Bis-(Heteroarylmethoxyphenyl)cycloalkyl carboxylates as inhibito

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Having -c- – wherein x is chalcogen – bonded directly to...

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514249, 514367, 544353, 546152, 546174, 548156, A61K 3147, C07D40112

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056913516

ABSTRACT:
Compounds having the structure ##STR1## where m is an integer of from one to nine; n is an integer of from one to four; W is selected from substituted or unsubstituted quinolyl, benzothiazolyl, or quinoxalyl, X is selected from C.sub.1-6 alkylene, C.sub.2-6 alkenylene and C.sub.2-6 alkynylene; Y is selected from halogen, C.sub.1-6 alkyl and C.sub.1-6, alkoxy; and Z is selected from --C(O)B; --C(R.sub.2).sup.2 --O--N.dbd.A--C(O)B; and --C(R.sup.2).dbd.N--O--A--C(O)B where A is C.sub.1-6 alkylene and B is --OH, --O--M.sup.+, --OD where D is a metabolically cleavable group, --OR.sup.6 where R.sup.6 is hydrogen or C.sub.1-6 alkyl, --NR.sup.6 R.sup.7 where R.sup.7 is hydrogen, C.sub.1-6 alkyl, hydroxy or C.sub.1-6 alkoxy, or where R.sup.6 and R.sup.7 taken together form a five to eight membered ring optionally containing one heteroatom selected from nitrogen, oxygen or sulfur, are inhibitors of leukotriene biosynthesis.

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Bashir-Hashemi, A., et al., Regioselectivity in Photochemical Chlorocarbonylation of Carbonyl Compounds, J. Org. Chem, vol. 59, No. 8, 1994, pp. 2132-2134.
Curran, D. P., et al., Tandem Transannular Radical Cyclizations. Total Synthesis of (+/-)-Modhephene and (+/-)-Epi-Modhephane, Tetrahedron, vol. 49, No. 4, 1993, pp. 755-770.
Miur, H., et al., Synthese von 5-substituierten Cyclooctynen, Communications, Aug., 1978, pp.596-598.

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