Mukdenia rossii - Unknown
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Internal ID UUID64404e15d2db2245474129
Scientific name Mukdenia rossii
Authority (Oliv.) Koidz.
First published in Acta Phytotax. Geobot. 4: 120 (1935)

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

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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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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

Links to other databases Top

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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)!
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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
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
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
β-Peltoboykinolic Acid from Astilbe rubra Attenuates TGF-β1-Induced Epithelial-to-Mesenchymal Transitions in Lung Alveolar Epithelial Cells Bang IJ, Kim HR, Jeon Y, Jeong MH, Park YJ, Kwak JH, Chung KH Molecules 15-Jul-2019
PMCID:PMC6680586
doi:10.3390/molecules24142573
PMID:31311194
Astragalin: A Bioactive Phytochemical with Potential Therapeutic Activities Riaz A, Rasul A, Hussain G, Zahoor MK, Jabeen F, Subhani Z, Younis T, Ali M, Sarfraz I, Selamoglu Z Adv Pharmacol Sci 02-May-2018
PMCID:PMC5954929
doi:10.1155/2018/9794625
PMID:29853868

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 / 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
(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,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-2008-1074534
https://doi.org/10.1055/S-2002-32565
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
3-Oxooleana-12-ene-27-oic 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/10.1248/CPB.55.1376
https://doi.org/10.1055/S-2002-32565
3beta-Hydroxyurs-12-ene-27-oic 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
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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