Apilimod mesylate

Highest phase reached
Drug type
Small molecule

Listing at source
Listed
Highest phase reached

Drug type
Small molecule
Drug name
Apilimod mesylate
Molecular weight
Structure (SMILES)
COc1ccc(-c2nc(S(C)(=O)=O)[nH]c2-c2ccc(OC)cc2)cc1.CS(=O)(=O)O.CS(=O)(=O)O

  • apilimod bis mesylate
  • Apilimod bis-mesylate
  • apilimod dimesylate
  • Apilimod dimesylate
  • Apilimod dimesylate [WHO-DD]
  • apilimod dimesylate capsule
  • Apilimod Dimesylate Capsule
  • apilimod dimesylate who dd
  • apilimod mesilate
  • Apilimod mesilate
  • apilimod mesylate
  • Apilimod mesylate
  • APILIMOD MESYLATE [USAN]
  • apilimod mesylate usan
  • benzaldehyde 3 methyl 2 6 4 morpholinyl 2 2 2 pyridinyl ethoxy 4 pyrimidinyl hydrazone methanesulfonate 1 2
  • benzaldehyde 3 methyl 2 6 4 morpholinyl 2 2 2 pyridinyl ethoxy 4 pyrimidinyl hydrazone methanesulphonate 1 2
  • benzaldehyde 3 methyl 6 4 morpholinyl 2 2 2 pyridinyl ethoxy 4 pyrimidinyl hydrazone dimethanesulfonate
  • benzaldehyde 3 methyl 6 4 morpholinyl 2 2 2 pyridinyl ethoxy 4 pyrimidinyl hydrazone dimethanesulphonate
  • benzaldehyde 3 methyl 6 4 morpholinyl 2 2 2 pyridinyl ethoxy 4 pyrimidinyl hydrazone mesilate
  • benzaldehyde 3 methyl 6 4 morpholinyl 2 2 2 pyridinyl ethoxy 4 pyrimidinyl hydrazone mesylate
  • BENZALDEHYDE, 3-METHYL-, (6-(4-MORPHOLINYL)-2-(2-(2-PYRIDINYL)ETHOXY)-4-PYRIMIDINYL)HYDRAZONE MESILATE
  • BENZALDEHYDE, 3-METHYL-, (6-(4-MORPHOLINYL)-2-(2-(2-PYRIDINYL)ETHOXY)-4-PYRIMIDINYL)HYDRAZONE MESYLATE
  • BENZALDEHYDE, 3-METHYL-, (6-(4-MORPHOLINYL)-2-(2-(2-PYRIDINYL)ETHOXY)-4-PYRIMIDINYL)HYDRAZONE, DIMETHANESULFONATE
  • BENZALDEHYDE, 3-METHYL-, (6-(4-MORPHOLINYL)-2-(2-(2-PYRIDINYL)ETHOXY)-4-PYRIMIDINYL)HYDRAZONE, DIMETHANESULPHONATE
  • BENZALDEHYDE, 3-METHYL-, 2-(6-(4-MORPHOLINYL)-2-(2-(2-PYRIDINYL)ETHOXY)-4-PYRIMIDINYL)HYDRAZONE METHANESULFONATE (1:2)

And 13 more, listed on the interactive page.

CAS registry numbers
  • 870087-36-8
ChEMBL ID
CHEMBL6067997
InChIKey
QAFWUMUPMXXFFK-UHFFFAOYSA-N
FDA ingredient codes (UNII)
  • 5G3P5OK11S

  • 11527330
  • 177644613

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

Drug name stem
-imod

Mechanisms of action

  • Mechanism
    1-phosphatidylinositol 3-phosphate 5-kinase inhibitor
    Action type
    Inhibitor
    Target
    1-phosphatidylinositol 3-phosphate 5-kinase
    Protein identifier
    Q9Y2I7

Open Targets mechanisms

  • Mechanism
    1-phosphatidylinositol 3-phosphate 5-kinase inhibitor
    Action type
    Inhibitor
    Target
    1-phosphatidylinositol 3-phosphate 5-kinase

  • Condition
    Crohn Disease
    Highest recorded phase
    2
    Condition identifier
    EFO:0000384
    Subject identifier
    D003424
  • Condition
    Arthritis, Rheumatoid
    Highest recorded phase
    2
    Condition identifier
    EFO:0000685
    Subject identifier
    D001172

  • Condition identifier
    EFO_0000384
    Highest recorded phase
    2
  • Condition identifier
    EFO_0005952
    Highest recorded phase
    2
  • Condition identifier
    HP_0004386
    Highest recorded phase
    1
  • Condition identifier
    MONDO_0004976
    Highest recorded phase
    2
  • Condition identifier
    MONDO_0005011
    Highest recorded phase
    2
  • Condition identifier
    MONDO_0008383
    Highest recorded phase
    2
  • Condition identifier
    MONDO_0015517
    Highest recorded phase
    1
  • Condition identifier
    MONDO_0018908
    Highest recorded phase
    2

Hydrogen bond acceptors
5
Hydrogen bond donors
1
Polar surface area
81.28
Calculated partition coefficient (ALogP)
3.16
Prodrug
No
Chirality
Achiral
Inorganic
No
Rule-of-five violations
0
Rotatable bonds
5
Heavy atoms
35
Molecular formula
C20H26N2O10S3
Monoisotopic mass
550.07495855
Natural product
No

Related records

Trials (25)

In development for (3)

Targets (1)