摘要:
Derivatives of benzo[5,6]cyclohepta pyridine, and pharmaceutically acceptable salts and solvates thereof are disclosed, which possess anti-allergic and anti-inflammatory activity. Methods for preparing and using the compounds are also described.
摘要:
Derivatives of 6,11-dihydro-11-(4-piperidylidene)-5H-benzo[5,6]cyclohepta[1,2-b]pyridine, and pharmaceutically acceptable salts and solvates thereof are disclosed, which possess anti-allergic and anti-inflammatory activity. Methods for preparing and using the compounds are also described.
摘要:
A selected one of a plurality of unique N-bit digital code words that corresponds to an associated signaling message is continuously transmitted until it is desired to transmit a different signaling message. Decoder logic in the receiver looks at a new group of N-signaling bits during each signaling bit interval, without reference to the start of a transmitted code word, and makes a decision during each signaling bit interval as to what signaling message was transmitted. In this manner a keep-alive signal is virtually continuously provided in the receiver. Latch circuitry repeats the previous decision from the decoder logic when the current group of N-signaling bits does not correspond to one of the unique code words or an ordered permutation thereof. In an alternate embodiment a memory circuit requires that the decoder logic repeat the same decision as to what signaling message was transmitted for P consecutive groups of N-signaling bits (i.e., for P consecutive signaling bit intervals) before the latch circuit will indicate that a different signaling message is being transmitted.
摘要:
A selected one of a plurality of unique N-bit digital code words that corresponds to an associated signaling message is continuously transmitted until it is desired to transmit a different signaling message. Decoder logic in the receiver looks at a new group of N-signaling bits during each signaling bit interval, without reference to the start of a transmitted code word, and makes a decision during each signaling bit interval as to what signaling message was transmitted. In this manner a keep-alive signal is virtually continuously provided in the receiver. Latch circuitry repeats the previous decision from the decoder logic when the current group of N-signaling bits does not correspond to one of the unique code words or an ordered permutation thereof. In an alternate embodiment a memory circuit requires that the decoder logic repeat the same decision as to what signaling message was transmitted for P consecutive groups of N-signaling bits (i.e., for P consecutive signaling bit intervals) before the latch circuit will indicate that a different signaling message is being transmitted.
摘要:
A lubricant composition for use alone or in a lubricating base, comprising a finely divided carbonate of Group IIA metal and a halogenated organic lubricant.
摘要:
Novel 3,20-dioxo-7.alpha.-halogeno-1,4-pregnadienes are described and their use as anti-inflammatory agents. Preferred are 7.alpha.-bromo- and 7.alpha.-chloro- derivatives, particularly 7.alpha.-bromo- and 7.alpha.-chloro-1,4-pregnadienes-11.beta.,17.alpha.,21-triol-3,20-dione 17,21-dihydrocarboncarboxylates, the 16-methyl and 16-methylene derivatives thereof being particularly valuable as topical anti-inflammatory agents.
摘要:
21-Halogeno-17.alpha.-acyloxy-20-keto-4-pregnenes having physiological properties are prepared by the reaction of a 17.alpha.,21-dihydroxy-20-keto-4-pregnene 17.alpha.,21-orthoester with a halide reagent selected from the group consisting of triarylsilyl halides and tri-lower alkylsilyl halides in an organic solvent, said halide being chloride or bromide. Preferred reagents are tri-lower alkylsilyl halides, particularly trimethylsilyl chloride.
摘要:
21-Desoxy-17.alpha.-acyloxy-20-keto-4-pregnenes having physiological properties are prepared by the reaction of a 17.alpha.,21-dihydroxy-20-keto-4-pregnene 17.alpha.,21-orthoester or a 21-iodo-21-desoxy-17.alpha.-acyloxy-20-keto-4-pregnene with an iodide reagent selected from the group consisting of triphenylsilyl iodide, tri-lower alkylsilyl iodide and triphenylmethyl iodide. When said 17.alpha.,21-dihydroxy-20-keto-4-pregnene 17.alpha.,21-orthoester is reacted with less than two molar equivalents of a tri-lower alkylsilyl iodide reagent there is also formed a 21-iodo-21-desoxy-17-.alpha. -acyloxy-20-keto-4-pregnene, a useful intermediate, which, upon reaction with additional iodide reagent, is converted to the corresponding 21-desoxy-17.alpha.-acyloxy-20-keto-4-pregnene.
摘要:
(17R)-Spiro-[androstane-17,1'-cyclobutan]-2'-ones are prepared by the reaction of a 17-oxo androstane, wherein all other ketones are blocked, with a cyclopropylarylsulfide or with a cyclopropylarylsulfonium salt having a non-nucleophilic anion, in an organic solvent together with a strong base, followed by reaction in situ of the intermediate thereby formed with aqueous acid or water.Some (17R)-spiro-[androstan-17,1'-cyclobutan]-2'-ones are useful as intermediates in preparing (17R)-spiro-[3-oxo-4-androstene-17,1'-cyclobutan]-2'-ones which are aldosterone antagonists. Additionally, (17R)-spiro-[androstane-17,1'-cyclobutan]-2'-ones are useful as intermediates in preparing known 17.alpha.-pregnane-21,17.beta.-carbolactones, valuable aldosterone blocking agents.