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Cyclic GMP

Catalog No. TN9056 Copy Product Info
Purity: 99.99%
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Cyclic GMP (cGMP) belongs to the class of endogenous metabolites and is a pivotal intracellular second messenger that mediates extracellular signals such as nitric oxide (NO) and natriuretic peptides (NPs). The effects of Cyclic GMP are primarily executed through three main target groups: cGMP-dependent protein kinases (PKGs), cGMP-gated cation channels, and phosphodiesterases (PDEs). Cyclic GMP is capable of inhibiting platelet adhesion and aggregation and participates in enhancing antiviral immune responses.

Cyclic GMP

Copy Product Info
🥰Excellent
Catalog No. TN9056

Cyclic GMP (cGMP) belongs to the class of endogenous metabolites and is a pivotal intracellular second messenger that mediates extracellular signals such as nitric oxide (NO) and natriuretic peptides (NPs). The effects of Cyclic GMP are primarily executed through three main target groups: cGMP-dependent protein kinases (PKGs), cGMP-gated cation channels, and phosphodiesterases (PDEs). Cyclic GMP is capable of inhibiting platelet adhesion and aggregation and participates in enhancing antiviral immune responses.

Cyclic GMP
Cas No. 7665-99-8
Pack SizePriceUSA StockGlobal StockQuantity
1 mg$45-In Stock
5 mg$106-In Stock
10 mg$163-In Stock
25 mg$328-In Stock
50 mg$463-In Stock
100 mg$648-In Stock
For In stock only · Estimated delivery: USA Stock (1-2 days) Global Stock (5-7 days)
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For research use only—not for human use. No sales to individuals. Use as intended only.
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Purity:99.99%
Appearance:Solid
Color:White
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Product Introduction

Bioactivity
Description
Cyclic GMP (cGMP) belongs to the class of endogenous metabolites and is a pivotal intracellular second messenger that mediates extracellular signals such as nitric oxide (NO) and natriuretic peptides (NPs). The effects of Cyclic GMP are primarily executed through three main target groups: cGMP-dependent protein kinases (PKGs), cGMP-gated cation channels, and phosphodiesterases (PDEs). Cyclic GMP is capable of inhibiting platelet adhesion and aggregation and participates in enhancing antiviral immune responses.
In vitro
In vitro studies on cardiac cells show that Cyclic GMP (1 microM) accumulation stimulated by ACh acts synergistically with Isoprenaline to activate cGMP-stimulated phosphodiesterases. This process inhibits cAMP-induced inward calcium current (ICa) and shortens action potentials. Additionally, its conjugate cGAMP induces IRF3 phosphorylation and nuclear translocation[1].
In vivo
In anesthetized rat models, Cyclic GMP has been demonstrated to effectively prevent renal platelet accumulation following ischemia-reperfusion, a protective effect not shared by cAMP, indicating its specificity in maintaining microcirculatory stability[1].
Chemical Properties
Molecular Weight345.21
FormulaC10H12N5O7P
Cas No.7665-99-8
SmilesO=C1C2=C(N(C=N2)[C@H]3[C@H](O)[C@]4([C@](O3)(COP(=O)(O)O4)[H])[H])NC(N)=N1
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year
Solubility Information
H2O: 4.00 mg/mL (11.59 mM), Sonication is recommended.
Solution Preparation Table
H2O
1mg5mg10mg50mg
1 mM2.8968 mL14.4839 mL28.9679 mL144.8394 mL
5 mM0.5794 mL2.8968 mL5.7936 mL28.9679 mL
10 mM0.2897 mL1.4484 mL2.8968 mL14.4839 mL
Note : The dilution table applies only to solid products. For liquid products, please calculate the stock solution based on the stated concentration and/or density.

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In Vivo Formulation Calculator (Clear solution)

Please enter your animal experiment information in the following box and click Calculate to obtain the stock solution preparation method and in vivo formula preparation method:
TargetMol | Animal experiments For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, TargetMol | Animal experiments and a total of 10 animals are to be administered, using a formulation of TargetMol | reagent 10% DMSO+ 40% PEG300+ 5% Tween 80+ 45% Saline/PBS/ddH2O , the resulting working solution concentration would be 2 mg/mL.
Stock Solution Preparation:

Dissolve 2 mg of the compound in 100 μL DMSOTargetMol | reagent to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.

Preparation of the In Vivo Formulation:

1) Add 100 μL of the DMSOTargetMol | reagent stock solution to 400 μL PEG300TargetMol | reagent and mix thoroughly until the solution becomes clear.

2) Add 50 μL Tween 80 and mix well until fully clarified.

3) Add 450 μL Saline,PBS or ddH2OTargetMol | reagent and mix thoroughly until a homogeneous solution is obtained.

This example is provided solely to demonstrate the use of the In Vivo Formulation Calculator and does not constitute a recommended formulation for any specific compound. Please select an appropriate dissolution and formulation strategy based on your experimental model and route of administration.
All co-solvents required for this protocol, includingDMSO, PEG300/PEG400, Tween 80, SBE-β-CD, and Corn oil, are available for purchase on the TargetMol website.
1 Enter information below:
mg/kg
g
μL
2 Enter the in vivo formulation:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

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Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc
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