Structural Characterization of Terpenoids from Abies holophylla Using Computational and Statistical Methods and Their Biological Activities (Q90661212)

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15 April 2020

title

Structural Characterization of Terpenoids from Abies holophylla Using Computational and Statistical Methods and Their Biological Activities (English)

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15 April 2020

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methyl 3-[(3R,3aR,5aS,6S,7S,9bR)-3a,6,9b-trimethyl-3-[(2R)-1-[(2R,4R)-4-methyl-5-oxooxolan-2-yl]propan-2-yl]-7-prop-1-en-2-yl-1,2,3,4,5,5a,7,8-octahydrocyclopenta[a]naphthalen-6-yl]propanoate

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(E,6R)-6-[(1'S,3R,6S,7S,7aS)-7-(2-carboxyethyl)-1',7-dimethyl-3'-methylidene-6-prop-1-en-2-ylspiro[2,5,6,7a-tetrahydro-1H-indene-3,2'-cyclopentane]-1'-yl]-2-methyl-4-oxohept-2-enoic acid

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(6R)-6-[(1'S,3R,6S,7S,7aS)-7-(2-carboxyethyl)-1',7-dimethyl-3'-methylidene-6-prop-1-en-2-ylspiro[2,5,6,7a-tetrahydro-1H-indene-3,2'-cyclopentane]-1'-yl]-2-methylidene-4-oxoheptanoic acid

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methyl 3-[(3S,5aS,6S,7S,9bS)-3,6,9b-trimethyl-3-[(2R)-1-[(2R,4R)-4-methyl-5-oxooxolan-2-yl]propan-2-yl]-7-prop-1-en-2-yl-1,2,5,5a,7,8-hexahydrocyclopenta[a]naphthalen-6-yl]propanoate

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(E,4R)-5-[(1R,2R,4aS,8aS)-2-hydroxy-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpent-2-ene-1,4-diol

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(12R,13R)-8,13-Epoxylabd-14-en-12-ol

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(2E,6R)-6-[(1S,3R,6S,8R,11S,12S,15R,16R)-6-hydroxy-7,7,12,16-tetramethylpentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-15-yl]-2-methylhept-2-enoic acid

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(9beta,13alpha,17S)-3alpha,23,23-Trihydroxy-17-methyl-30-nor-5alpha-lanosta-7,14,24-triene-26-oic acid 26,23-lactone

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(2R,6R)-6-[(3S,3aS,5aS,6R,7S)-6-(2-carboxyethyl)-3,3a,6-trimethyl-7-prop-1-en-2-yl-1,2,4,5,5a,7-hexahydrocyclopenta[a]naphthalen-3-yl]-2-methyl-4-oxoheptanoic acid

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13-Keto-8(14)-Podocarpen-18-oic acid

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(1S,2R,6R,7R,12S,15S)-12-hydroxy-2,6,13,13-tetramethyl-14-oxatetracyclo[8.6.0.02,7.012,15]hexadec-10-ene-6-carboxylic acid

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(6R)-2-methylidene-4-oxo-6-[(5R,9S,10R,13R,14R,17R)-4,4,10,13,14-pentamethyl-3-oxo-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl]heptanoic acid

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(E,4S)-5-[(1R,2R,4aS,8aS)-2-hydroxy-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpent-2-ene-1,4-diol

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(E,6R)-6-[(3R,5R,9S,10R,13S,17S)-3-hydroxy-4,4,10,13-tetramethyl-1,2,3,5,6,9,11,12,16,17-decahydrocyclopenta[a]phenanthren-17-yl]-2-methyl-4-oxohept-2-enoic acid

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Desmethylabietospiran

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(2R)-2-[(2R,3aR,5aS,9aS,9bR)-2,3a,6,6,9a-pentamethyl-1,4,5,5a,7,8,9,9b-octahydrobenzo[e][1]benzofuran-2-yl]but-3-en-2-ol

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5-hydroxy-3-methyl-5-[(2R)-2-[(5R,9S,10R,13R,14R,17R)-4,4,10,13,14-pentamethyl-3-oxo-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl]propyl]furan-2-one

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(E)-4-[(2R,4aS,8aS)-2-hydroxy-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]but-3-en-2-one

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1

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15 April 2020

Kang Ro Lee

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author name string

Joonseok Oh

2

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15 April 2020

Lalita Subedi

3

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15 April 2020

Sun Yeou Kim

4

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15 April 2020

Sang Un Choi

5

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publication date

31 July 2018

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Journal of Natural Products

15 April 2020

published in

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volume

81

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issue

8

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page(s)

1795-1802

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Immortalization of murine microglial cells by a v-raf/v-myc carrying retrovirus

15 April 2020

cites work

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Phytochemical and biological studies of Abies species

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9 March 2024

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Novel lanostane and rearranged lanostane-type triterpenoids from Abies sachalinensis - II -.

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12 April 2024

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Rearranged lanostane triterpenoids from Abies sachalinensis (III).

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12 April 2024

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Triterpenoids from species ofAbies hill. II. Abiesolidic acid — A new 3,4-secolanostanoid from the oleoresin ofAbies sibirica

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11 May 2024

https://opencitations.net/index/api/v1/citations/10.1007/BF00598342

Triterpenoids from Abies species VII. New lanostane lactones from Siberian fir needles

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11 May 2024

https://opencitations.net/index/api/v1/citations/10.1007/BF00598406

Triterpenoids fromAbies species. I. Abiesonic acid — A triterpenoid with a new carbon skeleton from the oleoresin ofAbies sibirica

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11 May 2024

https://opencitations.net/index/api/v1/citations/10.1007/BF00599258

Triterpenoids from Abies species X. Two new 3,4-secotriterpene acids from the oleoresin of the silver fir

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11 May 2024

https://opencitations.net/index/api/v1/citations/10.1007/BF00630074

Identifiers

DOI

10.1021/ACS.JNATPROD.8B00245

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15 April 2020

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