The present invention provides an agent for the prophylaxis or treatment of complications after coronary-artery bypass surgery or cardiac diseases, autoimmune diseases, central nervous system diseases, inflammatory diseases, sepsis, severe sepsis or septic shock in a patient who undergoes coronary-artery bypass surgery, which comprises a compound represented by the formula (I):
wherein each symbol is as defined in the specification, or a compound represented by the formula (II):
wherein each symbol is as defined in the specification, or a salt thereof or a prodrug thereof, and an agent for the prophylaxis or treatment of sepsis and the like, as well as complications after coronary-artery bypass surgery, which is prepared for administration of ethyl (6R)-6-[(2-chloro-4-fluoroanilino)sulfonyl]-1-cyclohexene-1-carboxylate or a salt thereof or a prodrug thereof in a specific dose at a specific administration time.
The present invention relates to a pharmaceutical agent containing an anti-sepsis drug (e.g., cycloalkene compound), and at least one kind of drug selected from the group consisting of an antibacterial agent, an antifungal agent, a non-steroidal antiinflammatory drug, a steroid and an anticoagulant in combination.
The present invention provides an emulsion composition comprising (A) a compound stable in an acidic range, and (B) a buffer, wherein the pH is adjusted from about 3.7 to about 5.5.
An emulsion composition containing a compound represented by the formula:
1
wherein R is an aliphatic hydrocarbon group optionally having substituents, an aromatic hydrocarbon group optionally having substituents, a heterocyclic group optionally having substituents, a group represented by the formula: —OR
1
(wherein R
1
is a hydrogen atom or an aliphatic hydrocarbon group optionally having substituents) or a group represented by the formula:
2
wherein R
1b
is a hydrogen atom or an aliphatic hydrocarbon group optionally having substituents, R
1c
is the same as or different from R
1b
and is a hydrogen atom or an aliphatic hydrocarbon group optionally having substituents, R
0
is a hydrogen atom or an aliphatic hydrocarbon group, or R and R
0
in combination represent a bond, Ar is an aromatic hydrocarbon group optionally having substituents
3
and the like, and n is an integer of 1 to 4, a salt thereof or a prodrug thereof, wherein the composition is adjusted to have a pH of not more than about 6, shows improved stability of the compound, a salt thereof or a prodrug thereof, and realizes expression of superior efficacy.
CYCLOALKENE DERIVATIVES, PROCESS FOR PRODUCING THE SAME, AND USE
申请人:Takeda Chemical Industries, Ltd.
公开号:EP1063228A1
公开(公告)日:2000-12-27
Compounds represented by formula (1a) or salts thereof, which are preventives/remedies for heart diseases, autoimmune diseases, inflammatory diseases, septic shock, etc., wherein R represents an optionally substituted aliphatic hydrocarbon group, optionally substituted aromatic hydrocarbon group, optionally substituted heterocyclic group, group represented by OR1 (wherein R1 represents hydrogen or an optionally substituted aliphatic hydrocarbon group), or group represented by formula (A) (wherein R1b band R1c are the same or different and each represents hydrogen or an optionally substituted aliphatic hydrocarbon group); R0 represents hydrogen or an aliphatic hydrocarbon group, or R and R0 in combination represent a bond; Ar represents an optionally substituted aromatic hydrocarbon group; and (B) or (C) where n is an integer of 1 to 4.
式(1a)代表的化合物或其盐,可预防/治疗心脏病、自身免疫性疾病、炎症性疾病、脓毒性休克等、其中 R 代表任选取代的脂肪族烃基、任选取代的芳香族烃基、任选取代的杂环基、由 OR1 代表的基团(其中 R1 代表氢或任选取代的脂肪族烃基)或由式(A)代表的基团(其中 R1b 带 R1c 相同或不同,且各自代表氢或任选取代的脂肪族烃基);R0 代表氢或脂族烃基,或 R 和 R0 结合代表键; Ar 代表任选取代的芳族烃基;以及 (B) 或 (C) 其中 n 为 1 至 4 的整数。