Antiproliferative 1,2,3-thiadiazole compounds

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Heterocyclic carbon compounds containing a hetero ring...

Reexamination Certificate

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C514S361000, C544S134000, C548S127000

Reexamination Certificate

active

07022702

ABSTRACT:
Pharmaceutical compositions and compounds are provided. The compounds of the invention have anti-proliferative activity, and may promote apoptosis in cells lacking normal regulation of cell cycle and death. In one embodiment of the invention, formulations of the compounds in combination with a physiologically acceptable carrier are provided. The pharmaceutical formulations are useful in the treatment of hyperproliferative disorders, which disorders include tumor growth, lymphoproliferative diseases, angiogenesis. The compounds of the invention are 1,2,3-thiadiazoles having the structure:and including stereoisomers, solvates, and pharmaceutically acceptable salts thereof, wherein each of R1, R22 , R3and R4is independently selected from hydrogen, R5R6, and R7, R5is selected from alkyl, heteroalkyl, aryl and heteroaryl; R6is selected from (R5)n-alkylene, (R5)n-heteroalkylene, (R5)n-arylene and (R5)n-heteroarylene; R7is selected from (R6)n-alkylene, (R6)n-heteroalkylene, (R6)n-arylene, and (R6)n-heteroarylene; and n is selected from 0, 1, 2, 3, 4 and 5, where R1and R2may together form a heterocyclic structure including the nitrogen to which they are both attached, and R3and R4may together form a heterocyclic structure including the nitrogen to which they are both attached; and each of L1and L2is independently selected from -A1-A2-A3- where each of Al, A2, and A3 is independently selected from a direct bond, alkylene, heteroalkylene, arylene and heteroarylene.

REFERENCES:
patent: 3787434 (1974-01-01), Volpp et al.
patent: 3874873 (1975-04-01), Volpp et al.
patent: 4101548 (1978-07-01), Crenshaw et al.
patent: 4171363 (1979-10-01), Crenshaw et al.
patent: 5098918 (1992-03-01), Thomas et al.
patent: 5674886 (1997-10-01), Okada et al.
patent: WO 96/29871 (1996-10-01), None
Bakulev et al., “Two Directions of Cyclization of α-Diazo-β-Dithioamides. New Rearrangements of 1,2,3-Triazole-4-Carbothiamides,”Tetrahedron(1989), vol. 45, pp 7329-7340.
Delcommenne et al., “Phosphoinositide-3-OH Kinase-Dependent Regulation of Glycogen Synthase Kinase 3 and Protein Kinase B/AKT by the Integrin-Linked Kinase,”Proceedings of the National Academy of Sciences, USA(Sep. 1998), vol. 95, pp 11211-11216.
Kandeel et al., “Oxidative Transformation of Pyrazole into Triazole. Novel Syntheses of 4-Cyano-2H-1,2,3-Triazole Derivatives,”Journal of the Chemical Society, Perkins Transaction 1(1986), pp 1379-1381.
Kandeel et al., “Activated Nitriles in Heterocyclic Synthesis: Reaction of Cyanogen Bromide with Some Functionally Substituted Enamines,”Journal of the Chemical Society, Perkins Transaction 1(1985), pp 1499-1501.
Kolobov et al., “Reactions of Diazoacetonitrile Derivatives,”Journal of Organic Chemistry of the USSR(1987), vol. 23, pp 1011-1012.
Mitchell et al., “Inhibitors of Angiogenesis”,Annual Reports in Medicinal Chemistry(1992), vol. 27, pp. 139-148.
Bakulev et al., “Domino-type Rearrangements in Conjugated 5-(1,2,3-Triazol-4-yl)1,2,3-thiadiazoles”, abstract provided fromChemical Abstracts Database, Accession No. 1998:55442. See alsoBull. Soc. Chim. Belg. (1997), vol. 106, pp 643-645.
Bakulev et al., “Synthesis and Study of the Rearrangements of 5-(1,2,3,-Triazol-4-yl)-1,2,3-thiadiazoles”, abstract provided fromChemical Abstracts Database, Accession No. 1998:454928. See alsoTetrahedron(1998), vol. 54, pp 8501-8514.
Tarasov et al., “C-Nucleophilic Substitution of 5-Halo-1,2,3-thiadiazoles As An Approach to Fused Pyridones and Pyranones”, abstract provided fromChemical Abstracts Database, Accession No. 1997:727791. See alsoJ. Chem. Res., Synop. (1997), vol. 11, pp 396-397.
Kuroda et al., “Preparation of Thiadiazole Derivatives as Agricultural Microbicides”, abstract provided fromChemical Abstracts Database, Accession No. 1996:694344. See also PCT Int. App. WO 96/29871.
Crenshaw et al. “Quinazoline Derivatives”, abstract provided fromChemical Abstracts Database, Accession No. 1978:597604. See also German Patent No. DE 2807392.
Dankova et al., “Investigation of Malonodithioamide Cyclization Direction As A Method for Study of .alpha.-Diazothioacetamide Reactivity”, abstract provided fromChemical Abstracts Database, Accession No. 1993:517183. See alsoKhim. Geterotsikl. Soedin. (1992), vol. 8, pp 1106-1112.
Dankova et al., “Methylation of 1,2,3-Thiadiazole-4-carbothioamides”, abstract provided fromChemical Abstracts Database, Accession No. 1990:532096. See alsoIvz. Akad. Nauk SSSR, Ser. Khim. (1990), vol. 4, pp. 938-940.
Lebedev et al., “Mass Spectra of 4,5-Disubstituted 1,2,3-Thiadiazoles”,Chemistry of Heterocyclic Compounds. (1988), vol. 24, pp 99-103. (translation).
Morzherin et al., “Study of the Characteristics of Rearrangements of 5-Amino-1,2,3-thiadiazole-4-carbothioamides”,Chemistry of Heterocycles(1994), vol. 30, pp 483-488.
Morzherin et al., “Nucleophilic Substitution in 1,2,3-Thiadiazoles”,Chemistry of Heterocyclic Compounds(1994), vol. 30, pp 489-494.

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