Amino acid derivatives

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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C514S227500, C514S357000, C514S365000, C514S374000, C514S399000, C514S448000, C544S054000, C544S058100, C544S058400, C546S323000, C548S200000, C548S236000, C548S333500, C549S072000

Reexamination Certificate

active

10154780

ABSTRACT:
A compound of the formula (I):[wherein R1is (substituted) alkyl, alkoxy, phenyl, hetero ring etc.; A is bond, CO, SO2; R2is H, (substituted) alkyl etc.; D is alkylene etc.; E is COO, OCO, O, S, SO, SO2etc.; R3is (substituted) alkyl, carbocyclic ring, hetero ring; J is O, NR16(R16is H, substituted alkyl); R4is (substituted) alkyl, carbocyclic ring, hetero ring.] or non-toxic salt thereof, and an N-type calcium channel blocker comprising it as an active ingredient.The compounds of the formula (I) possess an inhibitory action on N-type calcium channel, so they are useful as agent for the prevention and/or treatment of cerebral infarct, transient ischemic attack, encephalomyelopathy after cardiac operation, spinal angiopathy, hypertension with stress, neurosis or epilepsy etc. or agent for the treatment of pain.

REFERENCES:
patent: 4962225 (1990-10-01), Okada et al.
patent: 5596000 (1997-01-01), Esser et al.
patent: 5731340 (1998-03-01), Bras et al.
patent: 6605608 (2003-08-01), Seko et al.
patent: 0 194 464 (1986-09-01), None
patent: 0 237 082 (1987-09-01), None
patent: 0 405 391 (1991-01-01), None
patent: 0 520 200 (1992-12-01), None
patent: 0 697 403 (1996-02-01), None
patent: 0 757 037 (1997-02-01), None
patent: 0 780 386 (1997-06-01), None
patent: 0 805 147 (1997-11-01), None
patent: 6-80696 (1994-03-01), None
patent: 8-208690 (1996-08-01), None
patent: 8-217671 (1996-08-01), None
patent: 8-217751 (1996-08-01), None
patent: WO 89/02431 (1989-03-01), None
patent: WO 91/01976 (1991-02-01), None
patent: WO 93/15047 (1993-08-01), None
patent: WO 94/07815 (1994-04-01), None
patent: WO 94/12181 (1994-06-01), None
patent: WO 96/11940 (1996-04-01), None
patent: WO 97/49679 (1997-12-01), None
patent: WO 98/54123 (1998-12-01), None
CAS printout for Wolfe et al. Chem. Abs. 110:18385 (1989).
Gillessen et al., Chemical Abstracts, vol. 72:67256, 1970.
Poroshin et al., Chemical Abstracts, vol. 63:89274, 1965.
Gasc et al., Chemical Abstracts, vol. 114:82543, 1991.
Shengeliya et al., Chemical Abstracts, vol. 107:77510, 1987.
Kowollik et al., Chemical Abstracts, vol. 103:105274, 1985.
Lau et al., Chemical Abstracts, vol. 99:64868, 1983.
CAS printout for Connell et al, Oct. 1993, Chemical Abstracts, vol. 121:109676.
CAS printout for Ravi, et al, Apr. 1984, Chemical Abstracts, vol. 103:2340.
CAS printout for Bodanszky, et al, Feb. 1972, Chemical Abstracts, vol. 77:75449.
CAS printout for Aubury, et al, May 1987, Chemical Abstracts, vol. 109:73893.
PCT International Preliminary Examination Report, 1998.
CAS printout for Connell et al, Oct. 1993.
CAS printout for Ravi, et al, Apr. 1984.
CAS printout for Bodanszky, et al, Feb. 1972.
CAS printout for Aubry, et al, May 1987.
PCT International Preliminary Examination Report, 1998.
M. Ashraf Shalaby et al., “Thiopeptide Synthesis. α-Amino Thionoacid Derivatives of Nitrobenzotriazole as Thioacylating Agents,”J. Org. Chem., (1996) 61(25), 9045-9048.
Kosaku Noda et al., “A facile method for preparation of t-butyloxycarbonylamino acid p-nitroanilides,”Int. j. Peptide Protein Res(1990) 36(2), 197-200.
Shi Pu-Tao et al., “Opiate Multiple Receptor Binding Activity of Enkephalin Analogs,” ACTA Biochimica and Biophysica Sinica (Jan. 1983), vol. 15, No. 1, 67-76.
Castelhano et al., “Synthesis, Chemistry, and Absolute Configuration of Novel Transglutaminase Inhibitors Containing a 3-Halo-4,5-dihydroisoxazole,”Bioorganic Chemistry(1988), 16(3), 335-40.
V.F. Pozdnev et al., “Activation of carboxylic acids by pyrocarbonates. Synthesis of arylamides of N-protected amino acids and small peptides using dialkylk pyrocarbonates as condensing reagents,”Int. J. Peptide Protein Res. (1994) 44(1), 36-48.
Våclav Ċe{dot over (r)}ovsky, et al., “Papain-Catalyzed Synthesis of 2-Naphthylamdes of N-Acylamino Acids and Dipeptides,”Collection Czech Chem. Comm. (1987), vol. 52, 2309-16.
F. Orosz et al., “Derivatives of DL-1,2,3,4-Tetrahydro-2-Naphthylamine Acylated with Amino Acids,” Acta Chimica Academiac Scientiarum Hungaricae (1966) 49(3), 291-302.
Michio Namikoshi et al., “Use of Tetrabutylammonium Fluoride as a Facile Deprotecting Reagent for 4-Nitrobenzyl, 2,2,2-Tricholorethyl, and Phenacyl Esters of Amino Acids,”J. Org. Chem(1991), 56, 5464-5466.
Tohru Sugawara et al., “Application of a Unique Automated Synthesis System for Solution-phase Peptide Synthesis,”Chem. Pharm. Bull. (1995), 43(8), 1272-1280.
Nobutaka Fujii et al., “Studies on Peptides. CXXXII. Evaluation of Two β-Carboxyl Protecting Groups of Aspartic Acid, Cycloheptyl and Cycloctyl, for Peptide Synthesis,”Chem. Pharm. Bull(1985), 34(2), 864-8.
Haruaka Yajima et al Chem. Pharm. Bull., “Studies ofn Peptides. CXLIII. Evaluation of β-Menthylaspartate for Peptide Synthesis,” (1986), 34(10) 4356-61.
Tam et al., “Mechanisms of Aspartimide Formation: The effects of Protecting Groups, Acid, Base, Temperature and Time,”Peptide Research(1988), 1(1) 6-18.

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