Navitoclax, 99.97%

cas: 923564-51-6 — see every product listed under this CAS number, including other names

Navitoclax, 99.97% (CAS 923564-51-6) is a chemical reagent available from Chemat. Available pack sizes: 100 mg, 500 mg, 50 mg, 10mM/1mL, 5 mg, 200 mg, 25 mg, 10 mg. Offered by: MedChemExpress.

brandMedChemExpress
catalog numberHY-10087-100 mg
cas923564-51-6
size100 mg
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Available pack sizes

brand size price
MedChemExpress 100 mg 1318.15 Pln
MedChemExpress 500 mg 3955.94 Pln
MedChemExpress 50 mg 983.78 Pln
MedChemExpress 10mM/1mL 477.59 Pln
MedChemExpress 5 mg 361.49 Pln
MedChemExpress 200 mg 2037.97 Pln
MedChemExpress 25 mg 742.30 Pln
MedChemExpress 10 mg 454.37 Pln

properties

delivery time over 3 weeks
purity99.97%

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

Identity
Molecular formulaC47H55ClF3N5O6S3
Molecular weight974.6 g/mol
IUPAC name4-[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
InChIKeyJLYAXFNOILIKPP-KXQOOQHDSA-N
SMILESCC1(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)

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