摘要:
The invention relates to a peptide consisting of 7-17 adjoining amino acids and comprising the hexamer TX 1 EX 2 X 3 E, where X 1 , X 2 and X 3 can each be a natural or non-natural amino acid, wherein the peptide has no TNF receptor binding activity and is cyclized, for preventing and treating the hyperpermeability of epithelial cells and endothelial cells.
摘要翻译:描述了一种肽,其由7-17个相邻氨基酸组成并且包含六聚体TX EX XE,其中X,X和X可以是任何天然或非天然氨基酸,其中所述肽不具有TNF受体结合活性,并且是 环化,用于预防和治疗上皮细胞和内皮细胞的高渗透性。
摘要:
The invention relates to a protein which is selected from the amino acid sequence of the region valine Val(91) to glycine Gly(121) of the mature, human tumor necrosis factor, or a part thereof, provided that the protein comprises at least the amino acid sequence of the region lysine Lys(98) to glutamic acid Glu(116), the cysteine Cys(101) being replaced by a glycine and an amide bond being formed between the amino group of the side chain of the lysine Lys(98) and the carboxyl group of the side chain of the glutamic acid Glu(116). The protein activates epithelial ion channels and improves the pulmonary function and can be used to produce drugs for the treatment of diseases that are associated with the pulmonary function, such as oedema.
摘要:
Disclosed is a dry-powder peptide medicament with a non-typical concentration of carbohydrate excipient, as well as said medicament for use in treatment or prevention of a disease or condition, as well as methods for manufacturing said medicament.
摘要:
where X1 includes an amino acid sequence with 1 to 4 members having one or more natural or unnatural amino acids selected from: C, KSP, K, ornithin, 4-amino butanoic acid, β-alanine, 6-amino-hexanoic acid, and 7-amino-heptanoic acid; where X2 is one natural amino acid selected from: C, D, G and E; and where prior to cyclization, X1 is the N-terminus and X2 is the C-terminus.
摘要:
A method of conditioning/improving lung functions extracorporeally by treatment of a lung ex vivo with a cyclized compound of the amino acid sequence of formula X1-GQRETPEGAEAKPWY-X2 I wherein X1 comprises an amino acid (sequence) with 1 to 4 members, comprising natural or unnatural amino acids, and X2 comprises one amino acid, selected from natural amino acids; and a pharmaceutical composition, comprising a peptide of formula I as defined in any one of claims 1 to 7, in a form, which is appropriate for spraying to obtain an aerosol for inhalation, or which is appropriate for the preparation of a spray to obtain an aerosol upon spraying, which is appropriate for inhalation.