Londamocitinib

Highest phase reached
Drug type
Small molecule

Listing at source
Listed
Highest phase reached

Drug type
Small molecule
Drug name
Londamocitinib
Molecular weight
Structure (SMILES)
COC[C@H](C(=O)Nc1cccc2c(-c3nc(Nc4cccc(S(C)(=O)=O)c4F)ncc3F)c[nH]c12)N1CCN(C)CC1

  • (R)-N-(3-(5-Fluoro-2-((2-fluoro-3-(methylsulfonyl)phenyl)amino)pyrimidin-4-yl)-1H-indol-7-yl)-3-methoxy-2-(4-methylpiperazin-1-yl)propanamide
  • azd 4604
  • AZD-4604
  • azd4604
  • Azd4604
  • AZD4604
  • londamocitinib
  • Londamocitinib
  • londamocitinib [INN]
  • LONDAMOCITINIB [USAN]
  • Londamocitinib [WHO-DD]
  • londamocitinib inn
  • londamocitinib usan
  • londamocitinib who dd
  • r n 3 5 fluoro 2 2 fluoro 3 methylsulfonyl phenyl amino pyrimidin 4 yl 1h indol 7 yl 3 methoxy 2 4 methylpiperazin 1 yl propanamide

CAS registry numbers
  • 2241039-81-4
ChEMBL ID
CHEMBL4447181
InChIKey
JNUZADQZHYFJGW-JOCHJYFZSA-N
PubChem compound IDs
  • 135240395
FDA ingredient codes (UNII)
  • JAC34RRR7S

First in class
No
Orphan designation
No

Pharmacology name
londamocitinib
Type
Synthetic organic
Drug name stem
-tinib

  • Action
    Inhibition
    Action type
    Inhibitor
    Target
    Janus kinase 2
    Gene symbol
    JAK2
    Protein identifier
    O60674
    Median affinity
    5.91
    Affinity units
    pIC50
  • Action
    Inhibition
    Action type
    Inhibitor
    Target
    Janus kinase 1
    Gene symbol
    JAK1
    Protein identifier
    P23458
    Median affinity
    8.52
    Affinity units
    pIC50

Open Targets indications

  • Condition identifier
    MONDO_0004979
    Highest recorded phase
    2

Hydrogen bond acceptors
9
Hydrogen bond donors
3
Polar surface area
132.55
Calculated partition coefficient (ALogP)
3.25
Calculated partition coefficient (XLogP)
2.2
Prodrug
No
Chirality
Single enantiomer
Inorganic
No
Rule-of-five violations
1
Rotatable bonds
9
Heavy atoms
42
Molecular formula
C28H31F2N7O4S
Monoisotopic mass
599.21262999
Natural product
No

Recorded assays
56
Active assays
14

Active assay types

  • Confirmatory

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Related records

Trials (6)

In development for (1)