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Tenovin-6 p53 activator

Cat.No.S4900

Tenovin-6 is a small molecule activator of p53 transcriptional activity and inhibits dihydroorotate dehydrogenase (DHODH). This compound is also an inhibitor of SirT1 and SirT2.
Tenovin-6 p53 activator Chemical Structure

Chemical Structure

Molecular Weight: 454.63

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Quality Control

Batch: S490001 DMSO]98 mg/mL]false]Water]98 mg/mL]false]Ethanol]Insoluble]false Purity: 99.68%
99.68

Solubility

In vitro
Batch:

DMSO : 98 mg/mL (215.55 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO.)

Water : 98 mg/mL

Ethanol : Insoluble

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In vivo
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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.

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Chemical Information, Storage & Stability

Molecular Weight 454.63 Formula

C25H34N4O2S

Storage (From the date of receipt)
CAS No. 1011557-82-6 Download SDF Storage of Stock Solutions

Synonyms N/A Smiles CC(C)(C)C1=CC=C(C=C1)C(=O)NC(=S)NC2=CC=C(C=C2)NC(=O)CCCCN(C)C

Mechanism of Action

Targets/IC50/Ki
DHODH
p53
SIRT2
10 μM
SIRT1
21 μM
SIRT3
67 μM
In vitro

Tenovin-6 is a more water-soluble analog of tenovin-1. This compound acts through inhibition of the protein-deacetylating activities of SirT1 and SirT2. It inhibits the protein deacetylase activities of purified human SIRT1, SIRT2, and SIRT3 in vitro with IC50 of 21 μM, 10 μM, and 67 μM, respectively.

References

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