Iclepertin

Highest phase reached
Drug type
Small molecule

Listing at source
Listed
Highest phase reached

Drug type
Small molecule
Drug name
Iclepertin
Molecular weight
Structure (SMILES)
C[C@@H](Oc1ccc(S(C)(=O)=O)cc1C(=O)N1C[C@@H]2C[C@]2(c2cc(C(F)(F)F)on2)C1)C(F)(F)F

  • bi 425809
  • BI 425809
  • BI 425809 tablet
  • iclepertin
  • Iclepertin
  • iclepertin (BI 425809)
  • iclepertin [INN]
  • ICLEPERTIN [USAN]
  • Iclepertin [WHO-DD]
  • iclepertin inn
  • iclepertin usan
  • iclepertin who dd

CAS registry numbers
  • 1421936-85-7
ChEMBL ID
CHEMBL5314576
InChIKey
MYHDQTVHHMSLEF-DDBGAENHSA-N
PubChem compound IDs
  • 155259577
FDA ingredient codes (UNII)
  • M43ZDU10DD

First in class
No
Orphan designation
No

Pharmacology name
iclepertin
Type
Synthetic organic
Drug name stem
-pertin

Mechanisms of action

  • Action
    Inhibition
    Action type
    Inhibitor
    Target
    GlyT1
    Gene symbol
    SLC6A9
    Protein identifier
    P48067
    Median affinity
    8.3
    Affinity units
    pIC50

  • Condition
    Renal Insufficiency
    Highest recorded phase
    1
    Condition identifier
    HP:0000083
    Subject identifier
    D051437
  • Condition
    Cognitive Dysfunction
    Highest recorded phase
    1
    Condition identifier
    HP:0001268
    Subject identifier
    D060825
  • Condition
    Alzheimer Disease
    Highest recorded phase
    2
    Condition identifier
    MONDO:0004975
    Subject identifier
    D000544
  • Condition
    Schizophrenia
    Highest recorded phase
    3
    Condition identifier
    MONDO:0005090
    Subject identifier
    D012559

  • Condition identifier
    HP_0000083
    Highest recorded phase
    1
  • Condition identifier
    HP_0001268
  • Condition identifier
    HP_0001399
    Highest recorded phase
    1
  • Condition identifier
    HP_0100543
    Highest recorded phase
    1
  • Condition identifier
    MONDO_0004975
  • Condition identifier
    MONDO_0004975
    Highest recorded phase
    2
  • Condition identifier
    MONDO_0005090
    Highest recorded phase
    3

Hydrogen bond acceptors
6
Hydrogen bond donors
0
Polar surface area
89.71
Calculated partition coefficient (ALogP)
3.84
Calculated partition coefficient (XLogP)
3.5
Prodrug
No
Chirality
Single enantiomer
Inorganic
No
Rule-of-five violations
1
Rotatable bonds
5
Heavy atoms
34
Molecular formula
C20H18F6N2O5S
Monoisotopic mass
512.08406182
Natural product
No

Recorded assays
11
Active assays
1

Active assay types

  • Confirmatory

Related records

Trials (27)

In development for (3)