In vitro and in silico studies of 7′′,8′′-buddlenol D anti-inflammatory lignans from Carallia brachiata as p38 MAP kinase inhibitors
暂无分享,去创建一个
T. Rungrotmongkol | Hsun-Shuo Chang | C. Chansriniyom | Nakuntwalai Wisidsri | Ho-Cheng Wu | Nonthaneth Nalinratana | Preeyaporn Poldorn | Utid Suriya | Chanyanuch Laprasert | Wacharee Limpanasitthikul | N. Wisidsri | Chaisak Chansriniyom
[1] P. Pancorbo-Hidalgo,et al. The Role of Antioxidants on Wound Healing: A Review of the Current Evidence , 2021, Journal of clinical medicine.
[2] Ya-Ping Liu,et al. Chemical constituents from Melodinus cochinchinensis (Lour.) Merr. and their chemotaxonomic significance , 2021 .
[3] J. Molphy,et al. The influence of environmental and core temperature on cyclooxygenase and PGE2 in healthy humans , 2021, Scientific Reports.
[4] C. Chansriniyom,et al. S-deoxydihydroglyparvin from Glycosmis parva inhibits lipopolysaccharide induced murine macrophage activation through inactivating p38 mitogen activated protein kinase , 2021, Journal of advanced pharmaceutical technology & research.
[5] V. Patrone,et al. Lignans and Gut Microbiota: An Interplay Revealing Potential Health Implications , 2020, Molecules.
[6] M. Rudrapal,et al. Antidiabetic activity of Carallia brachiata Lour. leaves hydro-alcoholic extract (HAE) with antioxidant potential in diabetic rats , 2020, Indian Journal of Natural Products and Resources.
[7] Rahman,et al. IN VIVO EVALUATION OF ANALGESIC, ANTI-INFLAMMATORY AND ANTI- DIABETIC ACTIVITIES OF METHANOL EXTRACT OF CARALLIA BRACHIATA L. LEAVES , 2020 .
[8] H. Puthalakath,et al. Sepsis: Inflammation Is a Necessary Evil , 2019, Front. Cell Dev. Biol..
[9] Yong-Deok Jeon,et al. Apoptotic effect of enterodiol, the final metabolite of edible lignans, in colorectal cancer cells. , 2019, Journal of the science of food and agriculture.
[10] Andreas Eckert,et al. ProTox-II: a webserver for the prediction of toxicity of chemicals , 2018, Nucleic Acids Res..
[11] Ling Zhao,et al. Inflammatory responses and inflammation-associated diseases in organs , 2015, Oncotarget.
[12] Nam‐Jung Kim,et al. Recent Advances in the Inhibition of p38 MAPK as a Potential Strategy for the Treatment of Alzheimer’s Disease , 2017, Molecules.
[13] P. Lan,et al. A New Spiro Compound from Caragana acanthophylla , 2017, Chemistry of Natural Compounds.
[14] Olivier Michielin,et al. SwissADME: a free web tool to evaluate pharmacokinetics, drug-likeness and medicinal chemistry friendliness of small molecules , 2017, Scientific Reports.
[15] H. Korashy,et al. Dexamethasone Attenuates LPS-induced Acute Lung Injury through Inhibition of NF-κB, COX-2, and Pro-inflammatory Mediators , 2016, Immunological investigations.
[16] Gaozhi Chen,et al. Curcumin Analog L48H37 Prevents Lipopolysaccharide-Induced TLR4 Signaling Pathway Activation and Sepsis via Targeting MD2 , 2015, The Journal of Pharmacology and Experimental Therapeutics.
[17] Thomas Sander,et al. DataWarrior: An Open-Source Program For Chemistry Aware Data Visualization And Analysis , 2015, J. Chem. Inf. Model..
[18] P. Lograsso,et al. Structural Basis and Biological Consequences for JNK2/3 Isoform Selective Aminopyrazoles , 2015, Scientific Reports.
[19] S. Knapp,et al. A unique inhibitor binding site in ERK1/2 is associated with slow binding kinetics , 2014, Nature chemical biology.
[20] F. Peri,et al. Toll-like receptor 4 (TLR4) modulation by synthetic and natural compounds: an update. , 2014, Journal of medicinal chemistry.
[21] D. Brandeis,et al. A Review of Current Evidence , 2014 .
[22] S. Turk,et al. Novel toll-like receptor 4 (TLR4) antagonists identified by structure- and ligand-based virtual screening. , 2013, European journal of medicinal chemistry.
[23] Soo‐Young Choi,et al. Suppression of iNOS and COX-2 expression by flavokawain A via blockade of NF-κB and AP-1 activation in RAW 264.7 macrophages. , 2013, Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association.
[24] L. Mosyak,et al. Crystal Structure of a Human IκB Kinase β Asymmetric Dimer , 2013, The Journal of Biological Chemistry.
[25] J. de Vlieg,et al. X-ray structure of p38α bound to TAK-715: comparison with three classic inhibitors. , 2012, Acta crystallographica. Section D, Biological crystallography.
[26] V. Dixit,et al. Signaling in innate immunity and inflammation. , 2012, Cold Spring Harbor perspectives in biology.
[27] Keunwan Park,et al. Structure-Based Rational Design of a Toll-like Receptor 4 (TLR4) Decoy Receptor with High Binding Affinity for a Target Protein , 2012, PloS one.
[28] Sheng Lin,et al. Lignans and neolignans from Sinocalamus affinis and their absolute configurations. , 2011, Journal of natural products.
[29] Yue-Hu Wang,et al. Two dimeric lignans with an unusual α,β-unsaturated ketone motif from Zanthoxylum podocarpum and their inhibitory effects on nitric oxide production. , 2011, Bioorganic & medicinal chemistry letters.
[30] Qin Liu,et al. MicroRNA-101 Targets MAPK Phosphatase-1 To Regulate the Activation of MAPKs in Macrophages , 2010, The Journal of Immunology.
[31] A. Kuglstatter,et al. X-ray crystal structure of JNK2 complexed with the p38alpha inhibitor BIRB796: insights into the rational design of DFG-out binding MAP kinase inhibitors. , 2010, Bioorganic & medicinal chemistry letters.
[32] Guangying Chen,et al. A new flavonol from the stem-bark of Premna fulva , 2010 .
[33] J. Yadav,et al. Total synthesis of (+)-pseudohygroline , 2010 .
[34] B. Krishnaveni,et al. Wound Healing Activity of Carallia brachiata Bark , 2009, Indian journal of pharmaceutical sciences.
[35] S. Hong,et al. A new furofuran lignan from Isodon japonicus , 2009, Archives of pharmacal research.
[36] Da Yeon Lee,et al. In vitro anti-inflammatory activity of lignans isolated from Magnolia fargesii. , 2009, Bioorganic & medicinal chemistry letters.
[37] Sheng Lin,et al. Glycosides from the root of Iodes cirrhosa. , 2008, Journal of natural products.
[38] J. N. Sharma,et al. Role of nitric oxide in inflammatory diseases , 2007, Inflammopharmacology.
[39] Hayyoung Lee,et al. Crystal Structure of the TLR4-MD-2 Complex with Bound Endotoxin Antagonist Eritoran , 2007, Cell.
[40] C. Abad-Zapatero,et al. Discovery of a new class of 4-anilinopyrimidines as potent c-Jun N-terminal kinase inhibitors: Synthesis and SAR studies. , 2007, Bioorganic & medicinal chemistry letters.
[41] T. Pakkanen,et al. Phenolic compounds in silver birch (Betula pendula Roth) wood , 2006 .
[42] K. Miyake,et al. Inhibition of homodimerization of Toll-like receptor 4 by curcumin. , 2006, Biochemical pharmacology.
[43] P. Phuwapraisirisan,et al. Reactive radical scavenging and xanthine oxidase inhibition of proanthocyanidins from Carallia brachiata , 2006, Phytotherapy research : PTR.
[44] T. Tanaka,et al. A new diglycosyl megastigmane from Carallia brachiata. , 2004, Fitoterapia.
[45] D. Hommes,et al. Mitogen activated protein (MAP) kinase signal transduction pathways and novel anti-inflammatory targets , 2003, Gut.
[46] L. Tong,et al. Inhibition of p38 MAP kinase by utilizing a novel allosteric binding site , 2002, Nature Structural Biology.
[47] J. Coleman. Nitric oxide in immunity and inflammation. , 2001, International immunopharmacology.
[48] M. Belvisi,et al. Role of p38 MAP kinase in LPS‐induced airway inflammation in the rat , 2001, British journal of pharmacology.
[49] Jiahuai Han,et al. The p38 signal transduction pathway: activation and function. , 2000, Cellular signalling.
[50] Lin,et al. Involvement of p38 mitogen‐activated protein kinase in lipopolysaccharide‐induced iNOS and COX‐2 expression in J774 macrophages , 1999, Immunology.
[51] J. Frelek,et al. [Rh2(OCOCF3)4] as an auxiliary chromophore in chiroptical studies on steroidal alcohols , 1999 .
[52] B. K. English,et al. Specific inhibitors of p38 and extracellular signal-regulated kinase mitogen-activated protein kinase pathways block inducible nitric oxide synthase and tumor necrosis factor accumulation in murine macrophages stimulated with lipopolysaccharide and interferon-gamma. , 1999, The Journal of infectious diseases.
[53] M. Rawat,et al. Proanthocyanidins from Prunus armeniaca roots , 1999 .
[54] K. Wilson,et al. A single amino acid substitution makes ERK2 susceptible to pyridinyl imidazole inhibitors of p38 MAP kinase , 1998, Protein science : a publication of the Protein Society.
[55] C. Teng,et al. Bioactive constitutents from the stems of Annona montana. , 1995, Planta medica.
[56] G. Snatzke,et al. Circular dichroism, XCIII determination of the absolute configuration of alcohols, olefins, epoxides, and ethers from the CD of their “in situ” complexes with [Rh2(O2CCF3)4]. , 1990 .
[57] P. Houghton. Lignans and neolignans from Buddleja davidii , 1985 .
[58] K. Johnson. An Update. , 1984, Journal of food protection.
[59] G. Snatzke,et al. Circular dichroism—XLVII: Influence of substitution pattern on the benzene 1Lb-band Cotton effect , 1972 .
[60] J. Fitzgerald. (+)-Hygroline, the major alkaloid of Carallia brachiata (Rhizophoraceae) , 1965 .