General Information of Drug (ID: DMPXK27)

Drug Name
PBI-4050 Drug Info
Synonyms
setogepram; (3-pentylphenyl)acetic acid; 2-(3-Pentylphenyl)acetic acid; 1002101-19-0; 3-Pentylbenzeneacetic acid; UNII-879OVM0Y1S; Benzeneacetic acid, 3-pentyl-; 879OVM0Y1S; 1002101-19-0 (free acid); Fezagepras; SCHEMBL289216; CHEMBL4297635; GTPL10043; PBI4050; ZINC113492390; DB15447; HY-100775A; AS-59875; CS-0062694; A1-19258; Q27895887
Indication
Disease Entry ICD 11 Status REF
Idiopathic pulmonary fibrosis CB03.4 Phase 2 [1]
Cross-matching ID
PubChem CID
24749700
CAS Number
CAS 1002101-19-0
TTD Drug ID
DMPXK27

Molecule-Related Drug Atlas

Molecule-Related Drug Atlas
Molecule Type:
DTT
Drug Status:
Clinical Trial Drug(s)
Preclinical Drug(s)
Investigative Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
TAK-875 DMIM5AP Type-2 diabetes 5A11 Phase 3 [3]
Fasiglifam hemihydrate DMTGYSO Type-2 diabetes 5A11 Phase 3 [4]
P-1736 DMEYQPN Diabetic complication 5A2Y Phase 2 [5]
JTT-851 DMED5J6 Type-2 diabetes 5A11 Phase 2 [6]
SHR0534 DMGFTAI Type 2 diabetes 5A11 Phase 1 [7]
LY-2881835 DM5EXJV Type-2 diabetes 5A11 Phase 1 [6]
P11187 DMXZOI0 Type-2 diabetes 5A11 Phase 1 [6]
CPL207-280CA DMFMGZR Type 2 diabetes 5A11 Phase 1 [7]
LY2922470 DMGLTE2 Type 2 diabetes 5A11 Phase 1 [8]
CNX-011-67 DM1H8D6 Type 2 diabetes 5A11 Preclinical [9]
⏷ Show the Full List of 10 Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
SHR0534 DMGFTAI Type 2 diabetes 5A11 Phase 1 [7]
3-hydroxy capric acid DMC70P1 Discovery agent N.A. Investigative [10]
2-hydroxy capric acid DMJAN52 Discovery agent N.A. Investigative [10]
6-n-octylaminouracil DMXJFCQ Discovery agent N.A. Investigative [10]
3-hydroxylauric acid DMNMB6V Discovery agent N.A. Investigative [10]
2-hydroxylauric acid DMCNW3M Discovery agent N.A. Investigative [10]
undecanoic acid DMFOIPL Discovery agent N.A. Investigative [11]
⏷ Show the Full List of 7 Drug(s)

Molecular Interaction Atlas of This Drug

Molecular Interaction Atlas

Drug Therapeutic Target (DTT)
DTT Name DTT ID UniProt ID MOA REF
Free fatty acid receptor 1 (GPR40) TTB8FUC FFAR1_HUMAN Agonist [2]
Inflammation-related GPCR EX33 (GPR84) TTG0MQD GPR84_HUMAN Antagonist [2]

References

1 Clinical pipeline report, company report or official report of Liminal BioSciences.
2 Phase 2 clinical trial of PBI-4050 in patients with idiopathic pulmonary fibrosis. Eur Respir J. 2019 Mar 18;53(3):1800663.
3 Efficacy and safety of fasiglifam (TAK-875), a G protein-coupled receptor 40 agonist, in Japanese patients with type 2 diabetes inadequately controlled by diet and exercise: a randomized, double-blind, placebo-controlled, phase III trial. Diabetes Obes Metab. 2015 Jul;17(7):675-81.
4 A novel antidiabetic drug, fasiglifam/TAK-875, acts as an ago-allosteric modulator of FFAR1. PLoS One. 2013 Oct 10;8(10):e76280.
5 Discovery of p1736, a novel antidiabetic compound that improves peripheral insulin sensitivity in mice models. PLoS One. 2013 Oct 23;8(10):e77946.
6 Treatment of Type 2 Diabetes by Free Fatty Acid Receptor Agonists. Front Endocrinol (Lausanne) 2014; 5: 137.
7 Targeting metabolic dysregulation for fibrosis therapy. Nat Rev Drug Discov. 2020 Jan;19(1):57-75.
8 The Discovery, Preclinical, and Early Clinical Development of Potent and Selective GPR40 Agonists for the Treatment of Type 2 Diabetes Mellitus (LY2881835, LY2922083, and LY2922470). J Med Chem. 2016 Dec 22;59(24):10891-10916.
9 CNX-011-67, a novel GPR40 agonist, enhances glucose responsiveness, insulin secretion and islet insulin content in n-STZ rats and in islets from type 2 diabetic patients. BMC Pharmacol Toxicol. 2014 Mar 25;15:19.
10 Medium-chain fatty acid-sensing receptor, GPR84, is a proinflammatory receptor. J Biol Chem. 2013 Apr 12;288(15):10684-91.
11 Medium-chain fatty acids as ligands for orphan G protein-coupled receptor GPR84. J Biol Chem. 2006 Nov 10;281(45):34457-64.