Naronapride

Highest phase reached
Drug type
Small molecule

Listing at source
Listed
Highest phase reached

Drug type
Small molecule
Drug name
Naronapride
Molecular weight
Structure (SMILES)
COc1cc(N)c(Cl)cc1C(=O)N[C@@H]1CCN(CCCCCC(=O)O[C@H]2CN3CCC2CC3)C[C@@H]1OC

  • 1 piperidinehexanoic acid 4 4 amino 5 chloro 2 methoxybenzoyl amino 3 methoxy 1 azabicyclo 2 2 2 oct 3 yl ester 3s 4r
  • 1-PIPERIDINEHEXANOIC ACID, 4-((4-AMINO-5-CHLORO-2-METHOXYBENZOYL)AMINO)-3-METHOXY-, 1-AZABICYCLO(2.2.2)OCT-3-YL ESTER, (3S,4R)-
  • 20 mg ati 7505
  • 20 mg ATI 7505
  • 40 mg ATI 7505
  • 80 mg ATI 7505
  • ati 7505
  • ATI-7505
  • ati7505
  • ATI7505
  • naronaprida
  • Naronaprida
  • naronapride
  • Naronapride
  • naronapride [INN]
  • NARONAPRIDE [USAN]
  • Naronapride [WHO-DD]
  • naronapride inn
  • naronapride usan
  • naronapride who dd

CAS registry numbers
  • 860174-12-5
ChEMBL ID
CHEMBL2103858
InChIKey
VGDDOIZXGFJDRC-VJTSUQJLSA-N
PubChem compound IDs
  • 11237985
FDA ingredient codes (UNII)
  • 058896B00B

First in class
No
Orphan designation
No

Drug name stem
-pride

Mechanisms of action

  • Mechanism
    Serotonin 4 (5-HT4) receptor agonist
    Action type
    Agonist
    Target
    5-hydroxytryptamine receptor 4
    Protein identifier
    Q13639

Open Targets mechanisms

  • Mechanism
    Serotonin 4 (5-HT4) receptor agonist
    Action type
    Agonist
    Target
    5-hydroxytryptamine receptor 4

Investigated indications

  • Condition
    Gastroparesis
    Highest recorded phase
    2
    Condition identifier
    EFO:1000948
    Subject identifier
    D018589

  • Condition identifier
    EFO_0003948
    Highest recorded phase
    2
  • Condition identifier
    EFO_1000948
    Highest recorded phase
    2
  • Condition identifier
    HP_0002019
    Highest recorded phase
    2
  • Condition identifier
    HP_0012450
    Highest recorded phase
    2
  • Condition identifier
    MONDO_0006769
    Highest recorded phase
    2
  • Condition identifier
    MONDO_0007186
    Highest recorded phase
    2

Trial references

Hydrogen bond acceptors
8
Hydrogen bond donors
2
Polar surface area
106.36
Calculated partition coefficient (ALogP)
2.95
Calculated partition coefficient (XLogP)
2.8
Prodrug
No
Chirality
Single enantiomer
Inorganic
No
Rule-of-five violations
1
Rotatable bonds
11
Heavy atoms
37
Molecular formula
C27H41ClN4O5
Monoisotopic mass
536.2765481
Natural product
Yes

Related records

Trials (4)

In development for (2)

Targets (1)