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    • 2. 发明授权
    • Intake system for vehicle internal combustion engine
    • 汽车内燃机进气系统
    • US08137425B2
    • 2012-03-20
    • US12524621
    • 2008-01-29
    • Haruhiko SaitoTatsuya Oyama
    • Haruhiko SaitoTatsuya Oyama
    • B01D46/00
    • F02M35/10321F02B27/005F02M35/02F02M35/10013F02M35/108F02M35/161Y02T10/146
    • An intake system (10, 20) for a vehicle internal combustion engine is provided in which a first air intake duct (16), having an air intake inlet (16a) to inhale external air, is connected to an air cleaner box (14). A second air intake duct (17, 27) is also connected to the air cleaner box. The air intake inlet is closer to the air cleaner box than the second air intake duct is. The cross section area of a second air intake duct is greater than the cross section area of the first air intake duct. The center axis of the second air intake duct at an end on the side of a second air intake opening (12, 22) intersects with the center axis of the first air intake duct at an end on the side of a first air intake opening (11).
    • 提供了一种用于车辆内燃机的进气系统(10,20),其中具有吸入外部空气的进气口(16a)的第一进气管道(16)连接到空气滤清器箱(14) 。 第二进气管道(17,27)也连接到空气滤清器箱。 进气口比第二进气管更靠近空气滤清器箱。 第二进气管道的横截面面积大于第一进气管道的横截面面积。 在第二进气口(12,22)侧的端部处的第二进气管道的中心轴线与第一进气口侧的端部处的第一进气管道的中心轴线相交 11)。
    • 4. 发明授权
    • Heteroaryl derivatives
    • 杂芳基衍生物
    • US08217031B2
    • 2012-07-10
    • US12593566
    • 2008-03-28
    • Masato MatsuokaTatsuya Oyama
    • Masato MatsuokaTatsuya Oyama
    • A61K31/55C07D223/16
    • C07D491/048C07D495/04
    • The present invention relates to a compound represented by formula [1] or a pharmaceutically acceptable salt thereof: In formula [1], one of X and Y is CH and the other is oxygen or sulfur; R is hydrogen, etc.; Z is hydrogen, etc.; Ar is phenyl, etc.; and n is 1 or 2 and or m is 1 or 2, excluding compounds where n is 2 and m is 2 simultaneously. Also provided is a pharmaceutical composition comprising a compound of formula [1] or a pharmaceutically acceptable salt thereof as an active ingredient. The composition is usable as an agent for the prevention or treatment of depression, panic disorder, anxiety, obsessive-compulsive disorder, chronic pain, fibromyalgia, obesity, stress urinary incontinence, and overactive bladder.
    • 本发明涉及由式[1]表示的化合物或其药学上可接受的盐:在式[1]中,X和Y之一是CH,另一个是氧或硫; R是氢等; Z是氢等; Ar是苯基等; n为1或2,m为1或2,不包括n为2,m为2的化合物。 还提供了包含式[1]化合物或其药学上可接受的盐作为活性成分的药物组合物。 该组合物可用作预防或治疗抑郁症,恐慌症,焦虑症,强迫症,慢性疼痛,纤维肌痛,肥胖,压力性尿失禁和膀胱过动症的药剂。
    • 5. 发明申请
    • Antipruritics
    • 止痒药
    • US20080103162A1
    • 2008-05-01
    • US11981315
    • 2007-10-30
    • Tatsuya OyamaKyoko Sakana
    • Tatsuya OyamaKyoko Sakana
    • A61K31/517A61P17/04
    • C07D401/06A61K31/00A61K31/517C07D239/94
    • The present invention relates to an antipruritic agent comprising a nociceptine antagonist as an active ingredient. The nociceptine antagonist can be used as a preventive or remedy for diseases associated with itching (for example, atopic dermatitis and urticaria), local pruritus cutaneous caused by insect excretion and secretion, nodular prurigo, kidney dialysis, diabetes, blood disease, liver disease, kidney disease, incretion and metabolic disorder, viscera malignant tumor, hyperthyroidism, autoimmune disease, multiple sclerosis, neurologic disease, psychoneurosis, allergic conjunctivitis, spring catarrh, atopic keratoconjunctivitis, or itching caused by excess use of laxuries and drugs because it has excellent scratching behavior suppressing effect, that is, antiitching effect and antipruritic effect.
    • 本发明涉及含有止痛剂拮抗剂作为活性成分的止痒剂。 伤害性疼痛拮抗剂可用作与瘙痒相关疾病(例如特应性皮炎和荨麻疹)的预防或治疗,由昆虫排泄和分泌引起的皮肤局部瘙痒,结节性瘙痒,肾透析,糖尿病,血液病,肝脏疾病, 肾脏疾病,增生和代谢紊乱,内脏恶性肿瘤,甲状腺功能亢进,自身免疫性疾病,多发性硬化,神经系统疾病,精神病,过敏性结膜炎,春季卡他症,特应性角膜结膜炎,或过度使用松弛症和药物引起的瘙痒,因为它具有优异的划痕行为 抑制作用,即防止止痛作用和止痒作用。
    • 8. 发明申请
    • QUINAZOLINE DERIVATIVES AND PHARMACEUTICAL COMPOSITIONS THEREOF
    • 喹诺酮衍生物及其药物组合物
    • US20100022566A1
    • 2010-01-28
    • US12089087
    • 2006-10-03
    • Masahiko OkanoTatsuya Oyama
    • Masahiko OkanoTatsuya Oyama
    • A61K31/517C07D239/72A61P17/02A61P17/06
    • C07D239/94C07D401/12C07D401/14C07D403/12C07D405/12C07D405/14C07D413/12C07D413/14
    • The present invention relates to novel quinazoline derivatives with less skin irritation and an excellent action of strongly suppressing scratching behavior, and pharmaceutical compositions containing a quinazoline derivative as an active ingredient. The present invention is directed to the quinazoline derivatives represented by the general formula [1] or pharmaceutically acceptable salts thereof. In the general formula [1], R1 represents hydrogen or the like; R2 represents hydrogen or the like; R3 and R4 are the same or different and represent hydrogen, alkyl, alkoxy or halogen; R5 is combined with R6 to represent alkylene or represents hydrogen, hydroxy, alkyl, phenyl or alkoxy; R6 represents alkyl, cycloalkyl, phenyl, a 5- to 10-membered aromatic heterocyclic group containing one to three heteroatoms selected from the group consisting of a nitrogen atom, an oxygen atom and a sulfur atom, or —N(R6-1)(R6-2).
    • 本发明涉及具有较少皮肤刺激性和强烈抑制划伤行为的优异作用的新型喹唑啉衍生物以及含有喹唑啉衍生物作为活性成分的药物组合物。 本发明涉及由通式[1]表示的喹唑啉衍生物或其药学上可接受的盐。 在通式[1]中,R 1表示氢等; R2表示氢等; R3和R4相同或不同,代表氢,烷基,烷氧基或卤素; R5与R6结合表示亚烷基或代表氢,羟基,烷基,苯基或烷氧基; R6表示烷基,环烷基,苯基,含有1至3个选自氮原子,氧原子和硫原子的杂原子的5至10元芳族杂环基或-N(R 6-1)( R6-2)。
    • 9. 发明授权
    • Quinazoline derivatives and pharmaceutical compositions thereof
    • 喹唑啉衍生物及其药物组合物
    • US08431586B2
    • 2013-04-30
    • US12089087
    • 2006-10-03
    • Masahiko OkanoTatsuya Oyama
    • Masahiko OkanoTatsuya Oyama
    • A61K31/517
    • C07D239/94C07D401/12C07D401/14C07D403/12C07D405/12C07D405/14C07D413/12C07D413/14
    • The present invention relates to novel quinazoline derivatives with less skin irritation and an excellent action of strongly suppressing scratching behavior, and pharmaceutical compositions containing a quinazoline derivative as an active ingredient. The present invention is directed to the quinazoline derivatives represented by the general formula [1] or pharmaceutically acceptable salts thereof. In the general formula [1], R1 represents hydrogen or the like; R2 represents hydrogen or the like; R3 and R4 are the same or different and represent hydrogen, alkyl, alkoxy or halogen; R5 is combined with R6 to represent alkylene or represents hydrogen, hydroxy, alkyl, phenyl or alkoxy; R6 represents alkyl, cycloalkyl, phenyl, a 5- to 10-membered aromatic heterocyclic group containing one to three heteroatoms selected from the group consisting of a nitrogen atom, an oxygen atom and a sulfur atom, or —N(R6-1)(R6-2).
    • 本发明涉及具有较少皮肤刺激性和强烈抑制划伤行为的优异作用的新型喹唑啉衍生物以及含有喹唑啉衍生物作为活性成分的药物组合物。 本发明涉及由通式[1]表示的喹唑啉衍生物或其药学上可接受的盐。 在通式[1]中,R 1表示氢等; R2表示氢等; R3和R4相同或不同,代表氢,烷基,烷氧基或卤素; R5与R6结合表示亚烷基或代表氢,羟基,烷基,苯基或烷氧基; R6表示烷基,环烷基,苯基,含有1至3个选自氮原子,氧原子和硫原子的杂原子的5至10元芳族杂环基或-N(R 6-1)( R6-2)。