Phytochemistry and molecular systematics of Triaenophora rupestris and Oreosolen wattii (Scrophulariaceae). (Q46503624)

22 December 2017

title

Phytochemistry and molecular systematics of Triaenophora rupestris and Oreosolen wattii (Scrophulariaceae). (English)

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22 December 2017

[4-Acetyloxy-5-hydroxy-2-[[2-(hydroxymethyl)-10-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-5-yl]oxy]-6-methyloxan-3-yl] 3-phenylprop-2-enoate

main subject

Triaenophora rupestris

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(2S,3R,4S,5S,6R)-2-{[(1S,4aR,5R,7S,7aS)-5,7-dihydroxy-7-methyl-1H,4aH,5H,6H,7aH-cyclopenta[c]pyran-1-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

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6-O-trans-p-Coumaroyl ajugol

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[(2S,3R,4R,5S,6S)-4-acetyloxy-5-hydroxy-2-[[(1S,2S,4S,5S,6S,10S)-2-(hydroxymethyl)-10-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-5-yl]oxy]-6-methyloxan-3-yl] (E)-3-phenylprop-2-enoate

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(1S,4aR,5R,7S,7aR)-7-methyl-1-[(2R,3S,4R,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,5,6,7a-tetrahydrocyclopenta[c]pyran-4a,5,7-triol

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(2R,3S,4S,5S,6R)-2-[[(1S,4aS,5R,7S,7aS)-5,7-dihydroxy-7-methyl-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-1-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol

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1 reference

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[(1S,4aS,5R,7S,7aS)-7-hydroxy-7-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-5-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

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(2S,3R,4S,5S,6R)-2-[[(1S,4aR,5R,7S,7aS)-5,7-dihydroxy-7-methyl-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-1-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol

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LHEWQIBORVAWFM-VZPLGYOJSA-N

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[(1S,4aR,5R,7S,7aS)-4a,5-dihydroxy-7-methyl-1-[(2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,5,6,7a-tetrahydrocyclopenta[c]pyran-7-yl] (E)-3-phenylprop-2-enoate

1 reference

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(2S,3R,4S,5S,6R)-2-[[(1S,2S,4S,5S,6S,10S)-5-hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol

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(1S,4aS,6S,7S,7aR)-6-hydroxy-7-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylic acid

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1 reference

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(2S,3R,4S,5R,6R)-2-[[(1S,4aS,5R,7aS)-5-hydroxy-7-(hydroxymethyl)-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-1-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol

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LHEWQIBORVAWFM-FIBGQUEGSA-N

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molecular phylogenetics

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Scrophulariaceae

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based on heuristic

inferred from title

Scrophularia scorodonia

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Scrophularia buergeriana

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Scrophularia lepidota

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Scrophularia ningpoensis

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author

Charlotte H. Gotfredsen

4

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22 December 2017

Søren Rosendal Jensen

1

object named as

Søren Rosendal Jensen

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22 December 2017

author name string

Hong-Qing Li

2

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22 December 2017

Dirk C Albach

3

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22 December 2017

publication date

August 2008

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16 September 2022

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22 December 2017

volume

69

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22 December 2017

issue

11

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22 December 2017

page(s)

2162-2166

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22 December 2017

https://api.unpaywall.org/v2/10.1016/[email protected]

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19 March 2024

access restriction status

open access

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based on heuristic

inferred from online access status

cites work

Über Triterpene, XXXIII. Über das Saponin der Blüten vonVerbascum phlomoides L.

1 reference

9 March 2024

https://opencitations.net/index/api/v1/citations/10.1002/CBER.19801130510

Ilwensisaponins A, B, C, and D: Triterpene Saponins fromScrophularia ilwensis

1 reference

9 March 2024

https://opencitations.net/index/api/v1/citations/10.1002/HLCA.19930760322

Iridoids from Scrophularia genus.

1 reference

12 April 2024

https://opencitations.net/index/api/v1/citations/10.1515/ZNC-2001-7-807

Iridoid Glycosides from Verbascum thapsus L.

1 reference

12 April 2024

https://opencitations.net/index/api/v1/citations/10.1248/CPB.39.3261

Buddlejasaponins I-IV, four new oleanane-triterpene saponins from the aerial parts of Buddleja japonica Hemsl.

1 reference

12 April 2024

https://opencitations.net/index/api/v1/citations/10.1248/CPB.39.2764

Scrophulasaponins II-IV, new saikosaponin homologs from Scrophularia kakudensis FRANCH

1 reference

12 April 2024

https://opencitations.net/index/api/v1/citations/10.1248/CPB.41.1780

Identifiers

DOI

10.1016/J.PHYTOCHEM.2008.05.010

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22 December 2017

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22 December 2017