Details of the Drug-Related molecule(s) Interaction Atlas

General Information of DTT (ID: TTWELHI)

• DTT Name: Stress-activated protein kinase (p38) DTT Info
• Gene Name: p38

Molecule-Related Drug & Molecule List

9 Clinical Trial Drug(s) Transported by This DTP

Drug Name	Drug ID	Indication	ICD 11	Highest Status	REF
PF-07265803	DM3E6Q4	Dilated cardiomyopathy	BC43.0	Phase 3	[1]
ARRY-797	DMJ48AB	Dilated cardiomyopathy	BC43.0	Phase 2	[2]
AZD7624	DMEW3K9	Chronic obstructive pulmonary disease	CA22	Phase 2	[3]
BMS-582949	DMGYXFP	Atherosclerosis	BD40	Phase 2	[4]
GSK2269557	DMIN0SV	Asthma	CA23	Phase 2	[5]
MW150	DMBRVXB	Alzheimer disease	8A20	Phase 2	[6]
TAK-715	DMZKPI8	Rheumatoid arthritis	FA20	Phase 2	[7]
LY-2228820	DMHXTNW	Solid tumour/cancer	2A00-2F9Z	Phase 1/2	[8]
PUR1800	DM6H10N	Chronic obstructive pulmonary disease	CA22	Phase 1	[9]

6 Discontinued Drug(s) Transported by This DTP

Drug Name	Drug ID	Indication	ICD 11	Highest Status	REF
ARRY-614	DMXD93K	Arthritis	FA20	Discontinued in Phase 1	[10]
AVE-9940	DMIB3AT	Rheumatoid arthritis	FA20	Discontinued in Phase 1	[11]
AZD-6703	DM9KLD3	Rheumatoid arthritis	FA20	Discontinued in Phase 1	[12]
SB-281832	DMYTAJW	Asthma	CA23	Discontinued in Phase 1	[13]
TA-5493	DMFES2K	Inflammation	1A00-CA43.1	Discontinued in Phase 1	[14]
AMG-548	DMYIPLH	Inflammation	1A00-CA43.1	Terminated	[15]

References

• [1] Clinical pipeline report, company report or official report of Pfizer
• [2] Clinical pipeline report, company report or official report of the Pharmaceutical Research and Manufacturers of America (PhRMA)
• [3] Investigational p38 inhibitors for the treatment of chronic obstructive pulmonary disease. Expert Opin Investig Drugs. 2015 Mar;24(3):383-92.
• [4] Synthesis and evaluation of carbamoylmethylene linked prodrugs of BMS-582949, a clinical p38alpha inhibitor. Bioorg Med Chem Lett. 2013 May 15;23(10):3028-33.
• [5] Evaluation of WO2012032067 and WO2012055846: two selective PI3Kdelta inhibitors, which is GSK-2269557. Expert Opin Ther Pat. 2012 Aug;22(8):965-70.
• [6] p38alpha MAPK signaling drives pharmacologically reversible brain and gastrointestinal phenotypes in the SERT Ala56 mouse. Proc Natl Acad Sci U S A. 2018 Oct 23;115(43):E10245-E10254.
• [7] Inhibition of Wnt/beta-catenin signaling by p38 MAP kinase inhibitors is explained by cross-reactivity with casein kinase Idelta/ . Chem Biol. 2011 Apr 22;18(4):485-94.
• [8] URL: http://www.guidetopharmacology.org Nucleic Acids Res. 2015 Oct 12. pii: gkv1037. The IUPHAR/BPS Guide to PHARMACOLOGY in 2016: towards curated quantitative interactions between 1300 protein targets and 6000 ligands. (Ligand id: 7959).
• [9] Clinical pipeline report, company report or official report of Pulmatrix Lexington, MA
• [10] Cmpany report (Arraybiopharma)
• [11] US patent application no. 2008,0119,498, Therapeutic agent for pruritus comprising p38 map kinase inhibitor as the active ingredient.
• [12] The discovery of N-cyclopropyl-4-methyl-3-[6-(4-methylpiperazin-1-yl)-4-oxoquinazolin-3(4H)-yl]benzamide (AZD6703), a clinical p38alpha MAP kinase inhibitor for the treatment of inflammatory diseases. Bioorg Med Chem Lett. 2012 Jun 15;22(12):3879-83.
• [13] p38 MAPK inhibitors ameliorate target organ damage in hypertension: Part 1. p38 MAPK-dependent endothelial dysfunction and hypertension. J Pharmacol Exp Ther. 2003 Dec;307(3):932-8.
• [14] US patent application no. 2008,0269,123, Methods for treating polycystic kidney disease (pkd) or other cyst forming diseases.
• [15] p38 MAP kinase inhibitors: many are made, but few are chosen. Curr Opin Drug Discov Devel. 2005 Jul;8(4):421-30.