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Differential effects of Vitamin D analogs on bone formation and resorption

The Journal of steroid biochemistry and molecular biology, 2006, Vol.98 (1), p.72-77

2006

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Pharmacological properties and procognitive effects of ABT-288, a potent and selective histamine H3 receptor antagonist

The Journal of pharmacology and experimental therapeutics, 2012-10, Vol.343 (1), p.233

2012

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(-)-(9S)-9-(3-Bromo-4-fluorophenyl)-2,3,5,6,7,9-hexahydrothieno[3,2-b]quinolin-8(4H)-one 1,1-dioxide (A-278637): a novel ATP-sensitive potassium channel opener efficacious in suppressing urinary bladder contractions. II. in vivo characterization

The Journal of pharmacology and experimental therapeutics, 2002-10, Vol.303 (1), p.387-394

2002

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Discovery and Metabolic Stabilization of Potent and Selective 2-Amino-N-(adamant-2-yl) Acetamide 11β-Hydroxysteroid Dehydrogenase Type 1 Inhibitors

Journal of medicinal chemistry, 2007-01, Vol.50 (1), p.149-164

2007

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Zotarolimus, a Novel Sirolimus Analogue With Potent Anti-proliferative Activity on Coronary Smooth Muscle Cells and Reduced Potential for Systemic Immunosuppression

Journal of cardiovascular pharmacology, 2007-04, Vol.49 (4), p.228-235

2007

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Effects of ATP-sensitive K+ channel openers and tolterodine on involuntary bladder contractions in a pig model of partial bladder outlet obstruction

Neurourology and urodynamics, 2003, Vol.22 (2), p.147-155

2003

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Discovery and Pharmacological Evaluation of Growth Hormone Secretagogue Receptor Antagonists

Journal of medicinal chemistry, 2006-07, Vol.49 (15), p.4459-4469

2006

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2,4-Diaminopyrimidine Derivatives as Potent Growth Hormone Secretagogue Receptor Antagonists

Journal of medicinal chemistry, 2006-04, Vol.49 (8), p.2568-2578

2006

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Structure−Activity Studies of Novel Cyanoguanidine ATP-Sensitive Potassium Channel Openers for the Treatment of Overactive Bladder

Journal of medicinal chemistry, 2007-11, Vol.50 (24), p.6265-6273

2007

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Pharmacological characterization of urinary bladder smooth muscle contractility following partial bladder outlet obstruction in pigs

European journal of pharmacology, 2006-02, Vol.532 (1), p.107-114

2006

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Pharmacological Properties and Procognitive Effects of ABT-288, a Potent and Selective Histamine H 3 Receptor Antagonist

The Journal of pharmacology and experimental therapeutics, 2012-10, Vol.343 (1), p.233-245

2012

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Cardiovascular disease in chronic kidney failure: the role of VDR activators

Current opinion in investigational drugs (London, England : 2000), 2006-03, Vol.7 (3), p.206

2006

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Synthesis and Structure−Activity Relationships of a Novel Series of 2,3,5,6,7,9-Hexahydrothieno[3,2-b]quinolin-8(4H)-one 1,1-Dioxide KATP Channel Openers: Discovery of (−)-(9S)-9-(3-Bromo-4-fluorophenyl)-2,3,5,6,7,9- hexahydrothieno[3,2-b]quinolin-8(4H)-one 1,1-Dioxide (A-278637), a Potent KATP Opener That Selectively Inhibits Spontaneous Bladder Contractions

Journal of medicinal chemistry, 2004-06, Vol.47 (12), p.3163-3179

2004

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Nephrotoxicity studies of the immunosuppressants tacrolimus (FK506) and ascomycin in rat models

Toxicology (Amsterdam), 1998-02, Vol.125 (2-3), p.169-181

1998

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Discovery of less nephrotoxic FK506 analogs and determining immunophilin dependence of immunosuppressant nephrotoxicity with a novel single-dose rat cisplatin potentiation assay

The Journal of pharmacology and experimental therapeutics, 1997-12, Vol.283 (3), p.1509

1997

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Improved Methods for Transplanting Split-heart Neonatal Cardiac Grafts Into the Ear Pinna of Mice and Rats

Journal of pharmacological and toxicological methods, 1998-02, Vol.39 (1), p.9-17

1998

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Synthesis and Structure−Activity Relationships of a Novel Series of 2,3,5,6,7,9-Hexahydrothieno[3,2- b ]quinolin-8(4 H )-one 1,1-Dioxide K ATP Channel Openers: Discovery of (−)-(9 S )-9-(3-Bromo-4-fluorophenyl)-2,3,5,6,7,9- hexahydrothieno[3,2- b ]quinolin-8(4 H )-one 1,1-Dioxide (A-278637), a Potent K ATP Opener That Selectively Inhibits Spontaneous Bladder Contractions

Journal of medicinal chemistry, 2004-06, Vol.47 (12), p.3163-3179

2004

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DUNAIMYCINS, A NEW COMPLEX OF SPIROKETAL 24-MEMBERED MACROLIDES WITH IMMUNOSUPPRESSIVE ACTIVITY: III. IMMUNOSUPPRESSIVE ACTIVITIES OF DUNAIMYCINS

The Journal of Antibiotics, 1991/12/25, Vol.44(12), pp.1331-1341

1991

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Discovery and metabolic stabilization of potent and selective 2-amino-N-(adamant-2-yl) acetamide 11beta-hydroxysteroid dehydrogenase type 1 inhibitors

Journal of medicinal chemistry, 2007-01, Vol.50 (1), p.149-164

2007

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Synthesis and structure-activity relationships of a novel series of 2,3,5,6,7,9-hexahydrothieno[3,2-b]quinolin-8(4H)-one 1,1-dioxide K(ATP) channel openers: discovery of (-)-(9S)-9-(3-bromo-4-fluorophenyl)-2,3,5,6,7,9- hexahydrothieno[3,2-b]quinolin-8(4H)-one 1,1-dioxide (A-278637), a potent K(ATP) opener that selectively inhibits spontaneous bladder contractions

Journal of medicinal chemistry, 2004-06, Vol.47 (12), p.3163-3179

2004

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Identification of Receptor-Binding Residues in the Inflammatory Complement Protein C5a by Site-Directed Mutagenesis

Proceedings of the National Academy of Sciences - PNAS, 1989-01, Vol.86 (1), p.292-296

1989

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A Macrolactam Inhibitor of T Helper Type 1 and T Helper Type 2 Cytokine Biosynthesis for Topical Treatment of Inflammatory Skin Diseases

Journal of investigative dermatology, 1999-05, Vol.112 (5), p.729-738

1999

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Discovery of ascomycin analogs with potent topical but weak systemic activity for treatment of inflammatory skin diseases

Current pharmaceutical design, 1998-10, Vol.4 (5), p.367-379

1998

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A Macrolactam Inhibitor of T Helper Type 1 and T Helper Type 2 Cytokine Biosynthesis for Topical Treatment of Inflammatory Skin Diseases1

Journal of investigative dermatology, 1999-05, Vol.112 (5), p.729-738

1999

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Ex vivo assessment of immunosuppression in undiluted whole blood from pigs dosed with tacrolimus (FK506)

Clinical immunology (Orlando, Fla.), 1999-01, Vol.90 (1), p.133

1999

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Differential effects of Vitamin D analogs on bone formation and resorption

Pharmacological properties and procognitive effects of ABT-288, a potent and selective histamine H3 receptor antagonist

(-)-(9S)-9-(3-Bromo-4-fluorophenyl)-2,3,5,6,7,9-hexahydrothieno[3,2-b]quinolin-8(4H)-one 1,1-dioxide (A-278637): a novel ATP-sensitive potassium channel opener efficacious in suppressing urinary bladder contractions. II. in vivo characterization

Discovery and Metabolic Stabilization of Potent and Selective 2-Amino-N-(adamant-2-yl) Acetamide 11β-Hydroxysteroid Dehydrogenase Type 1 Inhibitors

Zotarolimus, a Novel Sirolimus Analogue With Potent Anti-proliferative Activity on Coronary Smooth Muscle Cells and Reduced Potential for Systemic Immunosuppression

Effects of ATP-sensitive K+ channel openers and tolterodine on involuntary bladder contractions in a pig model of partial bladder outlet obstruction

Discovery and Pharmacological Evaluation of Growth Hormone Secretagogue Receptor Antagonists

2,4-Diaminopyrimidine Derivatives as Potent Growth Hormone Secretagogue Receptor Antagonists

Structure−Activity Studies of Novel Cyanoguanidine ATP-Sensitive Potassium Channel Openers for the Treatment of Overactive Bladder

Pharmacological characterization of urinary bladder smooth muscle contractility following partial bladder outlet obstruction in pigs

Pharmacological Properties and Procognitive Effects of ABT-288, a Potent and Selective Histamine H 3 Receptor Antagonist

Cardiovascular disease in chronic kidney failure: the role of VDR activators

Nephrotoxicity studies of the immunosuppressants tacrolimus (FK506) and ascomycin in rat models

Discovery of less nephrotoxic FK506 analogs and determining immunophilin dependence of immunosuppressant nephrotoxicity with a novel single-dose rat cisplatin potentiation assay

Improved Methods for Transplanting Split-heart Neonatal Cardiac Grafts Into the Ear Pinna of Mice and Rats

DUNAIMYCINS, A NEW COMPLEX OF SPIROKETAL 24-MEMBERED MACROLIDES WITH IMMUNOSUPPRESSIVE ACTIVITY: III. IMMUNOSUPPRESSIVE ACTIVITIES OF DUNAIMYCINS

Discovery and metabolic stabilization of potent and selective 2-amino-N-(adamant-2-yl) acetamide 11beta-hydroxysteroid dehydrogenase type 1 inhibitors

Identification of Receptor-Binding Residues in the Inflammatory Complement Protein C5a by Site-Directed Mutagenesis

A Macrolactam Inhibitor of T Helper Type 1 and T Helper Type 2 Cytokine Biosynthesis for Topical Treatment of Inflammatory Skin Diseases

Discovery of ascomycin analogs with potent topical but weak systemic activity for treatment of inflammatory skin diseases

A Macrolactam Inhibitor of T Helper Type 1 and T Helper Type 2 Cytokine Biosynthesis for Topical Treatment of Inflammatory Skin Diseases1

Ex vivo assessment of immunosuppression in undiluted whole blood from pigs dosed with tacrolimus (FK506)

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