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PHARMACEUTICAL COMPOUNDS HAVING HSP90 INHIBITORY OR MODULATING ACTIVITY

机译:具有HSP90抑制作用或调节活性的药物

摘要

The invention provides a compound for use in medicine, the compound being a compound of the formula (VI0) or a salt, solvate, tautomer or N-oxide thereof: wherein the bicyclic group: is selected from the structures C1, C5 and C6: wherein n is 0, 1, 2 or 3; R1 is hydrogen, hydroxy, or ORz; R2a is hydroxy, methoxy or ORz; provided that at least one of R1 and R2a is ORz; Rz is Lp-Rp1; SO3H; a glucuronide residue; a mono-, di- or tripeptide residue; or Lp is a bond, CO, (CO)O, (CO)NRp1 or S(O)xNRp1; x is 1 or 2; Rp1 is hydrogen or a an optionally substituted C1-25 hydrocarbyl group containing 0, 1 or 2 carbocyclic rings and 0, 1, 2, 3, 4, 5 or 6 carbon-carbon multiple bonds, provided that Rp1 is not hydrogen when Lp is a bond, CO or (CO)O; and provided also that ORz does not contain an OO moiety; and excluding compounds wherein R1 is hydroxy and R2a is methoxy; Rp2 and Rp3 are the same or different and each is a group Rp1; and R3, R4a, R8 and R10 are defined in the claims. The compounds of formula (VI0) are pro-drugs of parent compounds wherein R1 and/or R2a are hydroxy, wherein the parent compounds have Hsp90 inhibiting activity.
机译:本发明提供了用于医学的化合物,该化合物为式(VI0)的化合物或其盐,溶剂化物,互变异构体或N-氧化物:其中双环基团选自结构C1,C5和C6:其中n为0、1、2或3; R1是氢,羟基或ORz; R2a是羟基,甲氧基或ORz;前提是R1和R2a中的至少一个是ORz; Rz是Lp-Rp1; SO3H;葡糖醛酸残基;单,二或三肽残基;或Lp为键,CO,(CO)O,(CO)NRp1或S(O)xNRp1; x是1或2; Rp1是氢或含有0、1或2个碳环和0、1、2、3、4、5或6个碳-碳多键的任选取代的C1-25烃基,条件是当Lp为键,CO或(CO)O;并且还规定ORz不包含OO部分; R1是羟基,R2a是甲氧基的化合物; Rp2和Rp3相同或不同,各自为基团Rp1; R3,R4a,R8和R10在权利要求中定义。式(VI0)化合物为母体化合物的前药,其中R1和/或R2a为羟基,其中母体化合物具有Hsp90抑制活性。

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