Actaea japonica - Unknown
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Internal ID UUID64400735e646a347327592
Scientific name Actaea japonica
Authority Thunb.
First published in Syst. Veg., ed. 14 (J. A. Murray). 488. 1784 [May-Jun 1784]

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Synonyms Top

Scientific name Authority First published in
Thalictrodes japonica Kuntze Revis. Gen. Pl. 1: 4 (1891)
Actaea acerina Prantl Bot. Jahrb. Syst. 9(3): 246. 1887 [30 Dec 1887]
Actaea japonica var. acutiloba (H.Hara) J.Compton Taxon 47: 620 (1998)
Cimicifuga acerina (Siebold & Zucc.) Tanaka Bult. Sci. Fak. Terk. Kjusu Imp. Univ. 1(4): 203, 209 (1925).
Cimicifuga acerina f. hispidula P.K.Hsiao Acta Phytotax. Sin., Addit. 1: 54 1965
Cimicifuga acerina var. intermedia H.Hara Acta Phytotax. Geobot. 13: 200 1943
Cimicifuga acerina var. peltata (Makino) H.Hara Acta Phytotax. Geobot. 13: 201 1943
Cimicifuga chinensis Koidz. Bot. Mag. (Tokyo) 44: 102 (1930)
Cimicifuga japonica Spreng. Syst. Veg. 2: 628 (1825)
Cimicifuga japonica var. acutiloba H.Hara Acta Phytotax. Geobot. 13: 200 1943
Cimicifuga japonica var. macrophylla (Koidz.) H.Hara J. Jap. Bot. 60: 137 (1985)
Cimicifuga japonica f. peltata Makino Bot. Mag. (Tokyo) 24: 140 1910
Cimicifuga japonica var. peltata (Makino) H.Hara J. Jap. Bot. 60: 137 (1985)
Cimicifuga macrophylla Koidz. Bot. Mag. (Tokyo) 44: 101 (1930)
Cimicifuga peltata Koidz. Bot. Mag. (Tokyo) 44: 101 (1930)
Pityrosperma acerinum Siebold & Zucc. Abh. Math.-Phys. Cl. Königl. Bayer. Akad. Wiss. 3(3): 735. 1843

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Language Common/alternative name
Japanese オオバショウマ
Tamil அக்டேயா யபோனிகா
Chinese 小升麻

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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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Maintain seeds at 20°C for 3 months, then transfer to 4°C for another 3 months.

Distribution (via POWO/KEW) Top

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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000519087
Tropicos 50213130
KEW urn:lsid:ipni.org:names:708008-1
The Plant List kew-2620541
Open Tree Of Life 988749
NCBI Taxonomy 64035
IPNI 927381-1
iNaturalist 742170
GBIF 7278076
EPPO CIMJA
USDA GRIN 411897
Wikipedia Actaea_japonica

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
Nonadaptive molecular evolution of plastome during the speciation of Actaea purpurea and its relatives Zhang D, Ren Y, Zhang J Ecol Evol 17-Sep-2022
PMCID:PMC9482002
doi:10.1002/ece3.9321
PMID:36177132
Paving the way towards effective plant-based inhibitors of hyaluronidase and tyrosinase: a critical review on a structure–activity relationship Gębalski J, Graczyk F, Załuski D J Enzyme Inhib Med Chem 26-Apr-2022
PMCID:PMC9045780
doi:10.1080/14756366.2022.2061966
PMID:35470749
Benefits of Black Cohosh (Cimicifuga racemosa) for Women Health: An Up-Close and In-Depth Review Mohapatra S, Iqubal A, Ansari MJ, Jan B, Zahiruddin S, Mirza MA, Ahmad S, Iqbal Z Pharmaceuticals (Basel) 23-Feb-2022
PMCID:PMC8953734
doi:10.3390/ph15030278
PMID:35337076
Ethnobotanical study on herbal market at the Dragon Boat Festival of Chuanqing people in China Wang Q, Zhao L, Gao C, Zhao J, Ren Z, Shen Y, Yao R, Yin H J Ethnobiol Ethnomed 23-Mar-2021
PMCID:PMC7985747
doi:10.1186/s13002-021-00447-y
PMID:33757555
Anti-angiogenic activity of ShengMaBieJia decoction in vitro and in acute myeloid leukaemia tumour-bearing mouse models Wang M, Ma B, Dai X, Zhang H, Dai H, Wang J, Liu L, Sun X Pharm Biol 20-May-2020
PMCID:PMC7301716
doi:10.1080/13880209.2020.1764059
PMID:32432951
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
Do Herbal Formulas Influence the International Normalized Ratio of Patients Taking Warfarin? A Retrospective Study Lu HY, Cho SY, Park SU, Jung WS, Moon SK, Park JM, Ko CN Evid Based Complement Alternat Med 10-Mar-2015
PMCID:PMC4377386
doi:10.1155/2015/213927
PMID:25861354
Phenolic constituents of the aerial parts of Cimicifuga simplex and Cimicifuga japonica. Iwanaga A, Kusano G, Warashina T, Miyase T J Nat Prod 23-Apr-2010
doi:10.1021/NP900752T
PMID:20184336
Structures of Two New Cyclolanostanol Xylosides, Cimiacerosides A and B Genjiro Kusano, Akiko Kusano, Masayuki Takahira, Makio Shibano, Toshio Miyase, Toru Okuyama The Japan Institute of Heterocyclic Chemistry 24-Mar-2009
doi:10.3987/COM-98-8121
Growth inhibitory activity of extracts and compounds from Cimicifuga species on human breast cancer cells. Einbond LS, Wen-Cai Y, He K, Wu HA, Cruz E, Roller M, Kronenberg F Phytomedicine 01-Jun-2008
PMCID:PMC2612939
doi:10.1016/J.PHYMED.2007.09.017
PMID:17980565
Growth inhibitory activity of extracts and compounds from Cimicifuga species on human breast cancer cells Einbond LS, Wen-Cai Y, He K, Wu HA, Cruz E, Roller M, Kronenberg F Phytomedicine 05-Nov-2007
PMCID:PMC2612939
doi:10.1016/j.phymed.2007.09.017
PMID:17980565
Floral benzenoid carboxyl methyltransferases: From in vitro to in planta function Effmert U, Saschenbrecker S, Ross J, Negre F, Fraser CM, Noel JP, Dudareva N, Piechulla B Phytochemistry 01-Jun-2005
PMCID:PMC2864587
doi:10.1016/j.phytochem.2005.03.031
PMID:15946712
Floral fragrances in Cimicifuga: Chemical polymorphism and incipient speciation in Cimicifuga simplex Inga groth, Gunnar Bergstrom, Olle Pellmyrt Elsevier BV 10-Feb-2003
doi:10.1016/0305-1978(87)90058-5
Phenolic constituents of Iris milesii rhizomes V.K. Agarwal, R.K. Thappa, S.G. Agarwal, K.L. Dhar Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)80460-4
Piscidic acid and fukiic acid esters from Cimicifuga simplex1Part 24 in the series “Constituents of Cimicifuga spp.”, and Part 2 in the series “Phenolics of Cimicifuga spp.” For part 23 see Ref.[1].1 Masayukui Takahira, Akiko Kusano, Makio Shibano, Genjiro Kusano, Toshio Miyase Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(98)00407-5

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 / Monoterpenoids / Bicyclic monoterpenoids
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1016/0305-1978(87)90058-5
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1016/0305-1978(87)90058-5
Sabinen 18818 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown https://doi.org/10.1016/0305-1978(87)90058-5
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
(1R,2R,3S,4R,7S,9S,12S,14S,17R,18R,19R,21R,22R)-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]tetracosane-2,9-diol 134688430 Click to see CC1CC2C(OC3(C1C4(CCC56CC57CCC(C(C7CCC6C4(C3O)C)(C)C)O)C)O2)C(C)(C)O 488.70 unknown https://doi.org/10.1080/10286029908039890
(1R,3R,6S,8R,12R,15R,16R)-7,7,12,16-tetramethyl-15-[(2S)-6-methylhept-5-en-2-yl]pentacyclo[9.7.0.01,3.03,8.012,16]octadec-10-en-6-ol 163001066 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2=CCC5C3(C4)CCC(C5(C)C)O)C)C 424.70 unknown https://doi.org/10.1248/YAKUSHI1947.90.1_64
(2R,3S,9S,12R,14S,17R,19R,22S)-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]tetracosane-2,9-diol 5315871 Click to see CC1CC2C(OC3(C1C4(CCC56CC57CCC(C(C7CCC6C4(C3O)C)(C)C)O)C)O2)C(C)(C)O 488.70 unknown https://doi.org/10.1080/10286029908039890
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 CC1CC2C(OC3(C1C4(CCC56CC57CCC(C(C7CCC6C4(C3O)C)(C)C)O)C)O2)C(C)(C)O 488.70 unknown https://doi.org/10.1248/YAKUSHI1947.87.12_1569
2-[(21,22-Dihydroxy-1,6,6,15,17,20,20-heptamethyl-19,23-dioxaheptacyclo[13.10.0.02,12.05,10.010,12.016,24.018,22]pentacos-2-en-7-yl)oxy]oxane-3,4,5-triol 73808750 Click to see CC1C2C(CC3(C2(CCC45C3=CCC6C4(C5)CCC(C6(C)C)OC7C(C(C(CO7)O)O)O)C)C)OC8(C1OC(C8O)(C)C)O 618.80 unknown https://doi.org/10.1016/S0031-9422(98)00407-5
2-[(21,22-Dihydroxy-1,6,6,15,17,20,20-heptamethyl-19,23-dioxaheptacyclo[13.10.0.02,12.05,10.010,12.016,24.018,22]pentacosan-7-yl)oxy]oxane-3,4,5-triol 73088411 Click to see CC1C2C(CC3(C2(CCC45C3CCC6C4(C5)CCC(C6(C)C)OC7C(C(C(CO7)O)O)O)C)C)OC8(C1OC(C8O)(C)C)O 620.80 unknown https://doi.org/10.1016/S0031-9422(98)00407-5
2-[[(1R,5R,7S,10R,12R,15R,16R,17S,18R,21R,22R,24S)-21,22-dihydroxy-1,6,6,15,17,20,20-heptamethyl-19,23-dioxaheptacyclo[13.10.0.02,12.05,10.010,12.016,24.018,22]pentacos-2-en-7-yl]oxy]oxane-3,4,5-triol 398800 Click to see CC1C2C(CC3(C2(CCC45C3=CCC6C4(C5)CCC(C6(C)C)OC7C(C(C(CO7)O)O)O)C)C)OC8(C1OC(C8O)(C)C)O 618.80 unknown https://doi.org/10.3987/COM-98-8121
8-(1,2-Dihydroxy-2-methylpropyl)-18-hydroxy-4,6,12,17,17-pentamethyl-9-oxahexacyclo[11.9.0.01,21.04,12.05,10.016,21]docosan-11-one 76795796 Click to see CC1CC(OC2C1C3(CCC45CC46CCC(C(C6CCC5C3(C2=O)C)(C)C)O)C)C(C(C)(C)O)O 488.70 unknown https://doi.org/10.1248/CPB.49.1468
Cimiaceroside A 21591249 Click to see CC1C2C(CC3(C2(CCC45C3=CCC6C4(C5)CCC(C6(C)C)OC7C(C(C(CO7)O)O)O)C)C)OC8(C1OC(C8O)(C)C)O 618.80 unknown https://doi.org/10.1016/S0031-9422(98)00407-5
Cimiaceroside B 398801 Click to see CC1C2C(CC3(C2(CCC45C3CCC6C4(C5)CCC(C6(C)C)OC7C(C(C(CO7)O)O)O)C)C)OC8(C1OC(C8O)(C)C)O 620.80 unknown https://doi.org/10.3987/COM-98-8121
Cimigenol 16020000 Click to see CC1CC2C(OC3(C1C4(CCC56CC57CCC(C(C7CCC6C4(C3O)C)(C)C)O)C)O2)C(C)(C)O 488.70 unknown https://doi.org/10.1248/YAKUSHI1947.87.12_1569
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins / Cucurbitacin glycosides
Cimigenoside 71098420 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://www.ncbi.nlm.nih.gov/pmc/articles/PMC2612939/
https://doi.org/10.1080/10286029908039890
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8R,9R,10R,13R,14R,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-ol 11870456 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1248/YAKUSHI1947.86.11_1006
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/10.1248/YAKUSHI1947.86.11_1006
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
5-[(2S,3R,4S,5S,6R)-6-(benzoyloxymethyl)-3,4,5-trihydroxyoxan-2-yl]oxy-2-hydroxybenzoic acid 46210881 Click to see C1=CC=C(C=C1)C(=O)OCC2C(C(C(C(O2)OC3=CC(=C(C=C3)O)C(=O)O)O)O)O 420.40 unknown https://doi.org/10.1021/NP900752T
5-[6-(Benzoyloxymethyl)-3,4,5-trihydroxyoxan-2-yl]oxy-2-hydroxybenzoic acid 75149598 Click to see C1=CC=C(C=C1)C(=O)OCC2C(C(C(C(O2)OC3=CC(=C(C=C3)O)C(=O)O)O)O)O 420.40 unknown https://doi.org/10.1021/NP900752T
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(2R,3S)-3-[3-(3,4-dimethoxyphenyl)prop-2-enoyloxy]-2-hydroxy-2-[(4-hydroxyphenyl)methyl]butanedioic acid 162869894 Click to see COC1=C(C=C(C=C1)C=CC(=O)OC(C(=O)O)C(CC2=CC=C(C=C2)O)(C(=O)O)O)OC 446.40 unknown https://doi.org/10.1021/NP900752T
(2S,3R)-2-[(3,4-dihydroxyphenyl)methyl]-3-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-2-hydroxybutanedioic acid 162905687 Click to see C1=CC(=C(C=C1CC(C(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)(C(=O)O)O)O)O 434.30 unknown https://doi.org/10.1021/NP900752T
2-Benzyl-3-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-2-hydroxybutanedioic acid 75149538 Click to see C1=CC=C(C=C1)CC(C(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)(C(=O)O)O 402.40 unknown https://doi.org/10.1021/NP900752T
Cimicifugic acid A 6449879 Click to see COC1=C(C=CC(=C1)C=CC(=O)OC(C(=O)O)C(CC2=CC(=C(C=C2)O)O)(C(=O)O)O)O 448.40 unknown https://doi.org/10.1016/S0031-9422(00)80460-4
Cimicifugic acid G 162905688 Click to see C1=CC(=C(C=C1CC(C(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)(C(=O)O)O)O)O 434.30 unknown https://doi.org/10.1021/NP900752T
Cimiracemate A 5315874 Click to see COC1=C(C=C(C=C1)C=CC(=O)OCC(=O)CC2=CC(=C(C=C2)O)O)O 358.30 unknown https://doi.org/10.1016/S0031-9422(00)80460-4
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
(2R,3S)-2-hydroxy-2-[(4-hydroxyphenyl)methyl]-3-[3-(4-hydroxyphenyl)prop-2-enoyloxy]butanedioic acid 162869588 Click to see C1=CC(=CC=C1CC(C(C(=O)O)OC(=O)C=CC2=CC=C(C=C2)O)(C(=O)O)O)O 402.40 unknown https://doi.org/10.1021/NP900752T
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-(4-Hydroxy-3-methoxyphenyl)prop-2-enoic acid 709 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O 194.18 unknown https://doi.org/10.1021/NP900752T
Caffeic Acid 689043 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown https://doi.org/10.1021/NP900752T
Ferulic acid 445858 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O 194.18 unknown https://doi.org/10.1021/NP900752T
Isoferulic acid 736186 Click to see COC1=C(C=C(C=C1)C=CC(=O)O)O 194.18 unknown https://doi.org/10.1016/S0031-9422(00)80460-4
p-Coumaric acid 637542 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown https://doi.org/10.1016/S0031-9422(00)80460-4
> Phenylpropanoids and polyketides / Phenylpropanoic acids
Fukiic acid 161871 Click to see C1=CC(=C(C=C1CC(C(C(=O)O)O)(C(=O)O)O)O)O 272.21 unknown https://doi.org/10.1016/S0031-9422(00)80460-4

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