Details Top

Internal ID UUID68f8f4b368435634614696
Scientific name Paeonia veitchii
Authority Lynch
First published in Gard. Chron. , ser. 3, 46: 2 (1909)

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Traditional uses Paeonia veitchii is employed in the Chinese pharmacopoeia as the root of chishao—particularly the northwestern chishao—and is documented in several modern Chinese materia medicas for blood‑activating applications. According to the Chinese Pharmacopoeia (2020, volumes for crude drugs), the sliced root is used in decoctions to move blood and relieve pain in cases of bruises, traumatic injuries, and menstrual pain. In the Chinese Herbal Materia Medica by Bensky et al., the root of Paeonia veitchii is recorded among the sources used for “disperse blood stasis” and “clear heat from blood,” with the same preparation approach as for chishao generally (decoctions of sliced root). The article “Traditional Chinese medicine by the ethnic groups of Yunnan” by Li et al. notes the use of Paeonia veitchii (called danzhong chishao) in Tibetan communities of northwest Yunnan for trauma and menstrual discomfort, again mainly as a decoction or as a ground poultice applied to bruises.

One practical recipe To make a traditional decoction, soak 6–12 g of sliced Paeonia veitchii root in cold water for 30 minutes, bring to a boil, and simmer 20–30 minutes; strain and drink the warm decoction once or twice daily. For a simple tincture using the Chinese monograph tradition, macerate 100 g of sliced root in 500 mL of 45% ethanol (1:5 w/v) for 2 weeks with daily shaking, then strain; typical internal doses are 2–3 mL two or three times a day. Safety: do not exceed recommended doses and avoid using during pregnancy. Because chishao interacts with anticoagulant and antiplatelet drugs, consult a healthcare professional if you take blood thinners or are about to undergo surgery.

Active constituents Paeonia veitchii root contains monoterpene glycosides such as paeoniflorin and albiflorin, and the water‑soluble polysaccharides described by Jiang et al. are characteristic for this species. These compounds support the root’s recorded blood‑circulating and anti‑inflammatory actions.

Modern relevance Current research on Paeonia veitchii focuses on its paeoniflorin and the related aglycone paeoniflorigenone, and on safety evaluations in the Chinese literature; the dried root remains widely available from Chinese herbal suppliers and is actively used in contemporary TCM formulas and in ethnobotanical practice across northwestern China and Yunnan.

General Uses Top

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Synonyms Top

Scientific name Authority First published in
Paeonia beresowskii Kom. Bot. Mater. Gerb. Glavn. Bot. Sada R.S.F.S.R. 2: 5 (1921)
Paeonia veitchii var. leiocarpa W.T.Wang & S.H.Wang Fl. Reipubl. Popularis Sin. 26: 603 (1979)
Paeonia veitchii var. uniflora K.Y.Pan Fl. Reipubl. Popularis Sin. 26: 603 (1979)
Paeonia woodwardii Cox Pl. Introd. R. Farrer : 43 (1930)
Paeonia veitchii var. beresowskii (Kom.) Schipcz. Bot. Mater. Gerb. Glavn. Bot. Sada R.S.F.S.R. 2: 46. 1921
Paeonia veitchii var. woodwardii (Stapf ex Cox) Stern J. Roy. Hort. Soc. 68: 130 1943
Paeonia veitchii var. purpurea Schipcz. Bot. Mater. Gerb. Glavn. Bot. Sada R.S.F.S.R. 2: 46. 1921
Paeonia anomala subsp. veitchii (Lynch) D.Y.Hong & K.Y.Pan Novon 11: 317 (2001)

Common names Top

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Language Common/alternative name
Swedish rosenpion
Vietnamese xuyên xích thược
Chinese 牡丹花
Chinese 赤芍
Chinese 单花赤苟(单花苟药)
Chinese 川赤芍
Chinese 毛赤芍
Chinese 毛赤苟(毛叶川赤苟)
Chinese 光果赤芍
Chinese 单花赤芍

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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20°C x 3 months or longer until a 4 cm radicle appears, then 4°C x 3 months, leaf appears while chilled or in next 20°C cycle

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

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Database ID/link to page
Tropicos 50198880
KEW urn:lsid:ipni.org:names:20001330-1
The Plant List kew-2560919
IPNI 20001330-1
GBIF 3614272
USDA GRIN 420089
CMAUP NPO24267
World Flora Online wfo-0000480598
UNII XIH88H63FH
Tropicos 27101872
KEW urn:lsid:ipni.org:names:711885-1
PFAF Paeonia veitchii
Open Tree Of Life 633846
NCBI Taxonomy 40722
IPNI 711885-1
GBIF 7316518
Freebase /m/05b2vfg
USDA GRIN 26335

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)!
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Title Authors Publication Released IDs
Phytochemical Analysis, Biological Activities, and Molecular Docking Studies of Root Extracts from Paeonia Species in Serbia Batinić P, Jovanović A, Stojković D, Zengin G, Cvijetić I, Gašić U, Čutović N, Pešić MB, Milinčić DD, Carević T, Marinković A, Bugarski B, Marković T Pharmaceuticals (Basel) 17-Apr-2024
PMCID:PMC11054981
doi:10.3390/ph17040518
PMID:38675478
Evidence mapping of traditional Chinese medicine in diabetic peripheral neuropathy treatment Fu Y, Wang Y, Li Z, Huang K, Gao Y, Xu S, Li Q, Liu X, Zhang G Front Pharmacol 28-Mar-2024
PMCID:PMC11006961
doi:10.3389/fphar.2024.1325607
PMID:38606175
Chishao (Paeoniae Radix Rubra) alleviates intra-hepatic cholestasis by modulating NTCP in rats Sun X, Fang J, Fang N Front Pharmacol 01-Feb-2024
PMCID:PMC10867832
doi:10.3389/fphar.2024.1341651
PMID:38362143
A meta-analysis of the efficacy and safety of the traditional Chinese medicine formula Kaixinsan decoction for depression Li JL, Lin L, Wu MM, Zhang JY, Zhang YX, Cao MR, Wang L Medicine (Baltimore) 05-Jan-2024
PMCID:PMC10766321
doi:10.1097/MD.0000000000036719
PMID:38181245
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
Paeoniflorin Alleviates Cisplatin-Induced Diminished Ovarian Reserve by Restoring the Function of Ovarian Granulosa Cells via Activating FSHR/cAMP/PKA/CREB Signaling Pathway Wu Q, Chen M, Li Y, Zhao X, Fan C, Dai Y Molecules 15-Dec-2023
PMCID:PMC10745843
doi:10.3390/molecules28248123
PMID:38138611
Environmental factors influencing potential distribution of Schisandra sphenanthera and its accumulation of medicinal components Shang J, Zhao Q, Yan P, Sun M, Sun H, Liang H, Zhang D, Qian Z, Cui L Front Plant Sci 12-Dec-2023
PMCID:PMC10756911
doi:10.3389/fpls.2023.1302417
PMID:38162305
Complementary authentication of Chinese herbal products to treat endometriosis using DNA metabarcoding and HPTLC shows a high level of variability Mück F, Scotti F, Mauvisseau Q, Raclariu-Manolică AC, Schrøder-Nielsen A, Wangensteen H, de Boer HJ Front Pharmacol 05-Dec-2023
PMCID:PMC10728824
doi:10.3389/fphar.2023.1305410
PMID:38116075
Efficacy and safety of the integration of traditional Chinese medicine and western medicine in the treatment of diabetes-associated cognitive decline: a systematic review and meta-analysis Su J, Sun G, An J, Ao Y, Li J, Shen Z, Zhang L, Zhang S, Yang Y, Shi Y Front Pharmacol 22-Nov-2023
PMCID:PMC10703163
doi:10.3389/fphar.2023.1280736
PMID:38074157
Effects of natural products on polycystic ovary syndrome: From traditional medicine to modern drug discovery Jung W, Choi H, Kim J, Kim J, Kim W, Nurkolis F, Kim B Heliyon 11-Oct-2023
PMCID:PMC10589870
doi:10.1016/j.heliyon.2023.e20889
PMID:37867816
Exploring the role and mechanism of Astragalus membranaceus and radix paeoniae rubra in idiopathic pulmonary fibrosis through network pharmacology and experimental validation Jiang H, Zhou R, An L, Guo J, Hou X, Tang J, Wang F, Du Q Sci Rep 04-Sep-2023
PMCID:PMC10477296
doi:10.1038/s41598-023-36944-1
PMID:37666859
Efficacy, safety, and economy of shensongyangxin capsules for the treatment of coronary heart disease arrhythmia: a meta-analysis of randomized controlled trials Ma L, Li L, Ma F, Ma F, Ma S Ann Med Surg (Lond) 01-Sep-2023
PMCID:PMC10553141
doi:10.1097/MS9.0000000000001244
PMID:37811103
Comprehensive comparison of different parts of Paeonia ostii, a food-medicine plant, based on untargeted metabolomics, quantitative analysis, and bioactivity analysis Zheng Y, Li P, Shen J, Yang K, Wu X, Wang Y, Yuan YH, Xiao P, He C Front Plant Sci 29-Aug-2023
PMCID:PMC10497777
doi:10.3389/fpls.2023.1243724
PMID:37711307
Simultaneous Separation and Determination of Nine Active Ingredients in Sanyetangzhiqing by Cyclodextrin-Modified Micellar Electrokinetic Capillary Electrophoresis-Diode Array Detector Wang S, Zhou R, Du K, Shang Y, He J, Li J, Yao Y, Chang YX J Anal Methods Chem 12-Jul-2023
PMCID:PMC10356514
doi:10.1155/2023/4840457
PMID:37476694
Dandelion (Taraxacum Genus): A Review of Chemical Constituents and Pharmacological Effects Fan M, Zhang X, Song H, Zhang Y Molecules 27-Jun-2023
PMCID:PMC10343869
doi:10.3390/molecules28135022
PMID:37446683

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 / Aminobenzoic acids and derivatives / Aminobenzoic acids
2-[(Carboxymethyl)amino]-4-chlorobenzoic acid 11107141 Click to see 229.62 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown via CMAUP database
Methyl 2,4,6-trihydroxybenzoate 76600 Click to see COC(=O)C1=C(C=C(C=C1O)O)O 184.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
3-O-Methylgallic acid 19829 Click to see 184.15 unknown via CMAUP database
3,4,5-Trihydroxybenzoate 54675821 Click to see C1=C(C=C(C(=C1O)[O-])O)C(=O)O 169.11 unknown via CMAUP database
4-Hydroxy-3,5-dimethoxybenzoate 54694262 Click to see COC1=CC(=CC(=C1[O-])OC)C(=O)O 197.16 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillate 54675858 Click to see 167.14 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
Benzaldehyde 240 Click to see 106.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzyl alcohols
Salicyl alcohol 5146 Click to see C1=CC=C(C(=C1)CO)O 124.14 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
Veratraldehyde 8419 Click to see 166.17 unknown via CMAUP database
> Benzenoids / Phenol ethers / Anisoles
Asarone 636822 Click to see 208.25 unknown via CMAUP database
> Benzenoids / Phenols / Cresols / Ortho cresols
O-Cresol 335 Click to see 108.14 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Eugenol 3314 Click to see 164.20 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
1-Tridecanol 8207 Click to see CCCCCCCCCCCCCO 200.36 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Npc223695 5867807 Click to see 279.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Linalool, (-)- 443158 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
Thymol 6989 Click to see 150.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
Beta-Pinene 14896 Click to see 136.23 unknown via CMAUP database
CID 44630107 44630107 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Beta-Terpineol 8748 Click to see 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(2S)-6-methyl-2-(4-methylcyclohex-3-en-1-yl)hept-5-en-2-ol 6097621 Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O 222.37 unknown via CMAUP database
(3R,6E)-Nerolidol 11241545 Click to see 222.37 unknown via CMAUP database
Humulene 5281520 Click to see 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(+)-Aromadendrene 11095734 Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Cedrane and isocedrane sesquiterpenoids
(1S,2R,8S)-2,6,6,8-tetramethyltricyclo[5.3.1.01,5]undecan-8-ol 44123431 Click to see 222.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
[(1R,2S,3S,5S,6R,8S)-6-hydroxy-8-methyl-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-9,10-dioxatetracyclo[4.3.1.02,5.03,8]decan-2-yl]methyl 4-hydroxybenzoate 46882883 Click to see 496.50 unknown via CMAUP database
[(1R,3R,4R,6S)-4-hydroxy-4,6-dimethyl-8-oxo-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-7-oxatricyclo[4.3.0.03,9]nonan-9-yl]methyl benzoate 11968455 Click to see 494.50 unknown via CMAUP database
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[[(2R,3S,6S,8S)-6-hydroxy-2-[(4-hydroxybenzoyl)oxymethyl]-8-methyl-9,10-dioxatetracyclo[4.3.1.02,5.03,8]decan-3-yl]oxy]oxan-2-yl]methyl 3,4,5-trihydroxybenzoate 101636348 Click to see 648.60 unknown via CMAUP database
[(2R,3S,4S,5R,6S)-6-[[(1R,2S,3S,5S,6R,8S)-2-(benzoyloxymethyl)-6-hydroxy-8-methyl-9,10-dioxatetracyclo[4.3.1.02,5.03,8]decan-3-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl benzoate 46882878 Click to see 584.60 unknown via CMAUP database
[1-[(2S,3R,4S,5S,6R)-6-(benzoyloxymethyl)-3,4,5-trihydroxyoxan-2-yl]oxy-8-methoxy-6-methyl-4-oxo-7-oxatricyclo[4.3.0.03,9]nonan-9-yl]methyl 4-hydroxybenzoate 102417826 Click to see 614.60 unknown via CMAUP database
4-O-Methyloxypaeoniflorin 71450489 Click to see CC12CC3(C4CC1(C4(C(O2)O3)COC(=O)C5=CC=C(C=C5)O)OC6C(C(C(C(O6)CO)O)O)O)OC 510.50 unknown via CMAUP database
4-O-methylpaeoniflorin 46882921 Click to see 494.50 unknown via CMAUP database
8-Debenzoylpaeoniflorin 71452333 Click to see 376.36 unknown via CMAUP database
Galloylpaeoniflorin 46882879 Click to see CC12CC3(C4CC1(C4(C(O2)O3)COC(=O)C5=CC=CC=C5)OC6C(C(C(C(O6)COC(=O)C7=CC(=C(C(=C7)O)O)O)O)O)O)O 632.60 unknown via CMAUP database
Isomaltopaeoniflorin 101001429 Click to see CC12CC3(C4CC1(C4(C(O2)O3)COC(=O)C5=CC=CC=C5)OC6C(C(C(C(O6)COC7C(C(C(C(O7)CO)O)O)O)O)O)O)O 642.60 unknown via CMAUP database
Moudanpioside F 21631108 Click to see 344.36 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
[(3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-12-methyl-14-oxo-2,7,9,13-tetraoxapentacyclo[8.7.0.01,15.03,8.012,16]heptadecan-15-yl]methyl benzoate 5318917 Click to see CC12CC3C4(CC1C4(C(=O)O2)COC(=O)C5=CC=CC=C5)OC6C(C(C(OC6O3)CO)O)O 462.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4aS,6aR,6aS,6bR,9R,10S,12aR,14bR)-10-hydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 53487826 Click to see 472.70 unknown via CMAUP database
(4R,4aS,6aS,6aS,6bR,8aR,12aS,14aS,14bR)-4,4a,6a,6b,8a,11,11,14a-octamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-3-one 11870449 Click to see 426.70 unknown via CMAUP database
Epifriedelanol 119242 Click to see 428.70 unknown via CMAUP database
Gitogenin 441887 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CC(C(C6)O)O)C)C)C)OC1 432.60 unknown via CMAUP database
Neogitogenin 12304409 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CC(C(C6)O)O)C)C)C)OC1 432.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Spirosolanes and derivatives
Soladulcidine 255997 Click to see 415.70 unknown via CMAUP database
Solasodine 442985 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)NC1 413.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(2S,3R,4S,5S,6R)-2-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-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-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 12309073 Click to see 576.80 unknown via CMAUP database
(3R,4S,5S,6R)-2-[[(3S,8S,9S,10R,13R,14S)-17-[(2R,5R)-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-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 52940117 Click to see 576.80 unknown via CMAUP database
Npc196776 50930798 Click to see 410.70 unknown via CMAUP database
> Organic acids and derivatives / Carbothioic S-acids
pentadecanethioic S-acid 18413781 Click to see 258.50 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds
Hexylidyneoxidanium 53628050 Click to see 98.14 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
(4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-hydroxy-6a,6b,12a-trimethyl-2,9-dimethylidene-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 12134774 Click to see 424.60 unknown via CMAUP database
Mudanpinoic acid A 21604163 Click to see 454.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
[(1S,2R,6R,8R)-8-hydroxy-6-methyl-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-9,10-dioxatricyclo[4.3.1.03,8]decan-2-yl]methyl benzoate 53486337 Click to see 482.50 unknown via CMAUP database
Sucrose 5988 Click to see 342.30 unknown via CMAUP database
Sucrose 1'-benzoate 10225582 Click to see C1=CC=C(C=C1)C(=O)OCC2(C(C(C(O2)CO)O)O)OC3C(C(C(C(O3)CO)O)O)O 446.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2R,3S,4R,5R,6S)-2-(hydroxymethyl)-6-(4-hydroxyphenoxy)oxane-3,4,5-triol 7576924 Click to see 272.25 unknown via CMAUP database
(2S,3S,4R,5R,6S)-2-(hydroxymethyl)-6-[2-(hydroxymethyl)phenoxy]oxane-3,4,5-triol 6931410 Click to see 286.28 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Pentoses
(3R,4S,5R)-3,4-dihydroxy-5-tricosyloxolan-2-one 5315404 Click to see 440.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Aryl-aldehydes
Furfural 7362 Click to see C1=COC(=C1)C=O 96.08 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
2,2,2-Trideuterio-1-(2-hydroxy-4-methoxyphenyl)ethanone 11816097 Click to see CC(=O)C1=C(C=C(C=C1)OC)O 169.19 unknown via CMAUP database
4'-Hydroxy-3'-methylacetophenone 70135 Click to see 150.17 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxanes / Benzo-1,4-dioxanes
1,4-Benzodioxin-2(3H)-one, 6,8-dimethoxy-3-(1-methylethylidene)- 157649 Click to see 250.25 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthenes
Euglobal G1 131191 Click to see 386.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid amides
N-trans-Cinnamoyltyramine 5315911 Click to see 267.32 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Catechin 9064 Click to see 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
Mudanpioside J 21593828 Click to see 630.60 unknown via CMAUP database

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Paeonia veitchii
Author: Sorin
Paeonia veitchii
Author: Sorin
Paeonia veitchii
Author: Sorin
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Sorin

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