DIDS is a dual inhibitor of ABCA1 and VDAC1. DIDS also inhibits RAD51, inhibiting RAD51-mediated homologous pairing and strand exchange reactions. DIDS inhibits anion exchange and binding to red blood cell membranes, inhibits the activation of caspase-3 and -9, and can be used in cancer research[1][2][3][4].
Molecular Weight:
454.52
CAS Number:
[53005-05-3]
Formula:
C16H10N2O6S4
Target:
RAD51,VDAC
Application Notes:
MCE Product type: Reference compound
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