PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 8064808-9 1994 At 1 mg/kg po in rats, 18 and 92 (L-162,234) produced 85-87% peak inhibition of the AII pressor response with duration exceeding 6 h. The identification of triazolinone-based sulfonamide derivatives combining high AT1 affinity, considerably enhanced AT2 potency, and favorable in vivo properties provides insights relevant to the design of dual AT1/AT2 receptor antagonists. Sulfonamides 175-186 angiotensin II receptor, type 1a Rattus norvegicus 214-217 8064808-4 1994 Certain other acidic sulfonamides, such as sulfonylcarbamates and disulfimides also displayed high affinity for the AT1 receptor. Sulfonamides 21-33 angiotensin II receptor, type 1a Rattus norvegicus 116-119 8064808-9 1994 At 1 mg/kg po in rats, 18 and 92 (L-162,234) produced 85-87% peak inhibition of the AII pressor response with duration exceeding 6 h. The identification of triazolinone-based sulfonamide derivatives combining high AT1 affinity, considerably enhanced AT2 potency, and favorable in vivo properties provides insights relevant to the design of dual AT1/AT2 receptor antagonists. Sulfonamides 175-186 angiotensin II receptor, type 1a Rattus norvegicus 345-348