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Drug ReportsTipifarnib
Tipifarnib
Tipifarnib is a small molecule pharmaceutical. It is currently being investigated in clinical studies. The pharmaceutical is active against CHURC1-FNTB protein.
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Financial
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Events Timeline
5D
1M
3M
6M
YTD
1Y
2Y
5Y
Max
Events
FDA approval date
EMA approval date
Patent expiration date
Study first post date
Last update post date
Start date
Primary completion date
Completion date
Results first post date
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Commercial
No data
Clinical
Clinical Trials
89 clinical trials
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Indications Phases 4
No data
Indications Phases 3
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Myeloid leukemia acuteD015470—C92.0492—115
Myelodysplastic syndromesD009190—D46472——11
LeukemiaD007938—C95622——9
Megakaryoblastic leukemia acuteD007947—C94.2451——9
Monocytic leukemia acuteD007948——451——9
Myelomonocytic leukemia acuteD015479—C92.5451——9
Erythroblastic leukemia acuteD004915EFO_1001257C94.0451——9
Pancreatic neoplasmsD010190EFO_0003860C25131——5
Indications Phases 2
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Breast neoplasmsD001943EFO_0003869C50310———10
GlioblastomaD005909EFO_0000515—44———6
Myeloid leukemiaD007951—C9234———6
Multiple myelomaD009101—C90.033———4
GliosarcomaD018316——32———4
Myelomonocytic leukemia chronicD015477—C93.133———4
Basophilic leukemia acuteD015471—C94.822———3
Eosinophilic leukemia acuteD015472——22———3
Non-hodgkin lymphomaD008228—C85.9—3———3
MedulloblastomaD008527———3———3
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Indications Phases 1
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
NeoplasmsD009369—C807————7
Blast crisisD001752——1————1
Myeloproliferative disordersD009196—D47.11————1
LymphomaD008223—C85.91————1
Plasma cell neoplasmsD054219——1————1
Refractory anemiaD000753—D46.41————1
Indications Without Phase
No data
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameTipifarnib
INNtipifarnib
Description
Tipifarnib is a quinolone that is 1-methylquinolin-2-one which carries a 3-chlorophenyl and an amino(4-chlorophenyl)(1-methyl-imidazol-5-yl)methyl groups at the 4 and 6 positions, respectively (the R-isomer). It has a role as an antineoplastic agent, an EC 2.5.1.58 (protein farnesyltransferase) inhibitor and an apoptosis inducer. It is a quinolone, a member of monochlorobenzenes, a member of imidazoles and a primary amino compound.
Classification
Small molecule
Drug classfarnesyl transferase inhibitor
Image (chem structure or protein)Loading
Structure (InChI/SMILES or Protein Sequence)
Cn1cncc1[C@@](N)(c1ccc(Cl)cc1)c1ccc2c(c1)c(-c1cccc(Cl)c1)cc(=O)n2C
Identifiers
PDB—
CAS-ID192185-72-1
RxCUI—
ChEMBL IDCHEMBL289228
ChEBI ID—
PubChem CID159324
DrugBankDB04960
UNII IDMAT637500A (ChemIDplus, GSRS)
Target
Agency Approved
CHURC1-FNTB
CHURC1-FNTB
Organism
Homo sapiens
Gene name
CHURC1-FNTB
Gene synonyms
NCBI Gene ID
Protein name
CHURC1-FNTB protein
Protein synonyms
CAAX farnesyltransferase subunit beta, Protein farnesyltransferase subunit beta, Ras proteins prenyltransferase subunit beta
Uniprot ID
Mouse ortholog
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Alternate
No data
Variants
No data
Financial
No data
Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 2,424 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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74 adverse events reported
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