(Q40405655)

20 September 2017

New eudesmane derivatives and other sesquiterpenes from the epigeal parts of Dittrichia graveolens (English)

1 reference

20 September 2017

Dittrichia graveolens

1 reference

2-(8-Hydroxy-4a,8-dimethyldecahydro-2-naphthalenyl)acrylic acid

1 reference

1 reference

(1R,3R,5S,6R,7S,9R)-7-methyl-12-methylidene-5-(2-oxopropyl)-4,10-dioxatricyclo[7.3.0.03,6]dodecan-11-one

1 reference

2-[(4aS,8abeta)-4aalpha,8-Dimethyl-7beta,8beta-dihydroxydecalin-2alpha-yl]acrylic acid methyl ester

1 reference

1 reference

2-[(2R,4aS,6R,8aR)-6-hydroxy-4a,8-dimethyl-2,3,4,5,6,8a-hexahydro-1H-naphthalen-2-yl]prop-2-enoic acid

1 reference

4a,8-Dimethyl-3-methylidene-2,5-dioxo-2,3,3a,4,4a,5,7a,8,9,9a-decahydroazuleno[6,5-b]furan-4-yl acetate

1 reference

(3aR,7S,8aR)-6-[(1R)-1-hydroxy-2-oxopropyl]-7-methyl-3-methylidene-4,7,8,8a-tetrahydro-3aH-cyclohepta[b]furan-2-one

1 reference

1 reference

(1S,3aR,5S,5aS,8aS,9aR)-1,5,8a-trimethyl-3a,4,5,5a,6,7,9,9a-octahydro-1H-azuleno[6,7-b]furan-2,8-dione

1 reference

(3aR,7S,8aR)-6-[(E)-3-hydroxybut-1-enyl]-7-methyl-3-methylidene-4,5,6,7,8,8a-hexahydro-3aH-cyclohepta[b]furan-2-one

1 reference

methyl 2-[(2R,4aS,7R,8S,8aR)-7-acetyloxy-8-hydroxy-4a,8-dimethyl-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl]prop-2-enoate

1 reference

2-[(2R,4aS,8R,8aR)-8-hydroxy-4a,8-dimethyl-1,2,3,4,5,8a-hexahydronaphthalen-2-yl]prop-2-enoic acid

1 reference

1 reference

1 reference

2-[(2R,4aS,6R,8aS)-6-hydroxy-4a-methyl-2,3,4,5,6,8a-hexahydro-1H-naphthalen-2-yl]prop-2-enoic acid

1 reference

6-(1-hydroxy-3-oxobutyl)-7-methyl-3-methylidene-4,5,6,7,8,8a-hexahydro-3aH-cyclohepta[b]furan-2-one

1 reference

(3aR,6R,7S,8aR)-6-[(1S)-1-hydroxy-3-oxobutyl]-7-methyl-3-methylidene-4,5,6,7,8,8a-hexahydro-3aH-cyclohepta[b]furan-2-one

1 reference

2-(6-hydroxy-4a,8-dimethyl-2,3,4,5,6,8a-hexahydro-1H-naphthalen-2-yl)prop-2-enoic acid

1 reference

2-[(2R,4aR,8R,8aR)-8-hydroxy-4a,8-dimethyl-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl]prop-2-enoic acid

1 reference

1 reference

2-[(2R,4aS,6R,8S,8aR)-6,8-dihydroxy-4a-methyl-2,3,4,5,6,7,8,8a-octahydro-1H-naphthalen-2-yl]prop-2-enoic acid

1 reference

2-[(2R,4aR,8aR)-4a,8-dimethyl-2,3,4,5,6,8a-hexahydro-1H-naphthalen-2-yl]prop-2-enoic acid

1 reference

7-Methyl-12-methylidene-5-(2-oxopropyl)-4,10-dioxatricyclo[7.3.0.03,6]dodecan-11-one

1 reference

methyl 2-[(2R,4aS,7R,8S,8aR)-7,8-dihydroxy-4a-methyl-2,3,4,5,6,7,8,8a-octahydro-1H-naphthalen-2-yl]prop-2-enoate

1 reference

Methyl 2-(7,8-dihydroxy-4a,8-dimethyl-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl)prop-2-enoate

1 reference

2-[(2R,4aS,6R,8S,8aR)-6,8-dihydroxy-4a,8-dimethyl-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl]prop-2-enoic acid

1 reference

(3aR,6R,7S,8aS)-7-methyl-3-methylidene-6-(3-oxobutyl)-4,5,6,7,8,8a-hexahydro-3aH-cyclohepta[b]furan-2-one

1 reference

(3R,3aR,8aR)-3,7-dimethyl-6-(3-oxobutyl)-3a,4,8,8a-tetrahydro-3H-cyclohepta[b]furan-2,5-dione

1 reference

2-[(2R,4aR,8aS)-4a-methyl-2,3,4,5,6,8a-hexahydro-1H-naphthalen-2-yl]prop-2-enoic acid

1 reference

2-(6,8-Dihydroxy-4a,8-dimethyl-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl)prop-2-enoic acid

1 reference

1 reference

7-methyl-3-methylidene-6-(3-oxobutyl)-4,5,6,7,8,8a-hexahydro-3aH-cyclohepta[b]furan-2-one

1 reference

1 reference

1 reference

2-[(2R,4aS)-4a,8-dimethyl-2,3,4,5,6,7-hexahydro-1H-naphthalen-2-yl]prop-2-enoic acid

1 reference

Azuleno[6,5-b]furan-2,5-dione, decahydro-4a,8-dimethyl-3-methylene-, [3aR-(3aalpha,4abeta,7aalpha,8beta,9aalpha)]-

1 reference

2-(7-Hydroxy-4a-methyl-8-methylidene-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl)prop-2-enoic acid

1 reference

2-(4a,8-dimethyl-2,3,4,5,6,8a-hexahydro-1H-naphthalen-2-yl)prop-2-enoic acid

1 reference

1 reference

8-Epi-xanthatin-1,5alpha-epoxide

1 reference

3alpha-Hydroxyilicic acid

1 reference

1 reference

Ahmad Muhamad Abou-Douh

series ordinal

1

1 reference

PubMed ID

18981602

retrieved

20 September 2017

language of work or name

English

1 reference

Chemical & Pharmaceutical Bulletin

publication date

2008

3 references

16 September 2022

16 September 2022

full work available at URL

https://www.jstage.jst.go.jp/article/cpb/56/11/56_11_1535/_pdf

1 reference

19 March 2024

https://api.unpaywall.org/v2/10.1248/cpb.56.1535?email=unpaywall_01@example.com

published in

Chemical & Pharmaceutical Bulletin

1 reference

20 September 2017

56

1 reference

20 September 2017

11

1 reference

20 September 2017

1535-1545

1 reference

https://api.unpaywall.org/v2/10.1248/cpb.56.1535?email=unpaywall_01@example.com

20 September 2017

1 reference

19 March 2024

access restriction status

open access

1 reference

based on heuristic

inferred from online access status

cites work

Cytotoxic sesquiterpene lactones from Centaurothamnus maximus and Vicoa pentanema.

1 reference

https://opencitations.net/index/api/v1/citations/10.1002/PTR.1258

COCI

reference URL

retrieved

10 April 2024

Eremophilane derivatives and other constituents from Haeckeria species and further Australian inuleae

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1248/CPB.56.1535

Chemical constituents of plants from the genus Inula

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1248/CPB.56.1535

Carrageenin-induced edema in hind paw of the rat as an assay for antiiflammatory drugs

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1248/CPB.56.1535

New sesquiterpene lactones from Inula species

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1248/CPB.56.1535

Quantitative structure-activity relationship of sesquiterpene lactones as inhibitors of the transcription factor NF-kappaB

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1248/CPB.56.1535

Oxygenated nerolidol esters and eudesmane acids fromInula viscosa

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1248/CPB.56.1535

Investigations on the Steroidal Anti-Inflammatory Activity of Triterpenoids fromDiospyros leucomelas*

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1248/CPB.56.1535

Eudesmane derivatives and other sesquiterpenes from Laggera alata

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1248/CPB.56.1535

Further sesquiterpene lactones from the genus Dittrichia

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1248/CPB.56.1535

New sesquiterpenoids from the jordanian medicinal plant inula viscosa

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1248/CPB.56.1535

Ichthyotoxic sesquiterpenes and xanthanolides from Dittrichia graveolens

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1248/CPB.56.1535

Antimycobacterial eudesmanolides from Inula helenium and Rudbeckia subtomentosa

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1248/CPB.56.1535

Biological activities of sesquiterpene lactones

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1248/CPB.56.1535

Gastroprotection and Prostaglandin E2Generation in Rats by Flavonoids ofDittrichia viscosa

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1248/CPB.56.1535

A New Eudesmane Acid from Dittrichia (Inula) viscosa

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1248/CPB.56.1535

Epi-Ililic acid from Alcantara Ekmaniana

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1248/CPB.56.1535

Sesquiterpenoids from Tithonia diversifolia with potential cancer chemopreventive activity

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1248/CPB.56.1535

Cytotoxic germacranolide sesquiterpene from Inula cappa

2 references

12 April 2024

https://opencitations.net/index/api/v1/references/10.1248/CPB.56.1535

12 April 2024

https://opencitations.net/index/api/v1/citations/10.1248/CPB.55.1258

A mechanistic approach to the in vivo anti-inflammatory activity of sesquiterpenoid compounds isolated from Inula viscosa

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1248/CPB.56.1535

Sesquiterpene acids from Inula Viscosa

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1248/CPB.56.1535

Assessment of the adrenergic beta-blocking activity of Inula racemosa

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1248/CPB.56.1535

Cytotoxic sesquiterpene lactones from Inula britannica.

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1248/CPB.56.1535

Analgesic, Anti-Inflammatory, Antipyretic and Haematological Effects of Aethiopinone, ano-Naphthoquinone Diterpenoid fromSalvia aethiopisRoots and two Hemisynthetic Derivatives

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1248/CPB.56.1535

Antiproliferative sesquiterpene lactones from the roots of Inula helenium

2 references

12 April 2024

https://opencitations.net/index/api/v1/references/10.1248/CPB.56.1535

12 April 2024

https://opencitations.net/index/api/v1/citations/10.1248/BPB.25.1370

A eudesmanolide and other constituents fromInula graveolens

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1248/CPB.56.1535

Xanthanolides from Xanthium indicum

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1248/CPB.56.1535

Cytotoxic and antibacterial sesquiterpenes from Inula graveolens

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1248/CPB.56.1535

12-carboxyeudesma-3,11(13)-diene. A novel sesquiterpenic acid with a narrow antifungal spectrum

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1248/CPB.56.1535

Chemical Profle of theDittrichia graveolens(Desf.) Greuter Essential Oil of Lebanese Origin

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1248/CPB.56.1535

High-field FT NMR application of Mosher's method. The absolute configurations of marine terpenoids

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1248/CPB.56.1535

Analgesic and antipyretic activities of an aqueous extract and of the flavone linarin of Buddleia cordata

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1248/CPB.56.1535

A glycosyl analogue of diacylglycerol and other antiinflammatory constituents from Inula viscosa

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1248/CPB.56.1535

Further eudesmanolides and xanthanolides from Telekia speciosa

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1248/CPB.56.1535

Cytotoxic and antibacterial activities of sesquiterpene lactones isolated from Tanacetum praeteritum subsp. praeteritum

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1248/CPB.56.1535

Sesquiterpene lactones from Artemisia herba-alba

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1248/CPB.56.1535

Identifiers

DOI

10.1248/CPB.56.1535

1 reference

20 September 2017

1 reference