422(93)85102-W
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,2R,4aS,6aR,6aS,6bR,8aR,9R,12aR,14bS)-1-hydroxy-9-methoxy-1,2,6a,6b,9,12a-hexamethyl-10-oxo-3,4,5,6,6a,7,8,8a,11,12,13,14b-dodecahydro-2H-picene-4a-carboxylic acid 162883867 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)OC)C)C)C2C1(C)O)C)C(=O)O 486.70 unknown https://doi.org/10.1016/S0031-9422(00)00493-3
[(3R,4aR,6aR,6bR,8aR,11S,12S,12aS,14aS,14bR)-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-yl] acetate 162999321 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)C 468.80 unknown https://doi.org/10.1016/0031-9422(93)85102-W
1-hydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-10-oxo-3,4,5,6,6a,7,8,8a,11,12,13,14b-dodecahydro-2H-picene-4a-carboxylic acid 22297554 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)CO)C)C)C2C1(C)O)C)C(=O)O 486.70 unknown https://doi.org/10.1016/S0031-9422(00)00493-3
19alpha,24-Dihydroxyurs-12-en-3-on-28-oic acid 10600994 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)CO)C)C)C2C1(C)O)C)C(=O)O 486.70 unknown https://doi.org/10.1016/S0031-9422(00)00493-3
> Lipids and lipid-like molecules / Steroids and steroid derivatives
1-hydroxy-9-methoxy-1,2,6a,6b,9,12a-hexamethyl-10-oxo-3,4,5,6,6a,7,8,8a,11,12,13,14b-dodecahydro-2H-picene-4a-carboxylic acid 162883866 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)OC)C)C)C2C1(C)O)C)C(=O)O 486.70 unknown https://doi.org/10.1016/S0031-9422(00)00493-3
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Pregnane steroids / Gluco/mineralocorticoids, progestogins and derivatives
[(3R,5S,8S,9S,10S,11R,13R,14S,17R)-17-ethenyl-3-hydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-11-yl] acetate 25180961 Click to see CC(=O)OC1CC2(C(CCC2C3C1C4(CCC(CC4CC3)O)C)C=C)C 360.50 unknown https://doi.org/10.1016/0031-9422(93)85102-W
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-3-O-glycosides
(2S,5S)-2-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromenylium-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 44256715 Click to see C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O 449.40 unknown https://doi.org/10.1016/0031-9422(93)85102-W
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-5-O-glycosides
(2S,3R,4S,5S,6S)-2-[2-(3,4-dihydroxyphenyl)-7-hydroxy-3-[(2S,3R,4S,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromenylium-5-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 163186830 Click to see C1=CC(=C(C=C1C2=C(C=C3C(=CC(=CC3=[O+]2)O)OC4C(C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)CO)O)O)O)O)O 611.50 unknown https://doi.org/10.1016/S0031-9422(00)85196-1
(3S,4S,6S)-2-(hydroxymethyl)-6-[7-hydroxy-3-[(2S,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2-(3,4,5-trihydroxyphenyl)chromenylium-5-yl]oxyoxane-3,4,5-triol 44256888 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C=C3C(=CC(=CC3=[O+]2)O)OC4C(C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)CO)O)O)O 627.50 unknown https://doi.org/10.1016/0031-9422(93)85102-W
2-[2-(3,4-Dihydroxyphenyl)-7-hydroxy-3-(3,4,5-trihydroxyoxan-2-yl)oxychromenylium-5-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 163192821 Click to see C1C(C(C(C(O1)OC2=C([O+]=C3C=C(C=C(C3=C2)OC4C(C(C(C(O4)CO)O)O)O)O)C5=CC(=C(C=C5)O)O)O)O)O 581.50 unknown https://doi.org/10.1016/0031-9422(93)85102-W
Cyanidin 3-galactoside-5-glucoside 44256703 Click to see C1=CC(=C(C=C1C2=C(C=C3C(=CC(=CC3=[O+]2)O)OC4C(C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)CO)O)O)O)O)O 611.50 unknown https://doi.org/10.1016/0031-9422(93)85102-W
Cyanin 441688 Click to see C1=CC(=C(C=C1C2=C(C=C3C(=CC(=CC3=[O+]2)O)OC4C(C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)CO)O)O)O)O)O 611.50 unknown https://doi.org/10.1016/0031-9422(93)85102-W
> 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/10.1016/0031-9422(93)85102-W
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-2,3-dihydrochromen-4-one 5317364 Click to see C1C(C(C(C(O1)OC2C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 436.40 unknown https://doi.org/10.1016/0031-9422(93)85102-W
7-Hydroxy-5-methoxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy-2-(3,4,5-trihydroxyphenyl)chromen-4-one 74978355 Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C2=O)C(=CC(=C3)O)OC)C4=CC(=C(C(=C4)O)O)O)O)O)O 478.40 unknown https://doi.org/10.1007/BF02977686
7-hydroxy-5-methoxy-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2-(3,4,5-trihydroxyphenyl)chromen-4-one 163091467 Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C2=O)C(=CC(=C3)O)OC)C4=CC(=C(C(=C4)O)O)O)O)O)O 478.40 unknown https://doi.org/10.1016/S0031-9422(00)85196-1
Astilbin 119258 Click to see CC1C(C(C(C(O1)OC2C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 450.40 unknown https://doi.org/10.1016/0031-9422(93)85102-W
Azaleatin 3-galactoside 44259528 Click to see COC1=CC(=CC2=C1C(=O)C(=C(O2)C3=CC(=C(C=C3)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 478.40 unknown https://doi.org/10.1016/0031-9422(93)85102-W
Azaleatin 3-rhamnoside 44259531 Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C2=O)C(=CC(=C3)O)OC)C4=CC(=C(C=C4)O)O)O)O)O 462.40 unknown https://doi.org/10.1016/0031-9422(93)85102-W
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 https://doi.org/10.1016/0031-9422(93)85102-W
Isoastilbin 316844 Click to see CC1C(C(C(C(O1)OC2C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 450.40 unknown https://doi.org/10.1016/0031-9422(93)85102-W
Myricitrin 5281673 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)O 464.40 unknown https://doi.org/10.1016/0031-9422(93)85102-W
Quercitrin 5280459 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 https://doi.org/10.1016/0031-9422(93)85102-W
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
(2S)-7-[(2R,3S,4R,5R,6S)-6-[[(2S,3S,4S)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-5-hydroxy-2-(4-methoxyphenyl)-6,8-dimethyl-2,3-dihydrochromen-4-one 163191237 Click to see CC1=C(C2=C(C(=C1OC3C(C(C(C(O3)COC4C(C(CO4)(CO)O)O)O)O)O)C)OC(CC2=O)C5=CC=C(C=C5)OC)O 608.60 unknown https://doi.org/10.1016/S0031-9422(00)00493-3
(2S)-7-[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-5-hydroxy-2-(4-methoxyphenyl)-6,8-dimethyl-2,3-dihydrochromen-4-one 637072 Click to see CC1=C(C2=C(C(=C1OC3C(C(C(C(O3)COC4C(C(CO4)(CO)O)O)O)O)O)C)OC(CC2=O)C5=CC=C(C=C5)OC)O 608.60 unknown https://doi.org/10.1016/S0031-9422(00)00493-3
(2S)-7-[(2S,3S,4S,5S,6R)-6-[[(2R,3S,4S)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-5-hydroxy-2-(4-methoxyphenyl)-6,8-dimethyl-2,3-dihydrochromen-4-one 162892125 Click to see CC1=C(C2=C(C(=C1OC3C(C(C(C(O3)COC4C(C(CO4)(CO)O)O)O)O)O)C)OC(CC2=O)C5=CC=C(C=C5)OC)O 608.60 unknown https://doi.org/10.1016/S0031-9422(00)00493-3
7-[6-[[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-5-hydroxy-2-(4-methoxyphenyl)-6,8-dimethyl-2,3-dihydrochromen-4-one 20979903 Click to see CC1=C(C2=C(C(=C1OC3C(C(C(C(O3)COC4C(C(CO4)(CO)O)O)O)O)O)C)OC(CC2=O)C5=CC=C(C=C5)OC)O 608.60 unknown https://doi.org/10.1016/S0031-9422(00)00493-3
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
(2R)-5,7-dihydroxy-2-(4-methoxyphenyl)-6,8-dimethyl-chroman-4-one 49770782 Click to see CC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=CC=C(C=C3)OC)C)O 314.30 unknown https://doi.org/10.1016/S0031-9422(00)00493-3
5,7-Dihydroxy-6,8-dimethyl-4'-methoxyflavanone 602155 Click to see CC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=CC=C(C=C3)OC)C)O 314.30 unknown https://doi.org/10.1016/S0031-9422(00)00493-3
Matteucinol 160490 Click to see CC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=CC=C(C=C3)OC)C)O 314.30 unknown https://doi.org/10.1016/S0031-9422(00)00493-3

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