1. GPCR/G Protein Neuronal Signaling
  2. Neurokinin Receptor
  3. [Glp5,(Me)Phe8,Sar9] Substance P (5-11)

[Glp5,(Me)Phe8,Sar9] Substance P (5-11)  (Synonyms: DiMe-C7)

Cat. No.: HY-P3801 Purity: 99.01%
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[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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[Glp5,(Me)Phe8,Sar9] Substance P (5-11) Chemical Structure

[Glp5,(Me)Phe8,Sar9] Substance P (5-11) Chemical Structure

CAS No. : 77128-69-9

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1 mg USD 50 In-stock
5 mg USD 120 In-stock
10 mg USD 180 In-stock
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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 addictive agent-seeking behavior in rats[1][2][3].

In Vivo

[Glp5,(Me)Phe8,Sar9] Substance P (5-11) (2 μg/side; inject into the ventral tegmental area; single) exhibits selective activation of mesolimbic and mesocortical dopamine metabolism in rat brain[1].
[Glp5,(Me)Phe8,Sar9] Substance P (5-11) (0.5, 1.5, 3 μg/side; inject into the ventral tegmental area; single) increases motor activity and induces recovery of addictive agent-seeking behavior in rats[2].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

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.
Molecular Weight

880.06

Formula

C43H61N9O9S

CAS No.
Appearance

Solid

Color

White to off-white

Sequence

pGlu-Gln-Phe-N-Methyl-Phe-Sar-Leu-Met-NH2

Sequence Shortening

pGlp-QF(-Me)F-Sar-LM-NH2

Shipping

Room temperature in continental US; may vary elsewhere.

Storage

Sealed storage, away from moisture

Powder -80°C 2 years
-20°C 1 year

*In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)

Solvent & Solubility
In Vitro: 

DMSO : ≥ 100 mg/mL (113.63 mM; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

*"≥" means soluble, but saturation unknown.

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 1.1363 mL 5.6814 mL 11.3629 mL
5 mM 0.2273 mL 1.1363 mL 2.2726 mL
View the Complete Stock Solution Preparation Table

* Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

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Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

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Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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Purity & Documentation
References

Complete Stock Solution Preparation Table

* Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

Optional Solvent Concentration Solvent Mass 1 mg 5 mg 10 mg 25 mg
DMSO 1 mM 1.1363 mL 5.6814 mL 11.3629 mL 28.4072 mL
5 mM 0.2273 mL 1.1363 mL 2.2726 mL 5.6814 mL
10 mM 0.1136 mL 0.5681 mL 1.1363 mL 2.8407 mL
15 mM 0.0758 mL 0.3788 mL 0.7575 mL 1.8938 mL
20 mM 0.0568 mL 0.2841 mL 0.5681 mL 1.4204 mL
25 mM 0.0455 mL 0.2273 mL 0.4545 mL 1.1363 mL
30 mM 0.0379 mL 0.1894 mL 0.3788 mL 0.9469 mL
40 mM 0.0284 mL 0.1420 mL 0.2841 mL 0.7102 mL
50 mM 0.0227 mL 0.1136 mL 0.2273 mL 0.5681 mL
60 mM 0.0189 mL 0.0947 mL 0.1894 mL 0.4735 mL
80 mM 0.0142 mL 0.0710 mL 0.1420 mL 0.3551 mL
100 mM 0.0114 mL 0.0568 mL 0.1136 mL 0.2841 mL
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  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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Product Name:
[Glp5,(Me)Phe8,Sar9] Substance P (5-11)
Cat. No.:
HY-P3801
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