Befotertinib

Highest phase reached
Drug type
Small molecule

Listing at source
Listed
Highest phase reached

Drug type
Small molecule
Drug name
Befotertinib
Molecular weight
Structure (SMILES)
C=CC(=O)Nc1cc(Nc2nccc(-c3cn(CC(F)(F)F)c4ccccc34)n2)c(OC)cc1N(C)CCN(C)C

  • 2 propenamide n 2 2 dimethylamino ethyl methylamino 4 methoxy 5 4 1 2 2 2 trifluoroethyl 1h indol 3 yl 2 pyrimidinyl amino phenyl
  • 2-PROPENAMIDE, N-(2-((2-(DIMETHYLAMINO)ETHYL)METHYLAMINO)-4-METHOXY-5-((4-(1-(2,2,2-TRIFLUOROETHYL)-1H-INDOL-3-YL)-2-PYRIMIDINYL)AMINO)PHENYL)-
  • befotertinib
  • Befotertinib
  • befotertinib [INN]
  • Befotertinib [WHO-DD]
  • befotertinib inn
  • befotertinib who dd
  • d 0316
  • D 0316
  • D-0316
  • D-0316 Capsule
  • d0316
  • D0316

CAS registry numbers
  • 1835667-63-4
ChEMBL ID
CHEMBL5095167
InChIKey
USOCZVZOXKTJTI-UHFFFAOYSA-N
PubChem compound IDs
  • 130412842
FDA ingredient codes (UNII)
  • 0XT2CPR891

First in class
No
Orphan designation
No

Pharmacology name
befotertinib
Type
Synthetic organic
Drug name stem
-tinib
Approval recorded by Guide to Pharmacology
Yes

Mechanisms of action

  • Action
    Inhibition
    Action type
    Inhibitor
    Target
    epidermal growth factor receptor
    Gene symbol
    EGFR
    Protein identifier
    P00533

Investigated indications

  • Condition
    Carcinoma, Non-Small-Cell Lung
    Highest recorded phase
    2
    Condition identifier
    EFO:0003060
    Subject identifier
    D002289

  • Condition identifier
    EFO_0003060
    Highest recorded phase
    3
  • Condition identifier
    MONDO_0005233
    Highest recorded phase
    3

Hydrogen bond acceptors
8
Hydrogen bond donors
2
Polar surface area
87.55
Calculated partition coefficient (ALogP)
5.54
Calculated partition coefficient (XLogP)
4.8
Prodrug
No
Chirality
Achiral
Inorganic
No
Rule-of-five violations
2
Rotatable bonds
11
Heavy atoms
41
Molecular formula
C29H32F3N7O2
Monoisotopic mass
567.25695778
Natural product
No

Related records

Trials (13)

In development for (1)