8 Results for "

Substance P analogue

" in MedChemExpress (MCE) Product Catalog:
Products (8)

8 Results for "Substance P analogue" in MCE Product Catalog:

Cat. No.: HY-P3801
CAS No.: 77128-69-9
Synonyms: DiMe-C7
[Glp5,(Me)Phe8,Sar9] Substance P (5-11) (DiMe-C7) is a Substance P (HY-P0201) analogue that has approximately the same effects as Substance P (HY-P0201) on neurokinin 1 receptor (NK1R) in rat brain, but with a much longer duration of action. [Glp5,(Me)Phe8,Sar9] Substance P (5-11) selectively activates dopamine metabolism in the mesencephalon and midbrain cortex of the rat brain. [Glp5,(Me)Phe8,Sar9] Substance P (5-11) also increases motor activity and induces recovery of addictive agent-seeking behavior in rats .
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Cat. No.: HY-P3799
CAS No.: 61123-13-5
Target:  

Neurokinin Receptor

Research Areas:  

Neurological Disease

[Glp6] Substance P (6-11) is an analogue of substance P (6-11). Substance P (6-11) stimulates [3H]-inositol monophosphate ([3H]-IP1) formation in rat urinary bladder by acting on the 'septide-sensitive' tachykinin receptors .
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Cat. No.: HY-P3905
CAS No.: 77128-78-0
Research Areas:  

Neurological Disease

[Glp5,Sar9] Substance P (5-11) is a neuropeptide Substance P (HY-P0201) analogue specifically designed to interact with the Neurokinin-1 (NK1) receptor. [Glp5,Sar9] Substance P (5-11) modulates pain perception and inflammatory responses.
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Cat. No.: HY-P1375
CAS No.: 89430-38-6
Target:  

nAChR

Research Areas:  

Endocrinology

[D-Trp7,9,10]-Substance P is a substance P analogue. Substance P stimulates substance P receptors but also inhibits ion conductance through nicotinic acetylcholine receptors .
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Cat. No.: HY-P11405
CAS No.: 122481-75-8
Target:  

Neurotensin Receptor

Research Areas:  

Neurological Disease Cancer

[D-Arg1, D-Trp5, 7, 9, Leu11]-Substance P is a potent inhibitor of cell growth in small cell lung cancer (SCLC). [D-Arg1, D-Trp5, 7, 9, Leu11]-Substance P is also a neuropeptide antagonist, capable of blocking colony formation stimulated by various neuropeptides (including vasopressin and bradykinin). [D-Arg1, D-Trp5, 7, 9, Leu11]-Substance P inhibits the mobilization of Ca 2+ and the activation of mitogen-activated protein kinases induced by vasopressin or bradykinin. [D-Arg1, D-Trp5, 7, 9, Leu11]-Substance P inhibits the growth of H-69 xenograft tumors in nude mice .
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Cat. No.: HY-P1375A
Target:  

mAChR

Research Areas:  

Endocrinology

[D-Trp7,9,10]-Substance P TFA is a substance P analogue. Substance P stimulates substance P receptors but also inhibits ion conductance through nicotinic acetylcholine receptors .
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Cat. No.: HY-P3808
CAS No.: 80434-86-2
Target:  

Neurokinin Receptor

Research Areas:  

Inflammation/Immunology

[D-Pro2,D-Trp7,9] Substance P, a Substance P (HY-P0201) analogue, is a weak agonist and a potent, specific, competitive Substance P antagonist .
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Cat. No.: HY-P3809
CAS No.: 77275-70-8
Target:  

Neurokinin Receptor

Research Areas:  

Neurological Disease

[D-Pro2,D-Phe7,D-Trp9] Substance P is a Substance P (HY-P0201) analogue. [D-Pro2,D-Phe7,D-Trp9] Substance P is an inhibitor of Substance P. [D-Pro2,D-Phe7,D-Trp9] Substance P contracts guinea-pig ileum (GPI) indirectly .
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