发明名称 SUPRAMETALLOGELS AND USES THEREOF
摘要 The disclosure provides nanostructures (e.g., nanospheres and nano-paddlewheels) formed through transition metal-ligand (e.g., Pd(II)-, Ni(II)-, or Fe(II)-ligand of Formula (A)) coordination and junction self-assembly. The disclosure also provides supramolecular complexes that include the nanostructures connected by divalent linkers Y. The provided supramolecular complexes are able to form gels (e.g., hydrogels). The gels are suprametallogels and exhibited excellent mechanical properties without sacrificing self-healing and showed high robustness and storage modulus. The present disclosure further provides compositions (e.g., gels) that include the nanostructures or supramolecular complexes and optionally an agent (e.g., small molecule), where the nanostructures and the nanostructure moieties of the supramolecular complexes may encapsulate and slowly release the agent. The nanostructures, supramolecular complex, and compositions may be useful in delivering an agent to a subject, tissue, or cell, as super-absorbent materials, and in treating a disease (e.g., a genetic diseases, proliferative disease (e.g., cancer or benign neoplasm), hematological disease, neurological disease, gastrointestinal disease (e.g., liver disease), spleen disease, respiratory disease (e.g., lung disease), painful condition, genitourinary disease, musculoskeletal condition, infectious disease, inflammatory disease, autoimmune disease, psychiatric disorder, or metabolic disorder).;
申请公布号 US2017073311(A1) 申请公布日期 2017.03.16
申请号 US201615270959 申请日期 2016.09.20
申请人 Massachusetts Institute of Technology 发明人 Johnson Jeremiah A.;Holten-Andersen Niels;Grindy Scott Charles;Kawamoto Ken;Zhukhovitskiy Aleksandr V.
分类号 C07D213/30;A61K47/22;C07F15/00 主分类号 C07D213/30
代理机构 代理人
主权项 1. A macromer of Formula (B): or a salt thereof, wherein: Ring A is a substituted or unsubstituted phenyl ring or a substituted or unsubstituted, 5- or 6-membered, monocyclic heteroaryl ring;XA is O, S, N, NRA1, C, or CRA2;XB is O, S, N, NRA1, C, or CRA2;XC is O, S, N, NRA1, C, or CRA2;XD is O, S, N, NRA1, C, or CRA2;XE is absent, N, or CRA2;each instance of RA1 is independently hydrogen, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted carbocyclyl, substituted or unsubstituted heterocyclyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, —C(═O)Ra, —C(═O)ORa, —C(═O)N(Ra)2, or a nitrogen protecting group;each instance of RA2 is independently hydrogen, halogen, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted carbocyclyl, substituted or unsubstituted heterocyclyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, —ORa, —N(Ra)2, —SRa, —CN, —SCN, —C(═NRa)Ra, —C(═NRa)ORa, —C(═NRa)N(Ra)2, —C(═O)Ra, —C(═O)ORa, —C(═O)N(Ra)2, —NO2, —NRaC(═O)Ra, —NRaC(═O)ORa, —NRaC(═O)N(Ra)2, —OC(═O)Ra, —OC(═O)ORa, or —OC(═O)N(Ra)2;each instance of Ra is independently hydrogen, substituted or unsubstituted acyl, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted carbocyclyl, substituted or unsubstituted heterocyclyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, a nitrogen protecting group when attached to a nitrogen atom, an oxygen protecting group when attached to an oxygen atom, or a sulfur protecting group when attached to a sulfur atom, or two instances of Ra are joined to form a substituted or unsubstituted heterocyclic or substituted or unsubstituted heteroaryl ring;each instance of RB is independently halogen, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted carbocyclyl, substituted or unsubstituted heterocyclyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, —ORa, —N(Ra)2, —SRa, —CN, —SCN, —C(═NRa)Ra, —C(═NRa)ORa, —C(═NRa)N(Ra)2, —C(═O)Ra, —C(═O)ORa, —C(═O)N(Ra)2, —NO2, —NRaC(═O)Ra, —NRaC(═O)ORa, —NRaC(═O)N(Ra)2, —OC(═O)Ra, —OC(═O)ORa, or —OC(═O)N(Ra)2;m is 0, 1, 2, 3, or 4, as valency permits;each instance of RC is independently halogen, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted carbocyclyl, substituted or unsubstituted heterocyclyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, —ORa, —N(Ra)2, —SRa, —CN, —SCN, —C(═NRa)Ra, —C(═NRa)ORa, —C(═NRa)N(Ra)2, —C(═O)Ra, —C(═O)ORa, —C(═O)N(Ra)2, —NO2, —NRaC(═O)Ra, —NRaC(═O)ORa, —NRaC(═O)N(Ra)2, —OC(═O)Ra, —OC(═O)ORa, or —OC(═O)N(Ra)2;n is 0, 1, 2, 3, or 4;ZA is a bond or a substituted or unsubstituted C1-4 hydrocarbon chain, optionally wherein one or more chain atoms are independently replaced with —O—, —S—, —NRZA—, —N═, or ═N—, wherein each instance of RZA is independently hydrogen, substituted or unsubstituted C1-6 alkyl, or a nitrogen protecting group;ZB is a bond or a substituted or unsubstituted C1-4 hydrocarbon chain, optionally wherein one or more chain atoms are independently replaced with —O—, —S—, or —NRZB—, wherein each instance of RZB is independently hydrogen, substituted or unsubstituted C1-6 alkyl, or a nitrogen protecting group; andY is a substituted or unsubstituted, saturated or unsaturated C30-3000 hydrocarbon chain, optionally wherein one or more chain atoms are independently replaced with —O—, —S—, —NRY—, ═N—, or —N═, wherein each instance of RY is independently hydrogen, substituted or unsubstituted C1-6 alkyl, or a nitrogen protecting group.
地址 Cambridge MA US