FIELD: chemistry.
SUBSTANCE: invention relates to novel compounds of formula (I) and formula (IV) or pharmaceutically acceptable salts thereof, which inhibit cystathionine -γ-lyase (CSE). In a compound of formula (I) having the structure R1 is H or unsubstituted C1-C6alkyl and A is selected from and -CONHSO2R4, where R4 is independently unsubstituted C1-C6alkyl or unsubstituted phenyl. In a compound of formula (IV) having the above structure A means and R1 is an optionally substituted or unsubstituted C2-C6alkyl, where C2-C6alkyl is independently optionally substituted with one or more additional groups independently selected from phenyl, C1-C4alkoxy, C1-C4alkylthio, halo-C1-C4alkyl, halo-C1-C4alkoxy, fluoro-C1-C4alkylamino, C1-C4alkylamino, di(C1-C4alkyl)amino.
EFFECT: compounds can be used to treat or prevent or reduce the incidence of a condition selected from nociceptive pain, acute postoperative pain, neuropathic pain, neuralgia of the trigeminal nerve (trigeminal neuralgia), diabetic peripheral neuropathy, herpetic neuralgia, postherpetic neuralgia, inflammatory pain, mixed neuropathic and inflammatory pain, rheumatoid arthritis, inflammatory bowel disease, irritable bowel syndrome, osteoarthritis, acute pancreatitis, chronic pancreatitis, pain associated with acute pancreatitis, pain associated with chronic pancreatitis, migraine, gout, ankylosing spondylitis, systemic lupus erythematosus (SLE), system inflammatory response syndrome (SIRS), multi-organ dysfunction syndrome (MODS), asthma, chronic obstructive pulmonary disease (COPD), sensitive skin, acne, rosacea (redheads), contact dermatitis and pain associated with cancer.
11 cl, 10 dwg, 1 tbl, 43 ex
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Authors
Dates
2018-07-20—Published
2013-07-23—Filed