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Drug ReportsNavitoclax
Navitoclax
Navitoclax is a small molecule pharmaceutical. It is currently being investigated in clinical studies. The pharmaceutical is active against apoptosis regulator Bcl-2 and bcl-2-like protein 1.
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Clinical
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Target
Variants
Financial
Trends
Safety
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
45 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
Primary myelofibrosisD055728—D47.4312—17
Indications Phases 2
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
B-cell chronic lymphocytic leukemiaD015451—C91.175———10
Precursor cell lymphoblastic leukemia-lymphomaD054198—C91.043——26
Non-hodgkin lymphomaD008228—C85.921———2
Small cell lung carcinomaD055752——22———2
Ovarian neoplasmsD010051EFO_0003893C5611———2
Myelodysplastic syndromesD009190—D4621———2
MelanomaD008545——11———1
Prostatic neoplasmsD011471—C61—1———1
Large b-cell lymphoma diffuseD016403—C83.3—1———1
Follicular lymphomaD008224—C8211———1
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Indications Phases 1
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
NeoplasmsD009369—C809————9
LymphomaD008223—C85.92————2
Myeloid leukemia acuteD015470—C92.02————2
Non-small-cell lung carcinomaD002289——1————1
Hematologic neoplasmsD019337——1————1
Healthy volunteers/patients———1————1
Liver cirrhosisD008103EFO_0001422K74.01————1
Hepatocellular carcinomaD006528—C22.01————1
Liver neoplasmsD008113EFO_1001513C22.01————1
Hepatitis bD006509——1————1
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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
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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
PDB—
CAS-ID923564-51-6
RxCUI—
ChEMBL IDCHEMBL443684
ChEBI ID—
PubChem CID24978538
DrugBankDB12340
UNII IDXKJ5VVK2WD (ChemIDplus, GSRS)
Target
Agency Approved
BCL2L1
BCL2L1
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
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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100 adverse events reported
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