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Tenovin-3

CAS# 1011301-27-1

Tenovin-3

2D Structure

Catalog No. BCC3889----Order now to get a substantial discount!

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Tenovin-3: 5mg $529 In Stock
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3D structure

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Tenovin-3

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Chemical Properties of Tenovin-3

Cas No. 1011301-27-1 SDF Download SDF
PubChem ID 24772097 Appearance Powder
Formula C18H21N3OS M.Wt 327.44
Type of Compound N/A Storage Desiccate at -20°C
Solubility DMSO : ≥ 31 mg/mL (94.67 mM)
*"≥" means soluble, but saturation unknown.
Chemical Name N-[(4-aminophenyl)carbamothioyl]-4-tert-butylbenzamide
SMILES CC(C)(C)C1=CC=C(C=C1)C(=O)NC(=S)NC2=CC=C(C=C2)N
Standard InChIKey NLAXTZPUTNGRDU-UHFFFAOYSA-N
Standard InChI InChI=1S/C18H21N3OS/c1-18(2,3)13-6-4-12(5-7-13)16(22)21-17(23)20-15-10-8-14(19)9-11-15/h4-11H,19H2,1-3H3,(H2,20,21,22,23)
General tips For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months.
We recommend that you prepare and use the solution on the same day. However, if the test schedule requires, the stock solutions can be prepared in advance, and the stock solution must be sealed and stored below -20℃. In general, the stock solution can be kept for several months.
Before use, we recommend that you leave the vial at room temperature for at least an hour before opening it.
About Packaging 1. The packaging of the product may be reversed during transportation, cause the high purity compounds to adhere to the neck or cap of the vial.Take the vail out of its packaging and shake gently until the compounds fall to the bottom of the vial.
2. For liquid products, please centrifuge at 500xg to gather the liquid to the bottom of the vial.
3. Try to avoid loss or contamination during the experiment.
Shipping Condition Packaging according to customer requirements(5mg, 10mg, 20mg and more). Ship via FedEx, DHL, UPS, EMS or other couriers with RT, or blue ice upon request.

Biological Activity of Tenovin-3

DescriptionTenovin-3 is able to increase p53 levels, determined in MCF-7 cells treated for 6 hr at 10 μM. Target: p53 in vitro: Tenovins inhibit the activities of human SirT1 and SirT2, two members of the NAD+-dependent class III histone deacetylases that also belong to the sirtuin family.[1]

References:
[1]. Lain S, et al. Discovery, in vivo activity, and mechanism of action of a small-molecule p53 activator. Cancer Cell. 2008 May;13(5):454-63.

Tenovin-3 Dilution Calculator

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Tenovin-3 Molarity Calculator

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Preparing Stock Solutions of Tenovin-3

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 3.054 mL 15.27 mL 30.5399 mL 61.0799 mL 76.3499 mL
5 mM 0.6108 mL 3.054 mL 6.108 mL 12.216 mL 15.27 mL
10 mM 0.3054 mL 1.527 mL 3.054 mL 6.108 mL 7.635 mL
50 mM 0.0611 mL 0.3054 mL 0.6108 mL 1.2216 mL 1.527 mL
100 mM 0.0305 mL 0.1527 mL 0.3054 mL 0.6108 mL 0.7635 mL
* Note: If you are in the process of experiment, it's necessary to make the dilution ratios of the samples. The dilution data above is only for reference. Normally, it's can get a better solubility within lower of Concentrations.

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Background on Tenovin-3

Tenovin SAR Studies Aimed at Increasing Water Solubility

ID
p53 Increasea K40Ac Tubulin Increaseb SirT2 Inhibitionc
R1 R2
Tenovin-1 tBu NHCOCH3 + + +
Tenovin-2 tBu NHCOCH(CH3)2 + + +
Tenovin-3 tBu NH2 + + +
Tenovin-4 N3 NHCOCH3
Tenovin-5 tBu NHCOPh + + +
Tenovin-6 tBu NHCO(CH2)4NMe2.HCl + + +
a     Ability to increase p53 levels was determined in MCF-7 cells treated for 6 hr at 10 μM.
b     Ability to increase K40 Ac-tubulin levels was determined in H1299 cells treated
c     SirT2 inhibition assessed using a compound concentration of 10 or 30 μM depending on the compound's solubility in the assay buffer.
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Description

Tenovin-3 is able to increase p53 levels, determined in MCF-7 cells treated for 6 hr at 10 μM.

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