Zidesamtinib

Highest phase reached
Drug type
Small molecule

Listing at source
Listed
Highest phase reached

Drug type
Small molecule
Drug name
Zidesamtinib
Molecular weight
Structure (SMILES)
CCn1ncc2c1-c1cnc(N)c(c1)O[C@H](C)c1cc(F)ccc1-c1nn(C)nc1C2

  • jideytro
  • JIDEYTRO
  • nu 0002362
  • nu 0002362 006
  • nu 0002362 009
  • nu 2362 010
  • nu 520
  • NU-0002362
  • NU-0002362-006
  • NU-0002362-009
  • NU-2362-010
  • NU-520
  • nuv 520
  • NUV-520
  • nvl 520
  • Nvl-520
  • NVL-520
  • zidesamtinib
  • Zidesamtinib
  • Zidesamtinib (NVL-520)
  • Zidesamtinib [INN]
  • Zidesamtinib [USAN]
  • Zidesamtinib [WHO-DD]
  • zidesamtinib inn
  • zidesamtinib usan

And 1 more, listed on the interactive page.

CAS registry numbers
  • 2739829-00-4
ChEMBL ID
CHEMBL5314497
InChIKey
DTWUUAFTYSMNQX-GFCCVEGCSA-N
PubChem compound IDs
  • 166560233
FDA ingredient codes (UNII)
  • MX5KQV5XHC

Patents
0
Designations
1
First in class
No
Fast track
No
Breakthrough designation
Yes
Orphan designation
No
Priority review
No
Orphan exclusivity
No
Accelerated approval
No

Pharmacology name
zidesamtinib
Type
Synthetic organic
Drug name stem
-tinib

  • Action
    Inhibition
    Action type
    Inhibitor
    Target
    neurotrophic receptor tyrosine kinase 1
    Gene symbol
    NTRK1
    Protein identifier
    P04629
    Affinity units
    pKi
  • Action
    Inhibition
    Action type
    Inhibitor
    Target
    c-ros oncogene 1, receptor tyrosine kinase
    Gene symbol
    ROS1
    Protein identifier
    P08922
    Median affinity
    9.15
    Affinity units
    pIC50
  • Action
    Inhibition
    Action type
    Inhibitor
    Target
    c-ros oncogene 1, receptor tyrosine kinase
    Gene symbol
    ROS1
    Protein identifier
    P08922
    Median affinity
    7.3
    Affinity units
    pKi

  • Condition
    Neoplasms
    Highest recorded phase
    2
    Condition identifier
    EFO:0000616
    Subject identifier
    D009369
  • Condition
    Neoplasms
    Highest recorded phase
    2
    Condition identifier
    MONDO:0004992
    Subject identifier
    D009369

  • Condition identifier
    EFO_0000616
  • Condition identifier
    MONDO_0005070
  • Condition identifier
    MONDO_0005233
    Highest recorded phase
    1

Trial references

Hydrogen bond acceptors
8
Hydrogen bond donors
1
Polar surface area
96.67
Calculated partition coefficient (ALogP)
3.53
Calculated partition coefficient (XLogP)
2.8
Prodrug
No
Chirality
Single enantiomer
Inorganic
No
Rule-of-five violations
0
Rotatable bonds
1
Heavy atoms
31
Molecular formula
C22H22FN7O
Monoisotopic mass
419.18698651
Natural product
No

  • 85001-101
  • 85001-102

Recorded assays
59
Active assays
4

Active assay types

  • Confirmatory

Related records

Trials (2)

In development for (2)