Anti-cancer compound
US-9486444-B1 · Nov 8, 2016 · US
US9822128B1 · US · B1
| Field | Value |
|---|---|
| Publication number | US-9822128-B1 |
| Application number | US-201715611771-A |
| Country | US |
| Kind code | B1 |
| Filing date | Jun 1, 2017 |
| Priority date | Jun 1, 2017 |
| Publication date | Nov 21, 2017 |
| Grant date | Nov 21, 2017 |
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The substituted spirooxindoles are MDM2-p53 inhibitors bearing a benzylidine (styryl) arm and have a complex fused ring system ideally suited for binding to the MDM2 protein, thereby interrupting its protein-protein interaction (PPI). Sixteen compounds, designated 4a-4p, were synthesized in a simple smooth method using an asymmetric 1,3-dipolar reaction as the key step. Testing showed that the compounds exhibit anti-cancer activity against various forms of cancer cells affecting humans.
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We claim: 1. A substituted spirooxindole for cancer treatment, comprising a compound having the formula: wherein R 1 and R 4 are independently hydrogen or chlorine; R 2 is hydrogen, chlorine, fluorine bromine, trifluoromethyl, methyl, or methoxy; R 3 is hydrogen, nitro (NO 2 ), fluorine, or bromine; and R 5 is hydrogen, chlorine, or bromine. 2. A substituted spirooxindole for cancer treatment, comprising a compound having the formula: wherein X is sulfur or oxygen. 3. A substituted spirooxindole for cancer treatment, comprising a compound having the formula:
Spiro-condensed systems · CPC title
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