Australian New Crops Info 2016
Supported by the Rural Industries Research and Development Corporation

Listing of Interesting Plants of the World:

Ajuga decumbens

 

 

This species is usually known as:

Ajuga decumbens, Ajuga decumbens var. decumbens

 

This species has also been known as:

Ajuga decumbens f. condensata, Ajuga decumbens var. glabrescens, Ajuga decumbens var. pallescens, Ajuga decumbens var. rosea, Ajuga decumbens var. sinuata, Ajuga decumbens var. vegeta

 

Common names:

Kiransou

 

 

Trends (five databases) 1901-2013:
[Number of papers mentioning Ajuga decumbens: 104]

 

Ajuga decumbens.jpg

 

Popularity of Ajuga decumbens over time
[Left-hand Plot: Plot of numbers of papers mentioning Ajuga decumbens (histogram and left hand axis scale of left-hand plot) and line of best fit, 1901 to 2013 if there are sufficient numbers of papers (equation and % variation accounted for in box); Right-hand Plot: Plot of a proportional micro index, derived from numbers of papers mentioning Ajuga decumbens as a proportion (scaled by multiplying by one million) of the approximate total number of papers available in databases for that year (frequency polygon and left-hand axis scale of right-hand plot) and line of best fit, 1901 to 2013 if there are sufficient numbers of papers (equation and % variation accounted for in box)] 

[For larger charts showing the numbers of papers that have mentioned this species over years, select this link; there are links to come back from there]

 

Keywords

[Total number of keywords included in the papers that mentioned this species: 404]

 

Ajuga decumbens (7), Labiatae (6), Iridoid glycosides (5), neo-clerodane diterpenoids (5), Ajuga iva (4), Inhibitory activities on NO production (4), 20-Hydroxyecdysone (3), Ajuga reptans (3), Cytotoxicity (3), Diterpenes (3), Diterpenoids (3), ecdysteroid (3), Iridoid (3), Neo-clerodane diterpenes (3), 4-Hydroxy-E-globularinin (2), 8-Acetylharpagide (2), Abietane diterpenoids (2), Aging (2), Ajudecumins A–D (2), Ajuga (2), Ajuga bracteosa (2), Ajuga ciliata (2), Ajuga ciliata Bunge (2), Anthocyanin (2), anti-complement activity (2), Athalia rosae ruficornis (2), Caenorhabditis elegans (2), Cancer chemopreventive activity (2), C-glycosylflavones (2), Chinese herbal medicine (2), Clerodendrin (2), Clerodendrum bungei (2), Cytotoxic (2), Deciduous forest (2), defense substance (2), Disease modifying anti-rheumatic drugs (2), fragmentation (2), Free radicals (2), Hydrological regimes (2), Iridaceae (2), Iris rossii (2), Lamiaceae (2), Life span (2), Liver fibrosis (2), Luteolin (2), Macrophage (2), Metabolite (2), neo-clerodane (2), neo-Clerodane diterpene (2), Neuroprotective activities (2), Paederia scandens (2), pharmacophagy (2), phenylpropanoid glycosides (2), Phylogeny (2), Pioneer species (2), Planting (2), Post-dam riparian vegetation (2), Pre-dam riparian vegetation (2), Radix Scrophulariae (2), Reactive oxygen species (2), Revegetation (2), Rheumatoid arthritis (2), RRLC/DAD-ESI-TOF MS (2), Scrophulariaceae (2), Seed bank (2), structural characterization (2), Systematic review (2), Tenthredinidae (2), Three Gorges Reservoir (2), Topsoil (2), turnip sawfly (2), Verbenaceae (2), Water-level-fluctuation zone (2), Winter flooding (2), Xanthones (2), 11-oxo-mogroside V (1), 14,15-Dihydroajugachin B (1), 14-Hydro-15-methoxyajugachin B (1), 15-Epilupulin (1), 3-hydroxykynurenine (1), 4-O-[beta]--glucopyranosyldihydroferulic acid (1), 8-acetylharpagidep-coumaroyl ester (1), 8-O-acetylharpagide (1), acetylation (1), Acetylcholinesterase (1), acetylscopine (1).....

 

[If all keywords are not here (as indicated by .....), they can be accessed from this link; there are links to come back from there]

 

 

Most likely scope for crop use/product (%):
[Please note: When there are only a few papers mentioning a species, care should be taken with the interpretation of these crop use/product results; as well, a mention may relate to the use of a species, or the context in which it grows, rather than a product]

 

medicinal (67.44), timber (5.24), revegetation (3.04), fruit (2.90), poison (2.52), ornamental (2.43), weed (1.95), sweetener (1.13), grain legume (1.08), shade (0.99).....

 

[To see the full list of crop use/product outcomes, from searching abstracts of the papers that have mentioned this species, select this link; details of the analysis process have also been included; there are links to come back from there]

 

 

Recent mentions of this species in the literature:
[since 2012, with links to abstracts; The references from 1901-2013 which have been used for the trend, keyword and crop use/product analyses below, are listed below these references]

 

Cheng J, Xiao S and Liu T (2016) Analysis of active patents to investigate the frequency and patterns of Chinese herbal extract combinations claiming to treat heart disease. Journal of Traditional Chinese Medical Sciences 3, 81-90. http://www.sciencedirect.com/science/article/pii/S2095754816300849

Islam MT, da Mata AMOF, de Aguiar RPS, Paz MFCJ, de Alencar MVOB, Ferreira PMP and de Carvalho Melo-Cavalcante AA (2016) Therapeutic Potential of Essential Oils Focusing on Diterpenes. Phytotherapy Research 30, 1420-1444. http://dx.doi.org/10.1002/ptr.5652

Lu X, Qiu H, Yang L, Zhang J, Ma S and Zhen L (2016) Anti-proliferation effects, efficacy of cyasterone in vitro and in vivo and its mechanism. Biomedicine & Pharmacotherapy 84, 330-339. http://www.sciencedirect.com/science/article/pii/S0753332216306151

Nasu H and Momohara A (2016) The beginnings of rice and millet agriculture in prehistoric Japan. Quaternary International 397, 504-512. http://www.sciencedirect.com/science/article/pii/S1040618215006436

Yan H, Wei P, Song J, Jia X and Zhang Z (2016) Enhanced anticancer activity in vitro and in vivo of luteolin incorporated into long-circulating micelles based on DSPE-PEG2000 and TPGS. Journal of Pharmacy and Pharmacology 68, 1290-1298. http://dx.doi.org/10.1111/jphp.12598

(2015) Contents (graphical abstracts and research highlights). Phytochemistry Letters 13, v-xxiii. http://www.sciencedirect.com/science/article/pii/S1874390015001354

Bajguz A, Bąkała I and Talarek M (2015) Chapter 5 - Ecdysteroids in Plants and their Pharmacological Effects in Vertebrates and Humans. In ‘Studies in Natural Products Chemistry’. (Ed.^(Eds Atta ur R) pp. 121-145. (Elsevier). http://www.sciencedirect.com/science/article/pii/B9780444634733000058

Kim M-B, Kim C, Chung W-S, Cho J-H, Nam D, Kim S-H and Ahn KS (2015) The Hydrolysed Products of Iridoid Glycosides Can Enhance Imatinib Mesylate-Induced Apoptosis in Human Myeloid Leukaemia Cells. Phytotherapy Research 29, 434-443. http://dx.doi.org/10.1002/ptr.5272

Lin T, Wang G, Zeng D and Chen H (2015) Cytotoxic metabolites from Botryotinia fuckeliana A-S-3: An endophytic fungus from Ajuga decumbens. Phytochemistry Letters 13, 206-211. http://www.sciencedirect.com/science/article/pii/S1874390015300136

Ma F, Gong X, Zhou X, Zhao Y and Li M (2015) An UHPLC–MS/MS method for simultaneous quantification of gallic acid and protocatechuic acid in rat plasma after oral administration of Polygonum capitatum extract and its application to pharmacokinetics. Journal of Ethnopharmacology 162, 377-383. http://www.sciencedirect.com/science/article/pii/S0378874114009489

(2014) Graphical contents list. Bioorganic & Medicinal Chemistry Letters 24, 2393-2403. http://www.sciencedirect.com/science/article/pii/S0960894X14004752

(2014) All in One - Complete Issue: ChemInform 40/2014. ChemInform 45, no-no. http://dx.doi.org/10.1002/chin.201494001

Chen H, Wang H, Yang B, Jin D-Q, Yang S, Wang M, Xu J, Ohizumi Y and Guo Y (2014) Diterpenes inhibiting NO production from Euphorbia helioscopia. Fitoterapia 95, 133-138. http://www.sciencedirect.com/science/article/pii/S0367326X14000732

Lee R-Y, Jang H-D, Kim Y-Y, Yang S-G, Choi H-J, Ji S-J and Oh B-U (2014) Flora of vascular plants in the Chilgapsan Provincial Park, Korea. Journal of Asia-Pacific Biodiversity 7, 237-247. http://www.sciencedirect.com/science/article/pii/S2287884X14000399

Lin T, Wang G, Shan W, Zeng D, Ding R, Jiang X, Zhu D, Liu X, Yang S and Chen H (2014) Myrotheciumones: Bicyclic cytotoxic lactones isolated from an endophytic fungus of Ajuga decumbens. Bioorganic & Medicinal Chemistry Letters 24, 2504-2507. http://www.sciencedirect.com/science/article/pii/S0960894X14003527

Lin T, Wang G, Shan W, Zeng D, Ding R, Jiang X, Zhu D, Liu X, Yang S and Chen H (2014) ChemInform Abstract: Myrotheciumones: Bicyclic Cytotoxic Lactones Isolated from an Endophytic Fungus of Ajuga decumbens. ChemInform 45, no-no. http://dx.doi.org/10.1002/chin.201440216

Lin T, Wang G, Zhou Y, Zeng D, Liu X, Ding R, Jiang X, Zhu D, Shan W and Chen H (2014) Structure Elucidation and Biological Activity of Two New Trichothecenes from an Endophyte, Myrothecium roridum. Journal of agricultural and food chemistry. 62, 5993-6000. http://dx.doi.org/10.1021/jf501724a

Liu Y, Nielsen M, Staerk D and Jäger AK (2014) High-resolution bacterial growth inhibition profiling combined with HPLC–HRMS–SPE–NMR for identification of antibacterial constituents in Chinese plants used to treat snakebites. Journal of Ethnopharmacology 155, 1276-1283. http://www.sciencedirect.com/science/article/pii/S0378874114005236

Lv H, Luo J and Kong L (2014) A new neo-clerodane diterpene from Ajuga decumbens. Natural product research. 28, 196-200. http://dx.doi.org/10.1080/14786419.2013.866114

Maliński MP, Michalska AD, Tomczykowa M, Tomczyk M and Thiem B (2014) Ragged Robin (Lychnis flos-cuculi) - a plant with potential medicinal value. Revista Brasileira de Farmacognosia 24, 722-730. http://www.sciencedirect.com/science/article/pii/S0102695X15000071

Oh J-H and Lee Y-J (2014) Sample Preparation for Liquid Chromatographic Analysis of Phytochemicals in Biological Fluids. Phytochemical Analysis 25, 314-330. http://dx.doi.org/10.1002/pca.2484

Park S, Son MJ, Yook C-S, Jin C, Lee YS and Kim HJ (2014) Chemical constituents from aerial parts of Caryopteris incana and cytoprotective effects in human HepG2 cells. Phytochemistry 101, 83-90. http://www.sciencedirect.com/science/article/pii/S0031942214000752

Sipahi H, Becker K, Gostner JM, Charehsaz M, Kirmizibekmez H, Schennach H, Aydin A and Fuchs D (2014) Effects of globularifolin on cell survival, nuclear factor-κB activity, neopterin production, tryptophan breakdown and free radicals in vitro. Fitoterapia 92, 85-92. http://www.sciencedirect.com/science/article/pii/S0367326X1300289X

Yang W, Li H, Zhang T, Sen L and Ni W (2014) Classification and identification of metal-accumulating plant species by cluster analysis. Environmental science and pollution research international. 21, 10626-10637. http://dx.doi.org/10.1007/s11356-014-3102-6

Di X-X, Wang S-Q, Zhang X-L, Wang B, Lou H-X and Wang X-N (2013) Diterpenoids from the aerial parts of Orthosiphon aristatus var. aristatus. Phytochemistry Letters 6, 412-417. http://www.sciencedirect.com/science/article/pii/S1874390013000876

Hwang H-S, Jang J-W, Jung S-Y, Lee H-J, Oh S-H and Yang J-C (2013) Distributional Characteristics of Plants in Hajo Island of Jeollanam-do, South Korea. Journal of Asia-Pacific Biodiversity 6, 435-448. http://www.sciencedirect.com/science/article/pii/S2287884X14600315

Hwang H-S, Yang J-C, Oh S-H, Lee Y-M and Chang K-S (2013) A Study on the Flora of 15 Islands in the Western Sea of Jeollanamdo Province, Korea. Journal of Asia-Pacific Biodiversity 6, 281-310. http://www.sciencedirect.com/science/article/pii/S2287884X14600169

Inomata Y, Terahara N, Kitajima J, Kokubugata G and Iwashina T (2013) Flavones and anthocyanins from the leaves and flowers of Japanese Ajuga species (Lamiaceae). Biochemical Systematics and Ecology 51, 123-129. http://www.sciencedirect.com/science/article/pii/S0305197813001580

Jung S-Y, Park S-H, Nam C-H, Lee H-J, Lee Y-M and Chang K-S (2013) The Distribution of Vascular Plants in Ulleungdo and Nearby Island Regions (Gwaneumdo, Jukdo), Korea. Journal of Asia-Pacific Biodiversity 6, 123-156. http://www.sciencedirect.com/science/article/pii/S2287884X14600066

Lee CH, Shin HT, Kwon YH, Yi MH, Yoon JW, Kim GS, Park GH and Sung JW (2013) The Vascular Plant Species in the Korean Demilitarized zone (DMZ). Journal of Asia-Pacific Biodiversity 6, 31-81. http://www.sciencedirect.com/science/article/pii/S2287884X14600029

Lu C-C, Wang J-H, Fang D-M and Wu Z-J (2013) Electrospray ionization tandem mass spectrometry of isomeric iridoid glucoside dimers. Rapid Communications in Mass Spectrometry 27, 503-506. http://dx.doi.org/10.1002/rcm.6470

Lu C-C, Wang J-H, Fang D-M, Wu Z-J and Zhang G-L (2013) Analyses of the Iridoid Glucoside Dimers in Paederia scandens Using HPLC–ESI–MS/MS. Phytochemical Analysis 24, 407-412. http://dx.doi.org/10.1002/pca.2424

Park KS (2013) Aucubin, a naturally occurring iridoid glycoside inhibits TNF-α-induced inflammatory responses through suppression of NF-κB activation in 3T3-L1 adipocytes. Cytokine 62, 407-412. http://www.sciencedirect.com/science/article/pii/S1043466613001531

Wen B, He R, Li P, Xu Q, Lu Y, Peng B and Li J (2013) Pharmacokinetics of 8-O-acetylharpagide and harpagide after oral administration of Ajuga decumbens Thunb extract in rats. Journal of Ethnopharmacology 147, 503-508. http://www.sciencedirect.com/science/article/pii/S0378874113002043

Wu Z-J, Wang J-H, Fang D-M and Zhang G-L (2013) Analysis of iridoid glucosides from Paederia scandens using HPLC–ESI-MS/MS. Journal of Chromatography B 923–924, 54-64. http://www.sciencedirect.com/science/article/pii/S1570023213000810

Yoon JW, Shin HT and Yi MH (2013) Distribution of Vascular Plants in the Ulleung Forest Trail Area, Korea. Journal of Asia-Pacific Biodiversity 6, 1-30. http://www.sciencedirect.com/science/article/pii/S2287884X14600017

(2012) Contents. Phytochemistry Letters 5, iii-xiii. http://www.sciencedirect.com/science/article/pii/S1874390012000778

Duffy R, Wade C and Chang R (2012) Discovery of anticancer drugs from antimalarial natural products: a MEDLINE literature review. Drug Discovery Today 17, 942-953. http://www.sciencedirect.com/science/article/pii/S1359644612001171

Guo P, Li Y, Jin D-q, Xu J, He Y, Zhang L and Guo Y (2012) neo-Clerodane diterpenes from Ajuga ciliata and their inhibitory activities on LPS-induced NO production. Phytochemistry Letters 5, 563-566. http://www.sciencedirect.com/science/article/pii/S1874390012001085

Han J-P, Shi L-C, Chen X-C and Lin Y-L (2012) Comparison of four DNA barcodes in identifying certain medicinal plants of Lamiaceae. Journal of Systematics and Evolution 50, 227-234. http://dx.doi.org/10.1111/j.1759-6831.2012.00184.x

Mizuno T, Okuyama Y and Iwashina T (2012) Phenolic compounds from Iris rossii, and their chemotaxonomic and systematic significance. Biochemical Systematics and Ecology 44, 157-160. http://www.sciencedirect.com/science/article/pii/S0305197812000889

Shukla V, Yadav D, Phulara SC, Gupta MM, Saikia SK and Pandey R (2012) Longevity-promoting effects of 4-hydroxy-E-globularinin in Caenorhabditis elegans. Free Radical Biology and Medicine 53, 1848-1856. http://www.sciencedirect.com/science/article/pii/S0891584912011112

Sun Z, Li Y, Jin D, Guo P, Song H, Xu J, Guo Y and Zhang L (2012) neo-Clerodane diterpenes from Ajuga decumbens and their inhibitory activities on LPS-induced NO production. Fitoterapia 83, 1409-14.

Sun Z, Li Y, Jin D, Guo P, Xu J, Guo Y and Zhang L (2012) Structure elucidation and inhibitory effects on NO production of clerodane diterpenes from Ajuga decumbens. Planta Med 78, 1579-93.

Sun Z, Li Y, Jin D-q, Guo P, Song H, Xu J, Guo Y and Zhang L (2012) neo-Clerodane diterpenes from Ajuga decumbens and their inhibitory activities on LPS-induced NO production. Fitoterapia 83, 1409-1414. http://www.sciencedirect.com/science/article/pii/S0367326X12002134

Wang B, Wang X-N, Shen T, Wang S-Q, Guo D-X and Lou H-X (2012) Rearranged abietane diterpenoid hydroquinones from aerial parts of Ajuga decumbens Thunb. Phytochemistry Letters 5, 271-275. http://www.sciencedirect.com/science/article/pii/S1874390012000274

Yang F, Liu W-W, Wang J, Liao L and Wang Y (2012) Riparian vegetation’s responses to the new hydrological regimes from the Three Gorges Project: Clues to revegetation in reservoir water-level-fluctuation zone. Acta Ecologica Sinica 32, 89-98. http://www.sciencedirect.com/science/article/pii/S1872203212000091

 

 

References 1901-2013 (and links to abstracts):
[Number of papers mentioning Ajuga decumbens: 104; Any undated papers have been included at the end]

 

 

Di X-X, Wang S-Q, Zhang X-L, Wang B, Lou H-X, Wang X-N (2013) Diterpenoids from the aerial parts of Orthosiphon aristatus var. aristatus. Phytochemistry Letters 6, 412-7. http://www.sciencedirect.com/science/article/pii/S1874390013000876

Lu C-C, Wang J-H, Fang D-M, Wu Z-J (2013) Electrospray ionization tandem mass spectrometry of isomeric iridoid glucoside dimers. Rapid Communications in Mass Spectrometry 27, 503-6. http://dx.doi.org/10.1002/rcm.6470

Lu C-C, Wang J-H, Fang D-M, Wu Z-J, Zhang G-L (2013) Analyses of the Iridoid Glucoside Dimers in Paederia scandens Using HPLC–ESI–MS/MS. Phytochemical Analysis 24, 407-12. http://dx.doi.org/10.1002/pca.2424

Park KS (2013) Aucubin, a naturally occurring iridoid glycoside inhibits TNF-α-induced inflammatory responses through suppression of NF-κB activation in 3T3-L1 adipocytes. Cytokine 62, 407-12. http://www.sciencedirect.com/science/article/pii/S1043466613001531

Wen B, He R, Li P, Xu Q, Lu Y, Peng B, Li J (2013) Pharmacokinetics of 8-O-acetylharpagide and harpagide after oral administration of Ajuga decumbens Thunb extract in rats. Journal of Ethnopharmacology 147, 503-8. http://www.sciencedirect.com/science/article/pii/S0378874113002043

Wu Z-J, Wang J-H, Fang D-M, Zhang G-L (2013) Analysis of iridoid glucosides from Paederia scandens using HPLC–ESI-MS/MS. Journal of Chromatography B 923–924, 54-64. http://www.sciencedirect.com/science/article/pii/S1570023213000810

Anonymous (2012) Contents. Phytochemistry Letters 5, iii-xiii. http://www.sciencedirect.com/science/article/pii/S1874390012000778

Duffy R, Wade C, Chang R (2012) Discovery of anticancer drugs from antimalarial natural products: a MEDLINE literature review. Drug Discovery Today 17, 942-53. http://www.sciencedirect.com/science/article/pii/S1359644612001171

Guo P, Li Y, Jin D-q, Xu J, He Y, Zhang L, Guo Y (2012) neo-Clerodane diterpenes from Ajuga ciliata and their inhibitory activities on LPS-induced NO production. Phytochemistry Letters 5, 563-6. http://www.sciencedirect.com/science/article/pii/S1874390012001085

Han J-P, Shi L-C, Chen X-C, Lin Y-L (2012) Comparison of four DNA barcodes in identifying certain medicinal plants of Lamiaceae. Journal of Systematics and Evolution 50, 227-34. http://dx.doi.org/10.1111/j.1759-6831.2012.00184.x

Mizuno T, Okuyama Y, Iwashina T (2012) Phenolic compounds from Iris rossii, and their chemotaxonomic and systematic significance. Biochemical Systematics and Ecology 44, 157-60. http://www.sciencedirect.com/science/article/pii/S0305197812000889

Shukla V, Yadav D, Phulara SC, Gupta MM, Saikia SK, Pandey R (2012) Longevity-promoting effects of 4-hydroxy-E-globularinin in Caenorhabditis elegans. Free Radical Biology and Medicine 53, 1848-56. http://www.sciencedirect.com/science/article/pii/S0891584912011112

Sun Z, Li Y, Jin D, Guo P, Xu J, Guo Y, Zhang L (2012) Structure elucidation and inhibitory effects on NO production of clerodane diterpenes from Ajuga decumbens. Planta Med 78, 1579-93.

Sun Z, Li Y, Jin D-q, Guo P, Song H, Xu J, Guo Y, Zhang L (2012) neo-Clerodane diterpenes from Ajuga decumbens and their inhibitory activities on LPS-induced NO production. Fitoterapia 83, 1409-14. http://www.sciencedirect.com/science/article/pii/S0367326X12002134

Wang B, Wang X-N, Shen T, Wang S-Q, Guo D-X, Lou H-X (2012) Rearranged abietane diterpenoid hydroquinones from aerial parts of Ajuga decumbens Thunb. Phytochemistry Letters 5, 271-5. http://www.sciencedirect.com/science/article/pii/S1874390012000274

Yang F, Liu W-W, Wang J, Liao L, Wang Y (2012) Riparian vegetation’s responses to the new hydrological regimes from the Three Gorges Project: Clues to revegetation in reservoir water-level-fluctuation zone. Acta Ecologica Sinica 32, 89-98. http://www.sciencedirect.com/science/article/pii/S1872203212000091

Guo P, Li Y, Xu J, Guo Y, Jin D-Q, Gao J, Hou W, Zhang T (2011) neo-Clerodane diterpenes from Ajuga ciliata Bunge and their neuroprotective activities. Fitoterapia 82, 1123-7. http://www.sciencedirect.com/science/article/pii/S0367326X1100178X

Hsieh W-T, Liu Y-T, Lin W-C (2011) Anti-inflammatory properties of Ajuga bracteosa in vivo and in vitro study and their effects on mouse model of liver fibrosis. Journal of Ethnopharmacology 135, 116-25. http://www.sciencedirect.com/science/article/pii/S0378874111001309

Peng B, He R, Xu Q, Gao J, Lu Y, Li J (2011) [Correlation between antimetastatic action of Ajuga decumbens and expression of MMPs and TIMPs]. Zhongguo Zhong Yao Za Zhi 36, 3511-4.

Pungitore CR, García C, Martín VS, Tonn CE, Ardanaz CE (2011) Mass spectrometry studies of iridoid aglycone derivatives. Rapid Communications in Mass Spectrometry 25, 2099-105. http://dx.doi.org/10.1002/rcm.5079

Zhang C, Jiang M, Lu A (2011) Chinese herbal medicines versus disease modifying antirheumatic drugs for management of rheumatoid arthritis: A systematic review. European Journal of Integrative Medicine 3, e219-e31. http://www.sciencedirect.com/science/article/pii/S1876382011001193

Kim S-K, Cho S-B, Moon H-I (2010) Anti-complement activity of isolated compounds from the roots of Clerodendrum bungei Steud. Phytotherapy Research 24, 1720-3. http://dx.doi.org/10.1002/ptr.3254

Wu Q, Yuan Q, Liu EH, Qi L-W, Bi Z-M, Li P (2010) Fragmentation study of iridoid glycosides and phenylpropanoid glycosides in Radix Scrophulariae by rapid resolution liquid chromatography with diode-array detection and electrospray ionization time-of-flight mass spectrometry. Biomedical Chromatography 24, 808-19. http://dx.doi.org/10.1002/bmc.1368

Zhong L, Cheng Q, Tian X, Zhao L, Qin Z (2010) Characterization of the Replication, Transfer, and Plasmid/Lytic Phage Cycle of the Streptomyces Plasmid-Phage pZL12. J. Bacteriol. 192, 3747-54. http://jb.asm.org/cgi/content/abstract/192/14/3747

Dinan L (2009) The Karlson Lecture. Phytoecdysteroids: What use are they? Archives of Insect Biochemistry and Physiology 72, 126-41. http://dx.doi.org/10.1002/arch.20334

Kwon S-H, Kim H-C, Lee S-Y, Jang C-G (2009) Loganin improves learning and memory impairments induced by scopolamine in mice. European Journal of Pharmacology 619, 44-9. http://www.sciencedirect.com/science/article/pii/S0014299909006530

Zhang G-M, Gong G-Q, Li L-L, Yang L-N, Wang Y (2009) Effects of Luteolin on the Proliferation of Rat Lung Fibroblasts. Chinese Journal of Natural Medicines 7, 297-300. http://www.sciencedirect.com/science/article/pii/S1875536410600222

Anonymous (2008) Subject Index. Helvetica Chimica Acta 91, 2399-446. http://dx.doi.org/10.1002/hlca.200890259

Anonymous (2008) Contents: HCA 4/2008. Helvetica Chimica Acta 91, n/a-n/a. http://dx.doi.org/10.1002/hlca.200890080

Anonymous (2008) Author Index. Helvetica Chimica Acta 91, 2379-98. http://dx.doi.org/10.1002/hlca.200890258

Bouderbala S, Lamri-Senhadji M, Prost J, Lacaille-Dubois MA, Bouchenak M (2008) Changes in antioxidant defense status in hypercholesterolemic rats treated with Ajuga iva. Phytomedicine 15, 453-61. http://www.sciencedirect.com/science/article/pii/S0944711307002541

Grace MH, Cheng DM, Raskin I, Lila MA (2008) Neo-clerodane diterpenes from Ajuga turkestanica. Phytochemistry Letters 1, 81-4. http://www.sciencedirect.com/science/article/pii/S187439000800027X

Huang X-C, Qin S, Guo Y-W, Krohn K (2008) Four New Neoclerodane Diterpenoids from Ajuga decumbens. Helvetica Chimica Acta 91, 628-34. http://dx.doi.org/10.1002/hlca.200890066

Inagaki H, Yamaguchi A, Kato K, Kageyama C, Iyozumi H, Oki Y (2008) Screening of weed extracts for antifungal properties against Colletotrichum lagenarium, the causal agent of anthracnose in cucumber. Weed Biology and Management 8, 276-83. http://dx.doi.org/10.1111/j.1445-6664.2008.00308.x

Koyama J, Morita I, Kobayashi N, Konoshima T, Takasaki M, Osakai T, Tokuda H (2008) Correlation between oxidation potentials and inhibitory effects on Epstein-Barr virus activation of flavonoids. Cancer Letters 263, 61-6. http://www.sciencedirect.com/science/article/pii/S0304383507006271

Ono Y, Fukaya Y, Imai S, Yamakuni T (2008) Beneficial effects of Ajuga decumbens on osteoporosis and arthritis. Biol Pharm Bull 31, 1199-204.

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Grateful acknowledgment is made to the following: for plant names: Australian Plant Name Index, Australian National Herbarium http://www.anbg.gov.au/cpbr/databases/apni-search-full.html; ; The International Plant Names Index, Royal Botanic Gardens, Kew/Harvard University Herbaria/Australian National Herbarium http://www.ipni.org/index.html; Plants Database, United States Department of Agriculture, National Resources Conservation Service http://plants.usda.gov/;DJ Mabberley (1997) The Plant Book, Cambridge University Press (Second Edition); JH Wiersma and B Leon (1999) World Economic Plants, CRC Press; RJ Hnatiuk (1990) Census of Australian Vascular Plants, Australian Government Publishing Service; for information: Science Direct http://www.sciencedirect.com/; Wiley Online Library http://onlinelibrary.wiley.com/advanced/search; High Wire http://highwire.stanford.edu/cgi/search; Oxford Journals http://services.oxfordjournals.org/search.dtl; USDA National Agricultural Library http://agricola.nal.usda.gov/booleancube/booleancube_search_cit.html; for synonyms: The Plant List http://www.theplantlist.org/; for common names: http://en.wikipedia.org/wiki/Main_Page; etc.


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