摘要:
Ectoparasitic insect pest controllers for animals, containing hydrazine derivatives of the general formula (I) as the active ingredient, and methods for application of the same: (I) [wherein A is (II), (III), (IV), (V) (wherein R4 and R5 are each H, C1-6 alkyl, or the like; and X is H, or one to five substituents selected from among halogeno and optionally halogenated C1-6 alkyl groups); R1 is H or C1-6 alkyl; R2 and R3 are each H, OH, C1-6 alkyl, phenylcarbonyl, or the like; Y is H, or one to five substituents selected from among halogeno, nitro, and cyano; Z is halogeno, cyano, C1-6 alkyl, or the like; and W is O or S]. The insect pest controllers exert remarkable controlling effects on parasitic insect pests harmful to domestic or pet animals, e.g. fleas, lice, ticks.
摘要:
The present invention relates to urethanes and the thio and dithio analogues thereof of general formula 1 wherein m, n, A, X, Y and R1 to R8 are defined as in claim 1, the enantiomers, diastereomers and the salts thereof, particularly the physiologically acceptable acid addition salts thereof which have valuable properties, particularly an inhibitory effect on cholesterol biosynthesis, pharmaceutical compositions containing these compounds, their use and processes for preparing them.
摘要:
The present invention provides therapeutically useful substituted guanidines and methods of treatment and pharmaceutical compositions that utilize or comprise one or more of such guanidines.
摘要:
The present invention provides therapeutically useful substituted guanidines and methods of treatment and pharmaceutical compositions that utilize or comprise one or more of such guanidines.
摘要:
A novel N-phenylcarbamate compound or its salt where possible, which is useful as the active ingredient of a biocidal composition for control of harmful organisms, is represented by the following general formula (I): ##STR1## wherein R.sup.1 is unsubstituted or substituted alkyl; R.sup.2 is H, unsubstituted or substituted alkyl, alkenyl, alkynyl or cycloalkyl, or --COX.sup.1 wherein X.sup.1 is unsubstituted or substituted alkyl, alkenyl, alkynyl, cycloalkyl or alkoxy; Z is --CH.sub.2 S--, --SCH.sub.2 --, --CH.sub.2 O--, --OCH.sub.2 --, --CH.sub.2 CH.sub.2 --, --CH.dbd.CH--, --C.tbd.C--, --CH.sub.2 SO--, --CH.sub.2 SO.sub.2 --, --CH.sub.2 SCH.sub.2 --, or --CH.sub.2 O--N.dbd.C(R.sup.4)--; R.sup.3 is unsubstituted or substituted phenyl, pyridyl, benzothiazolyl, benzoxazolyl, benzimidazolyl, imidazopyridyl, naphthyl, pyrimidinyl, thienyl, furyl, thiazolinyl, oxazolinyl, pyrazinyl, thiazolyl, oxazolyl, imidazolyl, pyrazolyl, quinolyl, indolyl, pyrrolyl, benzofuryl, benzothienyl, indanyl, tetrahydronaphthyl, dihydrobenzofuryl, dihydrobenzothienyl, benzoxazinyl, benzothiazinyl or benzoyl.
摘要翻译:一种新颖的N-苯基氨基甲酸酯化合物或其盐,其可用作用作控制有害生物的杀生物组合物的活性成分,由以下通式(I)表示:其中R 1为未取代的 或取代的烷基; R2是H,未取代或取代的烷基,烯基,炔基或环烷基,或-COX1,其中X1是未取代或取代的烷基,烯基,炔基,环烷基或烷氧基; Z是-CH 2 S - , - CH 2 - , - CH 2 O - , - OCH 2 - , - CH 2 CH 2 - , - CH = CH-, - C 3BOND C - , - CH 2 SO-, - CH 2 SO 2 - N = C(R 4) - ; R 3是未取代或取代的苯基,吡啶基,苯并噻唑基,苯并恶唑基,苯并咪唑基,咪唑并吡啶基,萘基,嘧啶基,噻吩基,呋喃基,噻唑啉基,恶唑啉基,吡嗪基,噻唑基,恶唑基,咪唑基,吡唑基,喹啉基,吲哚基,吡咯基,苯并呋喃基,苯并噻吩基, 二氢苯并噻吩基,苯并恶嗪基,苯并噻嗪基或苯甲酰基。
摘要:
Compounds of formula I ##STR1## and their salts in which R.sub.1 is optionally substituted phenyl, R.sub.2 is alkyl, cycloalkyl or optionally substituted amino, or R.sub.2 and R.sub.3 together with the nitrogen and carbon atoms to which they are attached form an optionally substituted heterocyclic ring or R.sub.3 and R.sub.4 together with the nitrogen atom to which they are attached form an optionally substituted heterocyclic ring and R.sub.5 is H, halo, alkyl, alkoxy, trifluoromethyl or a group of formula S(O).sub.m R.sub.8 in which m is 0, 1 or 2 and R.sub.8 is alkyl have utility in the treatment of diabetes particularly in the treatment of hyperglycaemia.
摘要翻译:式Ⅰ的化合物及其盐,其中R 1为任选取代的苯基,R 2为烷基,环烷基或任选取代的氨基,或R 2和R 3与它们所连接的氮原子和碳原子一起形成任选取代的杂环 环或R3和R4与它们所连接的氮原子一起形成任选取代的杂环,R 5是H,卤素,烷基,烷氧基,三氟甲基或式S(O)m R 8基团,其中m是0,1 或2和R8是烷基,可用于治疗糖尿病,特别是治疗高血糖症。
摘要:
Heat-sensitive recording materials contain an electron-donating chromogenic compound and an electron-attracting compound. The recording materials also contain at least one compound represented by the following formula: ##STR1## wherein R.sub.1 and R.sub.3 mean a hydrogen atom or an alkyl, aralkyl or aryl group, R.sub.2 and R.sub.4 denote an alkyl, alkenyl, aralkyl or aryl group, X.sub.1, X.sub.2, Y.sub.1 and Y.sub.2 stand for an oxygen or a sulfur atom, and --Z.sub.1 -- and --Z.sub.2 -- are a specific aromatic group. Also provided are phenol compounds represented by the following formula: ##STR2## wherein R.sub.1, R.sub.2, X.sub.1 and Y.sub.1 have the same meanings as defined above; R.sub.5 and R.sub.6 are a hydrogen or halogen atom or an alkyl, alkoxy, aralkyl, aryl or hydroxyl group; p and q stand for an integer of 1-4; R.sub.5 and R.sub.6 may be either the same or different when p and q represent an integer of 2 or greater; and --Z.sub.3 -- means a specific divalent group.
摘要:
The invention concerns novel (oxamido- and ureido-phenylsulfonyl)nitromethane derivatives and pharmaceutically acceptable salts thereof which are inhibitors of the enzyme aldose reductase and are of value, for example, in the treatment of certain peripheral effects of diabetes and galactosemia. Also disclosed are pharmaceutical compositions containing one of the derivatives and processes for the manufacture and use of the derivatives.
摘要:
There is disclosed a silver halide color photographic material having a silver halide emulsion layer on a base which comprises a novel cyan coupler. According to the disclosure, a silver halide color photographic material containing a cyan coupler that has high coupling reactivity and high color density, resulting color image being hardly susceptible to reduction fading and is excellent in heat fast can be obtained.