摘要:
Disclosed herein are non-natural amino acids and polypeptides that include at least one non-natural amino acid, and methods for making such non-natural amino acids and polypeptides. The non-natural amino acids, by themselves or as a part of a polypeptide, can include a wide range of possible functionalities, but typical have at least one oxime, carbonyl, dicarbonyl, and/or hydroxylamine group. Also disclosed herein are non-natural amino acid polypeptides that are further modified post-translationally, methods for effecting such modifications, and methods for purifying such polypeptides. Typically, the modified non-natural amino acid polypeptides include at least one oximine, carbonyl, dicarbonyl, and/or hydroxylamine group. Further disclosed are methods for using such non-natural amino acid polypeptides and modified non-natural amino acid polypeptides, including therapeutic, diagnostic, and other biotechnology uses.
摘要:
The invention relates to the compounds of formula (I) or its pharmaceutical acceptable salts, as well as polymorphs, solvates, enantiomers, stereoisomers and hydrates thereof. The pharmaceutical compositions comprising an effective amount of compounds of formula (I), and methods for the treatment of metabolic syndrome may be formulated for oral, buccal, rectal, topical, transdermal, transmucosal, intravenous, parenteral administration, syrup, or injection. Such compositions may be used to treatment of hyperuricemia, gout; dyslipidemia, obesity, urea cycle disorders, hyperglycemia, insulin resistance, diabetes mellitus, diabetes insipidus, type 1 diabetes, type 2 diabetes, microvascular complications,.macrovascular complications, lipid disorders, prediabetes., obesity, arrhythmia, myocardial infarction, stroke, neuropathy, renal complications, hypertriglyceridemia, cardiovascular complications, and post prandial hyperglycemia.
摘要:
The present invention provides processes for the preparation of amorphous and crystalline candesartan cilexetil with quality that complies to Ph.Eur./ICH Guidelines by an economical way using easy accessible substances and pure starting compounds.
摘要:
The invention relates to blends of organic material, to the use of said blends in organic electroluminescent devices and to organic electroluminescent devices containing said blends.
摘要:
The invention relates to 1,2,3,6,7,8-hexahydro-s-indacene-derivatives and 6,7-dihydro-5H-indeno[5,6-d][1,3]dioxol-derivatives of formula (I), wherein R1, A1, Z1, n, X and Y have the meaning defined in the claims. The invention also relates to the use thereof as component(s) in liquid-crystal substances. The invention further relates to liquid-crystal and electro-optical display elements which contain the inventive liquid-crystal substances.
摘要:
Disclosed is a process for the production of cyclopropylmethyl halides (CPMX) such as cyclopropylmethyl chloride (CPMCl) and cyclopropylmethyl bromide (CPMBr) wherein cyclopropanemethanol (CPMO) is contacted with a complex comprising a dialkyl sulfide and an N-halosuccinimide in the presence of an organic solvent.
摘要:
Disclosed is a process for the production of cyclopropylmethyl halides (CPMX) such as cyclopropylmethyl chloride (CPMCl) and cyclopropylmethyl bromide (CPMBr) wherein cyclopropanemethanol (CPMO) is contacted with a complex comprising a dialkyl sulfide and an N-halosuccinimide in the presence of an organic solvent.
摘要:
Disclosed is a process for the production of cyclopropylmethyl halides (CPMX) such as cyclopropylmethyl chloride (CPMCI) and cyclopropylmethyl bromide (CPMBr) wherein cyclopropanemethanol (CPMO) is contacted with an aqueous solution of a hydrogen halide (HX) at a temperature in the range of -30 °C to 35 °C. Also disclosed is a three-step process wherein CPMO is converted to a CPMX, the CPMX is separated as a liquid organic phase from the aqueous hydrogen halide by decantation and then is subjected to fractional distillation to provide CPMX in high purity. Finally, a process for the co-production of a CPMX and a cyclobutyl halide (CBX) is disclosed.
摘要:
The invention concerns a process for halogenating cyclopropylmethyl ketone with at least one dihalogen triorganophosphorane of the general formula (I): R3PHal2, in which the R groups can be the same or different and designate a saturated or unsaturated aliphatic C1-C20 hydrocarbon group, a phenyl or C1-C4 alkylphenyl group which can optionally be further substituted by one to two fluorine, chlorine and/or nitro groups, P means phosphorus and Hal means chlorine, bromine or iodine, at 80 to 130 °C, the dihalogen triorganophosphorane of the general formula (I) being prepared in situ from triorganophosphane oxide or triorganophosphane sulphide of the general formula (II), R3PA, in which R has the meaning given under formula (I) and A stands for oxygen or sulphur, with a halogenation reagent. The process is characterized in that the triorganophosphane oxide or triorganophosphane sulphide is used in catalytic amounts. The invention also concerns the halogenation product of the cyclopropyl ketone obtained according to this process and a process for reacting it to form cyclopropylacetylene.