发明名称 Means and methods of enhancing delivery to biological systems
摘要 This invention relates to a peptide or polypeptide (a) which is esterified or thio-esterified (i) at the carboxylate of the C-terminus with a guanidinium alkanol, a guanidinium alkanethiol, a PEG substituted with a guanidinium group and having a free hydroxyl group, or a PEG substituted with a guanidinium group and a sulfhydryl group; (ii) at a side-chain carboxylate of one or more Asp or GIu residues, if present, with a guanidinium alkanol, a guanidinium alkanethiol, a PEG substituted with a guanidinium group and having a free hydroxyl group, or a PEG substituted with a guanidinium group and a sulfhydryl group; (iii) at a hydroxyl group of one or more Ser, Thr or Tyr residues, if present, with a guanidinium alkanoic acid or a PEG substituted with a guanidinium group and a carboxyl group; (iv) at a sulfhydryl group of one or more Cys residues, if present, with a guanidinium alkanoic acid or a PEG substituted with a guanidinium group and a carboxyl group; and/or (v) at the N-terminus with a guanidinium alkanoic acid or a PEG substituted with a guanidinium group and a carboxyl group, wherein said N-terminus is previously amidated with an alpha- or beta-hydroxy acid, and wherein the ester is formed between the hydroxy group of said alpha- or beta-hydroxy acid and the carboxylic group of said guanidinium alkanoic acid or said PEG substituted with a guanidinium group and a carboxyl group; and/or (b) which contains one or more disulfides, the disulfide being formed between the sulfhydryl group of a Cys reside, if present, and a guanidinium alkanethiol or a PEG substituted with a guanidinium group and a sulfhydryl group.
申请公布号 US9211340(B2) 申请公布日期 2015.12.15
申请号 US200712443236 申请日期 2007.09.26
申请人 发明人 Botti Paolo
分类号 A61K47/48 主分类号 A61K47/48
代理机构 Pillsbury Winthrop Shaw Pittman LLP 代理人 Pillsbury Winthrop Shaw Pittman LLP
主权项 1. A nucleic acid (a) which is esterified at one or more phosphates with a guanidinium alkanol or a PEG substituted with a guanidinium group and having a free hydroxyl group; wherein the guanidinium alkanol has a structure of: HO—(CR1R2)n—N(R3)—C(═NR4)—NHR5  (Formula I) wherein the PEG substituted with a guanidinium group and having a free hydroxyl group has a structure of: HO—(CH2CH2(OCH2CH2)k—N(R3)—C(═NR4)—NHR5  (Formula V) wherein: n is an integer from 2 to 15; k is an integer from 1 to 12; each occurrence of R1 and R2 is independently selected from H; halogen; NH2; alkyl with 1 to 5 carbon atoms; R3 is H or alkyl with 1 to 5 carbon atoms; and R4 and R5 are each independently selected from H; alkyl with 1 to 5 carbon atoms; aryl; heteroaryl, wherein the N bearing the R4 or R5 group may be a ring atom of the heteroaryl; and/or a heteroaryl ring formed by R4 and R5.
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