PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 9406969-4 1997 All the responses to DVN injections of AII were totally prevented by DVN injection of 1 nmol of losartan, a mammalian non-peptide AII subtype 1 (AT1) receptor antagonist. Losartan 96-104 NLR family pyrin domain containing 3 Homo sapiens 39-42 9406969-4 1997 All the responses to DVN injections of AII were totally prevented by DVN injection of 1 nmol of losartan, a mammalian non-peptide AII subtype 1 (AT1) receptor antagonist. Losartan 96-104 NLR family pyrin domain containing 3 Homo sapiens 130-133 8172070-6 1994 The discovery of simple benzyl-substituted imidazoles, which possess weak but highly selective A-II receptor antagonistic properties, led to the development of losartan (DuP 753). Losartan 160-168 NLR family pyrin domain containing 3 Homo sapiens 95-99 8172070-6 1994 The discovery of simple benzyl-substituted imidazoles, which possess weak but highly selective A-II receptor antagonistic properties, led to the development of losartan (DuP 753). Losartan 170-177 NLR family pyrin domain containing 3 Homo sapiens 95-99 8172070-7 1994 Losartan is a potent, orally active, specific, competitive nonpeptide A-II receptor antagonist that appears to be an effective antihypertensive agent both in animal studies and in preliminary clinical trials. Losartan 0-8 NLR family pyrin domain containing 3 Homo sapiens 70-74 8172070-10 1994 Furthermore, losartan, a selective A-II type 1 (AT1) receptor antagonist, has also been a valuable pharmacologic probe for studying the mechanism of A-II stimulation of its receptors. Losartan 13-21 NLR family pyrin domain containing 3 Homo sapiens 35-39 8172070-10 1994 Furthermore, losartan, a selective A-II type 1 (AT1) receptor antagonist, has also been a valuable pharmacologic probe for studying the mechanism of A-II stimulation of its receptors. Losartan 13-21 NLR family pyrin domain containing 3 Homo sapiens 149-153 15629544-6 2005 Losartan infused into the portal vein abolishes PHR to AII but not the metabolic response; when infused via both pathways it abolishes the hypertensive responses and inhibits the metabolic effects. Losartan 0-8 NLR family pyrin domain containing 3 Homo sapiens 55-58 15629544-11 2005 Hemodynamic responses to AII are losartan-dependent but metabolic responses are partially losartan-independent. Losartan 33-41 NLR family pyrin domain containing 3 Homo sapiens 25-28 12034692-13 2002 Losartan (1 microM) significantly blocked the AII induced BK channel activation (p=0.0131), the Ca(2+)(I) response (p<10(-4)), and the AII induced volume effect (p=0.0046). Losartan 0-8 NLR family pyrin domain containing 3 Homo sapiens 46-49 15025837-0 2004 AII antagonists in hypertension, heart failure, and diabetic nephropathy: focus on losartan. Losartan 83-91 NLR family pyrin domain containing 3 Homo sapiens 0-3 12034692-13 2002 Losartan (1 microM) significantly blocked the AII induced BK channel activation (p=0.0131), the Ca(2+)(I) response (p<10(-4)), and the AII induced volume effect (p=0.0046). Losartan 0-8 NLR family pyrin domain containing 3 Homo sapiens 138-141 11026543-3 2000 The conformations of compounds with a good binding activity are quite similar to that of DuP753, a prototype of AII antagonist, suggesting that these compounds also bind to the same site of AII receptor. Losartan 89-95 NLR family pyrin domain containing 3 Homo sapiens 112-115 11026543-3 2000 The conformations of compounds with a good binding activity are quite similar to that of DuP753, a prototype of AII antagonist, suggesting that these compounds also bind to the same site of AII receptor. Losartan 89-95 NLR family pyrin domain containing 3 Homo sapiens 190-193 10971280-9 2000 Responses to AII in strips from children under 3 years old were antagonized by the AT1 receptor antagonist losartan (1 micromol/L) but not by the AT2 receptor antagonist PD 123319 (1 micromol/L), indicating interaction with the AT1 receptor. Losartan 107-115 NLR family pyrin domain containing 3 Homo sapiens 13-16