General Information of Drug (ID: DM68D3O)

Drug Name
PG-545 Drug Info
Synonyms
PG-457; PG-500; PG-501; PG-502; PG-503; PG-504; PG-505; PG-506; PG-507; PG-508; PG-509; PG-510; PG-511; PG-512; PG-513; PG-514;PG-536; PG-546; PG-547; PG-554; PG-562; PG-500 series (heparan sulfate mimetics), Progen
Indication
Disease Entry ICD 11 Status REF
Ocular disease 1F00.1Z Phase 1 [1]
Cross-matching ID
PubChem CID
57412324
CAS Number
CAS 1144492-69-2
TTD Drug ID
DM68D3O

Molecule-Related Drug Atlas

Molecule-Related Drug Atlas
Molecule Type:
DTT
Drug Status:
Clinical Trial Drug(s)
Discontinued Drug(s)
Drug(s) Targeting Heparanase (HPSE)
Drug Name Drug ID Indication ICD 11 Highest Status REF
Suramin DMTOUY9 African trypanosomiasis 1F51 Phase 1 [2]
Neutralase DMXHWK6 Angiogenesis disorder BE2Z Discontinued in Phase 3 [3]

Molecular Interaction Atlas of This Drug

Molecular Interaction Atlas

Drug Therapeutic Target (DTT)
DTT Name DTT ID UniProt ID MOA REF
Heparanase (HPSE) TTR7GJO HPSE_HUMAN Modulator [1]

References

1 PG545, a dual heparanase and angiogenesis inhibitor, induces potent anti-tumour and anti-metastatic efficacy in preclinical models. Br J Cancer. 2011 Feb 15;104(4):635-42.
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: 1728).
3 Heparanase neutralizes the anticoagulation properties of heparin and low-molecular-weight heparin. J Thromb Haemost. 2006 Mar;4(3):560-5.