About 9 results found for searched term "Neurotensin Receptor" (0.545 seconds)
Cat.No. | Name | Target |
---|---|---|
M7330 | Meclinertant | Neurotensin Receptor |
SR 48692 | ||
Meclinertant (SR 48692) is an effective, selective, non-peptide and oral antagonist of active neurotensin receptor (NTS1). Meclinertant competitively antagonizes neurotensin-induced intracellular Ca2+ mobilization in human colon cancer cells, with a pA2 value of 8.13. Meclinertant has anti-anxiety, anti-addiction and memory disorder effects. | ||
M7888 | Levocabastine hydrochloride | Others |
Non-peptide histamine H1 receptor antagonist; neurotensin NTS2 receptor ligand. | ||
M8205 | SR 142948A | Others |
SR 142948A is a non-peptide Neurotensin receptor antagonist. | ||
M10171 | JMV 449 acetate | Neurotensin Receptor |
JMV449 | ||
JMV 449 acetate is a potent neurotensin receptor agonist. | ||
M10571 | Neurotensin | Neurotensin Receptor |
H-Pyr-Leu-Tyr-Glu-Asn-Lys-Pro-Arg-Arg-Pro-Tyr-Ile-Leu-OH | ||
Neurotensin is a gut tridecapeptide with many central and peripheral functions, acts as a potent cellular mitogen for various colorectal and pancreatic cancers which possess high-affinity neurotensin receptors(NTR). | ||
M30352 | Neurotensin(8-13) | Neurotensin Receptor |
(8-13) | ||
Neurotensin (8-13) is an active fragment of Neurotensin. Neurotensin(8-13) results in a decrease in cell-surface NT1 receptors (NTR1) density. | ||
M30621 | Levocabastine | Histamine Receptor |
R 50547 | ||
Levocabastine (R 50547) is a potent and selective histamine H1-receptor antagonist. Levocabastine hydrochloride is also a selective, high affinity neurotensin receptor subtype 2 (NTR2) antagonist, with a Ki of 17 nM for mNTR2. Levocabastine can act as a VLA-4 antagonist, interferes with conjunctival eosinophil infiltration in allergic conjunctivitis (AC). | ||
M53001 | JMV 449 | Neurotensin Receptor |
JMV 449 is a potent neurotensin receptor agonist. | ||
M53973 | [Lys8, Lys9]-Neurotensin (8-13) | Neurotensin Receptor |
[Lys8, Lys9]-Neurotensin (8-13) (JMV438), a Neurotensin analog, exerts its analgesic effects through activation of the G protein-coupled receptors NTS1 and NTS2. |
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