Exploring the Anti-Cancer Mechanism of Novel 3,4'-Substituted Diaryl Guanidinium Derivatives
We previously identified a guanidinium-based lead compound that inhibited BRAF through a hypothetic type-III allosteric mechanism. Considering the pharmacophore identified in this lead compound (i.e., "lipophilic group", "di-substituted guanidine", "phenylguanidine polar end...
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Main Authors: | , , , , , |
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Format: | Book |
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MDPI AG,
2020-12-01T00:00:00Z.
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A1234.567 |
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Copy 1 | Available |