TDZD-8

Synonyms: NP 01139

TDZD-8 (NP 01139) is a non-ATP competitive GSK-3β inhibitor with IC50 of 2 μM; minimal inhibitory effect observed on CDK1, casein kinase II, PKA and PKC.

TDZD-8 Chemical Structure

TDZD-8 Chemical Structure

CAS: 327036-89-5

Selleck's TDZD-8 has been cited by 8 Publications

1 Customer Review

Purity & Quality Control

Batch: S292601 DMSO] 44.5 mg/mL] false] Ethanol] 44.5 mg/mL] false] Water] Insoluble] false Purity: 99.95%
99.95

TDZD-8 Related Products

Signaling Pathway

Choose Selective GSK-3 Inhibitors

Biological Activity

Description TDZD-8 (NP 01139) is a non-ATP competitive GSK-3β inhibitor with IC50 of 2 μM; minimal inhibitory effect observed on CDK1, casein kinase II, PKA and PKC.
Targets
GSK-3β [1]
2 μM
In vitro
In vitro TDZD-8 acts as a noncompetitive inhibitor of ATP or GS-1 binding. TDZD-8 shows no inhibition of PKA, PKC, Cdk-1/cyclin B or CK-II in kinase assays. [1] TDZD-8 specifically induces cell death of primary leukemia specimens. TDZD-8 ablates leukemia progenitor and stem cells. TDZD-8 treatment induces oxidative stress. TDZD-8 induces cell death with extremely rapid cell death kinetics showing loss of membrane integrity. TDZD-8 inhibits PKC and FLT3 in primary AML specimens. [2]

Chemical Information & Solubility

Molecular Weight 222.26 Formula

C10H10N2O2S

CAS No. 327036-89-5 SDF Download TDZD-8 SDF
Smiles CN1C(=O)N(C(=O)S1)CC2=CC=CC=C2
Storage (From the date of receipt)

In vitro
Batch:

DMSO : 44.5 mg/mL ( (200.21 mM); Moisture-absorbing DMSO reduces solubility. Please use fresh DMSO.)

Ethanol : 44.5 mg/mL

Water : Insoluble


Molecular Weight Calculator

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

Tel: +1-832-582-8158 Ext:3
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