摘要:
The present invention provides compounds of formula (I) in which R is as defined in the specification, or a pharmaceutically acceptable metabolically labile ester or amide thereof, or a pharmaceutically acceptable salt thereof, which are useful as antagonists of one or more of the actions of L-glutamate at metabotropic excitatory amino acid receptors.
摘要:
Novel pesticidal compositions, which are characterized by biodegradability and do not bioaccumulate to an unacceptable level in fats and tissues of animals, fowl and fish, containing active compounds and optionally a carrier suitable for administering said compounds to a pest by contact, ingestion or inhalation, are disclosed. Such compositions comprise in addition to the carrier compounds of formula (I), where R is H, Cl or other Hal, hydroxyl, lower alkoxyl, lower alkyl, cyano, CONR2 or NR2, where R2 is H or lower alkyl; X and Y may be R, and when taken together may be -0- or a saturated or unsaturated monocyclic or bicyclic group which may be substituted with R, epoxide, carboxy or carboxymethyl group; and the unsaturated analogs thereof wherein the unsaturation occurs at at least one of the 2 or the 5 positions, and wherein unsaturation may occur optionally in the ring formed by X and Y taken together; with the further proviso that said compound has between 4 and 6 halogens; and a carrier for said compound. Methods of using such pesticides to kill or disable pests are disclosed. Certain novel compounds within the group and novel methods of making said compounds are disclosed.
摘要:
Novel pesticidal compositions, which are characterized by biodegradability and do not bioaccumulate to an unacceptable level in fats and tissues of animals, fowl and fish, containing active compounds and optionally a carrier suitable for administering said compounds to a pest by contact, ingestion or inhalation, are disclosed. Such compositions comprise in addition to the carrier compounds of formula (I), where R is H, Cl or other Hal, hydroxyl, lower alkoxyl, lower alkyl, cyano, CONR2 or NR2, where R2 is H or lower alkyl; X and Y may be R, and when taken together may be -0- or a saturated or unsaturated monocyclic or bicyclic group which may be substituted with R, epoxide, carboxy or carboxymethyl group; and the unsaturated analogs thereof wherein the unsaturation occurs at at least one of the 2 or the 5 positions, and wherein unsaturation may occur optionally in the ring formed by X and Y taken together; with the further proviso that said compound has between 4 and 6 halogens; and a carrier for said compound. Methods of using such pesticides to kill or disable pests are disclosed. Certain novel compounds within the group and novel methods of making said compounds are disclosed.
摘要:
L'invention concerne de nouvelles compositions pesticides, caractérisées par une biodégradabilité et ne se bioaccumulant pas à un niveau inacceptable dans des matières grasses et des tissus d'animaux, de volailles et de poissons, contenant des composés actifs et facultativement un support adapté pour l'administration desdits composés aux parasites par contact, ingestion ou inhalation. Lesdites compositions comprennent, en plus du support, des composés de la formule (I), dans laquelle R représente H, Cl ou encore Hal, hydroxyle, alkoxy inférieur, alkyle inférieur, cyano, CONR2 ou NR2 ou R2 représente H ou alkyle inférieur; X et Y peuvent représenter R, et lorsqu'on les prend ensemble ils peuvent représenter -0- ou un groupe monocyclique ou bicyclique saturé ou non saturé pouvant être à substitution de R, d'un groupe époxyde, carboxy ou carboxyméthyle, ainsi que leurs analogues non saturés dans lesquels l'état insaturé peut avoir lieu facultativement dans l'anneau formé par X et Y pris ensemble; avec en plus la condition que ledit composé comporte 4 à 6 halogènes; ainsi qu'un support pour ledit composé. L'invention concerne en outre des procédés d'utilisation desdits pesticides afin de tuer ou d'annihiler les parasites, ainsi que certains composés nouveaux dans le groupe et certains nouveaux procédés de fabrication desdits composés.
摘要:
New compounds are described that fall within the general formula I wherein R' is hydrogen or a methoxy, ethoxy, propoxy, butoxy, tetrafluoroethoxy, methylthio, ethylthio, propylthio, fluoro, chloro, bromo, methyl, ethyl, or nitro group, and R 2 is hydrogen or a methyl group, or R' and R 2 together form a methylenedioxy group; and R 3 is hydrogen, or halogen or an esterifying group, as well as other derivatives of the acid. The I esterifying group may be a lower alkyl group, or one of the following groups (a) to (f):-
and Y 1 , y 2 , Y 3 , Y 4 , Y 5 and Y 6 are the same or different groups and each is hydrogen or a fluoro, bromo or chloro group, with the proviso that when R' is fluoro, chloro, bromo or methyl and R 2 is hydrogen, then one of Y' to Y 6 is other than hydrogen. Processes of making the compounds are described. The compounds in which R 3 is one of groups (a) to (f) are insecticides and insecticidal methods and compositions containing them are described.
摘要:
Compounds illustrated by general formula (I) useful as PDE IV inhibitors and for inhibiting the production of Tumor Necrosis Factor (TNF) are disclosed herein. In formula (I) R1 is C1-12 alkyl unsubstituted or substituted by 1 or more halogens; C3-6 cyclic alkyl unsubstituted or substituted by 1 to 3 methyl groups or one ethyl group; C4-6 cycloalkyl containing one or two unsaturated bonds; C7-11 polycycloalkyl, -(CR14R14)nC(O)-O-(CR14R14)m-R10, -(CR14R14)nC(O)-O-(CR14R14)r-R11, -(CR14R14)xOH, -(CR14R14)sO(CR14R14)m-R10, -(CR14R14)sO(CR14R14)r-R11, -(CR14R14)n-(C(O)NR14)-(CR14R14)m-R10, -(CR14R14)n-(C(O)NR14)-(CR14R14)r-R11, -(CR14R14)y-R11 or -(CR14R14)z-R10; X2 is O or NR14; X3 is hydrogen or X; X is YR2, halogen, nitro, NR14R14 or formamide; Y is O or S(O)m; R2 is -CH3 or -CH2CH3, each may be unsubstituted or substituted by 1 to 5 fluorines; A is (a), (b), (c), (d) or (e); B is >C=Z or C=S.