| Cat.No. | Name | Information |
|---|---|---|
| M52943 | CTOP | CTOP is a potent and highly selective μ-opioid receptor antagonist. |
| M52942 | Hypocretin (70-98), human | Hypocretin (70-98), human is a polypeptide that is capable of binding to an orexin receptor OX1R and promotes apoptosis. |
| M52941 | Xenopus orexin A | Xenopus orexin A is a neuropeptides that identified as an endogenous ligands for an orphan G-protein-coupled receptor. |
| M52940 | Xenopus orexin B | Xenopus orexin B is a neuropeptides that identified as an endogenous ligands for an orphan G-protein-coupled receptor. |
| M52939 | Orexin B, human | Orexin B, human is an endogenous agonist at Orexin receptor with Kis of 420 and 36 nM for OX1 and OX2, respectively. |
| M52938 | (d(CH2)51, Tyr(Me)2, Thr4, Orn8, Tyr-NH29)-Vasotocin | (d(CH2)51,Tyr(Me)2,Thr4,Orn8,Tyr-NH29)-Vasotocin is an oxytocin antagonist and can be used for the research of sexual behavior. |
| M52937 | (d(CH2)51, Tyr(Me)2, Orn8)-Oxytocin | (d(CH2)51,Tyr(Me)2,Orn8)-Oxytocin (OVT) is an oxytocin receptor antagonist. |
| M52936 | (Val3, Pro8)-Oxytocin | (Val3,Pro8)-Oxytocin is the Gq-dependent pathway agonist. |
| M52935 | (d(CH2)51, Tyr(Me)2, Thr4, Orn8, des-Gly-NH29)-Vasotocin | (d(CH2)51,Tyr(Me)2,Thr4,Orn8,des-Gly-NH29)-Vasotocin, an oxytocin receptor antagonist, abolishes oxytocin-enhanced inhibitory postsynaptic currents in CA1 pyramidal neurons. |
| M52934 | Demoxytocin | Demoxytocin, a heterodetic cyclic peptide, is an analog of oxytocin. |
| M52933 | Cargutocin | Cargutocin, an oxytocin analogue, targets the oxytocin receptor and acts as a uterine contraction agent. |
| M52932 | Barusiban | Barusiban (FE-200440) is an oxytocin receptor (OT-R) antagonist (Ki=0.8 nM), inhibits OT-induced contraction. |
| M52931 | L-366682 | L-366682, a cyclic hexapeptide, possesses antagonism of oxytocin. |
| M52930 | [Arg-15, 20, 21, Leu17]-PACAP-Gly-Lys-Arg-NH2 | [Arg-15,-20,-21,Leu17]-PACAP-Gly-Lys-Arg-NH2 (BM-PACAP) is a synthetic PACAP 1-27 analogue with relaxant effect. |
| M52929 | PACAP-38 (16-38), human, mouse, rat | PACAP-38 (16-38), human, mouse, rat demonstrates potent, efficacious, and sustained stimulatory effects on sympathetic neuronal NPY and catecholamine production. |
| M52928 | PACAP (6-38), human, ovine, rat | PACAP (6-38), human, ovine, rat is a potent PACAP receptor antagonist with IC50s of 30, 600, and 40 nM for PACAP type I receptor, PACAP type II receptor VIP1, and PACAP type II receptor VIP2, respectively. |
| M52927 | PACAP (1-38) free acid | PACAP (1-38) free acid is an endogenous neuropeptide. |
| M52926 | Antiflammin 2 | Antiflammin 2 inhibits the synthesis of platelet-activating factor (PAF) with the IC50 of 100 nM. |
| M52925 | Parstatin(human) | Parstatin(human), a cell-penetrating PAR-1 thrombin receptor agonist peptide, is a potent inhibitor of angiogenesis. |
| M52924 | Parstatin(mouse) | Parstatin(mouse), a cell-penetrating PAR-1 thrombin receptor agonist peptide, is a potent inhibitor of angiogenesis. |
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