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Actaea yunnanensis

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 UUID6440073826f54857215695
Scientific name Actaea yunnanensis
Authority (P.K.Hsiao) J.Compton
First published in Taxon 47: 621 (1998)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Cimicifuga yunnanensis P.K.Hsiao Acta Phytotax. Sin., Addit. 1: 55 (1965)

Common names Top

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Language Common/alternative name
Chinese 云南升麻

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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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-0000519148
Tropicos 50213137
KEW urn:lsid:ipni.org:names:1002882-1
The Plant List kew-2620598
Open Tree Of Life 512689
NCBI Taxonomy 64043
IPNI 1002882-1
iNaturalist 742179
GBIF 5616552

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
Traditional uses, phytochemistry, pharmacology, quality control and clinical studies of Cimicifugae Rhizoma: a comprehensive review Zhang Q, Wei W, Jin X, Lu J, Chen S, Ogaji OD, Wang S, Du K, Chang Y, Li J Chin Med 07-May-2024
PMCID:PMC11075223
doi:10.1186/s13020-024-00937-7
PMID:38715120
New triterpenes from Cimicifuga yunnanensis down-regulating the mRNA expression of CD147, MMP-2, and MMP-9 Lu NH, Li J, Yang YR, Liu HL, Du YR RSC Adv 17-Nov-2021
PMCID:PMC9043592
doi:10.1039/d1ra07828c
PMID:35494395
Antitumor Profile of Carbon-Bridged Steroids (CBS) and Triterpenoids Dembitsky VM, Gloriozova TA, Poroikov VV Mar Drugs 03-Jun-2021
PMCID:PMC8228860
doi:10.3390/md19060324
PMID:34205074
Chemical Authentication of Botanical Ingredients: A Review of Commercial Herbal Products Ichim MC, Booker A Front Pharmacol 15-Apr-2021
PMCID:PMC8082499
doi:10.3389/fphar.2021.666850
PMID:33935790
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
Anticancer efficiency of cycloartane triterpenoid derivatives isolated from Cimicifuga yunnanensis Hsiao on triple-negative breast cancer cells Li X, Wang W, Fan Y, Wei Y, Yu LQ, Wei JF, Wang YF Cancer Manag Res 06-Dec-2018
PMCID:PMC6289211
doi:10.2147/CMAR.S185387
PMID:30584366
Natural Products Research in China From 2015 to 2016 Liu H, Zhu G, Fan Y, Du Y, Lan M, Xu Y, Zhu W Front Chem 20-Mar-2018
PMCID:PMC5869933
doi:10.3389/fchem.2018.00045
PMID:29616210
Antiacetylcholinesterase triterpenes from the fruits of Cimicifuga yunnanensis Nian Y, Lu NH, Liu XL, Li DS, Zhou L, Qiu MH RSC Adv 19-Feb-2018
PMCID:PMC9078504
doi:10.1039/c8ra00291f
PMID:35539105
Anticancer Chemodiversity of Ranunculaceae Medicinal Plants: Molecular Mechanisms and Functions Hao DC, He CN, Shen J, Xiao PG Curr Genomics 01-Feb-2017
PMCID:PMC5321773
doi:10.2174/1389202917666160803151752
PMID:28503089
Novel cycloartane triterpenoid from Cimicifuga foetida (Sheng ma) induces mitochondrial apoptosis via inhibiting Raf/MEK/ERK pathway and Akt phosphorylation in human breast carcinoma MCF-7 cells Sun HY, Liu BB, Hu JY, Xu LJ, Chan SW, Chan CO, Mok DK, Zhang DM, Ye WC, Chen SB Chin Med 11-Jan-2016
PMCID:PMC4709995
doi:10.1186/s13020-015-0073-6
PMID:26759603
New Anti-angiogenic Leading Structure Discovered in the Fruit of Cimicifuga yunnanensis Nian Y, Yang J, Liu TY, Luo Y, Zhang JH, Qiu MH Sci Rep 12-Mar-2015
PMCID:PMC4356973
doi:10.1038/srep09026
PMID:25762443
Four New 9,19‐Cyclolanostane Derivatives from the Rhizomes of <i>Cimicifuga yunnanensis</i><scp>Hsiao</scp> Yin Nian, Jian‐Chao Chen, Lu Lu, Xian‐Ming Zhang, Lin Zhou, Ming‐Hua Qiu Wiley 29-Jan-2009
doi:10.1002/HLCA.200800231
Evaluation of the Botanical Authenticity and Phytochemical Profile of Black Cohosh Products by High-Performance Liquid Chromatography with Selected Ion Monitoring Liquid Chromatography–Mass Spectrometry Jiang B, Kronenberg F, Nuntanakorn P, Qiu MH, Kennelly EJ J Agric Food Chem 03-May-2006
PMCID:PMC3204370
doi:10.1021/jf0606149
PMID:16637680

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 / Steroids and steroid derivatives / Cycloartanols and derivatives
(18'-Hydroxy-1,4',6',12',17',17'-hexamethylspiro[3,6-dioxabicyclo[3.1.0]hexane-4,8'-9-oxahexacyclo[11.9.0.01,21.04,12.05,10.016,21]docosane]-3'-yl) acetate 162889708 Click to see CC1CC2(C3C(O3)(CO2)C)OC4C1C5(C(CC67CC68CCC(C(C8CCC7C5(C4)C)(C)C)O)OC(=O)C)C 528.70 unknown https://doi.org/10.1002/HLCA.200800231
(1S,2R,3S,4R,7R,12R,14R,16R,17R,18R,19R,21R,22S)-2,16-dihydroxy-22-(2-hydroxypropan-2-yl)-3,8,8,17,19-pentamethyl-23,24-dioxaheptacyclo[19.2.1.01,18.03,17.04,14.07,12.012,14]tetracosan-9-one 162890806 Click to see 502.70 unknown https://doi.org/10.1002/HLCA.200800231
(1S,2R,3S,4R,7R,12S,14R,16R,17R,18R,19R,21R,22S)-2,16-dihydroxy-22-(2-hydroxypropan-2-yl)-3,8,8,17,19-pentamethyl-23,24-dioxaheptacyclo[19.2.1.01,18.03,17.04,14.07,12.012,14]tetracos-10-en-9-one 162917340 Click to see 500.70 unknown https://doi.org/10.1002/HLCA.200800231
[(1R)-1-[(1S,4R,5R,6R,8R,10R,11R,12S,13R,16R,18S,21R)-10,11-dihydroxy-4,6,12,17,17-pentamethyl-18-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-9-oxahexacyclo[11.9.0.01,21.04,12.05,10.016,21]docosan-8-yl]-2-methylprop-2-enyl] acetate 162911793 Click to see CC1CC(OC2(C1C3(CCC45CC46CCC(C(C6CCC5C3(C2O)C)(C)C)OC7C(C(C(CO7)O)O)O)C)O)C(C(=C)C)OC(=O)C 662.80 unknown https://doi.org/10.1002/HLCA.200800231
[(1S,1'R,3'R,4S,4'R,5S,5'R,6'R,10'S,12'S,13'S,16'R,18'S,21'R)-1,4',6',12',17',17'-hexamethyl-18'-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyspiro[3,6-dioxabicyclo[3.1.0]hexane-4,8'-9-oxahexacyclo[11.9.0.01,21.04,12.05,10.016,21]docosane]-3'-yl] acetate 10963368 Click to see CC1CC2(C3C(O3)(CO2)C)OC4C1C5(C(CC67CC68CCC(C(C8CCC7C5(C4)C)(C)C)OC9C(C(C(CO9)O)O)O)OC(=O)C)C 660.80 unknown https://doi.org/10.1002/HLCA.200800231
[(1S,1'R,3'R,4S,4'R,5S,5'R,6'R,10'S,12'S,13'S,16'R,18'S,21'R)-18'-hydroxy-1,4',6',12',17',17'-hexamethylspiro[3,6-dioxabicyclo[3.1.0]hexane-4,8'-9-oxahexacyclo[11.9.0.01,21.04,12.05,10.016,21]docosane]-3'-yl] acetate 162889709 Click to see 528.70 unknown https://doi.org/10.1002/HLCA.200800231
[(1S,3R)-1-[(2S)-3,3-dimethyloxiran-2-yl]-3-[(1S,3R,6S,8R,11R,12S,13R,15R,16R)-13-hydroxy-7,7,12,16-tetramethyl-14-oxo-6-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-15-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]butyl] acetate 162976666 Click to see 662.80 unknown https://doi.org/10.1002/HLCA.200800231
[1-[10,11-Dihydroxy-4,6,12,17,17-pentamethyl-18-(3,4,5-trihydroxyoxan-2-yl)oxy-9-oxahexacyclo[11.9.0.01,21.04,12.05,10.016,21]docosan-8-yl]-2-methylprop-2-enyl] acetate 162911792 Click to see 662.80 unknown https://doi.org/10.1002/HLCA.200800231
[1,4',6',12',17',17'-Hexamethyl-18'-(3,4,5-trihydroxyoxan-2-yl)oxyspiro[3,6-dioxabicyclo[3.1.0]hexane-4,8'-9-oxahexacyclo[11.9.0.01,21.04,12.05,10.016,21]docosane]-3'-yl] acetate 73079472 Click to see CC1CC2(C3C(O3)(CO2)C)OC4C1C5(C(CC67CC68CCC(C(C8CCC7C5(C4)C)(C)C)OC9C(C(C(CO9)O)O)O)OC(=O)C)C 660.80 unknown https://doi.org/10.1002/HLCA.200800231
[1,4',6',12',17',17'-Hexamethyl-2-oxo-18'-(3,4,5-trihydroxyoxan-2-yl)oxyspiro[3,6-dioxabicyclo[3.1.0]hexane-4,8'-9-oxahexacyclo[11.9.0.01,21.04,12.05,10.016,21]docosane]-3'-yl] acetate 78200716 Click to see 674.80 unknown https://doi.org/10.1002/HLCA.200800231
[2-Hydroxy-3,8,8,17,19-pentamethyl-22-prop-1-en-2-yl-9-(3,4,5-trihydroxyoxan-2-yl)oxy-23,24-dioxaheptacyclo[19.2.1.01,18.03,17.04,14.07,12.012,14]tetracosan-16-yl] acetate 85320078 Click to see 660.80 unknown https://doi.org/10.1002/HLCA.200800231
11-(2-Hydroxypropan-2-yl)-1,1,7a,8,13a-pentamethyloctadecahydro-5H-10,12a-epoxycyclopropa[1',8a']naphtho[2',1':4,5]indeno[2,1-b]oxepine-2,13-diol 23504335 Click to see 488.70 unknown https://doi.org/10.1002/HLCA.200800231
15-[4-(3,3-Dimethyloxiran-2-yl)-4-oxobutan-2-yl]-13,18-dihydroxy-7,7,12,16-tetramethyl-6-(3,4,5-trihydroxyoxan-2-yl)oxypentacyclo[9.7.0.01,3.03,8.012,16]octadec-10-en-14-one 85155713 Click to see 632.80 unknown https://doi.org/10.1002/HLCA.200800231
15alpha-hydroxycimicidanol-3-O-xyloside 162895006 Click to see 632.80 unknown https://doi.org/10.1002/HLCA.200800231
2,16-Dihydroxy-22-(2-hydroxypropan-2-yl)-3,8,8,17,19-pentamethyl-23,24-dioxaheptacyclo[19.2.1.01,18.03,17.04,14.07,12.012,14]tetracos-10-en-9-one 162917339 Click to see 500.70 unknown https://doi.org/10.1002/HLCA.200800231
2,16-Dihydroxy-22-(2-hydroxypropan-2-yl)-3,8,8,17,19-pentamethyl-23,24-dioxaheptacyclo[19.2.1.01,18.03,17.04,14.07,12.012,14]tetracosan-9-one 162890805 Click to see 502.70 unknown https://doi.org/10.1002/HLCA.200800231
23-O-Acetyl shengmanol xyloside 13071462 Click to see 662.80 unknown https://doi.org/10.1002/HLCA.200800231
acetylacteol-3-O-beta-D-xyloside 124928652 Click to see 676.80 unknown https://doi.org/10.1002/HLCA.200800231
Cimigenol 16020000 Click to see 488.70 unknown https://doi.org/10.1002/HLCA.200800231
Cimiracemoside K 10930352 Click to see 660.80 unknown https://doi.org/10.1002/HLCA.200800231
Cimiracemoside P 91827183 Click to see CC1CC2(C3C(O3)(C(=O)O2)C)OC4C1C5(C(CC67CC68CCC(C(C8CCC7C5(C4)C)(C)C)OC9C(C(C(CO9)O)O)O)OC(=O)C)C 674.80 unknown https://doi.org/10.1002/HLCA.200800231
Shengmating; Spiro[5H-cyclopropa[1',8'a]naphth[2',1':4,5]indeno[2,1-b]pyran-10(2H),2'-[3,6]dioxabicyclo[3.1.0]hexane] |A-D-xylopyranoside deriv 15558324 Click to see 676.80 unknown https://doi.org/10.1002/HLCA.200800231
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
(1S,2S,4R,5R,6R,9R,10S,11R,12R,16R,18S,21R)-2,9,10,11-tetrahydroxy-4,6,12,17,17-pentamethyl-18-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyhexacyclo[11.9.0.01,21.04,12.05,10.016,21]docos-13-en-8-one 10008613 Click to see CC1CC(=O)C(C2(C1C3(CC(C45CC46CCC(C(C6CC=C5C3(C2O)C)(C)C)OC7C(C(C(CO7)O)O)O)O)C)O)O 592.70 unknown https://doi.org/10.1002/HLCA.200800231
2,9,10,11-Tetrahydroxy-4,6,12,17,17-pentamethyl-18-(3,4,5-trihydroxyoxan-2-yl)oxyhexacyclo[11.9.0.01,21.04,12.05,10.016,21]docos-13-en-8-one 85090814 Click to see CC1CC(=O)C(C2(C1C3(CC(C45CC46CCC(C(C6CC=C5C3(C2O)C)(C)C)OC7C(C(C(CO7)O)O)O)O)C)O)O 592.70 unknown https://doi.org/10.1002/HLCA.200800231
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins / Cucurbitacin glycosides
(2S,3R,4S,5R)-2-[[(1S,2R,3S,4R,7R,9S,12R,14S,17R,18R,19R,21R,22S)-22-(2-butoxypropan-2-yl)-2-hydroxy-3,8,8,17,19-pentamethyl-23,24-dioxaheptacyclo[19.2.1.01,18.03,17.04,14.07,12.012,14]tetracosan-9-yl]oxy]oxane-3,4,5-triol 131844764 Click to see 676.90 unknown https://doi.org/10.1002/HLCA.200800231
[(1S)-1-[(1S,4R,5R,6R,8R,10R,11R,12S,13R,16R,18S,21R)-10,11-dihydroxy-4,6,12,17,17-pentamethyl-18-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-9-oxahexacyclo[11.9.0.01,21.04,12.05,10.016,21]docosan-8-yl]-2-hydroxy-2-methylpropyl] acetate 58901565 Click to see 680.90 unknown https://doi.org/10.1002/HLCA.200800231
[(1S)-1-[(1S,4R,5R,6R,8R,10R,11R,12S,13R,16R,18S,21R)-10,11-dihydroxy-4,6,12,17,17-pentamethyl-18-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-9-oxahexacyclo[11.9.0.01,21.04,12.05,10.016,21]docosan-8-yl]-2-methoxy-2-methylpropyl] acetate 162915170 Click to see 694.90 unknown https://doi.org/10.1002/HLCA.200800231
[1-[10,11-Dihydroxy-4,6,12,17,17-pentamethyl-18-(3,4,5-trihydroxyoxan-2-yl)oxy-9-oxahexacyclo[11.9.0.01,21.04,12.05,10.016,21]docosan-8-yl]-2-hydroxy-2-methylpropyl] acetate 13071466 Click to see CC1CC(OC2(C1C3(CCC45CC46CCC(C(C6CCC5C3(C2O)C)(C)C)OC7C(C(C(CO7)O)O)O)C)O)C(C(C)(C)O)OC(=O)C 680.90 unknown https://doi.org/10.1002/HLCA.200800231
[1-[10,11-Dihydroxy-4,6,12,17,17-pentamethyl-18-(3,4,5-trihydroxyoxan-2-yl)oxy-9-oxahexacyclo[11.9.0.01,21.04,12.05,10.016,21]docosan-8-yl]-2-methoxy-2-methylpropyl] acetate 85286528 Click to see CC1CC(OC2(C1C3(CCC45CC46CCC(C(C6CCC5C3(C2O)C)(C)C)OC7C(C(C(CO7)O)O)O)C)O)C(C(C)(C)OC)OC(=O)C 694.90 unknown https://doi.org/10.1002/HLCA.200800231
[2-Hydroxy-2-methyl-1-[4,6,12,17,17-pentamethyl-11-oxo-18-(3,4,5-trihydroxyoxan-2-yl)oxy-9-oxahexacyclo[11.9.0.01,21.04,12.05,10.016,21]docosan-8-yl]propyl] acetate 73020168 Click to see 662.80 unknown https://doi.org/10.1002/HLCA.200800231
2-[[2,16-Dihydroxy-22-(2-hydroxypropan-2-yl)-3,8,8,17,19-pentamethyl-23,24-dioxaheptacyclo[19.2.1.01,18.03,17.04,14.07,12.012,14]tetracosan-9-yl]oxy]oxane-3,4,5-triol 53463575 Click to see 636.80 unknown https://doi.org/10.1002/HLCA.200800231
2-[[22-(2-Butoxypropan-2-yl)-2-hydroxy-3,8,8,17,19-pentamethyl-23,24-dioxaheptacyclo[19.2.1.01,18.03,17.04,14.07,12.012,14]tetracosan-9-yl]oxy]oxane-3,4,5-triol 162988878 Click to see 676.90 unknown https://doi.org/10.1002/HLCA.200800231
2-[2-Hydroxy-3,8,8,17,19-pentamethyl-9-(3,4,5-trihydroxyoxan-2-yl)oxy-23,24-dioxaheptacyclo[19.2.1.01,18.03,17.04,14.07,12.012,14]tetracosan-22-yl]propan-2-yl acetate 72799835 Click to see CC1CC2C(OC3(C1C4(CCC56CC57CCC(C(C7CCC6C4(C3O)C)(C)C)OC8C(C(C(CO8)O)O)O)C)O2)C(C)(C)OC(=O)C 662.80 unknown https://doi.org/10.1002/HLCA.200800231
24-Acetoxyisodahurinol 3-O-xylopyranoside 21606550 Click to see CC1CC(OC2C1C3(CCC45CC46CCC(C(C6CCC5C3(C2=O)C)(C)C)OC7C(C(C(CO7)O)O)O)C)C(C(C)(C)O)OC(=O)C 662.80 unknown https://doi.org/10.1002/HLCA.200800231
25-O-Acetylcimigenol xyloside 91826996 Click to see CC1CC2C(OC3(C1C4(CCC56CC57CCC(C(C7CCC6C4(C3O)C)(C)C)OC8C(C(C(CO8)O)O)O)C)O2)C(C)(C)OC(=O)C 662.80 unknown https://doi.org/10.1002/HLCA.200800231
Cimigenol 3-O-beta-D-xylopyranoside 71098420 Click to see 620.80 unknown https://doi.org/10.1002/HLCA.200800231
Cimigenol xyloside 16088242 Click to see CC1CC2C(OC3(C1C4(CCC56CC57CCC(C(C7CCC6C4(C3O)C)(C)C)OC8C(C(C(CO8)O)O)O)C)O2)C(C)(C)O 620.80 unknown https://doi.org/10.1002/HLCA.200800231
Cimiside A 10054869 Click to see 636.80 unknown https://doi.org/10.1002/HLCA.200800231

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