| Cat.No. | Name | Information |
|---|---|---|
| M52888 | Angiopeptin | Angiopeptin, a cyclic octapeptide analogue of somatostatin, is a weak sst2/sst5 receptor partial agonist with IC50 values of 0.26 nM and 6.92 nM, respectively. |
| M52887 | Ilatreotide | Ilatreotide (SDZ CO61), glycated somatostatin derivative, is a highly potent glycated analog of somatostatin with improved oral activity. |
| M52886 | BIM-23190 | BIM-23190, a somatostatin analog, a selective SSTR2 and SSTR5 agonist, exhibits Ki values of 0.34 nM and 11.1 nM for SSTR2 and SSTR5, respectively. |
| M52885 | [Orn5]-URP | [Orn5]-URP is a potent and selective pure antagonist of Urotensin-II receptor (UT), with an pEC50 of 7.24. |
| M52883 | Urotensin II, mouse | Urotensin II, mouse is an endogenous ligand for the orphan G-protein-coupled receptor GPR14 or SENR. |
| M52882 | UFP-803 | UFP-803 is a potent urotensin-II receptor (UT) ligand. |
| M52881 | [Orn8]-Urotensin II (human) | [Orn8]-Urotensin II (human), a peptide analog of urotensin II, is a UT receptor agonist. |
| M52880 | Big Endothelin-1 (1-38), human | Big Endothelin-1 (1-38), human is the precursor of endothelin-1. |
| M52879 | (d(CH2)51, Tyr(Me)2, Arg8)-Vasopressin | (d(CH2)51,Tyr(Me)2,Arg8)-Vasopressin (SKF 100273) is a vasopressin V1 receptor selective antagonist. |
| M52878 | [Asu1, 6-Arg8]Vasopressin | [Asu1,6-Arg8]Vasopressin is an vasopressin agonist which potentiates cyclic AMP accumulation and ACTH release induced by corticotropin-releasing factor (CRF) in rat anterior pituitary cells in culture. |
| M52877 | Big Endothelin-1 (1-39), porcine | Big Endothelin-1 (1-39), porcine is the precursor of endothelin-1. |
| M52876 | D[LEU4, LYS8]-VP | D[LEU4,LYS8]-VP is a selective agonist of vasopressin V1b receptor, with the Kis of 0.16 nM, 0.52 nM, and 0.1.38 nM for rat, human and mouse V1b receptor, respectively. |
| M52875 | (D-Arg8)-Inotocin | (D-Arg8)-Inotocin is a potent, selective and competitive antagonist of vasopressin receptor (V1aR), with a Ki of 1.3 nM. |
| M52874 | [Deamino-Pen1, Val4, D-Arg8]-vasopressin | [Deamino-Pen1,Val4,D-Arg8]-vasopressin (AVP-A) is an arginine-vasopressin (AVP) antagonist. |
| M52873 | [8-L-arginine] deaminovasopressin | [8-L-arginine] deaminovasopressin (dAVP) is a vasopressin analog. |
| M52872 | (Phe2, Orn8)-Oxytocin | (Phe2,Orn8)-Oxytocin is a selective V1 vasopressin agonist. |
| M52871 | (d(CH2)51, Tyr(Me)2, Dab5, Arg8)-Vasopressin | (d(CH2)51,Tyr(Me)2,Dab5,Arg8)-Vasopressin (d(CH2)5[Tyr(Me)2, Dab5]AVP) is a specific antagonist of vasopressin V1a receptor, with a pA2 of 6.71. |
| M52870 | Desamino(D-3-(3′-pyridyl)-Ala2, Arg8)-Vasopressin | Desamino(D-3-(3′-pyridyl)-Ala2,Arg8)-Vasopressin, a synthetic analog of vasopressin (AVP), is a weak agonist at antidiuretic receptor. |
| M52869 | (Phenylac1, D-Tyr(Et)2, Lys6, Arg8, des-Gly9)-Vasopressin | (Phenylac1,D-Tyr(Et)2,Lys6,Arg8,des-Gly9)-Vasopressin is a potent vasopressin V1 receptor (VP V1R) antagonist. |
| M52868 | 2-(3-Trifluoromethylphenyl)glycine hydrochloride | 2-(3-Trifluoromethylphenyl)glycine hydrochloride is a precursor of substituted 2-acetamido-5-aryl-l, 2,4-triazolones. |
Products are for research use only. Not for human use. We do not sell to patients.
© Copyright 2010-2024 AbMole BioScience. All Rights Reserved.
