Assay ID | Title | Year | Journal | Article |
AID1144906 | Agonist activity at NK1 receptor in Sprague-Dawley rat pituitary gland assessed as change in FSH release at 1000 ng/ml by radioimmunoassay in presence of LH-RH (Rvb = 613 +/- 203 ng/ml) | 1976 | Journal of medicinal chemistry, Feb, Volume: 19, Issue:2
| Synthesis and some biological activities of the tyrosine-8 analog of substance P. |
AID1144905 | Agonist activity at NK1 receptor in Sprague-Dawley rat pituitary gland assessed as change in LH release at 100000 ng/ml by radioimmunoassay in presence of LH-RH (Rvb = -11 +/- 27 ng/ml) | 1976 | Journal of medicinal chemistry, Feb, Volume: 19, Issue:2
| Synthesis and some biological activities of the tyrosine-8 analog of substance P. |
AID1144909 | Antagonist activity at NK1 receptor in Sprague-Dawley rat pituitary gland assessed as inhibition of LH release by radioimmunoassay in presence of LH-RH | 1976 | Journal of medicinal chemistry, Feb, Volume: 19, Issue:2
| Synthesis and some biological activities of the tyrosine-8 analog of substance P. |
AID1144912 | Effect on prolactin release in Sprague-Dawley rat pituitary gland at 100 ug/ml by radioimmunoassay | 1976 | Journal of medicinal chemistry, Feb, Volume: 19, Issue:2
| Synthesis and some biological activities of the tyrosine-8 analog of substance P. |
AID1144904 | Agonist activity at NK1 receptor in Sprague-Dawley rat pituitary gland assessed as change in LH release at 10000 ng/ml by radioimmunoassay in presence of LH-RH (Rvb = -11 +/- 27 ng/ml) | 1976 | Journal of medicinal chemistry, Feb, Volume: 19, Issue:2
| Synthesis and some biological activities of the tyrosine-8 analog of substance P. |
AID1144920 | Decrease in systemic arterial blood pressure in dog at 10 ng/kg, iv measured for 2 to 20 mins after drug dosage (Rvb = 140 mmHg) | 1976 | Journal of medicinal chemistry, Feb, Volume: 19, Issue:2
| Synthesis and some biological activities of the tyrosine-8 analog of substance P. |
AID1144915 | Retardation factor of the compound using CHCl3-MeOH-concentrated NH4OH at ratio of 60:45:20 as solvent system by thin layer chromatography | 1976 | Journal of medicinal chemistry, Feb, Volume: 19, Issue:2
| Synthesis and some biological activities of the tyrosine-8 analog of substance P. |
AID1144911 | Effect on growth hormone release in Sprague-Dawley rat pituitary gland at 100 ug/ml by radioimmunoassay | 1976 | Journal of medicinal chemistry, Feb, Volume: 19, Issue:2
| Synthesis and some biological activities of the tyrosine-8 analog of substance P. |
AID1144918 | Retardation factor of the compound using n-PrOH-1N HOAc at ratio of 2:1 as solvent system by thin layer chromatography | 1976 | Journal of medicinal chemistry, Feb, Volume: 19, Issue:2
| Synthesis and some biological activities of the tyrosine-8 analog of substance P. |
AID1144910 | Antagonist activity at NK1 receptor in Sprague-Dawley rat pituitary gland assessed as inhibition of FSH release by radioimmunoassay in presence of LH-RH | 1976 | Journal of medicinal chemistry, Feb, Volume: 19, Issue:2
| Synthesis and some biological activities of the tyrosine-8 analog of substance P. |
AID1144913 | Effect on thyrotropin hormone release in Sprague-Dawley rat pituitary gland at 100 ug/ml by radioimmunoassay | 1976 | Journal of medicinal chemistry, Feb, Volume: 19, Issue:2
| Synthesis and some biological activities of the tyrosine-8 analog of substance P. |
AID1144908 | Agonist activity at NK1 receptor in Sprague-Dawley rat pituitary gland assessed as change in FSH release at 100000 ng/ml by radioimmunoassay in presence of LH-RH (Rvb = 613 +/- 203 ng/ml) | 1976 | Journal of medicinal chemistry, Feb, Volume: 19, Issue:2
| Synthesis and some biological activities of the tyrosine-8 analog of substance P. |
AID1144916 | Retardation factor of the compound using EtOH-H2O at ratio of 7:3 as solvent system by thin layer chromatography | 1976 | Journal of medicinal chemistry, Feb, Volume: 19, Issue:2
| Synthesis and some biological activities of the tyrosine-8 analog of substance P. |
AID1144914 | Retardation factor of the compound using EtOAc-Pyr-HOAc-H2O at ratio of 5:5:1:3 as solvent system by thin layer chromatography | 1976 | Journal of medicinal chemistry, Feb, Volume: 19, Issue:2
| Synthesis and some biological activities of the tyrosine-8 analog of substance P. |
AID1144901 | Decrease in systemic arterial blood pressure in dog at >5 ng/kg, iv measured for 2 to 20 mins after drug dosage | 1976 | Journal of medicinal chemistry, Feb, Volume: 19, Issue:2
| Synthesis and some biological activities of the tyrosine-8 analog of substance P. |
AID1144902 | Agonist activity at NK1 receptor in guinea pig ileum assessed as increase in muscle tone | 1976 | Journal of medicinal chemistry, Feb, Volume: 19, Issue:2
| Synthesis and some biological activities of the tyrosine-8 analog of substance P. |
AID1144903 | Agonist activity at NK1 receptor in Sprague-Dawley rat pituitary gland assessed as change in LH release at 1000 ng/ml by radioimmunoassay in presence of LH-RH (Rvb = -11 +/- 27 ng/ml) | 1976 | Journal of medicinal chemistry, Feb, Volume: 19, Issue:2
| Synthesis and some biological activities of the tyrosine-8 analog of substance P. |
AID1144907 | Agonist activity at NK1 receptor in Sprague-Dawley rat pituitary gland assessed as change in FSH release at 10000 ng/ml by radioimmunoassay in presence of LH-RH (Rvb = 613 +/- 203 ng/ml) | 1976 | Journal of medicinal chemistry, Feb, Volume: 19, Issue:2
| Synthesis and some biological activities of the tyrosine-8 analog of substance P. |
AID1144917 | Retardation factor of the compound using n-BuOH-HOAc-EtOAc-H2O at ratio of 1:1:1:1 as solvent system by thin layer chromatography | 1976 | Journal of medicinal chemistry, Feb, Volume: 19, Issue:2
| Synthesis and some biological activities of the tyrosine-8 analog of substance P. |
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023] |