cas: 923564-51-6 — see every product listed under this CAS number, including other names
ABT–263 (Navitoclax) (CAS 923564-51-6) is a chemical reagent available from Chemat. Available pack sizes: 10mg, 100mg, 5mg, 10mM (in 1ml dmso), 50mg. Offered by: GLPBio.
| brand | GLPBio |
|---|---|
| catalog number | GC12405-10 |
| cas | 923564-51-6 |
| size | 10mg |
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| brand | size | price | |
|---|---|---|---|
| GLPBio | 10mg | 662.57 Pln | |
| GLPBio | 100mg | 1565.90 Pln | |
| GLPBio | 5mg | 597.04 Pln | |
| GLPBio | 10mM (in 1ml dmso) | 760.86 Pln | |
| GLPBio | 50mg | 1121.26 Pln |
| purity | No data |
|---|---|
| delivery time | To be confirmed by Chemat |
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 antineoplastic agent and an apoptosis inducer. It is a member of piperazines, an aryl sulfide, a sulfone, an organofluorine compound, a member of morpholines, a secondary amino compound, a tertiary amino compound, a member of monochlorobenzenes and a N-sulfonylcarboxamide.
Source: ChEBI
| Molecular formula | C47H55ClF3N5O6S3 |
|---|---|
| Molecular weight | 974.6 g/mol |
| IUPAC name | 4-[4-[[2-(4-chlorophenyl)-5,5-dimethylcyclohexen-1-yl]methyl]piperazin-1-yl]-N-[4-[[(2R)-4-morpholin-4-yl-1-phenylsulfanylbutan-2-yl]amino]-3-(trifluoromethylsulfonyl)phenyl]sulfonylbenzamide |
| InChIKey | JLYAXFNOILIKPP-KXQOOQHDSA-N |
| SMILES | CC1(CCC(=C(C1)CN2CCN(CC2)C3=CC=C(C=C3)C(=O)NS(=O)(=O)C4=CC(=C(C=C4)N[C@H](CCN5CCOCC5)CSC6=CC=CC=C6)S(=O)(=O)C(F)(F)F)C7=CC=C(C=C7)Cl)C |
Computed by PubChem (NCBI)