摘要:
The present invention relates to an improved, cost effective, eco-friendly and easy t handle process to manufacture substantially pure form of (2E)-2-Cyano-3-(3,4-dihydroxy-5 nitrophenyl)-N,N-diethyl-2-propenamide or (E)- N,N-diethyl-2-cyano-3-(3,4-dihyroxy-5 nitroρhenyl)-acrylamide polymorphic form A commonly known as (E)-Entacapone represente by Formula I, using ammonium acetate as a base.
摘要:
The present invention relates to biphenylyl derivatives, processes for their production, their uses and pharmaceutical compositions containing them.
摘要:
Compounds represented by the following general formula [I]: wherein A, R, X, Y and n are each as defined in the description; salts thereof, and insecticides/miticides characterized by containing one or more members selected from the above compounds and salts thereof as the active ingredient.
摘要:
A compound of general formula (I), or pharmaceutically acceptable salts, solvates or polymorphs thereof; wherein R is independ ently CF3, OCF3, C1-C4alkylthio or C1-C4alkoxy; n is 1, 2 or 3; and the other variables are as defined in the claims. These compounds inhibit monoamine re-uptake and in particular exhibit activity as selective serotonin re-uptake inhibitors. They are useful in disorders such as depression, attention deficit hyperactivity disorder, obsessive-compulsive disorder, post-traumatic stress disorder, substance abuse disorders and sexual dysfunction including premature ejaculation.
摘要:
A photostable UV absorbent with maximum absorption above 340 nm having formula (I), wherein R is -CO(R2) or phenyl optionally substituted with lower alkyl and/or lower alkoxy; R2 is -alkyl, -O(C2+ alkyl), (1) or (2); n has a value of from 2 to 8; S and T each independently are hydroxy, lower alkyl, lower alkoxy or, when R2 is alkyl or alkoxy, S can also be phenyl and when R2 is alkoxy, T is alkoxy, or S + T taken with the phenyl ring form a naphthyl radical or a fused benzodioxol-5-yl heterocyclic radical; k + 1 has a value of from 0 to 3 with the proviso that, when R2 is -O(alkyl), T is -O(lower alkyl) and the value of 1 is 2 or 3; R3 is hydrogen or lower alkylene; R4, R5, and R6 are each independently C1 to C18 alkyl or one of R4, R5 and R6 can be phenyl and A is an anion.
摘要:
The disclosure provides crystalline compositions comprising D-metyrosine and L- metyrosine, pharmaceutical formulation comprising one or more crystalline composition described herein and a pharmaceutically acceptable excipient, methods for treating cancer in a patient in need thereof, the method comprising administering to the patient one or more composition described herein, and methods for preparing the compositions described herein.
摘要:
Described herein are compounds of formula (I), related compositions, and their use, for example in the formation of a-amino acids or a precursor thereof such as an a-aminonitrile.
摘要:
Novel multibinding compounds are disclosed. The compounds of this invention comprise 2 - 10 ligands covalently connected, each of the ligands being capable of binding to a ligand binding site in a Ca channel, thereby modulating the biological activities thereof.
摘要:
Process for the preparation of a diastereomerically enriched phenylglycine amide derivative in which an enantiomerically enriched phenylglycine amide is converted into the corresponding Schiff base with the aid of compound R2-C(O)-R3, and the Schiff base obtained is subsequently converted into the diastereomerically enriched phenylglycine amide derivative with the aid of a cyanide source, a reducing agent or an allyl organometallic compound. The phenylglycine amide derivatives obtained are interesting starting materials for the preparation of for example enantiomerically enriched alpha - and/or beta -amino acids and derivatives thereof, such as amides and esters, and amines.