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77128-69-9

77128-69-9 structure
77128-69-9 structure
  • Name: (Pyr5,N-Me-Phe8,Sar9)-Substance P (5-11)
  • Chemical Name: G Substance P (5-11)
  • CAS Number: 77128-69-9
  • Molecular Formula: C43H61N9O9S
  • Molecular Weight: 880.064
  • Catalog: Signaling Pathways GPCR/G Protein Neurokinin Receptor
  • Create Date: 2018-12-29 20:32:25
  • Modify Date: 2025-08-22 22:07:09
  • [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 cocaine-seeking behavior in rats[1][2][3].

Name G Substance P (5-11)
Synonyms 5-Oxo-L-prolyl-L-glutaminyl-L-phenylalanyl-N-methyl-L-phenylalanyl-N-methylglycyl-L-leucyl-L-methioninamide
PGLU5,MEPHE8,SAR9-SUBSTANCE P FRAGMENT*5-11
PGLU-GLN-PHE-N-METHYL-PHE-SAR-LEU-MET-NH2
DiMe-C7
PYR-GLN-PHE-N-ME-PHE-SAR-LEU-MET-NH2
SUBSTANCE P (PGLU5,MEPHE8,SAR9)-*FRAGMEN T 5-11
L-Methioninamide, 5-oxo-L-prolyl-L-glutaminyl-L-phenylalanyl-N-methyl-L-phenylalanyl-N-methylglycyl-L-leucyl-
[GLP5,(ME)PHE8,SAR9] SUBSTANCE P (5-11)
GLP-GLN-PHE-(NME)PHE-SAR-LEU-MET-NH2
[pGlu5,MePhe8,Sar9]substance P(5-11)
(PYR5,N-ME-PHE8,SAR9)-SUBSTANCE P (5-11)
substance P (5-11),pGlu(5)-MePhe(8)-MeGly(9)
Description [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 cocaine-seeking behavior in rats[1][2][3].
Related Catalog
In Vivo [Glp5,(Me)Phe8,Sar9] Substance P (5-11) (2 µg/side; inject into the ventral tegmental area; single) 选择性地激活大鼠大脑间脑和中脑皮层的多巴胺代谢[1]。 [Glp5,(Me)Phe8,Sar9] Substance P (5-11) (0.5, 1.5, 3 µg/side; inject into the ventral tegmental area; single) 增加大鼠运动活性,诱导可卡因寻求行为的恢复[2]。 Animal Model: Male Sprague-Dawley rats (300-350 g)[1]. Dosage: 2 µg/side Administration: Inject into the ventral tegmental area; single Result: Selectively activated mesolimbic and mesocortical dopamine metabolism. Animal Model: Male Wistar rats (300-350 g)[2]. Dosage: 0.5, 1.5, 3 µg/side Administration: Inject into the ventral tegmental area; single Result: Significantly increased locomotor activity when at 3 µg/side.
References

[1]. Elliott PJ, et al. Selective activation of mesolimbic and mesocortical dopamine metabolism in rat brain by infusion of a stable substance P analogue into the ventral tegmental area. Brain Res. 1986 Jan 15;363(1):145-7.  

[2]. Eison AS, et al. Substance P analog, DiMe-C7: evidence for stability in rat brain and prolonged central actions. Science. 1982 Jan 8;215(4529):188-90.  

[3]. Placenza FM, et al. Infusion of the substance P analogue, DiMe-C7, into the ventral tegmental area induces reinstatement of cocaine-seeking behaviour in rats. Psychopharmacology (Berl). 2004 Dec;177(1-2):111-20.  

Density 1.3±0.1 g/cm3
Boiling Point 1291.2±65.0 °C at 760 mmHg
Molecular Formula C43H61N9O9S
Molecular Weight 880.064
Flash Point 734.7±34.3 °C
Exact Mass 879.431274
PSA 297.60000
LogP 1.66
Vapour Pressure 0.0±0.3 mmHg at 25°C
Index of Refraction 1.580
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