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Carbon Nanotube Substrates Boost Neuronal Electrical Signaling

Nano letters, 2005-06, Vol.5 (6), p.1107-1110

2005

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2,7-Dimethyl-3,8-dinitrodipyrazolo[1,5-a:1′,5′-d]pyrazine-4,9-dione: A new labelling reagent for liquid chromatographic analysis of amino acids

Analytica chimica acta, 2006-10, Vol.579 (2), p.152-157

2006

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Fluorosulfonyl- and Bis-(β-chloroethyl)amino-phenylamino Functionalized Pyrazolo[4,3-e]1,2,4-triazolo[1,5-c]pyrimidine Derivatives: Irreversible Antagonists at the Human A3 Adenosine Receptor and Molecular Modeling Studies

Journal of medicinal chemistry, 2001-08, Vol.44 (17), p.2735-2742

2001

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Autocorrelation of molecular electrostatic potential surface properties combined with partial least squares analysis as new strategy for the prediction of the activity of human A(3) adenosine receptor antagonists

Journal of medicinal chemistry, 2005-09, Vol.48 (18), p.5698-5704

2005

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7-Substituted 5-Amino-2-(2-furyl)pyrazolo[4,3-e]-1,2,4-triazolo[1,5-c]pyrimidines as A2A Adenosine Receptor Antagonists: A Study on the Importance of Modifications at the Side Chain on the Activity and Solubility

Journal of medicinal chemistry, 2002-01, Vol.45 (1), p.115-126

2002

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Synthesis, Biological Activity, and Molecular Modeling Investigation of New Pyrazolo[4,3-e]-1,2,4-triazolo[1,5-c]pyrimidine Derivatives as Human A3 Adenosine Receptor Antagonists

Journal of medicinal chemistry, 2002-02, Vol.45 (4), p.770-780

2002

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Binding affinity of adenosine receptor agonists and antagonists at human cloned A3 adenosine receptors

Life sciences (1973), 1998, Vol.63 (5), p.PL 81-PL87

1998

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Oligonucleotides and oligonucleotide conjugates: a new approach for cancer treatment

Current medicinal chemistry, 2005, Vol.12 (1), p.71

2005

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CC-1065 and the duocarmycins: recent developments

Expert opinion on therapeutic patents, 2000-12, Vol.10 (12), p.1853-1871

2000

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Heterocyclic analogs of DNA minor groove alkylating agents

Current pharmaceutical design, 1998-06, Vol.4 (3), p.249

1998

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DNA minor groove alkylating agents structurally related to distamycin A

Expert opinion on therapeutic patents, 2000-06, Vol.10 (6), p.891-904

2000

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A3 Adenosine Receptor Ligands: History and Perspectives

Medicinal research reviews, 2000-03, Vol.20 (2), p.103-128

2000

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Demystifying the three dimensional structure of G protein-coupled receptors (GPCRs) with the aid of molecular modeling

Chemical communications (Cambridge, England), 2003-12 (24), p.2949-2956

2003

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Facile and Versatile Route to the Synthesis of Fused 2-Pyridones: Useful Intermediates for Polycyclic Sytems

Synthetic communications, 2006-05, Vol.36 (9), p.1173-1183

2006

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[(3)H]MRE 3008F20: a novel antagonist radioligand for the pharmacological and biochemical characterization of human A(3) adenosine receptors

Molecular pharmacology, 2000-05, Vol.57 (5), p.968-975

2000

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Synthesis, biological and modeling studies of 1,3-di- n-propyl-2,4-dioxo-6-methyl-8-(substituted) 1,2,3,4-tetrahydro [1,2,4]-triazolo [3,4-f]-purines as adenosine receptor antagonists

Farmaco (Società chimica italiana : 1989), 2005-08, Vol.60 (8), p.643-651

2005

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Highlights on the Development of A2A Adenosine Receptor Agonists and Antagonists

ChemMedChem, 2007-03, Vol.2 (3), p.260-281

2007

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Medicinal chemistry of A2A adenosine receptor antagonists

Current topics in medicinal chemistry, 2003, Vol.3 (4), p.403

2003

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Pyrazolo[4,3-e]1,2,4-triazolo[1,5-c]pyrimidine Derivatives as Highly Potent and Selective Human A3 Adenosine Receptor Antagonists: Influence of the Chain at the N8 Pyrazole Nitrogen

Journal of medicinal chemistry, 2000-12, Vol.43 (25), p.4768-4780

2000

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Synthesis, biological properties, and molecular modeling investigation of the first potent, selective, and water-soluble human A(3) adenosine receptor antagonist

Journal of medicinal chemistry, 2002-08, Vol.45 (17), p.3579-3582

2002

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A(3) adenosine receptor ligands: history and perspectives

Medicinal research reviews, 2000-03, Vol.20 (2), p.103-128

2000

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Design, Radiosynthesis, and Biodistribution of a New Potent and Selective Ligand for in Vivo Imaging of the Adenosine A2A Receptor System Using Positron Emission Tomography

Journal of medicinal chemistry, 2000-11, Vol.43 (23), p.4359-4362

2000

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Nitrile Oxide [3 + 2] Cycloaddition: Application to the Synthesis of 6-Substituted 3(2H)-Pyridazinones and 6-Substituted 4,5-Dihydro-4-hydroxy-3(2H)-pyridazinones

Synthesis (Stuttgart), 1994, Vol.1994 (11), p.1158-1162

1994

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Pyrazolo[4,3-e]-1,2,4-triazolo[1,5-c]pyrimidine Derivatives as Highly Potent and Selective Human A3 Adenosine Receptor Antagonists

Journal of medicinal chemistry, 1999-11, Vol.42 (22), p.4473-4478

1999

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Design, radiosynthesis, and biodistribution of a new potent and selective ligand for in vivo imaging of the adenosine A(2A) receptor system using positron emission tomography

Journal of medicinal chemistry, 2000-11, Vol.43 (23), p.4359-4362

2000

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Carbon Nanotube Substrates Boost Neuronal Electrical Signaling

2,7-Dimethyl-3,8-dinitrodipyrazolo[1,5-a:1′,5′-d]pyrazine-4,9-dione: A new labelling reagent for liquid chromatographic analysis of amino acids

Fluorosulfonyl- and Bis-(β-chloroethyl)amino-phenylamino Functionalized Pyrazolo[4,3-e]1,2,4-triazolo[1,5-c]pyrimidine Derivatives: Irreversible Antagonists at the Human A3 Adenosine Receptor and Molecular Modeling Studies

Autocorrelation of molecular electrostatic potential surface properties combined with partial least squares analysis as new strategy for the prediction of the activity of human A(3) adenosine receptor antagonists

7-Substituted 5-Amino-2-(2-furyl)pyrazolo[4,3-e]-1,2,4-triazolo[1,5-c]pyrimidines as A2A Adenosine Receptor Antagonists: A Study on the Importance of Modifications at the Side Chain on the Activity and Solubility

Synthesis, Biological Activity, and Molecular Modeling Investigation of New Pyrazolo[4,3-e]-1,2,4-triazolo[1,5-c]pyrimidine Derivatives as Human A3 Adenosine Receptor Antagonists

Binding affinity of adenosine receptor agonists and antagonists at human cloned A3 adenosine receptors

Oligonucleotides and oligonucleotide conjugates: a new approach for cancer treatment

CC-1065 and the duocarmycins: recent developments

Heterocyclic analogs of DNA minor groove alkylating agents

DNA minor groove alkylating agents structurally related to distamycin A

A3 Adenosine Receptor Ligands: History and Perspectives

Demystifying the three dimensional structure of G protein-coupled receptors (GPCRs) with the aid of molecular modeling

Facile and Versatile Route to the Synthesis of Fused 2-Pyridones: Useful Intermediates for Polycyclic Sytems

[(3)H]MRE 3008F20: a novel antagonist radioligand for the pharmacological and biochemical characterization of human A(3) adenosine receptors

Synthesis, biological and modeling studies of 1,3-di- n-propyl-2,4-dioxo-6-methyl-8-(substituted) 1,2,3,4-tetrahydro [1,2,4]-triazolo [3,4-f]-purines as adenosine receptor antagonists

Highlights on the Development of A2A Adenosine Receptor Agonists and Antagonists

Medicinal chemistry of A2A adenosine receptor antagonists

Pyrazolo[4,3-e]1,2,4-triazolo[1,5-c]pyrimidine Derivatives as Highly Potent and Selective Human A3 Adenosine Receptor Antagonists: Influence of the Chain at the N8 Pyrazole Nitrogen

Synthesis, biological properties, and molecular modeling investigation of the first potent, selective, and water-soluble human A(3) adenosine receptor antagonist

A(3) adenosine receptor ligands: history and perspectives

Design, Radiosynthesis, and Biodistribution of a New Potent and Selective Ligand for in Vivo Imaging of the Adenosine A2A Receptor System Using Positron Emission Tomography

Nitrile Oxide [3 + 2] Cycloaddition: Application to the Synthesis of 6-Substituted 3(2H)-Pyridazinones and 6-Substituted 4,5-Dihydro-4-hydroxy-3(2H)-pyridazinones

Pyrazolo[4,3-e]-1,2,4-triazolo[1,5-c]pyrimidine Derivatives as Highly Potent and Selective Human A3 Adenosine Receptor Antagonists

Design, radiosynthesis, and biodistribution of a new potent and selective ligand for in vivo imaging of the adenosine A(2A) receptor system using positron emission tomography

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