摘要:
A protein having amino acid sequence in SEQ ID No.:1 of the Sequence Listing derived from human MP52, and a dimer protein thereof. A homodimer protein described above can be obtained by constructing a plasmid containing DNA coding amino acid sequence in SEQ ID No.:1 of the Sequence Listing with a methionine at the N-terminus, introducing the plasmid into E . coli for transformation, solubilizing inclusion bodies obtained by culturing the transformant, purifying the monomer protein from the solubilized solution, refolding the monomer protein into a dimer protein and purifying the same. The homodimer protein described above is useful as a pharmaceutical composition for treating cartilage and bone diseases.
摘要翻译:衍生自人MP52的序列表的SEQ ID No.1中具有氨基酸序列的蛋白质及其二聚体蛋白质。 可以通过在N末端构建含有序列表SEQ ID No.1的DNA编码氨基酸序列的质粒与甲硫氨酸,将质粒导入大肠杆菌进行转化,溶解包合物来获得上述同型二聚体蛋白 通过培养转化体获得的物质,从溶解的溶液中纯化单体蛋白质,将单体蛋白质重新折叠成二聚体蛋白质并将其纯化。 上述同型二聚体蛋白质可用作治疗软骨和骨疾病的药物组合物。
摘要:
The invention concerns steroid compounds of general formula (I) in which n = 2, 3, either R1 and R2 = H, (C1-C4) alkyl, or R1 and R2 form with nitrogen a heterocyclic compound, X = OH optionally esterified, Y = (C1-C4)alkyl, and their additive salts, the method for preparing them, their application as medicine and the pharmaceutical compositions containing them.
摘要:
The invention concerns compounds of formula (I) in which R represents an alkyl radical optionally substituted or (CH2)nAr, n representing a whole number ranging from 0 to 6 and Ar representing an aryl or heteroaryl radical optionally substituted, and Z represents a hydrogen atom or the radical of a carboxylic acid. The compounds of formula (I) have very interesting antibiotic properties.
摘要:
The present invention relates to a novel process for the preparation of physostigmine carbamate derivatives and to pharmaceutically acceptable salts thereof. The present invention further relates to a novel process for the preparation of eseroline derivatives and to pharmaceutically acceptable salts thereof.
摘要:
The present invention relates to novel heterocyclic substituted pyrrolidine amide derivatives of formula (1), and stereoisomers and pharmaceutically acceptable salts thereof and their use as tachykinin receptor antagonists. Such antagonists are useful in the treatment of tachykinin-mediated diseases and conditions disclosed herein including: asthma, cough, and bronchitis.
摘要:
Die vorliegende Erfindung betrift ein verbessertes Verfahren zur Gewinnung eines Vorläufers von Insulinen oder Insulinderivaten mit korrekt verbundenen Cystinbrücken in Gegenwart von Cystein oder Cysteinhydrochlorid und von einem chaotropen Hilfsstoff.
摘要:
A mouse anti-human MP52 monoclonal antibody which binds to dimeric human MP52 but not to monomeric human MP52. This mouse monoclonal antibody comprising IgG and having a high specificity can be obtained by sensitizing mice with human MP52 (CHO-MP52) produced in CHO cells and human MP52 (rhMP52) produced in escherichia coli . This antibody is useful in, for example, purifying or assaying human MP52 produced b genetic engineering techniques.
摘要:
Die vorliegende Erfindung betrifft substituierte Imidazolidinderivate der Formel I, in der B, E, W, Y, R, R 2 , R 3 , R 30 , e und h die in den Ansprüchen angegebenen Bedeutungen haben. Die Verbindungen der Formel I sind wertvolle Arzneimittelwirkstoffe, die sich zum Beispiel zur Therapie und Prophylaxe von Entzündungserkrankungen, beispielsweise der rheumatoiden Arthritis, oder von allergischen Erkrankungen eignen. Die Verbindungen der Formel I sind Inhibitoren der Adhäsion und Migration von Leukozyten und/oder Antagonisten des zur Gruppe der Integrine gehörenden Adhäsionsrezeptors VLA-4. Sie eignen sich generell zur Therapie oder Prophylaxe von Krankheiten, die durch ein unerwünschtes Ausmaß an Leukozytenadhäsion und/oder Leukozytenmigration verursacht werden oder damit verbunden sind oder bei denen Zell-Zell- oder Zell-Matrix-Interaktionen eine Rolle spielen, die auf Wechselwirkungen von VLA-4-Rezeptoren mit ihren Liganden beruhen. Die Erfindung betrifft weiterhin Verfahren zur Herstellung der Verbindungen der Formel I, ihre Verwendung, insbesondere als Arzneimittelwirkstoffe, und pharmazeutische Präparate, die Verbindungen der Formel I enthalten.
摘要:
A process for producing a muturation bone morphogenetic protein by the action of a processing enzyme on a bone morphogenetic protein precursor, which comprisis either introducing an expression vector of a bone morphogenetic protein precursor and an expression vector of a processing enzyme into an animal cell strains, culturing the resultant strain to yield a maturation bone morphogenietc protein, and separating the same from the culture, or alternatively adding a solution of a processing enzyme to a solution of a bone morphogenetic protein precursor and incubating the obtained solution mixture. A suitable process comprises introducing an expression vector of a human MP52 precusor and an expression vector of a secretory furin variant into an established animal cell strain, culturing the resultant strain to yield a muturation bone morphogenetic protein, and separating the same from the culture.
摘要:
Verbindungen der Formel I mit den in den Ansprüchen angegebenen Bedeutungen der Substituenten sind hervorragend wirksame Substanzen zum Herstellen von Medikamenten zur Prophylaxe und zur Therapie von Herz-Kreislauferkrankungen, insbesondere Arrhythmien, zur Behandlung von Ulcera des Magen-Darm-Bereichs oder zur Behandlung von Durchfallerkrankungen.