Yeats inhibitors and methods of use thereof

A compound or a pharmaceutically acceptable salt thereof comprising a base oligomer and a side chain,

• wherein the compound is defined according to Formula (I):
• wherein A is CR2 or N;
• wherein each instance of B1 and B2 is an independently selected bivalent linking unit, wherein the bivalent linking units are connected by amide, ester, thioester, thioamide, imidate, imide, sulfonate, or sulfonamide linkage in a head-to-tail manner;
• wherein D1 is H or unsubstituted or substituted hydrocarbyl, carbocyclyl or heterocyclyl;
• wherein D2 is H, NH2, NHR15, NR16R17, OH, OR18, or unsubstituted or substituted hydrocarbyl, carbocyclyl or heterocyclyl;
• wherein X is unsubstituted or substituted C1-10 alkyl, C1-10 alkenyl, C1-10 alkynyl, C1-10 carbocyclyl, C1-10 heteroalkyl, C1-10 heteroalkenyl, C1-10 heteroalkynyl, or C1-10 heterocyclyl;
• wherein Y is NR3, O, or S;
• wherein Z is —CO—, —CS—, —CNR4—, —SO—, or —SO2—;
• wherein R2, R3, and R4 are independently H or C1-10 hydrocarbyl, C1-10 carbocyclyl, or C1-10 heterocyclyl;
• wherein R1 is a conjugated/delocalized group, such as an unsubstituted or substituted, heterocyclic or carbocyclic, aromatic ring (monocyclic, bicyclic, tricyclic, tetracyclic) or unsubstituted or substituted alkenyl or alkynyl;
• wherein R15, R16, R17, and R18 can be H or alkyl, alkenyl, alkynyl, substituted alkyl, substituted alkenyl, substituted alkynyl, alkoxy, alkylamino, dialkylamino, hydroxy, aryl, substituted aryl, heteroaryl, substituted heteroaryl, substituted alkoxy, carboxyl, substituted carboxyl, amino, substituted amino, amido, substituted amido, C3-C20 cyclic, substituted C3-C20 cyclic, heterocyclic, or substituted heterocyclic;
• and
• wherein m and n are each independently integers from 0 to 10, wherein at least one of m or n is not 0.