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Tubulysin compounds with high cytotoxicity, pharmaceutical compositions thereof, and method of use thereof
专利权人:
Matteo Zanda
发明人:
Matteo Zanda,Monica Sani,Paolo Lazzari
申请号:
US12841976
公开号:
US08580820B2
申请日:
2010.07.22
申请国别(地区):
US
年份:
2013
代理人:
摘要:
Tubulysine compounds of formula (A) having a high cytotoxicitywherein:B is selected from CH2, CH2—CH2 or CH2—CH2—CH2,D is an aromatic linker,X1 is alkyl or alkenyl,X2 is selected from the X2a, substituted or non substituted, selected from: aryl, heteroaryl, arylalkyl, cycloalkylalkyl, heterocycloalkylalkyl, or heteroarylalkyl,X2b: alkylene-O-alkyl, wherein alkylene is C2-C10,X2c: CH2—O-alkyl,X3 is selected from H, or together with X4 forms the group ═O,X4 is selected from H, halogen, OH, SH, alkyl, alkenyl, (OR5)n—OR6, OC(O)R7, NR6R7, or together with X4 forms the group ═O,R5 is an alkylene,n is zero or an integer from 1 to 10,R6 and R7, equal to or different from each other, have the following meanings:z1: H, alkyl,z2 substituted or non substituted: aryl, heteroaryl, cycloalkyl, heterocycloalkyl, arylalkyl, heteroarylalkyl, cycloalkylalkyl, heterocycloalkyl-alkyl,X5 is z2, or has the meaning of z3-alkyl, alkenyl,X6 is selected from NR8R9, OR8, NH—NR8R9, SR8, R10, wherein R8 and R9, equal to or different from each other, have the same meanings of R6, R10 has the same meanings as R6 but excluding H,X7 is z3 or H,X8 is selected from z3, H, halogen, OH, SH, OCH3.
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