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Salvia digitaloides

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 UUID643febab53be3777193668
Scientific name Salvia digitaloides
Authority Diels
First published in Notes Roy. Bot. Gard. Edinburgh 5: 234 (1912)

Ethnobotanical Use Top

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General Uses Top

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Common products:
- Live plants (potted or bare‑root) sold by nurseries for landscape and garden use.
- Seed packets marketed for propagation.
- Soft‑wood cuttings supplied by specialty nurseries.

Properties relevant to use:
- Perennial herbaceous plant, 0.2–0.3 m tall, forming a compact clump.
- Leaves silvery‑green, ovate, aromatic when crushed.
- Inflorescence: pinkish‑purple to violet flower spikes, 5–10 cm long, blooming in early to mid‑summer (June–July).
- Natural habitat: rocky slopes and forest edges at 2000–3500 m altitude in southwestern China, indicating preference for well‑drained, gravely soils.
- Climate: cold‑hardy in temperate regions; listed in horticultural references as hardy to USDA zones 6–9.
- Suitable for rock gardens, alpine plantings, and container displays; provides seasonal ornamental interest for 3–4 months.
- Propagation by seed or soft‑wood cuttings.

Standards and regulation:
- Horticultural nomenclature follows the International Code of Nomenclature for Cultivated Plants (ICNCP); material is sold under the species name or registered cultivar names.
- Retail sales in the EU and US are subject to general plant‑health regulations requiring phytosanitary certificates for interstate/international movement.
- Seed packets must meet national labeling standards for germination rate, purity, and country of origin (e.g., US Federal Seed Act, EU Seed Marketing Directive).
- The American Nursery Stock Standard (ANSI/ANLA) provides quality‑control guidelines for ornamental plant identification and labeling.

Sustainability and sourcing:
- Commercial production relies primarily on cultivated seed and cuttings; wild collection for trade is not commonly reported.
- Small‑scale propagation by specialty nurseries reduces pressure on natural populations.
- Responsible sourcing is recommended from nurseries that maintain traceability and follow good propagation practices.

Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Chinese 丹参
Chinese 银紫丹参
Chinese 毛地黄鼠尾草
Chinese 玉名喇叭
Chinese 白元参
Chinese 毛地黃鼠尾草

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Salvia digitaloides var. digitaloides Unknown
Salvia digitaloides var. glabrescens E.Peter Acta Horti Gothob. 9: 114 (1934)

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000300863
Tropicos 17606597
KEW urn:lsid:ipni.org:names:456106-1
The Plant List kew-182516
Open Tree Of Life 287418
NCBI Taxonomy 268902
IPNI 456106-1
iNaturalist 1231621
GBIF 3903995
Freebase /m/05c1zlk
EOL 2894171
Wikipedia Salvia_digitaloides
CMAUP NPO26049

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
A Comprehensive Review of the Classification, Sources, Phytochemistry, and Pharmacology of Norditerpenes Zeng N, Zhang Q, Yao Q, Fu G, Su W, Wang W, Li B Molecules 21-Dec-2023
PMCID:PMC10780140
doi:10.3390/molecules29010060
PMID:38202643
Ethnobotanical, Phytochemical, and Pharmacological Properties of the Subfamily Nepetoideae (Lamiaceae) in Inflammatory Diseases Ortiz-Mendoza N, Martínez-Gordillo MJ, Martínez-Ambriz E, Basurto-Peña FA, González-Trujano ME, Aguirre-Hernández E Plants (Basel) 02-Nov-2023
PMCID:PMC10648697
doi:10.3390/plants12213752
PMID:37960108
Leucosceptosides A and B: Two Phenyl-Ethanoid Glycosides with Important Occurrence and Biological Activities Frezza C, De Vita D, Toniolo C, Sciubba F, Tomassini L, Venditti A, Bianco A, Serafini M, Foddai S Biomolecules 02-Dec-2022
PMCID:PMC9775335
doi:10.3390/biom12121807
PMID:36551235
A new strategy for osteoarthritis therapy: Inhibition of glycolysis Tan C, Li L, Han J, Xu K, Liu X Front Pharmacol 10-Nov-2022
PMCID:PMC9685317
doi:10.3389/fphar.2022.1057229
PMID:36438808
Microhabitat and Pollinator Differentiation Drive Reproductive Isolation between Two Sympatric Salvia Species (Lamiaceae) Ling TC, Phokasem P, Sinpoo C, Yang YP, Disayathanoowat T Plants (Basel) 16-Sep-2022
PMCID:PMC9506227
doi:10.3390/plants11182423
PMID:36145824
Correction to: Isoprenylated Flavonoids as Cav3.1 Low Voltage-Gated Ca2+ Channel Inhibitors from Salvia digitaloides Zhao JJ, Li SY, Xia F, Hu YL, Nian Y, Xu G Nat Prod Bioprospect 12-May-2021
PMCID:PMC8599561
doi:10.1007/s13659-021-00308-x
PMID:33978931
Isoprenylated Flavonoids as Cav3.1 Low Voltage-Gated Ca2+ Channel Inhibitors from Salvia digitaloides Zhao JJ, Li SY, Xia F, Hu YL, Nian Y, Xu G Nat Prod Bioprospect 24-Apr-2021
PMCID:PMC8599534
doi:10.1007/s13659-021-00307-y
PMID:33893991
Structure-Dependent Activity of Plant-Derived Sweeteners Ҫiçek SS Molecules 22-Apr-2020
PMCID:PMC7221985
doi:10.3390/molecules25081946
PMID:32331403
Five New Iridoids from Roots of Salvia digitaloides Wu SJ, Chan YY Molecules 29-Sep-2014
PMCID:PMC6270932
doi:10.3390/molecules191015521
PMID:25268712
Two Diterpenoids and a Cyclopenta[c]pyridine Derivative from Roots of Salvia digitaloids Wu SJ, Huang CH, Chan YY, Liao YR, Hwang TL, Wu TS Int J Mol Sci 27-Jun-2014
PMCID:PMC4139800
doi:10.3390/ijms150711566
PMID:24979137
Pollen sensitivity to ultraviolet-B (UV-B) suggests floral structure evolution in alpine plants Zhang C, Yang YP, Duan YW Sci Rep 31-Mar-2014
PMCID:PMC3970119
doi:10.1038/srep04520
PMID:24682234
Sweet and bitter glycosides of the Chinese plant drug, Bai-Yun-Shen (roots of Salvia digitaloides). Takashi Tanaka, Osamu Tanaka, ZhongWen Lin, Jun Zhou, Hiroyuki Ageta Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.31.780
Diterpenoid constituents of the roots of Salvia digitaloides. Xu G, Yang J, Wang YY, Peng LY, Yang XW, Pan ZH, Liu ED, Li Y, Zhao QS J Agric Food Chem 08-Dec-2010
doi:10.1021/JF103366G
PMID:21073172
Salviatalin A and salvitrijudin A, two diterpenes with novel skeletons from roots of Salvia digitaloides and anti-inflammatory evaluation Shwu-Jen Wu, Hsiu-Hui Chan, Tsong-Long Hwang, Keduo Qian, Susan Morris-Natschke, Kuo-Hsiung Lee, Tian-Shung Wu Elsevier BV 17-Jun-2010
doi:10.1016/J.TETLET.2010.06.048
Staminal Evolution in the Genus Salvia (Lamiaceae): Molecular Phylogenetic Evidence for Multiple Origins of the Staminal Lever Walker JB, Sytsma KJ Ann Bot 22-Aug-2006
PMCID:PMC2735309
doi:10.1093/aob/mcl176
PMID:16926227

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 / Diterpenoids / Colensane and clerodane diterpenoids
(2S,4aS,8aR)-5-[2-(furan-3-yl)ethyl]-1,1,4a,6-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-2-ol 13876994 Click to see 302.50 unknown https://doi.org/10.1248/CPB.31.780
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Tanshinones, isotanshinones, and derivatives
(1R)-1,6,6-trimethyl-1,2,6,7,8,9-hexahydrophenanthro[1,2-b]furan-10,11(3aH,11aH)-dione 25181389 Click to see CC1COC2C1C(=O)C(=O)C3=C2C=CC4=C3CCCC4(C)C 298.40 unknown via CMAUP database
(S)-6-(Hydroxymethyl)-1,6-dimethyl-6,7,8,9-tetrahydrophenanthro[1,2-b]furan-10,11-dione 9926694 Click to see CC1=COC2=C1C(=O)C(=O)C3=C2C=CC4=C3CCCC4(C)CO 310.30 unknown via CMAUP database
1,6,6-Trimethyl-1,2,6,7,8,9-hexahydrophenanthro(1,2-b)furan-10,11-dione 496348 Click to see 296.40 unknown via CMAUP database
Dihydrotanshinone 5316743 Click to see CC1COC2=C1C(=O)C(=O)C3=C2C=CC4=C(C=CC=C43)C 278.30 unknown https://doi.org/10.1021/JF103366G
Dihydrotanshinone I 11425923 Click to see 278.30 unknown via CMAUP database
Methuyl tanshinonate 624381 Click to see CC1=COC2=C1C(=O)C(=O)C3=C2C=CC4=C3CCCC4(C)C(=O)OC 338.40 unknown via CMAUP database
Npc85771 622085 Click to see 292.30 unknown via CMAUP database
Tanshinone I 114917 Click to see CC1=C2C=CC3=C(C2=CC=C1)C(=O)C(=O)C4=C3OC=C4C 276.30 unknown https://doi.org/10.1021/JF103366G
Tanshinone IIA 164676 Click to see CC1=COC2=C1C(=O)C(=O)C3=C2C=CC4=C3CCCC4(C)C 294.30 unknown https://doi.org/10.1021/JF103366G
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
(2R,3S,4S,5S)-2-[(2R,3R,4S,5S,6R)-2-[[(2S,4aS,8aS)-5-[2-(furan-3-yl)ethyl]-1,1,4a,6-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-2-yl]oxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxyoxane-3,4,5-triol 162896920 Click to see 596.70 unknown https://doi.org/10.1248/CPB.31.780
(2S,3R,4S,5R)-2-[(2R,3R,4S,5S,6R)-2-[[(2S,4aS,8aR)-5-[2-(furan-3-yl)ethyl]-1,1,4a,6-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-2-yl]oxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxyoxane-3,4,5-triol 21636206 Click to see CC1=C(C2(CCC(C(C2CC1)(C)C)OC3C(C(C(C(O3)CO)O)O)OC4C(C(C(CO4)O)O)O)C)CCC5=COC=C5 596.70 unknown https://doi.org/10.1248/CPB.31.780
(2S,3R,4S,5R)-2-[(2R,3R,4S,5S,6R)-2-[[(2S,4aS,8aS)-5-[2-(furan-3-yl)ethyl]-1,1,4a,6-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-2-yl]oxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxyoxane-3,4,5-triol 162896919 Click to see CC1=C(C2(CCC(C(C2CC1)(C)C)OC3C(C(C(C(O3)CO)O)O)OC4C(C(C(CO4)O)O)O)C)CCC5=COC=C5 596.70 unknown https://doi.org/10.1248/CPB.31.780
2-[2-[[5-[2-(Furan-3-yl)ethyl]-1,1,4a,6-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-2-yl]oxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxyoxane-3,4,5-triol 13889923 Click to see 596.70 unknown https://doi.org/10.1248/CPB.31.780
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
Barlerin 162823 Click to see 448.40 unknown https://doi.org/10.1248/CPB.31.780
methyl 7-acetyloxy-5-hydroxy-7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylate 18759764 Click to see 448.40 unknown https://doi.org/10.1248/CPB.31.780
Shanzhiside methyl ester 13892722 Click to see CC1(CC(C2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O)O 406.40 unknown https://doi.org/10.1248/CPB.31.780
Shanzhiside methylester [M+H]+ 13892721 Click to see 406.40 unknown https://doi.org/10.1248/CPB.31.780
Shanzhiside-methylester 3085296 Click to see 406.40 unknown https://doi.org/10.1248/CPB.31.780
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxasteroids and derivatives / Tanshinlactones and derivatives
Neo-tanshinlactone 10264769 Click to see 264.27 unknown https://doi.org/10.1021/JF103366G
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
(1S,2S,6S,7R,9S,10S)-2,6-dimethyl-11,15-dioxo-14-oxapentacyclo[8.8.0.01,9.02,7.012,16]octadec-12(16)-ene-6-carboxylic acid 46895103 Click to see 344.40 unknown https://doi.org/10.1016/J.TETLET.2010.06.048
(2S,6S,7R)-2,6-dimethyl-11,15-dioxo-14-oxatetracyclo[8.8.0.02,7.012,16]octadeca-1(10),12(16)-diene-6-carboxylic acid 46895102 Click to see CC12CCCC(C1CCC3=C2CCC4=C(C3=O)COC4=O)(C)C(=O)O 344.40 unknown https://doi.org/10.1016/J.TETLET.2010.06.048
2,6-Dimethyl-11,15-dioxo-14-oxapentacyclo[8.8.0.01,9.02,7.012,16]octadec-12(16)-ene-6-carboxylic acid 75230160 Click to see CC1(CCCC2(C1CC3C24C3C(=O)C5=C(CC4)C(=O)OC5)C)C(=O)O 344.40 unknown https://doi.org/10.1016/J.TETLET.2010.06.048
2,6-Dimethyl-11,15-dioxo-14-oxatetracyclo[8.8.0.02,7.012,16]octadeca-1(10),12(16)-diene-6-carboxylic acid 75230159 Click to see CC12CCCC(C1CCC3=C2CCC4=C(C3=O)COC4=O)(C)C(=O)O 344.40 unknown https://doi.org/10.1016/J.TETLET.2010.06.048
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
3,5,3',4'-Tetrahydroxy-6,7,8-trimethoxyflavone 44260067 Click to see 376.30 unknown via CMAUP database
3,5,7-Trihydroxy-2-(4-hydroxy-3-methoxyphenyl)-6,8-dimethoxy-4H-1-benzopyran-4-one 12311234 Click to see 376.30 unknown via CMAUP database
3,5,7,3',4'-Pentahydroxy-6,8-dimethoxyflavone 14483219 Click to see 362.30 unknown via CMAUP database
Kaempferol 5280863 Click to see 286.24 unknown via CMAUP database
Quercetin 5280343 Click to see 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 13871824 Click to see 432.40 unknown via CMAUP database
5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[(2R,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 57511421 Click to see 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
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 via CMAUP database
Vitexin 5280441 Click to see 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Cacticin 5318644 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 478.40 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
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
2-(3,4-Dihydroxyphenyl)-5,7,8-trihydroxy-3-methoxy-4H-chromen-4-one 5386958 Click to see 332.26 unknown via CMAUP database
3-Methoxyluteolin 5280681 Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 316.26 unknown via CMAUP database
5,7,8,4'-Tetrahydroxy-3-methoxyflavone 5319442 Click to see COC1=C(OC2=C(C1=O)C(=CC(=C2O)O)O)C3=CC=C(C=C3)O 316.26 unknown via CMAUP database
Gossypetin 3,3'-dimethyl ether 21676153 Click to see 346.30 unknown via CMAUP database
Quercetagetin 3-methyl ether 5320475 Click to see COC1=C(OC2=C(C1=O)C(=C(C(=C2)O)O)O)C3=CC(=C(C=C3)O)O 332.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
5,7,2'-Trihydroxy-3,6,4',5'-tetramethoxyflavone 44259895 Click to see 390.30 unknown via CMAUP database
5,7,3'-Trihydroxy-3,6,4',5'-tetramethoxyflavone 44258045 Click to see 390.30 unknown via CMAUP database
5,7,3',4'-Tetrahydroxy-3,6,5'-trimethoxyflavone 44258041 Click to see 376.30 unknown via CMAUP database
5,7,3',4',5'-Pentahydroxy-3,6-dimethoxyflavone 44259884 Click to see 362.30 unknown via CMAUP database
5,7,8,3',4'-Pentahydroxy-3,6-dimethoxyflavone 21676156 Click to see COC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=CC(=C(C=C3)O)O)OC)O)O 362.30 unknown via CMAUP database
5,7,8,4'-Tetrahydroxy-3,6-dimethoxyflavone 44260054 Click to see 346.30 unknown via CMAUP database
6-Hydroxykaempferol 3,6-dimethyl ether 5352032 Click to see 330.29 unknown via CMAUP database
Axillarin 5281603 Click to see 346.30 unknown via CMAUP database
Jaceidin 5464461 Click to see 360.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Benthamitin 44259900 Click to see 432.40 unknown via CMAUP database
Casticin 5315263 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)O 374.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
3',4',5,7-Tetrahydroxy-3,8-dimethoxyflavone 5748553 Click to see COC1=C(C=C(C2=C1OC(=C(C2=O)OC)C3=CC(=C(C=C3)O)O)O)O 346.30 unknown via CMAUP database
5-Hydroxy-3,6,7,8,3',4',5'-heptamethoxyflavone 44260077 Click to see 448.40 unknown via CMAUP database
5,2'-Dihydroxy-3,6,7,8,4',5'-hexamethoxyflavone 44260086 Click to see 434.40 unknown via CMAUP database
5,3'-Dihydroxy-3,6,7,8,4'-pentamethoxyflavone 369954 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)OC)O 404.40 unknown via CMAUP database
5,3',4'-Trihydroxy-3,6,7,8-tetramethoxyflavone 54799 Click to see COC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=CC(=C(C=C3)O)O)OC)OC)OC 390.30 unknown via CMAUP database
5,3',5'-Trihydroxy-3,6,7,8,4'-pentamethoxyflavone 44260074 Click to see COC1=C(C=C(C=C1O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)OC)O 420.40 unknown via CMAUP database
5,4'-Dihydroxy-3,6,7,8,3'-pentamethoxyflavone 100625 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)OC)O 404.40 unknown via CMAUP database
5,6,3',5'-Tetrahydroxy-3,7,8,4'-tetramethoxyflavone 44260073 Click to see COC1=C(C=C(C=C1O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)O)O)OC)O 406.30 unknown via CMAUP database
5,7-Dihydroxy-2-(4-hydroxy-3-methoxy-phenyl)-3,6,8-trimethoxy-chromen-4-one 5386959 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC)O 390.30 unknown via CMAUP database
5,7-Dihydroxy-3,6,8,3',4',5'-hexamethoxyflavone 5386963 Click to see 434.40 unknown via CMAUP database
5,7,2'-Trihydroxy-3,6,8,4',5'-pentamethoxyflavone 5487077 Click to see COC1=C(C=C(C(=C1)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC)O)OC 420.40 unknown via CMAUP database
5,7,2',4'-Tetrahydroxy-3,6,8,5'-tetramethoxyflavone 21676158 Click to see 406.30 unknown via CMAUP database
5,7,2',4'-Tetrahydroxy-3,8,5'-trimethoxyflavone 44260043 Click to see COC1=C(C=C(C(=C1)C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)OC)OC)O)O 376.30 unknown via CMAUP database
5,7,2',4'-Tetrahydroxy-8,5'-dimethoxyflavone 44258626 Click to see COC1=C(C=C(C(=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC)O)O 346.30 unknown via CMAUP database
5,7,2',5'-Tetrahydroxy-3,6,8,4'-tetramethoxyflavone 44260085 Click to see COC1=C(C=C(C(=C1)O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC)O 406.30 unknown via CMAUP database
5,7,3'-Trihydroxy-3,6,8,4'-Tetramethoxyflavone 21599528 Click to see 390.30 unknown via CMAUP database
5,7,3'-Trihydroxy-3,6,8,4',5'-pentamethoxyflavone 5352085 Click to see COC1=CC(=CC(=C1OC)O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC 420.40 unknown via CMAUP database
5,7,3',4'-Tetrahydroxy-3,6,8-trimethoxyflavone 5386962 Click to see 376.30 unknown via CMAUP database
5,7,3',4'-Tetrahydroxy-3,6,8,5'-tetramethoxyflavone 44260072 Click to see 406.30 unknown via CMAUP database
5,7,3',4',5'-Pentahydroxy-3,6,8-trimethoxyflavone 11383767 Click to see 392.30 unknown via CMAUP database
5,7,3',5'-Tetrahydroxy-3,6,8,4'-tetramethoxyflavone 44260071 Click to see COC1=C(C=C(C=C1O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC)O 406.30 unknown via CMAUP database
5,7,4'-Trihydroxy-3,6,8,3',5'-pentamethoxyflavone 21676159 Click to see 420.40 unknown via CMAUP database
5,7,4'-Trihydroxy-3,8-dimethoxyflavone 13983738 Click to see 330.29 unknown via CMAUP database
Agecorynin D 14162688 Click to see COC1=C(C=C(C(=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)O)O 390.30 unknown via CMAUP database
Calycopterin 10429470 Click to see 374.30 unknown via CMAUP database
Conyzatin 13916282 Click to see 404.40 unknown via CMAUP database
Digicitrin 10071564 Click to see COC1=CC(=CC(=C1OC)O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)OC 434.40 unknown via CMAUP database
Gossypetin 3,8,3'-trimethyl ether 5386961 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)OC)OC)O 360.30 unknown via CMAUP database
Hibiscetin 3,8,4'-trimethyl ether 44260037 Click to see 376.30 unknown via CMAUP database
Sarothrin 5386960 Click to see 360.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
methyl (1S,4aS,5R,7S,7aS)-7-acetyloxy-5-(4-hydroxy-3,5-dimethoxybenzoyl)oxy-7-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylate 70690438 Click to see CC(=O)OC1(CC(C2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)OC(=O)C4=CC(=C(C(=C4)OC)O)OC)C 628.60 unknown https://doi.org/10.1248/CPB.31.780
methyl 7-acetyloxy-5-(4-hydroxy-3,5-dimethoxybenzoyl)oxy-7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylate 77913352 Click to see CC(=O)OC1(CC(C2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)OC(=O)C4=CC(=C(C(=C4)OC)O)OC)C 628.60 unknown https://doi.org/10.1248/CPB.31.780

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