Salvia splendens - Unknown
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Author: Public Domain - WikiMedia

Salvia splendens - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

Salvia splendens - Leaf
Part: Leaf
Author: Sorin

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Details Top

Internal ID UUID643febf50cbd7405114579
Scientific name Salvia splendens
Authority Sellow ex Schult.
First published in Mant. 1 (Schultes) 1: 185. 1822 [late 1822]

Description Top

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Salvia splendens, also known as scarlet sage, is a tender herbaceous perennial plant native to Brazil. It grows at high elevations with warm temperatures and high humidity. While the wild form can reach up to 1.3 meters tall, smaller cultivars are more commonly seen as bedding plants in shopping malls and public gardens worldwide. This plant was first described in 1822 and has since been selected for dwarf sizes and different colors, ranging from white to dark purple. It is a popular ornamental plant, but does not survive freezing temperatures and is often grown as an annual. Some notable cultivars include 'Alba' with white flowers, 'Atropurpurea' with dark violet to purple flowers, and 'Grandiflora' with large red flowers. Two cultivars, 'Vanguard' and 'Van-Houttei', have received the Royal Horticultural Society's Award of Garden Merit.

Synonyms Top

Scientific name Authority First published in
Jungia splendens (Sellow ex Schult.) Soják Čas. Nár. Muz. Praze, Rada Přír. 152(1): 21. 1983
Salvia brasiliensis Spreng. Syst. Veg. 1: 56 (1824)
Salvia colorans hort. ex Benth. Labiat. Gen. Spec. : 287 (1833)
Fenixanthes splendens Raf. Autik. Bot. : 122 (1840)

Common names Top

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Language Common/alternative name
English tropical sage
English scarlet sage
Belarusian Сальвія
Belarusian Шалфей цудоўны
Bulgarian обикновено пламъче
Catalan coral·lí
Catalan coral·lins
Czech šalvěj zářivá
German feuer-salbei
German feuersalbei
Estonian leeksalvei
Persian سالویا اسپلندنز
Finnish tulisalvia
Hebrew מרווה הדורה
Upper Sorbian pyšna želbija
Armenian Եղեսպակ փայլուն
Japanese 来路花
Japanese ヒゴロモソウ
Japanese スカーレットセージ
Japanese サルビア・スプレンデンス
Japanese 緋衣草
Japanese サルビア
Korean 샐비어
Korean 깨꽃
Lithuanian raudonžiedis šalavijas
Macedonian жарче
Dutch vuursalie
Polish szałwia błyszcząca
Romanian Salvie
Russian Шалфей блестящий
Russian Шалфей тропический
Russian Шалфей сверкающий
Swedish praktsalvia
Tonga teʻekosi sivilaise
Turkish ateş çiçeği
Chinese 地梗鼠尾
Chinese 象牙红
Chinese 一串紅
Chinese 一串红
Chinese 墙下红
Chinese 炮仔花
Chinese 西洋红
Chinese 象牙海棠
Chinese 鼠尾草
Chinese 赛尔维亚

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

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-0000302359
USDA Plants SASP6
Tropicos 50293092
INPN 639059
Flora of Italy 8605
KEW urn:lsid:ipni.org:names:60466516-2
The Plant List kew-183912
Plantarium 33541
Missouri Botanical Garden 281427
Open Tree Of Life 294217
Observations.org 145594
NCBI Taxonomy 180675
NBN Atlas NHMSYS0000463193
Nature Serve 2.136267
IPNI 60452620-2
iNaturalist 143203
GBIF 2927029
Freebase /m/06_spk
WisFlora 7626
EPPO SALSP
EOL 579412
Elurikkus 215082
USDA GRIN 70596
Wikipedia Salvia_splendens

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCF_004379255.2 SspV2 Chromosome Beijing Forestry University 2021-05-20 100.0x 768.60 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
An R2R3-MYB Transcriptional Factor LuMYB314 Associated with the Loss of Petal Pigmentation in Flax (Linum usitatissimum L.) Guo D, Jiang H, Xie L Genes (Basel) 18-Apr-2024
PMCID:PMC11050253
doi:10.3390/genes15040511
PMID:38674445
Genetic linkage mapping and quantitative trait locus (QTL) analysis of sweet basil (Ocimum basilicum L.) to identify genomic regions associated with cold tolerance and major volatiles Brindisi LJ, Mattera R III, Mudiyala S, Honig J, Simon JE PLoS One 09-Apr-2024
PMCID:PMC11003626
doi:10.1371/journal.pone.0299825
PMID:38593174
The complete chloroplast genome of Lagochilus ilicifolius Bunge ex Bentham, Labiat. Gen. 1834 (Lamiaceae) and its phylogenetic analysis Hou WJ, Men WX, Xing YP, Yang YY, Xu L, Kang TG, Song YY Mitochondrial DNA B Resour 02-Apr-2024
PMCID:PMC10993758
doi:10.1080/23802359.2024.2334013
PMID:38586511
Isolation, Characterization, and Expression Analysis of NAC Transcription Factor from Andrographis paniculata (Burm. f.) Nees and Their Role in Andrographolide Production Kumar R, Kumar C, Roy Choudhury D, Ranjan A, Raipuria RK, Dubey KK, Mishra A, Kumar C, Manzoor MM, Kumar A, Kumari A, Singh K, Singh GP, Singh R Genes (Basel) 28-Mar-2024
PMCID:PMC11049156
doi:10.3390/genes15040422
PMID:38674357
Chromosome-level genome assembly provides insights into the genome evolution and functional importance of the phenylpropanoid–flavonoid pathway in Thymus mongolicus Dang Z, Xu Y, Zhang X, Mi W, Chi Y, Tian Y, Liu Y, Ren W BMC Genomics 19-Mar-2024
PMCID:PMC10949689
doi:10.1186/s12864-024-10202-8
PMID:38504151
Chromosome-level genome of Thymus mandschuricus reveals molecular mechanism of aroma compounds biosynthesis Jia L, Xu N, Xia B, Gao W, Meng Q, Li Q, Sun Y, Xu S, He M, Gu H Front Plant Sci 13-Mar-2024
PMCID:PMC10965588
doi:10.3389/fpls.2024.1368869
PMID:38545395
High-quality genome assembly enables prediction of allele-specific gene expression in hybrid poplar Shi TL, Jia KH, Bao YT, Nie S, Tian XC, Yan XM, Chen ZY, Li ZC, Zhao SW, Ma HY, Zhao Y, Li X, Zhang RG, Guo J, Zhao W, El-Kassaby YA, Müller N, Van de Peer Y, Wang XR, Street NR, Porth I, An X, Mao JF Plant Physiol 27-Feb-2024
PMCID:PMC11060683
doi:10.1093/plphys/kiae078
PMID:38412470
The PGPR Bacillus aryabhattai promotes soybean growth via nutrient and chlorophyll maintenance and the production of butanoic acid Mun BG, Hussain A, Park YG, Kang SM, Lee IJ, Yun BW Front Plant Sci 19-Feb-2024
PMCID:PMC10909845
doi:10.3389/fpls.2024.1341993
PMID:38439982
Integrating Transcriptome and Chemical Analyses to Provide Insights into Biosynthesis of Terpenoids and Flavonoids in the Medicinal Industrial Crop Andrographis paniculate and Its Antiviral Medicinal Parts Yu K, Liang P, Yu H, Liu H, Guo J, Yan X, Li Z, Li G, Wang Y, Wang C Molecules 14-Feb-2024
PMCID:PMC10893308
doi:10.3390/molecules29040852
PMID:38398604
A digital PCR approach to assess the purity of oregano Cottenet G, Blancpain C, Holzwarth J Heliyon 11-Feb-2024
PMCID:PMC10900423
doi:10.1016/j.heliyon.2024.e25985
PMID:38420487
A haplotype-resolved gap-free genome assembly provides novel insight into monoterpenoid diversification in Mentha suaveolens ‘Variegata’ Yang H, Wang C, Zhou G, Zhang Y, He T, Yang L, Wu Y, Wang Z, Tang X, Chen G, Liu Z, Tang H, Zhou H, Kang X, Zhang S, Leng L, Chen S, Song C Hortic Res 17-Jan-2024
PMCID:PMC10925848
doi:10.1093/hr/uhae022
PMID:38469381
Recurrent symmetrical bendings cause dwarfing in Hydrangea through spatial molecular regulation of xylem cell walls Ley-Ngardigal B, Roman H, Brouard N, Huché-Thélier L, Guérin V, Leduc N Front Plant Sci 16-Jan-2024
PMCID:PMC10826399
doi:10.3389/fpls.2023.1268272
PMID:38293622
Subgenome phasing for complex allopolyploidy: case-based benchmarking and recommendations Zhang RG, Shang HY, Jia KH, Ma YP Brief Bioinform 06-Jan-2024
PMCID:PMC10772947
doi:10.1093/bib/bbad513
PMID:38189536
Reference genome of the nutrition-rich orphan crop chia (Salvia hispanica) and its implications for future breeding Gupta P, Geniza M, Elser J, Al-Bader N, Baschieri R, Phillips JL, Haq E, Preece J, Naithani S, Jaiswal P Front Plant Sci 14-Dec-2023
PMCID:PMC10757625
doi:10.3389/fpls.2023.1272966
PMID:38162307
The SmERF1b-like regulates tanshinone biosynthesis in Salvia miltiorrhiza hairy root Li D, Liu Y, Chen G, Yan Y, Bai Z AoB Plants 08-Dec-2023
PMCID:PMC10799320
doi:10.1093/aobpla/plad086
PMID:38249522

Phytochemical Profile Top

Add a new one!
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
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
[(1R)-2-[(6aR,7R,8S,9R,10aS)-9-[(2R,3S,5R,6R)-3,5-dihydroxy-6-(hydroxymethyl)-4-oxooxan-2-yl]oxy-7,8-dimethyl-3-oxo-5,6,6a,8,9,10-hexahydro-1H-benzo[d][2]benzofuran-7-yl]-1-(furan-3-yl)ethyl] acetate 53348973 Click to see CC1C(CC23COC(=O)C2=CCCC3C1(C)CC(C4=COC=C4)OC(=O)C)OC5C(C(=O)C(C(O5)CO)O)O 548.60 unknown https://doi.org/10.1002/HLCA.201000203
[2-[9-[3,5-dihydroxy-6-(hydroxymethyl)-4-oxooxan-2-yl]oxy-7,8-dimethyl-3-oxo-5,6,6a,8,9,10-hexahydro-1H-benzo[d][2]benzofuran-7-yl]-1-(furan-3-yl)ethyl] acetate 76019168 Click to see CC1C(CC23COC(=O)C2=CCCC3C1(C)CC(C4=COC=C4)OC(=O)C)OC5C(C(=O)C(C(O5)CO)O)O 548.60 unknown https://doi.org/10.1002/HLCA.201000203
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(6aR,7S,8R,10aS)-7-[(2R)-2-hydroxy-2-(5-oxo-2H-furan-3-yl)ethyl]-7,8-dimethyl-5,6,6a,8,9,10-hexahydro-1H-benzo[d][2]benzofuran-3-one 162906744 Click to see CC1CCC23COC(=O)C2=CCCC3C1(C)CC(C4=CC(=O)OC4)O 346.40 unknown https://doi.org/10.1021/NP068036D
[(1R)-2-[(6aR,7S,8S,9R,10aS)-9-hydroxy-7,8-dimethyl-3-oxo-5,6,6a,8,9,10-hexahydro-1H-benzo[d][2]benzofuran-7-yl]-1-(furan-3-yl)ethyl] acetate 163106183 Click to see CC1C(CC23COC(=O)C2=CCCC3C1(C)CC(C4=COC=C4)OC(=O)C)O 388.50 unknown https://doi.org/10.1021/NP068036D
CID 12313706 12313706 Click to see CC1CCC23COC(=O)C2=CCCC3C1(C)CC(C4=CC(=O)OC4)O 346.40 unknown https://doi.org/10.1021/NP068036D
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
[(1S,4S,7S,8R,9R,10S,11R,14R)-8-acetyloxy-7-[(2S)-2-hydroxy-5-oxo-2H-furan-4-yl]-9-methyl-5,15-dioxo-6,16-dioxatetracyclo[8.7.0.01,14.04,9]heptadec-12-en-11-yl] acetate 162983118 Click to see CC(=O)OC1C=CC2C(=O)OCC23C1C4(C(CC3)C(=O)OC(C4OC(=O)C)C5=CC(OC5=O)O)C 490.50 unknown https://doi.org/10.1016/S0031-9422(97)00180-5
[8-acetyloxy-7-(2-hydroxy-5-oxo-2H-furan-4-yl)-9-methyl-5,15-dioxo-6,16-dioxatetracyclo[8.7.0.01,14.04,9]heptadec-12-en-11-yl] acetate 162983117 Click to see CC(=O)OC1C=CC2C(=O)OCC23C1C4(C(CC3)C(=O)OC(C4OC(=O)C)C5=CC(OC5=O)O)C 490.50 unknown https://doi.org/10.1016/S0031-9422(97)00180-5
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
1,8-Dihydroxy-2,6-dimethoxy-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyxanthen-9-one 163014324 Click to see COC1=C(C2=C(C=C1)OC3=C(C2=O)C(=CC(=C3OC4C(C(C(C(O4)CO)O)O)O)OC)O)O 466.40 unknown https://doi.org/10.1016/S0031-9422(97)00180-5
https://doi.org/10.1021/NP068036D
https://doi.org/10.1002/HLCA.201000203
https://doi.org/10.1002/MRC.1869
> Organoheterocyclic compounds / Naphthofurans
(1S,4S,6R,8R,9S,11R)-6-(furan-3-yl)-11-hydroxy-4,8-dimethyl-5,15-dioxatetracyclo[7.7.0.01,13.04,8]hexadec-12-en-14-one 16099457 Click to see CC12CCC34COC(=O)C3=CC(CC4C1(CC(O2)C5=COC=C5)C)O 344.40 unknown https://doi.org/10.1002/HLCA.201000203
https://doi.org/10.1021/NP068036D
(1S,4S,6S,8R,9S,11R)-6-(furan-3-yl)-11-hydroxy-4,8-dimethyl-5,15-dioxatetracyclo[7.7.0.01,13.04,8]hexadec-12-en-14-one 162975323 Click to see CC12CCC34COC(=O)C3=CC(CC4C1(CC(O2)C5=COC=C5)C)O 344.40 unknown https://doi.org/10.1021/NP068036D
6-(Furan-3-yl)-11-hydroxy-4,8-dimethyl-5,15-dioxatetracyclo[7.7.0.01,13.04,8]hexadec-12-en-14-one 162975322 Click to see CC12CCC34COC(=O)C3=CC(CC4C1(CC(O2)C5=COC=C5)C)O 344.40 unknown https://doi.org/10.1002/HLCA.201000203
https://doi.org/10.1021/NP068036D
> Organoheterocyclic compounds / Naphthopyrans
(1S,4S,7R,9R,10R,11R,14R)-7-(furan-3-yl)-11-hydroxy-9-methyl-6,16-dioxatetracyclo[8.7.0.01,14.04,9]heptadec-12-ene-5,15-dione 73350928 Click to see CC12CC(OC(=O)C1CCC34C2C(C=CC3C(=O)OC4)O)C5=COC=C5 358.40 unknown https://doi.org/10.1021/NP068036D
https://doi.org/10.1002/HLCA.201000203
https://doi.org/10.1016/S0031-9422(97)00180-5
https://doi.org/10.1002/MRC.1869
(1S,4S,7S,8R,9R,10S,11R,14R)-7-(furan-3-yl)-8,11-dihydroxy-9-methyl-6,16-dioxatetracyclo[8.7.0.01,14.04,9]heptadec-12-ene-5,15-dione 52914116 Click to see CC12C(CCC34C1C(C=CC3C(=O)OC4)O)C(=O)OC(C2O)C5=COC=C5 374.40 unknown https://doi.org/10.1002/HLCA.201000203
(1S,4S,7S,8R,9R,10S,14R)-7-(furan-3-yl)-8-hydroxy-9-methyl-6,16-dioxatetracyclo[8.7.0.01,14.04,9]heptadec-12-ene-5,15-dione 16099452 Click to see CC12C(CCC34C1CC=CC3C(=O)OC4)C(=O)OC(C2O)C5=COC=C5 358.40 unknown https://doi.org/10.1021/NP068036D
https://doi.org/10.1002/HLCA.201000203
(1S,4S,7S,8R,9R,10S)-7-(furan-3-yl)-8-hydroxy-9-methyl-6,16-dioxatetracyclo[8.7.0.01,14.04,9]heptadec-12-ene-5,15-dione 163186470 Click to see CC12C(CCC34C1CC=CC3C(=O)OC4)C(=O)OC(C2O)C5=COC=C5 358.40 unknown https://doi.org/10.1021/NP068036D
(1S,7S,8R,9R,10S,14R)-7-(furan-3-yl)-8-hydroxy-9-methyl-6,16-dioxatetracyclo[8.7.0.01,14.04,9]heptadeca-3,12-diene-5,15-dione 16099456 Click to see CC12C3CC=CC4C3(CC=C1C(=O)OC(C2O)C5=COC=C5)COC4=O 356.40 unknown https://doi.org/10.1021/NP068036D
[(1S,4S,7S,8R,9R,10S,11R,14R)-8-acetyloxy-7-(furan-3-yl)-9-methyl-5,15-dioxo-6,16-dioxatetracyclo[8.7.0.01,14.04,9]heptadec-12-en-11-yl] acetate 101939043 Click to see CC(=O)OC1C=CC2C(=O)OCC23C1C4(C(CC3)C(=O)OC(C4OC(=O)C)C5=COC=C5)C 458.50 unknown https://doi.org/10.1002/HLCA.201000203
https://doi.org/10.1002/MRC.1869
https://doi.org/10.1016/S0031-9422(97)00180-5
https://doi.org/10.1021/NP068036D
[(1S,4S,7S,8R,9R,10S,14R)-7-(furan-3-yl)-9-methyl-5,15-dioxo-6,16-dioxatetracyclo[8.7.0.01,14.04,9]heptadec-12-en-8-yl] acetate 102589440 Click to see CC(=O)OC1C(OC(=O)C2C1(C3CC=CC4C3(CC2)COC4=O)C)C5=COC=C5 400.40 unknown https://doi.org/10.1002/MRC.1869
https://doi.org/10.1002/HLCA.201000203
https://doi.org/10.1021/NP068036D
https://doi.org/10.1016/S0031-9422(97)00180-5
[(1S,7S,8R,9R,10S,11R,14R)-7-(furan-3-yl)-8-hydroxy-9-methyl-5,15-dioxo-6,16-dioxatetracyclo[8.7.0.01,14.04,9]heptadeca-3,12-dien-11-yl] acetate 53348972 Click to see CC(=O)OC1C=CC2C(=O)OCC23C1C4(C(C(OC(=O)C4=CC3)C5=COC=C5)O)C 414.40 unknown https://doi.org/10.1002/HLCA.201000203
[7-(Furan-3-yl)-8-hydroxy-9-methyl-5,15-dioxo-6,16-dioxatetracyclo[8.7.0.01,14.04,9]heptadeca-3,12-dien-11-yl] acetate 76019167 Click to see CC(=O)OC1C=CC2C(=O)OCC23C1C4(C(C(OC(=O)C4=CC3)C5=COC=C5)O)C 414.40 unknown https://doi.org/10.1002/HLCA.201000203
7-(Furan-3-yl)-11-hydroxy-9-methyl-6,16-dioxatetracyclo[8.7.0.01,14.04,9]heptadec-12-ene-5,15-dione 162845576 Click to see CC12CC(OC(=O)C1CCC34C2C(C=CC3C(=O)OC4)O)C5=COC=C5 358.40 unknown https://doi.org/10.1002/MRC.1869
https://doi.org/10.1002/HLCA.201000203
https://doi.org/10.1021/NP068036D
https://doi.org/10.1016/S0031-9422(97)00180-5
7-(Furan-3-yl)-8-hydroxy-9-methyl-6,16-dioxatetracyclo[8.7.0.01,14.04,9]heptadec-12-ene-5,15-dione 162892325 Click to see CC12C(CCC34C1CC=CC3C(=O)OC4)C(=O)OC(C2O)C5=COC=C5 358.40 unknown https://doi.org/10.1002/HLCA.201000203
https://doi.org/10.1021/NP068036D
7-(Furan-3-yl)-8-hydroxy-9-methyl-6,16-dioxatetracyclo[8.7.0.01,14.04,9]heptadeca-3,12-diene-5,15-dione 162843560 Click to see CC12C3CC=CC4C3(CC=C1C(=O)OC(C2O)C5=COC=C5)COC4=O 356.40 unknown https://doi.org/10.1021/NP068036D
7-(Furan-3-yl)-8,11-dihydroxy-9-methyl-6,16-dioxatetracyclo[8.7.0.01,14.04,9]heptadec-12-ene-5,15-dione 75952095 Click to see CC12C(CCC34C1C(C=CC3C(=O)OC4)O)C(=O)OC(C2O)C5=COC=C5 374.40 unknown https://doi.org/10.1002/HLCA.201000203
Salviarin 329251 Click to see CC12CC(OC(=O)C1CCC34C2CC=CC3C(=O)OC4)C5=COC=C5 342.40 unknown https://doi.org/10.1016/S0031-9422(97)00180-5
https://doi.org/10.1021/NP068036D
https://doi.org/10.1002/HLCA.201000203
https://doi.org/10.1002/MRC.1869
Splendidin 433422 Click to see CC(=O)OC1C=CC2C(=O)OCC23C1C4(C(CC3)C(=O)OC(C4OC(=O)C)C5=COC=C5)C 458.50 unknown https://doi.org/10.1002/HLCA.201000203
https://doi.org/10.1016/S0031-9422(97)00180-5
https://doi.org/10.1021/NP068036D
https://doi.org/10.1002/MRC.1869
ZT72DJ66LU 15705466 Click to see CC12CC(OC(=O)C1CCC34C2CC=CC3C(=O)OC4)C5=COC=C5 342.40 unknown https://doi.org/10.1002/HLCA.201000203
https://doi.org/10.1002/MRC.1869
https://doi.org/10.1021/NP068036D
https://doi.org/10.1016/S0031-9422(97)00180-5
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanidin 3-O-p-coumaroyl glycosides / Anthocyanidin 3-O-6-p-coumaroyl glycosides
[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-[7-hydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2-(3,4,5-trihydroxyphenyl)chromenylium-3-yl]oxyoxan-2-yl]methyl (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 154496255 Click to see C1=CC(=C(C=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=C([O+]=C4C=C(C=C(C4=C3)OC5C(C(C(C(O5)CO)O)O)O)O)C6=CC(=C(C(=C6)O)O)O)O)O)O)O)O 789.70 unknown https://doi.org/10.1016/S0040-4039(00)70662-9
[(2R,3S,4S,5S,6S)-3,4,5-trihydroxy-6-[7-hydroxy-5-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2-(3,4,5-trihydroxyphenyl)chromenylium-3-yl]oxyoxan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate 154496223 Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=C([O+]=C4C=C(C=C(C4=C3)OC5C(C(C(C(O5)CO)O)O)O)O)C6=CC(=C(C(=C6)O)O)O)O)O)O)O 773.70 unknown https://doi.org/10.1016/S0031-9422(01)00415-0
3-[[(2S,3S,4R,5R,6S)-3-(2-carboxyacetyl)oxy-6-[3-[(2S,3S,4S,5S,6S)-6-[[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-7-hydroxy-2-(3,4,5-trihydroxyphenyl)chromenylium-5-yl]oxy-4,5-dihydroxyoxan-2-yl]methoxy]-3-oxopropanoic acid 154497407 Click to see C1=CC(=C(C=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=C([O+]=C4C=C(C=C(C4=C3)OC5C(C(C(C(O5)COC(=O)CC(=O)O)OC(=O)CC(=O)O)O)O)O)C6=CC(=C(C(=C6)O)O)O)O)O)O)O)O 961.80 unknown https://doi.org/10.1016/S0040-4039(00)70662-9
3-[[(2S,3S,4S,5S,6S)-6-[3-[(2S,3R,4R,5S,6R)-6-[[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-7-hydroxy-2-(3,4,5-trihydroxyphenyl)chromenylium-5-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-3-oxopropanoic acid 154497021 Click to see C1=CC(=C(C=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=C([O+]=C4C=C(C=C(C4=C3)OC5C(C(C(C(O5)COC(=O)CC(=O)O)O)O)O)O)C6=CC(=C(C(=C6)O)O)O)O)O)O)O)O 875.70 unknown https://doi.org/10.1016/S0040-4039(00)70662-9

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