Search Results - "Haider, Shozeb M"
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A structural analysis of G-quadruplex/ligand interactions
Published in Biochimie (01-08-2011)“…This focused review article discusses in detail, all available high-resolution small molecule ligand/G-quadruplex structural data derived from crystallographic…”
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A molecular model for drug binding to tandem repeats of telomeric G-quadruplexes
Published in Biochemical Society transactions (01-06-2009)“…The extreme 3'-ends of human telomeres consist of 150-250 nucleotides of single-stranded DNA sequence together with associated proteins. Small-molecule ligands…”
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Selectivity in small molecule binding to human telomeric RNA and DNA quadruplexes
Published in Chemical communications (Cambridge, England) (01-01-2009)“…Quadruplex RNAs are less well understood than their DNA counterparts, yet of potentially high biological relevance. The interactions of several…”
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4
Molecular Dynamics Studies of the STAT3 Homodimer:DNA Complex: Relationships between STAT3 Mutations and Protein–DNA Recognition
Published in Journal of chemical information and modeling (25-05-2012)“…Signal Transducers and Activators of Transcription (STAT) proteins are a group of latent cytoplasmic transcription factors involved in cytokine signaling…”
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5
Selective recognition of c-MYC Pu22 G-quadruplex by a fluorescent probe
Published in Nucleic acids research (18-03-2019)“…Abstract Nucleic acid mimics of fluorescent proteins can be valuable tools to locate and image functional biomolecules in cells. Stacking between the internal…”
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crystallographic and modelling study of a human telomeric RNA (TERRA) quadruplex
Published in Nucleic acids research (01-09-2010)“…DNA telomeric repeats in mammalian cells are transcribed to guanine-rich RNA sequences, which adopt parallel-stranded G-quadruplexes with a propeller-like…”
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Targeting Multiple Effector Pathways in Pancreatic Ductal Adenocarcinoma with a G‑Quadruplex-Binding Small Molecule
Published in Journal of medicinal chemistry (22-03-2018)“…Human pancreatic ductal adenocarcinoma (PDAC) involves the dysregulation of multiple signaling pathways. A novel approach to the treatment of PDAC is…”
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Rational Design of Acridine-Based Ligands with Selectivity for Human Telomeric Quadruplexes
Published in Journal of the American Chemical Society (08-09-2010)“…Structure-based modeling methods have been used to design a series of disubstituted triazole-linked acridine compounds with selectivity for human telomeric…”
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Evaluation of by disubstituted acridone derivatives as telomerase inhibitors: the importance of G-quadruplex binding
Published in Bioorganic & medicinal chemistry letters (06-12-2004)“…[Display omitted] The synthesis and evaluation of a group of 2,6-, 2,7- and 3,6-bis-aminoalkylamido acridones are reported, which show a similar level of…”
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A G-quadruplex-binding compound showing anti-tumour activity in an in vivo model for pancreatic cancer
Published in Scientific reports (16-06-2015)“…We report here that a tetra-substituted naphthalene-diimide derivative (MM41) has significant in vivo anti-tumour activity against the MIA PaCa-2 pancreatic…”
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Targeting Human Gastrointestinal Stromal Tumor Cells with a Quadruplex-Binding Small Molecule
Published in Journal of medicinal chemistry (25-06-2009)“…Most of human gastrointestinal stromal tumors (GIST) are driven by activating mutations in the proto-oncogene KIT, a tyrosine kinase receptor. Clinical…”
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12
Phosphorylation of Histone Deacetylase 8: Structural and Mechanistic Analysis of the Phosphomimetic S39E Mutant
Published in Biochemistry (Easton) (12-11-2019)“…Histone deacetylase (HDAC) enzymes that catalyze removal of acetyl-lysine post-translational modifications are frequently post-translationally modified. HDAC8…”
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13
Modular synthesis of functional libraries by accelerated SuFEx click chemistry
Published in Chemical science (Cambridge) (13-03-2024)“…Accelerated SuFEx Click Chemistry (ASCC) is a powerful method for coupling aryl and alkyl alcohols with SuFEx-compatible functional groups. With its hallmark…”
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Sequence occurrence and structural uniqueness of a G-quadruplex in the human c-kit promoter
Published in Nucleic acids research (01-09-2007)“…The 22-nt c-kit87 promoter sequence is unique within the human genome. Its fold and tertiary structure have recently been determined by NMR methods [Phan,A.T.,…”
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Surface area accessibility and the preferred topology of telomeric DNA quadruplex–ligand complexes
Published in Biochimie (01-08-2011)“…Solvent-accessible surface area calculations have been performed on two human telomeric quadruplex structures, the parallel crystal structure and an (3 + 1)…”
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16
Structure of a G-quadruplex–Ligand Complex
Published in Journal of molecular biology (07-02-2003)“…Stabilisation of G-quadruplex structures formed from telomeric DNA, by means of quadruplex-selective ligands, is a means of inhibiting the telomerase enzyme…”
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Molecular Modeling on Inhibitor Complexes and Active-Site Dynamics of Cytochrome P450 C17, a Target for Prostate Cancer Therapy
Published in Journal of molecular biology (30-07-2010)“…A molecular model for the P450 enzyme cytochrome P450 C17 (CYP17) is presented based on sequence alignments of multiple template structures and homology…”
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Biaryl polyamides as a new class of DNA quadruplex-binding ligands
Published in Chemical communications (Cambridge, England) (01-01-2009)“…We report a novel class of biaryl polyamides highly selective for G-quadruplex DNA, and with significant cytotoxicity in several cancer cell lines; they form…”
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N-substituted Piperazinopyridylsteroid Derivatives as Abiraterone Analogues Inhibit Growth and Induce Pro-apoptosis in Human Hormone-independent Prostate Cancer Cell Lines
Published in Chemical biology & drug design (01-11-2013)“…Nine new 17‐(piperazin‐1‐yl)pyridin‐5‐yl)steroids as abiraterone analogues were synthesized. Compounds 5d and 5g showed selective activities against…”
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Bis-guanylhydrazone diimidazo[1,2-a:1,2-c]pyrimidine as a novel and specific G-quadruplex binding motif
Published in Chemical communications (Cambridge, England) (21-08-2010)“…A bis-guanylhydrazone derivative of diimidazo[1,2-a:1,2-c]pyrimidine has unexpectedly been found to be a potent stabiliser of several quadruplex DNAs, whereas…”
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