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Salvia przewalskii

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 UUID643febe38351d844835331
Scientific name Salvia przewalskii
Authority Maxim.
First published in Bull. Acad. Imp. Sci. Saint-Pétersbourg , sér. 3, 27: 526 (1882)

Ethnobotanical Use Top

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General Uses Top

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No verified non-medicinal uses were identified in the consulted sources for Salvia przewalskii. The species is primarily noted in the taxonomic and horticultural literature; commercial/industrial, culinary, craft, fragrance/cosmetics, colorant/tanning, or material-science applications are not documented for this taxon in accessible authoritative references. If such uses are reported in future primary literature, they will require explicit citation to reliable sources before inclusion.

Synonyms Top

Scientific name Authority First published in
Salvia feddei H.Lév. Repert. Spec. Nov. Regni Veg. 12: 532 (1913)
Salvia labellifera H.Lév. Repert. Spec. Nov. Regni Veg. 12: 532 (1913)
Salvia mandarinorum Diels Bot. Jahrb. Syst. 29: 557 (1900)
Salvia przewalskii var. alba X.L.Huang & H.W.Li Acta Phytotax. Sin. 19: 245 (1981)
Salvia przewalskii var. glabrescens E.Peter Acta Horti Gothob. 9: 115. 1934
Salvia przewalskii var. mandarinorum (Diels) E.Peter Acta Horti Gothob. 9: 115. 1934
Salvia przewalskii var. rubrobrunnea C.Y.Wu Fl. Yunnanica 1: 662 (1977)
Salvia tatsienensis Fraanch. Bull. Annuel Soc. Philom. Paris , sér. 8, 3: 150 (1891)
Salvia thibetica H.Lév. Repert. Spec. Nov. Regni Veg. 9: 219 (1911)
Salvia przewalskii f. albiflora Y.H.Wu J. Wuhan Bot. Res. 23: 235 (2005)
Salvia transhimalaica Yonek. Fl. Mustang [Nepal] : 265 (2008)

Common names Top

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Language Common/alternative name
Arabic قصعين برزفالسكي
Chinese 丹参
Chinese 红根草
Chinese 甘西鼠尾草
Chinese 甘西鼠尾草（高原丹参）
Chinese 紫丹参
Chinese 红秦艽
Chinese 高原丹参

Subspecies (abbr. subsp./ssp.) Top

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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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • Tibet

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000302023
KEW urn:lsid:ipni.org:names:457025-1
The Plant List kew-183597
Open Tree Of Life 547902
NCBI Taxonomy 342060
IPNI 457025-1
iNaturalist 821033
GBIF 7307728
Freebase /m/05mqlhc
EOL 2894205
USDA GRIN 32956
Wikipedia Salvia_przewalskii
Tropicos 100254326
KEW urn:lsid:ipni.org:names:60450162-2
The Plant List kew-374960
Open Tree Of Life 6083633
IPNI 60450162-2
GBIF 3885304
CMAUP NPO25813

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
In vitro micropropagation and conservation of endangered medicinal plant Nepeta asterotricha Rech.f. (Lamiaceae): genetic fidelity, phytochemical and biological assessment Zamani M, Sonboli A, Goldansaz M, Mirjalili MH Physiol Mol Biol Plants 23-Feb-2024
PMCID:PMC10901756
doi:10.1007/s12298-024-01416-x
PMID:38435858
Accumulation of Polyphenols and Associated Gene Expression in Hairy Roots of Salvia viridis Exposed to Methyl Jasmonate Grzegorczyk-Karolak I, Krzemińska M, Grąbkowska R, Gomulski J, Żekanowski C, Gaweda-Walerych K Int J Mol Sci 07-Jan-2024
PMCID:PMC10815010
doi:10.3390/ijms25020764
PMID:38255839
Expression and regulation of HIF-1a in hypoxic pulmonary hypertension: Focus on pathological mechanism and Pharmacological Treatment Wan JJ, Yi J, Wang FY, Zhang C, Dai AG Int J Med Sci 01-Jan-2024
PMCID:PMC10750340
doi:10.7150/ijms.88216
PMID:38164358
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
Yield and Composition of the Essential Oil of Clinopodium nepeta subsp. spruneri as Affected by Harvest Season and Cultivation Method, i.e., Outdoor, Greenhouse and In Vitro Culture Vlachou G, Papafotiou M, Daferera DJ, Tarantilis PA Plants (Basel) 07-Dec-2023
PMCID:PMC10747734
doi:10.3390/plants12244098
PMID:38140425
The complete chloroplast genome sequence of Plectranthus hadiensis (Lamiaceae) and phylogenetic analysis Hao J, Lu Y, Dang M, Xia R, Xu L, Zhu Z, Yu Y Mitochondrial DNA B Resour 05-Oct-2023
PMCID:PMC10557565
doi:10.1080/23802359.2023.2262689
PMID:37810612
Promising Natural Medicines for the Treatment of High-Altitude Illness Li L, Lin L, Wen B, Zhao PC, Liu DS, Pang GM, Wang ZR, Tan Y, Lu C High Alt Med Biol 12-Sep-2023
PMCID:PMC10516238
doi:10.1089/ham.2022.0139
PMID:37504973
Functional divergence of CYP76AKs shapes the chemodiversity of abietane-type diterpenoids in genus Salvia Hu J, Qiu S, Wang F, Li Q, Xiang CL, Di P, Wu Z, Jiang R, Li J, Zeng Z, Wang J, Wang X, Zhang Y, Fang S, Qiao Y, Ding J, Jiang Y, Xu Z, Chen J, Chen W Nat Commun 04-Aug-2023
PMCID:PMC10403556
doi:10.1038/s41467-023-40401-y
PMID:37542034
Unveiling the spatial distribution and molecular mechanisms of terpenoid biosynthesis in Salvia miltiorrhiza and S. grandifolia using multi-omics and DESI–MSI Xia J, Lou G, Zhang L, Huang Y, Yang J, Guo J, Qi Z, Li Z, Zhang G, Xu S, Song X, Zhang X, Wei Y, Liang Z, Yang D Hortic Res 31-May-2023
PMCID:PMC10419090
doi:10.1093/hr/uhad109
PMID:37577405
Oxidative Stress Inducers in Cancer Therapy: Preclinical and Clinical Evidence Nizami ZN, Aburawi HE, Semlali A, Muhammad K, Iratni R Antioxidants (Basel) 26-May-2023
PMCID:PMC10295724
doi:10.3390/antiox12061159
PMID:37371889
Application of Rosmarinic Acid with Its Derivatives in the Treatment of Microbial Pathogens Kernou ON, Azzouz Z, Madani K, Rijo P Molecules 22-May-2023
PMCID:PMC10220798
doi:10.3390/molecules28104243
PMID:37241981
Editorial: Bone and Cartilage Diseases – The Role and Potential of Natural Products, Volume II Pei M, Xu D, Wu L Front Pharmacol 02-May-2023
PMCID:PMC10185899
doi:10.3389/fphar.2023.1194875
PMID:37201019
Exploring the pharmacological aspects of natural phytochemicals against SARS-CoV-2 Nsp14 through an in silico approach De A, Bhattacharya S, Debroy B, Bhattacharya A, Pal K In Silico Pharmacol 28-Apr-2023
PMCID:PMC10141836
doi:10.1007/s40203-023-00143-7
PMID:37131867
Hairy Root Cultures as a Source of Phenolic Antioxidants: Simple Phenolics, Phenolic Acids, Phenylethanoids, and Hydroxycinnamates Malarz J, Yudina YV, Stojakowska A Int J Mol Sci 07-Apr-2023
PMCID:PMC10138958
doi:10.3390/ijms24086920
PMID:37108084
Natural Products for the Treatment of Pulmonary Hypertension: Mechanism, Progress, and Future Opportunities Zeng Z, Wang X, Cui L, Wang H, Guo J, Chen Y Curr Issues Mol Biol 13-Mar-2023
PMCID:PMC10047369
doi:10.3390/cimb45030152
PMID:36975522

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 / Anthracenes / Anthraquinones
1,5-Dihydroxy-3-methoxy-7-methylanthraquinone 15138599 Click to see 284.26 unknown https://doi.org/10.1016/0031-9422(92)90069-3
1,5-Dihydroxy-3-methylanthraquinone 5316800 Click to see 254.24 unknown https://doi.org/10.1016/0031-9422(92)90069-3
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
Protocatechuic Acid 72 Click to see 154.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
Veratraldehyde 8419 Click to see 166.17 unknown via CMAUP database
> Benzenoids / Phenanthrenes and derivatives
(+)-Przewalskin 132966659 Click to see 272.40 unknown https://doi.org/10.1248/CPB.53.1575
(1R,8S,10R)-5,11,11-trimethyl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2(7),3,5-trien-4-ol 138113846 Click to see 272.40 unknown https://doi.org/10.1016/0031-9422(91)80121-G
(1S,8R,10R)-4-hydroxy-11,11-dimethyl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2(7),3,5-triene-5-carbaldehyde 162913607 Click to see CC1(CCCC23C1CC(C4=C2C=C(C(=C4)C=O)O)OC3)C 286.40 unknown https://doi.org/10.1002/HLCA.200800293
4-Hydroxy-11,11-dimethyl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2(7),3,5-triene-5-carbaldehyde 162913606 Click to see 286.40 unknown https://doi.org/10.1002/HLCA.200800293
CID 14139389 14139389 Click to see 272.40 unknown via CMAUP database
> Hydrocarbon derivatives / Tropones
4-Acetyl-5,10,16-trihydroxy-12,12-dimethyl-6-propan-2-yl-17-oxatetracyclo[7.6.2.01,11.02,8]heptadeca-2(8),4,6-trien-3-one 73240473 Click to see 402.50 unknown https://doi.org/10.1021/OL061609T
Przewalskin A 16090911 Click to see 402.50 unknown https://doi.org/10.1021/OL061609T
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
gamma-Linolenic acid 5280933 Click to see CCCCCC=CCC=CCC=CCCCCC(=O)O 278.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(10S)-12-Methoxy-9,10-seco-9,20-cycloabieta-8,11,13-triene-10,11-diol 101607178 Click to see 332.50 unknown https://doi.org/10.1248/CPB.53.1575
(11R)-12,12-dimethyl-6-propan-2-yltricyclo[9.4.0.03,8]pentadeca-1(15),3,5,7-tetraen-5-ol 14587208 Click to see 284.40 unknown via CMAUP database
(11S)-12,12-dimethyl-6-propan-2-yltricyclo[9.4.0.03,8]pentadeca-1(15),3,5,7-tetraen-5-ol 14587207 Click to see 284.40 unknown https://doi.org/10.1248/CPB.53.1575
(11S)-12,12-Dimethyl-6-propan-2-yltricyclo[9.4.0.03,8]pentadeca-1(15),3,5,7-tetraene-4,5-diol 10040486 Click to see 300.40 unknown https://doi.org/10.1248/CPB.53.1575
(1R,8S,10S)-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2(7),5-diene-3,4-dione 102280560 Click to see 314.40 unknown https://doi.org/10.1002/HLCA.200800293
(4aS)-6-hydroxy-1,1,4a-trimethyl-7-propan-2-yl-3,4,10,10a-tetrahydro-2H-phenanthren-9-one 5321549 Click to see 300.40 unknown via CMAUP database
1,2-Dihydrotanshinquinone 105119 Click to see CC1=CCCC2=C1C=CC3=C2C(=O)C(=O)C4=C3OC=C4C 278.30 unknown https://doi.org/10.1248/CPB.53.1575
11,11-Dimethyl-5-propan-2-yl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2(7),5-diene-3,4-dione 163041876 Click to see 314.40 unknown https://doi.org/10.1002/HLCA.200800293
12,12-Dimethyl-6-propan-2-yltricyclo[9.4.0.03,8]pentadeca-1,3,5,7,14-pentaene-4,5-diol 11514927 Click to see 298.40 unknown https://doi.org/10.1248/CPB.53.1575
12,12-Dimethyl-6-propan-2-yltricyclo[9.4.0.03,8]pentadeca-1(15),3,5,7-tetraen-5-ol 11011523 Click to see CC(C)C1=C(C=C2CC3=CCCC(C3CCC2=C1)(C)C)O 284.40 unknown https://doi.org/10.1248/CPB.53.1575
12,12-Dimethyl-6-propan-2-yltricyclo[9.4.0.03,8]pentadeca-3,5,7-triene-1,5-diol 4022498 Click to see 302.50 unknown https://doi.org/10.1248/CPB.53.1575
4aH-Dibenzo[a,d]cycloheptene-4a,6,7-triol, 1,2,3,4,5,10,11,11a-octahydro-1,1-dimethyl-8-(1-methylethyl)-, trans-(9CI) 11809306 Click to see 318.40 unknown https://doi.org/10.1248/CPB.53.1575
5-Methoxy-12,12-dimethyl-6-propan-2-yltricyclo[9.4.0.03,8]pentadeca-3,5,7-triene-1,4-diol 14526919 Click to see 332.50 unknown https://doi.org/10.1248/CPB.53.1575
6-Hydroxy-1,1,4A-trimethyl-7-(propan-2-YL)-1,2,3,4,4A,9,10,10A-octahydrophenanthren-9-one 275529 Click to see 300.40 unknown https://doi.org/10.1248/CPB.53.1575
6,7-Dehydroferruginol 10978982 Click to see CC(C)C1=C(C=C2C(=C1)C=CC3C2(CCCC3(C)C)C)O 284.40 unknown https://doi.org/10.1248/CPB.53.1575
9-Methoxy-12,12-dimethyl-6-propan-2-yltricyclo[9.4.0.03,8]pentadeca-1(15),3,5,7-tetraene-4,5-diol 73009331 Click to see 330.50 unknown https://doi.org/10.1248/CPB.53.1575
Abieta-9(11),8(14),12-trien-12-ol 521330 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C)O 286.50 unknown via CMAUP database
Barbatusol 627133 Click to see 300.40 unknown https://doi.org/10.1248/CPB.53.1575
Danshenxinkun D 127172 Click to see 336.40 unknown via CMAUP database
DELTA6-Dehydroferruginol 14165048 Click to see 284.40 unknown https://doi.org/10.1248/CPB.53.1575
Demethylsalvicanol 11666872 Click to see 318.40 unknown https://doi.org/10.1248/CPB.53.1575
Ferruginol 442027 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C)O 286.50 unknown https://doi.org/10.1248/CPB.53.1575
From the seeds of Chamaecyparis pisifera 355228 Click to see 302.50 unknown via CMAUP database
Lanigerol 188496 Click to see CC(C)C1=C(C=C2CC3(CCCC(C3CCC2=C1)(C)C)O)O 302.50 unknown https://doi.org/10.1248/CPB.53.1575
Przewalskin C 11566132 Click to see 330.50 unknown https://doi.org/10.1248/CPB.53.1575
Przewalskin D 101375853 Click to see CC(C)C1=C(C(=C2C=C3C=CCC(C3CCC2=C1)(C)C)O)O 298.40 unknown https://doi.org/10.1248/CPB.53.1575
Sugiol 94162 Click to see 300.40 unknown https://doi.org/10.1248/CPB.53.1575
> 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
(1S,6R,19R,22R,28S,30S)-19-hydroxy-13,22,31,31-tetramethyl-19-(2-oxopropyl)-25-propan-2-yl-5,7,23,35-tetraoxanonacyclo[26.6.1.01,30.03,27.04,24.06,22.08,21.09,18.012,17]pentatriaconta-3,8(21),9(18),10,12,14,16,24,26-nonaen-20-one 57404390 Click to see 648.80 unknown via CMAUP database
(6R)-6-(hydroxymethyl)-1,6-dimethyl-8,9-dihydro-7H-naphtho[1,2-g][1]benzofuran-10,11-dione 56967682 Click to see CC1=COC2=C1C(=O)C(=O)C3=C2C=CC4=C3CCCC4(C)CO 310.30 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 https://doi.org/10.1248/CPB.53.1575
https://doi.org/10.1080/10826079708010970
Cryptotanshinone 160254 Click to see 296.40 unknown https://doi.org/10.1248/CPB.53.1575
https://doi.org/10.1021/NP800119K
https://doi.org/10.1080/10826079708010970
Danshenol A 3083514 Click to see 336.40 unknown via CMAUP database
Danshenxinkun A 149138 Click to see 296.30 unknown via CMAUP database
Dehydrodanshenol A 71816415 Click to see CC1=C2C=CC3=C(C2=CC=C1)C(C(=O)C4=C3OC=C4C)(CC(=O)C)O 334.40 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 via CMAUP database
Dihydrotanshinone I 11425923 Click to see 278.30 unknown https://doi.org/10.1080/10826079708010970
Isograndifoliol 71816417 Click to see 302.40 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
Miltipolone 10086184 Click to see 300.40 unknown via CMAUP database
Miltirone 160142 Click to see 282.40 unknown via CMAUP database
Npc85771 622085 Click to see 292.30 unknown via CMAUP database
Przewaquinone A 619402 Click to see 310.30 unknown https://doi.org/10.1016/0031-9422(91)80121-G
https://doi.org/10.1021/NP800119K
Przewaquinone C 56967683 Click to see 296.30 unknown via CMAUP database
Tanshindiol B 5321620 Click to see 312.30 unknown via CMAUP database
Tanshindiol C 126072 Click to see 312.30 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/10.1248/CPB.53.1575
https://doi.org/10.1016/0031-9422(91)80121-G
Tanshinone IIA 164676 Click to see CC1=COC2=C1C(=O)C(=O)C3=C2C=CC4=C3CCCC4(C)C 294.30 unknown https://doi.org/10.1248/CPB.53.1575
https://doi.org/10.1080/10826079708010970
https://doi.org/10.1016/0031-9422(91)80121-G
Tanshinone Iib 318797 Click to see 310.30 unknown https://doi.org/10.1016/0031-9422(91)80121-G
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(1R,8R,9S)-3,4,9-trihydroxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2,4,6-trien-15-one 100934562 Click to see 346.40 unknown via CMAUP database
(1R,8S)-3,4-dihydroxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2,4,6-trien-15-one 6324890 Click to see 330.40 unknown via CMAUP database
(1R)-3,4-Dihydroxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2,4,6-trien-15-one 2579 Click to see 330.40 unknown https://doi.org/10.1248/CPB.53.1575
Carnosol 442009 Click to see 330.40 unknown https://doi.org/10.1248/CPB.53.1575
Rosmanol 13966122 Click to see 346.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,2R,4aS,6aR,6aS,6bR,8aR,10R,12aR)-1,10-dihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 9956482 Click to see 472.70 unknown via CMAUP database
3-Hydroxyolean-12-en-28-oic acid 619166 Click to see 456.70 unknown https://doi.org/10.1016/0031-9422(88)80642-3
Npc62469 49867942 Click to see 456.70 unknown via CMAUP database
Oleanolic Acid 10494 Click to see 456.70 unknown https://doi.org/10.1016/0031-9422(88)80642-3
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxasteroids and derivatives / Tanshinlactones and derivatives
Tanshinlactone 5321617 Click to see CC1=C2C=CC3=C(C2=CC=C1)C(=O)OC4=C3OC=C4C 264.27 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/0031-9422(91)80121-G
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1016/0031-9422(91)80121-G
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2R)-2-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy-3-[4-hydroxy-3-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]propanoic acid 25245849 Click to see 522.50 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
3-Hydroxybenzaldehyde 101 Click to see C1=CC(=CC(=C1)O)C=O 122.12 unknown via CMAUP database
> Organoheterocyclic compounds / Benzofurans
(-)-Rosmadial 72996596 Click to see 344.40 unknown https://doi.org/10.1248/CPB.53.1575
Rosmadial 15801061 Click to see 344.40 unknown https://doi.org/10.1248/CPB.53.1575
> Organoheterocyclic compounds / Naphthofurans
(1S,4'R)-4',7-dimethylspiro[benzo[e][2]benzofuran-1,2'-oxolane]-3-one 163023712 Click to see 268.31 unknown https://doi.org/10.1248/CPB.53.1575
13-Hydroxy-5,5-dimethyl-15-propan-2-yl-11-oxatetracyclo[8.6.0.01,13.04,9]hexadeca-8,15-diene-12,14-dione 163002166 Click to see CC(C)C1=CC23CCC4C(=CCCC4(C)C)C2OC(=O)C3(C1=O)O 330.40 unknown https://doi.org/10.1021/OL062748D
4',7-Dimethylspiro[benzo[e][2]benzofuran-1,2'-oxolane]-3-one 163023711 Click to see 268.31 unknown https://doi.org/10.1248/CPB.53.1575
CID 56932940 56932940 Click to see 556.60 unknown via CMAUP database
Cryptoacetalide 46896125 Click to see CC1CC2(C3=C(C4=C(C=C3)C(CCC4)(C)C)C(=O)O2)OC1 286.40 unknown https://doi.org/10.1248/CPB.53.1575
Danshinspiroketallactone 56956598 Click to see 268.31 unknown via CMAUP database
Epidanshenspiroketallactone 102004791 Click to see 268.31 unknown via CMAUP database
Przewalskin B 51002763 Click to see 330.40 unknown https://doi.org/10.1021/OL062748D
Salprzelactone 71816414 Click to see CC1COC(=O)C1C2C3=C(C4=CC=CC(=C4C=C3)C)C(=O)O2 296.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(2S,3S)-4-[(E)-3-[(1S)-1-carboxy-2-(3,4-dihydroxyphenyl)ethoxy]-3-oxoprop-1-enyl]-2-(3,4-dihydroxyphenyl)-7-hydroxy-2,3-dihydro-1-benzofuran-3-carboxylic acid 95359683 Click to see 538.50 unknown https://doi.org/10.1021/NP0501031
2-[[4-[(E)-3-[1-carboxy-2-(3,4-dihydroxyphenyl)ethoxy]-3-oxoprop-1-enyl]-2-(3,4-dihydroxyphenyl)-6-hydroxy-2,3-dihydro-1-benzofuran-3-yl]-hydroxymethoxy]-3-(3,4-dihydroxyphenyl)propanoic acid 56677421 Click to see 720.60 unknown via CMAUP database
Dimethyl lithospermate B 11422787 Click to see COC(=O)C(CC1=CC(=C(C=C1)O)O)OC(=O)C=CC2=C3C(C(OC3=C(C=C2)O)C4=CC(=C(C=C4)O)O)C(=O)OC(CC5=CC(=C(C=C5)O)O)C(=O)OC 746.70 unknown https://doi.org/10.1016/S0031-9422(01)00415-0
Lithospermic Acid 6441498 Click to see 538.50 unknown via CMAUP database
Przewalskinic acid A 9975641 Click to see 358.30 unknown https://doi.org/10.1016/S0031-9422(01)00415-0
Salvianolic Acid B 6451084 Click to see 718.60 unknown https://doi.org/10.1021/NP0501031
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(S)-Rosmarinic acid 639655 Click to see 360.30 unknown via CMAUP database
Rosmarinic Acid 5281792 Click to see 360.30 unknown https://doi.org/10.1021/NP0501031
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
(Z)-3-[2-(carboxymethyl)-3,4-dihydroxy-phenyl]prop-2-enoic acid 49770696 Click to see C1=CC(=C(C(=C1C=CC(=O)O)CC(=O)O)O)O 238.19 unknown via CMAUP database
3-(3,4-Dihydroxyphenyl)prop-2-enoate 54710367 Click to see 179.15 unknown via CMAUP database
3-(3,4-Dihydroxyphenyl)Prop-2-Enoic Acid 2518 Click to see 180.16 unknown via CMAUP database
Isoferulic Acid 736186 Click to see 194.18 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
5,6,4'-Trihydroxy-7,3'-dimethoxyflavone 10359254 Click to see 330.29 unknown via CMAUP database
Jaranol 5318869 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC=C(C=C3)O)O 314.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Phenylpropanoic acids
2-[(E)-3-(3,4-dihydroxycyclohexa-1,5-dien-1-yl)-1-hydroxy-allyloxy]-3-(3,4-dihydroxyphenyl)propanoic acid 49770232 Click to see C1=CC(=CC(C1O)O)C=CC(O)OC(CC2=CC(=C(C=C2)O)O)C(=O)O 364.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
(2S)-3-(3,4-dihydroxyphenyl)-2-[(Z)-3-[2-[(E)-2-(3,4-dihydroxyphenyl)ethenyl]-3,4-dihydroxyphenyl]prop-2-enoyl]oxypropanoic acid 9913656 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=C(C(=C(C=C2)O)O)C=CC3=CC(=C(C=C3)O)O)O)O 494.40 unknown via CMAUP database

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