Azenosertib (Zn-C3)

Azenosertib (Zn-C3) is an oral active, highly effective and selective Wee1 inhibitor with IC50 of 3.9 nM, which can be used in cancer research.

Azenosertib (Zn-C3) Chemical Structure

Azenosertib (Zn-C3) Chemical Structure

CAS No. 2376146-48-2

Purity & Quality Control

Products often used together with Azenosertib (Zn-C3)

Adavosertib (MK-1775)


ZN-c3 has a higher selectivity and better safety profiles compared to Adavosertib, making it particularly well-suited for combination therapies.

Bukhari AB, et al. Front Oncol. 2022 Feb 17;12:828684.

RP-6306


Zn-C3 and RP-306 combined inhibition of WEE1 and PKMYT1 exhibits synergism in killing of U2OS cells.

Benada J, et al. NAR Cancer. 2023 Jun 13;5(3):zcad029.

Azenosertib (Zn-C3) Related Products

Signaling Pathway

Biological Activity

Description Azenosertib (Zn-C3) is an oral active, highly effective and selective Wee1 inhibitor with IC50 of 3.9 nM, which can be used in cancer research.
Targets
Wee1 [1]
3.9 nM
NCT Number Recruitment Conditions Sponsor/Collaborators Start Date Phases
NCT05743036 Recruiting
Metastatic Colorectal Cancer
K-Group Beta Inc. a wholly owned subsidiary of Zentalis Pharmaceuticals Inc|Pfizer
February 27 2023 Phase 1|Phase 2
NCT05682170 Recruiting
Acute Myeloid Leukemia (AML)
K-Group Alpha Inc. a wholly owned subsidiary of Zentalis Pharmaceuticals Inc.
December 1 2022 Phase 1|Phase 2
NCT05431582 Withdrawn
Tumors|Ovarian Cancer|Breast Cancer|Lung Cancer|Pancreatic Cancer
M.D. Anderson Cancer Center|Zentalis Pharmaceuticals
December 14 2022 Phase 1
NCT05198804 Recruiting
Ovarian Cancer|Platinum-resistant Ovarian Cancer|Primary Peritoneal Carcinoma|Fallopian Tube Cancer
K-Group Beta Inc. a wholly owned subsidiary of Zentalis Pharmaceuticals Inc
January 27 2022 Phase 1|Phase 2

Chemical Information & Solubility

Molecular Weight 526.63 Formula

C29H34N8O2

CAS No. 2376146-48-2 SDF --
Smiles CCC1(O)CCC2=CC=C(N=C12)N3N(CC=C)C(=O)C4=CN=C(NC5=CC=C(C=C5)N6CCN(C)CC6)N=C34
Storage (From the date of receipt) 3 years -20°C powder

In vitro
Batch:

DMSO : 100 mg/mL ( (189.88 mM) Moisture-absorbing DMSO reduces solubility. Please use fresh DMSO.)

Ethanol : 100 mg/mL

Water : Insoluble


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In vivo
Batch:

Add solvents to the product individually and in order.


In vivo Formulation Calculator

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In vivo Formulation Calculator (Clear solution)

Step 1: Enter information below (Recommended: An additional animal making an allowance for loss during the experiment)

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Working concentration: mg/ml;

Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )

Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.

Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

Note: 1. Please make sure the liquid is clear before adding the next solvent.
2. Be sure to add the solvent(s) in order. You must ensure that the solution obtained, in the previous addition, is a clear solution before proceeding to add the next solvent. Physical methods such
as vortex, ultrasound or hot water bath can be used to aid dissolving.

Tech Support

Answers to questions you may have can be found in the inhibitor handling instructions. Topics include how to prepare stock solutions, how to store inhibitors, and issues that need special attention for cell-based assays and animal experiments.

Handling Instructions

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