Seltorexant

Highest phase reached
Drug type
Small molecule

Listing at source
Listed
Highest phase reached

Drug type
Small molecule
Drug name
Seltorexant
Molecular weight
Structure (SMILES)
Cc1cc(C)nc(N2CC3CN(C(=O)c4c(F)cccc4-n4nccn4)CC3C2)n1

  • ((3AR,6AS)-5-(4,6-DIMETHYLPYRIMIDIN- 2-YL)HEXAHYDROPYRROLO(3,4-C)PYRROL-2(1H)-YL)(2-FLUORO- 6-(2H-1,2,3-TRIAZOL-2-YL)PHENYL)METHANONE OREXIN RECEPTOR ANTAGONIST
  • 3ar 6as 5 4 6 dimethylpyrimidin 2 yl hexahydropyrrolo 3 4 c pyrrol 2 1h yl 2 fluoro 6 2h 1 2 3 triazol 2 yl phenyl methanone orexin receptor antagonist
  • jnj 42847922
  • jnj 42847922 10 mg
  • jnj 42847922 20 mg
  • jnj 42847922 20mg
  • jnj 42847922 40 mg
  • jnj 42847922 40mg
  • jnj 42847922 5 mg
  • JNJ-42847922
  • JNJ-42847922 20mg
  • JNJ-42847922 40mg
  • methanone 3ar 6as 5 4 6 dimethyl 2 pyrimidinyl hexahydropyrrolo 3 4 c pyrrol 2 1h yl 2 fluoro 6 2h 1 2 3 triazol 2 yl phenyl rel
  • METHANONE, ((3AR,6AS)-5-(4,6-DIMETHYL-2-PYRIMIDINYL)HEXAHYDROPYRROLO(3,4-C)PYRROL-2(1H)-YL)(2-FLUORO-6-(2H-1,2,3-TRIAZOL-2-YL)PHENYL)-, REL-
  • min 202
  • MIN-202
  • seltorexant
  • Seltorexant
  • seltorexant [INN]
  • SELTOREXANT [USAN]
  • Seltorexant [WHO-DD]
  • seltorexant 20 mg
  • Seltorexant 20 mg
  • seltorexant 40 mg
  • Seltorexant 40 mg

And 3 more, listed on the interactive page.

CAS registry numbers
  • 1452539-75-1
ChEMBL ID
CHEMBL3597971
InChIKey
SQOCEMCKYDVLMM-UHFFFAOYSA-N
FDA ingredient codes (UNII)
  • AIS8N3O50B

  • 67116280
  • 86278359

First in class
No
Orphan designation
No

Pharmacology name
seltorexant
Type
Synthetic organic

  • Action
    Antagonist
    Action type
    Antagonist
    Target
    OX1 receptor
    Gene symbol
    HCRTR1
    Protein identifier
    O43613
    Median affinity
    6.3
    Affinity units
    pKB
  • Action
    Antagonist
    Action type
    Antagonist
    Target
    OX1 receptor
    Gene symbol
    HCRTR1
    Protein identifier
    O43613
    Median affinity
    6.1
    Affinity units
    pKi
  • Action
    Antagonist
    Action type
    Antagonist
    Target
    OX2 receptor
    Gene symbol
    HCRTR2
    Protein identifier
    O43614
    Median affinity
    8.8
    Affinity units
    pKB
  • Action
    Antagonist
    Action type
    Antagonist
    Target
    OX2 receptor
    Gene symbol
    HCRTR2
    Protein identifier
    O43614
    Median affinity
    8
    Affinity units
    pKi
    Primary target
    Yes
  • Mechanism
    Orexin receptor 2 antagonist
    Action type
    Antagonist
    Target
    Orexin receptor type 2
    Protein identifier
    O43614

Open Targets mechanisms

  • Mechanism
    Orexin receptor 2 antagonist
    Action type
    Antagonist
    Target
    Orexin receptor type 2

  • Condition
    Liver Diseases
    Highest recorded phase
    1
    Condition identifier
    EFO:0001421
    Subject identifier
    D008107
  • Condition
    Kidney Diseases
    Highest recorded phase
    1
    Condition identifier
    EFO:0003086
    Subject identifier
    D007674
  • Condition
    Depressive Disorder, Major
    Highest recorded phase
    3
    Condition identifier
    EFO:0003761
    Subject identifier
    D003865
  • Condition
    Sleep Apnea, Obstructive
    Highest recorded phase
    1
    Condition identifier
    EFO:0003918
    Subject identifier
    D020181
  • Condition
    Sleep Initiation and Maintenance Disorders
    Highest recorded phase
    2
    Condition identifier
    EFO:0004698
    Subject identifier
    D007319
  • Condition
    Depressive Disorder, Major
    Highest recorded phase
    3
    Condition identifier
    MONDO:0002009
    Subject identifier
    D003865
  • Condition
    Alzheimer Disease
    Highest recorded phase
    2
    Condition identifier
    MONDO:0004975
    Subject identifier
    D000544

  • Condition identifier
    EFO_0001421
    Highest recorded phase
    1
  • Condition identifier
    EFO_0003086
    Highest recorded phase
    1
  • Condition identifier
    EFO_0003918
    Highest recorded phase
    1
  • Condition identifier
    EFO_0004698
    Highest recorded phase
    2
  • Condition identifier
    MONDO_0002009
    Highest recorded phase
    3
  • Condition identifier
    MONDO_0004975
    Highest recorded phase
    2
  • Condition identifier
    MONDO_0007147
    Highest recorded phase
    1
  • Condition identifier
    MONDO_0013600
    Highest recorded phase
    3

Hydrogen bond acceptors
7
Hydrogen bond donors
0
Polar surface area
80.04
Calculated partition coefficient (ALogP)
2.02
Calculated partition coefficient (XLogP)
2.8
Prodrug
No
Chirality
Achiral
Inorganic
No
Rule-of-five violations
0
Rotatable bonds
3
Heavy atoms
30
Molecular formula
C21H22FN7O
Monoisotopic mass
407.18698651
Natural product
No

Recorded assays
116
Active assays
29

  • Confirmatory
  • Other

These details could not be displayed.

Related records

Trials (34)

In development for (6)

Targets (2)