Assay ID | Title | Year | Journal | Article |
AID1148688 | Antidiuretic activity in iv dosed rat | 1978 | Journal of medicinal chemistry, Sep, Volume: 21, Issue:9
| Design of potent antagonists of the vasopressor response to arginine-vasopressin. |
AID277896 | Vasopressor activity in rat | 2007 | Journal of medicinal chemistry, Feb-22, Volume: 50, Issue:4
| Design and synthesis of the first selective agonists for the rat vasopressin V(1b) receptor: based on modifications of deamino-[Cys1]arginine vasopressin at positions 4 and 8. |
AID1598498 | Agonist activity at recombinant human V2 receptor expressed in HEK293 cells measured after 5 hrs by cAMP response element driven luciferase reporter gene assay | | | |
AID1150192 | Ratio of arginine-vasopressin to compound for antidiuretic activity in sc dosed Brattleboro rat hereditary hypothalamic diabetes insipidus model | 1977 | Journal of medicinal chemistry, Sep, Volume: 20, Issue:9
| [1-deaminopenicillamine,4-valine]-8-D-arginine-vasopressin, a highly potent inhibitor of the vasopressor response to arginine-vasopressin. |
AID1150141 | Ratio of antidiuretic activity in Brattleboro rat to vasopressor activity in rat | 1977 | Journal of medicinal chemistry, Sep, Volume: 20, Issue:9
| [1-(L-2-hydroxy-3-mercaptopropanoic acid)] analogues of arginine-vasopressin, [8-D-arginine]vasopressin, and [4-valine,8-D-arginine]vasopressin. |
AID1150133 | Oxytocic activity in rat uterus in presence of Mg2+ | 1977 | Journal of medicinal chemistry, Sep, Volume: 20, Issue:9
| [1-(L-2-hydroxy-3-mercaptopropanoic acid)] analogues of arginine-vasopressin, [8-D-arginine]vasopressin, and [4-valine,8-D-arginine]vasopressin. |
AID1150135 | Vasopressor activity in rat | 1977 | Journal of medicinal chemistry, Sep, Volume: 20, Issue:9
| [1-(L-2-hydroxy-3-mercaptopropanoic acid)] analogues of arginine-vasopressin, [8-D-arginine]vasopressin, and [4-valine,8-D-arginine]vasopressin. |
AID1150893 | Activity at oxytocin receptor in rat uterus | 1976 | Journal of medicinal chemistry, Jun, Volume: 19, Issue:6
| Synthesis and some pharmacological properties of deamino(4-threonine,8-D-arginine)vasopressin and deamino(8-D-arginine)vasopressin, highly potent and specific antidiuretic peptides, and (8-D-arginine)vasopressin and deamino-arginine-vasopressin. |
AID1598501 | Agonist activity at recombinant human V1B receptor expressed in HEK293 cells measured after 5 hrs by luciferase reporter gene assay | | | |
AID277900 | Displacement of [3H]AVP from vasopressin V1a receptor in rat liver membrane | 2007 | Journal of medicinal chemistry, Feb-22, Volume: 50, Issue:4
| Design and synthesis of the first selective agonists for the rat vasopressin V(1b) receptor: based on modifications of deamino-[Cys1]arginine vasopressin at positions 4 and 8. |
AID1598506 | Clearance in Sprague-Dawley rat at 0.1 mg/kg, iv administered as cassette dose by LC-MS/MS analysis | | | |
AID1150187 | Antidiuretic activity in sc dosed Brattleboro rat hereditary hypothalamic diabetes insipidus model measured over 6 hrs | 1977 | Journal of medicinal chemistry, Sep, Volume: 20, Issue:9
| [1-deaminopenicillamine,4-valine]-8-D-arginine-vasopressin, a highly potent inhibitor of the vasopressor response to arginine-vasopressin. |
AID1150894 | Activity at oxytocin receptor in rat uterus in presence of Mg2+ | 1976 | Journal of medicinal chemistry, Jun, Volume: 19, Issue:6
| Synthesis and some pharmacological properties of deamino(4-threonine,8-D-arginine)vasopressin and deamino(8-D-arginine)vasopressin, highly potent and specific antidiuretic peptides, and (8-D-arginine)vasopressin and deamino-arginine-vasopressin. |
AID1598499 | Agonist activity at human OTR stably expressed in CHOK1 cells by NFAT-luciferase reporter gene assay | | | |
AID197144 | Tested for intravenous anti-oxytocic effect in the absence of Mg2+ in rats; agonist at concentration of 8 units/kg | 1980 | Journal of medicinal chemistry, Apr, Volume: 23, Issue:4
| [1-beta-Mercapto-beta,beta-cyclopentamethylenepropionic acid),2-(O-methyl)tyrosine ]argine-vasopressin and [1-beta-mercapto-beta,beta-cyclopentamethylenepropionic acid)]argine-vasopressine, two highly potent antagonists of the vasopressor response to argi |
AID1598529 | Antidiuretic activity in iv dosed rat assessed as suppression of urine output relative to control | | | |
AID230908 | Ratio of antidiuretic to vasopressor agonistic activity; Infinite | 1989 | Journal of medicinal chemistry, Jan, Volume: 32, Issue:1
| 2-O-alkyltyrosine derivatives of 1-deamino-arginine-vasopressin: highly specific and potent antidiuretic agonists. |
AID168452 | Compound was tested for its antidiuretic activity | 1989 | Journal of medicinal chemistry, Jan, Volume: 32, Issue:1
| 2-O-alkyltyrosine derivatives of 1-deamino-arginine-vasopressin: highly specific and potent antidiuretic agonists. |
AID1150140 | Antidiuretic activity in sc dosed Brattleboro rat assessed as spontaneous urine output measured every 1 hr for 24 hrs | 1977 | Journal of medicinal chemistry, Sep, Volume: 20, Issue:9
| [1-(L-2-hydroxy-3-mercaptopropanoic acid)] analogues of arginine-vasopressin, [8-D-arginine]vasopressin, and [4-valine,8-D-arginine]vasopressin. |
AID172987 | Tested for intravenous antidiuretic activity in rats | 1980 | Journal of medicinal chemistry, Apr, Volume: 23, Issue:4
| [1-beta-Mercapto-beta,beta-cyclopentamethylenepropionic acid),2-(O-methyl)tyrosine ]argine-vasopressin and [1-beta-mercapto-beta,beta-cyclopentamethylenepropionic acid)]argine-vasopressine, two highly potent antagonists of the vasopressor response to argi |
AID1150897 | Ratio of antidiuretic activity in rat to vasopressor activity in rat | 1976 | Journal of medicinal chemistry, Jun, Volume: 19, Issue:6
| Synthesis and some pharmacological properties of deamino(4-threonine,8-D-arginine)vasopressin and deamino(8-D-arginine)vasopressin, highly potent and specific antidiuretic peptides, and (8-D-arginine)vasopressin and deamino-arginine-vasopressin. |
AID1148687 | Antivasopressor activity in iv dosed phenoxybenzamine treated rat assessed as inhibition of arginine-vasopressin-induced effect | 1978 | Journal of medicinal chemistry, Sep, Volume: 21, Issue:9
| Design of potent antagonists of the vasopressor response to arginine-vasopressin. |
AID197146 | Tested for intravenous anti-vasopressor pA2 effect in rats | 1980 | Journal of medicinal chemistry, Apr, Volume: 23, Issue:4
| [1-beta-Mercapto-beta,beta-cyclopentamethylenepropionic acid),2-(O-methyl)tyrosine ]argine-vasopressin and [1-beta-mercapto-beta,beta-cyclopentamethylenepropionic acid)]argine-vasopressine, two highly potent antagonists of the vasopressor response to argi |
AID173420 | Dose that reduces the response seen with 2x units of agonist to equal the response seen with 1x unit of agonist administered before antagonist | 1989 | Journal of medicinal chemistry, Jan, Volume: 32, Issue:1
| 2-O-alkyltyrosine derivatives of 1-deamino-arginine-vasopressin: highly specific and potent antidiuretic agonists. |
AID1150184 | Oxytocic activity in Sherman albino rat uterus assessed as contraction | 1977 | Journal of medicinal chemistry, Sep, Volume: 20, Issue:9
| [1-deaminopenicillamine,4-valine]-8-D-arginine-vasopressin, a highly potent inhibitor of the vasopressor response to arginine-vasopressin. |
AID1150895 | Antidiuretic activity in rat | 1976 | Journal of medicinal chemistry, Jun, Volume: 19, Issue:6
| Synthesis and some pharmacological properties of deamino(4-threonine,8-D-arginine)vasopressin and deamino(8-D-arginine)vasopressin, highly potent and specific antidiuretic peptides, and (8-D-arginine)vasopressin and deamino-arginine-vasopressin. |
AID1598508 | Protein binding in rat plasma at 200 to 1000 ng/ml measured after 15 mins by UC-LC/MS/MS analysis | | | |
AID277895 | Antidiuretic activity in rat | 2007 | Journal of medicinal chemistry, Feb-22, Volume: 50, Issue:4
| Design and synthesis of the first selective agonists for the rat vasopressin V(1b) receptor: based on modifications of deamino-[Cys1]arginine vasopressin at positions 4 and 8. |
AID196969 | In vitro anti-oxytocic activity on isolated estrogen treated rat uteri without Mg+2; Agonist | 1989 | Journal of medicinal chemistry, Jan, Volume: 32, Issue:1
| 2-O-alkyltyrosine derivatives of 1-deamino-arginine-vasopressin: highly specific and potent antidiuretic agonists. |
AID1598505 | Agonist activity at recombinant human V1a receptor expressed in HEK293 cells up to 1000 nM measured after 5 hrs by luciferase reporter gene assay | | | |
AID1132554 | Antidiuretic activity in iv dosed rat assessed as agonist activity on arginine-vasopressin-induced effect | 1978 | Journal of medicinal chemistry, Mar, Volume: 21, Issue:3
| [1-(beta-mercapto-beta,beta-cyclopentamethylenepropionic acid),4-valine,-8-D-arginine]vasopressin, a potent and selective inhibitor of the vasopressor response to arginine-vasopressin. |
AID1132555 | Antivasopressor activity in iv dosed phenoxybenzamine treated rat assessed as antagonist activity on arginine-vasopressin-induced effect | 1978 | Journal of medicinal chemistry, Mar, Volume: 21, Issue:3
| [1-(beta-mercapto-beta,beta-cyclopentamethylenepropionic acid),4-valine,-8-D-arginine]vasopressin, a potent and selective inhibitor of the vasopressor response to arginine-vasopressin. |
AID277899 | Displacement of [3H]AVP from vasopressin V2 receptor in rat kidney membranes | 2007 | Journal of medicinal chemistry, Feb-22, Volume: 50, Issue:4
| Design and synthesis of the first selective agonists for the rat vasopressin V(1b) receptor: based on modifications of deamino-[Cys1]arginine vasopressin at positions 4 and 8. |
AID196847 | In vitro anti-oxytocic activity on isolated estrogen treated rat uteri with 0.5 mM Mg+2; Agonist | 1989 | Journal of medicinal chemistry, Jan, Volume: 32, Issue:1
| 2-O-alkyltyrosine derivatives of 1-deamino-arginine-vasopressin: highly specific and potent antidiuretic agonists. |
AID196810 | Binding affinity was determined | 1989 | Journal of medicinal chemistry, Jan, Volume: 32, Issue:1
| 2-O-alkyltyrosine derivatives of 1-deamino-arginine-vasopressin: highly specific and potent antidiuretic agonists. |
AID1598503 | Selectivity ratio of EC50 for human OTR stably expressed in CHOK1 cells to EC50 for recombinant human V2 receptor expressed in HEK293 cells | | | |
AID1598500 | Agonist activity at human OTR stably expressed in CHOK1 cells by NFAT-luciferase reporter gene assay relative to control | | | |
AID1150189 | Antivasopressor activity in iv dosed phenoxybenzamine-treated rat assessed as inhibition of arginine-vasopressin-induced vasopressor response | 1977 | Journal of medicinal chemistry, Sep, Volume: 20, Issue:9
| [1-deaminopenicillamine,4-valine]-8-D-arginine-vasopressin, a highly potent inhibitor of the vasopressor response to arginine-vasopressin. |
AID1150132 | Oxytocic activity in rat uterus in absence of Mg2+ | 1977 | Journal of medicinal chemistry, Sep, Volume: 20, Issue:9
| [1-(L-2-hydroxy-3-mercaptopropanoic acid)] analogues of arginine-vasopressin, [8-D-arginine]vasopressin, and [4-valine,8-D-arginine]vasopressin. |
AID1598504 | Selectivity ratio of EC50 for recombinant human V1B receptor expressed in HEK293 cells to EC50 for recombinant human V2 receptor expressed in HEK293 cells | | | |
AID1598502 | Agonist activity at recombinant human V1B receptor expressed in HEK293 cells measured after 5 hrs by luciferase reporter gene assay relative to control | | | |
AID1150896 | Vasopressor activity in rat | 1976 | Journal of medicinal chemistry, Jun, Volume: 19, Issue:6
| Synthesis and some pharmacological properties of deamino(4-threonine,8-D-arginine)vasopressin and deamino(8-D-arginine)vasopressin, highly potent and specific antidiuretic peptides, and (8-D-arginine)vasopressin and deamino-arginine-vasopressin. |
AID1598507 | Non-renal clearance in nephrectomized Sprague-Dawley rat at 0.1 mg/kg, iv administered as cassette dose by LC-MS/MS analysis | | | |
AID277897 | Activity at OT receptor assessed as oxytocic activity in absence of magnesium | 2007 | Journal of medicinal chemistry, Feb-22, Volume: 50, Issue:4
| Design and synthesis of the first selective agonists for the rat vasopressin V(1b) receptor: based on modifications of deamino-[Cys1]arginine vasopressin at positions 4 and 8. |
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023] |