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AZD-5597

Name: AZD-5597
Brand: TargetMol
SKU: T21544
Price: 52 USD
Availability: InStock
Rating: 5 (10 reviews)

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Catalog No. T21544Cas No. 924641-59-8

Alias (S)-(4-((5-Fluoro-4-(1-isopropyl-2-methyl-1H-imidazol-5-yl)pyrimidin-2-yl)amino)phenyl)(3-(methylamino)pyrrolidin-1-yl)methanone

AZD-5597 ((S)-(4-((5-Fluoro-4-(1-isopropyl-2-methyl-1H-imidazol-5-yl)pyrimidin-2-yl)amino)phenyl)(3-(methylamino)pyrrolidin-1-yl)methanone) is a potent imidazole pyrimidine amide CDK inhibitor.

AZD-5597

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Purity: 98.01%

Catalog No. T21544Alias (S)-(4-((5-Fluoro-4-(1-isopropyl-2-methyl-1H-imidazol-5-yl)pyrimidin-2-yl)amino)phenyl)(3-(methylamino)pyrrolidin-1-yl)methanoneCas No. 924641-59-8

AZD-5597 ((S)-(4-((5-Fluoro-4-(1-isopropyl-2-methyl-1H-imidazol-5-yl)pyrimidin-2-yl)amino)phenyl)(3-(methylamino)pyrrolidin-1-yl)methanone) is a potent imidazole pyrimidine amide CDK inhibitor.

Pack Size	Price	USA Warehouse	Global Warehouse
1 mg	$52	In Stock	-
5 mg	$123	In Stock	-
10 mg	$197	In Stock	-
25 mg	$438	In Stock	-
50 mg	$689	In Stock	-
100 mg	$973	In Stock	-
1 mL x 10 mM (in DMSO)	$147	In Stock	In Stock

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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]

All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.

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Batch Information

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Purity:98.01%

Appearance:solid

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COA LCMS HNMR

Product Introduction

AZD-5597 AI Summary

AZD-5597 exhibits potent bioactivities including the inhibition of CDK2 and CDK1 with an IC50 of 2.0 nM each. It also shows significant antiproliferative activity against human LoVo cells with an IC50 of 39.0 nM and inhibits human ERG with an activity of 95.0 μM. In vivo, it demonstrates substantial antitumor activity, inhibiting tumor volume by 55.0% in human SW620 cell xenografted nude mice at a dosage of 15 mg/kg, administered intraperitoneally thrice a week for 3 weeks. These findings suggest AZD-5597 has potential anti-cancer properties through the inhibition of key cell cycle regulators..

Note: Summary generated by AI. Data source: ChEMBL

Bioactivity

Description	AZD-5597 ((S)-(4-((5-Fluoro-4-(1-isopropyl-2-methyl-1H-imidazol-5-yl)pyrimidin-2-yl)amino)phenyl)(3-(methylamino)pyrrolidin-1-yl)methanone) is a potent imidazole pyrimidine amide CDK inhibitor.
Synonyms	(S)-(4-((5-Fluoro-4-(1-isopropyl-2-methyl-1H-imidazol-5-yl)pyrimidin-2-yl)amino)phenyl)(3-(methylamino)pyrrolidin-1-yl)methanone

Chemical Properties

Molecular Weight	437.51
Formula	C₂₃H₂₈FN₇O
Cas No.	924641-59-8
Smiles	CN[C@H]1CCN(C1)C(=O)c1ccc(Nc2ncc(F)c(n2)-c2cnc(C)n2C(C)C)cc1
Relative Density.	1.32 g/cm3

Storage & Solubility Information

Storage

Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.

Solubility Information

DMSO: 55 mg/mL (125.71 mM), Sonication is recommended.

In Vivo Formulation

10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (4.57 mM), Sonication is recommended.

Please add the solvents sequentially, clarifying the solution as much as possible before adding the next one. Dissolve by heating and/or sonication if necessary. Working solution is recommended to be prepared and used immediately. The formulation provided above is for reference purposes only. In vivo formulations may vary and should be modified based on specific experimental conditions.

Solution Preparation Table

DMSO

	1mg	5mg	10mg	50mg
1 mM	2.2857 mL	11.4283 mL	22.8566 mL	114.2831 mL
5 mM	0.4571 mL	2.2857 mL	4.5713 mL	22.8566 mL
10 mM	0.2286 mL	1.1428 mL	2.2857 mL	11.4283 mL
20 mM	0.1143 mL	0.5714 mL	1.1428 mL	5.7142 mL
50 mM	0.0457 mL	0.2286 mL	0.4571 mL	2.2857 mL
100 mM	0.0229 mL	0.1143 mL	0.2286 mL	1.1428 mL

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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:

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 DMSO TargetMol | 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 DMSO TargetMol | reagent stock solution to 400 μL PEG300 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 ddH₂O TargetMol | 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.

Dose Conversion

You can also refer to dose conversion for different animals. More Dose Conversion

Tech Support

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