Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Rheumatoid arthritis | D001172 | EFO_0000685 | M06.9 | 1 | 2 | — | — | — | 3 |
Arthritis | D001168 | HP_0001369 | M05-M14 | 1 | 2 | — | — | — | 3 |
Multiple myeloma | D009101 | — | C90.0 | — | 2 | — | — | — | 2 |
Plasma cell neoplasms | D054219 | — | — | — | 2 | — | — | — | 2 |
Myelodysplastic syndromes | D009190 | — | D46 | — | 1 | — | — | — | 1 |
Hematologic diseases | D006402 | EFO_0005803 | D75.9 | — | 1 | — | — | — | 1 |
Preleukemia | D011289 | — | — | — | 1 | — | — | — | 1 |
Bone marrow diseases | D001855 | — | — | — | 1 | — | — | — | 1 |
Syndrome | D013577 | — | — | — | 1 | — | — | — | 1 |
Bone marrow neoplasms | D019046 | — | — | — | 1 | — | — | — | 1 |
Drug common name | TALMAPIMOD |
INN | talmapimod |
Description | Talmapimod is an indolecarboxamide obtained by formal condensation of the carboxy group of 6-chloro-3-[(dimethylamino)(oxo)acetyl]-1-methylindole-5-carboxylic acid with the secondary amino group of (2S,5R)-1-[(4-fluorophenyl)methyl]-2,5-dimethylpiperazine. It is a potent inhibitor of MAPK and exhibits anti-cancer properties. It has a role as an EC 2.7.11.24 (mitogen-activated protein kinase) inhibitor, an apoptosis inducer and an antineoplastic agent. It is a N-acylpiperazine, a N-alkylpiperazine, an aromatic amide, a member of monofluorobenzenes, a chloroindole, an indolecarboxamide, a dicarboxylic acid diamide and an aromatic ketone. |
Classification | Small molecule |
Drug class | immunomodulators: mitogen-activated protein (MAP) kinase inhibitors |
Image (chem structure or protein) | |
Structure (InChI/SMILES or Protein Sequence) | C[C@H]1CN(C(=O)c2cc3c(C(=O)C(=O)N(C)C)cn(C)c3cc2Cl)[C@H](C)CN1Cc1ccc(F)cc1 |
PDB | — |
CAS-ID | 309913-83-5 |
RxCUI | — |
ChEMBL ID | CHEMBL514201 |
ChEBI ID | 90683 |
PubChem CID | — |
DrugBank | — |
UNII ID | B1E00KQ6NT (ChemIDplus, GSRS) |