General Information of Drug (ID: DMRJBH4)

Drug Name
ISIS 13730 Drug Info
Indication
Disease Entry ICD 11 Status REF
Discovery agent N.A. Investigative [1]
Cross-matching ID
TTD Drug ID
DMRJBH4

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
MLN2480 DMBR8NF Solid tumour/cancer 2A00-2F9Z Phase 2 [2]
RG7304 DMGFAVQ Solid tumour/cancer 2A00-2F9Z Phase 1 [3]
SPN-803 DM8O2AQ Parkinson disease 8A00.0 Phase 1 [2]
PLX-4720 DMBK9AM Cutaneous melanoma 2C30 Phase 1 [4]
L-779450 DM51B74 Discovery agent N.A. Investigative [5]
ZM-336372 DMD5JYQ Discovery agent N.A. Investigative [6]
PLX-ORI3 DMZG1L5 Solid tumour/cancer 2A00-2F9Z Investigative [2]
2-(Phenylamino)-6-(3-acetamidophenyl)pyrazine DMPUARE Discovery agent N.A. Investigative [7]
ISIS 13741 DMC7Q38 Discovery agent N.A. Investigative [1]
ISIS 14144 DMWIKD5 Discovery agent N.A. Investigative [1]
⏷ 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
B-Raf messenger RNA (BRAF mRNA) TT0EOB8 BRAF_HUMAN Not Available [1]

References

1 US patent application no. 5,981,731, Antisense oligonucleotide modulation of B-raf gene expression.
2 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: 1943).
3 Clinical pipeline report, company report or official report of Roche.
4 Comprehensive analysis of kinase inhibitor selectivity. Nat Biotechnol. 2011 Oct 30;29(11):1046-51.
5 The identification of potent and selective imidazole-based inhibitors of B-Raf kinase. Bioorg Med Chem Lett. 2006 Jan 15;16(2):378-81.
6 The selectivity of protein kinase inhibitors: a further update. Biochem J. 2007 Dec 15;408(3):297-315.
7 Novel inhibitors of B-RAF based on a disubstituted pyrazine scaffold. Generation of a nanomolar lead. J Med Chem. 2006 Jan 12;49(1):407-16.