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GPR41/FFAR3 and GPR43/FFAR2 as Cosensors for Short-Chain Fatty Acids in Enteroendocrine Cells vs FFAR3 in Enteric Neurons and FFAR2 in Enteric Leukocytes
GPR41/FFAR3 and GPR43/FFAR2 as Cosensors for Short-Chain Fatty Acids in Enteroendocrine Cells vs FFAR3 in Enteric Neurons and FFAR2 in Enteric Leukocytes
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GPR41/FFAR3 and GPR43/FFAR2 as Cosensors for Short-Chain Fatty Acids in Enteroendocrine Cells vs FFAR3 in Enteric Neurons and FFAR2 in Enteric Leukocytes

Nøhr, Mark K ; Pedersen, Maria H ; Gille, Andreas ; Egerod, Kristoffer L ; Engelstoft, Maja S ; Husted, Anna Sofie ; Sichlau, Rasmus M ; Grunddal, Kaare V ; Seier Poulsen, Steen ; Han, Sangdon ; Jones, Robert M ; Offermanns, Stefan ; Schwartz, Thue W

Endocrinology (Philadelphia), 2013-10, Vol.154 (10), p.3552-3564 [Periódico revisado por pares]

Chevy Chase, MD: Endocrine Society

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2
Embelin and its derivatives unravel the signaling, proinflammatory and antiatherogenic properties of GPR84 receptor
Embelin and its derivatives unravel the signaling, proinflammatory and antiatherogenic properties of GPR84 receptor
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Embelin and its derivatives unravel the signaling, proinflammatory and antiatherogenic properties of GPR84 receptor

Gaidarov, Ibragim ; Anthony, Todd ; Gatlin, Joel ; Chen, Xiaohua ; Mills, David ; Solomon, Michelle ; Han, Sangdon ; Semple, Graeme ; Unett, David J.

Pharmacological research, 2018-05, Vol.131, p.185-198 [Periódico revisado por pares]

Netherlands: Elsevier Ltd

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3
Discovery of APD371: Identification of a Highly Potent and Selective CB2 Agonist for the Treatment of Chronic Pain
Discovery of APD371: Identification of a Highly Potent and Selective CB2 Agonist for the Treatment of Chronic Pain
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Discovery of APD371: Identification of a Highly Potent and Selective CB2 Agonist for the Treatment of Chronic Pain

Han, Sangdon ; Thoresen, Lars ; Jung, Jae-Kyu ; Zhu, Xiuwen ; Thatte, Jayant ; Solomon, Michelle ; Gaidarov, Ibragim ; Unett, David J ; Yoon, Woo Hyun ; Barden, Jeremy ; Sadeque, Abu ; Usmani, Amin ; Chen, Chuan ; Semple, Graeme ; Grottick, Andrew J ; Al-Shamma, Hussein ; Christopher, Ronald ; Jones, Robert M

ACS medicinal chemistry letters, 2017-12, Vol.8 (12), p.1309-1313 [Periódico revisado por pares]

American Chemical Society

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4
Therapeutic Utility of Cannabinoid Receptor Type 2 (CB2) Selective Agonists
Therapeutic Utility of Cannabinoid Receptor Type 2 (CB2) Selective Agonists
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Therapeutic Utility of Cannabinoid Receptor Type 2 (CB2) Selective Agonists

Han, Sangdon ; Thatte, Jayant ; Buzard, Daniel J ; Jones, Robert M

Journal of medicinal chemistry, 2013-11, Vol.56 (21), p.8224-8256 [Periódico revisado por pares]

United States: American Chemical Society

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5
Total Syntheses and Structures of Angular [6]- and [7]Phenylene: The First Helical Phenylenes (Heliphenes)
Total Syntheses and Structures of Angular [6]- and [7]Phenylene: The First Helical Phenylenes (Heliphenes)
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Total Syntheses and Structures of Angular [6]- and [7]Phenylene: The First Helical Phenylenes (Heliphenes)

Han, Sangdon ; Bond, Andrew D ; Disch, Raymond L ; Holmes, Daniel ; Schulman, Jerome M ; Teat, Simon J ; Vollhardt, K. Peter C ; Whitener, Glenn D

Angewandte Chemie (International ed.), 2002-09, Vol.41 (17), p.3223-3227 [Periódico revisado por pares]

Weinheim: Wiley-VCH Verlag

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6
Total Syntheses of Angular [7]-, [8]-, and [9]Phenylene by Triple Cobalt-Catalyzed Cycloisomerization: Remarkably Flexible Heliphenes
Total Syntheses of Angular [7]-, [8]-, and [9]Phenylene by Triple Cobalt-Catalyzed Cycloisomerization: Remarkably Flexible Heliphenes
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Total Syntheses of Angular [7]-, [8]-, and [9]Phenylene by Triple Cobalt-Catalyzed Cycloisomerization: Remarkably Flexible Heliphenes

Han, Sangdon ; Anderson, D. Ryan ; Bond, Andrew D ; Chu, Hiufung V ; Disch, Raymond L ; Holmes, Daniel ; Schulman, Jerome M ; Teat, Simon J ; Vollhardt, K. Peter C ; Whitener, Glenn D

Angewandte Chemie (International ed.), 2002-09, Vol.41 (17), p.3227-3230 [Periódico revisado por pares]

Weinheim: Wiley-VCH Verlag

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7
Discovery of nonpeptide 3,4-dihydroquinazoline-4-carboxamides as potent and selective sst2 agonists
Discovery of nonpeptide 3,4-dihydroquinazoline-4-carboxamides as potent and selective sst2 agonists
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Discovery of nonpeptide 3,4-dihydroquinazoline-4-carboxamides as potent and selective sst2 agonists

Zhao, Jian ; Wang, Shimiao ; Han, Sangdon ; Kim, Sun Hee ; Kusnetzow, Ana Karin ; Nguyen, Julie ; Rico-Bautista, Elizabeth ; Tan, Hannah ; Betz, Stephen F. ; Scott Struthers, R. ; Zhu, Yunfei

Bioorganic & medicinal chemistry letters, 2020-09, Vol.30 (17), p.127391-127391, Article 127391 [Periódico revisado por pares]

England: Elsevier Ltd

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8
Discovery of CRN04894: A Novel Potent Selective MC2R Antagonist
Discovery of CRN04894: A Novel Potent Selective MC2R Antagonist
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Discovery of CRN04894: A Novel Potent Selective MC2R Antagonist

Kim, Sun Hee ; Han, Sangdon ; Zhao, Jian ; Wang, Shimiao ; Kusnetzow, Ana Karin ; Reinhart, Greg ; Fowler, Melissa A. ; Markison, Stacy ; Johns, Michael ; Luo, Rosa ; Struthers, R. Scott ; Zhu, Yunfei ; Betz, Stephen F.

ACS medicinal chemistry letters, 2024-04, Vol.15 (4), p.478-485 [Periódico revisado por pares]

United States: American Chemical Society

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9
Discovery of 4-(3-aminopyrrolidinyl)-3-aryl-5-(benzimidazol-2-yl)-pyridines as potent and selective SST5 agonists for the treatment of congenital hyperinsulinism
Discovery of 4-(3-aminopyrrolidinyl)-3-aryl-5-(benzimidazol-2-yl)-pyridines as potent and selective SST5 agonists for the treatment of congenital hyperinsulinism
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Discovery of 4-(3-aminopyrrolidinyl)-3-aryl-5-(benzimidazol-2-yl)-pyridines as potent and selective SST5 agonists for the treatment of congenital hyperinsulinism

Zhao, Jian ; Wang, Shimiao ; Hee Kim, Sun ; Han, Sangdon ; Rico-Bautista, Elizabeth ; Sturchler, Emmanuel ; Nguyen, Julie ; Tan, Hannah ; Staley, Christine ; Karin Kusnetzow, Ana ; Betz, Stephen F. ; Johns, Michael ; Goulet, Lance ; Luo, Rosa ; Fowler, Melissa ; Athanacio, Jon ; Markison, Stacy ; Scott Struthers, R. ; Zhu, Yunfei

Bioorganic & medicinal chemistry letters, 2022-09, Vol.71, p.128807-128807, Article 128807 [Periódico revisado por pares]

England: Elsevier Ltd

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10
Discovery of Paltusotine (CRN00808), a Potent, Selective, and Orally Bioavailable Non-peptide SST2 Agonist
Discovery of Paltusotine (CRN00808), a Potent, Selective, and Orally Bioavailable Non-peptide SST2 Agonist
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Discovery of Paltusotine (CRN00808), a Potent, Selective, and Orally Bioavailable Non-peptide SST2 Agonist

Zhao, Jian ; Wang, Shimiao ; Markison, Stacy ; Kim, Sun Hee ; Han, Sangdon ; Chen, Mi ; Kusnetzow, Ana Karin ; Rico-Bautista, Elizabeth ; Johns, Michael ; Luo, Rosa ; Struthers, R. Scott ; Madan, Ajay ; Zhu, Yunfei ; Betz, Stephen F.

ACS medicinal chemistry letters, 2023-01, Vol.14 (1), p.66-74 [Periódico revisado por pares]

United States: American Chemical Society

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