Enlicitide chloride

Highest phase reached
Drug type

Listing at source
Listed
Highest phase reached

Drug type
Drug name
Enlicitide chloride
Molecular weight
Structure (SMILES)
COc1ccc(C[C@@H]2NC(=O)[C@H]([C@@H](C)O)NC(=O)[C@@H]3[C@@H]4CCN3C(=O)[C@@H]3Cc5cn(c6ccc(F)cc56)CCCCCCN(Cc5ccc(cc5)CCNC(=O)[C@]5(C)CCCN5C2=O)C(=O)CCC(=O)N[C@@H](C)C(=O)N[C@H](CNC(=O)CCCCC[N+](C)(C)C)C(=O)N[C@@H](Cc2cccc(c2)CNC(=O)CO4)C(=O)N3)cc1.[Cl-]

  • chlorure d enlicitide
  • Chlorure d'enlicitide
  • chloruro de enlicitida
  • Chloruro de enlicitida
  • enlicitide chloride
  • Enlicitide chloride
  • enlicitide chloride [INN]
  • enlicitide chloride inn

CAS registry numbers
  • 2407527-16-4
ChEMBL ID
CHEMBL6067978
InChIKey
CLOLWQCFULXMAR-QQCDJELVSA-N
PubChem compound IDs
  • 166642685
FDA ingredient codes (UNII)
  • 3D2DNA8NXK

First in class
No
Orphan designation
No

Pharmacology name
enlicitide
Type
Peptide
Drug name stem
-tide

Mechanisms of action

  • Action
    Binding
    Action type
    Binding
    Target
    proprotein convertase subtilisin/kexin type 9
    Gene symbol
    PCSK9
    Protein identifier
    Q8NBP7
    Median affinity
    11.3
    Affinity units
    pKi

  • Condition identifier
    HP_0003124
    Highest recorded phase
    1
  • Condition identifier
    HP_0003124
    Highest recorded phase
    3
  • Condition identifier
    MONDO_0005439
    Highest recorded phase
    3
  • Condition identifier
    MONDO_0021187
    Highest recorded phase
    3

Prodrug
No
Chirality
Single enantiomer
Inorganic
No
Heavy atoms
113
Molecular formula
C82H110ClFN14O15
Monoisotopic mass
1584.7947647
Natural product
No

Related records

Trials (18)