General Information of Drug (ID: DMV7TMB)

Drug Name
Benzimidazole derivative 6 Drug Info
Synonyms PMID28270010-Compound-Figure7-1
Indication
Disease Entry ICD 11 Status REF
Solid tumour/cancer 2A00-2F9Z Patented [1]
Cross-matching ID
PubChem CID
57345941
CAS Number
CAS 1357920-84-3
TTD Drug ID
DMV7TMB

Molecule-Related Drug Atlas

Molecule-Related Drug Atlas
Molecule Type:
DTT
Drug Status:
Approved Drug(s)
Clinical Trial Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
Entrectinib DMMPTLH Non-small cell lung cancer 2C25 Approved [2]
Larotrectinib DM26CQR Solid tumour/cancer 2A00-2F9Z Approved [3]
MIM-D3 DMZHN5B Alzheimer disease 8A20 Phase 3 [4]
SNA-120 DMPN314 Plaque psoriasis EA90.0 Phase 2 [5]
CT 327 DMQXL1T Plaque psoriasis EA90.0 Phase 2 [6]
TPX-0005 DM9FB2T Solid tumour/cancer 2A00-2F9Z Phase 1/2 [7]
ONO-7579 DMXLPYE Solid tumour/cancer 2A00-2F9Z Phase 1/2 [7]
Altiratinib DMUJCBT Solid tumour/cancer 2A00-2F9Z Phase 1 [1]
PLX7486 DM0IVGU Pancreatic cancer 2C10 Phase 1 [8]
DS-6051 DM0RD4F Solid tumour/cancer 2A00-2F9Z Phase 1 [9]
⏷ Show the Full List of 10 Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
Crizotinib DM4F29C Non-small-cell lung cancer 2C25.Y Approved [10]
Lorlatinib DMICDLV Non-small-cell lung cancer 2C25.Y Approved [3]
Entrectinib DMMPTLH Non-small cell lung cancer 2C25 Approved [2]
Brigatinib DM7W94S Anaplastic large cell lymphoma 2A90.A Approved [11]
Ceritinib DMB920Z Non-small-cell lung cancer 2C25.Y Approved [12]
Alectinib DMP1I6Y Lung cancer 2C25.0 Approved [13]
Ensartinib DMIKDCQ Non-small-cell lung cancer 2C25.Y Phase 3 [7]
PF-06463922 DMKM7EW Non-small-cell lung cancer 2C25.Y Phase 2 [14]
AP26113 DMYBQEF Solid tumour/cancer 2A00-2F9Z Phase 2 [15]
TPX-0005 DM9FB2T Solid tumour/cancer 2A00-2F9Z Phase 1/2 [7]
⏷ Show the Full List of 10 Drug(s)

Molecular Interaction Atlas of This Drug

Molecular Interaction Atlas

Drug Therapeutic Target (DTT)
DTT Name DTT ID UniProt ID MOA REF
ALK tyrosine kinase receptor (ALK) TTPMQSO ALK_HUMAN Inhibitor [1]
Tropomyosin-related kinase A (TrkA) TTTDVOJ NTRK1_HUMAN Inhibitor [1]

References

1 Tropomyosin receptor kinase inhibitors: an updated patent review for 2010-2016 - Part I.Expert Opin Ther Pat. 2017 Jun;27(6):733-751.
2 Drugs@FDA. U.S. Food and Drug Administration. U.S. Department of Health Human Services. 2019
3 2018 FDA drug approvals.Nat Rev Drug Discov. 2019 Feb;18(2):85-89.
4 Safety and efficacy of MIM-D3 ophthalmic solutions in a randomized, placebo-controlled Phase 2 clinical trial in patients with dry eye. Clin Ophthalmol. 2013; 7: 1275-1285.
5 Clinical pipeline report, company report or official report of the Pharmaceutical Research and Manufacturers of America (PhRMA)
6 Topical TrkA Kinase Inhibitor CT327 is an Effective, Novel Therapy for the Treatment of Pruritus due to Psoriasis: Results from Experimental Studies, and Efficacy and Safety of CT327 in a Phase 2b Clinical Trial in Patients with Psoriasis. Acta Derm Venereol. 2015 May;95(5):542-8.
7 Clinical pipeline report, company report or official report of the Pharmaceutical Research and Manufacturers of America (PhRMA)
8 National Cancer Institute Drug Dictionary (drug id 747694).
9 National Cancer Institute Drug Dictionary (drug id 766123).
10 Drugs@FDA. U.S. Food and Drug Administration. U.S. Department of Health & Human Services. 2015
11 2017 FDA drug approvals.Nat Rev Drug Discov. 2018 Feb;17(2):81-85.
12 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: 7397).
13 CH5424802, a selective ALK inhibitor capable of blocking the resistant gatekeeper mutant. Cancer Cell. 2011 May 17;19(5):679-90.
14 PF-06463922, an ALK/ROS1 Inhibitor, Overcomes Resistance to First and Second Generation ALK Inhibitors in Preclinical Models. Cancer Cell. 2015 Jul 13;28(1):70-81.
15 Interpreting expression profiles of cancers by genome-wide survey of breadth of expression in normal tissues. Genomics 2005 Aug;86(2):127-41.