Suramin

Highest phase reached
Drug type
Small molecule

Listing at source
Listed
Highest phase reached

Drug type
Small molecule
Drug name
Molecular weight
Structure (SMILES)
Cc1ccc(C(=O)Nc2ccc(S(=O)(=O)O)c3cc(S(=O)(=O)O)cc(S(=O)(=O)O)c23)cc1NC(=O)c1cccc(NC(=O)Nc2cccc(C(=O)Nc3cc(C(=O)Nc4ccc(S(=O)(=O)O)c5cc(S(=O)(=O)O)cc(S(=O)(=O)O)c45)ccc3C)c2)c1

  • 8 8 carbonylbis imino 3 1 phenylenecarbonylimino 4 methyl 3 1 phenylene carbonylimino bis 1 3 5 naphthalenetrisulfonic acid
  • 8 8 ureylenebis m phenylenecarbonylimino 4 methyl m phenylene carbonylimino di 1 3 5 naphthalenetrisulfonic acid
  • 8,8'-(CARBONYLBIS(IMINO-3,1-PHENYLENECARBONYLIMINO(4-METHYL-3,1-PHENYLENE)CARBONYLIMINO))BIS-1,3,5-NAPHTHALENETRISULFONIC ACID
  • 8,8'-(UREYLENEBIS(M-PHENYLENECARBONYLIMINO(4-METHYL-M-PHENYLENE)CARBONYLIMINO))DI-1,3,5-NAPHTHALENETRISULFONIC ACID
  • farma
  • Farma
  • farma 939
  • FARMA-939
  • fourneau
  • Fourneau
  • metaret
  • Metaret
  • naganol
  • Naganol
  • nsc 34936
  • NSC-34936
  • suramin
  • Suramin
  • Suramin [WHO-DD]
  • suramin who dd
  • suramine
  • Suramine

CAS registry numbers
  • 145-63-1
ChEMBL ID
CHEMBL265502
InChIKey
FIAFUQMPZJWCLV-UHFFFAOYSA-N
RxNorm IDs (RxCUI)
  • 10256
FDA ingredient codes (UNII)
  • 6032D45BEM

  • 5361
  • 4261196
  • 135973538

Patents
0
Designations
2
First in class
No
Fast track
No
Breakthrough designation
No
Orphan designation
No
Priority review
No
Orphan exclusivity
No
Accelerated approval
No

Pharmacology name
suramin
Type
Synthetic organic
Approval recorded by Guide to Pharmacology
Yes

  • Action
    Activator
    Action type
    ACTIVATOR
    Target
    RyR1
    Gene symbol
    RYR1
    Protein identifier
    P21817
  • Action
    Activator
    Action type
    ACTIVATOR
    Target
    RyR2
    Gene symbol
    RYR2
    Protein identifier
    Q92736
  • Action
    Antagonist
    Action type
    Antagonist
    Target
    P2Y2 receptor
    Gene symbol
    P2RY2
    Protein identifier
    P41231
    Median affinity
    4.3
    Affinity units
    pIC50
  • Action
    Antagonist
    Action type
    Antagonist
    Target
    P2Y1 receptor
    Gene symbol
    P2RY1
    Protein identifier
    P47900
    Median affinity
    5.3
    Affinity units
    pKi
  • Action
    Antagonist
    Action type
    Antagonist
    Target
    P2X3
    Gene symbol
    P2RX3
    Protein identifier
    P56373
    Median affinity
    4.83
    Affinity units
    pIC50
  • Action
    Antagonist
    Action type
    Antagonist
    Target
    P2Y6 receptor
    Gene symbol
    P2RY6
    Protein identifier
    Q15077
    Median affinity
    4
    Affinity units
    pKB
  • Action
    Antagonist
    Action type
    Antagonist
    Target
    P2Y11 receptor
    Gene symbol
    P2RY11
    Protein identifier
    Q96G91
    Affinity units
    pIC50
  • Action
    Antagonist
    Action type
    Antagonist
    Target
    P2Y13 receptor
    Gene symbol
    P2RY13
    Protein identifier
    Q9BPV8
    Median affinity
    5.6
    Affinity units
    pIC50

Open Targets mechanisms

  • Mechanism
    Acidic fibroblast growth factor inhibitor
    Action type
    Inhibitor
    Target
    Fibroblast growth factor 1

  • Action type
    Antagonist
    Gene symbol
    P2RY2
    Protein identifier
    P41231
    Organism
    Homo sapiens
    Target development level
    Clinical
  • Action type
    Antagonist
    Gene symbol
    P2RY1
    Protein identifier
    P47900
    Organism
    Homo sapiens
    Target development level
    Chemical evidence
  • Action type
    Antagonist
    Gene symbol
    P2RY6
    Protein identifier
    Q15077
    Organism
    Homo sapiens
    Target development level
    Chemical evidence
  • Action type
    Antagonist
    Gene symbol
    P2RY11
    Protein identifier
    Q96G91
    Organism
    Homo sapiens
    Target development level
    Biological evidence
  • Action type
    Antagonist
    Gene symbol
    P2RY13
    Protein identifier
    Q9BPV8
    Organism
    Homo sapiens
    Target development level
    Chemical evidence

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
    2
  • Condition identifier
    EFO_0005225
    Highest recorded phase
    1
  • Condition identifier
    MONDO_0005233
    Highest recorded phase
    2
  • Condition identifier
    MONDO_0005258
    Highest recorded phase
    2
  • Condition identifier
    MONDO_0005459
    Highest recorded phase
    1

  • Event
    chest pain
    Reports
    4
    Reporting signal score
    11.5054
  • Event
    electromyogram abnormal
    Reports
    1
    Reporting signal score
    7.73814

Trial references

Calculated partition coefficient (XLogP)
1.5
Prodrug
No
Chirality
Achiral
Inorganic
No
Heavy atoms
86
Molecular formula
C51H40N6O23S6
Monoisotopic mass
1296.0469086
Natural product
Yes

Recorded assays
1,785
Active assays
275

  • Confirmatory
  • Other
  • Screening

Distribution coefficient (LogD)

Median
0.00023
Mean
0.00023
Minimum
0.00023
Maximum
0.00023
Unit
unitless
Assays
1
Standard deviation
0
Summary method
median
Censored results excluded
0
Other units excluded
0
Unknown units excluded
0

Measurement types

  • LogD

Related records

Trials (21)

In development for (2)

Targets (1)