Search Results - "Kiselyov, Alexander S"
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Novel inhibitors of VEGF receptors-1 and -2 based on azole-5-carboxamide templates
Published in Bioorganic & medicinal chemistry letters (01-07-2007)“…We have developed a series of novel potent 1-(2-(pyridin-4-yl)ethyl)-1 H-azole-5-carboxamides active against kinases VEGFR-2 and -1. Both specific and dual…”
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2
Arylphthalazines. Part 2: 1-(Isoquinolin-5-yl)-4-arylamino phthalazines as potent inhibitors of VEGF receptors I and II
Published in Bioorganic & medicinal chemistry letters (15-03-2006)“…The synthesis and structure–activity relationships for a sub-class of arylphthalazine derivatives which have found use as inhibitors of VEGF receptors I and II…”
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3
Virtual and biomolecular screening converge on a selective agonist for GPR30
Published in Nature chemical biology (01-04-2006)“…Estrogen is a hormone critical in the development, normal physiology and pathophysiology of numerous human tissues. The effects of estrogen have traditionally…”
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4
Chemistry of N-fluoropyridinium salts
Published in Chemical Society reviews (01-12-2005)“…This tutorial review deals with developments in the chemistry of N-fluoropyridinium salts in the past decade, including both synthetic and mechanistic aspects…”
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5
Quantitative 3D reconstruction of viral vector distribution in rodent and ovine brain following local delivery
Published in Neuroimage. Reports (01-12-2024)“…Viral vectors are an active area of research and development to treat diseases of the central nervous system (CNS). However, systemic delivery of…”
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6
DNA triple-helix specific intercalators as antigene enhancers: Unfused aromatic cations
Published in Biochemistry (Easton) (12-10-1993)“…Triple-helical structures involving the interaction of an oligonucleotide third strand with a duplex nucleic acid sequence have recently gained attention as a…”
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7
3,4-Disubstituted isothiazoles: Novel potent inhibitors of VEGF receptors 1 and 2
Published in Bioorganic & medicinal chemistry letters (15-02-2009)“…Novel derivatives of isothiazoles are described as potent ATP-competitive inhibitors of vascular endothelial growth factor receptors I and II (VEGFR-1/2)…”
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8
(1,2,3-Triazol-4-yl)benzenamines: Synthesis and activity against VEGF receptors 1 and 2
Published in Bioorganic & medicinal chemistry letters (01-03-2009)“…Both synthesis and activity of the novel derivatives of (1,2,3-triazol-4-yl)benzenamines are described. Selected molecules of these series are potent and…”
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9
One-pot synthesis of polysubstituted pyrimidines
Published in Tetrahedron letters (07-03-2005)“…[Display omitted] A series of polysubstituted pyrimidines were synthesized from in situ generated α,β-unsaturated imines and the corresponding amidine or…”
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10
The o-Amino-Trifluoromethyl Functionality as a Novel Synthon for 4-Fluoroquinolines
Published in Journal of organic chemistry (01-10-1994)Get full text
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11
Oxadiazole derivatives as a novel class of antimitotic agents: Synthesis, inhibition of tubulin polymerization, and activity in tumor cell lines
Published in Bioorganic & medicinal chemistry letters (01-03-2006)“…The synthesis, SAR studies, and pharmacokinetic properties of oxadiazole based tubulin inhibitor class are reported. This class of compounds binds to the…”
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12
Efficient Syntheses of the anti- and syn-Diol Epoxide Metabolites of the Carcinogenic Polycyclic Aromatic Hydrocarbon Benzo[g]chrysene
Published in Journal of organic chemistry (01-09-1995)Get full text
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13
Arylphthalazines as potent, and orally bioavailable inhibitors of VEGFR-2
Published in Bioorganic & medicinal chemistry (15-01-2009)“…A series of arylphthalazine derivatives were synthesized and evaluated as antagonists of VEGF receptor II (VEGFR-2). IM-094482 57, which was prepared in two…”
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14
Discovery of Dual VEGFR-2 and Tubulin Inhibitors with in Vivo Efficacy
Published in ACS medicinal chemistry letters (09-12-2010)“…In an effort to develop potent, orally bioavailable compounds for the treatment of neoplastic diseases, we developed a class of dual VEGFR-2 kinase and tubulin…”
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15
Design and chemical synthesis of [1,2,4]triazol[1,5- c]pyrimidin-5-yl amines, a novel class of VEGFR-2 kinase inhibitors
Published in Tetrahedron letters (01-07-2009)“…The Letter describes a facile approach to 7,8-dihydro[1,2,4]triazol[1,5- c]pyrimidin-5-yl amines, a novel class of potent inhibitors of vascular endothelial…”
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16
1-[4-(1 H-Benzoimidazol-2-yl)-phenyl]-3-[4-(1 H-benzoimidazol-2-yl)-phenyl]-urea derivatives as small molecule heparanase inhibitors
Published in Bioorganic & medicinal chemistry letters (15-01-2006)“…The development of small molecule heparanase inhibitor 7a (IC 50 = 0.27 μM) is reported. A novel class of 1-[4-(1 H-benzoimidazol-2-yl)-phenyl]-3-[4-(1…”
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17
Hetaryl imidazoles: A novel dual inhibitors of VEGF receptors I and II
Published in Bioorganic & medicinal chemistry letters (01-03-2006)“…Novel potent derivatives of hetaryl imidazoles are described as inhibitors of vascular endothelial growth factor receptor II (VEGFR-2). Many compounds display…”
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18
Synthesis and structure–activity relationships of 1,2,4-triazoles as a novel class of potent tubulin polymerization inhibitors
Published in Bioorganic & medicinal chemistry letters (01-12-2005)“…The synthesis and SAR studies on triazole-containing tubulin inhibitor class are reported. A novel triazole-containing chemical series was shown to inhibit…”
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19
4-(Azolylphenyl)-phthalazin-1-amines: Novel Inhibitors of VEGF Receptors I and II
Published in Chemical biology & drug design (01-12-2006)“…Novel potent derivatives of phthalazine are described as ATP‐competitive inhibitors of vascular endothelial growth factor receptors I and II (VEGFR‐1/2). A…”
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20
Arylphthalazines: Identification of a new phthalazine chemotype as inhibitors of VEGFR kinase
Published in Bioorganic & medicinal chemistry letters (01-11-2005)“…The synthesis and structure–activity relationships for a new class of arylphthalazine derivatives, which have found use as inhibitors of VEGFR-2 kinase, are…”
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