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As vascularization promotes cancer progression, soluble VEGFR-1 and -2 could act as decoys impeding VEGF-VEGFR-2 binding on the surface of target cells

Pfeiffer, J., Johnson, D

Comparative studies in obese mice showed that AOD-9604 produced slightly greater fat reduction than the unmodified fragment at equivalent doses

Under neutral pH, the surface was negatively charged, but in acidic tumour tissues or endosomes, protonation caused a charge reversal to positive, facilitating cell binding and internalisation, which improved drug accumulation within tumour cells [21]