Protein tyrosine phosphatase 1B inhibitors isolated from Artemisia roxburghiana

References

• Tonks NK. Protein tyrosine phosphatases: from genes, to function, to disease. Nat Rev Mol Cell Biol 2006;7:833–46
   PubMed Web of Science ®Google Scholar
• Fisher EH, Charbonneau H, Tonks NK. Protein tyrosine phosphatases: a diverse family of intracellular and transmembrane enzymes. Science 1991;253:401–6
   PubMed Web of Science ®Google Scholar
• Hunter T. Protein kinases and phosphatases: the Yin and Yang of protein phosphorylation and signaling. Cell 1995;80:225–36
   PubMed Web of Science ®Google Scholar
• Bialy L, Waldmann H. Inhibitors of protein tyrosine phosphatases: next-generation drugs? Angew Chem 2005;44:3814–39
   Google Scholar
• Koren S, Fantus IG. Inhibition of the protein tyrosine phosphatase PTP1B: potential therapy for obesity, insulin resistance and type-2 diabetes mellitus. Best Pract Res Clin Endocrinol Metabol 2007;21:621–40
   PubMed Web of Science ®Google Scholar
• Elchebly M, Payette P, Michaliszyn E, Cromlish W. Increased insulin sensitivity and obesity resistance in mice lacking the protein tyrosine phosphatase-1B gene. Science 1999;283:1544–8
   PubMed Web of Science ®Google Scholar
• Ali MI, Ketsawatsomkron P, Chantemele EJ, et al. Deletion of protein tyrosine phosphatase 1b improves peripheral insulin resistance and vascular function in obese, leptin-resistant mice via reduced oxidant tone. Circ Res 2009;105:1013–22
   PubMed Web of Science ®Google Scholar
• Dua VK, Verma G, Agarwal DD, et al. Antiprotozoal activities of traditional medicinal plants from the Garhwal region of North West Himalaya, India. J Ethnopharmacol 2011;136:123–8
   PubMed Web of Science ®Google Scholar
• Ashraf M, Hayat MQ, Jabeen S, et al. Artemisia L. species recognized by the local community of northern areas of Pakistan as folk therapeutic plants. J Med Plant Res 2010;4:112–19
   Google Scholar
• Hussain Z, Waheed A, Qureshi RA, et al. The effect of medicinal plants of Islamabad and Murree region of Pakistan on insulin secretion from INS-1 cells. Phytother Res 2004;18:73–7
   PubMed Web of Science ®Google Scholar
• Bicchi C, Rubiolo P, Marschall H, et al. Constituents of Artemisia roxburghiana Besser essential oil. Flavour Fragrance J 1998;13:40–6
   Web of Science ®Google Scholar
• Gohari AR, Ebrahimi H, Saeidnia S, et al. Flavones and flavone glycosides from Salvia macrosiphon Boiss. Iranian J Pharma Res 2011;10:247–51
   PubMed Web of Science ®Google Scholar
• Ogihara K, Higa M, Hokama K, Suga T. Triterpenes from the leaves of Parsonsia laevigata. Phytochemistry 1987;26:783–5
   Web of Science ®Google Scholar
• Sharma P, Gupta YK, Sharma MC, Dobhal MP.Two new compounds from the stem of Nerium oleander. Indian J Chem Sect B Org Chem Med Chem 2010;49B:374–8
   Google Scholar
• Ayatollahi AM, Ghanadian M, Afsharypour S, et al. Pentacyclic triterpenes in Euphorbia microsciadia with their T-cell proliferation activity. Iranian J Pharma Res 2011;10:287–94
   PubMed Web of Science ®Google Scholar
• Ting Z, Yan Y, Guanhua D, Ruoyun C. Study on chemical constituents from the roots of Saussurea lappa. Zhongguo Zhongyao Zazhi 2011;36:1620–2
   PubMedGoogle Scholar
• Chen JX, Huang SH, Wang Y, et al. Studies on the chemical constituents from Lobelia chinensis. J Chinese Med Mat 2010;33:1721–4
   Google Scholar
• Khan I, Nisar M, Shah MR, et al. Anti-inflammatory activities of Taxusabietane A isolated from Taxus wallichiana Zucc. Fitoterapea 2011;82:1003–7
   PubMed Web of Science ®Google Scholar
• Rizvi SUF, Siddiqui HL, Nisar M, et al. Discovery and molecular docking of quinolyl-thienyl chalcones as anti-angiogenic agents targeting VEGFR-2 tyrosine kinase. Bioorg Med Chem Lett 2012;22:942–4
   PubMed Web of Science ®Google Scholar
• Khan I, Nisar M, Khan N, et al. Structural insights to investigate Conypododiol as a dual cholinesterase inhibitor from Asparagus adscendens. Fitoterapia 2010;81:1020–5
   PubMed Web of Science ®Google Scholar
• Nisar M, Kaleem WA, Khan I, et al. Molecular simulations probing Kushecarpin A as a new lipoxygenase inhibitor. Fitoterapia 2011;82:1008–11
   PubMed Web of Science ®Google Scholar
• Khan I, Samad A, Khan AZ, et al. Molecular interactions of 4-acetoxy-plakinamine B with peripheral anionic and other catalytic subsites of the aromatic gorge of acetylcholinesterase: computational and structural insights. Pharma Biol 2013;51:722–7
   PubMed Web of Science ®Google Scholar
• Zhang W, Hong D, Zhou Y, et al. Ursolic acid and its derivative inhibit protein tyrosine phosphatase 1B, enhancing insulin receptor phosphorylation and stimulating glucose uptake. Biochim Biophys Acta 2006;1760:1505–12
   PubMed Web of Science ®Google Scholar
• Choi JY, Na MK, Hwang IH, et al. Isolation of betulinic acid, its methyl ester and guaiane sesquiterpenoids with protein tyrosine phosphatase 1B inhibitory activity from the roots of Saussurea lappa C.B.Clarke. Molecules 2009;14:266–72
   PubMed Web of Science ®Google Scholar
• Shah MR, Shamim A, White LS, et al. The anti-inflammatory properties of Au–scopoletin nanoconjugates. New J Chem 2014;38:5566–72
   Web of Science ®Google Scholar
• Kim J, Lee YS, Kim C-S, Kim JS. Betulinic acid has an inhibitory effect on pancreatic lipase and induces adipocyte lipolysis. Phytother Res 2012;26:1003–6
   PubMed Web of Science ®Google Scholar
• Castellano JM, Guinda A, Delgado T, et al. Biochemical basis of the antidiabetic activity of oleanolic acid and related pentacyclic triterpenes. Diabetes 2013;62:1791--9
   PubMed Web of Science ®Google Scholar
• Tang JJ, Li JG, Qi W, et al. Inhibition of SREBP by a small molecule, betulin, improves hyperlipidemia and insulin resistance and reduces atherosclerotic plaques. Cell Metab 2011;13:44–56
   PubMed Web of Science ®Google Scholar
• Ramírez-Espinosa JJ, Rios MY, López-Martínez S, et al. Antidiabetic activity of some pentacyclic acid triterpenoids, role of PTP–1B: in vitro, in silico, and in vivo approaches. Eur J Med Chem 2011;46:2243–51
   PubMed Web of Science ®Google Scholar
• Fazal-Ur-Rehman, Khan MF, Khan I, et al. Molecular interactions of an alkaloid euchrestifoline as a new acetylcholinesterase inhibitor. Bangladesh J Pharmacol 2013;8:361–4
   Web of Science ®Google Scholar
• Rehman UU, Shah J, Khan MA, et al. Molecular docking of taraxerol acetate as a new COX inhibitor. Bangladesh J Pharmacol 2013;8:194–7
   Web of Science ®Google Scholar
• Ali S, Nisar M, Iriti M, et al. Biotransformation of finasteride by Ocimum sanctum L., and tyrosinase inhibitory activity of transformed: experimental and computational insights. Steroids 2014;92:20–4
   PubMed Web of Science ®Google Scholar
• Khan I, Nisar M, Khan AZ, et al. Molecular insights to explore abietane diterpenes as new LOX inhibitors. Chem Res 2013;22:5809–13
   Google Scholar
• Uddin G, Rauf A, Collina S, et al. Pistagremic acid, a glucosidase inhibitor from Pistacia integerrima. Fitoterapia 2012;83:1648–52
   PubMed Web of Science ®Google Scholar