General Information of Drug (ID: DM740BS)

Drug Name
BI 1358894 Drug Info
Indication
Disease Entry ICD 11 Status REF
Depression 6A70-6A7Z Phase 2 [1]
Cross-matching ID
TTD Drug ID
DM740BS

Molecule-Related Drug Atlas

Molecule-Related Drug Atlas
Molecule Type:
DTT
Drug Status:
Clinical Trial Drug(s)
Investigative Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
GFB-887 DM2IJWG Diabetic nephropathy GB61.Z Phase 2 [3]
2-APB DM9AKVR Discovery agent N.A. Investigative [4]
daidzein DMRFTJX Discovery agent N.A. Investigative [5]
lysophosphatidylcholine DMOGFVH Discovery agent N.A. Investigative [5]
KB-R7943 DMMD5W3 Discovery agent N.A. Investigative [6]
BTP2 DMNM63G Discovery agent N.A. Investigative [5]
bromoenol lactone DMKQ0CA Discovery agent N.A. Investigative [7]
ML204 DM15YL0 Discovery agent N.A. Investigative [8]
(-)-englerin A DMPQBWY Discovery agent N.A. Investigative [9]
⏷ Show the Full List of 9 Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
2-APB DM9AKVR Discovery agent N.A. Investigative [10]
ML204 DM15YL0 Discovery agent N.A. Investigative [8]
(-)-englerin A DMPQBWY Discovery agent N.A. Investigative [9]

Molecular Interaction Atlas of This Drug

Molecular Interaction Atlas

Drug Therapeutic Target (DTT)
DTT Name DTT ID UniProt ID MOA REF
Short transient receptor potential channel 4 (TRPC4) TTX0H5W TRPC4_HUMAN Inhibitor [2]
Short transient receptor potential channel 5 (TRPC5) TT32NQ1 TRPC5_HUMAN Inhibitor [2]

References

1 ClinicalTrials.gov (NCT04423757) A Home-based Study Using Mobile Technology to Test Whether BI 1358894 is Effective in People With Depression. U.S. National Institutes of Health.
2 Clinical pipeline report, company report or official report of Boehringer Ingelheim.
3 Safety and Efficacy of GFB-887, a TRPC5 Channel Inhibitor, in Patients With Focal Segmental Glomerulosclerosis, Treatment-Resistant Minimal Change Disease, or Diabetic Nephropathy: TRACTION-2 Trial Design. Kidney Int Rep. 2021 Jul 23;6(10):2575-2584.
4 Block of TRPC5 channels by 2-aminoethoxydiphenyl borate: a differential, extracellular and voltage-dependent effect. Br J Pharmacol. 2005 Jun;145(4):405-14.
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: 490).
6 The Na+/Ca2+ exchange inhibitor KB-R7943 potently blocks TRPC channels. Biochem Biophys Res Commun. 2007 Sep 14;361(1):230-6.
7 Bromoenol lactone inhibits voltage-gated Ca2+ and transient receptor potential canonical channels. J Pharmacol Exp Ther. 2011 Nov;339(2):329-40.
8 Identification of ML204, a novel potent antagonist that selectively modulates native TRPC4/C5 ion channels. J Biol Chem. 2011 Sep 23;286(38):33436-46.
9 (-)-Englerin is a potent and selective activator of TRPC4 and TRPC5 calcium channels. Angew Chem Int Ed Engl. 2015 Mar 16;54(12):3787-91.
10 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: 489).