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Magnetic-activated carbon composites derived from iron sludge and biological sludge for sulfonamide antibiotic removal

Environmental science and pollution research international, 2020-04, Vol.27 (12), p.13436-13446

2020

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Backpulsing technology applied in MF and UF processes for membrane fouling mitigation: A review

Journal of membrane science, 2019-10, Vol.587, p.117136, Article 117136

2019

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The use of ligand-based de novo design for scaffold hopping and sidechain optimization: Two case studies

Bioorganic & medicinal chemistry, 2008, Vol.16 (1), p.422-427

2008

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A Point Mutation in the Human Melanin Concentrating Hormone Receptor 1 Reveals an Important Domain for Cellular Trafficking

Molecular endocrinology (Baltimore, Md.), 2005-10, Vol.19 (10), p.2579-2590

2005

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Discovery of a potent, selective, and less flexible selective norepinephrine reuptake inhibitor (sNRI)

Bioorganic & medicinal chemistry, 2008-07, Vol.18 (14), p.4224-4227

2008

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Research on a transmission line defect identification method based on voiceprint recognition

Journal of physics. Conference series, 2024-08, Vol.2814 (1), p.12031

2024

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3-[(2R)-Amino-2-phenylethyl]-1-(2,6-difluorobenzyl)-5-(2-fluoro-3-methoxyphenyl)- 6-methylpyrimidin-2,4-dione (NBI 42902) as a Potent and Orally Active Antagonist of the Human Gonadotropin-Releasing Hormone Receptor. Design, Synthesis, and in Vitro and in Vivo Characterization

Journal of medicinal chemistry, 2005-02, Vol.48 (4), p.1169-1178

2005

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Fused tricyclic indoles as S1P1 agonists with robust efficacy in animal models of autoimmune disease

Bioorganic & medicinal chemistry letters, 2012-07, Vol.22 (13), p.4404-4409

2012

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4-{(2R)-[3-Aminopropionylamido]-3-(2,4-dichlorophenyl)propionyl}-1-{2-[(2-thienyl)ethylaminomethyl]phenyl}piperazine as a Potent and Selective Melanocortin-4 Receptor AntagonistDesign, Synthesis, and Characterization

Journal of medicinal chemistry, 2004-12, Vol.47 (27), p.6821-6830

2004

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Research on online monitoring system of fusion transmission line based on multi-source data

Journal of physics. Conference series, 2022-11, Vol.2360 (1), p.12021

2022

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Synthesis and structure-activity relationships of selective norepinephrine reuptake inhibitors (sNRI) with improved pharmaceutical characteristics

Bioorganic & medicinal chemistry, 2008-12, Vol.18 (23), p.6151-6155

2008

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A broad activity screen in support of a chemogenomic map for kinase signalling research and drug discovery

Biochemical journal, 2013-04, Vol.451 (2), p.313-328

2013

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The synthesis of sialylated oligosaccharides using a CMP-Neu5Ac synthetase/sialyltransferase fusion

Nature biotechnology, 1998-08, Vol.16 (8), p.769-772

1998

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A multivariate study of backpulsing for membrane fouling mitigation in produced water treatment

Journal of environmental chemical engineering, 2021-04, Vol.9 (2), p.104839, Article 104839

2021

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Synthesis and Structure−Activity Relationships of 1-Arylmethyl-5-aryl-6-methyluracils as Potent Gonadotropin-Releasing Hormone Receptor Antagonists

Journal of medicinal chemistry, 2004-02, Vol.47 (5), p.1259-1271

2004

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Determination of the Binding Mode of Thienopyrimidinedione Antagonists to the Human Gonadotropin Releasing Hormone Receptor Using Structure−Activity Relationships, Site-Directed Mutagenesis, and Homology Modeling

Journal of medicinal chemistry, 2006-10, Vol.49 (21), p.6170-6176

2006

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Design and Structure−Activity Relationships of 2-Alkyl-3-aminomethyl-6-(3-methoxyphenyl)-7-methyl-8-(2-fluorobenzyl)imidazolo[1,2-a]pyrimid-5-ones as Potent GnRH Receptor Antagonists

Journal of medicinal chemistry, 2003-04, Vol.46 (9), p.1769-1772

2003

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Identification of 1-Arylmethyl-3- (2-aminoethyl)-5-aryluracil as Novel Gonadotropin-Releasing Hormone Receptor Antagonists

Journal of medicinal chemistry, 2003-05, Vol.46 (11), p.2023-2026

2003

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Synthesis and initial structure–Activity relationships of a novel series of imidazolo[1,2- a]pyrimid-5-ones as potent GnRH receptor antagonists

Bioorganic & medicinal chemistry letters, 2002-08, Vol.12 (16), p.2179-2183

2002

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Initial Structure–Activity Relationship Studies of a Novel Series of Pyrrolo[1,2- a]pyrimid-7-ones as GnRH Receptor Antagonists

Bioorganic & medicinal chemistry letters, 2002-02, Vol.12 (3), p.399-402

2002

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PHOTODEGRADATION OF SULFAMETHOXAZOLE AND PHOTOLYSIS ACTIVE SPECIES IN WATER UNDER UV-VIS LIGHT IRRADIATION

Fresenius environmental bulletin, 2015-01 (5)

2015

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Synthesis and Structure–Activity relationships of 1-arylmethyl-3-(2-aminopropyl)-5-aryl-6-methyluracils as potent GnRH receptor antagonists

Bioorganic & medicinal chemistry letters, 2003-10, Vol.13 (19), p.3311-3315

2003

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Design, synthesis and structure–Activity relationships of novel imidazolo[1,2- a]pyrimid-5-ones as potent GnRH receptor antagonists

Bioorganic & medicinal chemistry letters, 2002-08, Vol.12 (16), p.2185-2187

2002

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Abstract 1242: A broad activity screen in support of a chemogenomic map for kinase signaling research and drug discovery

Cancer research (Chicago, Ill.), 2012-04, Vol.72 (8_Supplement), p.1242-1242

2012

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Quinoline-Carboxylic acids are potent inhibitors that inhibit the binding of insulin-Like growth factor (IGF) to IGF-Binding proteins

Bioorganic & medicinal chemistry letters, 2003-06, Vol.13 (11), p.1931-1934

2003

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Magnetic-activated carbon composites derived from iron sludge and biological sludge for sulfonamide antibiotic removal

Backpulsing technology applied in MF and UF processes for membrane fouling mitigation: A review

The use of ligand-based de novo design for scaffold hopping and sidechain optimization: Two case studies

A Point Mutation in the Human Melanin Concentrating Hormone Receptor 1 Reveals an Important Domain for Cellular Trafficking

Discovery of a potent, selective, and less flexible selective norepinephrine reuptake inhibitor (sNRI)

Research on a transmission line defect identification method based on voiceprint recognition

3-[(2R)-Amino-2-phenylethyl]-1-(2,6-difluorobenzyl)-5-(2-fluoro-3-methoxyphenyl)- 6-methylpyrimidin-2,4-dione (NBI 42902) as a Potent and Orally Active Antagonist of the Human Gonadotropin-Releasing Hormone Receptor. Design, Synthesis, and in Vitro and in Vivo Characterization

Fused tricyclic indoles as S1P1 agonists with robust efficacy in animal models of autoimmune disease

4-{(2R)-[3-Aminopropionylamido]-3-(2,4-dichlorophenyl)propionyl}-1-{2-[(2-thienyl)ethylaminomethyl]phenyl}piperazine as a Potent and Selective Melanocortin-4 Receptor AntagonistDesign, Synthesis, and Characterization

Research on online monitoring system of fusion transmission line based on multi-source data

Synthesis and structure-activity relationships of selective norepinephrine reuptake inhibitors (sNRI) with improved pharmaceutical characteristics

A broad activity screen in support of a chemogenomic map for kinase signalling research and drug discovery

The synthesis of sialylated oligosaccharides using a CMP-Neu5Ac synthetase/sialyltransferase fusion

A multivariate study of backpulsing for membrane fouling mitigation in produced water treatment

Synthesis and Structure−Activity Relationships of 1-Arylmethyl-5-aryl-6-methyluracils as Potent Gonadotropin-Releasing Hormone Receptor Antagonists

Determination of the Binding Mode of Thienopyrimidinedione Antagonists to the Human Gonadotropin Releasing Hormone Receptor Using Structure−Activity Relationships, Site-Directed Mutagenesis, and Homology Modeling

Design and Structure−Activity Relationships of 2-Alkyl-3-aminomethyl-6-(3-methoxyphenyl)-7-methyl-8-(2-fluorobenzyl)imidazolo[1,2-a]pyrimid-5-ones as Potent GnRH Receptor Antagonists

Identification of 1-Arylmethyl-3- (2-aminoethyl)-5-aryluracil as Novel Gonadotropin-Releasing Hormone Receptor Antagonists

Synthesis and initial structure–Activity relationships of a novel series of imidazolo[1,2- a]pyrimid-5-ones as potent GnRH receptor antagonists

Initial Structure–Activity Relationship Studies of a Novel Series of Pyrrolo[1,2- a]pyrimid-7-ones as GnRH Receptor Antagonists

PHOTODEGRADATION OF SULFAMETHOXAZOLE AND PHOTOLYSIS ACTIVE SPECIES IN WATER UNDER UV-VIS LIGHT IRRADIATION

Synthesis and Structure–Activity relationships of 1-arylmethyl-3-(2-aminopropyl)-5-aryl-6-methyluracils as potent GnRH receptor antagonists

Design, synthesis and structure–Activity relationships of novel imidazolo[1,2- a]pyrimid-5-ones as potent GnRH receptor antagonists

Abstract 1242: A broad activity screen in support of a chemogenomic map for kinase signaling research and drug discovery

Quinoline-Carboxylic acids are potent inhibitors that inhibit the binding of insulin-Like growth factor (IGF) to IGF-Binding proteins

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