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Navitoclax
Navitoclax is a small molecule pharmaceutical. It is currently being investigated in clinical studies. The pharmaceutical is active against bcl-2-like protein 1 and apoptosis regulator Bcl-2.
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Commercial
Therapeutic Areas
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Trade Name
FDA
EMA
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Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
No data
Labels
FDA
EMA
No data
Indications
FDA
EMA
No data
Agency Specific
FDA
EMA
No data
Patent Expiration
No data
ATC Codes
No data
HCPCS
No data
Clinical
Clinical Trials
43 clinical trials
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Mock data
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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
Primary myelofibrosisD055728D47.431217
Indications Phases 2
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
B-cell chronic lymphocytic leukemiaD015451C91.17510
Precursor cell lymphoblastic leukemia-lymphomaD054198C91.04326
Non-hodgkin lymphomaD008228C85.9212
Small cell lung carcinomaD055752222
Ovarian neoplasmsD010051EFO_0003893C56112
Myelodysplastic syndromesD009190D46212
MelanomaD008545111
Prostatic neoplasmsD011471C6111
Large b-cell lymphoma diffuseD016403C83.311
Follicular lymphomaD008224C82111
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Indications Phases 1
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
NeoplasmsD009369C8099
LymphomaD008223C85.922
Myeloid leukemia acuteD015470C92.022
Non-small-cell lung carcinomaD00228911
Hematologic neoplasmsD01933711
Healthy volunteers/patients11
Liver cirrhosisD008103EFO_0001422K74.011
Hepatocellular carcinomaD006528C22.011
Liver neoplasmsD008113EFO_1001513C22.011
Hepatitis bD00650911
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Indications Without Phase
No data
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameNAVITOCLAX
INNnavitoclax
Description
Navitoclax is a N-sulfonylcarboxamide resulting from the formal condensation of the carboxy group of 4-{4-[(4'-chloro-4,4-dimethyl-3,4,5,6-tetrahydro[biphenyl]-2-yl)methyl]piperazin-1-yl}benzoic acid with the amino group of 4-{[(2R)-4-(morpholin-4-yl)-1-(phenylsulfanyl)butan-2-yl]amino}-3-[(trifluoromethyl)sulfonyl]benzenesulfonamide. It is a BH3-mimetic drug which targets the anti-apoptotic B-cell lymphoma-2 (BCL-2) family proteins, including BCL-2, BCL-xL, and BCL-w, and induces apoptosis in cancer cells. Currently under clinical investigation as treatment for solid tumors and hematologic malignancies. It has a role as a B-cell lymphoma 2 inhibitor, an apoptosis inducer and an antineoplastic agent. It is a member of piperazines, a member of monochlorobenzenes, a member of morpholines, an aryl sulfide, a N-sulfonylcarboxamide, a sulfone, an organofluorine compound, a secondary amino compound and a tertiary amino compound.
Classification
Small molecule
Drug classbcl-2 (B-cell lymphoma 2) inhibitors
Image (chem structure or protein)
Structure (InChI/SMILES or Protein Sequence)
CC1(C)CCC(c2ccc(Cl)cc2)=C(CN2CCN(c3ccc(C(=O)NS(=O)(=O)c4ccc(N[C@H](CCN5CCOCC5)CSc5ccccc5)c(S(=O)(=O)C(F)(F)F)c4)cc3)CC2)C1
Identifiers
PDB4LVT
CAS-ID923564-51-6
RxCUI
ChEMBL IDCHEMBL443684
ChEBI ID
PubChem CID24978538
DrugBankDB12340
UNII IDXKJ5VVK2WD (ChemIDplus, GSRS)
Target
Agency Approved
BCL2L1
BCL2L1
BCL2
BCL2
Organism
Homo sapiens
Gene name
BCL2L1
Gene synonyms
BCL2L, BCLX
NCBI Gene ID
Protein name
bcl-2-like protein 1
Protein synonyms
Apoptosis regulator Bcl-X, protein phosphatase 1, regulatory subunit 52
Uniprot ID
Mouse ortholog
Bcl2l1 (12048)
bcl-2-like protein 1 (Q64373)
Alternate
No data
Variants
Clinical Variant
No data
Financial
No data
Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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90 adverse events reported
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