General Information of Drug (ID: DMJX6SM)

Drug Name
CKD-712 Drug Info
Indication
Disease Entry ICD 11 Status REF
Solid tumour/cancer 2A00-2F9Z Phase 1 [1]
Cross-matching ID
PubChem CID
9861304
TTD Drug ID
DMJX6SM

Molecule-Related Drug Atlas

Molecule-Related Drug Atlas
Molecule Type:
DTT
Drug Status:
Clinical Trial Drug(s)
Patented Agent(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
WP-1066 DMUGHWR Recurrent glioblastoma 2A00.00 Phase 1/2 [2]
Aminotriazolopyridine derivative 1 DMW2LZ0 N. A. N. A. Patented [3]
Imidazo[4,5-c]pyridine derivative 2 DMFDRJT N. A. N. A. Patented [3]
PMID27774824-Compound-Figure11Example1up DMH1W8F N. A. N. A. Patented [3]
Imidazo[4,5-c]pyridine derivative 1 DM4KBZQ N. A. N. A. Patented [3]

Molecular Interaction Atlas of This Drug

Molecular Interaction Atlas

Drug Therapeutic Target (DTT)
DTT Name DTT ID UniProt ID MOA REF
JAK-STAT signaling pathway (JAK-STAT pathway) TTKAWRQ NOUNIPROTAC Inhibitor [1]

References

1 HO-1 and JAK-2/STAT-1 signals are involved in preferential inhibition of iNOS over COX-2 gene expression by newly synthesized tetrahydroisoquinoline alkaloid, CKD712, in cells activated with lipopolysacchride. Cell Signal. 2008 Oct;20(10):1839-47.
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. (Ligand id: 7972).
3 Inhibitors of JAK-family kinases: an update on the patent literature 2013-2015, part 1.Expert Opin Ther Pat. 2017 Feb;27(2):127-143.