摘要:
The present invention relates to functional 1,3-dihydrogeno disilazanes of formula: ##STR1## in which: R and R.sub.1, identical or different, represent an atom of hydrogen or a hydrocarbon such as an alkyl, alkenyl or alkynyl, cycloalkyl or cycloalkenyl, aryl, alkylaryl, alkenylaryl, alkynylaryl, arylalkyl, arylalkenyl or arylalkynyl radical, possibly functional, R also being able to represent a radical ##STR2## and R.sub.2 represents an atom of halogen, an OR group or an --NRR.sub.1 group, when R and R.sub.1 are both hydrocarbon radicals.
摘要:
The present invention relates to copolymers containing --Si--N-- and --Si--Si-- bonds, which are obtained by the polycondensation ofat least one silane of the formula RR.sub.1 SiCl.sub.2and at least one disilazane of the formula ##STR1## in which formulae: R.sub.2 is a halogen atom, preferably Br and Cl, andR, R.sub.1 and R.sub.3, which are identical or different, represent a hydrogen atom or an alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, aryl, alkylaryl or alkenylaryl hydrocarbon radical which may be functional,to a process for the preparation of the said copolymers,to the polycarbosilazanes obtained by thermolysis of the said copolymers and to the silicon carbonitrides obtained by heating the said polycarbosilazanes.
摘要:
The present invention relates to a process for preparing disilylmethanes, wherein the magnesian reaction is carried out between methylene chloride and at least one chlorosilane in a donor solvent.
摘要:
The present invention discloses and claims pharmaceutical compositions comprising Group A streptogramin derivatives of formula (I) and salts thereof in combination with at least one natural group B streptogramin derivative
摘要:
The present invention relates to the use of 2-aminothiazoline derivatives of formula: in which either R1 is a hydrogen atom or an alkyl radical and R2 is an alkyl, -alk—NH2, —CH2—R3, —CH2—S—R4 or phenyl radical substituted with a nitro or —NH— C (═NH) CH3 radical, or R1 is an alkyl radical and R2 is a hydrogen atom, R3 is a (3-6C) cycloalkyl, pyridyl, pyridyl N-oxide, thienyl, thiazolyl, imidazolyl, pyrazinyl, triazolyl or phenyl radical or a phenyl radical substituted with a nitro, hydroxy or carboxyl radical, R4 represents a pyridyl or pyridyl N-oxide radical, alk represents an alkylene radical, or pharmaceutically acceptable salts thereof, as inhibitors of inducible NO-synthase.
摘要:
This invention relates to a novel 1,8 benzo[b]naphythyridine derivative of general formula (I), ##STR1## wherein R is H or a hydroxy, amino or alkylamino radical optionally substituted by amino or hydroxy, or R is dialkylamino of which the alkyl portions may form, with the nitrogen atom, a 5- or 6-membered heterocyclic ring which optionally contains a further heteroatom chosen from nitrogen, oxygen or sulphur, or R is C.sub.3-6 cycloalkylamino or an alkanylamino, N-alkyl N-alkanylamino or aminoalkylphenylamino radical; R.sub.1 and R.sub.2, which are the same or different, are in positions 2 and 3 and represent H, alkyl, C.sub.2-4 alkenyl, phenyl, or substituted phenyl, or R.sub.1 and R.sub.2 are in position 2 and represent alkyl; R.sub.3 is H or alkyl, fluoroalkyl, carboxyalkyl, C.sub.3-6 cycloalkyl, fluorophenyl, difluorophenyl, alkyloxy or alkylamino; and R.sub.4 is H or F, wherein the C.sub.1-4 alkanyl and alkyl radicals are linear or branched; stereoisomeric forms thereof or mixtures of these; and salts and hydrated forms thereof. These novel derivatives are useful as antimicrobials.
摘要:
The present invention relates to imidazolone derivatives of formula (I) to methods of preparing such derivatives, intermediates thereto, pharmaceutical compositions comprising such derivatives, and methods of inhibiting protein kinase, and methods of treatment comprising administration of such derivatives.
摘要:
Group A streptogramin derivatives of formula (I) and salts thereof: and Group A streptogramin derivatives of formula (III) and salts thereof: as well as processes for preparing such streptogramins, and pharmaceutical compositions comprising such streptogramins, alone or combined with at least one group B streptogramin derivative.
摘要:
The present invention relates to the use of 2-amino-4-heteroarylethyl-thiazoline derivatives of formula (I) in which Het represents a thienyl, pyrimidyl, pyridyl or thiazolyl radical or pharmaceutically acceptable salts thereof as inhibitors of inducible NO-synthase.
摘要:
Group A streptogramin derivatives of formula (I): the salts thereof, and mixtures of stereoisomers thereof, as well as processes for preparing them and pharmaceutical compositions comprising them are disclosed.