摘要:
The invention relates to biocidal compounds of the formula RCH 2 NHR 1 or monomethyl or monoethyl ethers thereof, the compounds including the said ethers containing no more than 30 carbon atoms in total; esters thereof; salts thereof; wherein R = C 15-22 carbocyclic fused ring system containing 3-5 aromatic rings optionally substituted by 1-2 substituents, said substituents (containing ≤ 4 carbon atoms in total) being halogen; cyano; C 1-4 alkyl or C 1-4 alkoxy, each optionally substituted by OH or C 1-2 alkoxy; halogen substituted C 1-2 alkyl or C 1-2 alkoxy; S(O) n R 2 n = 0-2 and R 2 is C 1-2 alkyl optionally substituted by OH or C 1-2 alkoxy; or R is optionally substituted by NR 3 R 4 (which contains ≤ 5 carbons) wherein R 3 and R 4 = C 1 3 alkyl group or NR 3 R 4 forms a 5- or 6- membered heterocyclic ring optionally containing 1-2 additional heteroatoms; R 1 contains ≤ 8 carbons and is wherein m is 0 or 1; R 5 and R 6 = H or C 1-5 alkyl optionally substituted by OH; R 7 and R 8 = H, C 1-3 alkyl; -C-C-is a five-or-six-membered saturated carbocyclic ring; R 9 is H, CH 3 or CH 2 OH; R 10 , R 11 and R 12 = H or CH 3 ; R 13 = H, CH 3 , OH or CH 2 0H with the proviso that R is not substituted or unsubstituted perylene, fluoranthene, chrysene, pyrene or triphenylene. Also disclosed are formations containing the compounds, methods for their preparation, chemical intermediates in their preparation and the use of the compounds in the treatment of tumors and as antipathogenic agents particularly antifungal agents.
摘要:
Disclosed herein are novel D-(threo)-1-aryl-2-acylamido-3-fluoro-1-propanols of the general formula I and specified salts thereof, where R represents a specified alkyl, haloalkyl, halodeuteroalkyl, azidomethyl or methylsulfonylmethyl group, X and X' independently represent a hydrogen or halogen atom, a nitro, cyano or a substituted or unsubstituted phenyl group or represent a group R 1 (A) n in which group n is zero or 1, A is oxygen, sulfur, carbonyl, sulfinyl or sulfonyl and R is a specified lower alkyl, amino or lower alkyl amino group and Z is hydrogen or a specified acyl group. The novel compounds exhibit antibacterial activity and their use for this purpose is disclosed. Also disclosed are methods for the preparation of the novel compounds as well as certain novel intermediates therefor.
摘要:
A compound of formula (I): or a pharmaceutically acceptable salt thereof, wherein R A is a group of formula (a): wherein T represents a group of formula (b): wherein Q is , and where R' is a hydrogen or halogen atom or a -CF 3 , OR 4 , NHR 4 , -NHCOR 4 , -NHCONH 2 , NHSO 2 R 4 , CH 2 OR 4 or -CH 2 SO 2 R 4 group: R 2 is a hydrogen or halogen atom or an -OR 4 group; R 3 is a hydrogen or halogen atome; and R 4 is hydrogen, C 1-6 alkyl or benzyl; X' is a bond or -OCH 2 -; X 2 is a group of formula -CR 5 R 6 -CH 2 -A-wherein R 5 and R 6 are independently hydrogen or methyl; and A is a bond, -CH 2 -, or O; T' represents a hydrogen atom or a group of formula (b) as defined above in respect of T, such that T' and T may be the same or different; R C represents a group (a) as defined above in respect of R A , such that R C and R A may be the same or different; provided that when R A and R C each represent a group of formula: wherein R is oH or -O-benzyl; then when A is a bond, -CH 2 - or -0, R' is not -CH 2 OH or NHSO 2 -C 1-4 alkyl; processes for the preparation of such compounds and their use in medicine and agriculture.
摘要:
Disclosed herein are novel D-(threo)-1-aryl-2-acylamido-3-fluoro-1-propanols of the general formula I and specified salts thereof, where R represents a specified alkyl, haloalkyl, halodeuteroalkyl, azidomethyl or methylsulfonylmethyl group, X and X' independently represent a hydrogen or halogen atom, a nitro, cyano or a substituted or unsubstituted phenyl group or represent a group R 1 (A) n in which group n is zero or 1, A is oxygen, sulfur, carbonyl, sulfinyl or sulfonyl and R is a specified lower alkyl, amino or lower alkyl amino group and Z is hydrogen or a specified acyl group. The novel compounds exhibit antibacterial activity and their use for this purpose is disclosed. Also disclosed are methods for the preparation of the novel compounds as well as certain novel intermediates therefor.
摘要:
N 6 -Substittuted diarylalkyladenosines of the formula: are disclosed. Processes for their manufacture and pharmaceutical compositions containing the same are also disclosed. The compounds have highly desirable central- nervous system and cardio-vascular properties.
摘要:
A method for the preparation of an animal feed composition comprising admixing an animal feed with from 0.01 to 400 grams per ton of feed of a compound of the following formula wherein X, Y, Z, R,, R2, R 3 and R 4 are as defined in the text. Some new compounds with the same general formula are claimed. These phenylethanol amine derivatives and their acid addition salts act as growth promotors and fat reducing agents in farm and companion animals.