Constituents of cimicifugae rhizoma II. Isolation and structures of new cycloartenol triterpenoids and related compounds from Cimicifuga foetida L (Q104388227)

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scientific article published on 25 April 2003

Language	Label	Description	Also known as
English	Constituents of cimicifugae rhizoma II. Isolation and structures of new cycloartenol triterpenoids and related compounds from Cimicifuga foetida L	scientific article published on 25 April 2003

Statements

scholarly article

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Constituents of cimicifugae rhizoma II. Isolation and structures of new cycloartenol triterpenoids and related compounds from Cimicifuga foetida L (English)

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Actaea cimicifuga

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Cimicidanol 3-O-alpha-L-arabinoside

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2-[(1S,2R,3S,4R,7R,9S,12R,14S,17R,18R,19R,21R,22R)-2-hydroxy-3,8,8,17,19-pentamethyl-9-[(2S,3R,4S,5R)-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

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15-(5,6-Dihydroxy-6-methyl-4-oxoheptan-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

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Cimicifugoside H2

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(2R,3S,4R,5S)-2-[[(1R,2R,3S,4R,7R,9S,12S,14R,17R,18R,19R,21R,22R)-2-hydroxy-3,8,8,17,19-pentamethyl-22-prop-1-en-2-yl-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

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[(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

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[2-Hydroxy-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

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NEWMWGLPJQHSSQ-XWXUZQMCSA-N

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(1S,2S,4R,5R,6R,9R,10R,12R,16R,18S,21R)-2,9,10,18-tetrahydroxy-4,6,12,17,17-pentamethylhexacyclo[11.9.0.01,21.04,12.05,10.016,21]docos-13-en-8-one

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(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

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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

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(2S)-4-hydroxy-7-(hydroxymethyl)-2-(2-hydroxypropan-2-yl)-2H,3H-furo[3,2-g]chromen-5-one

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[15-[4-(3,3-Dimethyloxiran-2-yl)-4-oxobutan-2-yl]-7,7,12,16-tetramethyl-14-oxo-6-(3,4,5-trihydroxyoxan-2-yl)oxy-17-pentacyclo[9.7.0.01,3.03,8.012,16]octadec-10-enyl] acetate

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2,9,10-Trihydroxy-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

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[(1S,3R,6S,8R,12S,15R,16R,17R)-15-[(2R)-4-[(2R)-3,3-dimethyloxiran-2-yl]-4-oxobutan-2-yl]-7,7,12,16-tetramethyl-14-oxo-6-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-17-pentacyclo[9.7.0.01,3.03,8.012,16]octadec-10-enyl] acetate

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(1S,3R,6S,8R,12R,13R,15R,16R,18S)-15-[(2R,5R)-5,6-dihydroxy-6-methyl-4-oxoheptan-2-yl]-13,18-dihydroxy-7,7,12,16-tetramethyl-6-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxypentacyclo[9.7.0.01,3.03,8.012,16]octadec-10-en-14-one

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(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

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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

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(1S,3R,6S,8R,12R,15R,16R,18S)-15-[(2R)-4-[(2R)-3,3-dimethyloxiran-2-yl]-4-oxobutan-2-yl]-18-hydroxy-7,7,12,16-tetramethyl-6-[(2S,3S,4R,5R)-3,4,5-trihydroxyoxan-2-yl]oxypentacyclo[9.7.0.01,3.03,8.012,16]octadec-10-en-14-one

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isoferulic acid

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(2S,3R,4S,5S)-2-[[(1S,3R,8S,10R,17S,18R,19R,21S,22R)-22-(2-hydroxypropan-2-yl)-3,9,9,17,19-pentamethyl-23,24-dioxahexacyclo[19.2.1.01,18.03,17.05,15.08,13]tetracosa-5,12,15-trien-10-yl]oxy]oxane-3,4,5-triol

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HXXZFHABSSZFHB-UNCLGPHQSA-N

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Cimicifuga foetida

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based on heuristic

inferred from title

author name string

Shigetoshi Kadota

1

1 reference

http://api.crossref.org/works/10.1016%2F0040-4020%2894%2901015-r

Jian Xin Li

2

1 reference

http://api.crossref.org/works/10.1016%2F0040-4020%2894%2901015-r

Ken Tanaka

3

1 reference

http://api.crossref.org/works/10.1016%2F0040-4020%2894%2901015-r

Tsuneo Namba

4

1 reference

http://api.crossref.org/works/10.1016%2F0040-4020%2894%2901015-r

publication date

January 1995

3 references

16 September 2022

16 September 2022

1 reference

http://api.crossref.org/works/10.1016%2F0040-4020%2894%2901015-r

51

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http://api.crossref.org/works/10.1016%2F0040-4020%2894%2901015-r

4

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http://api.crossref.org/works/10.1016%2F0040-4020%2894%2901015-r

1143-1166

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http://api.crossref.org/works/10.1016%2F0040-4020%2894%2901015-r

[Contents of Cimicifuga racemosa. 3. On the constitution of the rings A, B and C of actein]

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9 March 2024

https://opencitations.net/index/api/v1/citations/10.1002/ARDP.19673001203

Studies on the costituents of Cimicifuga spp. II. Constituents of Cimicifuga acerina. 2. Structure of cimigenol

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12 April 2024

https://opencitations.net/index/api/v1/citations/10.1248/YAKUSHI1947.87.12_1569

Studies on the Constituents of Cimicifuga Species. XIV. A New Xyloside from the Aerial Parts of Cimicifuga simplex WORMSK.

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12 April 2024

https://opencitations.net/index/api/v1/citations/10.1248/CPB.42.1106

Constituents of Cimicifugae Rhizoma. I. Isolation and Characterization of Ten New Cycloartenol Triterpenes from Cimicifuga heracleifolia Komarov.

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12 April 2024

https://opencitations.net/index/api/v1/citations/10.1248/CPB.41.832

Studies on the Chinese crude drug "Shoma." VIII. Two new triterpenol bisdesmosides, 3-arabinosyl-24-O-acetylhydroshengmanol 15-glucoside and 3-xylosyl-24-O-acetylhydroshengmanol 15-glucoside, from Cimicifuga dahurica

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12 April 2024

https://opencitations.net/index/api/v1/citations/10.1248/CPB.42.48

Studies on the constituents of orchidaceous plants. V Isolation, structure, and C-13 signal assignments of novel methylsterols from Nervilia purpurea Schlechter.

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12 April 2024

https://opencitations.net/index/api/v1/citations/10.1248/CPB.34.3183

Spasmolytic substances from Cimicifuga dahurica maxim

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12 April 2024

https://opencitations.net/index/api/v1/citations/10.1248/CPB.24.580

Identifiers

10.1016/0040-4020(94)01015-R

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