Molecule Details
InChIKeyLJJKNPQAGWVLDQ-SNVBAGLBSA-N
Compound NameThiorphan, (S)-
Canonical SMILESO=C(O)CNC(=O)[C@@H](CS)Cc1ccccc1
Clinical Status Data-mined Candidate
Targets (Human+Pathogen)3
Pfam Stratification Cross-Family
Avg pChEMBL7.82
SourceBindingDB;ChEMBL
2D Structure
2D structure
Activity Profile
DrugBank Annotations
DrugBank ID DB08626
Drug NameThiorphan
CAS Number76721-89-6
Groups experimental
ATC Codes nan
DescriptionA potent inhibitor of membrane metalloendopeptidase (enkephalinase). Thiorphan potentiates morphine-induced analgesia and attenuates naloxone-precipitated withdrawal symptoms.

Categories: Amino Acids Amino Acids, Peptides, and Proteins Amino Acids, Sulfur Enzyme Inhibitors N-substituted Glycines Protease Inhibitors Sulfur Compounds
Cross-references: BindingDB: 50024102 CHEMBL298827 ChemSpider: 3571959 C01619 PDB: TIO PubChem:4369380 PubChem:99445097 Wikipedia: Thiorphan ZINC: ZINC000003872336
Target Activities (3)
Target Gene Organism Category Pfam pChEMBL Type Source
P08473 MME Homo sapiens Human PF01431 PF05649 8.5 IC50 ChEMBL;BindingDB
P42892 ECE1 Homo sapiens Human PF01431 PF05649 8.1 IC50 BindingDB
P12821 ACE Homo sapiens Human PF01401 6.8 IC50 ChEMBL;BindingDB
DrugBank Target Actions (1)
Target Gene Target Name Action Type
P08473 MME Neprilysin inhibitor targets