Search Results - "Sagineedu, Sreenivasa Rao"
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Andrographolide derivatives inhibit guanine nucleotide exchange and abrogate oncogenic Ras function
Published in Proceedings of the National Academy of Sciences - PNAS (18-06-2013)“…Aberrant signaling by oncogenic mutant rat sarcoma (Ras) proteins occurs in ∼15% of all human tumors, yet direct inhibition of Ras by small molecules has…”
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Pharmacological Modulation of Apoptosis and Autophagy in Pancreatic Cancer Treatment
Published in Mini reviews in medicinal chemistry (01-01-2022)“…Pancreatic cancer is a fatal malignant neoplasm with infrequent signs and symptoms until a progressive stage. In 2020, GLOBOCAN reported that pancreatic cancer…”
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The impact of cycleanine in cancer research: a computational study
Published in Journal of molecular modeling (01-11-2022)“…Cancer is imposing a global health burden because of the steady increase in new cases. Moreover, current anticancer therapeutics are associated with many…”
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In silico and saturation transfer difference NMR approaches to unravel the binding mode of an andrographolide derivative to K-Ras oncoprotein
Published in Future medicinal chemistry (01-09-2020)“…Andrographolide and its benzylidene derivatives, SRJ09 and SRJ23, potentially bind oncogenic K-Ras to exert anticancer activity. Their molecular interactions…”
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A classical genetic solution to enhance the biosynthesis of anticancer phytochemicals in Andrographis paniculata Nees
Published in PloS one (25-02-2014)“…Andrographolides, the diterpene lactones, are major bioactive phytochemicals which could be found in different parts of the medicinal herb Andrographis…”
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Edible foxtail millet flour stabilises and retain the in vitro activity of blueberry bioactive components
Published in International journal of food science & technology (01-07-2018)“…Summary Blueberries, a functional food, are rich in bioactive polyphenols and anthocyanins. However, the shelf life is short and requires cold storage. This…”
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In vitro 3D colon tumor penetrability of SRJ09, a new anti-cancer andrographolide analog
Published in Investigational new drugs (01-10-2014)“…Summary Limited tumor penetrability of anti-cancer drugs is recognized as one of the major factors that lead to poor anti-tumor activity. SRJ09…”
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Advances and challenges in developing andrographolide and its analogues as cancer therapeutic agents
Published in Drug discovery today (01-09-2019)“…•New semisynthetic molecules derived from AGP in recent years to target cancer have not been discussed in any review thus far.•With 20 years of research…”
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A K‐RAS Inhibitor Abrogates Self‐Renewal of Pancreatic Cancer Stem Cells via K‐RAS – NF‐κB – SOX2 Axis
Published in The FASEB journal (01-04-2020)“…Abstract only…”
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Microarray-based identification of differentially expressed genes associated with andrographolide derivatives-induced resistance in colon and prostate cancer cell lines
Published in Toxicology and applied pharmacology (15-08-2021)“…Chemoresistance poses a major hurdle to cancer treatments. Andrographolide-derived SRJ09 and SRJ23 were reported to exhibit potent, selective inhibitory…”
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More than just a KRAS inhibitor: DCAI abrogates the self-renewal of pancreatic cancer stem cells in vitro
Published in Oncologie (Paris, France) (24-11-2023)Get full text
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SRS06, a new semisynthetic andrographolide derivative with improved anticancer potency and selectivity, inhibits nuclear factor-κB nuclear binding in the A549 non-small cell lung cancer cell line
Published in Pharmacology (01-01-2015)“…Andrographolide has been reported with anticancer and anti-inflammatory properties through the inhibition of the activity of signaling molecules such as v-Src,…”
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Salt stress-induced protein pattern associated with photosynthetic parameters and andrographolide content in Andrographis paniculata Nees
Published in Bioscience, biotechnology, and biochemistry (02-01-2015)“…Andrographis paniculata is a multifunctional medicinal plant and a potent source of bioactive compounds. Impact of environmental stresses such as salinity on…”
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SRJ09, a promising anticancer drug lead: Elucidation of mechanisms of antiproliferative and apoptogenic effects and assessment of in vivo antitumor efficacy
Published in Pharmacological research (01-05-2016)“…[Display omitted] SRJ09 (3,19-(2-bromobenzylidene)andrographolide), a semisynthetic andrographolide (AGP) derivative, was shown to induce G1 cell cycle arrest…”
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Quantitative analysis of andrographolide, a biomarker of Andrographis paniculata, using qNMR spectroscopy
Published in Frontiers in pharmacology (2019)“…Abstract only…”
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Quantitative analysis of andrographolide, a biomarker of Andrographis paniculata, using qNMR spectroscopy
Published in Frontiers in pharmacology (2019)“…Abstract only…”
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Analysis of the Anticancer Phytochemicals in Andrographis paniculata Nees. under Salinity Stress
Published in BioMed research international (01-01-2013)“…Salinity causes the adverse effects in all physiological processes of plants. The present study aimed to investigate the potential of salt stress to enhance…”
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Abstract 4454: SRJ09, a semisynthetic anticancer agent, targets Ras-MAPK signaling pathway: assessment in breast and colon cancer cell lines
Published in Cancer research (Chicago, Ill.) (01-10-2014)“…SRJ09 (3,19-(2-bromobenzylidene)andrographolide) was shown to be more selective towards breast and colon cancers in USA NCI 60 cancer cell line screen, thus…”
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NCI in vitro and in silico anticancer screen, cell cycle pertubation and apoptosis-inducing potential of new acylated, benzylidene and isopropylidene derivatives of andrographolide
Published in Environmental toxicology and pharmacology (01-09-2014)“…Highlights • Andrographolide (AGP) has been shown to possess promising anticancer activity. • We evaluated the anticancer potential of newer AGP derivatives. •…”
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SRJ23, a new semisynthetic andrographolide derivative: in vitro growth inhibition and mechanisms of cell cycle arrest and apoptosis in prostate cancer cells
Published in Cell biology and toxicology (01-10-2014)“…Purpose 3,19-(3-Chloro-4-fluorobenzylidene)andrographolide (SRJ23), a new semisynthetic derivative of andrographolide (AGP), exhibited selectivity against…”
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