摘要:
A non-reciprocal circuit device comprising a magnetic plate F1; center conductors L1, L2, and L3 that are mutually insulated and disposed so as to intersect on magnetic plate F1; a plane conductor P1 that is disposed facing the center conductors with magnetic plate F1 placed therebetween, the plane conductor being connected to first ends of all the center conductors; matching capacitors C1 to C3 that have first ends grounded electrically and second ends connected to second ends of the center conductors; first matching circuits that have first ends connected to the second ends of the center conductors and second ends that are input/output ports; and a second matching circuit that has a first end connected to or integrated with the plane conductor and a second end grounded electrically.
摘要:
An objective of the present invention is to provide compounds having antitumor activity. According to the present invention, there is provided compounds represented by formula (I) and pharmaceutically acceptable salts thereof, and solvates thereof: wherein R1 represents H or a substitutable unsaturated five- or six-membered heterocyclic ring; R2 represents H; X represents CH or N; Z represents O or S; E is absent or represents halogen, alkyl, or alkoxy; J represents S or O; and T represents phenyl, an unsaturated five- or six-membered heterocyclic ring, an unsaturated nine- or ten-membered bicyclic carbocyclic ring or heterocyclic ring.
摘要:
There are provided compounds which can be used in the treatment of diseases mediated by the autophosphorylation of a PDGF receptor, specifically, compounds which can inhibit neointima formation hypertrophy. The compounds are those represented by formula (I) or pharmacologically acceptable salts or solvates thereof: wherein R1 and R2 represent hydrogen, alkyl or the like; R3, R4, R5, and R6 represent hydrogen, halogen, alkyl, alkoxy or the like; R11 and R12 represent hydrogen, alkyl, alkylcarbonyl or the like; and A represents any one of formulae (i) to (x), provided that compounds wherein R3, R4, R5 and R6 represent hydrogen and A represents group (v) wherein u is 0 (zero) and R19 represents phenyl optionally substituted by halogen, alkyl, or alkoxy are excluded.
摘要翻译:提供的化合物可用于治疗由PDGF受体的自磷酸化介导的疾病,特别是可抑制新内膜形成肥大的化合物。 化合物是由式(I)表示的化合物或其药学上可接受的盐或溶剂化物:其中R 1和R 2代表氢,烷基等; R 3,R 4,R 5和R 6代表氢,卤素,烷基,烷氧基或 喜欢; R 11和R 12代表氢,烷基,烷基羰基等; 并且A表示式(i)至(x)中的任何一个,条件是其中R 3,R 4,R 5和R 5的化合物 代表氢,A代表其中u为0(零)且R 19表示任选被卤素,烷基或烷氧基取代的苯基的基团(ⅴ)。
摘要:
A first line stub SB1 and one end of each of two switches SW1 and SW2 are connected to a transmission line 11L at spacings L1, L2 and L3 in order from the input end of the transmission line 11L, the other ends of the two switches are connected to a second line stub SB2, the first and second line stubs have an open end or short-circuit end, and matching at any of four frequency bands can be selected by combining on and off of the two switches SW1 and SW2.
摘要:
An irreversible circuit element is configured by including a magnetic substance, a plurality of central conductors L1 to L3, one ends of which are connected to different input/output ports, arranged on the magnetic substance so as to intersect each other while being insulated from each other, a first conductor P1 connected to the other ends of all the central conductors L1 to L3, a second conductor, a plurality of matching capacitors (each configured by C1 to C3) connecting the one end of the central conductors L1 to L3 and the second conductor and a variable matching mechanism V1, one end of which is connected or integrated with the second conductor, capable of changing reactance between the one end and the other end thereof.
摘要:
An irreversible circuit element is configured by including a magnetic substance, a plurality of central conductors L1 to L3, one ends of which are connected to different input/output ports, arranged on the magnetic substance so as to intersect each other while being insulated from each other, a first conductor P1 connected to the other ends of all the central conductors L1 to L3, a second conductor, a plurality of matching capacitors (each configured by C1 to C3) connecting the one end of the central conductors L1 to L3 and the second conductor and a variable matching mechanism V1, one end of which is connected or integrated with the second conductor, capable of changing reactance between the one end and the other end thereof.
摘要:
A ring-fused heterocyclic derivative represented by the following general formula (I) or a pharmaceutically acceptable salt thereof having a T-type calcium channel regulatory effect and useful as a pruritus therapeutic and/or preventive agent, and the like are provided. In the general formula (I), R1 represents optionally substituted lower alkyl, and the like; R2 represents an optionally substituted cycloalkyl, and the like; Q represents a hydrogen atom, and the like; R3 represents —C(═O)NR8R9 (wherein R8 and R9 may be the same or different, and each represents a hydrogen atom, and the like), and the like; L1 represents —CR11AR11B— (wherein R11A and R11B may be the same or different, and each represents a hydrogen atom, and the like), and the like; and W1 and W2 may be the same or different, and each represents C—R12 (wherein R12 represents a hydrogen atom, and the like), and the like.
摘要翻译:提供由具有T型钙通道调节作用并可用作瘙痒治疗和/或预防剂的由以下通式(I)表示的环稠合杂环衍生物或其药学上可接受的盐。 在通式(I)中,R 1表示任选取代的低级烷基等; R2表示任选取代的环烷基等; Q表示氢原子等; R 3表示-C(= O)NR 8 R 9(其中R 8和R 9可以相同或不同,各自表示氢原子等)等。 L1表示-CR11AR11B-(其中R11A和R11B可以相同或不同,各自表示氢原子等)等。 并且W1和W2可以相同或不同,并且各自表示C-R12(其中R12表示氢原子等)等。
摘要:
The present invention provides a nitrogen-containing aromatic heterocyclic derivative represented by formula (I): [wherein W represents CR3 (wherein R3 represents a hydrogen atom or the like) or the like, R4 represents a hydrogen atom or the like, R5 represents a hydrogen atom or the like, R9 represents substituted imidazolyl, R12 and R13 may be the same or different, each represent a hydrogen atom or the like, R22 and R23 may be the same or different, each represent a hydrogen atom or the like, R24 represents a hydrogen atom or the like, Y represents C—R25 (wherein R25 represents a hydrogen atom or the like) or the like] or a pharmaceutically acceptable salt thereof and a FGFR inhibitor comprising, as an active ingredient, the nitrogen-containing aromatic heterocyclic derivative or the pharmaceutically acceptable salt thereof, or the like.
摘要:
A PAPR observation unit that measures PAPR in a distributed output of an input signal and PAPR in a combined output of a linear transmission path and a third order distortion generation path, a distortion observation unit that observes distortion in the output of a power amplifier, and a controller are provided, where the controller includes a third order out-of-band distortion compensation coefficient control unit that adjusts coefficients corresponding to an outside of an input signal band among frequency characteristic compensator coefficients on the basis of distortion observed by the distortion observation unit and a third order in-band distortion coefficient control unit that adjusts coefficients corresponding to an inside of the input signal band among frequency characteristic compensator coefficients on the basis of the observed PAPR.
摘要:
A first line stub SB1 and one end of each of two switches SW1 and SW2 are connected to a transmission line 11L at spacings L1, L2 and L3 in order from the input end of the transmission line 11 L, the other ends of the two switches are connected to a second line stub SB2, the first and second line stubs have an open end or short-circuit end, and matching at any of four frequency bands can be selected by combining on and off of the two switches SW1 and SW2.