General Information of DTT (ID: TTK0FEA)

DTT Name Leucine-rich repeat kinase 2 (LRRK2) DTT Info
Gene Name LRRK2

Molecule-Related Drug & Molecule List

Molecule-Related Drug List
Molecule Type:
DTT
DTP
DME
Drug Status:
Clinical Trial Drug(s)
Patented Agent(s)
Investigative Drug(s)
3 Clinical Trial Drug(s) Transported by This DTP
Drug Name Drug ID Indication ICD 11 Highest Status REF
BIIB094 DMLUO5K Parkinson disease 8A00.0 Phase 1 [1]
DNL151 DMZT89C Parkinson disease 8A00.0 Phase 1 [2]
DNL201 DMFEORD Parkinson disease 8A00.0 Phase 1 [2]
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32 Patented Agent(s) Transported by This DTP
Drug Name Drug ID Indication ICD 11 Highest Status REF
Aminopyridine derivative 2 DMUGZNL N. A. N. A. Patented [3]
Aminopyridine derivative 3 DMSLJE8 N. A. N. A. Patented [3]
Azaindazole derivative 1 DM3S0LI N. A. N. A. Patented [3]
Azaindazole derivative 2 DMEYS3V N. A. N. A. Patented [3]
Azaindazole derivative 3 DMOV9XA N. A. N. A. Patented [3]
Azaindazole derivative 4 DMX3MNT N. A. N. A. Patented [3]
Bidentate ligands of Markush derivative 1 DMB08D3 N. A. N. A. Patented [3]
Bidentate ligands of Markush derivative 2 DM2QNMC N. A. N. A. Patented [3]
Fused thiophene derivative 1 DMV7IX4 N. A. N. A. Patented [3]
Hydrazide derivative 3 DM3U79M N. A. N. A. Patented [3]
Hydrazide derivative 4 DM1HI8Q N. A. N. A. Patented [3]
Hydrazide derivative 5 DM6RLVB N. A. N. A. Patented [3]
Oxindole derivative 2 DM6ZYMC N. A. N. A. Patented [3]
Oxindole derivative 3 DM0ENF3 N. A. N. A. Patented [3]
Oxindole derivative 4 DM3U58I N. A. N. A. Patented [3]
PMID28117607-Compound-20 DMAXS57 N. A. N. A. Patented [3]
PMID28117607-Compound-21 DMS8OTG N. A. N. A. Patented [3]
PMID28117607-Compound-4 DMVIY73 N. A. N. A. Patented [3]
PMID28117607-Compound-5 DMPBNFM N. A. N. A. Patented [3]
PMID28117607-Compound-6 DM68B1R N. A. N. A. Patented [3]
PMID28117607-Compound-7 DMJZREU N. A. N. A. Patented [3]
Pyridopyrimidinone derivative 1 DMZ6TSD N. A. N. A. Patented [3]
Pyridopyrimidinone derivative 2 DMUF63N N. A. N. A. Patented [3]
Pyridopyrimidinone derivative 3 DMHSDUR N. A. N. A. Patented [3]
Pyrrolo-pyridazine derivative 1 DMQ2U54 N. A. N. A. Patented [3]
Pyrrolo-pyridine derivative 1 DM9K5CI N. A. N. A. Patented [3]
Pyrrolo-pyridine derivative 2 DMVNY5I N. A. N. A. Patented [3]
Pyrrolo-pyrimidine derivative 1 DMEVXT0 N. A. N. A. Patented [3]
Pyrrolo-pyrimidine derivative 10 DMR0ZU6 N. A. N. A. Patented [3]
Pyrrolo-pyrimidine derivative 11 DMEIDC0 N. A. N. A. Patented [3]
Pyrrolo-pyrimidine derivative 8 DMZH27I N. A. N. A. Patented [3]
Pyrrolo-pyrimidine derivative 9 DMJEV86 N. A. N. A. Patented [3]
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⏷ Show the Full List of 32 Patented Agent(s)
6 Investigative Drug(s) Transported by This DTP
Drug Name Drug ID Indication ICD 11 Highest Status REF
GNE-7915 DMYWM56 Discovery agent N.A. Investigative [4]
GNE-9605 DMLXR90 Discovery agent N.A. Investigative [4]
HMS3229G13 DMUPS48 Discovery agent N.A. Investigative [5]
PF-06447475 DMEUT0W Discovery agent N.A. Investigative [6]
PF-06454589 DMWIVM3 Discovery agent N.A. Investigative [6]
URMC-099 DMCJXWK Discovery agent N.A. Investigative [7]
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⏷ Show the Full List of 6 Investigative Drug(s)
Molecule Interaction Atlas

References

1 Clinical pipeline report, company report or official report of Ionis
2 Clinical pipeline report, company report or official report of the Pharmaceutical Research and Manufacturers of America (PhRMA)
3 Leucine-rich repeat kinase 2 inhibitors: a patent review (2014-2016).Expert Opin Ther Pat. 2017 Jun;27(6):667-676.
4 Discovery of highly potent, selective, and brain-penetrant aminopyrazole leucine-rich repeat kinase 2 (LRRK2) small molecule inhibitors. J Med Chem. 2014 Feb 13;57(3):921-36.
5 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. (Target id: 2059).
6 Discovery and preclinical profiling of 3-[4-(morpholin-4-yl)-7H-pyrrolo[2,3-d]pyrimidin-5-yl]benzonitrile (PF-06447475), a highly potent, selective, brain penetrant, and in vivo active LRRK2 kinase inhibitor. J Med Chem. 2015 Jan 8;58(1):419-32.
7 Discovery, synthesis, and characterization of an orally bioavailable, brain penetrant inhibitor of mixed lineage kinase 3. J Med Chem. 2013 Oct 24;56(20):8032-48.