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    • 5. 发明申请
    • TEMPLATE FIXED ΒΕΤΑ-HAIRPIN LOOP MIMETICS AND THEIR USE IN PHAGE DISPLAY
    • 模板固定的BetaEpsilonTauAlpha-HAIRPIN环状物质及其在PHAGE显示中的使用
    • WO2005047503A1
    • 2005-05-26
    • PCT/EP2003/012783
    • 2003-11-15
    • POLYPHOR LTD.UNIVERSITÄT ZÜRICHVRIJBLOED, Jan, WimOBRECHT, DanielLOCURIO, SergioGOMBERT, Frank, OttoLUDIN, ChristianJUNG, Françoise
    • VRIJBLOED, Jan, WimOBRECHT, DanielLOCURIO, SergioGOMBERT, Frank, OttoLUDIN, ChristianJUNG, Françoise
    • C12N15/10
    • C07K1/047C12N15/1037C40B40/02
    • Template-fixed β-hairpin mimetics of the general formula R 1 -Cys-Z-Cys-R 2 (I) wherein the two Cys residues are bridged by a disulfide bond thereby forming a cyclic peptide; R l and R 2 are preferably Glu-Thr and Thr-Lys; or Lys-Thr and Thr-Glu; or Thr-Glu and Lys-Thr; or Thr-Lys and Glu-Thr; or Leu-Glu and Lys-Val; or Val-Lys and Glu-Leu; or Glu-Leu and Val-Lys; or Lys-Leu and Val-Glu; or Asn-Gly and Lys-Val; or Val-Gly and Lys-Asn; or Gly-Asn and Val-Lys; or Gly-Val and Asn-Lys; or Gly-Gly and Gly-Gly; or Glu-Leu-Lys and Glu-Val-Lys; or Lys-Val-Glu and Lys-Leu-Glu; or Leu-Glu-Lys and Glu-Lys-Val; or Val-Lys-Glu and Lys-Glu-Leu; or Glu-Lys-Leu and Val-Glu-Lys; or Lys-Glu-Val and Leu-Lys-Glu; or Lys-Glu-Leu and Val-Lys-Glu; or Glu-Lys-Val and Leu-Glu-Lys; or Lys-Val-Gly and Gly-Leu-Glu; or Glu-Leu-Gly and Gly-Val-Lys; or Val-Lys-Gly and Gly-Glu-Leu; or Leu-Glu-Gly and Gly-Lys-Val; or Val-Gly-Lys and Glu-Gly-Leu; or Leu-Gly-Glu and Lys-Gly-Val; or Gly-Gly-Gly and Gly-Gly-Gly; and Z is a chain of n amino acid residues with n being an integer form 4 to 20 and with each of these n amino acid residues being, independently, derived from any naturally occurring L­- α-amino acid are provided. Libraries comprising a plurality of these templates can be used for the construction of phage display derived template-fixed β-hairpin mimetics generating phage display libraries with very high binding constants to targets, thus combining the advantage of screening of large phage display derived template-fixed β-hairpin libraries which in turn considerably facilitates structure-activity studies, and hence the discovery of new molecules with potent activities and with novel selectivities towards different types of targets.
    • 通式R 1 -Cys-Z-Cys-R 2(I)的模板固定的β-发夹模拟物,其中两个Cys残基被二硫键桥接,从而形成环肽; R 1和R 2优选为Glu-Thr和Thr-Lys; 或Lys-Thr和Thr-Glu; 或Thr-Glu和Lys-Thr; 或Thr-Lys和Glu-Thr; 或Leu-Glu和Lys-Val; 或Val-Lys和Glu-Leu; 或Glu-Leu和Val-Lys; 或Lys-Leu和Val-Glu; 或Asn-Gly和Lys-Val; 或Val-Gly和Lys-Asn; 或Gly-Asn和Val-Lys; 或Gly-Val和Asn-Lys; 或Gly-Gly和Gly-Gly; 或Glu-Leu-Lys和Glu-Val-Lys; 或Lys-Val-Glu和Lys-Leu-Glu; 或Leu-Glu-Lys和Glu-Lys-Val; 或Val-Lys-Glu和Lys-Glu-Leu; 或Glu-Lys-Leu和Val-Glu-Lys; 或Lys-Glu-Val和Leu-Lys-Glu; 或Lys-Glu-Leu和Val-Lys-Glu; 或Glu-Lys-Val和Leu-Glu-Lys; 或Lys-Val-Gly和Gly-Leu-Glu; 或Glu-Leu-Gly和Gly-Val-Lys; 或Val-Lys-Gly和Gly-Glu-Leu; 或Leu-Glu-Gly和Gly-Lys-Val; 或Val-Gly-Lys和Glu-Gly-Leu; 或Leu-Gly-Glu和Lys-Gly-Val; 或Gly-Gly-Gly和Gly-Gly-Gly; 并且Z是n个氨基酸残基的链,其中n是4至20的整数,并且这些n个氨基酸残基中的每一个独立地衍生自任何天然存在的L-α-氨基酸。 包含多个这些模板的文库可用于构建噬菌体展示衍生的模板固定的β-发夹模拟物,其产生具有非常高的结合常数的靶标的噬菌体展示文库,因此结合筛选大噬菌体展示衍生模板固定的优点 β-发夹文库反过来极大地促进结构活性研究,从而发现具有有效活性和对不同类型靶标具有新选择性的新分子。
    • 6. 发明申请
    • BETA-HAIRPIN PEPTIDOMIMETIC WITH ELASTASE INHIBITORY ACTIVITY AND AEROSOL DOSAGE FORMS THEREOF
    • 具有弹性蛋白酶抑制活性和气溶胶剂型的β-HAIRPIN肽制剂
    • WO2017207117A1
    • 2017-12-07
    • PCT/EP2017/025156
    • 2017-05-31
    • POLYPHOR AG
    • LUDIN, ChristianKELLER, Manfred
    • A61K8/64A61K38/12A61K9/00C07K7/64
    • The present invention relates to pharmaceutical aerosols comprising a β-hairpin peptidomimetic of formula cyclo(-OctG-Glu-Thr-Ala-Ser-lle-Pro-Pro-Gln-Lys-Tyr- D Pro-Pro-), or a pharmaceutically acceptable salt thereof, having inhibitory activity against human neutrophil elastase. It further relates to solid or liquid pharmaceutical compositions and kits for preparing and administering such aerosols. The invention can be used for the prevention, management or treatment of pulmonary diseases, such as alpha-1 antitrypsin deficiency (AATD), cystic fibrosis (CF), non-cystic fibrosis bronchiactasis (NCFB), or chronic obstructive pulmonary disease (COPD), or infections, or diseases, or conditions of the lungs, being mediated by or resulting from human neutrophil elastase activity. Thus, the invention further relates to a pharmaceutical composition or a pharmaceutical aerosol comprising the active compound cyclo(-OctG-Glu-Thr-Ala-Ser-lle-Pro-Pro-Gln-Lys-Tyr- D Pro-Pro-), or any pharmaceutically acceptable salt thereof, for use in a method for the prevention, management or treatment of diseases or conditions of the lungs being mediated by or resulting from human neutrophil elastase activity in a subject.
    • 本发明涉及药物气雾剂,其包含式环(-OctG-Glu-Thr-Ala-Ser-Ile-Pro-Pro-Gln-Lys-Tyr-)的β-发夹肽模拟物 Pro-Pro-)或其药学上可接受的盐,其对人嗜中性粒细胞弹性蛋白酶具有抑制活性。 它还涉及用于制备和施用这种气雾剂的固体或液体药物组合物和试剂盒。 本发明可用于预防,治疗或治疗肺部疾病,如α-1抗胰蛋白酶缺乏症(AATD),囊性纤维化(CF),非囊性纤维化支气管扩张症(NCFB)或慢性阻塞性肺病(COPD) ,或由人嗜中性粒细胞弹性蛋白酶活性介导或由其产生的感染,或肺的疾病或病症。 因此,本发明进一步涉及包含活性化合物环(-OctG-Glu-Thr-Ala-Ser-Ile-Pro-Pro-Gln-Lys-Tyr-D-D)的药物组合物或药用气雾剂。 Pro-Pro-)或其任何药学上可接受的盐,用于预防,管理或治疗受试者中由人嗜中性粒细胞弹性蛋白酶活性介导或由其产生的肺疾病或病症的方法。
    • 7. 发明申请
    • BETA-HAIRPIN PEPTIDOMIMETICS AS SELECTIVE ELASTASE INHIBITORS
    • BETA-HAIRPIN PEPTIDOMIMETICS作为选择性弹性酶抑制剂
    • WO2015096873A1
    • 2015-07-02
    • PCT/EP2013/078073
    • 2013-12-27
    • POLYPHOR AG
    • GOMBERT, Frank OttoOBRECHT, DanielSELLIER-KESSLER, OdileLEDERER, AlexanderLUDIN, ChristianSCHMITT-BILLET, ManuelaWEINBRENNER, Steffen
    • C07K14/81
    • C07K7/64A61K38/00C07K14/811
    • β-Hairpin peptidomimetics of the general formula cyclo(-Xaa 1 -Xaa 2 -Thr 3 -Xaa 4 -Ser 5 -Xaa 6 -Xaa 7 -Xaa 8 -Xaa 9 -Xaa 10 -Xaa 11 -Xaa 12 -Xaa 13 -) and pharmaceutically acceptable salts thereof, with Xaa 1 , Xaa 2 , Xaa 4 , Xaa 6 , Xaa 7 , Xaa 8 , Xaa 9 , Xaa 10 , Xaa 11 , Xaa 12 and Xaa 13 being amino acid residues of certain types which are defined in the description and the claims, have elastase inhibitory properties, especially against human neutrophil elastase, and can be used for preventing infections or diseases related to such infections in healthy individuals or for slowing infections in infected patients. The compounds of the invention can further be used where cancer, or immunological diseases, or pulmonary diseases, or cardiovascular diseases, or neurodegenerative diseases, or inflammation, or diseases related to inflammation, are mediated or resulting from elastase activity. These peptidomimetics can be manufactured by a process which is based on a mixed solid- and solution phase synthetic strategy.
    • 通式为(Xaa1-Xaa2-Thr3-Xaa4-Ser5-Xaa6-Xaa7-Xaa8-Xaa9-Xaa10-Xaa11-Xaa12-Xaa13-)的β-发夹肽模拟物及其药学上可接受的盐与Xaa1,Xaa2,Xaa4 作为在说明书和权利要求书中定义的某些类型的氨基酸残基的Xaa6,Xaa7,Xaa8,Xaa9,Xaa10,Xaa11,Xaa12和Xaa13具有弹性蛋白酶抑制性质,特别是针对人嗜中性粒细胞弹性蛋白酶,并且可用于预防 感染或与健康个体感染有关的疾病或感染患者感染减缓。 本发明的化合物可以进一步用于由弹性蛋白酶活性介导或由弹性蛋白酶活性介导的癌症或免疫疾病或肺部疾病或心血管疾病或神经变性疾病或炎症或与炎症有关的疾病。 这些肽模拟物可以通过基于混合固相和溶液相合成策略的方法制造。
    • 9. 发明申请
    • DYE CONJUGATES OF TEMPLATE-FIXED PEPTIDOMIMETICS
    • 模板固定肽的DYE结合
    • WO2006117011A1
    • 2006-11-09
    • PCT/EP2005/004751
    • 2005-05-02
    • POLYPHOR Ltd.UNIVERSITÄT ZÜRICHDE MARCO, Steven, J.GOMBERT, FrankOBRECHT, DanielLUDIN, ChristianROMAGNOLI, Barbara
    • DE MARCO, Steven, J.GOMBERT, FrankOBRECHT, DanielLUDIN, ChristianROMAGNOLI, Barbara
    • C07K7/64A61K38/04G01N33/68
    • C07K7/64A61K38/4886
    • Dye conjugates of template-fixed β-hairpin peptidomimetics of the general formula (I) wherein Z is a template-fixed chain of 14 α-amino acid residues which, depending on their positions in the chain (counted starting from the N-terminal amino acid), are Gly, or Pro or of certain types which, as the remaining symbols in the above formula, are defined in the description and the claims, and salts thereof, have CXCR4 antagonizing properties, and are useful for cancer therapy; diagnostic imaging; for detection of tumors and other abnormalties; for photoacoustic tumor imaging, detection and therapy; and for sonofluorescence tumor imaging, detection and therapy. The various dyes forming part of these conjugates are useful over the range of 300-1200 nm, the exact range being dependent upon the particular dye. These dye conjugates of β-hairpin peptidomimetic can be manufactured by processes which are based on a mixed solid- and solution phase synthetic strategy.
    • 通式(I)的模板固定的β-发夹肽模拟物的染料缀合物,其中Z是14个氨基酸残基的模板固定链,其取决于其在链中的位置(从N-末端氨基开始计数 酸)是Gly或Pro或某些类型,其作为上述式中的其余符号在说明书和权利要求书及其权利要求书中定义及其盐具有CXCR4拮抗性质,并且可用于癌症治疗; 诊断成像; 用于检测肿瘤等异常; 用于光声肿瘤成像,检测和治疗; 并用于超声荧光肿瘤成像,检测和治疗。 形成这些共轭物的一部分的各种染料在300-1200nm的范围内是有用的,确切的范围取决于特定的染料。 β-发夹肽模拟物的这些染料缀合物可以通过基于混合固相和溶液相合成策略的方法制备。