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Scott A. Long

Scott A. Long,Medicinal Chemistry,Organic Chemistry

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Scott A. Long

Publications: 9 | Citations: 40

Fields: Medicinal Chemistry, Organic Chemistry

Collaborated with 70 co-authors from 1996 to 2011 | Cited by 215 authors

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Publications (9)

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Discovery of novel spirocyclic inhibitors of fatty acid amide hydrolase (FAAH). Part 2. Discovery of 7-azaspiro[3.5]nonane urea PF04862853, an orally efficacious inhibitor of fatty acid amide hydrolase (FAAH) for pain

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Journal: Bioorganic & Medicinal Chemistry Letters - BIOORG MEDICINAL CHEM LETTER , vol. 21, no. 21, pp. 6545-6553, 2011

Discovery of novel spirocyclic inhibitors of fatty acid amide hydrolase (FAAH). Part 1: Identification of 7-azaspiro[3.5]nonane and 1-oxa-8-azaspiro[4.5]decane as lead scaffolds

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Journal: Bioorganic & Medicinal Chemistry Letters - BIOORG MEDICINAL CHEM LETTER , vol. 21, no. 21, pp. 6538-6544, 2011

Structure-based drug design enables conversion of a DFG-in binding CSF1R kinase inhibitor to a DFG-out binding mode (Citations: 3)

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Journal: Bioorganic & Medicinal Chemistry Letters - BIOORG MEDICINAL CHEM LETTER , vol. 20, no. 5, pp. 1543-1547, 2010

Discovery of (3 S ,3a R )-2-(3-Chloro-4-cyanophenyl)-3-cyclopentyl-3,3a,4,5-tetrahydro-2 H -benzo[ g ]indazole-7-carboxylic Acid (PF3882845), an Orally Efficacious Mineralocorticoid Receptor (MR) Antagonist for Hypertension and Nephropathy (Citations: 2)

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Journal: Journal of Medicinal Chemistry - J MED CHEM , vol. 53, no. 16, pp. 5979-6002, 2010

Benzothiophene inhibitors of MK2. Part 2: Improvements in kinase selectivity and cell potency (Citations: 2)

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Journal: Bioorganic & Medicinal Chemistry Letters - BIOORG MEDICINAL CHEM LETTER , vol. 19, no. 16, pp. 4882-4884, 2009

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Citations (40 times by 39 publications)

Dynamic Changes in the Copy Number of Pluripotency and Cell Proliferation Genes in Human ESCs and iPSCs during Reprogramming and Time in Culture (Citations: 45)

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Journal: Cell Stem Cell , vol. 8, no. 1, pp. 106-118, 2011

Multidimensional Profiling of CSF1R Screening Hits and Inhibitors: Assessing Cellular Activity, Target Residence Time, and Selectivity in a Higher Throughput Way

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Journal: Journal of Biomolecular Screening - J BIOMOL SCREEN , vol. 16, no. 9, pp. 1007-1017, 2011

A theoretical entropy score as a single value to express inhibitor selectivity

Journal: BMC Bioinformatics , vol. 12, no. 1, pp. 94-11, 2011

Numerical methods with fourth-order spatial accuracy for variable-order nonlinear Stokes’ first problem for a heated generalized second grade fluid

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Journal: Computers & Mathematics With Applications - COMPUT MATH APPL , vol. 62, no. 3, pp. 971-986, 2011

Combinatorial protocol in multiple linear regression/partial least-squares directed rationale for the caspase-3 inhibition activity of isoquinoline-1,3,4-trione derivatives (Citations: 1)

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Journal: Sar and Qsar in Environmental Research - SAR QSAR ENVIRON RES , vol. 21, no. 1-2, pp. 169-185, 2010

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Co-authors (70)

Journals (3)

Keywords (13)

Scott A. Long,Medicinal Chemistry,Organic Chemistry

Publications (9)

BibTeX | RIS | RefWorks Download

Discovery of novel spirocyclic inhibitors of fatty acid amide hydrolase (FAAH). Part 2. Discovery of 7-azaspiro[3.5]nonane urea PF04862853, an orally efficacious inhibitor of fatty acid amide hydrolase (FAAH) for pain

Discovery of novel spirocyclic inhibitors of fatty acid amide hydrolase (FAAH). Part 1: Identification of 7-azaspiro[3.5]nonane and 1-oxa-8-azaspiro[4.5]decane as lead scaffolds

Structure-based drug design enables conversion of a DFG-in binding CSF1R kinase inhibitor to a DFG-out binding mode (Citations: 3)

Discovery of (3 S ,3a R )-2-(3-Chloro-4-cyanophenyl)-3-cyclopentyl-3,3a,4,5-tetrahydro-2 H -benzo[ g ]indazole-7-carboxylic Acid (PF3882845), an Orally Efficacious Mineralocorticoid Receptor (MR) Antagonist for Hypertension and Nephropathy (Citations: 2)

Benzothiophene inhibitors of MK2. Part 2: Improvements in kinase selectivity and cell potency (Citations: 2)

Citations (40 times by 39 publications)

Dynamic Changes in the Copy Number of Pluripotency and Cell Proliferation Genes in Human ESCs and iPSCs during Reprogramming and Time in Culture (Citations: 45)

Multidimensional Profiling of CSF1R Screening Hits and Inhibitors: Assessing Cellular Activity, Target Residence Time, and Selectivity in a Higher Throughput Way

A theoretical entropy score as a single value to express inhibitor selectivity

Numerical methods with fourth-order spatial accuracy for variable-order nonlinear Stokes’ first problem for a heated generalized second grade fluid

Combinatorial protocol in multiple linear regression/partial least-squares directed rationale for the caspase-3 inhibition activity of isoquinoline-1,3,4-trione derivatives (Citations: 1)


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Scott A. Long,Medicinal Chemistry,Organic Chemistry

Publications (9) BibTeX | RIS | RefWorks Download

Structure-based drug design enables conversion of a DFG-in binding CSF1R kinase inhibitor to a DFG-out binding mode (Citations: 3)

Discovery of (3 S ,3a R )-2-(3-Chloro-4-cyanophenyl)-3-cyclopentyl-3,3a,4,5-tetrahydro-2 H -benzo[ g ]indazole-7-carboxylic Acid (PF3882845), an Orally Efficacious Mineralocorticoid Receptor (MR) Antagonist for Hypertension and Nephropathy (Citations: 2)

Benzothiophene inhibitors of MK2. Part 2: Improvements in kinase selectivity and cell potency (Citations: 2)

Dynamic Changes in the Copy Number of Pluripotency and Cell Proliferation Genes in Human ESCs and iPSCs during Reprogramming and Time in Culture (Citations: 45)

Combinatorial protocol in multiple linear regression/partial least-squares directed rationale for the caspase-3 inhibition activity of isoquinoline-1,3,4-trione derivatives (Citations: 1)

Publications (9)

BibTeX | RIS | RefWorks Download