FIELD: pharmacology.
SUBSTANCE: invention relates to a compound of the formula
where R1 represents a hydrogen atom, C1-6 alkyl group, C1-6 alkoxy group, di-C1-6 alkylamino group; each of L1 and L2 independently represents a single bond, NR2, O, S or a C1-6alkylene group; B is a C3-11 cycloalkylene group, a C3-11 cycloalkenylene group, a 3 to 11-membered heterocyclylene group containing 1 to 5 heteroatoms as ring-forming atoms (the hetero atom is a nitrogen atom, an oxygen atom or a sulfur atom), a C6-10 arylene group, a 5 to 10 membered heteroarylene group containing 1 to 5 hetero atoms as ring-forming atoms (the hetero atom is a nitrogen atom, an oxygen atom or a sulfur atom), a C1-6 alkylene group or a C2-6 alkenylene group; A is a C1-6 alkyl group, a C3-11 cycloalkyl group, a C3-11 cycloalkenyl group, a 3 to 11-membered heterocyclyl group containing 1 to 5 heteroatoms as ring-forming atoms (the hetero atom is a nitrogen atom, an oxygen atom or a sulfur atom), a C6-10 aryl group or a 5 to 10 membered heteroaryl group containing 1 to 5 heteroatoms as ring-forming atoms (the hetero atom is a nitrogen atom, an oxygen atom or a sulfur atom); L3 is a C1-6 alkylene group; D is a C3-11 cycloalkyl group, a C3-11 cycloalkenyl group, a 3 to 11-membered heterocyclyl group containing 1 to 5 heteroatoms as ring-forming atoms (the heteroatom is a nitrogen atom, an oxygen atom or a sulfur atom), a C6-10 aryl group or a 5 to 10 membered heteroaryl group containing 1 to 5 heteroatoms as ring-forming atoms (the hetero atom is a nitrogen atom, an oxygen atom or a sulfur atom); the values of the remaining substituents are indicated in the claims. The invention also relates to a T-type calcium channel inhibitor, a prophylactic agent, a therapeutic agent for neuropathic pain, a medicament.
EFFECT: new compounds of the formula having inhibitory activity against T-type calcium channels are obtained.
37 cl, 43 tbl, 876 ex
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Authors
Dates
2018-02-16—Published
2013-03-29—Filed