Mukdenia rossii is a plant in the saxifrage family, Saxifragaceae. It is a herbaceous plant with basal, palmate leaves and white flowers that bloom in the spring. The plant is known for its fall foliage, which displays vibrant colors. It is also sometimes referred to as Saxifraga rossii. This plant is a member of the Saxifragaceae family and is native to Asia. It is commonly used as an ornamental plant in gardens and is a popular choice for its attractive foliage and delicate flowers.

Synonyms Top

Scientific name	Authority	First published in
Mukdenia acanthifolia	Nakai	J. Jap. Bot. 17: 684 (1941)
Aceriphyllum rossii	Engl.	Nat. Pflanzenfam. 3(2a): 52 (1891)
Saxifraga rossii	Oliv.	Hooker's Icon. Pl. 13: t. 1258 (1878)

Common names Top

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Filter by language:

Language	Common/alternative name
Finnish	vaahtera-angervo
Korean	돌단풍
Chinese	爬山虎
Chinese	槭叶草
Chinese	丹顶草
Chinese	腊八菜
Chinese	槭葉草

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 at 4°C for 3 weeks, then increase to 20°C.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- China
  - Manchuria
- Eastern Asia
  - Korea

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0001136020
Tropicos	29101442
KEW	urn:lsid:ipni.org:names:791989-1
The Plant List	tro-29101442
Missouri Botanical Garden	286944
Open Tree Of Life	756726
NCBI Taxonomy	29766
IPNI	791989-1
iNaturalist	542469
GBIF	7339206
Freebase	/m/03gql97
EOL	2887077
USDA GRIN	420062
Wikipedia	Mukdenia_rossii

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

Characteristics of the complete chloroplast genome of Saxifragaceae species Bergenia purpurascens (Hook. f. et Thoms.) Engl

Ao L, Li N, Fardous Mohammad Safiul A, Li S, Zhao T, Wang J, Zou Y, Li R, Chen S

Mitochondrial DNA B Resour

22-Dec-2023

PMCID:	PMC10763838
doi:	10.1080/23802359.2023.2294895
PMID:	38173921

Effects of Dietary Components on Mast Cells: Possible Use as Nutraceuticals for Allergies?

Kaag S, Lorentz A

Cells

10-Nov-2023

PMCID:	PMC10670325
doi:	10.3390/cells12222602
PMID:	37998337

Exploring plant polyphenols as anti-allergic functional products to manage the growing incidence of food allergy

Wu T, Li Z, Wu Y, Yang X, Li L, Chen S, Qi B, Wang Y, Li C, Zhao Y

Front Nutr

09-Jun-2023

PMCID:	PMC10290203
doi:	10.3389/fnut.2023.1102225
PMID:	37360292

Antibacterial and Antifungal Terpenes from the Medicinal Angiosperms of Asia and the Pacific: Haystacks and Gold Needles

Wiart C, Kathirvalu G, Raju CS, Nissapatorn V, Rahmatullah M, Paul AK, Rajagopal M, Sathiya Seelan JS, Rusdi NA, Lanting S, Sulaiman M

Molecules

04-May-2023

PMCID:	PMC10180233
doi:	10.3390/molecules28093873
PMID:	37175283

Cold Resistance of Euonymus japonicus Beihaidao Leaves and Its Chloroplast Genome Structure and Comparison with Celastraceae Species

Cai H, Gu X, Li Y, Ren Y, Yan S, Yang M

Plants (Basel)

20-Sep-2022

PMCID:	PMC9573587
doi:	10.3390/plants11192449
PMID:	36235317

Characterization of the complete chloroplast genome of Peltoboykinia tellimoides (Saxifragaceae)

Yang R, Li R, Dong M, Liu L

Mitochondrial DNA B Resour

03-May-2022

PMCID:	PMC9090422
doi:	10.1080/23802359.2022.2070040
PMID:	35558180

Flavonoids as inhibitors of human neutrophil elastase

Jakimiuk K, Gesek J, Atanasov AG, Tomczyk M

J Enzyme Inhib Med Chem

13-May-2021

PMCID:	PMC8128182
doi:	10.1080/14756366.2021.1927006
PMID:	33980119

Homegarden agroecosystems managed by Salar people on Qinghai-Tibet Plateau

Zhu M, Luo B, La B, Chen R, Liu F, Long C

J Ethnobiol Ethnomed

23-Mar-2021

PMCID:	PMC7989092
doi:	10.1186/s13002-021-00448-x
PMID:	33757541

Sequencing and comparative analysis of the chloroplast genome of Ribes odoratum provide insights for marker development and phylogenetics in Ribes

Wang L, Liang J, Sa W, Wang L

Physiol Mol Biol Plants

01-Feb-2021

PMCID:	PMC7873140
doi:	10.1007/s12298-021-00932-4
PMID:	33627964

Natural Compounds in Sex Hormone-Dependent Cancers: The Role of Triterpenes as Therapeutic Agents

Şoica C, Voicu M, Ghiulai R, Dehelean C, Racoviceanu R, Trandafirescu C, Roșca OJ, Nistor G, Mioc M, Mioc A

Front Endocrinol (Lausanne)

21-Jan-2021

PMCID:	PMC7859451
doi:	10.3389/fendo.2020.612396
PMID:	33552000

Anti-Inflammatory, Barrier-Protective, and Antiwrinkle Properties of Agastache rugosa Kuntze in Human Epidermal Keratinocytes

Lee Y, Lim HW, Ryu IW, Huang YH, Park M, Chi YM, Lim CJ

Biomed Res Int

26-Oct-2020

PMCID:	PMC7641687
doi:	10.1155/2020/1759067
PMID:	33195687

Degradation of key photosynthetic genes in the critically endangered semi-aquatic flowering plant Saniculiphyllum guangxiense (Saxifragaceae)

Folk RA, Sewnath N, Xiang CL, Sinn BT, Guralnick RP

BMC Plant Biol

08-Jul-2020

PMCID:	PMC7346412
doi:	10.1186/s12870-020-02533-x
PMID:	32640989

Plastome Evolution in Saxifragaceae and Multiple Plastid Capture Events Involving Heuchera and Tiarella

Liu LX, Du YX, Folk RA, Wang SY, Soltis DE, Shang FD, Li P

Front Plant Sci

24-Apr-2020

PMCID:	PMC7193090
doi:	10.3389/fpls.2020.00361
PMID:	32391025

The complete chloroplast genome of Philadelphus pekinensis Rupr. (Hydrangeaceae)

Fan Q, Li M, Zhou H, Liu W, Gong W

Mitochondrial DNA B Resour

27-Feb-2020

PMCID:	PMC7510828
doi:	10.1080/23802359.2020.1730725
PMID:	33366907

Next-Generation Genome Sequencing of Sedum plumbizincicola Sheds Light on the Structural Evolution of Plastid rRNA Operon and Phylogenetic Implications within Saxifragales

Ding H, Zhu R, Dong J, Bi D, Jiang L, Zeng J, Huang Q, Liu H, Xu W, Wu L, Kan X

Plants (Basel)

29-Sep-2019

PMCID:	PMC6843225
doi:	10.3390/plants8100386
PMID:	31569538

Phytochemical Profile Top

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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 / Triterpenoids
(1R,2R,5R,10R,11R,14R,15R,18R,23R)-2,7,7,10,14,18,21,21-octamethyl-6,8-dioxahexacyclo[12.12.0.02,11.05,10.015,24.018,23]hexacos-24-ene-15-carboxylic acid	23651014	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC6C5(COC(O6)(C)C)C)C)C)C2C1)C(=O)O)C)C	512.80	unknown	https://doi.org/10.1021/NP900273Z
(1S,2R,4aR,6aR,6aR,6bR,8aR,10S,12aR,14bR)-10-hydroxy-1,2,4a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-6a-carboxylic acid	12016585	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C(=O)O)C	456.70	unknown	https://doi.org/10.1055/S-2002-32565
(2R,4aS,6aR,6aS,6bR,8aR,9R,10S,12aR,14bR)-10-hydroxy-9-(hydroxymethyl)-2,4a,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-2-carboxylic acid	21123690	Click to see CC12CCC(CC1C3=CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)CO)O)C)(C)C(=O)O	472.70	unknown	https://doi.org/10.1021/NP900273Z
(2R,4aS,6aR,6aS,6bR,8aR,9S,10R,12aR,14bR)-10-acetyloxy-2,4a,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-2,9-dicarboxylic acid	44254604	Click to see CC(=O)OC1CCC2(C(C1(C)C(=O)O)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C(=O)O)C)C)C)C	528.70	unknown	https://doi.org/10.1021/NP900273Z
(2R,4aS,6aR,6aS,6bR,8aR,9S,10S,12aR,14bR)-10-hydroxy-2,4a,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-2,9-dicarboxylic acid	44254602	Click to see CC12CCC(CC1C3=CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C(=O)O)O)C)(C)C(=O)O	486.70	unknown	https://doi.org/10.1021/NP900273Z
(3alpha,4alpha,20alpha)-3-Hydroxyolean-12-ene-23,29-dioic acid	44254696	Click to see CC12CCC(CC1C3=CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C(=O)O)O)C)(C)C(=O)O	486.70	unknown	https://doi.org/10.1021/NP900273Z
(3R,4S,4aR,6aR,6bR,8aR,12aR,14aR,14bR)-3-acetyloxy-4,6a,8a,11,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4,6b-dicarboxylic acid	44254603	Click to see CC(=O)OC1CCC2(C(C1(C)C(=O)O)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C)C(=O)O)C)C	528.70	unknown	https://doi.org/10.1021/NP900273Z
(4aR,6aR,6aR,6bR,8aR,10R,12aR,14bR)-10-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy-2,2,4a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-6a-carboxylic acid	44254694	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C=CC6=CC(=C(C=C6)O)O)C)C)C2C1)C(=O)O)C)C	618.80	unknown	https://doi.org/10.1021/NP900273Z
(4aR,6aR,6aR,6bR,8aR,10R,12aR,14bR)-10-hydroxy-2,2,4a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-6a-carboxylic acid	21633160	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C(=O)O)C)C	456.70	unknown	https://doi.org/10.1248/CPB.55.1376 https://doi.org/10.1055/S-2002-32565
(4aR,6aR,6aR,6bR,8aR,12aR,14bR)-2,2,4a,6b,9,9,12a-heptamethyl-10-oxo-3,4,5,6,6a,7,8,8a,11,12,13,14b-dodecahydro-1H-picene-6a-carboxylic acid	21594119	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1)C(=O)O)C)C	454.70	unknown	https://doi.org/10.1021/NP900273Z https://doi.org/10.1055/S-2002-32565 https://doi.org/10.1248/CPB.55.1376
(4aR,6aR,6aR,6bR,8aR,9R,12aR,14bR)-9-(hydroxymethyl)-2,2,4a,6b,9,12a-hexamethyl-10-oxo-3,4,5,6,6a,7,8,8a,11,12,13,14b-dodecahydro-1H-picene-6a-carboxylic acid	23651015	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)CO)C)C)C2C1)C(=O)O)C)C	470.70	unknown	https://doi.org/10.1021/NP900273Z
(4aR,6aR,6aR,6bR,8aR,9S,10R,12aR,14bR)-9-formyl-10-hydroxy-2,2,4a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-6a-carboxylic acid	44254695	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C=O)O)C)C)C2C1)C(=O)O)C)C	470.70	unknown	https://doi.org/10.1021/NP900273Z
(4aS,6aS,6aS,6bR,8aS,10S,12aR,14bR)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	51892422	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C	456.70	unknown	https://doi.org/10.1248/CPB.55.1376
(4aS,6aS,6aS,6bS,8aS,10R,12aS,14bS)-10-hydroxy-2,2,4a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-6a-carboxylic acid	133611880	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C(=O)O)C)C	456.70	unknown	https://doi.org/10.1055/S-2002-32565 https://doi.org/10.1055/S-2008-1074534
10-Hydroxy-2,2,4a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-6a-carboxylic acid	12314032	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C(=O)O)C)C	456.70	unknown	https://doi.org/10.1055/S-2002-32565
10-Hydroxy-9-(hydroxymethyl)-2,2,4a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-6a-carboxylic acid	56667929	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1)C(=O)O)C)C	472.70	unknown	https://doi.org/10.1055/S-2002-32565
2,2,4a,6b,9,9,12a-heptamethyl-10-oxo-3,4,5,6,6a,7,8,8a,11,12,13,14b-dodecahydro-1H-picene-6a-carboxylic acid	73810219	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1)C(=O)O)C)C	454.70	unknown	https://doi.org/10.1055/S-2002-32565 https://doi.org/10.1055/S-2008-1074534
3-Epikatonic Acid	10434225	Click to see CC1(C2CCC3(C(C2(CCC1O)C)CC=C4C3(CCC5(C4CC(CC5)(C)C(=O)O)C)C)C)C	456.70	unknown	https://doi.org/10.1021/NP900273Z
aceriphyllic acid A	46191092	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1)C(=O)O)C)C	472.70	unknown	https://doi.org/10.1248/CPB.55.1376 https://doi.org/10.1055/S-2002-32565 https://doi.org/10.1021/NP900273Z https://doi.org/10.1055/S-2008-1074534
Aceriphyllic acid B.	163184149	Click to see CC12CCC(CC1C3=CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)CO)O)C)(C)C(=O)O	472.70	unknown	https://doi.org/10.1055/S-2002-32565
Azukisapogenol	73744576	Click to see CC12CCC(CC1C3=CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)CO)O)C)(C)C(=O)O	472.70	unknown	https://doi.org/10.1055/S-2002-32565
Beta-Peltoboykinolic Acid	12016584	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C(=O)O)C)C	456.70	unknown	https://doi.org/10.1021/NP900273Z https://doi.org/10.1055/S-2002-32565 https://doi.org/10.1248/CPB.55.1376
Gypsogenic acid	15560324	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C(=O)O)O)C)C)C2C1)C)C(=O)O)C	486.70	unknown	https://doi.org/10.1248/CPB.55.1376
Oleanolic Acid	10494	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C	456.70	unknown	https://doi.org/10.1021/NP900273Z
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Proline and derivatives
Lincomycin B	3081983	Click to see CCC1CC(N(C1)C)C(=O)NC(C2C(C(C(C(O2)SC)O)O)O)C(C)O	392.50	unknown	https://doi.org/10.1021/NP900273Z
> 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/10.1007/BF02980079
Astragalin	5282102	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O	448.40	unknown	https://doi.org/10.1007/BF02980079
Rutin	5280805	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O	610.50	unknown	https://doi.org/10.1007/BF02980079

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Mukdenia rossii

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top